(E)-2-Octenal

(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
(E)-2-Octenal Structure
(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)
FEMA 3215 | 2-OCTENAL
refractive index n20/D 1.45(lit.)
Fp 150 °F
storage temp. 2-8°C
solubility Chloroform (Soluble), Methanol (Slightly)
form neat
color Colourless
Odorat 1.00 % in dipropylene glycol. fresh cucumber fatty green herbal banana waxy green leaf
Odor Typefatty
Water Solubility Not miscible or difficult to mix in water. Soluble in alcohol and fixed oils.
Sensitive Air Sensitive
JECFA Number1363
Stability:Air Sensitive, Light Sensitive
LogP2.64
CAS DataBase Reference2548-87-0(CAS DataBase Reference)
NIST Chemistry Reference2-Octenal, (E)-(2548-87-0)
EPA Substance Registry System2-Octenal, (2E)- (2548-87-0)
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
Toxicitydnd-ham-fbr 250 mmol/l/1H MUREAV 497,185,2001
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
(E)-2-Octenal Usage And Synthesis
Chemical PropertiesColorless liquid
Usestrans-2-Octenal is one of the probable major contributors to the Californian long-grain cooked rice odor.
DefinitionChEBI: 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 DescriptionThe 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 ProfileMutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors.
(E)-2-Octenal Preparation Products And Raw materials
Preparation Products(2E,4E)-2,4-Octadienal
WIELAND-MIESCHER KETONE alpha-Ionone Ethisterone 5-ANDROSTENEDIOL Adrenosterone 16-methyl-20-oxopregna-5,16-dien-3-beta-yl acetate Prednisolone 17-Methyltestosterone Testosterone CORTISONE Prednisone METHANDIENONE 16-Dehydroprogesterone TRANS-2-OCTENOIC ACID Irisone (E)-2-Octenal Cortisone acetate Androsta-1,4-diene-3,17-dione

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.