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Hexadecanoic acid, 1-(hydroxymethyl)-2-(phenylmethoxy)ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22128-35-4

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22128-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22128-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,2 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22128-35:
(7*2)+(6*2)+(5*1)+(4*2)+(3*8)+(2*3)+(1*5)=74
74 % 10 = 4
So 22128-35-4 is a valid CAS Registry Number.

22128-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-benzyl-2-O-palmitoyl-rac-glycerol

1.2 Other means of identification

Product number -
Other names -

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:22128-35-4 SDS

22128-35-4Relevant academic research and scientific papers

Synthesis of 1-lyso-2-palmitoyl-rac-glycero-3-phosphocholine and its regioisomers and structural elucidation by NMR spectroscopy and FAB tandem mass spectrometry

Kim, Young-Ah,Park, Myoung-Soon,Kim, Young Hwan,Han, So-Yeop

, p. 2921 - 2928 (2007/10/03)

Three regioisomers of a naturally occurring lysophosphatidylcholine were chemically synthesized from glycerol. The phosphocholine moiety of the molecule was introduced by sequentially reacting with ethylene chlorophosphite, bromine, water, and trimethyl amine. Removal of a silyl protecting group of the hydroxyl group in the glycerol backbone was achieved without any accompanying acyl migration in the final stage of the synthesis by using NBS in a dimethyl sulfoxide-water cosolvent system. Structures of all regioisomers were compared by NMR spectroscopy and FAB tandem mass spectrometry.

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