trans-4,5-epoxy-2(E)-Decenal • 3-<wbr/>(3-<wbr/>pentyloxiranyl)-<wbr/>2E-<wbr/>propenal (CAS 134454-31-2) (Inchi key HIOMEXREAUSUBP-FNORWQNLSA-N) || Cayman Chemical | Supplier
trans-4,5-epoxy-2(E)-Decenal
Item № 10004257
CAS № 134454-31-2
Purity ≥95%
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1 mg $112.00 $0.00
5 mg $504.00 $0.00
10 mg $896.00 $0.00

Pricing updated 2015-08-29. Prices are subject to change without notice.

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Description
Synonyms
  • 3-(3-pentyloxiranyl)-2E-propenal

Polyunsaturated fatty acids such as arachidonate and linoeate, while essential to health maintenance, are subject to random peroxidation by ambient oxygen, resulting in fragmented and reactive decomposition products. One prominent autoxidation product of either trilinolein or arachidonic acid is trans-4,5-epoxy-2(E)-decenal. One prominent autoxidation product of either trilinolein or arachidonic acid is trans-4,5-epoxy-2(E)-decenal. This aldehyde is responsible for a pungent metallic flavor of decomposed lipids, with a detection threshold of 1.5 pg/l in air.1 trans-4,5-epoxy-2(E)-Decenal also reacts with nucleophiles (lysine amino groups) on proteins, leading to loss of cell function and viability.2 This reactive aldehyde is therefore a useful tool in elucidating the effects of peroxidative damage in experimental models.

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Technical Information
Formal Name 3-​[(2R,​3R)-​3-​pentyloxiranyl]-​2E-​propenal
CAS Number 134454-31-2
Synonyms
  • 3-(3-pentyloxiranyl)-2E-propenal
Molecular Formula C10H16O2
Formula Weight 168.2
Purity ≥95%
Formulation A solution in methyl acetate
λmax 218 nm
SMILES CCCCCC1OC1\C=C\C=O
InChI Code ​1S/C10H16O2/c1-2-3-4-6-9-10(12-9)​7-5-8-11/h5,7-10H,2-4,6H2,1H3/b7-5+
InChI Key HIOMEXREAUSUBP-FNORWQNLSA-N

WARNING - This product is not for human or veterinary use.

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Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere
Stability 1 year
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References & Background Reading
Product Description References

1. Lin, J., Fay, L.B., Welti, D.H., et al. Quantification of key odorants formed by autoxidation of arachidonic acid using isotope dilution assay. Lipids 36(7) 749-756 (2001).

2. Zamora, R., and Hidalgo, F.J. Modification of lysine amino groups by the lipid peroxidation product 4,5(E)-epoxy-2(E)-heptenal. Lipids 29 243-249 (1994).

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