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  2. 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.

  3. Butanediol - Wikipedia

    en.wikipedia.org/wiki/Butanediol

    2-methylpropane-1,2-diol; 2-methylpropane-1,3-diol; and one unstable geminal diol: 2-methylpropane-1,1-diol (not a glycol), hydrate of 2-methylpropanal (isobutyraldehyde) These three methylpropanediols are structural isomers of butanediols. They are not chiral.

  4. 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

  5. 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. With two alcohol functional groups, the molecule is classified as a diol.The compound is also chiral, but most studies do not distinguish the enantiomers.

  6. 1,4-Butanedithiol - Wikipedia

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

    Alkylation with geminal dihalides gives 1,3-dithiepanes. Oxidation gives the cyclic disulfide 1,2-dithiane: [3] HSCH 2 CH 2 CH 2 CH 2 SH + O → S 2 (CH 2) 4 + H 2 O. It forms self-assembled monolayers on gold. [4] It is also used in polyadditions along with 1,4-butanediol to form sulfur-containing polyester and polyurethanes containing ...

  7. 1,4-Butynediol - Wikipedia

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

    1,4-Butynediol is a precursor to 1,4-butanediol and 2-butene-1,4-diol by hydrogenation. It is also used in the manufacture of certain herbicides, textile additives, corrosion inhibitors, plasticizers, synthetic resins, and polyurethanes. It is the major raw material used in the synthesis of vitamin B 6. [5]

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  9. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    Examples include ethane-1,2-diol or ethylene glycol HO−(CH 2) 2 −OH, a common ingredient of antifreeze products. Another example is propane-1,2-diol, or alpha propylene glycol, HO−CH 2 −CH(OH)−CH 3, used in the food and medicine industry, as well as a relatively non-poisonous antifreeze product.

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