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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel 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.
Übersicht Usually used to synthesize ester imides.
Specifications Synonyme
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
Spezifikationen & Reinheit
≥98%
Namen und Kennungen Pubchem Sid 488183627 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183627 Kanonisches Lächeln C1C2CC3CC1CC(C2)C3O IUPAC Name adamantan-2-ol 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 Isomere SMILES C1C2CC3CC1CC(C2)C3O WGK Deutschland 3 Molekulargewicht 152.23 Beilstein 2498536 Reaxy-Rn 1903957 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.
Download SDS → ✅ 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.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic oxygen compounds Klasse 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 Beschreibung 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-Struktur Zugehörige Ziele (menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Soluble in Methanol Schmelzpunkt (°C) 264-269°C Molekulargewicht 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
FAQs und Artikel Citations of This Product Referenzen 1. Yao Wang, Junhua Qiu, Chengwei Wang, Ruiyu Yang, Fuyou Guo, Tian Li, Shili Li, Lei Yang, Wei Ding. (2026) Sustainable Strategy of Natural trans-Anethole in Controlling Bacterial Wilt: Virulence Suppression and Beneficial Microbiome Enrichment. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:41568748 ] [10.1021/acs.jafc.5c13627 ]
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