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  2. 1,4-Butanedithiol - Wikipedia

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

    1,4-Butanedithiol is an organosulfur compound with the formula HSCH 2 CH 2 CH 2 CH 2 SH. It is a malodorous, colorless liquid that is highly soluble in organic solvents.

  3. 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

  4. 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.

  5. 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.

  6. 1,4-Butanediol diglycidyl ether - Wikipedia

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

    1,4-Butanediol diglycidyl ether (B14DODGE) is an organic chemical in the glycidyl ether family. It is aliphatic and a colorless liquid. It has two epoxide (oxirane) groups per molecule. [1] Its main use is in modifying epoxy resins especially viscosity reduction. [2] It is REACH registered. [3] The IUPAC name is 2-[4-(oxiran-2-ylmethoxy ...

  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]

  8. Diacetyl - Wikipedia

    en.wikipedia.org/wiki/Diacetyl

    A distinctive feature of diacetyl (and other vicinal diketones) is the long C–C bond linking the carbonyl centers. This bond distance is about 1.54 Å, compared to 1.45 Å for the corresponding C–C bond in 1,3-butadiene. The elongation is attributed to repulsion between the polarized carbonyl carbon centers. [2]

  9. Butane-1-thiol - Wikipedia

    en.wikipedia.org/wiki/Butane-1-thiol

    Butane-1-thiol, also known as butyl mercaptan, is a volatile, clear to yellowish liquid with a fetid (extremely foul-smelling) odor, commonly described as "skunk" odor. In fact, 1-butanethiol is structurally similar to several major constituents of a skunk's defensive spray but is not actually present in the spray. [ 4 ]