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31970-86-2

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31970-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31970-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,7 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31970-86:
(7*3)+(6*1)+(5*9)+(4*7)+(3*0)+(2*8)+(1*6)=122
122 % 10 = 2
So 31970-86-2 is a valid CAS Registry Number.

31970-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[bis[4-(trimethylazaniumyl)phenyl]methyl]phenyl]-trimethylazanium,triiodide

1.2 Other means of identification

Product number -
Other names nona-N-methyl-4,4',4''-methanetriyl-tri-anilinium,tris iodide

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:31970-86-2 SDS

31970-86-2Relevant articles and documents

Structure-Resistance Relationships: Interrogating Antiseptic Resistance in Bacteria with Multicationic Quaternary Ammonium Dyes

Forman, Megan E.,Fletcher, Madison H.,Jennings, Megan C.,Duggan, Stephanie M.,Minbiole, Kevin P. C.,Wuest, William M.

supporting information, p. 958 - 962 (2016/05/24)

Bacterial resistance toward commonly used biocides is a widespread yet underappreciated problem, one which needs not only a deeper understanding of the mechanisms by which resistance proliferates, but also means for mitigation. To advance our understanding of this issue, we recognized a polyaromatic structural core analogous to activators of QacR, a negative transcriptional regulator of the efflux pump QacA, and envisioned a series of quaternary ammonium compounds (QACs) based on this motif. Using commercially available dye scaffolds, we synthesized and evaluated the antimicrobial activity of 52 novel QACs bearing 1-3 quaternary ammonium centers. Striking differences in antimicrobial activity against bacteria bearing QAC resistance genes have been observed, with up to a 125-fold increase in minimum inhibitory concentration (MIC) for select structures against bacteria known to bear efflux pumps. Based on these findings, general trends in structure-resistance relationships have been identified, laying the groundwork for future mechanistic studies.

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