Dipalmitoylphosphatidylserine

Base Information

• Chemical Name: Dipalmitoylphosphatidylserine
• CAS No.: 3036-82-6
• Molecular Formula: C₃₈H₇₄NO₁₀P
• Molecular Weight: 735.98
• UNII: HE802C2TFR
• DSSTox Substance ID: DTXSID201307601
• Nikkaji Number: J3.047.187C
• Wikidata: Q27896139
• Mol file: 3036-82-6.mol

Synonyms:dipalmitoylphosphatidylserine;DPPS

Chemical Property of Dipalmitoylphosphatidylserine

Chemical Property:

• Vapor Pressure: 7.46E-27mmHg at 25°C
• Boiling Point: 782.6°Cat760mmHg
• Flash Point: 427.1°C
• PSA: 181.49000
• Density: 1.057g/cm³
• LogP: 9.86960
• Storage Temp.: −20°C
• Solubility.: chloroform: 25 mg/mL, clear, colorless
• XLogP3: 9.9
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 40
• Exact Mass: 735.50503455
• Heavy Atom Count: 50
• Complexity: 875

Purity/Quality:

98%Min ^*data from raw suppliers

1,2-Dipalmitoyl-rac-glycero-3-phospho-L-serine ~98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(C(=O)O)N)OC(=O)CCCCCCCCCCCCCCC
• Isomeric SMILES: CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OC[C@@H](C(=O)O)N)OC(=O)CCCCCCCCCCCCCCC

Technology Process of Dipalmitoylphosphatidylserine

There total 12 articles about Dipalmitoylphosphatidylserine 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: 95.0%

O-benzyl O-[(S)-2-(benzyloxycarbonyl)-2-(benzyloxycarbonylamino)ethyl] O-[1,2-di-(O-palmitoyl)-sn-glycer-3-yl] phosphate (1240407-85-5) → dipalmitoylphosphatidyl-L-serine (3036-82-6,40290-42-4,40290-43-5,72904-02-0)

Guidance literature:

With palladium 10% on activated carbon; hydrogen; In acetic acid; at 20 ℃; for 48h;

DOI:10.1007/s00726-009-0447-0

Reference yield: 85.0%

1,2-dipalmitoyl-sn-glycerol-3-phosphoryl-N-Troc-serine → dipalmitoylphosphatidyl-L-serine (3036-82-6,40290-42-4,40290-43-5,72904-02-0)

Guidance literature:

With acetic acid; zinc; at 25 ℃; for 7h;

Reference yield:

O-(1,2-O-dipalmitoyl-sn-3-glyceryl) O- O-phenyl phosphate → dipalmitoylphosphatidyl-L-serine (3036-82-6,40290-42-4,40290-43-5,72904-02-0)

Guidance literature:

With hydrogen; platinum(IV) oxide;

upstream raw materials:

1,2-di-O-hexacecanoyl-3-O-benzyl-sn-glycerol

1,2-dipalmitoyl-sn-glycerol

1-hexadecylcarboxylic acid

O-benzyl O-[(S)-2-(benzyloxycarbonyl)-2-(benzyloxycarbonylamino)ethyl] O-[1,2-di-(O-palmitoyl)-sn-glycer-3-yl] phosphate

Downstream raw materials:

1,2-dipalmitoyl-sn-glycero-3-phosphatidic acid

C₃₇H₇₁O₁₁P

C₃₇H₇₁O₁₀P

C₃₇H₇₂NO₉P

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