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Documentos Principais

V0384

Sigma-Aldrich

cis-Vaccenic acid

≥97% (capillary GC), oil

Sinônimo(s):

cis-11-Octadecenoic acid

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About This Item

Fórmula linear:
CH3(CH2)5CH=CH(CH2)9CO2H
Número CAS:
Peso molecular:
282.46
Beilstein:
1726565
Número MDL:
Código UNSPSC:
12352211
ID de substância PubChem:
NACRES:
NA.25

fonte biológica

Macadamia integrifolia oil

Nível de qualidade

Ensaio

≥97% (capillary GC)

forma

oil

Impurezas

<0.5% Trans-11 isomer

índice de refração

n20/D 1.459 (lit.)

pb

150 °C/0.03 mmHg (lit.)

pf

14-15 °C (lit.)

densidade

0.887 g/mL at 25 °C (lit.)

grupo funcional

carboxylic acid

tipo de lipídio

unsaturated FAs

Condições de expedição

ambient

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CCCCCC\C=C/CCCCCCCCCC(O)=O

InChI

1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h7-8H,2-6,9-17H2,1H3,(H,19,20)/b8-7-

chave InChI

UWHZIFQPPBDJPM-FPLPWBNLSA-N

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Aplicação


  • Enhancing durability and sustainable preservation of Egyptian stone monuments using metabolites produced by Streptomyces exfoliatus.: This research investigates the use of microbial metabolites, including cis-Vaccenic acid, to enhance the preservation of historical monuments (Abd-Elhalim et al., 2023). (Abd-Elhalim et al., 2023).

Embalagem

Sealed ampule

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Nervonic acid &#8805;99% (capillary GC)

Sigma-Aldrich

N1514

Nervonic acid

&#947;-Linolenic acid analytical standard

Supelco

62174

γ-Linolenic acid

D Lipinsky et al.
Pflugers Archiv : European journal of physiology, 425(1-2), 140-149 (1993-10-01)
To dissect the cellular events responsible for the prolonged latency of the response to thyrotropin-releasing hormone (TRH) in Xenopus oocytes we interfered with different steps of the signal transduction pathway. Preincubation of oocytes with cis-vaccenic acid (a membrane-fluidizing agent) shortened
A Shibahara et al.
FEBS letters, 264(2), 228-230 (1990-05-21)
The novel pathways of oleic acid formation from cis-vaccenic (cis-11-octadecenoic) acid and of cis-vaccenic acid formation from oleic acid by enzymatic positional isomerization have been proposed in higher plants, based on stable-isotope experiments using [2,2-2H2]cis-vaccenate or [2,2-2H2]oleate as an immediate
Juan J Loor et al.
The British journal of nutrition, 90(6), 1039-1048 (2003-12-04)
Cis 9, trans 11 (c 9, t11)-18:2 and trans 10, cis 12 (t10, c12)-18:2 are the major conjugated linoleic acid (CLA) isomers in dietary supplements which reduce milk fat content in nursing women. The present study evaluated the effects of
Arturo Anadón et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(2), 591-598 (2009-11-26)
The acute oral toxicity of a trans-10 C18:1-rich milk fat (T10, 20% of total FA), and a trans-11 C18:1+cis-9 trans-11 C18:2-rich milk fat (T11-CLA, 14% and 4.8% of total FA, respectively) was studied in rats receiving a single oral dose
Jihane Gasmi et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 20(8-9), 734-742 (2013-03-05)
Plant-derived non-essential fatty acids are important dietary nutrients, and some are purported to have chemopreventive properties against various cancers, including that of the prostate. In this study, we determined the ability of seven dietary C-18 fatty acids to cause cytotoxicity

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