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19805-23-3

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19805-23-3 Usage

General Description

()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate is a chemical compound that belongs to the class of phosphonates. It is an ester derivative of hexadecanoic acid and contains a hydroxyphosphinoyloxy group attached to a 2-aminoethoxy substituted hydroxypropyl chain. ()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate has potential applications in the fields of pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. It may act as a surfactant, emulsifier, or stabilizer in various formulations, and further research may unveil its potential uses in drug delivery systems or as a corrosion inhibitor. However, further studies are required to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19805-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19805-23:
(7*1)+(6*9)+(5*8)+(4*0)+(3*5)+(2*2)+(1*3)=123
123 % 10 = 3
So 19805-23-3 is a valid CAS Registry Number.

19805-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1)-3-(((2-Aminoethoxy)hydroxyphosphinoyl)oxy)-2-hydroxypropyl hexadecanoate

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:19805-23-3 SDS

19805-23-3Downstream Products

19805-23-3Relevant articles and documents

Rapid tin-mediated access to a lysophosphatidylethanolamine (LPE) library: Application to positional LC/MS analysis for hepatic LPEs in non-alcoholic steatohepatitis model mice

Furukawa, Takayuki,Fuda, Hirotoshi,Miyanaga, Satoshi,Watanabe, Chinatsu,Chiba, Hitoshi,Hui, Shu-Ping

, p. 133 - 138 (2016/10/11)

Even though lysophospholipids have attracted much interest in recent years on account of their unique bioactivity, research related to lysophospholipids is usually hampered by problems associated with standard sample preparation and discrimination of regioisomers. Herein, we demonstrate a quick tin-chemistry-based synthetic route to lysophosphatidylethanolamines (LPEs) and its application in the positional analysis of hepatic LPEs in non-alcoholic steatohepatitis (NASH) model mice. We found that the preference of hepatic LPE regioisomer largely depends on the unsaturation of acyl chain in both control and NASH model mice. In addition, hepatic C18:2-LPE and C20:5-LPE levels were significantly lower in the NASH model mice than those in the control. The LC/MS technique based on the library of LPE regioisomers allows an accurate observation of hepatic LPE metabolism and might provide useful information to elucidate yet ambiguous pathogenesis of NASH.

The synthesis of phospholipids. I. Phosphatidyl and lysophosphatidyl ethanolamines.

Billimoria,Lewis

, p. 1404 - 1412 (2007/10/12)

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