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· · COA & SDS available for every product · Same-day shipping on in-stock items 2-Adamantanol - ≥98% , CAS No.700-57-2
Synonyms
2-Adamantanol, 97% | FT-0610989 | 2-Hydroxyadamantane | Z56757309 | InChI=1/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H | Adamantan-2-ol | NSC 193480 | EINECS 211-846-7 | W-104572 | HMS1787B03 | 2-Tricyclo[3.3.1.13, 7]decanol | A0720 | EN300-16725
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Usually used to synthesize ester imides.
Specifications Synonyms
2-Adamantanol, 97% | FT-0610989 | 2-Hydroxyadamantane | Z56757309 | InChI=1/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H | Adamantan-2-ol | NSC 193480 | EINECS 211-846-7 | W-104572 | HMS1787B03 | 2-Tricyclo[3.3.1.13, 7]decanol | A0720 | EN300-16725
Specifications & Purity
≥98%
Names and Identifiers Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488183627
Canonical Smiles
C1C2CC3CC1CC(C2)C3O
InChIKey
FOWDOWQYRZXQDP-UHFFFAOYSA-N
INCHI
1S/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H2
Isomeric SMILES
C1C2CC3CC1CC(C2)C3O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1903957&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
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✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
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Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic oxygen compounds Class Organooxygen compounds Subclass Alcohols and polyols Intermediate Tree Nodes Not available Direct Parent Cyclic alcohols and derivatives Alternative Parents Secondary alcohols Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Cyclic alcohol - Secondary alcohol - Hydrocarbon derivative - Aliphatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates (CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in Methanol Melt Point(°C) 264-269°C Molecular Weight 152.230 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 0 Exact Mass 152.12 Da Monoisotopic Mass 152.12 Da Topological Polar Surface Area 20.200 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 148.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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