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Key Documents

P9667

Sigma-Aldrich

Methyl palmitoleate

≥99% (capillary GC), liquid

Synonym(s):

Methyl cis-9-hexadecenoate, Palmitoleic acid methyl ester

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About This Item

Linear Formula:
CH3(CH2)5CH=CH(CH2)7COOCH3
CAS Number:
Molecular Weight:
268.43
Beilstein:
1726111
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

biological source

Macadamia integrifolia oil

Quality Level

Assay

≥99% (capillary GC)

form

liquid

refractive index

n20/D 1.451 (lit.)

bp

180-183 °C/1 mmHg (lit.)

mp

−0.5-0.5 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

functional group

ester

lipid type

unsaturated FAs

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCC\C=C/CCCCCCCC(=O)OC

InChI

1S/C17H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h8-9H,3-7,10-16H2,1-2H3/b9-8-

InChI key

IZFGRAGOVZCUFB-HJWRWDBZSA-N

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Application


  • Bioprospection of the Antarctic Diatoms Craspedostauros ineffabilis IMA082A and Craspedostauros zucchelli IMA088A.: This study investigates the bioprospective potential of Antarctic diatoms, identifying bioactive compounds including methyl palmitoleate that could be used in pharmaceuticals and nutraceuticals (Trentin et al., 2024).

Packaging

Sealed ampule.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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C Rentel et al.
Electrophoresis, 20(12), 2329-2336 (1999-09-28)
Miniaturized separation techniques such as capillary electrochromatography (CEC), pressurized capillary electrochromatography (pCEC) and capillary high performance liquid chromatography (CHPLC) have been coupled to a new detection technique: coordination ion spray mass spectrometry (CIS-MS). Electrospray ionization (ESI) has found widespread applications
P W Wertz et al.
Journal of dermatological science, 1(1), 33-37 (1990-01-01)
The goal of the present study was to determine whether topically applied fatty acid esters enter into epidermal lipid metabolism. Of special interest with respect to epidermal function were the linoleate-rich O-acylsphingolipids thought to be essential in maintenance of the
Eleftheria Diakogiannaki et al.
The Journal of endocrinology, 194(2), 283-291 (2007-07-21)
Long-chain saturated and monounsaturated fatty acids differ in their propensity to induce beta-cell death in vitro with palmitate (C16:0) being cytotoxic, whereas palmitoleate (C16:1n-7) is cytoprotective. We now show that this cytoprotective capacity extends to a poorly metabolised C16:1n-7 derivative
Saeedeh Noushini et al.
Scientific reports, 10(1), 19799-19799 (2020-11-15)
Diverse methods have been used to sample insect semiochemicals. Sampling methods can differ in efficiency and affinity and this can introduce significant biases when interpreting biological patterns. We compare common methods used to sample tephritid fruit fly rectal gland volatiles
Zsuzsanna Grózer et al.
Virulence, 6(1), 85-92 (2015-02-06)
Prostaglandins are C20 fatty acid metabolites with diverse biological functions. In mammalian cells, prostaglandins are produced from arachidonic acid (AA) via cyclooxygenases (COX1 and COX2). Although fungi do not possess cyclooxygenase homologues, several pathogenic species are able to produce prostaglandins from

Protocols

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

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