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Safety Information

P8180

Sigma-Aldrich

DL-α-Phosphatidylcholine, distearoyl

≥98%

Synonym(s):

1,2-Distearoyl-rac-glycero-3-phosphocholine

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About This Item

Empirical Formula (Hill Notation):
C44H88NO8P
CAS Number:
816-93-3
Molecular Weight:
790.15
MDL number:
MFCD00067532
UNSPSC Code:
12352211
PubChem Substance ID:
24898915
NACRES:
NA.25

Quality Level

200

Assay

≥98%

form

powder

functional group

phospholipid

lipid type

phosphoglycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC[N](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC

InChI

1S/C44H89NO8P/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,(H,48,49)

InChI key

OIBGDBRKAPVPMZ-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG8886
BCBW0789
BCBQ9446
BCBQ8834V
BCBQ8834

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PLoS neglected tropical diseases, 5(12), e1429-e1429 (2011-12-30)
Vaccines that activate strong specific Th1-predominant immune responses are critically needed for many intracellular pathogens, including Leishmania. The requirement for sustained and efficient vaccination against leishmaniasis is to formulate the best combination of immunopotentiating adjuvant with the stable antigen (Ag)
Yoshiyuki Hattori et al.
Chemical & pharmaceutical bulletin, 59(11), 1386-1392 (2011-11-02)
Histone deacetylase inhibitor (HDACI), suberoylanilide hydroxamic acid (SAHA), approved by the Food and Drug Administration (FDA) for the treatment of cutaneous T cell lymphoma, is a promising new treatment strategy for various cancers. In this study, we hypothesized that a
Alejandro Perdomo-Ortiz et al.
The journal of physical chemistry. B, 116(35), 10757-10770 (2012-08-14)
Two-dimensional fluorescence spectroscopy (2D FS) is applied to determine the conformation and femtosecond electronic population transfer in a dimer of magnesium meso tetraphenylporphyrin. The dimers are prepared by self-assembly of the monomer within the amphiphilic regions of 1,2-distearoyl-sn-glycero-3-phosphocholine liposomes. A
Xiaoming Xu et al.
International journal of pharmaceutics, 423(2), 410-418 (2011-12-31)
A mathematical model has been developed to predict the encapsulation efficiency of hydrophilic drugs in unilamellar liposomes, and will be useful in formulation development to rapidly achieve optimized formulations. This model can also be used to compare drug encapsulation efficiencies
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