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D2636

Sigma-Aldrich

Dipalmitin

≥99.0%

Synonym(s):

Glycerol 1,2(3)-dihexadecanoate

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About This Item

Empirical Formula (Hill Notation):
C35H68O5
CAS Number:
26657-95-4
Molecular Weight:
568.91
EC Number:
247-886-7
MDL number:
MFCD00216843
UNSPSC Code:
12352211
PubChem Substance ID:
329798747
NACRES:
NA.25

biological source

synthetic (organic)

Assay

≥99.0%

form

powder

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC

InChI

1S/2C35H68O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-31-33(36)32-40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-32-33(31-36)40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h2*33,36H,3-32H2,1-2H3

InChI key

UJTQAHPLAOYWPB-UHFFFAOYSA-N

Other Notes

Approx. 50% 1,2- and 50% 1,3-isomer.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Konstantin Balashev et al.
Biochimica et biophysica acta, 1768(1), 90-99 (2006-11-07)
An important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme structure and behaviour in organized molecular media that mimic in-vivo systems. In this study we demonstrate the use of AFM as a tool to study
S Handwerger et al.
Placenta, 13(1), 55-62 (1992-01-01)
The dynamics of prolactin release from human decidual explants were studied under basal conditions, in response to decidual prolactin-releasing factor (PRL-RF), and in response to PRL-RF in the presence of decidual prolactin release-inhibitory factor (PRL-IF) or other factors known to
H De Boeck et al.
Biochemistry, 28(18), 7439-7446 (1989-09-05)
The interaction of four diacylglycerols (DAGs) with multilamellar phospholipid bilayers consisting either of dipalmitoylphosphatidylcholine (DPPC) or of a mixture of DPPC and bovine liver phosphatidylcholine (BL-PC) extracts was investigated by a combination of 31P and 2H NMR spectrometry. We found
D R Kodali et al.
Chemistry and physics of lipids, 52(3-4), 163-170 (1990-02-01)
The acyl migration of 1,2-dipalmitoyl-sn-glycerol (1,2-DPG) to 1,3-dipalmitoylglycerol (1,3-DPG) in different states, neat, in the presence of egg yolk lecithin (sonicated and unsonicated) and on silica gel was studied. The isomerization was quantitated by scanning densitometry of charred TLC plates
E Randell et al.
Biochimica et biophysica acta, 1124(3), 273-278 (1992-03-25)
Production of [3H]1,2-dipalmitoylglycerol ([3H]DAG) from 1-palmitoyl-2-[9,10-3H]palmitoyl-sn-glycero-3-phosphocholine and [3H]phosphorylcholine from 1,2-dipalmitoyl-sn-glycero-3-[Me-3H]phosphocholine was studied using sonicated rat platelets. The formation of [3H]DAG and [3H]phosphorylcholine occurred at a comparable rate. [3H]Phosphorylcholine formation was dependent on the concentration of the substrate, platelet sonicates and
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