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P4273

Sigma-Aldrich

1,2-Diheptanoyl-sn-glycero-3-phosphocholine

solution, 20 mg/mL in chloroform, ~99% (GC)

Synonym(s):

L-α-Phosphatidylcholine, diheptanoyl

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About This Item

Empirical Formula (Hill Notation):
C22H44NO8P
CAS Number:
Molecular Weight:
481.56
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:

assay

~99% (GC)

form

solution

concentration

20 mg/mL in chloroform

storage temp.

−20°C

SMILES string

CCCCCCC(=O)OC[C@@H](COP(O)(=O)OCC[N](C)(C)C)OC(=O)CCCCCC

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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3

target_organs

Central nervous system, Liver,Kidney

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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J R Bian et al.
Biochemistry, 29(34), 7928-7935 (1990-08-28)
Small bilayer particles form spontaneously from gel-state long-chain phospholipids such as dipalmitoylphosphatidylcholine and 0.2 mol fraction short-chain lecithins (e.g., diheptanoyl-phosphatidylcholine). When the particles are incubated at temperatures greater than the Tm of the long-chain phosphatidylcholine (PC), the particles rapidly fuse
M Shinomiya et al.
Biochemical and biophysical research communications, 113(3), 811-816 (1983-06-29)
The effect of apolipoprotein C-II (apoC-II) on the lipoprotein lipase (LpL)-catalyzed hydrolysis of phospholipids was studied using purified bovine milk LpL and dihexanoyl (diC6) and diheptanoyl (diC7) phosphatidylcholine. In contrast to porcine pancreatic phospholipase A2, the LpL-catalyzed hydrolysis of these
B B Vinton et al.
The Biochemical journal, 330 ( Pt 3), 1433-1442 (1998-05-23)
The structure and phosphorylation of two protein kinase C (PKC) alpha substrate peptides were investigated in varying lipid systems using enzyme activity assays and circular dichroism (CD) spectroscopy. The alpha-peptide, which exhibits the typical PKC alpha substrate motif and is
M Y el-Sayed et al.
Biochimica et biophysica acta, 831(1), 133-141 (1985-09-20)
Phospholipase C (phosphatidylcholine cholinephosphohydrolase, EC 3.1.4.3) (Bacillus cereus) activity toward diheptanoylphosphatidylcholine is increased 50-100% by low concentrations of both positively and negatively charged detergents. Zwitterionic and nonionic detergents have no such activating effect. This charged detergent activation requires an interface
J P Ferreira et al.
Biochemistry, 32(32), 8098-8102 (1993-08-17)
Phospholipase A2 from Naja naja kaouthia venom was covalently coupled onto agarose beads using two different chemistries. The effect of micellar competitive inhibitors in the coupling media was evaluated. Enzyme bound to N-hydroxysuccinimide-activated agarose, which is reactive primarily toward epsilon-amino

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