Other grades of this product :
| Methyl Oleate Basic information |
| Methyl Oleate Chemical Properties |
| Melting point | -20 °C | | Boiling point | 218 °C/20 mmHg (lit.) | | density | 0.874 g/mL at 20 °C (lit.) | | vapor pressure | 10 mm Hg ( 205 °C) | | refractive index | n20/D 1.452(lit.) | | Fp | >230 °F | | storage temp. | -20°C | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | form | Oily Liquid | | color | Clear yellow to amber | | Specific Gravity | 0.875 (20/4℃) | | Water Solubility | Miscible with alcohol, ether and chloroform. Immiscible with water. | | Merck | 14,6828 | | BRN | 1727037 | | Stability: | Stable, but air and light sensitive. Incompatible with strong oxidizing agents. Combustible. | | InChIKey | QYDYPVFESGNLHU-KHPPLWFESA-N | | CAS DataBase Reference | 112-62-9(CAS DataBase Reference) | | NIST Chemistry Reference | 9-Octadecenoic acid (Z)-, methyl ester(112-62-9) | | EPA Substance Registry System | Methyl oleate (112-62-9) |
| Methyl Oleate Usage And Synthesis |
| Chemical Properties | colourless liquid | | Uses | Intermediate for detergents, emulsifiers, wet-ting agents, stabilizers, textile treatment, plasti-cizers for duplicating inks, rubbers, waxes, etc.;biochemical research, chromatographic referencestandard. | | Uses | 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 ink, rubber and wax. It finds application as lubricant and lubricant additive. | | Uses | Methyl oleate was used to study the catalytic potential of molybdenum oxide/bipyridinedicarboxylate hybrid material. | | Definition | ChEBI: A fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol. | | General Description | Clear to amber liquid. Insoluble in water. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | Esters, such as (Z)-9-Octadecenoic acid methyl ester, react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides | | Fire Hazard | Combustible | | Safety Profile | Questionable carcinogen with experimental tumorigenic data by skin contact. When heated to decomposition it emits acrid smoke and irritating fumes | | Purification Methods | Purify the oleate by fractional distillation under reduced pressure, and by low temperature crystallisation from acetone. Store it in the dark under N2. [Beilstein 2 IV 1649.] |
| Methyl Oleate Preparation Products And Raw materials |
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