• In industrial chemical synthesis, acetylene reacts with two equivalents of formaldehyde to form butyne-1,4-diol. (wikipedia.org)
  • LyondellBasell manufactures 1,4-butanediol in a multi-step process without the use of acetylene. (alchetron.com)
  • [13] Berthelot's empirical formula for acetylene (C 4 H 2 ), as well as the alternative name " quadricarbure d'hydrogène " (hydrogen quadricarbide), were incorrect because many chemists at that time used the wrong atomic mass for carbon (6 instead of 12). (zirconiumbia515.sbs)
  • They are used, for example, for the extraction of butadiene from C 4 fractions, of acetylene from C 2 cracking fractions and of aromatics from aliphatics. (justia.com)
  • CO2-oxidative dehydrogenation of propane (CO2-ODHP) provides a promising route for propylene production. (dicp.ac.cn)
  • It is co-produced together with ethylene in steam crackers and also by refinery cat-crackers and, increasingly, dehydrogenation of propane. (orbichem.com)
  • Butane-1,4-diol is rapidly converted into gamma-hydroxybutyric acid by the enzymes alcohol dehydrogenase and aldehyde dehydrogenase, and differing levels of these enzymes may account for differences in effects and side effects between users. (wikipedia.org)
  • However, potentiation of ethanol's effects may simply be caused by competition for the alcohol dehydrogenase and aldehyde dehydrogenase enzymes with co-administered 1,4-butanediol. (wikipedia.org)
  • Hydrogenation of this aldehyde yields 1,4-butanediol. (alchetron.com)
  • Ruihua's technology for butadiene production by oxygen-enriched dehydrogenation of butenes uses different feeding methods and different feed compositions to solve the blockage of the second-stage reactor of the traditional oxidative dehydrogenation process and extend the catalyst operation cycle. (ruihuaeng.com)
  • Butane-1,4-diol is also used as a recreational drug known by some users as "One Comma Four", "Liquid Fantasy", "One Four Bee" or "One Four B-D-O". A few Federal Courts have stated that 1,4-butanediol exerts effects similar to gamma-hydroxybutyrate (GHB), which is a metabolic product of 1,4-butanediol. (wikipedia.org)
  • Hydrogenation of butyne-1,4-diol gives butane-1,4-diol. (wikipedia.org)
  • In research conducted for a Carnot Network project, the CEA is developing innovative LOHCs that leverage the reversible hydrogenation-dehydrogenation reactions of certain non-toxic organic compounds. (cea.fr)
  • A continuous reactor test bench was also designed during this phase of the research for further testing of the GBL-BDO hydrogenation-dehydrogenation reactions. (cea.fr)
  • Hydrogenation of 1,4-butynediol gives 1,4-butanediol. (alchetron.com)
  • Not only can the GBL molecules be synthesized from renewable resources, but the molecule-catalyst combination also demonstrates lower dehydrogenation enthalpy (41 kJ/molH2) than that of conventional LOHCs. (cea.fr)
  • 1,4-Butanediol , colloquially known as BD , is the organic compound with the formula HOCH 2 CH 2 CH 2 CH 2 OH. (alchetron.com)
  • World production of butane-1,4-diol was claimed to be about one million metric tons per year and market price is about US$ 2,000 (€ 1,600) per ton (2005). (wikipedia.org)
  • At about 200 °C in the presence of soluble ruthenium catalysts, the diol undergoes dehydrogenation to form butyrolactone. (wikipedia.org)
  • 20. The antioxidant according to claim 16, in which the substituents R 3 and R 4 or R 4 and R 5 , together with a part-structure --O--CH 2 --NR 7 --CH 2 -- oxygen-attached via the substituent R 4 form a second tetrahydrooxazine ring. (patentsencyclopedia.com)
  • This is because the same enzymes that are responsible for metabolizing alcohol also metabolize 1,4-butanediol so there is a strong chance of a dangerous drug interaction. (wikipedia.org)
  • however there is a study suggesting that 1,4-butanediol may have potential alcohol-like pharmacological effects on its own. (wikipedia.org)
  • This contradicts the hypothesis of butane-1,4-diol having inherent alcohol-like pharmacological effects. (wikipedia.org)
  • The allyl alcohol is then hydroformylated to 4-hydroxybutyraldehyde. (alchetron.com)
  • however there is a study suggesting that 1,4-butanediol may have potential alcohol-like pharmacological effects that are not due to this conversion. (alchetron.com)
  • Individuals have been prosecuted for possession of 1,4-butanediol under the Federal Analog Act as substantially similar to GHB. (wikipedia.org)
  • Butane-1,4-diol is used industrially as a solvent and in the manufacture of some types of plastics, elastic fibers and polyurethanes. (wikipedia.org)
  • World production of butane-1,4-diol was claimed to be about one million metric tons per year and market price is about US$ 2,000 (€ 1,600) per ton (2005). (wikipedia.org)
  • Butane-1,4-diol is also used as a recreational drug known by some users as "One Comma Four", "Liquid Fantasy", "One Four Bee" or "One Four B-D-O". A few Federal Courts have stated that 1,4-butanediol exerts effects similar to gamma-hydroxybutyrate (GHB), which is a metabolic product of 1,4-butanediol. (wikipedia.org)
  • Butane-1,4-diol is rapidly converted into gamma-hydroxybutyric acid by the enzymes alcohol dehydrogenase and aldehyde dehydrogenase, and differing levels of these enzymes may account for differences in effects and side effects between users. (wikipedia.org)
  • Butane-1,4-diol seems to have two types of pharmacological actions. (wikipedia.org)
  • The study arrived at this conclusion based on the finding that butane-1,4-diol coadministered with ethanol led to potentiation of some of the behavioral effects of ethanol. (wikipedia.org)
  • Another study found no effect following intracerebroventricular injection of butane-1,4-diol in rats. (wikipedia.org)
  • This contradicts the hypothesis of butane-1,4-diol having inherent alcohol-like pharmacological effects. (wikipedia.org)
  • Like gamma-hydroxybutyric acid, butane-1,4-diol is safe only in small amounts. (wikipedia.org)
  • While butane-1,4-diol is not currently scheduled federally in the United States, a number of states have classified 1,4-butanediol as a controlled substance. (wikipedia.org)
  • 1,4-Butanediol (Tetramethylene glycol) is commonly used as a solvent in the chemical industry to manufacture gamma-butyrolactone and elastic fibers like spandex. (milestone-suppliers.com)
  • γ-Butyrolactone is produced industrially by dehydrogenation of 1,4-butanediol at a temperature of 180-300 °C and atmospheric pressure in the presence of a copper catalyst. (gblmagic.com)
  • The industrial production of γ-Butyrolactone involves the dehydrogenation of 1,4-butanediol, carried out at a temperature ranging from 180 to 300 degrees Celsius under atmospheric pressure. (researchem.net)
  • In the presence of phosphoric acid and high temperature, it dehydrates to the important solvent tetrahydrofuran.At about 200 °C in the presence of soluble ruthenium catalysts, the diol undergoes dehydrogenation to form butyrolactone. (milestone-suppliers.com)
  • In comparison, the related compound 1,4-butanediol (1,4-B) tends to be slightly less potent, slower to take effect, but longer-acting than GHB. (researchem.net)