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17966-25-5

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17966-25-5 Usage

Common Use

Ingredient in personal care products and cosmetics

Function

Surfactant and emulsifying agent

Purpose

Mixes oil and water-based ingredients in skincare products

Application

Lotions, creams, and cleansers

Primary Role

Stabilizes and binds different components of products

Consistency

Ensures a consistent and smooth texture

Additional Role

Acts as a skin conditioning agent

Effect on Skin

Softens and smooths the skin

Nature

Mild and gentle

Suitability

Wide range of skincare and cosmetic formulations

Check Digit Verification of cas no

The CAS Registry Mumber 17966-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,6 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17966-25:
(7*1)+(6*7)+(5*9)+(4*6)+(3*6)+(2*2)+(1*5)=145
145 % 10 = 5
So 17966-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C39H77O8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(40)45-35-37(36-46-48(42,43)44)47-39(41)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h37H,3-36H2,1-2H3,(H2,42,43,44)

17966-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-octadecanoyloxy-3-phosphonooxypropyl) octadecanoate

1.2 Other means of identification

Product number -
Other names 1,2-di-O-stearoyl-rac-3-glycerophosphate

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:17966-25-5 SDS

17966-25-5Relevant articles and documents

Protection of phosphate with the 9-fluorenylmethyl group. Synthesis of unsaturated-acyl phosphatidylinositol 4,5-bisphosphate

Watanabe, Yutaka,Nakamura, Tomoko,Mitsumoto, Hiroyuki

, p. 7407 - 7410 (2007/10/03)

Alkyl di-(9-fluorenylmethyl) phosphates obtained via phosphitylation were found to be suitable for protection of phosphoric monoesters, which were generated by treatment of the triesters with DBU or triethylamine This strategy and a hydroxyl protecting gr

A new approach to the synthesis of phosphatidic acids and their analogs

Smirnova, L.I.,Malenkovskaya, M. A.,Predvoditelev, D. A.,Nifant'ev, E. E.

, p. 1011 - 1019 (2007/10/02)

The synthesis of phosphatidic acids, their monoamides and dialkyl esters, and thiophosphatidic acids was realized on the basis of the amidophosphites of 1,2-diacylglycerols and 1,2-isopropylideneglycerol.

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