309931
Methyl palmitate
97%
Synonym(s):
n-Hexadecanoic acid methyl ester, Methyl hexadecanoate, Palmitic acid methyl ester
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About This Item
Linear Formula:
CH3(CH2)14CO2CH3
CAS Number:
Molecular Weight:
270.45
EC Number:
203-966-3
UNSPSC Code:
12352211
MDL number:
Beilstein/REAXYS Number:
1780973
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
InChI key
FLIACVVOZYBSBS-UHFFFAOYSA-N
SMILES string
CCCCCCCCCCCCCCCC(=O)OC
assay
97%
refractive index
n20/D 1.4512 (lit.)
bp
185 °C/10 mmHg (lit.)
mp
32-35 °C (lit.)
density
0.852 g/mL at 25 °C (lit.)
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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
Adriana Rodríguez-Rivera et al.
Journal of applied toxicology : JAT, 28(8), 1021-1026 (2008-07-16)
Liver fibrosis is characterized by an excess of collagen fiber deposition, and it is known that Kupffer cells play an important role by immunomodulation of the toxic response. Methyl palmitate (MP) is an effective Kupffer cell inhibitor. The aim of
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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