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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 ...
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. and one unstable geminal diol:
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 ...
1,4-Butanedithiol. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 1,4-Butanedithiol is an organosulfur compound with the formula HSCH2CH2CH2CH2SH. It is a malodorous, colorless liquid that is highly soluble in organic solvents.
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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]
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. The compound is a colorless, bittersweet, water-soluble liquid.
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