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Dichlorophosphinic acid 2-ethylhexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

45088-64-0

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45088-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 45088-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,0,8 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 45088-64:
(7*4)+(6*5)+(5*0)+(4*8)+(3*8)+(2*6)+(1*4)=130
130 % 10 = 0
So 45088-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Cl2O2P/c1-3-5-6-8(4-2)7-12-13(9,10)11/h8H,3-7H2,1-2H3

45088-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dichlorophosphoryloxymethyl)heptane

1.2 Other means of identification

Product number -
Other names 2-ethylhexyl phosphorodichloridate

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:45088-64-0 SDS

45088-64-0Upstream product

45088-64-0Relevant academic research and scientific papers

Relationship between aggregation properties and antimicrobial activities of alkylphosphocholines with branched alkyl chains

Luká?, Milo?,Garajová, Mária,Mrva, Martin,Bukovsky, Marián,Ondriska, Franti?ek,Máriássy, Eszter,Devínsky, Ferdinand,Lacko, Ivan

, p. 247 - 256 (2012)

Synthesis of five alkylphosphocholines with branched alkyl chains (Isophol-PCs) with different length of alkyl chains was described. Isophol 8-PC and Isophol12-PC represent new compounds. The physico-chemical properties of Isophol-PCs were determined, critical micelle concentration and types of formed aggregates in aqueous solutions were investigated. The biological activities of Isophol-PCs have been studied for the first time in the present study. Antimicrobial activities of alkylphosphocholines were studied against bacteria (Staphylococcus aureus, Escherichia coli), yeast (Candida albicans) and pathogenic free-living amoebae (Acanthamoeba lugdunensis and Acanthamoeba quina). A. lugdunensis and A. quina are relatively insusceptible to action of miltefosine (standard compound of alkylphosphocholines) and therefore they are good models for studies of amoebicidal action of the investigated compounds. Relationship between structure, physico-chemical and biological activities of Isophol-PCs was discussed. S. aureus and C. albicans were sensitive to action of Isophol 16-PC, Isophol20-PC. E. coli was not sensitive to action of all studied alkylphosphocholines in the concentrations equal to, or less than 10 mM. Among all the synthesized compounds, Isophol16-PC had the highest level of activity against both strains of Acanthamoeba. The minimum trophocidal concentrations of Isophol16-PC against A. lugdunensis and A. quina are about four times lower than the minimum trophocidal concentrations of miltefosine against booth strains.

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