(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate

(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate Structure
CAS No.
55774-32-8
Chemical Name:
(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate
Synonyms
EGVM;trans-7;Ai3-36730;7Z9E-12Ac;(E,Z)-7,9-DDDA;Einecs 259-812-0;(7Z,9E)-Dodecadienyl acetate;EGVM (European Grapevine Moth);(E,Z)-7,9-Dodecadienyl acetate;(Z,E)-7,9-Dodecadienyl acetate
CBNumber:
CB4498047
Molecular Formula:
C14H24O2
Molecular Weight:
224.34
MOL File:
55774-32-8.mol
MSDS File:
SDS
Modify Date:
2023/5/15 10:43:54

(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate Properties

Boiling point 309.6±21.0 °C(Predicted)
Density 0.896±0.06 g/cm3(Predicted)
vapor pressure 0.16 Pa (20 °C)
Flash point 61 °C
storage temp. −20°C
solubility Chloroform (Slightly), Methanol (Slightly)
Water Solubility 2.0 mg l-1(20 °C, est.)
form Oil
color Colourless
Stability Light Sensitive
EPA Substance Registry System 7,9-Dodecadien-1-ol, acetate, (7Z,9E)- (55774-32-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H411-H315
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  16-26-36

(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate Chemical Properties,Uses,Production

Uses

The pheromone is used for trapping and control of the European grapevine moth (Lubesia butrana).

Metabolic pathway

Facile hydrolysis to the alcohol (2) would be expected in alkaline solution. No published information is available but generally compounds of this class are rapidly degraded biologically and their behaviour is similar to that of typical long chain alkenoic acids.

Degradation

The effect of heat, sunlight, radicals and oxidants on isomerisation of the double bonds has been investigated. The compound is degraded by heating at 50 °C (6 mg remained of 100 mg after 6 days) but the process may be slowed by the addition of antioxidants. Isomerisation occurs readily in sunlight in the presence of a photosensitiser. Within 100 minutes an equilibrium mixture containing 76% E,E and 12-14% of each of the E,Z- and Z,E-isomers was formed. In the absence of photosensitiser, degradation was faster than photoequilibration. Photo-oxidation in the presence of Rose Bengal as a singlet oxygen generator gave a furan derivative (4) (see Scheme 1). This takes place after isomerisation of 1 to the E,E-isomer (3) (Shani et al., 1981).

(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate Preparation Products And Raw materials

Raw materials

Preparation Products

(7E,9Z)-Dodeca-7,9-dien-l-y1 acetate Suppliers

Global( 44)Suppliers
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TRANS-7, CIS-9-DODECADIENYL ACETATE trans-7 trans-7,cis-9-dodecadien-1-yl acetate (7E,9Z)-dodeca-7,9-dienyl acetate (E,Z)-7,9-DDDA (7Z,9E)-7,9-Dodecadien-1-ol acetate (E,Z)-7,9-Dodecadienyl acetate 7,9-Dodecadien-1-ol, acetate, (E,Z)- Ai3-36730 Einecs 259-812-0 EGVM (European Grapevine Moth) (7Z,9E)-7,9-Dodecadien-1-yl acetate (Z,E)-7,9-Dodecadienyl acetate EGVM (7Z,9E)-Dodecadienyl acetate 7Z9E-12Ac 7,9-Dodecadien-1-ol, acetate, (7Z,9E)- (7E,9Z)-Dodeca-7,9-dien-l-y1 acetate 7E, 9Z-Dodecadienyl Acetate CAS 55774-32-8 55774-32-8