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Methylpalmitat
97%
Synonym(e):
n-Hexadecansäuremethylester, Methyl-palmitat, Methylhexadecanoat
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About This Item
Lineare Formel:
CH3(CH2)14CO2CH3
CAS-Nummer:
Molekulargewicht:
270.45
Beilstein:
1780973
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352211
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Assay
97%
Brechungsindex
n20/D 1.4512 (lit.)
bp
185 °C/10 mmHg (lit.)
mp (Schmelzpunkt)
32-35 °C (lit.)
Dichte
0.852 g/mL at 25 °C (lit.)
SMILES String
CCCCCCCCCCCCCCCC(=O)OC
InChI
1S/C17H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h3-16H2,1-2H3
InChIKey
FLIACVVOZYBSBS-UHFFFAOYSA-N
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Tsutomu Ishioka et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(4), 671-680 (2003-03-01)
Normal mode analyses are made for methyl palmitate molecule having all-trans or conformational disorders around the ester head group, in order to explain characteristic observed frequency shifts in the wagging progressive region between all-trans and disorder chains in triglyceride molecules.
Ebtehal El-Demerdash
Toxicology and applied pharmacology, 254(3), 238-244 (2011-05-18)
Methyl palmitate (MP) has been shown earlier to inhibit Kupffer cells and rat peritoneal macrophages. To evaluate the potential of MP to inhibit the activation of other macrophages, RAW cells (macrophages of alveolar origin) were treated with varying concentrations of
Ari Gargir et al.
Biochimica et biophysica acta, 1569(1-3), 167-173 (2002-02-21)
The biological activities of many acylated molecules are lipid dependent. Lipids, however, are poorly immunogenic or non-immunogenic. We employed a phage display semi-synthetic human antibody library to isolate anti-lipid antibodies. Selection was done against methyl palmitate, a 16 carbon aliphatic
Eman M Mantawy et al.
Toxicology and applied pharmacology, 258(1), 134-144 (2011-11-15)
Fibrosis accompanies most chronic liver disorders and is a major factor contributing to hepatic failure. Therefore, the need for an effective treatment is evident. The present study was designed to assess the potential antifibrotic effect of MP and whether MP
Y N Wang et al.
Journal of economic entomology, 102(1), 196-202 (2009-03-04)
Walnut, Juglans regia L., is known for its insecticidal activities to a range of herbivores and microbes. Isolation and identification of bioactive compounds from walnut is a potential approach for the development of new pesticides. Laboratory experiments were carried out
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