1-OCTADECANOYL-2-[CIS-9-OCTADECENOYL]-SN-GLYCERO-3-PHOSPHOCHOLINE

Base Information

• Chemical Name: 1-OCTADECANOYL-2-[CIS-9-OCTADECENOYL]-SN-GLYCERO-3-PHOSPHOCHOLINE
• CAS No.: 56421-10-4
• Molecular Formula: C₄₄H₈₆NO₈P
• Molecular Weight: 788.142
• Mol file: 56421-10-4.mol

Synonyms:3,5,9-Trioxa-4-phosphaheptacosan-1-aminium,4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxo-9-octadecenyl)oxy]-, inner salt,4-oxide, [R-(Z)]-;3,5,9-Trioxa-4-phosphaheptacosan-1-aminium,4-hydroxy-N,N,N-trimethyl-10-oxo-7-[[(9Z)-1-oxo-9-octadecenyl]oxy]-, innersalt, 4-oxide, (7R)- (9CI);Choline phosphate, 3-ester with L-2-oleo-1-stearin(6CI);1-Stearoyl-2-oleoyl-sn-glycero-3-phosphocholine;L-a-1-Stearoyl-2-oleoyl lecithin;L-a-1-Stearoyl-2-oleoylphosphatidylcholine;

Chemical Property of 1-OCTADECANOYL-2-[CIS-9-OCTADECENOYL]-SN-GLYCERO-3-PHOSPHOCHOLINE

Chemical Property:

• PSA: 121.00000
• LogP: 13.01840
• Storage Temp.: −20°C

Purity/Quality:

98%min ^*data from raw suppliers

2-?Oleoyl-?1-?stearoyl-?sn-?glycero-?3-?phosphocholine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Description: SOPC; PC(18:0/18:1), also known as 1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine, is an asymmetrical phospholipid with saturated fatty acid (stearic acid/18:0) at sn-1 position and unsaturated fatty acid (oleic acid/18:1) at sn-2 position.
• Uses: 2-?Oleoyl-?1-?stearoyl-?sn-?glycero-?3-?phosphocholine is used in the assembly of various supported lipid bilayers.

Technology Process of 1-OCTADECANOYL-2-[CIS-9-OCTADECENOYL]-SN-GLYCERO-3-PHOSPHOCHOLINE

There total 1 articles about 1-OCTADECANOYL-2-[CIS-9-OCTADECENOYL]-SN-GLYCERO-3-PHOSPHOCHOLINE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

picric acid ; trimethyl-(2-bromo-ethyl)-ammonium picrate (57188-54-2) + Silber-benzyl-β-oleoyl-γ-stearoyl-L-α-glycerol-phosphat → 1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine (56421-10-4)

Guidance literature:

Multistep reaction; (i), (ii) NaI, Hg;

upstream raw materials:

picric acid ; trimethyl-(2-bromo-ethyl)-ammonium picrate