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Fenozan 27, also known as Fenpyroximate, is a novel insecticide belonging to the class of amidinohydrazones. It is specifically designed to target lepidopteran pests, such as caterpillars and moths, by disrupting their energy production within the mitochondria. Fenozan 27 is known for its unique mode of action, which involves inhibiting the electron transport chain in the respiratory process, leading to the death of the pest. This chemical is particularly effective against pests that have developed resistance to other commonly used insecticides, making it a valuable tool in integrated pest management strategies. It is also characterized by its low mammalian toxicity and minimal impact on beneficial insects, which contributes to its environmental friendliness.

6524-49-8

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6524-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6524-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,2 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6524-49:
(6*6)+(5*5)+(4*2)+(3*4)+(2*4)+(1*9)=98
98 % 10 = 8
So 6524-49-8 is a valid CAS Registry Number.

6524-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis-[4-hydroxy-3,5-di-t.-butylphenyl-propionic acid]-ethylene glycolester

1.2 Other means of identification

Product number -
Other names Ethylenglykol-bis-<3-(3.5-di-t-butyl-4-hydroxyphenyl)-propionat>

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:6524-49-8 SDS

6524-49-8Downstream Products

6524-49-8Relevant academic research and scientific papers

Process for the production of hydroxyalkylphenyl derivatives

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, (2008/06/13)

An improved process for the production of hydroxyalkylphenyl derivatives, especially esters and amides containing hydroxyalkylphenyl groups is disclosed, which process comprises gradually adding methyl acrylate, in the presence of an alkaline catalyst, to the alkyl substituted phenolic compound, and adding to the resultant reaction mixture a suitable alcohol or amine, optionally in the presence of a second catalyst which is different from the first catalyst. The improved process results in good yields and in a reduction of undesirable by-products while avoiding isolation of the intermediates.

Process for the production of hydroxyalkylphenyl derivatives

-

, (2008/06/13)

An improved process for the production of hydroxyalkylphenyl derivatives, especially esters containing hydroxyalkylphenyl groups is disclosed, which process comprises gradually adding methyl acrylate, in the presence of an alkaline catalyst, to the alkyl substituted phenolic compound and a suitable alcohol. The improved process results in good yields and in a reduction of undesirable by-products while avoiding isolation of the intermediates.

Polyalkylene glycol esters of hindered phenols substituted alkanoic acid

-

, (2008/06/13)

Compounds of the formula: EQU1 WHEREIN X is oxygen or sulfur, a is an integer from 2 to 6, b is an integer from 3 to 40, and R is SPC1 Wherein R1 is an alkyl group of 1 to 8 carbon atoms, R2 is hydrogen or an alkyl group of 1 to 8 carbon atoms, and X is an integer from 0 to 6 Are useful as antioxidants for organic materials normally subject to oxidative deterioration, such as polyacetals, polypropylene, and nylon, in amounts of from about 0.005 to about 5% by weight of the composition.

4-Hydroxy-3,5-di-alkyl-phenyl-propionic acid composition suitable as lipid lowering and anti-diabetic agents

-

, (2008/06/13)

Pharmaceutical compositions acting on the metabolism which contain as active derivatives of the 4-hydroxy-3,5-di-akylphenyl-propionic acid corresponding to the formula I and II EQU1 wherein R1 and R2 which may be identical or different, each stands for an alkylradical having 1 to 8 carbon atoms, R3 stands for an alkylene radical having 2 to 12 carbon atoms, X stands for hydroxy, alkoxy having 1 to 18 carbon atoms, phenalkoxy having 1 to 4 alkyl carbon atoms, cycloalkoxy having 5 to 8 carbon atoms, --NR4 R5 in which R4 stands for an alkyl group having 1 to 18 carbon atoms, R5 stands for a hydrogen atom or R4 and R5 may form with the nitrogen atom a heterocyclic six-membered ring which may carry another hetero atom and n is an integer from 2 to 4 and process for preparing them.

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