methyl linoleate

methyl linoleate

[′meth·əl lə′nō·lē‚āt]
(organic chemistry)
C19H34O2 A combustible, colorless liquid with a boiling point of 212°C; soluble in alcohol and ether; used in the manufacture of detergents, emulsifiers, lubricants, and textiles, and in medical research.
References in periodicals archive ?
Five ester compounds, namely methyl oleate, methyl linoleate, isopropyl myristate, methyl octadecanoate and methyl hexadecanoate except above a repellent response was found against all the three bedbug stages (Table 5).
To estimate the solubility parameters of the methyl esters, a mixture model with the five major components of methyl esters (methyl palmitate, methyl stearate, methyl oleate, methyl linoleate, and methyl linolenate) was created by using Amorphous Cell.
The scientists compared the formation of conjugated dienes from methyl linoleate in the presence of antioxidants to the control, which had no antioxidant.
An alternative synthesis procedure was developed by dissolving nonmodified or partially acetylated) sucrose or inulin in DMAA (n, N-dimethylacetamide), adding sunflower oil or methyl linoleate, and reacting the mixture at 140[degree]C.
The oxidative and crosslinking ability of iron salt combination with reducing agents was studied for model system consisting of either neat ethyl linoleate or methyl linoleate, in the case of diluted aqueous emulsions.
J, Ming, W, Oyman, ZO, van der Linde, R, "Oxidation of Methyl Linoleate in Micellar Solutions Induces by the Combination Iron (II)/Ascorbic Acid and Iron(II)/[H.
Butylated hydroxyanisole, butyl ptolyl sulfide, 6-methyl-4-chromanone, 5,6-dimethoxy1-indanone, palmitic acid, methyl linoleate, 5-methoxypsoralen were obtained from Aldrich (Milwaukee, WI, USA).
Several identified compounds (but ylated hydroxyanisole, butyl p-tolyl sulfide, 6-methyl-4chromanone, 5,6-dimethoxy- 1-indanone, palmitic acid, methyl linoleate, 5-methoxypsoralen) were commercially available and were tested for their antiproliferative activity.
These results suggest that the antiproliferative activity of butylated hydroxyanisole, 5,6-dimethoxy-1-indanone, palmitic acid and methyl linoleate is not associated to induction of differentiation; on the contrary, the antiproliferative activity of butyl-p-tolyl sulfide, 6-methyl-4-chromanone and 5-methoxypsolaren is associated to activation of the differentiation pattern of K562 cells.
The scientists compared the formation of conjugated diene from methyl linoleate in the presence of antioxidants to the control, which contained no antioxidants.