3-(3-PENTYLOXIRANYL)-2E-PROPENOL
3-(3-PENTYLOXIRANYL)-2E-PROPENOL Basic information
- Product Name:
- 3-(3-PENTYLOXIRANYL)-2E-PROPENOL
- Synonyms:
-
- 4,5-Epoxy-(E)-dec-2-enal
- FEMA 4037
- 3-[(2R,3R)-3-PENTYLOXIRANYL]-2E-PROPENAL
- 3-(3-PENTYLOXIRANYL)-2E-PROPENOL
- TRANS-4,5-EPOXY-2(E)-DECENAL
- epoxy-2-decenal,(E)-4,5-epoxy-(E)-2-decenal
- 4,5-EPOXY-(E)-2-DECENAL
- 2-Propenal, 3-[(2R,3R)-3-pentyl-2-oxiranyl]-, (2E)-rel-
- CAS:
- 134454-31-2
- MF:
- C10H16O2
- MW:
- 168.23
- Mol File:
- 134454-31-2.mol
3-(3-PENTYLOXIRANYL)-2E-PROPENOL Chemical Properties
- Boiling point:
- 273.3±15.0 °C(Predicted)
- Density
- 1.022±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): .2 mg/ml
- Odor
- citrus metallic green aldehydic
- Odor Type
- citrus
- JECFA Number
- 1570
- LogP
- 2.05
3-(3-PENTYLOXIRANYL)-2E-PROPENOL Usage And Synthesis
Description
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-
Uses
trans-4,5-Epoxy-(E)-2-decenal is an oxygenated α,β-unsaturated aldehyde found in mammalian blood that gives blood its characteristic metallic odor. It is used by predators to locate blood or prey[1].
References
[1] Lee SH,et al. 4,5-Epoxy-2(E)-decenal-induced formation of 1,N(6)-etheno-2'-deoxyadenosine and 1,N(2)-etheno-2'-deoxyguanosine adducts. Chem Res Toxicol. 2002 Mar;15(3):300-4. DOI:10.1021/tx010147j
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