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1-Dodecanoyl-sn-glycero-3-phosphocholine

Base Information
  • Chemical Name:1-Dodecanoyl-sn-glycero-3-phosphocholine
  • CAS No.:20559-18-6
  • Molecular Formula:C20H42 N O7 P
  • Molecular Weight:439.52
  • Hs Code.:2923900090
  • UNII:V4Z2U6E9RE
  • DSSTox Substance ID:DTXSID50942749
  • Wikidata:Q27145041
  • Metabolomics Workbench ID:14990
  • ChEMBL ID:CHEMBL566871
  • Mol file:20559-18-6.mol
1-Dodecanoyl-sn-glycero-3-phosphocholine

Synonyms:20559-18-6;1-Dodecanoyl-sn-glycero-3-phosphocholine;L-alpha-Lysophosphatidylcholine, lauroyl;1-lauroyl-sn-glycero-3-phosphocholine;1-Dodecanoyllysolecithin;L-ALPHA-LYSOPHOSPHATIDYLCHOLINE,LAUROYL;V4Z2U6E9RE;1-Dodecanoyl-sn-glycerol-3-phosphorylcholine;CHEBI:74966;PC(12:0/0:0);1-Lauroyl-2-hydroxy-sn-glycero-3-phosphocholine;1-Lauroyl-L-alpha-phosphorylcholine;[(2R)-3-dodecanoyloxy-2-hydroxypropyl] 2-(trimethylazaniumyl)ethyl phosphate;alpha-L-Lysophosphatidylcholine dodecyl;Choline, hydroxide, dihydrogen phosphate, inner salt, 3-ester with 1-monolaurin, L-;Laurin, 1-mono-, 3-(dihydrogen phosphate), monoester with choline hydroxide, inner salt, L-;MFCD00133434;1-Lauroyl-2-lysolecithin;LYSOPC 12;UNII-V4Z2U6E9RE;1-Lauroyllysophosphatidylcholine;CHEMBL566871;DTXSID50942749;1-dodecanoyllysophosphatidylcholine;C12-LYSOPHOSPHATIDYLCHOLINE;LMGP01050009;Lauroyl-L-alpha-Lysophosphatidylcholine;.alpha.-L-Lysophosphatidylcholine dodecyl;L-.alpha.-Lysophosphatidylcholine, lauroyl;E78450;Q27145041;(R)-3-(dodecanoyloxy)-2-hydroxypropyl 2-(trimethylammonio)ethyl phosphate;12:0 Lyso PC, 1-lauroyl-2-hydroxy-sn-glycero-3-phosphocholine, powder;3-(Dodecanoyloxy)-2-hydroxypropyl 2-(trimethylazaniumyl)ethyl phosphate;(2R)-3-(dodecanoyloxy)-2-hydroxypropyl 2-(trimethylazaniumyl)ethyl phosphate;(R)-3-(Dodecanoyloxy)-2-hydroxypropyl (2-(trimethylammonio)ethyl) phosphate;2-[[(2R)-3-dodecanoyloxy-2-hydroxy-propoxy]-hydroxy-phosphoryl]oxyethyl-trimethyl-ammonium;Dodecanoyl-sn-glycero-3-phosphocholine (isomer 1) (LPC(12:0) i1) dagger double dagger;3,5,9-TRIOXA-4-PHOSPHAHENEICOSAN-1-AMINIUM, 4,7-DIHYDROXY-N,N,N-TRIMETHYL-10-OXO-, INNER SALT, 4-OXIDE, (7R)-;3,5,9-Trioxa-4-phosphaheneicosan-1-aminium, 4,7-dihydroxy-N,N,N-trimethyl-10-oxo-, inner salt, 4-oxide, (R)-

Suppliers and Price of 1-Dodecanoyl-sn-glycero-3-phosphocholine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 17 raw suppliers
Chemical Property of 1-Dodecanoyl-sn-glycero-3-phosphocholine
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:114.93000 
  • Density:g/cm3 
  • LogP:4.08940 
  • Storage Temp.:−20°C 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:20
  • Exact Mass:439.26988968
  • Heavy Atom Count:29
  • Complexity:460
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O
  • Isomeric SMILES:CCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O
Technology Process of 1-Dodecanoyl-sn-glycero-3-phosphocholine

There total 2 articles about 1-Dodecanoyl-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:
Guidance literature:
L-glycero-3-phosphorylcholine; With di(n-butyl)tin oxide; In isopropyl alcohol; for 1h; Heating;
n-dodecanoyl chloride; With TEA; In isopropyl alcohol; at 20 ℃; for 0.583333h; Further stages.;
DOI:10.1039/b604636c
Guidance literature:
With water; phospholipase A2;
DOI:10.1021/j100288a018
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