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D8269

Sigma-Aldrich

Glyceryl 1,3-distearate

≥99% (TLC)

Synonym(s):

1,3-Dioctadecanoylglycerol, 1,3-Distearin, 1,3-Distearoylglycerol

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About This Item

Empirical Formula (Hill Notation):
C39H76O5
CAS Number:
504-40-5
Molecular Weight:
625.02
Beilstein:
1810306
EC Number:
207-992-6
MDL number:
MFCD00053741
UNSPSC Code:
12352211
PubChem Substance ID:
24894200
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

200

Assay

≥99% (TLC)

form

powder

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCC

InChI

1S/C39H76O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-35-37(40)36-44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h37,40H,3-36H2,1-2H3

InChI key

IZHVBANLECCAGF-UHFFFAOYSA-N

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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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G R Vantrappen et al.
Gastroenterology, 96(4), 1126-1134 (1989-04-01)
A synthetic "mixed" triglyceride (1,3-distearoyl,2[13C]octanoyl glycerol), having a medium-chain fatty acid in the 2 position, was evaluated as a substrate for an exocrine pancreatic function test by comparing the 13CO2 breath excretion with the lipase output in the duodenum in
H O Herrmann et al.
Molecular and biochemical parasitology, 3(5), 319-325 (1981-09-01)
A medium-chain O-alkylglycerol, 1-O-[1'-14C]dodecyl-sn-glycerol, has been found to be incorporated into plasmenyl ethanolamine by Leishmania donovani promastigotes as revealed by radio gas-liquid chromatography; however, the ether bond of the administered O-alkyl-glycerol was cleaved extensively as judged from the occurrence of
R Brasseur et al.
Biochemical and biophysical research communications, 127(3), 969-976 (1985-03-29)
Phorbol esters and diacylglycerols activate protein kinase C but specific structural parameters appear to be required for the enzyme activation. We have analyzed the conformation of potent and not potent diacylglycerols and phorbol esters. The orientation of the CH20H group
Richard O Adlof et al.
Journal of agricultural and food chemistry, 51(7), 2096-2099 (2003-03-20)
Symmetrical disaturated triacylglycerols of the structure SUS, where S is stearic acid (18:0) and U is an unsaturated fatty acid, either oleic (O; 9cis-18:1), linoleic (L; 9cis,12cis-18:2), or linolenic (Ln; 9cis,12cis,15cis-18:3), are important components providing functionality to interesterified fat blends
M C Luzardo et al.
Archives of biochemistry and biophysics, 363(1), 81-90 (1999-03-02)
The physical properties conferred to DPPC bilayers by including neoglycolipids composed by two different trisaccharides: mannose-mannose-mannose (3M) and glucose-mannose-glucose (GMG) attached to a cholesterol (cho) and a distearylglycerol (diC18) lipid moiety by a spacer were evaluated by means of the
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