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P5177

Sigma-Aldrich

Methyl palmitate

≥99% (capillary GC)

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Synonym(s):
n-Hexadecanoic acid methyl ester, Methyl hexadecanoate, Palmitic acid methyl ester
Linear Formula:
CH3(CH2)14CO2CH3
CAS Number:
Molecular Weight:
270.45
Beilstein/REAXYS Number:
1780973
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

biological source

plant (palm)

Quality Level

assay

≥99% (capillary GC)

form

solid

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.)

functional group

ester

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

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

InChI key

FLIACVVOZYBSBS-UHFFFAOYSA-N

Gene Information

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General description

Methyl palmitate (PAME), a fatty acid ester of palmitic acid, is a muscurinic receptors antagonist. Methyl palmitate functions as a vasodilator and relaxes the arterioles in retina upon electrical depolarization. In the superior cervical ganglion, methyl palmitate modulates nicotinic receptor. Endogenous methyl palmitate modulates nicotinic receptor-mediated transmission in the superior cervical ganglion. PAME activates Kv7 channels and promotes perivascular adipose tissue.

Application

Methyl palmitate has been used to test impact of cerebral blood flow using laser doppler flowmetry (LDF) experiments and as a standard to determine retention indices (RIs) using gas chromatograph−mass spectrometer

related product

Product No.
Description
Pricing

wgk_germany

WGK 1

flash_point_f

235.4 °F

flash_point_c

113.0 °C

ppe

Eyeshields, Gloves, type N95 (US)


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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Endogenous methyl palmitate modulates nicotinic receptor-mediated transmission in the superior cervical ganglion
Lin HW, et al.
Proceedings of the National Academy of Sciences of the USA, 1051(49), 19526-19531 (2008)
Palmitic acid methyl ester and its relation to control of tone of human visceral arteries and rat aortas by perivascular adipose tissue
Wang N, et al.
Frontiers in Physiology, 9 (2018)
Terminal double bonds in the alkenes and acetates of defensive secretion from the thrips Suocerathrips linguis Mound & Marullo, 1994 (Thysanoptera: Phlaeothripidae)
Gehlsen U, et al.
Chemoecology, 19(2), 97-102 (2009)
Jiao Liu et al.
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Protocols

Protocol for GC Analysis of Bacterial Acid Methyl Esters (BAMEs) on Equity®-1

Separation of Methyl decanoate; Methyl dodecanoate; Methyl myristate; Methyl palmitate; Methyl caprylate; Methyl oleate; Methyl linoleate; Methyl linolenate; Methyl stearate

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