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ETHIOFENCARB-SULFONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53380-23-7

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53380-23-7 Usage

Uses

Ethiofencarb Sulfone is a metabolite of Croneton, a carbamate insecticide.

Check Digit Verification of cas no

The CAS Registry Mumber 53380-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,8 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53380-23:
(7*5)+(6*3)+(5*3)+(4*8)+(3*0)+(2*2)+(1*3)=107
107 % 10 = 7
So 53380-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4S/c1-3-17(14,15)8-9-6-4-5-7-10(9)16-11(13)12-2/h4-7H,3,8H2,1-2H3,(H,12,13)

53380-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHIOFENCARB-SULFONE

1.2 Other means of identification

Product number -
Other names cronetonsulfone

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:53380-23-7 SDS

53380-23-7Upstream product

53380-23-7Downstream Products

53380-23-7Relevant academic research and scientific papers

Photodegradation of the Carbamate Insecticide Ethiofencarb

Kopf, Gudrun,Schwack, Wolfgang

, p. 303 - 310 (1995)

In order to study the photoreactivity and possible photodegradation pathways of ethiofencarb (2-ethylthiomethylphenyl methylcarbamate) on plant surfaces, model experiments in the presence of cyclohexane, cyclohexene and isopropanol were performed. Both artificial light (λ > 280 nm) and natural sunlight were used. Half-lives of the ethiofencarb photodegradation were in the order cyclohexane isopropanol cyclohexene and ranged from 75 min to more than 20 h. Depending on the solvent and the light source chosen, different photoproducts were obtained. When ethiofencarb was irradiated in the presence of cyclohexane, photooxidation to the corresponding sulfoxide was the main degradation pathway, followed by a cyclization reaction. In the case of isopropanol as model solvent, numerous photoproducts were detected as a result of photooxidation, hydrolysis and the addition to ethiofencarb of the solvent molecule.

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