Detail of "33956-49-9"

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CAS Number:
33956-49-9
Name:
8,10-Dodecadien-1-ol,(8E,10E)-
Molecular Structure:
Formula:
C12H22 O
Molecular Weight:
182.34
Deleted CAS:
76600-88-9
Synonyms:
8,10-Dodecadien-1-ol,(E,E)- (8CI); (8E,10E)-8,10-Dodecadien-1-ol; (8E,10E)-Dodecadien-1-ol;(E,E)-8,10-Dodecadien-1-ol; (E,E)-8,10-Dodecadien-l-ol;(E,E)-8,10-Dodecadienol; 8-trans,10-trans-Dodecadien-1-ol; CP-MK; Codlelure;Codlemone; Feroflon SR 2; Feroflor SR 2; trans-8,trans-10-Dodecadien-1-ol;trans-trans-8,10-Dodecadien-1-ol
Density:
0.862g/cm³
Melting Point:
30-32 °C
Boiling Point:
270.7°Cat760mmHg
Flash Point:
100.9°C
Hazard Symbols:
Risk Codes:
36/37/38
Safety:
Moderately toxic by ingestion. When heated to decomposition it emits acrid smoke and irritating vapors. Details

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Pheromone of Cydia pomonella (8E,10E)-dodeca-8,10-dien-1-ol General purity: 95% Isomeric purity: 98%

Supplier:TBD-Biodiscovery [ Estonia]

Integral
65

Tel:+372-747-2501

Address:Tiigi 61b, 50410, Tartu, ESTONIA

Supplier:Chemica, Inc [ Canada]

800 Integral
800

Tel:+1-310-532-7531

Address:316 West 130th Street, Los Angeles, CA 90061

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Control of the codling moth (Laspeyresia pomonella L: Control of the codling moth (Laspeyresia pomonella L.) with a synthetic sex pheromone by the [male disruption] method: first trial in a commercial apple orchard. Audemard, H.; Beauvais, Francoise; Descoins, C. (Stn. Zool. - Avignon, Inst. Natl. Rech. Agron., Montfavet, Fr.). Rev. Zool. Agric. Pathol. Veg., 76(1), 15-24 (French) 1977. CODEN: RZAPAZ. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemicals) Codling moths were controlled in an apple orchard by trapping with Codlemone [33956-49-9]. In addn., Dysaphis plantaginea was controlled by phosalone [2310-17-0], Aphis pomi by pirimicarb [23103-98-2], Panonychus ulmi by cyhexatin [13121-70-5], and Zeuzera pyrina by mevinphos [7786-34-7].

Photoisomerization of synthetic sex pheromones of insects: Photoisomerization of synthetic sex pheromones of insects. Part I. Dodecenyl acetates and trans-8, trans-10-dodecadien-1-ol. Nesterova, I. P. (VNII Biol. Metod. Zashch. Rast., USSR). Khim. Sel'sk. Khoz., (12), 28-9 (Russian) 1984. CODEN: KSKZAN. ISSN: 0023-1185. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Half-life of films of trans-9-dodecen-1-yl acetate (I) [35148-19-7] and cis-9-dodecen-1-yl acetate (II) [16974-11-1] under 365.6-nm UV was 8 and 15 h, resp. Within 30 h 78% I and 93% II vanished, and the proportion of newly formed II in I and I in II increased from 3 to 27 and 53%, resp. Half-life of I and II under sunlight was 65 and 40 h, resp. Half-life of trans-8, trans-10-dodecadien-1-ol (III) [33956-49-9] under UV was 4 h and residue after 35 h of irradn. was 24%. Decompn. of III under UV was combined with isomerization to trans-8, cis-10-dodecadien-1-ol [67992-60-3] and to an unidentified isomer whose combined content increased from 9 to 46% within 35 h. The residue of III after 152 h of solar exposure was 47%.