17351-34-7

Basic information

• Product Name: 14-Pentadecenoicacid
• Synonyms: 14-cis-Pentadecenoic acid;pentadec-14-enoic acid
• CAS NO: 17351-34-7
• Molecular Formula: C₁₅H₂₈O₂
• Molecular Weight: 240.38
• Mol File: 17351-34-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 170-190 °C(Press: 2 Torr)
• Appearance: /
• Density: 0.904±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.78±0.10(Predicted)
• CAS DataBase Reference: 14-Pentadecenoicacid(CAS DataBase Reference)
• NIST Chemistry Reference: 14-Pentadecenoicacid(17351-34-7)
• EPA Substance Registry System: 14-Pentadecenoicacid(17351-34-7)

Safety Data

• Hazardous Substances Data: 17351-34-7(Hazardous Substances Data)

Usage

Uses

ω-Pentadecenoic Acid, is a fatty acid that has been used in the fabrication of fibrous scaffold biomaterials for tissue engineering applications and for the construction of metallomesogenic side-chain polymers that coat capillary columns used in gas chromatography.

Upstream product

• 16339-75-6 12-tridecenyl alcohol 
• 105-53-3 diethyl malonate 
• 67-56-1 methanol 
• 627-91-8 adipic acid monomethyl ester 
• 111-81-9 Methyl 10-undecenoate 
• 505-54-4 thapsic acid 
• 112-38-9 10-undecenoic acid 
• 23550-12-1 5-Oxo-pentadecen-14-saeure-methylester 
• 13133-46-5 1-methanesulfinyl-dodec-11-en-2-one 
• 23550-13-2 5-oxo-pentadec-14-enoic acid 

Downstream Products

• 821-38-5 1,14-tetradecanedioic acid 
• 91400-78-1 pentadec-14-enoic acid methyl ester 
• 41240-35-1 dimethyl 2-ethylheptadecane-1,17-dioate 

Relevant articles and documents

Enzymatic Oxidative Tandem Decarboxylation of Dioic Acids to Terminal Dienes

The biocatalytic oxidative tandem decarboxylation of C7–C18dicarboxylic acids to terminal C5–C16dienes was catalyzed by the P450 monooxygenase OleT with conversions up to 29 % for 1,11-dodecadiene (0.49 g L–1). The sequential nature of the cascade was proven by the fact that decarboxylation of intermediate C6–C11ω-alkenoic acids and heptanedioic acid exclusively gave nonconjugated 1,4-pentadiene; scale-up allowed the isolation of 1,15-hexadecadiene and 1,11-dodecadiene; the system represents a short and green route to terminal dienes from renewable dicarboxylic acids.