392979

15-Hydroxypentadecanoic acid

97%

• Formule linéaire : HO(CH₂)₁₄CO₂H
• Numéro CAS: 4617-33-8
• Poids moléculaire : 258.40
• Numéro CE : 225-026-1
• Numéro MDL: MFCD00039535
• Code UNSPSC : 12352100
• ID de substance PubChem : 24864154
• Nomenclature NACRES : NA.22

Propriétés

• Niveau de qualité: 200
• Essai: 97%
• Pf: 85-89 °C (lit.)
• Groupe fonctionnel: carboxylic acid; hydroxyl
• Chaîne SMILES: OCCCCCCCCCCCCCCC(O)=O
• InChI: 1S/C15H30O3/c16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15(17)18/h16H,1-14H2,(H,17,18)
• Clé InChI: BZUNJUAMQZRJIP-UHFFFAOYSA-N

Description

Description générale

15-Hydroxypentadecanoic acid is an ω-hydroxy acid. One of the method reported for its synthesis is from 1,12-dodecanolide.[1] It is reported to be one of the bioactive component in Tagetes erecta L. leaf and flower extract.[2]

15-Hydroxypentadecanoic acid undergoes lactonization reaction catalyzed by Mucor javanicus L46 and Mucor miehei to afford macrocyclic mono- and oligolactone derivatives.[3] Its lipase-catalyzed synthesis from 15-tetracosenoic acid in Malania Olcifera Chum oil has been proposed. It also participates in the biosynthesis of pentadecanolide.[4]

Application

15-Hydroxypentadecanoic acid is suitable reagent used in the following studies:

• As an internal standard in the quantification of formation of 11-hydroxylauric acid by gas chromatography.[5]
• In the synthesis of [16-¹⁴C]16DCA (DCA= dicarboxylic acid) by one-carbon elongation procedure at C15.[6]
• As an internal standard for the normalization of intensities in the mass spectra of plant cutin polymer.[7]

It may be used in the synthesis of 5-pentadecanolide on dealuminated HY zeolite[8] and also fatty acid analog of podophyllotoxin.[9]

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)