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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 called it "tetramethylene glyco
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
The direct esterification of succinic acid with 1,4-butanediol is the most common way to produce PBS. It consists of a two step process. It consists of a two step process. First, an excess of the diol is esterified with the diacid to form PBS oligomers with elimination of water .
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 ...
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 ...
Example of a 1,2-diol (Ethyleneglycol, top),a 1,3-diol (1,3-Propanediol, middle)and a 1,4-diol (1,4-Butanediol, bottom).An alkanediol, composed of alkane and diol, are a group of substances consisting of linear or branched hydrocarbon chains containing exactly two hydroxy groups at different positions.
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.
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]