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25371-54-4

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25371-54-4 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 25371-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25371-54:
(7*2)+(6*5)+(5*3)+(4*7)+(3*1)+(2*5)+(1*4)=104
104 % 10 = 4
So 25371-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H43O3P/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24(21,22-2)23-3/h4-20H2,1-3H3

25371-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecylphosphonate de dimethyle

1.2 Other means of identification

Product number -
Other names DIMETHYL OCTADECYLPHOSPHONATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. CBI
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:25371-54-4 SDS

25371-54-4Relevant articles and documents

On the reaction of dimethyl hydrogen phosphite with long-chain industrial olefins

Nizamov,Ermolaev,Sergeenko,Nizamov,Batyeva,Al'Fonsov,Cherkasov

, p. 1978 - 1979 (2007)

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Boutevin,Hervaud,Jeanmaire,Boulahna,Elasri

, p. 1 - 14 (2007/10/03)

This paper describes the synthesis and the characterization by 1H and 31P NMR of several monosalts and monoacids issued from phosphonates bearing alkyl groups (C1 to C18) or alkylene groups (allyl or vinyl). Functional compounds (alcohol or acetate) were also used and the results demonstrate the reaction selectivity. The method involves sodium iodide in ketones (acetone or 2-butanone) under reflux. It is very selective for monosalts, but only methyl phosphonates are very reactive. The corresponding acids were then obtained in quantitative yields with a cation exchange resin (sulfate acid).

PHOSPHONATE-CONTAINING ANALOGS OF CHOLESTERYL ESTER AS NOVEL INHIBITORS OF CHOLESTERYL ESTER TRANSFER PROTEIN

Pietzonka, Thomas,Damon, Robert,Russell, Mary,Wattanasin, Sompong

, p. 1951 - 1954 (2007/10/03)

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