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P9667

Sigma-Aldrich

Methyl palmitoleate

≥99% (capillary GC), liquid

Sinônimo(s):

Methyl cis-9-hexadecenoate, Palmitoleic acid methyl ester

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About This Item

Fórmula linear:
CH3(CH2)5CH=CH(CH2)7COOCH3
Número CAS:
1120-25-8
Peso molecular:
268.43
Beilstein:
1726111
Número CE:
214-303-2
Número MDL:
MFCD00042911
Código UNSPSC:
12352211
ID de substância PubChem:
24899053
NACRES:
NA.25

fonte biológica

Macadamia integrifolia oil

Nível de qualidade

200

Ensaio

≥99% (capillary GC)

Formulário

liquid

índice de refração

n20/D 1.451 (lit.)

p.e.

180-183 °C/1 mmHg (lit.)

pf

−0.5-0.5 °C (lit.)

densidade

0.875 g/mL at 25 °C (lit.)

grupo funcional

ester

tipo de lipídio

unsaturated FAs

Condições de expedição

ambient

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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-

chave InChI

IZFGRAGOVZCUFB-HJWRWDBZSA-N

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Aplicação


  • 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).

Embalagem

Sealed ampule.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113.0 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
SLCL9246
SLCH0807
SLCF0841
SLBX9802
SLBT4523

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Sigma-Aldrich

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Supelco

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Palmitoleic acid ≥98.5% (GC), liquid

Sigma-Aldrich

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Sigma-Aldrich

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Supelco

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Methyl oleate

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
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
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
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
Xian-Guo Zou et al.
Journal of agricultural and food chemistry, 62(43), 10594-10603 (2014-10-10)
In the present study, a human milk fat substitute (HMFS) enriched in medium-chain fatty acids (MCFAs) was synthesized through acidolysis reaction from Cinnamomum camphora seed oil (CCSO) with oleic acid in a solvent-free system. A commercial immobilized lipase, Lipozyme RM
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