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About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and for production of methyl methacrylate and bisphenol A, which are precursors to widely used plastics. [23] [24] It is a common building block in organic chemistry. It serves as a solvent in household products such as nail polish remover and paint thinner.
Acetone is a vaporization additive, mainly used with methanol racing fuel; Butyl rubber (as polyisobutylene succinimide, detergent to prevent fouling of diesel fuel injectors) Ferrous picrate, used in diesel fuel to increase fuel conversion efficiency and reduce emissions; Two-stroke oil, for lubrication of small engines reliant on crankcase ...
This includes supplements which contain a listed chemical, regardless of their dosage form or packaging and regardless of whether the chemical mixture, drug product or dietary supplement is exempt from regulatory controls. For each chemical, its illicit manufacturing use is given in parentheses.
Acetone is a chemical used to remove nail polish from your nails or as a household cleaner. It also occurs naturally in your body, facilitating ketosis.
The chemical name acetone peroxide is most commonly used to refer to the cyclic trimer, the product of a reaction between two precursors, hydrogen peroxide and acetone, in an acid-catalyzed nucleophilic addition, although monomeric and dimeric forms are also possible. [18] [19] Synthesis of tri-cyclic acetone peroxide.
It can be used with nonpolar compounds, but cannot accommodate complex chemistry. Reichardt's dye, a solvatochromic dye that changes color in response to polarity, gives a scale of E T (30) values. E T is the transition energy between the ground state and the lowest excited state in kcal/mol, and (30) identifies the dye.
It used molasses as feedstock and had 96 fermenters with a volume of 96,000 gallons each. [8] After World War II, ABE fermentation became generally non-profitable, compared to the production of the same three solvents (acetone, butanol, ethanol) from petroleum. [1] During the 1950s and 1960s, ABE fermentation was replaced by petroleum chemical ...
General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]