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  2. 1,4-Butanediol - Wikipedia

    en.wikipedia.org/wiki/1,4-Butanediol

    1,4-Butanediol, also called Butane-1,4-diol (other names include 1,4-B, BD, BDO and 1,4-BD), [5] is a primary alcohol and an organic compound with the formula HOCH 2 CH 2 CH 2 CH 2 OH. . It is a colorless viscous liquid first synthesized in 1890 via acidic hydrolysis of N,N'-dinitro-1,4-butanediamine by Dutch chemist Pieter Johannes Dekkers, who called it "tetramethylene glyco

  3. Butanediol - Wikipedia

    en.wikipedia.org/wiki/Butanediol

    Isobutylene glycol may be considered a kind of butylene glycol, similarly to butane historically including n-butane and i-butane (isobutane). The modern name for the closely related type of compounds is methylpropanediol. There are two stable structural isomers: 2-methylpropane-1,2-diol; 2-methylpropane-1,3-diol

  4. 1,2-Butanediol - Wikipedia

    en.wikipedia.org/wiki/1,2-Butanediol

    1,2-Butanediol is a byproduct of the production of 1,4-butanediol from butadiene. [8] It is also a byproduct of the catalytic hydrocracking of starches and sugars such as sorbitol to ethylene glycol and propylene glycol. [9] It can also be obtained from the dihydroxylation of but-1-ene by OsO 4.

  5. 2,3-Butanediol - Wikipedia

    en.wikipedia.org/wiki/2,3-Butanediol

    2,3-Butanediol is the organic compound with the formula (CH 3 CHOH) 2. It is classified as a vic -diol ( glycol ). It exists as three stereoisomers, a chiral pair and the meso isomer.

  6. 1,4-Butanedithiol - Wikipedia

    en.wikipedia.org/wiki/1,4-Butanedithiol

    It is also used in polyadditions along with 1,4-butanediol to form sulfur-containing polyester and polyurethanes containing diisocyanate. [ 5 ] [ 6 ] [ 7 ] Several of these polymers are considered biodegradable and many of their components are sourced from non-petroleum oils.

  7. 1,3-Butanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Butanediol

    1,3-Butanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 OH, not to be confused with 1,4 Butanediol. With two alcohol functional groups, the molecule is classified as a diol . The compound without the R (or D) designation is racemic, which is what has been used in most studies before 2023.

  8. (R,R)-butanediol dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/(R,R)-butanediol_dehydrogenase

    Thus, the two substrates of this enzyme are (R,R)-butane-2,3-diol and NAD +, whereas its 3 products are (R)-acetoin, NADH, and H +. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor. The systematic name of this enzyme class is (R,R)-butane-2,3-diol:NAD ...

  9. Category:Butane - Wikipedia

    en.wikipedia.org/wiki/Category:Butane

    Pages in category "Butane" The following 11 pages are in this category, out of 11 total. ... 1,2-Butanediol; 2,3-Butanediol; D. Butane (data page) 1,4-Dichlorobutane ...