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Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH3)2CO. [ 22 ] It is the simplest and smallest ketone (>C=O). It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.
Carbon tetrachloride (data page) Butanone (data page) Vapor-liquid Equilibrium of Acetone/water[4] P = 760 mmHg. BP. Temp. °C. % by mole acetone. liquid.
Acetone peroxide (/ æsəˈtəʊn pɛrˈɒksaɪd / ⓘ also called APEX and mother of Satan[3][4]) is an organic peroxide and a primary explosive. It is produced by the reaction of acetone and hydrogen peroxide to yield a mixture of linear monomer and cyclic dimer, trimer, and tetramer forms. The monomer is dimethyldioxirane.
Acetone, the simplest ketone. In organic chemistry, a ketone / ˈkiːtoʊn / is an organic compound with the structure R−C (=O)−R', where R and R' can be a variety of carbon -containing substituents. Ketones contain a carbonyl group −C (=O)− (a carbon-oxygen double bond C=O).
Acetylacetone is an organic compound with the chemical formula CH3−C (=O)−CH2−C (=O)−CH3. It is classified as a 1,3- diketone. It exists in equilibrium with a tautomer CH3−C (=O)−CH=C (−OH)−CH3. The mixture is a colorless liquid. These tautomers interconvert so rapidly under most conditions that they are treated as a single ...
Deuterated acetone ( (CD 3) 2 CO), also known as acetone-d6, is a form (isotopologue) of acetone (CH 3) 2 CO in which the hydrogen atom (H) is replaced with deuterium (heavy hydrogen) isotope (2 H or D). Deuterated acetone is a common solvent used in NMR spectroscopy. [1]
Ketone bodies. Acetone. Acetoacetic acid. (R)- beta -Hydroxybutyric acid. Ketone bodies are water-soluble molecules or compounds that contain the ketone groups produced from fatty acids by the liver (ketogenesis). [1][2] Ketone bodies are readily transported into tissues outside the liver, where they are converted into acetyl-CoA (acetyl ...
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] The protecting group can be removed by hydrolysis of the ketal using dilute aqueous acid.
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