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1-O-HEXADECYL-2-ACETYL-SN-GLYCERO-3-PHOSPHOCHOLINE

Base Information
  • Chemical Name:1-O-HEXADECYL-2-ACETYL-SN-GLYCERO-3-PHOSPHOCHOLINE
  • CAS No.:74389-68-7
  • Molecular Formula:C26H54NO7P
  • Molecular Weight:523.691
  • Hs Code.:
  • UNII:42EWD89I80
  • DSSTox Substance ID:DTXSID00225377
  • Wikipedia:Platelet-activating_factor
  • Wikidata:Q420577
  • NCI Thesaurus Code:C16998
  • Pharos Ligand ID:NM8NKPBMTKJM
  • Metabolomics Workbench ID:14671
  • ChEMBL ID:CHEMBL1235246
  • Mol file:74389-68-7.mol
1-O-HEXADECYL-2-ACETYL-SN-GLYCERO-3-PHOSPHOCHOLINE

Synonyms:3,5,9-Trioxa-4-phosphapentacosan-1-aminium,7-(acetyloxy)-4-hydroxy-N,N,N-trimethyl-, inner salt, 4-oxide, (R)-;1-Hexadecyl-2-acetyl-sn-glycero-3-phosphocholine;1-O-Hexadecyl-2-O-acetyl-sn-glycero-3-phosphocholine;1-O-Hexadecyl-2-O-acetyl-sn-glyceryl-3-phosphorylcholine;1-O-Hexadecyl-2-acetyl-sn-glycero-3-phosphocholine;1-O-Hexadecyl-2-acetyl-sn-glycerophosphocholine;1-O-Hexadecyl-2-acetyl-sn-glyceryl-3-phosphorylcholine;1-O-Hexadecyl-platelet-activating factor; Blood platelet-activating factor;Blood platelet-activating factor acether; C16-PAF; C16-PAF acether; PAF; PAF16; PAF acether; Platelet-activating factor; Platelet-activating factor acether

Suppliers and Price of 1-O-HEXADECYL-2-ACETYL-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
  • TRC
  • PAF(C16)
  • 5mg
  • $ 140.00
  • Tocris
  • PAF(C16)
  • 1
  • $ 71.00
  • Sigma-Aldrich
  • β-Acetyl-γ-O-hexadecyl-L-α-phosphatidylcholine hydrate ≥98%
  • 5mg
  • $ 120.00
  • Sigma-Aldrich
  • β-Acetyl-γ-O-hexadecyl-L-α-phosphatidylcholine hydrate ≥98%
  • 1mg
  • $ 48.80
  • Sigma-Aldrich
  • Platelet Activating Factor-16
  • 1mg
  • $ 42.36
  • Sigma-Aldrich
  • β-Acetyl-γ-O-hexadecyl-L-α-phosphatidylcholine hydrate ≥98%
  • 10mg
  • $ 287.00
  • Sigma-Aldrich
  • Platelet Activating Factor-16
  • 5mg
  • $ 97.12
  • Sigma-Aldrich
  • β-Acetyl-γ-O-hexadecyl-L-α-phosphatidylcholine hydrate ≥98%
  • 25mg
  • $ 560.00
  • CSNpharm
  • PAF(C16)
  • 100mg
  • $ 703.00
  • Crysdot
  • PAF(C16) 95+%
  • 100mg
  • $ 703.00
Total 8 raw suppliers
Chemical Property of 1-O-HEXADECYL-2-ACETYL-SN-GLYCERO-3-PHOSPHOCHOLINE
Chemical Property:
  • Melting Point:247 °C 
  • PSA:103.93000 
  • LogP:6.69400 
  • Storage Temp.:−20°C 
  • Solubility.:Soluble in H2O or ethanol 
  • XLogP3:6.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:26
  • Exact Mass:523.36379006
  • Heavy Atom Count:35
  • Complexity:546
Purity/Quality:

97% *data from raw suppliers

PAF(C16) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22-38-40-48/20/22 
  • Safety Statements: 36/37-24/25-22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCCOCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)C
  • Isomeric SMILES:CCCCCCCCCCCCCCCCOC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)C
  • Uses PAF (C16) (cas# 74389-68-7) is a blood platelet-activating factor, used to study human airway smooth muscle cell line. C16-02:0 PC or 1-O-hexadecyl-2-acetyl-sn-glycero-3-phosphocholine may be used as a substrate in enzymatic lipoprotein-associated phospholipase A2 (Lp-PLA2) activity assay. It may also be used to study its physicochemical properties and its interaction with peptides derived from the C-terminal domains of human apolipoprotein E.
Technology Process of 1-O-HEXADECYL-2-ACETYL-SN-GLYCERO-3-PHOSPHOCHOLINE

There total 47 articles about 1-O-HEXADECYL-2-ACETYL-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:
In pyridine; at 50 ℃; for 8h;
Guidance literature:
Yield given. Multistep reaction;
DOI:10.1016/S0040-4039(00)87654-6
Guidance literature:
Yield given. Multistep reaction; deprotection and reacylation;
DOI:10.1016/S0040-4039(00)95277-8
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