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(+)-cis-Permethrin is a synthetic pyrethroid insecticide and acaricide that is commonly used for controlling pests in agriculture, as well as in residential and commercial settings. It is a fast-acting neurotoxin that targets the nervous systems of insects and mites, leading to paralysis and eventual death.
Used in Agriculture:
(+)-cis-Permethrin is used as a pest control agent for protecting crops from a wide range of insects and mites that can cause significant damage and reduce yield. Its fast-acting nature and effectiveness against various pests make it a valuable tool in ensuring a healthy and productive agricultural output.
Used in Residential and Commercial Settings:
(+)-cis-Permethrin is used as an insecticide and acaricide for controlling pests in homes, offices, and other commercial spaces. It helps to eliminate mosquitoes, ants, cockroaches, and ticks, which can be a nuisance and pose health risks. Its effectiveness in controlling these pests contributes to maintaining a clean and safe living and working environment.
However, it is important to handle and apply (+)-cis-Permethrin with caution, as it can be toxic to aquatic organisms and poses potential risks to human health and the environment. Proper application and adherence to safety guidelines are crucial to minimize any adverse effects.

54774-45-7

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54774-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54774-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54774-45:
(7*5)+(6*4)+(5*7)+(4*7)+(3*4)+(2*4)+(1*5)=147
147 % 10 = 7
So 54774-45-7 is a valid CAS Registry Number.

54774-45-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Phenoxybenzyl (1R,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopr opanecarboxylate

1.2 Other means of identification

Product number -
Other names CIS-PERMETHRIN STANDARD

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54774-45-7 SDS

54774-45-7Relevant academic research and scientific papers

Assignment of absolute configurations of permethrin and its synthon 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid by electronic circular dichroism, optical rotation, and X-ray crystallography

Bicker, Wolfgang,Kacprzak, Karol,Kwit, Marcin,Laemmerhofer, Michael,Gawronski, Jacek,Lindner, Wolfgang

experimental part, p. 1027 - 1035 (2009/10/10)

The availability of single stereoisomers of biologically/toxicologically relevant chiral compounds such as the pyrethroid-type insecticide permethrin (PM) and the reliable determination of their absolute configurations are of central importance for the de

Search for Routes of Synthesis of Permethrin and Chloropermethrin Starting from Halogen-containing Alkenoic Acids

Badanyan,Stepanyan,Mikaelyan,Ovivyan,Panosyan

, p. 34 - 41 (2007/10/03)

Promising procedures were developed for the synthesis of permethrin and I-chloropermethrin starting from acid chloride, nitrile, and esters of 3,3-dimethyl-2,2,4,6,6-pentachloro-5-alkenoic acid and 3,3-dimethyl-2,2,6,6-tetrachloro-5-alken-4-olide, which were prepared by adding derivatives of trichloroacetic acid to 1,1-dichloro-4-methyl-1,3-pentadiene in the presence of catalytic amounts of monovalent copper ions and amine.

New Chiral Agents for Resolution of Racemic cis-Permethric and cis-Z-cyhalothric Acids

Popov, Sergey A.,Tkachev, Alexey V.

, p. 1013 - 1018 (2007/10/03)

Resolution of racemic pyrethroid acids (cis-permethric and cis-Z-cyhalothric) using stable optically active amines derived from natural monoterpene (+)-3-carene and preparation of optically active esters of the pyrethroid acids are described.

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