{"title":"Quantimol Best Sellers","description":null,"products":[{"product_id":"nu2058-161058-83-9","title":"NU2058 [CAS 161058-83-9]","description":"\u003cdiv style=\"font-family: Arial, Helvetica, sans-serif; color: #233047; line-height: 1.7; width: 100%; max-width: 100%; margin: 0; padding: 0; box-sizing: border-box;\"\u003e\n\n  \u003c!-- HERO --\u003e\n  \u003cdiv style=\"background: linear-gradient(135deg, #16244a 0%, #21345f 100%); border-radius: 22px; padding: 32px 24px; margin-bottom: 28px; border: 1px solid #2f466f; box-shadow: 0 18px 45px rgba(22,36,74,0.18);\"\u003e\n    \u003cdiv style=\"display: inline-block; padding: 6px 12px; border-radius: 999px; background: rgba(73,168,208,0.16); color: #9ad8ee; font-size: 12px; font-weight: 700; letter-spacing: 0.08em; text-transform: uppercase; margin-bottom: 14px;\"\u003e\n      Quantimol Compound Profile\n    \u003c\/div\u003e\n    \u003ch2 style=\"margin: 0 0 10px 0; font-size: 30px; line-height: 1.2; color: #ffffff; font-weight: 800;\"\u003e\n      NU-2058\n    \u003c\/h2\u003e\n    \u003cdiv style=\"font-size: 16px; color: #c9d7ea; margin-bottom: 14px;\"\u003e\n      O6-Cyclohexylmethylguanine | 6-(cyclohexylmethoxy)-7H-purin-2-amine\n    \u003c\/div\u003e\n    \u003cdiv style=\"font-size: 15px; color: #dce7f5; max-width: 920px;\"\u003e\n      Purine-based small molecule presented with standardized identifiers, physicochemical parameters, external database cross-references, and selected safety and spectral information for research cataloging and analytical documentation.\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- STRUCTURE + OVERVIEW --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(320px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eStructure\u003c\/h3\u003e\n      \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px; text-align: center;\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/image\/imgsrv.fcgi?cid=4564\u0026amp;t=l\" alt=\"NU-2058 chemical structure\" style=\"max-width: 100%; height: auto; border-radius: 10px;\"\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 12px; font-size: 14px; color: #5d6b7e;\"\u003e\n        Public structure image based on PubChem CID 4564\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 14px;\"\u003e\n        \u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/4564\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #49a8d0; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-right: 10px; margin-bottom: 8px;\"\u003e\n          View PubChem Record\n        \u003c\/a\u003e\n        \u003ca href=\"https:\/\/commonchemistry.cas.org\/detail?cas_rn=161058-83-9\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #16244a; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-bottom: 8px;\"\u003e\n          View CAS Entry\n        \u003c\/a\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eProduct Overview\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047; margin-bottom: 14px;\"\u003e\n        NU-2058 is listed in the uploaded record with multiple recognized identifiers including CAS, EC number, UNII, ChEMBL, DrugBank, NSC, and PubChem cross-references. The record also provides a standardized IUPAC name, structure descriptors, computed physicochemical properties, a spectral thumbnail reference, and a GHS hazard summary.\n      \u003c\/div\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        This page format is suitable for compound identification, internal catalog consistency, technical documentation, and product presentation where customers need fast access to core molecular and reference data.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- KEY IDENTIFIERS --\u003e\n  \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eKey Chemical Identifiers\u003c\/h3\u003e\n    \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(220px,1fr)); gap: 14px;\"\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eCAS Number\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e161058-83-9\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eMolecular Formula\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003eC\u003csub\u003e12\u003c\/sub\u003eH\u003csub\u003e17\u003c\/sub\u003eN\u003csub\u003e5\u003c\/sub\u003eO\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eMolecular Weight\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e247.30 g\/mol\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003ePubChem CID\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e4564\u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- NAMES + DESCRIPTORS --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(320px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eNames \u0026amp; Synonyms\u003c\/h3\u003e\n\n      \u003cdiv style=\"margin-bottom: 12px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003ePreferred Name\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 16px; color: #233047; margin-top: 5px;\"\u003eNU-2058\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 12px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eIUPAC Name\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 15px; color: #233047; margin-top: 5px;\"\u003e\n          6-(cyclohexylmethoxy)-7H-purin-2-amine\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eCommon Synonyms\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 15px; color: #233047; margin-top: 5px;\"\u003e\n          NU 2058\u003cbr\u003e\n          O(6)-cyclohexylmethylguanine\u003cbr\u003e\n          O6-Cyclohexylmethylguanine\u003cbr\u003e\n          2-amino-6-[(cyclohexylmethyl)oxy]purine\u003cbr\u003e\n          6-(cyclohexylmethoxy)-9H-purin-2-amine\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eStructure Descriptors\u003c\/h3\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eSMILES\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          C1CCC(CC1)COC2=NC(=NC3=C2NC=N3)N\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eInChI\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 13px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          InChI=1S\/C12H17N5O\/c13-12-16-10-9(14-7-15-10)11(17-12)18-6-8-4-2-1-3-5-8\/h7-8H,1-6H2,(H3,13,14,15,16,17)\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eInChIKey\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          MWGXGTJJAOZBNW-UHFFFAOYSA-N\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eReference IDs\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px;\"\u003e\n          ChEMBL: CHEMBL269881\u003cbr\u003e\n          DrugBank: DB02407\u003cbr\u003e\n          UNII: 884MN6AR44\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- COMPUTED PROPERTIES --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eComputed Physicochemical Properties\u003c\/h3\u003e\n    \u003cdiv style=\"overflow-x: auto;\"\u003e\n      \u003ctable style=\"width: 100%; border-collapse: collapse; min-width: 680px;\"\u003e\n        \u003cthead\u003e\n          \u003ctr\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eProperty\u003c\/th\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eValue\u003c\/th\u003e\n          \u003c\/tr\u003e\n        \u003c\/thead\u003e\n        \u003ctbody\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eMolecular Weight\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e247.30 g\/mol\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eExact Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e247.14331018 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eMonoisotopic Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e247.14331018 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eXLogP3\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e2.1\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eTopological Polar Surface Area\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e89.7 Ų\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Donor Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e2\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Acceptor Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e5\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eRotatable Bond Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e3\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHeavy Atom Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e18\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eFormal Charge\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e0\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eComplexity\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e271\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003eCompound Canonicalized\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003eYes\u003c\/td\u003e\n\u003c\/tr\u003e\n        \u003c\/tbody\u003e\n      \u003c\/table\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- SAFETY + SPECTRAL --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(300px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eSafety Summary\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047; margin-bottom: 10px;\"\u003e\n        \u003cstrong\u003eSignal word:\u003c\/strong\u003e Warning\n      \u003c\/div\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047; margin-bottom: 10px;\"\u003e\n        \u003cstrong\u003eHazard statements:\u003c\/strong\u003e\u003cbr\u003e\n        H315: Causes skin irritation\u003cbr\u003e\n        H319: Causes serious eye irritation\u003cbr\u003e\n        H335: May cause respiratory irritation\n      \u003c\/div\u003e\n      \u003cdiv style=\"font-size: 14px; color: #5d6b7e;\"\u003e\n        Refer to the full SDS and institutional handling procedures before use.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eSpectral Reference\u003c\/h3\u003e\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/4cekgpILByR\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; color: inherit;\"\u003e\n        \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden;\"\u003e\n          \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/47129910_1\" alt=\"NU-2058 13C NMR spectrum thumbnail\" style=\"width: 100%; height: 180px; object-fit: cover; display: block;\"\u003e\n          \u003cdiv style=\"padding: 14px;\"\u003e\n            \u003cdiv style=\"font-size: 16px; color: #16244a; font-weight: 700;\"\u003e13C NMR Spectrum\u003c\/div\u003e\n            \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen external spectral reference\u003c\/div\u003e\n          \u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- CATALOG \/ DOCUMENTATION --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(280px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eCatalog \u0026amp; Documentation Value\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        The uploaded record includes standardized names, external database identifiers, hazard summary information, spectral reference availability, and PubChem-linked related records. This supports clear compound identity presentation across technical product pages and internal catalog systems.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eResearch Reference Connectivity\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        The record includes cross-references to ChEMBL, DrugBank, Open Targets, PubMed-linked literature, and related compound search views, making it useful for discovery support, compound traceability, and reference verification workflows.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- EXTERNAL LINKS --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eExternal Reference Links\u003c\/h3\u003e\n    \u003cul style=\"margin: 0; padding-left: 18px; color: #233047; font-size: 15px;\"\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/4564\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003ePubChem CID 4564\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/www.ebi.ac.uk\/chembl\/explore\/compound\/CHEMBL269881\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eChEMBL: CHEMBL269881\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/go.drugbank.com\/drugs\/DB02407\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eDrugBank: DB02407\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/platform.opentargets.org\/drug\/CHEMBL269881\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eOpen Targets\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/substance\/505539846\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003ePubChem Reference Collection SID\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/#query=CID4564%20structure\u0026amp;tab=similarity\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eSimilar Compounds Search\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli\u003e\u003ca href=\"https:\/\/dtp.cancer.gov\/dtpstandard\/servlet\/dwindex?searchtype=NSC\u0026amp;outputformat=html\u0026amp;searchlist=707619\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eNCI NSC 707619\u003c\/a\u003e\u003c\/li\u003e\n    \u003c\/ul\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- SEO \/ STRUCTURED DATA --\u003e\n  \u003cscript type=\"application\/ld+json\"\u003e\n  {\n    \"@context\": \"https:\/\/schema.org\",\n    \"@type\": \"Product\",\n    \"name\": \"NU-2058\",\n    \"alternateName\": [\n      \"NU 2058\",\n      \"O6-Cyclohexylmethylguanine\",\n      \"O(6)-cyclohexylmethylguanine\",\n      \"2-amino-6-[(cyclohexylmethyl)oxy]purine\",\n      \"6-(cyclohexylmethoxy)-9H-purin-2-amine\"\n    ],\n    \"description\": \"NU-2058 presented with standardized identifiers, structural descriptors, molecular formula, molecular weight, safety summary, and computed physicochemical properties for research cataloging and analytical reference use.\",\n    \"image\": \"https:\/\/pubchem.ncbi.nlm.nih.gov\/image\/imgsrv.fcgi?cid=4564\u0026t=l\",\n    \"sku\": \"NU-2058\",\n    \"category\": \"Research Chemicals\",\n    \"brand\": {\n      \"@type\": \"Brand\",\n      \"name\": \"Quantimol\"\n    },\n    \"additionalProperty\": [\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"CAS Number\",\n        \"value\": \"161058-83-9\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"PubChem CID\",\n        \"value\": \"4564\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"Molecular Formula\",\n        \"value\": \"C12H17N5O\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"Molecular Weight\",\n        \"value\": \"247.30 g\/mol\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"InChIKey\",\n        \"value\": \"MWGXGTJJAOZBNW-UHFFFAOYSA-N\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"SMILES\",\n        \"value\": \"C1CCC(CC1)COC2=NC(=NC3=C2NC=N3)N\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"UNII\",\n        \"value\": \"884MN6AR44\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"ChEMBL ID\",\n        \"value\": \"CHEMBL269881\"\n      }\n    ],\n    \"sameAs\": [\n      \"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/4564\",\n      \"https:\/\/www.ebi.ac.uk\/chembl\/explore\/compound\/CHEMBL269881\",\n      \"https:\/\/go.drugbank.com\/drugs\/DB02407\",\n      \"https:\/\/platform.opentargets.org\/drug\/CHEMBL269881\"\n    ]\n  }\n  \u003c\/script\u003e\n\n  \u003cscript type=\"application\/ld+json\"\u003e\n  {\n    \"@context\": \"https:\/\/schema.org\",\n    \"@type\": \"ChemicalSubstance\",\n    \"name\": \"NU-2058\",\n    \"alternateName\": [\n      \"NU 2058\",\n      \"O6-Cyclohexylmethylguanine\",\n      \"2-amino-6-[(cyclohexylmethyl)oxy]purine\"\n    ],\n    \"molecularFormula\": \"C12H17N5O\",\n    \"monoisotopicMolecularWeight\": \"247.14331018\",\n    \"inChI\": \"InChI=1S\/C12H17N5O\/c13-12-16-10-9(14-7-15-10)11(17-12)18-6-8-4-2-1-3-5-8\/h7-8H,1-6H2,(H3,13,14,15,16,17)\",\n    \"inChIKey\": \"MWGXGTJJAOZBNW-UHFFFAOYSA-N\",\n    \"smiles\": \"C1CCC(CC1)COC2=NC(=NC3=C2NC=N3)N\",\n    \"identifier\": [\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"CAS\",\n        \"value\": \"161058-83-9\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"PubChem CID\",\n        \"value\": \"4564\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"UNII\",\n        \"value\": \"884MN6AR44\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"ChEMBL ID\",\n        \"value\": \"CHEMBL269881\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"DrugBank ID\",\n        \"value\": \"DB02407\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"EC Number\",\n        \"value\": \"633-908-6\"\n      }\n    ]\n  }\n  \u003c\/script\u003e\n\n\u003c\/div\u003e","brand":"Quantimol","offers":[{"title":"5 mg","offer_id":53293934575953,"sku":"QM-0155256-01","price":56.05,"currency_code":"GBP","in_stock":true},{"title":"10 mg","offer_id":53293934608721,"sku":"QM-0155256-02","price":71.58,"currency_code":"GBP","in_stock":true},{"title":"25 mg","offer_id":53293934641489,"sku":"QM-0155256-03","price":127.38,"currency_code":"GBP","in_stock":true},{"title":"50 mg","offer_id":53293934674257,"sku":"QM-0155256-04","price":216.46,"currency_code":"GBP","in_stock":true},{"title":"100 mg","offer_id":53293934707025,"sku":"QM-0155256-05","price":301.5,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"diethyl-phthalate-standard-84-66-2","title":"Diethyl phthalate (Standard) [CAS 84-66-2]","description":"\u003cp\u003e\u003cstrong\u003eDiethyl phthalate (Standard)\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"100 mg","offer_id":53303648158033,"sku":"QM-0094605-01","price":57.09,"currency_code":"GBP","in_stock":true},{"title":"250 mg","offer_id":53303648190801,"sku":"QM-0094605-02","price":88.0,"currency_code":"GBP","in_stock":true},{"title":"500 mg","offer_id":53303648223569,"sku":"QM-0094605-03","price":119.5,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"1-2-propanediol-57-55-6","title":"(±) -1,2-Propanediol [CAS 57-55-6]","description":"\u003cp\u003e\u003cstrong\u003e(±) -1,2-Propanediol\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"100 mL","offer_id":53305130647889,"sku":"QM-0098075-01","price":94.75,"currency_code":"GBP","in_stock":true},{"title":"500 mL","offer_id":53305130680657,"sku":"QM-0098075-02","price":129.63,"currency_code":"GBP","in_stock":true},{"title":"1000 mL","offer_id":53305130713425,"sku":"QM-0098075-03","price":188.51,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"nadh-58-68-4","title":"NADH [CAS 58-68-4]","description":"\u003cdiv style=\"font-family: Arial, Helvetica, sans-serif; color: #233047; line-height: 1.7; width: 100%; max-width: 100%; margin: 0; box-sizing: border-box;\"\u003e\n\n  \u003cdiv style=\"background: linear-gradient(135deg, #16244a 0%, #21345f 100%); border-radius: 18px; padding: 30px 26px; border: 1px solid #dbe4ec; box-shadow: 0 18px 45px rgba(22, 36, 74, 0.16);\"\u003e\n\n    \u003cdiv style=\"display: flex; align-items: center; gap: 14px; flex-wrap: wrap; margin-bottom: 18px;\"\u003e\n      \u003cdiv style=\"width: 48px; height: 48px; border-radius: 14px; background: linear-gradient(135deg, #49a8d0 0%, #6ab7db 100%); display: flex; align-items: center; justify-content: center; color: #ffffff; font-size: 24px; font-weight: 700;\"\u003e\n        ⚡\n      \u003c\/div\u003e\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 28px; font-weight: 800; color: #ffffff; margin: 0;\"\u003e\n          NADH\n        \u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #d9e7f2; margin-top: 4px;\"\u003e\n          CAS: 58-68-4\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border-radius: 16px; padding: 26px 24px; border: 1px solid #dbe4ec;\"\u003e\n\n      \u003cdiv style=\"font-size: 22px; font-weight: 800; color: #16244a; margin-bottom: 18px;\"\u003e\n        Applications\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit, minmax(260px, 1fr)); gap: 16px;\"\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            1. Enzyme Activity Assays\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eWidely used as a coenzyme in dehydrogenase-based enzyme assays\u003c\/li\u003e\n            \u003cli\u003eSupports measurement of oxidoreductase activity in biochemical workflows\u003c\/li\u003e\n            \u003cli\u003eApplicable in kinetic studies and enzyme screening platforms\u003c\/li\u003e\n            \u003cli\u003eUseful in spectrophotometric assays based on NADH oxidation at 340 nm\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            2. Metabolism Research\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eCentral reagent for studies of cellular respiration and energy metabolism\u003c\/li\u003e\n            \u003cli\u003eUsed in research on glycolysis, the TCA cycle, and mitochondrial function\u003c\/li\u003e\n            \u003cli\u003eSupports redox balance and metabolic flux investigations\u003c\/li\u003e\n            \u003cli\u003eApplicable in cellular bioenergetics and metabolic regulation studies\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            3. Mitochondrial Function Studies\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eUsed in assays evaluating electron transport chain activity\u003c\/li\u003e\n            \u003cli\u003eRelevant in studies of oxidative phosphorylation and ATP production\u003c\/li\u003e\n            \u003cli\u003eSupports research on mitochondrial dysfunction and stress responses\u003c\/li\u003e\n            \u003cli\u003eUseful in disease models linked to metabolic and mitochondrial imbalance\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            4. Cell Biology \u0026amp; Redox Research\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eSupports studies of intracellular redox status and reducing capacity\u003c\/li\u003e\n            \u003cli\u003eUsed in investigations of oxidative stress and antioxidant systems\u003c\/li\u003e\n            \u003cli\u003eApplicable in viability, proliferation, and stress-response assays\u003c\/li\u003e\n            \u003cli\u003eRelevant to signaling pathways influenced by cellular redox balance\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            5. Diagnostic \u0026amp; Clinical Chemistry Research\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eUsed in reagent systems for biochemical and clinical assay development\u003c\/li\u003e\n            \u003cli\u003eApplicable in coupled enzymatic detection methods\u003c\/li\u003e\n            \u003cli\u003eSupports development of analytical kits for metabolite quantification\u003c\/li\u003e\n            \u003cli\u003eRelevant in research involving lactate, glucose, alcohol, and related analytes\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            6. Biosensor \u0026amp; Analytical Development\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eUsed in biosensor research involving dehydrogenase-coupled detection\u003c\/li\u003e\n            \u003cli\u003eSupports electrochemical and optical assay development\u003c\/li\u003e\n            \u003cli\u003eUseful in signal amplification strategies for metabolite analysis\u003c\/li\u003e\n            \u003cli\u003eApplicable in research on rapid analytical platforms and diagnostic devices\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            7. Drug Discovery \u0026amp; Screening\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eUsed in screening assays targeting NAD(H)-dependent enzymes\u003c\/li\u003e\n            \u003cli\u003eSupports inhibitor profiling and pathway-focused compound evaluation\u003c\/li\u003e\n            \u003cli\u003eRelevant in discovery workflows involving metabolic enzymes\u003c\/li\u003e\n            \u003cli\u003eUseful in assay platforms for mechanistic and pharmacological studies\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n        \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 14px; padding: 18px;\"\u003e\n          \u003cdiv style=\"font-size: 17px; font-weight: 700; color: #16244a; margin-bottom: 10px;\"\u003e\n            8. General Laboratory Research\n          \u003c\/div\u003e\n          \u003cul style=\"padding-left: 18px; margin: 0; color: #3a4a63;\"\u003e\n            \u003cli\u003eUseful as a standard biochemical reagent in academic and industrial laboratories\u003c\/li\u003e\n            \u003cli\u003eApplied in cofactor supplementation for in vitro reaction systems\u003c\/li\u003e\n            \u003cli\u003eSupports teaching, assay optimization, and mechanistic investigations\u003c\/li\u003e\n            \u003cli\u003eSuitable for broad use in biochemistry, molecular biology, and life science research\u003c\/li\u003e\n          \u003c\/ul\u003e\n        \u003c\/div\u003e\n\n      \u003c\/div\u003e\n\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\u003c\/div\u003e","brand":"Quantimol","offers":[{"title":"1 Each","offer_id":53306021216593,"sku":"QM-0099715","price":0.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"complete-freund-s-adjuvant-cfa-1-mg-ml-9007-81-2","title":"Complete Freund's adjuvant (CFA, 1 mg\/ml) [CAS 9007-81-2]","description":"\u003cdiv style=\"font-family: Arial, Helvetica, sans-serif; color: #233047; line-height: 1.7; width: 100%; max-width: 100%; margin: 0; padding: 0; box-sizing: border-box;\"\u003e\n\n  \u003c!-- HERO --\u003e\n  \u003cdiv style=\"background: linear-gradient(135deg, #16244a 0%, #21345f 100%); border-radius: 22px; padding: 32px 24px; margin-bottom: 28px; border: 1px solid #2f466f; box-shadow: 0 18px 45px rgba(22,36,74,0.18);\"\u003e\n    \u003cdiv style=\"display: inline-block; padding: 6px 12px; border-radius: 999px; background: rgba(73,168,208,0.16); color: #9ad8ee; font-size: 12px; font-weight: 700; letter-spacing: 0.08em; text-transform: uppercase; margin-bottom: 14px;\"\u003e\n      Quantimol Compound Profile\n    \u003c\/div\u003e\n    \u003ch2 style=\"margin: 0 0 10px 0; font-size: 30px; line-height: 1.2; color: #ffffff; font-weight: 800;\"\u003e\n      5-Fluorocytosine Arabinoside\n    \u003c\/h2\u003e\n    \u003cdiv style=\"font-size: 16px; color: #c9d7ea; margin-bottom: 14px;\"\u003e\n      Ara-FC | 5-Fluoro-D-cytidine\n    \u003c\/div\u003e\n    \u003cdiv style=\"font-size: 15px; color: #dce7f5; max-width: 920px;\"\u003e\n      A fluorinated nucleoside-type compound presented with standardized identifiers, structural descriptors, biologic line notation, and computed physicochemical properties for research cataloging, analytical reference, and compound documentation workflows.\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- STRUCTURE + OVERVIEW --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(320px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eStructure\u003c\/h3\u003e\n      \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px; text-align: center;\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/image\/imgsrv.fcgi?cid=352938\u0026amp;t=l\" alt=\"5-Fluorocytosine arabinoside chemical structure\" style=\"max-width: 100%; height: auto; border-radius: 10px;\"\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 12px; font-size: 14px; color: #5d6b7e;\"\u003e\n        Public structure image based on PubChem CID 352938\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 14px;\"\u003e\n        \u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/352938\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #49a8d0; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-right: 10px; margin-bottom: 8px;\"\u003e\n          View PubChem Record\n        \u003c\/a\u003e\n        \u003ca href=\"https:\/\/commonchemistry.cas.org\/detail?cas_rn=4298-10-6\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #16244a; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-bottom: 8px;\"\u003e\n          View CAS Entry\n        \u003c\/a\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eProduct Overview\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047; margin-bottom: 14px;\"\u003e\n        5-Fluorocytosine arabinoside is listed in the uploaded record with multiple recognized identifiers and cross-references, including PubChem, ChEMBL, HMDB, and NCI NSC entries. The record also includes biologic line notation and standardized computed descriptors, making it suitable for product-page documentation where clear identity presentation is important.\n      \u003c\/div\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        This format is useful for customers who want quick access to the compound name, synonym set, molecular formula, molecular weight, InChIKey, SMILES, and selected computed properties in a single product-page view.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- KEY IDENTIFIERS --\u003e\n  \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eKey Chemical Identifiers\u003c\/h3\u003e\n    \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(220px,1fr)); gap: 14px;\"\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eCAS Number\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e4298-10-6\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eMolecular Formula\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003eC\u003csub\u003e9\u003c\/sub\u003eH\u003csub\u003e12\u003c\/sub\u003eFN\u003csub\u003e3\u003c\/sub\u003eO\u003csub\u003e5\u003c\/sub\u003e\n\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003eMolecular Weight\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e261.21 g\/mol\u003c\/div\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; text-transform: uppercase; font-weight: 700;\"\u003ePubChem CID\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 6px;\"\u003e352938\u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- NAMES + DESCRIPTORS --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(320px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eNames \u0026amp; Synonyms\u003c\/h3\u003e\n\n      \u003cdiv style=\"margin-bottom: 12px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003ePreferred Name\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 16px; color: #233047; margin-top: 5px;\"\u003e5-Fluorocytosine arabinoside\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 12px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eIUPAC Name\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 15px; color: #233047; margin-top: 5px;\"\u003e\n          4-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-fluoropyrimidin-2-one\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eCommon Synonyms\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 15px; color: #233047; margin-top: 5px;\"\u003e\n          Ara-FC\u003cbr\u003e\n          5-Fluoro-D-cytidine\u003cbr\u003e\n          Fluorocytosine arabinoside\u003cbr\u003e\n          5-FCR\u003cbr\u003e\n          FCA\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eStructure Descriptors\u003c\/h3\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eSMILES\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          C1=C(C(=NC(=O)N1C2C(C(C(O2)CO)O)O)N)F\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eInChI\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 13px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          InChI=1S\/C9H12FN3O5\/c10-3-1-13(9(17)12-7(3)11)8-6(16)5(15)4(2-14)18-8\/h1,4-6,8,14-16H,2H2,(H2,11,12,17)\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eInChIKey\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003e\n          STRZQWQNZQMHQR-UHFFFAOYSA-N\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 13px; color: #5d6b7e; font-weight: 700; text-transform: uppercase;\"\u003eBiologic IUPAC \/ Condensed\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px;\"\u003e\n          5-fluoro-cytidine \/ fl5Cyt-Ribf\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- COMPUTED PROPERTIES --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eComputed Physicochemical Properties\u003c\/h3\u003e\n    \u003cdiv style=\"overflow-x: auto;\"\u003e\n      \u003ctable style=\"width: 100%; border-collapse: collapse; min-width: 680px;\"\u003e\n        \u003cthead\u003e\n          \u003ctr\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eProperty\u003c\/th\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eValue\u003c\/th\u003e\n          \u003c\/tr\u003e\n        \u003c\/thead\u003e\n        \u003ctbody\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eMolecular Weight\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e261.21 g\/mol\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eExact Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e261.07609865 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eMonoisotopic Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e261.07609865 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eXLogP3\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e-2.1\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eTopological Polar Surface Area\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e129 Ų\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Donor Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e4\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Acceptor Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e6\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eRotatable Bond Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e2\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHeavy Atom Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e18\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eFormal Charge\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e0\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eComplexity\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e426\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eUndefined Atom Stereocenter Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e4\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003eCompound Canonicalized\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003eYes\u003c\/td\u003e\n\u003c\/tr\u003e\n        \u003c\/tbody\u003e\n      \u003c\/table\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- RESEARCH \/ DOCUMENTATION CONTENT --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(280px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eCatalog \u0026amp; Documentation Value\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        This record includes a standardized name set, cross-database identifiers, structural notation, and computed molecular descriptors. That makes it well suited for internal catalog consistency, technical product pages, and customer-facing identity verification blocks.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px;\"\u003e\n      \u003ch3 style=\"margin: 0 0 14px 0; font-size: 20px; color: #16244a;\"\u003eDatabase Cross-References\u003c\/h3\u003e\n      \u003cdiv style=\"font-size: 15px; color: #233047;\"\u003e\n        The uploaded record includes linked identifiers in PubChem, ChEMBL, HMDB, and the NCI Developmental Therapeutics Program. These references can support traceability across discovery, curation, and archival workflows.\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- EXTERNAL LINKS --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eExternal Reference Links\u003c\/h3\u003e\n    \u003cul style=\"margin: 0; padding-left: 18px; color: #233047; font-size: 15px;\"\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/352938\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003ePubChem CID 352938\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/www.ebi.ac.uk\/chembl\/explore\/compound\/CHEMBL89342\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eChEMBL: CHEMBL89342\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/hmdb.ca\/metabolites\/HMDB0246793\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eHMDB0246793\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/dtp.cancer.gov\/dtpstandard\/servlet\/dwindex?searchtype=NSC\u0026amp;outputformat=html\u0026amp;searchlist=529180\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eNCI NSC 529180\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/#query=CID352938%20structure\u0026amp;tab=similarity\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eSimilar Compounds Search\u003c\/a\u003e\u003c\/li\u003e\n    \u003c\/ul\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- SEO \/ STRUCTURED DATA --\u003e\n  \u003cscript type=\"application\/ld+json\"\u003e\n  {\n    \"@context\": \"https:\/\/schema.org\",\n    \"@type\": \"Product\",\n    \"name\": \"5-Fluorocytosine arabinoside\",\n    \"alternateName\": [\n      \"Ara-FC\",\n      \"5-Fluoro-D-cytidine\",\n      \"Fluorocytosine arabinoside\",\n      \"5-FCR\",\n      \"FCA\"\n    ],\n    \"description\": \"5-Fluorocytosine arabinoside presented with standardized identifiers, structural descriptors, molecular formula, molecular weight, and computed physicochemical properties for research cataloging and analytical reference use.\",\n    \"image\": \"https:\/\/pubchem.ncbi.nlm.nih.gov\/image\/imgsrv.fcgi?cid=352938\u0026t=l\",\n    \"sku\": \"5-Fluorocytosine-arabinoside\",\n    \"category\": \"Research Chemicals\",\n    \"brand\": {\n      \"@type\": \"Brand\",\n      \"name\": \"Quantimol\"\n    },\n    \"additionalProperty\": [\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"CAS Number\",\n        \"value\": \"4298-10-6\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"PubChem CID\",\n        \"value\": \"352938\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"Molecular Formula\",\n        \"value\": \"C9H12FN3O5\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"Molecular Weight\",\n        \"value\": \"261.21 g\/mol\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"InChIKey\",\n        \"value\": \"STRZQWQNZQMHQR-UHFFFAOYSA-N\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"SMILES\",\n        \"value\": \"C1=C(C(=NC(=O)N1C2C(C(C(O2)CO)O)O)N)F\"\n      }\n    ],\n    \"sameAs\": 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\"value\": \"4298-10-6\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"PubChem CID\",\n        \"value\": \"352938\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"ChEMBL ID\",\n        \"value\": \"CHEMBL89342\"\n      },\n      {\n        \"@type\": \"PropertyValue\",\n        \"name\": \"HMDB ID\",\n        \"value\": \"HMDB0246793\"\n      }\n    ]\n  }\n  \u003c\/script\u003e\n\n\u003c\/div\u003e","brand":"Quantimol","offers":[{"title":"10 mL","offer_id":53306306101585,"sku":"QM-0100595","price":206.74,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"xylose-standard-58-86-6","title":"Xylose (Standard) [CAS 58-86-6]","description":"\u003cp\u003e\u003cstrong\u003eXylose (Standard)\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific 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mg","offer_id":53321784164689,"sku":"QM-0135305-01","price":62.26,"currency_code":"GBP","in_stock":true},{"title":"50 mg","offer_id":53321784197457,"sku":"QM-0135305-02","price":81.92,"currency_code":"GBP","in_stock":true},{"title":"100 mg","offer_id":53321784230225,"sku":"QM-0135305-03","price":118.38,"currency_code":"GBP","in_stock":true},{"title":"250 mg","offer_id":53321784262993,"sku":"QM-0135305-04","price":231.03,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"glucosamine-hydrochloride-66-84-2","title":"Glucosamine (hydrochloride) [CAS 66-84-2]","description":"\u003cp\u003e\u003cstrong\u003eGlucosamine (hydrochloride)\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"500 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g","offer_id":53331393085777,"sku":"QM-0160419-05","price":414.5,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"dimethyl-malonate-108-59-8","title":"Dimethyl malonate [CAS 108-59-8]","description":"\u003cp\u003e\u003cstrong\u003eDimethyl malonate\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"500 mg","offer_id":53335558521169,"sku":"QM-0185208-01","price":78.82,"currency_code":"GBP","in_stock":true},{"title":"10 mM - 1 mL","offer_id":53335558553937,"sku":"QM-0185208-02","price":89.13,"currency_code":"GBP","in_stock":true},{"title":"1 g","offer_id":53335558586705,"sku":"QM-0185208-03","price":94.75,"currency_code":"GBP","in_stock":true},{"title":"5 g","offer_id":53335558619473,"sku":"QM-0185208-04","price":135.25,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"fmoc-suberol-212783-75-0","title":"Fmoc-Suberol [CAS 212783-75-0]","description":"\u003cp\u003e\u003cstrong\u003eFmoc-Suberol\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"1 g","offer_id":53335570743633,"sku":"QM-0185266-01","price":51.91,"currency_code":"GBP","in_stock":true},{"title":"5 g","offer_id":53335570776401,"sku":"QM-0185266-02","price":78.82,"currency_code":"GBP","in_stock":true},{"title":"10 g","offer_id":53335570809169,"sku":"QM-0185266-03","price":118.38,"currency_code":"GBP","in_stock":true},{"title":"25 g","offer_id":53335570841937,"sku":"QM-0185266-04","price":250.47,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"methylnitronitrosoguanidine-70-25-7","title":"Methylnitronitrosoguanidine [CAS 70-25-7]","description":"\u003cdiv style=\"font-family: Arial, Helvetica, sans-serif; color: #233047; line-height: 1.7; width: 100%; max-width: 100%; margin: 0; padding: 0; box-sizing: border-box;\"\u003e\n\n  \u003c!-- Hero --\u003e\n  \u003cdiv style=\"background: linear-gradient(135deg, #16244a 0%, #21345f 100%); border-radius: 22px; padding: 30px 24px; margin-bottom: 28px; border: 1px solid #2f466f; box-shadow: 0 18px 45px rgba(22,36,74,0.18);\"\u003e\n    \u003cdiv style=\"display: inline-block; padding: 6px 12px; border-radius: 999px; background: rgba(73,168,208,0.16); color: #9ad8ee; font-size: 12px; font-weight: 700; letter-spacing: 0.08em; text-transform: uppercase; margin-bottom: 14px;\"\u003e\n      Quantimol Compound Profile\n    \u003c\/div\u003e\n    \u003ch2 style=\"margin: 0 0 10px 0; font-size: 30px; line-height: 1.2; color: #ffffff; font-weight: 800;\"\u003e\n      N-methyl-N'-nitro-N-nitrosoguanidine\n    \u003c\/h2\u003e\n    \u003cdiv style=\"font-size: 16px; color: #c9d7ea; margin-bottom: 14px;\"\u003e\n      Also listed as \u003cstrong style=\"color: #ffffff;\"\u003e1-methyl-2-nitro-1-nitrosoguanidine\u003c\/strong\u003e\n    \u003c\/div\u003e\n    \u003cdiv style=\"font-size: 15px; color: #dce7f5; max-width: 920px;\"\u003e\n      Structured identity, computed molecular properties, and direct access to public compound and spectral reference pages.\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- Structure + overview --\u003e\n  \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(320px,1fr)); gap: 24px; margin-bottom: 24px;\"\u003e\n    \n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eStructure\u003c\/h3\u003e\n      \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 16px; padding: 16px; text-align: center;\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/image\/imgsrv.fcgi?cid=6261\u0026amp;t=l\" alt=\"N-methyl-N'-nitro-N-nitrosoguanidine chemical structure\" style=\"max-width: 100%; height: auto; border-radius: 10px;\"\u003e\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 14px; font-size: 14px; color: #5d6b7e;\"\u003e\n        Public compound structure image\n      \u003c\/div\u003e\n      \u003cdiv style=\"margin-top: 14px;\"\u003e\n        \u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/6261\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #49a8d0; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-right: 10px; margin-bottom: 8px;\"\u003e\n          View PubChem Record\n        \u003c\/a\u003e\n        \u003ca href=\"https:\/\/commonchemistry.cas.org\/detail?cas_rn=70-25-7\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"display: inline-block; background: #16244a; color: #ffffff; text-decoration: none; padding: 10px 16px; border-radius: 999px; font-size: 14px; font-weight: 700; margin-bottom: 8px;\"\u003e\n          View CAS Entry\n        \u003c\/a\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 22px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n      \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eKey Identifiers\u003c\/h3\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eCAS Number\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 5px;\"\u003e70-25-7\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eMolecular Formula\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 5px;\"\u003eC\u003csub\u003e2\u003c\/sub\u003eH\u003csub\u003e5\u003c\/sub\u003eN\u003csub\u003e5\u003c\/sub\u003eO\u003csub\u003e3\u003c\/sub\u003e\n\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eMolecular Weight\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 18px; color: #16244a; font-weight: 700; margin-top: 5px;\"\u003e147.09 g\/mol\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eSMILES\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003eCN(C(=N[N+](=O)[O-])N)N=O\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv style=\"margin-bottom: 14px;\"\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eInChIKey\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 14px; color: #233047; margin-top: 5px; word-break: break-word;\"\u003eVZUNGTLZRAYYDE-UHFFFAOYSA-N\u003c\/div\u003e\n      \u003c\/div\u003e\n\n      \u003cdiv\u003e\n        \u003cdiv style=\"font-size: 12px; color: #5d6b7e; font-weight: 700; text-transform: uppercase; letter-spacing: 0.06em;\"\u003eHMDB ID\u003c\/div\u003e\n        \u003cdiv style=\"font-size: 15px; color: #233047; margin-top: 5px;\"\u003e\n          \u003ca href=\"https:\/\/hmdb.ca\/metabolites\/HMDB0243924\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eHMDB0243924\u003c\/a\u003e\n        \u003c\/div\u003e\n      \u003c\/div\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- Properties --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eComputed Physicochemical Properties\u003c\/h3\u003e\n    \u003cdiv style=\"overflow-x: auto;\"\u003e\n      \u003ctable style=\"width: 100%; border-collapse: collapse; min-width: 680px;\"\u003e\n        \u003cthead\u003e\n          \u003ctr\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eProperty\u003c\/th\u003e\n            \u003cth style=\"text-align: left; padding: 12px 14px; background: #16244a; color: #ffffff; font-size: 14px;\"\u003eValue\u003c\/th\u003e\n          \u003c\/tr\u003e\n        \u003c\/thead\u003e\n        \u003ctbody\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eExact Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e147.03923904 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eMonoisotopic Mass\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e147.03923904 Da\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eXLogP3\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e-0.2\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eTPSA\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e117 Ų\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Donors\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e1\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHydrogen Bond Acceptors\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e5\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eRotatable Bonds\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e1\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eHeavy Atom Count\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e10\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003eFormal Charge\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px; border-bottom: 1px solid #e4ecf3;\"\u003e0\u003c\/td\u003e\n\u003c\/tr\u003e\n          \u003ctr\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003eComplexity\u003c\/td\u003e\n\u003ctd style=\"padding: 12px 14px;\"\u003e170\u003c\/td\u003e\n\u003c\/tr\u003e\n        \u003c\/tbody\u003e\n      \u003c\/table\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- Spectral gallery --\u003e\n  \u003cdiv style=\"background: #f4f7fa; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; margin-bottom: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 18px 0; font-size: 22px; color: #16244a;\"\u003eSpectral Reference Gallery\u003c\/h3\u003e\n    \u003cdiv style=\"display: grid; grid-template-columns: repeat(auto-fit,minmax(220px,1fr)); gap: 18px;\"\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/9Flbwn5y86n\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/4936729_1\" alt=\"1H NMR spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003e1H NMR\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/38e4ZFSAENF\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/4936728_1\" alt=\"13C NMR spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003e13C NMR\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/GWD4ezOlf8s\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/36886356_1\" alt=\"GC-MS spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003eGC-MS\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/LEJKSwEHYw6\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/4936730_1\" alt=\"FTIR spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003eFTIR\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/7xlDZ0NBhPf\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/10444009_1\" alt=\"ATR-IR spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003eATR-IR\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n      \u003ca href=\"https:\/\/spectrabase.com\/spectrum\/7h7VBGy53q4\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"text-decoration: none; background: #ffffff; border: 1px solid #dbe4ec; border-radius: 16px; overflow: hidden; color: inherit; box-shadow: 0 8px 20px rgba(22,36,74,0.05);\"\u003e\n        \u003cimg src=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/rest\/pug_view\/data\/key\/10444011_1\" alt=\"Raman spectrum thumbnail\" style=\"width: 100%; height: 170px; object-fit: cover; display: block;\"\u003e\n        \u003cdiv style=\"padding: 14px;\"\u003e\n          \u003cdiv style=\"font-size: 16px; font-weight: 700; color: #16244a;\"\u003eRaman\u003c\/div\u003e\n          \u003cdiv style=\"font-size: 13px; color: #5d6b7e; margin-top: 4px;\"\u003eOpen spectrum reference\u003c\/div\u003e\n        \u003c\/div\u003e\n      \u003c\/a\u003e\n\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003c!-- External resources --\u003e\n  \u003cdiv style=\"background: #ffffff; border: 1px solid #dbe4ec; border-radius: 20px; padding: 24px; box-shadow: 0 10px 28px rgba(22,36,74,0.06);\"\u003e\n    \u003ch3 style=\"margin: 0 0 16px 0; font-size: 22px; color: #16244a;\"\u003eExternal Reference Links\u003c\/h3\u003e\n    \u003cul style=\"margin: 0; padding-left: 18px; color: #233047; font-size: 15px;\"\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/6261\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003ePubChem CID 6261\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/commonchemistry.cas.org\/detail?cas_rn=70-25-7\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eCAS Common Chemistry\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli style=\"margin-bottom: 8px;\"\u003e\u003ca href=\"https:\/\/hmdb.ca\/metabolites\/HMDB0243924\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003eHMDB Record\u003c\/a\u003e\u003c\/li\u003e\n      \u003cli\u003e\u003ca href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/135436526\" target=\"_blank\" rel=\"noopener noreferrer\" style=\"color: #49a8d0; text-decoration: none; font-weight: 700;\"\u003ePreferred Related PubChem Record\u003c\/a\u003e\u003c\/li\u003e\n    \u003c\/ul\u003e\n  \u003c\/div\u003e\n\n\u003c\/div\u003e","brand":"Quantimol","offers":[{"title":"1 g","offer_id":53336443748689,"sku":"QM-0142468-01","price":275.99,"currency_code":"GBP","in_stock":true},{"title":"5 g","offer_id":53336443781457,"sku":"QM-0142468-02","price":614.98,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"},{"product_id":"aminopicoline-695-34-1","title":"Aminopicoline [CAS 695-34-1]","description":"\u003cp\u003e\u003cstrong\u003eAminopicoline\u003c\/strong\u003e is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.\u003c\/p\u003e","brand":"Quantimol","offers":[{"title":"1 g","offer_id":53342545641809,"sku":"QM-0193706-01","price":51.91,"currency_code":"GBP","in_stock":true},{"title":"10 mM - 1 mL","offer_id":53342545674577,"sku":"QM-0193706-02","price":53.98,"currency_code":"GBP","in_stock":true},{"title":"25 g","offer_id":53342545707345,"sku":"QM-0193706-03","price":106.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/files\/quantimol-021.png?v=1773515276"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1030\/0211\/2337\/collections\/quantimol-032_a1a88abf-29c2-44ce-a289-399ee1ff4bf6.png?v=1773597839","url":"https:\/\/quantimol.com\/collections\/offer.oembed","provider":"Quantimol","version":"1.0","type":"link"}