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Phenoxyethanol is used as a perfume fixative; an insect repellent; an antiseptic; [7] a solvent for cellulose acetate, dyes, inks, and resins; a preservative for pharmaceuticals, cosmetics and lubricants; [8] an anesthetic in fish aquaculture; [9] [10] and in organic synthesis. It is an alternative to formaldehyde-releasing preservatives. [11]
At 25°C, it is soluble in phenoxyethanol, dimethyl capramide, ethoxydiglycol, dimethyl isosorbide, and alcohol , which are ingredients used in cosmetics. [1] [10] ...
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH.It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils.
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Phenoxyethanol; Tyrosol; 1-phenyl-1,2-ethanediol This page was last edited on 7 July 2018, at 13:10 (UTC). Text is available under the Creative Commons ...
Ethanol Butanol. A primary alcohol is an alcohol in which the hydroxy group is bonded to a primary carbon atom. It can also be defined as a molecule containing a “–CH 2 OH” group. [1]
The flammable nature of the exhalations of wine was already known to ancient natural philosophers such as Aristotle (384–322 BCE), Theophrastus (c. 371 –287 BCE), and Pliny the Elder (23/24–79 CE). [5]
Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters.The reaction mainly applies to primary and secondary alcohols.
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