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61423-61-8

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  • Phosphoric acid,mono(2-aminoethyl) mono[(2R)-2,3-bis(hexadecyloxy)propyl] ester

    Cas No: 61423-61-8

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61423-61-8 Usage

Description

L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN, also known as a dialkylglycerophosphoethanolamine, is a phospholipid with hexadecyl alkyl groups and an sn stereochemistry glycerol core with the phosphoethanolamine unit at position 3. It plays a crucial role in the structure and function of biological membranes.

Uses

Used in Pharmaceutical Industry:
L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN is used as a pharmaceutical excipient for its emulsifying and stabilizing properties. It helps in the formulation of drug delivery systems, such as liposomes and emulsions, to improve the solubility, bioavailability, and targeted delivery of therapeutic agents.
Used in Cosmetic Industry:
L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN is used as an emollient and emulsifier in cosmetic formulations. It helps to maintain the skin's moisture balance, providing a smooth and soft texture while also improving the stability and consistency of cosmetic products.
Used in Food Industry:
L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN is used as an emulsifier in the food industry to stabilize mixtures of oil and water, preventing separation and improving the texture and appearance of food products.
Used in Research Applications:
L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN is used as a model membrane component in biophysical and biochemical research. It helps scientists study the properties and behavior of biological membranes, as well as the interactions between membrane components and other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 61423-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61423-61:
(7*6)+(6*1)+(5*4)+(4*2)+(3*3)+(2*6)+(1*1)=98
98 % 10 = 8
So 61423-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C37H78NO6P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-32-41-35-37(36-44-45(39,40)43-34-31-38)42-33-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h37H,3-36,38H2,1-2H3,(H,39,40)/t37-/m1/s1

61423-61-8 Well-known Company Product Price

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  • Sigma

  • (37161)  1,2-Dihexadecyl-sn-glycero-3-phosphoethanolamine  ≥99.0% (TLC)

  • 61423-61-8

  • 37161-100MG

  • 3,058.38CNY

  • Detail
  • Sigma

  • (37161)  1,2-Dihexadecyl-sn-glycero-3-phosphoethanolamine  ≥99.0% (TLC)

  • 61423-61-8

  • 37161-1G

  • 18,298.80CNY

  • Detail

61423-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoethyl [(2R)-2,3-dihexadecoxypropyl] hydrogen phosphate

1.2 Other means of identification

Product number -
Other names 3-sn-Phosphatidylethanolamine,1,2-dihexadecyl

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:61423-61-8 SDS

61423-61-8Downstream Products

61423-61-8Relevant articles and documents

A lipid-lipase aggregate with ether linkage as a new type of immobilized enzyme for enantio-selective hydrolysis in organic solvents

Akita,Umezawa,Matsukura,Oishi

, p. 318 - 324 (2007/10/02)

For the purpose of carrying out smoothly enzymatic reaction of water-insoluble substrates in organic solvents, a new type of immobilized enzyme, a lipid-lipase aggregate, was developed. In order to prepare various kinds of lipid-lipase aggregates, 27 kinds of dialkyl ether-type phospholipid analogues were newly synthesized and used for the preparation of aggregates with lipase. Thus obtained lipid-lipase aggregates were found to catalyze the enantioselective hydrolysis of the (+)-α-acyloxy ester 2 much more efficiently than lipase immobilized with synthetic prepolymer (ENTP-4000) in water-saturated isopropyl ether. Namely, the reaction time became much shorter (2 to 3 d for completion as compared with 21 d) and the chemical and optical yields of the reaction products were found to be high.

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