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Citric acid 1-[2-hydroxy-3-(stearoyloxy)propyl] ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50825-78-0

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50825-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50825-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,2 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50825-78:
(7*5)+(6*0)+(5*8)+(4*2)+(3*5)+(2*7)+(1*8)=120
120 % 10 = 0
So 50825-78-0 is a valid CAS Registry Number.

50825-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-2-[2-(2-hydroxy-3-octadecanoyloxypropoxy)-2-oxoethyl]butanedioic acid

1.2 Other means of identification

Product number -
Other names Glyceryl stearate citrate

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:50825-78-0 SDS

50825-78-0Upstream product

50825-78-0Downstream Products

50825-78-0Relevant academic research and scientific papers

Method for preparing monofatty acid glyceride citrate in aqueous phase

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Paragraph 0028; 0031-0033; 0036-0038; 0041-0043; 0046-0048, (2019/07/04)

The invention provides a method for preparing monofatty acid glyceride citrate in an aqueous phase. The method comprises the steps: adding epichlorohydrin and citric acid as starting raw materials, and performing two steps of reactions including esterification and ring opening in the presence of a reaction aid in an aqueous phase so as to produce the monofatty acid glyceride citrate. According tothe method for preparing the monofatty acid glyceride citrate in an aqueous phase, the cheap and easily available epichlorohydrin is adopted as a starting raw material, a reaction is performed on theepichlorohydrin with citric acid in the presence of polytetrafluoroethylene particles (PTFE), a phase transfer catalyst and alkali in the aqueous environment so as to obtain a compound 1 quantitatively, and then the ring-opening reaction is performed on the compound 1 and stearic acid so as to prepare the monofatty acid glyceride citrate; and the preparation method has mild reaction conditions, easily available reaction reagents, a high reaction yield and high selectivity, and the final product has high purity and a broad commercial application prospect.

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