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103554-07-0

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103554-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103554-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103554-07:
(8*1)+(7*0)+(6*3)+(5*5)+(4*5)+(3*4)+(2*0)+(1*7)=90
90 % 10 = 0
So 103554-07-0 is a valid CAS Registry Number.

103554-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name trioctyl(6-trioctylphosphaniumylhexyl)phosphanium,dibromide

1.2 Other means of identification

Product number -
Other names -

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:103554-07-0 SDS

103554-07-0Downstream Products

103554-07-0Relevant articles and documents

Phosphonium-ammonium-based di-cationic ionic liquids as antibacterial over the ESKAPE group

Bolla, Jean-Michel,Camplo, Michel,Lautard, Christelle,Raimundo, Jean-Manuel,Brunel, Frédéric,Garzino, Frédéric

supporting information, (2020/07/23)

Emergence of antibioresistance is currently a major threat of public health worldwide. Hence there is an urge need of finding new antibacterial material. Herein, we report a simple and eco-friendly method to synthesize homo and heterodicationic ionic liquids based on quaternary phosphonium and ammonium salt. In order to investigate the structure activity relationship (SAR) we measured the MICs of a series of 16 derivatives with structural variations (nature of cations and counter-ions, size of linker and alkyl side chains as well as structural symmetry) over a range of Gram-positive and Gram-negative bacterial strains from the ESKAPE group. Some of the tested structures exhibit high antimicrobial activities (MIC = 0.5 mg/L) and are active over a wide range of bacteria from Gram-positive to Gram-negative. Overall, these results reveal the strong potential of di-cationic derivatives as antibacterial agents and the determination of activities from structural features gives decisive information for future synthesis of such di-cationic structures for biocidal purpose.

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