ChemicalBook--->CAS DataBase List--->41096-46-2

41096-46-2

41096-46-2 Structure

41096-46-2 Structure
IdentificationBack Directory
[Name]

HYDROPRENE
[CAS]

41096-46-2
[Synonyms]

zr512
zr-512
gencor
oms1696
altozar
ent70459
Altozar IGR
(2E,4E)-Hydroprene
Hydroprene=Altozar=Encotone=Gencor
ethyl3,7,11-trimethyl-2,4-dodecadienoate
ethyl3,7,11-trimethyldodeca-2,4-dienoate
(e,e)-ethyl3,7,11-trimethyl-2,4-dodecadienoate
ethyl(2e,4e)-3,7,11-trimethyl-dodeca-2-4-dienoate
3,7,11-trimethyl-,ethylester,(2e,4e)-dodeca-4-dienoicacid
(2E,4E)-3,7,11-Trimethyldodeca-2,4-dienoic acid ethyl ester
2,4-Dodecadienoic acid, 3,7,11-trimethyl-, ethyl ester, (2E,4E)-
[Molecular Formula]

C17H30O2
[MDL Number]

MFCD00233106
[MOL File]

41096-46-2.mol
[Molecular Weight]

266.42
Chemical PropertiesBack Directory
[Boiling point ]

bp0.03 95°
[density ]

0.8955
[refractive index ]

1.4510 (estimate)
[Henry's Law Constant]

5.1×10-2 mol/(m3Pa) at 25℃, Ebert et al. (2023)
[EPA Substance Registry System]

Hydroprene (41096-46-2)
Safety DataBack Directory
[HS Code ]

29161900
[Hazardous Substances Data]

41096-46-2(Hazardous Substances Data)
[Toxicity]

LD50 orally in rats: >34000 mg/kg (Edwards)
Hazard InformationBack Directory
[Description]

Hydroprene is an amenity and domestic insecticide. It has a low aqueous solubility, is quite volatile and, based on its chemical properties, it is slightly mobile but unlikely to leach to groundwater. It is not generally persistent in soil systems. It has a low mammalian toxicity. It shows a moderate level of toxicity to fish and daphnia but is relatively non-toxic to adult honeybees but may be harmful to bee larvae.
[Uses]

Hydroprene is used in the method for controlling pests of sugarcane, citrus, rapeseed, and potato plants.
[Definition]

ChEBI: The ethyl ester of (2E,4E)-3,7,11-trimethyldodeca-2,4-dienoic acid
[Production Methods]

Hydroprene is commercially synthesised through esterification of 3,7,11-trimethyl-2,4-dodecadienoic acid with ethanol. The production process begins with the preparation of the dodecadienoic acid backbone, which involves controlled oligomerization and selective methylation of linear precursors. This intermediate is then esterified with ethanol under acidic conditions to yield hydroprene. The final product is purified via distillation and stabilised for formulation
[Mechanism of action]

A juvenile hormone mimic. Contact and stomach action, acts by duplicating the action of juvenile hormones keeping the insect in an immature state
[Pesticide Type]

Insecticide; Insect Growth Regulator
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