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

83601-84-7

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83601-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83601-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83601-84:
(7*8)+(6*3)+(5*6)+(4*0)+(3*1)+(2*8)+(1*4)=127
127 % 10 = 7
So 83601-84-7 is a valid CAS Registry Number.

83601-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name endosulfan-sulphate

1.2 Other means of identification

Product number -
Other names endosulfdanesulfate

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:83601-84-7 SDS

83601-84-7Downstream Products

83601-84-7Relevant academic research and scientific papers

Photoinduced Reactions: Part IV - Studies on Photochemical Fate of 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide (Endosulphan), an Important Insecticide

Dureja, P.,Mukerjee, S. K.

, p. 411 - 413 (2007/10/02)

The photolysis of the cyclodiene insecticide endosulphan (6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide) has been examined under different conditions, including environmental.Two new photometabolites, photo-α-endosulphan and photo-β-endosulphan have been isolated from α- and β-isomers of endosulphan respectively and characterised on the basis of their 13C NMR spectra and other data.Irradiation in polar solvents gives metabolites similar to those formed under biotic conditions.When exposed to sunlight on plant leaves, α-endosulphane not only forms the photometabolite but also undergoes isomerisation to β-isomer.On the other hand β-isomer is relatively more stable.This explains the relatively longer persistence of β-endosulphan in the environment and may have some significance on their toxicity.

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