enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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]

  5. File:1,4-butanedithiol.svg - Wikipedia

    en.wikipedia.org/wiki/File:1,4-butanedithiol.svg

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses ...

  6. 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]

  7. Dithiane - Wikipedia

    en.wikipedia.org/wiki/Dithiane

    1,3-Dithiane is an organosulfur compound with the formula CH 2 S 2 C 3 H 6. It is one of three isomers of the formula (CH 2) 4 S 2. The 1,3-isomer arises by the reaction of 1,3-propanedithiol with formaldehyde. [1] 1,3-Dithianes are sometimes used as protecting group of carbonyl-containing compounds.

  8. 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 ]

  9. Dithioerythritol - Wikipedia

    en.wikipedia.org/wiki/Dithioerythritol

    Dithioerythritol (DTE) is a sulfur containing sugar alcohol derived from the corresponding 4-carbon monosaccharide erythrose. It is an epimer of dithiothreitol (DTT). The molecular formula for DTE is C 4 H 10 O 2 S 2 .

  1. Related searches 1 4 butanedithiol diacetate sds card for 100 free phone chat line numbers

    what is 1 4 butynediolbutane 1 4 diol