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· · COA & SDS available for every product · Same-day shipping on in-stock items ricinelaidic acid - Reagent grade , CAS No.7431-95-0
GRADE & PURITY Reagent Grade ? General reagent-grade purity suitable for most laboratory work. Use as a dependable default when no specific higher grade is required. Synonyms
12-hydroxyl-9-octadecenoic acid | FT-0774278 | RICINELAIDIC ACID FREE ACID | DTXSID20859274 | 9-Octadecenoic acid, 12-hydroxy-, (9Z,12R)- | FT-0607233 | MEGxp0_002003 | 12-hydroxyoctadec-9-enoic acid | ACon1_000440 | SB44559
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Why this grade Reagent grade Reagent Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
12-hydroxyl-9-octadecenoic acid | FT-0774278 | RICINELAIDIC ACID FREE ACID | DTXSID20859274 | 9-Octadecenoic acid, 12-hydroxy-, (9Z, 12R)- | FT-0607233 | MEGxp0_002003 | 12-hydroxyoctadec-9-enoic acid | ACon1_000440 | SB44559
Specifications & Purity
Reagent grade
Names and Identifiers Canonical Smiles CCCCCCC(CC=CCCCCCCCC(=O)O)O IUPAC Name 12-hydroxyoctadec-9-enoic acid InChIKey WBHHMMIMDMUBKC-UHFFFAOYSA-N INCHI 1S/C18H34O3/c1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21/h9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21) Isomeric SMILES CCCCCCC(CC=CCCCCCCCC(=O)O)O PubChem CID 8839 Molecular Weight 298.46
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 Lipids and lipid-like molecules Class Fatty Acyls Subclass Fatty acids and conjugates Intermediate Tree Nodes Not available Direct Parent Long-chain fatty acids Alternative Parents Hydroxy fatty acids Unsaturated fatty acids Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Long-chain fatty acid - Hydroxy fatty acid - Unsaturated fatty acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. 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 Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Flash Point(°F) Not applicable Flash Point(°C) Not applicable Molecular Weight 298.500 g/mol XLogP3 5.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 15 Exact Mass 298.251 Da Monoisotopic Mass 298.251 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 261.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 1 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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