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7057-92-3

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7057-92-3 Usage

General Description

Didodecyl hydrogen phosphate is a chemical compound with the formula C24H51O4P that is used as an emulsifying and stabilizing agent in various industrial applications. It is a long-chain alkyl phosphate ester, consisting of two dodecyl (C12) alkyl chains attached to a phosphate group. Didodecyl hydrogen phosphate is a surfactant, which means it has the ability to lower the surface tension between two substances and promote the formation of stable emulsions. It is commonly used in the production of personal care products, such as hair conditioners and lotions, as well as in the manufacturing of paints, coatings, and lubricants. Didodecyl hydrogen phosphate is also used in the formulation of agricultural products and in the textile industry as a fabric softener and antistatic agent. Additionally, it has potential applications in the pharmaceutical and food industries due to its emulsifying and stabilizing properties.

Check Digit Verification of cas no

The CAS Registry Mumber 7057-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,5 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7057-92:
(6*7)+(5*0)+(4*5)+(3*7)+(2*9)+(1*2)=103
103 % 10 = 3
So 7057-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H51O4P/c1-3-5-7-9-11-13-15-17-19-21-23-27-29(25,26)28-24-22-20-18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3,(H,25,26)

7057-92-3SDS

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 didodecyl hydrogen phosphate

1.2 Other means of identification

Product number -
Other names phosphoric acid didodecyl ester

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:7057-92-3 SDS

7057-92-3Downstream Products

7057-92-3Relevant articles and documents

pH-SENSITIVE CAPSULE MEMBRANES. REVERSIBLE PERMEABILITY CONTROL FROM THE DISSOCIATIVE BILAYER-COATED CAPSULE MEMBRANE BY AN AMBIENT pH CHANGE.

Okahata,Seki

, p. 8065 - 8070 (1984)

Nylon ultrathin capsules coated with synthetic bilayers having dissociative head groups (2C//1//2PO//4** minus , 2C//1//2-cys-2COO** minus , 2C//1//2-scu-COO** minus , and 2C//1//6-gly-NH//3** plus ) were prepared. Permeations through the membrane of a fluorescent probe trapped in the inner aqueous phase could be reduced by factors of 50-100 relative to that of the uncoated capsule and reversibly controlled by pH changes of the outer medium: in the case of the capsule coated with bilayers containing phosphate (2C//1//2PO//4** minus ) and carboxylate head groups (2C//1//2-cys-2COO** minus and 2C//1//2-suc-COO** minus ), the permeation was redused in the neutral medium, increased in the acidic medium, and reverted to the original slow rate in the neutral medium, depending on the dissociation of head groups of coating bilayers.

Two novel bi-functional hybrid materials constructed from POMs and a Schiff base with excellent third-order NLO and catalytic properties

Hu, Gonghao,Miao, Hao,Mei, Hua,Zhou, Shuai,Xu, Yan

supporting information, p. 7947 - 7951 (2016/06/01)

The first polyoxometalates modified by a porphyrin-resembling planar Schiff base have been successfully designed and synthesized under hydrothermal conditions. The third-order NLO responses indicated that they are excellent third-order NLO materials. Their catalytic performances are also investigated. The Royal Society of Chemistry.

POLYCATIONIZED PHOSPHOLIPID DERIVATIVES

-

Page/Page column 17, (2010/04/30)

The present invention provides novel phospholipid derivatives. Furthermore, the present invention provides lipid membrane structures excellent in gene/nucleic acid introduction efficiency into a cell.

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