A 15-carbon monounsaturated fatty acid
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Product Categories

Product Type

Biochemicals
Lipids
Fatty Acids

Research Area

Lipid Biochemistry
Fatty Acids

10(E)-Pentadecenoic Acid

Item No. 22467

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
10E-pentadecenoic acid
CAS Number
321744-58-5
Synonyms
  • FA 15:1
Molecular Formula
C15H28O2
Formula Weight
240.4
Purity
≥98%
Formulation (Request formulation change)
A 10 mg/ml solution in ethanol
Solubility(Learn about Variance in Solubility)
DMF: 25 mg/mlDMSO: 10 mg/mlEthanol: 25 mg/mlEthanol:PBS(pH 7.2) (1:1): 0.25 mg/ml
λmax
230 nm
SMILES
OC(CCCCCCCC/C=C/CCCC)=O
InChi Code
InChI=1S/C15H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17/h5-6H,2-4,7-14H2,1H3,(H,16,17)/b6-5+
InChi Key
APXSAEQXOXTDAM-AATRIKPKSA-N
Side Chain Carbon Sum
15:1
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    1 mg

    $36

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    5 mg

    $153

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    10 mg

    $268

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    25 mg

    $587

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    Product Description

    10(E)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. It inhibits IFN-γ-induced production of kynurenine in THP-1 cells by 14% when used at a concentration of 20 µM.1 10(E)-Pentadecenoic acid has been used in studies of alternative β-oxidation pathways.2,3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Costabile, M., Bassal, N.K., Gerber, J.P., et al. Inhibition of indoleamine 2,3-dioxygenase activity by fatty acids and prostaglandins: A structure function analysis. Prostaglandins Leukot. Essent. Fatty Acids 122, 7-15 (2017).

    2. Robert, J., Marchesini, S., Delessert, S., et al. Analysis of the β-oxidation of trans-unsaturated fatty acid in recombinant Saccharomyces cerevisiae expressing a peroxisomal PHA synthase reveals the involvement of a reductase-dependent pathway. Biochim. Biophys. Acta 1734(2), 169-177 (2005).

    3. Allenbach, L., and Poirier, Y. Analysis of the alternative pathways for the β-oxidation of unsaturated fatty acids using transgenic plants synthesizing polyhydroxyalkanoates in peroxisomes. Plant Physiol. 124(3), 1159-1168 (2000).