Extracted from atherosclerotic lesions; can be used as a standard
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13(R)-HODE cholesteryl ester

Item No. 38606

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
13R-hydroxy-9Z,11E-octadecadienoic acid, cholesteryl ester
CAS Number
330800-94-7
Molecular Formula
C45H76O3
Formula Weight
665.1
Purity
≥98%
Formulation (Request formulation change)
A 100 µg/ml solution in ethanol
Solubility(Learn about Variance in Solubility)
DMF: >50 mg/mlDMSO: >50 mg/mlEthanol: >50 mg/mlEthanol:PBS (1:10): <10 µg/ml
λmax
234 nm
SMILES
CCCCC[C@@H](O)\C=C\C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@H]23)C1
InChi Code
InChI=1S/C45H76O3/c1-7-8-16-22-37(46)23-17-14-12-10-9-11-13-15-18-24-43(47)48-38-29-31-44(5)36(33-38)25-26-39-41-28-27-40(35(4)21-19-20-34(2)3)45(41,6)32-30-42(39)44/h12,14,17,23,25,34-35,37-42,46H,7-11,13,15-16,18-22,24,26-33H2,1-6H3/b14-12-,23-17+/t35-,37-,38+,39+,40-,41+,42+,44+,45-/m1/s1
InChi Key
RZXYPSUQZUUHPD-SIOVVMIPSA-N
Side Chain Carbon Sum
18:2
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    25 µg

    $239

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    50 µg

    $325

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    100 µg

    $611

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    Product Description

    13(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions.1 It remains uncertain whether the oxidized fatty acid portion of the molecule results from enzymatic lipoxygenation or from random lipid peroxidation.2 13(R)-HODE cholesteryl ester can be used as a standard for analysis of chiral HODE cholesteryl esters.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Brooks, C.J.W., Harland, W.A., Steel, G., et al. Lipids of human atheroma: Isolation of hydroxyoctadecadienoic acids from advanced aortal lesions. Biochim. Biophys. Acta 202(3), 563-566 (1970).

    2. Belkner, J., Wiesner, R., Kühn, H., et al. The oxygenation of cholesterol esters by the reticulocyte lipoxygenase. FEBS Lett. 279(1), 110-114 (1991).