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22094-20-8

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22094-20-8 Usage

Uses

New lipids in food protein hydrolyzates.

Check Digit Verification of cas no

The CAS Registry Mumber 22094-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22094-20:
(7*2)+(6*2)+(5*0)+(4*9)+(3*4)+(2*2)+(1*0)=78
78 % 10 = 8
So 22094-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H41ClO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(24)25-19-20(23)18-22/h20,23H,2-19H2,1H3

22094-20-8SDS

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 1-chloro-3,3-dihydroxyhenicosan-4-one

1.2 Other means of identification

Product number -
Other names Octadecanoic acid,3-chloro-2-hydroxypropyl 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:22094-20-8 SDS

22094-20-8Downstream Products

22094-20-8Relevant articles and documents

Maerker et al.

, p. 2681,2686 (1961)

Synthesis of novel zwitterionic heterogemini surfactants derived from fatty acid and investigation of their behavior at the air-water interface

Yu, Erlei,Mamat, Xamxikamar,Zhang, Yagang,Eli, Wumanjiang

, p. 591 - 597 (2016/10/05)

A series of novel cationic-non-ionic heterogemini surfactants (Cn-1EC-s-Cm where n and m represents the hydrocarbon chain length of fatty acid and aliphatic amine, n=12, 14, 16, 18, m=12, 14, 16) were synthesized from fatty acid, epichlorohydrin and aldciphatic amine. The chemicals tructures of the surfactants were characterized by IR spectra, NMR, ESI-MS and elemental analysis. Their critical micelle concentrations (CMC) in the aqueous solutions were determined by surface-tension at 25°C.Relationship betweenγcmc and hydrophobic chain length was established which showed a large increase upon increasing of chain length with ester. The surface-tension measurements of Cn-1EC-s-Cm showed a low CMC, which greatly improve the efficiency in lowering the surface tension. Furthermore, adsorption and micellization behavior of Cn-1EC-s-Cm were investigated by measuring minimum average area per surfactant molecule and standard free energy.

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