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Mequinol is a common active ingredient in topical drugs used for skin depigmentation.As a topical drug mequinol is often mixed with tretinoin, a topical retinoid.A common formulation for this drug is an ethanolic solution of 2% mequinol and 0.01% tretinoin by mass. [1]
Its chemical names are based on considering the structure as either an acetyl (methyl-ketone) analog of anisole. Other names It can also be seen as a methyl ether analog of acetophenone. Acetanisole is found naturally in castoreum, the glandular secretion of the beaver. [1]
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Propylene glycol methyl ether acetate (PGMEA, 1-methoxy-2-propanol acetate) is a P-type glycol ether used in inks, coatings, and cleaners. It is sold by Dow Chemical under the name Dowanol PMA, [ 3 ] by Shell Chemical under the name methyl proxitol acetate, [ 4 ] [ 5 ] and by Eastman under the name PM Acetate.
2-Methoxyethanol, or methyl cellosolve, is an organic compound with formula C 3 H 8 O 2 that is used mainly as a solvent.It is a clear, colorless liquid with an ether-like odor.
Anisyl acetate (4-methoxybenzyl acetate) is an acetate ester of anisyl alcohol. It is a naturally occurring flavor found in various fruits and types of vanilla . [ 1 ] It is also used as a flavoring agent to produce a flavor profile described variously as sweet, smooth, fruity (cherry or plum) and vanilla or almond.
The conversion of methyl acetate back into its components, by an acid, is a first-order reaction with respect to the ester. The reaction of methyl acetate and a base, for example sodium hydroxide, is a second-order reaction with respect to both reactants. Methyl acetate is a Lewis base that forms 1:1 adducts with a variety of Lewis acids.
Olefin metathesis has been widely studied. One of the synthesis pathways for octyl methoxycinnamate includes cross metathesis. The high efficiency of the nitro-Grela catalyst has been used in the cross metathesis of trans-anethole with 2-ethylhexyl acrylate to produce octyl methoxycinnamate (86% yield).