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1-hexadecyl-2-palmitoyl-sn-glycero-3-phosphocholine is a type of 2-acyl-1-alkyl-sn-glycero-3-phosphocholine, which is a class of glycerophospholipids. It consists of a hexadecanoyl (palmitoyl) acyl group and a hexadecyl alkyl group. 1-hexadecyl-2-palmitoyl-sn-glycero-3-phosphocholine plays a crucial role in the structure and function of cell membranes.

88587-94-4

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88587-94-4 Usage

Uses

Used in Pharmaceutical Industry:
1-hexadecyl-2-palmitoyl-sn-glycero-3-phosphocholine is used as a pharmaceutical agent for its potential therapeutic effects. It has been studied for its ability to modulate cellular processes and may have applications in the treatment of various diseases.
Used in Cosmetic Industry:
In the cosmetic industry, 1-hexadecyl-2-palmitoyl-sn-glycero-3-phosphocholine is used as an emulsifying agent. It helps to stabilize formulations by reducing the surface tension between oil and water, allowing for the creation of homogeneous mixtures.
Used in Research:
1-hexadecyl-2-palmitoyl-sn-glycero-3-phosphocholine is also used in research settings as a model compound to study the properties and functions of glycerophospholipids in biological systems. This helps scientists to better understand the role of these lipids in cellular processes and their potential as therapeutic targets.

Check Digit Verification of cas no

The CAS Registry Mumber 88587-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,8 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88587-94:
(7*8)+(6*8)+(5*5)+(4*8)+(3*7)+(2*9)+(1*4)=204
204 % 10 = 4
So 88587-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C40H82NO7P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-35-45-37-39(38-47-49(43,44)46-36-34-41(3,4)5)48-40(42)33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h39H,6-38H2,1-5H3/t39-/m1/s1

88587-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexadecyl-2-hexadecanoyl-sn-glycero-3-phosphocholine

1.2 Other means of identification

Product number -
Other names L-1-hexadecyl-2-palmitoyl-phosphatidylcholine

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:88587-94-4 SDS

88587-94-4Downstream Products

88587-94-4Relevant academic research and scientific papers

Enzymatic Release of Antitumor Ether Lipids by Specific Phospholipase A2 Activation of Liposome-Forming Prodrugs

Andresen, Thomas L.,Davidsen, Jesper,Begtrup, Mikael,Mouritsen, Ole G.,J?rgensen, Kent

, p. 1694 - 1703 (2004)

An enzymatically activated liposome-based drug-delivery concept involving masked antitumor ether lipids (AELs) has been investigated. This concept takes advantage of the cytotoxic properties of AEL drugs as well as the membrane permeability enhancing prop

An Efficient Stereocontrolled Route to Both Enantiomers of Platelet Activating Factor and Analogues with Long-Chain Esters at C2: Saturated and Unsaturated Ether Glycerolipids by Opening of Glycidyl Arenesulfonates

Guivisdalsky, Pedro N.,Bittman, Robert

, p. 4643 - 4648 (2007/10/02)

Both enantiomers of various ether/ester glycerophospholines (R)- and (S)-1, including platelet activating factor (PAF, 2), have been synthesized from arenesulfonate derivatives of glycidol ((R)- and (S)-3) that are readily available in high enantiomeric p

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