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P9667

Sigma-Aldrich

Methyl palmitoleate

≥99% (capillary GC), liquid

Sinónimos:

Methyl cis-9-hexadecenoate, Palmitoleic acid methyl ester

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About This Item

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

origen biológico

Macadamia integrifolia oil

Ensayo

≥99% (capillary GC)

Formulario

liquid

índice de refracción

n20/D 1.451 (lit.)

bp

180-183 °C/1 mmHg (lit.)

mp

−0.5-0.5 °C (lit.)

densidad

0.875 g/mL at 25 °C (lit.)

grupo funcional

ester

tipo de lípido

unsaturated FAs

Condiciones de envío

ambient

temp. de almacenamiento

−20°C

cadena 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-

Clave InChI

IZFGRAGOVZCUFB-HJWRWDBZSA-N

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Aplicación


  • 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).

Envase

Sealed ampule.

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

235.4 °F - closed cup

Punto de inflamabilidad (°C)

113.0 °C - closed cup

Equipo de protección personal

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
SLCL9246
SLCH0807
SLCF0841
SLBX9802
SLBT4523

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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
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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