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(methylselenonyl)methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22089-69-6

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22089-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22089-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22089-69:
(7*2)+(6*2)+(5*0)+(4*8)+(3*9)+(2*6)+(1*9)=106
106 % 10 = 6
So 22089-69-6 is a valid CAS Registry Number.

22089-69-6SDS

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 methylselenonylmethane

1.2 Other means of identification

Product number -
Other names dimethyl selenoxide

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:22089-69-6 SDS

22089-69-6Downstream Products

22089-69-6Relevant academic research and scientific papers

Toxicity of oxyanions of selenium and of a proposed bioremediation intermediate, dimethyl selenone

Yu, Rui,Coffman, John P.,Van Fleet-Stalder, Verena,Chasteen, Thomas G.

, p. 140 - 145 (2007/10/03)

The relative toxicity of selenate, selenite, and dimethyl selenone were assessed by determining growth inhibition and growth rate inhibition of Pseudomonas fluorescens K27 and using the Microtox bioassay method at varying concentrations of these three selenium species. The results of EC50 vary depending on the organism tested and the method used; for P. fluorescens K27, EC50 increased in the order of dimethyl selenone selenate selenite. However, for Vibrio fisheri, EC50 increased in the order of selenite dimethyl selenone selenate. The possibility that different reduction mechanisms may dominate the remediation of the two selenium oxyanions with different oxidation states by P. fluorescens K27 is discussed, as is whether dimethyl selenone is a possible intermediate in selenium reduction and methylation.

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