532-87-6

Basic information

• Product Name: ALVASOL
• Synonyms: 4-(5-methyl-1-methylene-4-hexenyl)-1-(4-methyl-3-pentenyl)-cyclohexen;4-(5-methyl-1-methylene-4-hexenyl)-1-(4-methyl-3-pentenyl)-Cyclohexene;ALVASOL;DIMYRCENE;4-(5-methyl-1-methylene-4-hexenyl)-1-(4-methylpent-3-enyl)cyclohexene;Cyclohexene,4-(5-methyl-1-methylene-4-hexenyl)-1-(4-methyl-3-pentenyl)-;1-(4-Methyl-3-pentenyl)-4-(1-methylene-5-methyl-4-hexenyl)-1-cyclohexene;4-(5-Methyl-1-methylene-4-hexenyl)-1-(4-methyl-3-pentenyl)-1-cyclohexene
• CAS NO: 532-87-6
• Molecular Formula: C₂₀H₃₂
• Molecular Weight: 272.47
• EINECS: 208-546-3
• Mol File: 532-87-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 357.6°Cat760mmHg
• Flash Point: 163.1°C
• Appearance: /
• Density: 0.861g/cm³
• Vapor Pressure: 5.57E-05mmHg at 25°C
• Refractive Index: 1.49
• CAS DataBase Reference: ALVASOL(CAS DataBase Reference)
• NIST Chemistry Reference: ALVASOL(532-87-6)
• EPA Substance Registry System: ALVASOL(532-87-6)

Safety Data

• Hazardous Substances Data: 532-87-6(Hazardous Substances Data)

Usage

General Description

ALVASOL is a chemical combination of the active ingredients Alphacypermethrin and Imidacloprid. These ingredients work together as a powerful insecticide, providing broad-spectrum control of a wide range of insect pests including ants, termites, cockroaches, and other household pests. Alphacypermethrin acts as a fast-acting neurotoxin, causing paralysis and death in targeted insects, while Imidacloprid disrupts the nervous system and causes systemic toxicity. The combination of these two chemicals in ALVASOL provides an effective and long-lasting solution for pest control in residential and commercial settings.

InChI:InChI=1/C20H32/c1-16(2)8-6-10-18(5)20-14-12-19(13-15-20)11-7-9-17(3)4/h8-9,12,20H,5-7,10-11,13-15H2,1-4H3

Upstream product

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Downstream Products

• 22460-20-4 1-(1,5-Dimethyl-hexyl)-4-(4-methyl-pentyl)-benzene 
• 56009-20-2 cyclohexane, 1-(1,5-dimethylhexyl)-4-(4-methylpentyl)- 

Relevant articles and documents

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Synthesis of p-Camphorene

p-Camphorene is synthesised by the application of Wittig reaction with methylenetriphenylphosphorane on 1(4-methyl-3-pentenyl)-4-(5-methyl-4-hexe-1-one)cyclohex-1-ene (5), the cardinal intermediate, which was procured by the formation of β-ketosulphoxide and then its subsequent alkylation with 1-bromo-3-methyl-2-butene of the compound 1(4-methyl-3-pentenyl)-4-carbmethoxycyclohex-1-ene (3).The alkylated material was submitted to reductive cleavage with aluminium amalgam in aqueous THF at 65 deg to furnish 5.