392979

15-Hydroxypentadecanoic acid

97%

• Fórmula lineal: HO(CH₂)₁₄CO₂H
• Número de CAS: 4617-33-8
• Peso molecular: 258.40
• Número CE: 225-026-1
• Número MDL: MFCD00039535
• Código UNSPSC: 12352100
• ID de la sustancia en PubChem: 24864154
• NACRES: NA.22

Propiedades

• Nivel de calidad: 200
• Ensayo: 97%
• mp: 85-89 °C (lit.)
• grupo funcional: carboxylic acid; hydroxyl
• cadena 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)
• Clave InChI: BZUNJUAMQZRJIP-UHFFFAOYSA-N

Descripción

Descripción general

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]

Aplicación

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]

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)