61423-61-8

Basic information

• Product Name: L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN
• Synonyms: 2-aminoethyl (R)-2,3-bis(hexadecyloxy)propyl hydrogen phosphate;1,2-DI-O-HEXADECYL-SN-GLYCERO-3-PHOSPHATIYLETHANOLAMINE;3-sn-Phosphatidylethanolamine, 1,2-dihexadecyl, L-β,γ-Dihexadecyl-α-cephalin;Dihexadecylphosphatidylethanolamine;Phosphoric acid hydrogen (2-aminoethyl)[(R)-2,3-bis(hexadecyloxy)propyl] ester;L-b,g-Dihexadecyl-a-cephalin;L-β,γ-Dihexadecyl-α-cephalin;1,2-Di-O-hexadecyl-sn-glycero-3-phosphoethanolamine
• CAS NO: 61423-61-8
• Molecular Formula: C37H78NO6P
• Molecular Weight: 663.99
• EINECS: 262-782-1
• Mol File: 61423-61-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 699.2 ºC
• Flash Point: 376.6 ºC
• Appearance: /
• Density: 0.961 g/cm³
• Vapor Pressure: 2.12E-21mmHg at 25°C
• Refractive Index: 1.469
• Storage Temp.: −20°C
• BRN: 2029302
• CAS DataBase Reference: L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN(CAS DataBase Reference)
• NIST Chemistry Reference: L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN(61423-61-8)
• EPA Substance Registry System: L-BETA,GAMMA-DIHEXADECYL-ALPHA-CEPHALIN(61423-61-8)

Safety Data

• WGK Germany: 3
• F: 10-21
• Hazardous Substances Data: 61423-61-8(Hazardous Substances Data)

Usage

Definition

ChEBI: A dialkylglycerophosphoethanolamine in which the alkyl groups are hexadecyl and the glycerol core has sn stereochemistry with the phosphoethanolamine unit at position 3.

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

Upstream product

• 74123-29-8 1,2-di-O-hexadecyl-rac-glycero-3-phosphoric acid dichloride 
• 6076-35-3 1,2-dihexadecylglycerol 
• 124770-91-8 2-(2,3-Bis-hexadecyloxy-propoxy)-[1,3,2]oxazaphospholidine 2-oxide 

Relevant articles and documents

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

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.