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P9667

Sigma-Aldrich

Metil palmitoleato

≥99% (capillary GC), liquid

Sinonimo/i:

Metil cis-9-esadecenoato, Metil estere dell’acido palmitoleico

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About This Item

Formula condensata:
CH3(CH2)5CH=CH(CH2)7COOCH3
Numero CAS:
1120-25-8
Peso molecolare:
268.43
Beilstein:
1726111
Numero CE:
214-303-2
Numero MDL:
MFCD00042911
Codice UNSPSC:
12352211
ID PubChem:
24899053
NACRES:
NA.25

Origine biologica

Macadamia integrifolia oil

Livello qualitativo

200

Saggio

≥99% (capillary GC)

Forma fisica

liquid

Indice di rifrazione

n20/D 1.451 (lit.)

P. eboll.

180-183 °C/1 mmHg (lit.)

Punto di fusione

−0.5-0.5 °C (lit.)

Densità

0.875 g/mL at 25 °C (lit.)

Gruppo funzionale

ester

Tipo di lipide

unsaturated FAs

Condizioni di spedizione

ambient

Temperatura di conservazione

−20°C

Stringa SMILE

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-
IZFGRAGOVZCUFB-HJWRWDBZSA-N

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Applicazioni


  • 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).

Confezionamento

Sealed ampule.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113.0 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Methyl arachidate ≥99% (capillary GC)

Sigma-Aldrich

A3881

Methyl arachidate

Methyl tetracosanoate ≥99.0% (capillary GC)

Sigma-Aldrich

L6766

Methyl tetracosanoate

Methyl cis-13-docosenoate analytical standard

Supelco

45659

Methyl cis-13-docosenoate

Palmitoleic acid ≥98.5% (GC), liquid

Sigma-Aldrich

P9417

Palmitoleic acid

Methyl elaidate ≥99% (capillary GC)

Sigma-Aldrich

E4762

Methyl elaidate

Methyl oleate analytical standard

Supelco

75160

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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