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Molecule
ID:132698
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄₄H₈₈NO₈P
Molecular Mass
790.145181
Exact Mass
789.62475541
Charge
0
InChI
InChI=1S/C44H88NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h42H,6-41H2,1-5H3
InChIKey
NRJAVPSFFCBXDT-UHFFFAOYSA-N
Canonic Smiles
CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(OCC[N+](C)(C)C)[O-]
Isomeric Smiles
CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC
Calculated Properties
JChem
Acid pKa
1.8550572
H Acceptors
4
H Donor
0
LogD (pH = 5.5)
11.915575
LogD (pH = 7.4)
11.915671
Log P
9.892071
Molar Refractivity
234.2691
Polarizability
89.74931
Polar Surface Area
111.19
Rotatable Bonds
44
Lipinski's Rule of Five
false
Data Source
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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IUPAC name
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IUPAC Traditional name
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Synonyms
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MDL Number
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PubChem SID
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PubChem CID
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Product Information
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From Data Sources
Bioactivity
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Data Source
Academic Data
PubChem
65146
Commercial Catalog
Sigma Aldrich
P8180
Names and Identifiers
IUPAC name
(2-{[2,3-bis(octadecanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
IUPAC Traditional name
1,2-distearoyllecithin
Synonyms
1,2-Distearoyl-rac-glycero-3-phosphocholine
DL-α-Phosphatidylcholine, distearoyl
Registration numbers
CAS Number
816-93-3
MDL Number
MFCD00067532
PubChem SID
24898915
162226975
PubChem CID
65146
Properties
Safety Information
Storage Temperature
-20°C
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Product Information
Purity
≥98%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay