171597-35-6

Basic information

• Product Name: 1-stearoyl-2-benzylglycerophosphocholine
• Synonyms: 1-stearoyl-2-benzylglycerophosphocholine
• CAS NO: 171597-35-6
• Molecular Weight: 613.816
• Mol File: 171597-35-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-stearoyl-2-benzylglycerophosphocholine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-stearoyl-2-benzylglycerophosphocholine(171597-35-6)
• EPA Substance Registry System: 1-stearoyl-2-benzylglycerophosphocholine(171597-35-6)

Safety Data

• Hazardous Substances Data: 171597-35-6(Hazardous Substances Data)

Upstream product

• 55357-38-5 choline tosylate 
• 85647-89-8 (S)-1-stearoyl-2-O-benzyl-sn-glycerol 
• 171505-42-3 Octadecanoic acid (R)-2-benzyloxy-3-[(2-chloro-ethoxy)-hydroxy-phosphoryloxy]-propyl ester 
• 75-50-3 trimethylamine 
• 14690-00-7 2-O-benzylglycerol 
• 111-63-7 vinyl stearate 
• 171505-41-2 Octadecanoic acid (R)-2-benzyloxy-3-oxo-propyl ester 
• 57-11-4 stearic acid 

Downstream Products

• 27098-24-4 trimethyl (2-{[(2R)-2-[(9Z,12Z)-octadeca-9,12-dienoyloxy]-3-(octadecanoyloxy)propylphosphonato]oxy}ethyl)azanium 
• 143447-36-3 (9Z,11E)-(S)-13-(1-Methoxy-1-methyl-ethylperoxy)-octadeca-9,11-dienoic acid (R)-2-[((S)-2,3-dihydroxy-propoxy)-hydroxy-phosphoryloxy]-1-octadecanoyloxymethyl-ethyl ester; compound with ammonia 
• 143447-37-4 (9Z,11E)-(S)-13-Hydroperoxy-octadeca-9,11-dienoic acid (R)-2-[((S)-2,3-dihydroxy-propoxy)-hydroxy-phosphoryloxy]-1-octadecanoyloxymethyl-ethyl ester; compound with ammonia 
• 65886-80-8 (4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid (S)-1-hydroxymethyl-2-octadecanoyloxy-ethyl ester 
• 19420-57-6 1-stearoyl-sn-glycero-3-phosphocholine 

Relevant articles and documents

A Regioselective, Stereoselective Synthesis of a Diacylglycerophosphocholine Hydroperoxide by use of Lipoxygenase and Lipase

1-Stearoyl-2--sn-glycero-3-phosphocholine (11) was synthesized without contamination by any regio- and stereo-chemical isomers by a combination of lipoxygenase-catalysed peroxidation, lipase-catalysed stearo

Enzymatic synthesis of phosphatidylinositol bearing polyunsaturated acyl group

A new route for the synthesis of phosphatidylinositol (PI) having a polyunsaturated fatty acyl group was developed by using lipase and phospholipase C as biocatalysts to supplement the normal chemical reactions.

Asymmetric synthesis of diacylglycerophosphocholine hydroperoxide VIa, lipoxygenase-catalyzed hydroperoxidation of linoleic acid and lipase-catalyzed enantioselective stearoylation of 2-O-benzoyl-1,3-propanediol

Phosphatidylcholine hydroperoxide (11) bearing (S)-13-hydroperoxy-9Z,11E-octadecadienoic acid has been synthesized for the first time using lipoxygenase and lipase in addition to conventional chemical methods.As an extension of the study, lipase-catalyzed