Methyl oleate, 96%
Methyl oleate, 96%
Methyl oleate, 96%
Thermo Scientific Chemicals

Methyl oleate, 96%

CAS: 112-62-9 | C19H36O2 | 296.495 g/mol
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25 g
100 g
Catalog number H31358.14
also known as H31358-14
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150,00
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Quantity:
25 g
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Price (EUR)
150,00
Each
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Chemical Identifiers
CAS112-62-9
IUPAC Namemethyl (9E)-octadec-9-enoate
Molecular FormulaC19H36O2
InChI KeyQYDYPVFESGNLHU-ZHACJKMWSA-N
SMILESCCCCCCCC\C=C\CCCCCCCC(=O)OC
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥94.0%
Identification (FTIR)Conforms
Refractive Index1.4500-1.4560 @ 20°C
Methyl oleate is used as a chromatographic reference standard in biochemical research. It is also used as an intermediate for detergents, emulsifiers, wetting agents, stabilizers, textile treatments, plasticizers for duplicating inks, rubbers and waxes. It finds application as lubricants and lubricant additives.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Methyl oleate is used as a chromatographic reference standard in biochemical research. It is also used as an intermediate for detergents, emulsifiers, wetting agents, stabilizers, textile treatments, plasticizers for duplicating inks, rubbers and waxes. It finds application as lubricants and lubricant additives.

Solubility
Miscible with alcohol, ether and chloroform. Immiscible with water.

Notes
Air and light sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Zhao, H. Y.; Simon, S. L. Equilibrium free-radical polymerization of methyl methacrylate under nanoconfinement. Polymer 2015, 66, 173-178.
  2. Deruer, E.; Duguet, N.; Lemaire, M. Thiazolylidene-Catalyzed Cleavage of Methyl Oleate-Derived α-Hydroxy Ketone to the Corresponding Free Aldehydes. J. Neurosci. Methods 2015, 254, 86-93.