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Butanone, also known as methyl ethyl ketone (MEK) or ethyl methyl ketone, [a] is an organic compound with the formula CH 3 C(O)CH 2 CH 3. This colorless liquid ketone has a sharp, sweet odor reminiscent of acetone. It is produced industrially on a large scale, but occurs in nature only in trace amounts. [7]
Little is known about the long-term safety of raspberry ketone supplements, [15] [16] especially since little research has been done with humans. [17] Toxicological models indicate a potential for cardiotoxic effects, as well as effects on reproduction and development. [15]
1.3807 at 15.9 °C Abbe number: 32 Dielectric constant, ε r: 18.5 ε 0 at 20 °C Bond strength: 2.67 pa Bond length: r. Bond angle? Magnetic susceptibility? Surface tension: 23.9 dyn/cm at 25 °C Viscosity [1] 0.5429 mPa·s at 0 °C 0.4284 mPa·s at 20 °C 0.3490 mPa·s at 40 °C 0.2482 mPa·s at 80 °C
Butan-2-yl (sec-butyl) group is chiral. The carbon atom at position 2 is a stereocenter. It has four different groups attached: −H, −CH 3, −CH 2 −CH 3, and −R (the R group is not equal to those three groups). The names of the two chiral groups are: (2S)-butan-2-yl and (2R)-butan-2-yl.
1,2,3,4-Butanetetracarboxylic acid is an organic compound with the formula HO 2 CCH 2 CH(CO 2 H)CH(CO 2 H)CH 2 CO 2 H. It is one of the simplest stable tetracarboxylic acids. The compound exists as two diastereomers, meso and the (R,R)/(S,S) pair. All are white solids. The compound is produced by oxidation of tetrahydrophthalic anhydride. [1]
Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry.It is a colorless liquid with a slight peppermint or camphor odor. It is a precursor to triazolylpinacolone in the synthesis of the fungicide triadimefon and in synthesis of the herbicide metribuzin.
n-Butylamine is an organic compound (specifically, an amine) with the formula CH 3 (CH 2) 3 NH 2. This colourless liquid is one of the four isomeric amines of butane, the others being sec-butylamine, tert-butylamine, and isobutylamine. It is a liquid having the fishy, ammonia-like odor common to amines. The liquid acquires a yellow color upon ...
2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 (UTC). Text is available under the Creative Commons Attribution ...