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(E)-2-Octenal

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(E)-2-Octenal Basic information

Product Name:
(E)-2-Octenal
Synonyms:
  • (e)-2-octena
  • 2-(E)-octenal
  • oct-(E)-2-enal
  • oct-2(E)-enal
  • T2 OCTENAL
  • TRANS-2-OCTEN-1-AL
  • TRANS-2-OCTENAL
  • FEMA 3215
CAS:
2548-87-0
MF:
C8H14O
MW:
126.2
EINECS:
219-833-8
Product Categories:
  • O-P
  • Alphabetical Listings
  • aldehyde Flavor
  • Flavors and Fragrances
  • Aldehydes
  • C8
  • Carbonyl Compounds
Mol File:
2548-87-0.mol
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(E)-2-Octenal Chemical Properties

Melting point:
3.5°C (estimate)
Boiling point:
84-86 °C19 mm Hg(lit.)
Density 
0.846 g/mL at 25 °C(lit.)
vapor density 
>1 (vs air)
refractive index 
n20/D 1.45(lit.)
FEMA 
3215 | 2-OCTENAL
Flash point:
150 °F
storage temp. 
2-8°C
solubility 
Chloroform (Soluble), Methanol (Slightly)
color 
Colourless
Odor
at 1.00 % in dipropylene glycol. fresh cucumber fatty green herbal banana waxy green leaf
Odor Type
fatty
Water Solubility 
Not miscible or difficult to mix in water. Soluble in alcohol and fixed oils.
Sensitive 
Air Sensitive
JECFA Number
1363
Stability:
Air Sensitive, Light Sensitive
LogP
2.64
CAS DataBase Reference
2548-87-0(CAS DataBase Reference)
NIST Chemistry Reference
2-Octenal, (E)-(2548-87-0)
EPA Substance Registry System
2-Octenal, (2E)- (2548-87-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
RTECS 
RH2130000
TSCA 
Yes
HS Code 
29121900
Toxicity
dnd-ham-fbr 250 mmol/l/1H MUREAV 497,185,2001

MSDS

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(E)-2-Octenal Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

trans-2-Octenal is one of the probable major contributors to the Californian long-grain cooked rice odor.

Definition

ChEBI: The (E)-isomer of oct-2-enal.

Synthesis Reference(s)

The Journal of Organic Chemistry, 51, p. 2607, 1986 DOI: 10.1021/jo00363a043
Journal of the American Chemical Society, 93, p. 1724, 1971 DOI: 10.1021/ja00736a027
Tetrahedron, 39, p. 3207, 1983 DOI: 10.1016/S0040-4020(01)91568-6

General Description

The rate constant for the gas-phase reaction of the NO(3) radical with trans-2-octenal was studied using absolute rate method. The fungal volatile organic compound trans-2-octenal, caused locomotory defects and changes in green fluorescent protein (GFP) and antigen-labeled dopaminergic neurons in adult Drosophila melanogaster.

Safety Profile

Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors.

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