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Merck

75100

Sigma-Aldrich

Ethyl oleate

tested according to Ph. Eur.

Sinónimos:

Ethylis oleas, Oleic acid ethyl ester

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About This Item

Fórmula lineal:
CH3(CH2)7CH=CH(CH2)7COOC2H5
Número de CAS:
Peso molecular:
310.51
Beilstein:
1727318
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
En este momento no podemos mostrarle ni los precios ni la disponibilidad

Agency

tested according to Ph. Eur.

Formulario

liquid

índice de refracción

n20/D 1.451 (lit.)

bp

216-218 °C/15 mmHg

mp

−32 °C (lit.)

densidad

0.87 g/mL at 25 °C (lit.)

grupo funcional

ester

cadena SMILES

CCCCCCCC\C=C/CCCCCCCC(=O)OCC

InChI

1S/C20H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h11-12H,3-10,13-19H2,1-2H3/b12-11-

Clave InChI

LVGKNOAMLMIIKO-QXMHVHEDSA-N

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Aplicación

Ethyl oleate can be used as a reactant in the:
  • Bouveault−Blanc reduction to synthesize primary alcohols in the presence of stabilized alkali metals.[1]
  • Lipase-catalyzed synthesis of ceramides by reacting with phytosphingosine.[2]
  • Synthesis of amides via direct amidation with amines in the presence of transition metal catalyst.[3]

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves


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Chemical and thermochemical aspects of the ozonolysis of ethyl oleate: Decomposition enthalpy of ethyl oleate ozonide.
Cataldo F.
Chemistry and Physics of Lipids, 175, 41-49 (2013)
Michael D Hardy et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(27), 8187-8192 (2015-06-24)
Cell membranes are dynamic structures found in all living organisms. There have been numerous constructs that model phospholipid membranes. However, unlike natural membranes, these biomimetic systems cannot sustain growth owing to an inability to replenish phospholipid-synthesizing catalysts. Here we report
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Oxidative medicine and cellular longevity, 2020, 3938672-3938672 (2020-08-11)
Beta-hydroxy-beta-methylbutyrate (HMB), a naturally occurring leucine metabolite, has been shown to attenuate plantar flexor muscle loss and increase myogenic stem cell activation during reloading after a period of significant muscle wasting by disuse in old rodents. However, it was less
K J Dussan et al.
Bioresource technology, 101(24), 9542-9549 (2010-08-19)
Magnetic nanoparticles were prepared by coprecipitating Fe(2+) and Fe(3+) ions in a sodium hydroxide solution and used as support for lipase. The lipase-coated particles were applied in a reactive extraction process that allowed separation of the products formed during transesterification.
Shujauddin Changi et al.
ChemSusChem, 5(9), 1743-1757 (2012-08-29)
We examined the behavior of phenylalanine in high-temperature water (HTW) at 220, 250, 280, and 350 °C. Under these conditions, the major product is phenylethylamine. The minor products include styrene and phenylethanol (1-phenylethanol and 2-phenylethanol), which appear at higher temperatures and

Questions

  1. Is butylated hydroxyanisole (BHA) added as a preservative to the product with the number 75100-1L, Ethyl Oleate? This has been determined to be present through LC-MS analysis.

    1 answer
    1. The product contains butylated hydroxyanisole (BHA), with a maximum value of 0.012%.

      Helpful?

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