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  2. California Proposition 65 list of chemicals - Wikipedia

    en.wikipedia.org/wiki/California_Proposition_65...

    tert-Amyl methyl ether: 994-05-8 December 13, 2013 n-Butyl glycidyl ether: 2426-08-6 April 4, 2014 Chloramphenicol: 56-75-7 January 4, 2013 Chlorodibromomethane: 124-48-1 October 29, 1999 Chlorsulfuron: 64902-72-3 June 6, 2014 Cyclohexanol: 108-93-0 January 25, 2002 Diaminotoluene (mixed) – November 20, 2015 Dienestrol: 84-17-3 January 4 ...

  3. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    The tert-butoxide is a strong, non-nucleophilic base in organic chemistry. It readily abstracts acidic protons from substrates, but its steric bulk inhibits the group from participating in nucleophilic substitution, such as in a Williamson ether synthesis or an S N 2 reaction. tert-Butyl alcohol reacts with hydrogen chloride to form tert-butyl ...

  4. List of gasoline additives - Wikipedia

    en.wikipedia.org/wiki/List_of_gasoline_additives

    Isopropyl alcohol (IPA) n-butanol (BuOH) Gasoline grade t-butanol (GTBA) Ethers: Methyl tert-butyl ether (MTBE), now outlawed in many states of the U.S. for road use because of water contamination. Tertiary amyl methyl ether (TAME) Tertiary hexyl methyl ether (THEME) Ethyl tertiary butyl ether (ETBE) Tertiary amyl ethyl ether (TAEE) Diisopropyl ...

  5. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  6. tert-Butylthiol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylthiol

    tert-Butylthiol is the main ingredient in many gas odorant blends. [citation needed] It is always utilized as a blend of other compounds, typically dimethyl sulfide, methyl ethyl sulfide, tetrahydrothiophene or other mercaptans such as isopropyl mercaptan, sec-butyl mercaptan and/or n-butyl mercaptan, due to its rather high melting point of −0.5 °C (31.1 °F).

  7. VOC exempt solvent - Wikipedia

    en.wikipedia.org/wiki/VOC_exempt_solvent

    In the US, dimethyl carbonate was exempted under the definition of volatile organic compounds (VOCs) by the U.S. EPA in 2009. [9] Due to its classification as VOC exempt, dimethyl carbonate has grown in popularity and applications as a replacement for methyl ethyl ketone (MEK) and other solvents.

  8. P4-t-Bu - Wikipedia

    en.wikipedia.org/wiki/P4-t-Bu

    P 4-t-Bu is a readily accessible chemical from the group of neutral, peralkylated sterically hindered polyaminophosphazenes, which are extremely strong bases but very weak nucleophiles, with the formula (CH 3) 3 C−N=P(−N=P(−N(CH 3) 2) 3) 3. "t-Bu" stands for tert-butyl (CH 3) 3 C –. "P 4" stands for the fact that this molecule has 4 ...

  9. Comparison of psychoactive alcohols in alcoholic drinks

    en.wikipedia.org/wiki/Comparison_of_psychoactive...

    2-Methyl-2-butanol (2M2B), tert-Amyl alcohol (TAA, tert-amylol) Tertiary 75-85-4 2-Methylpropan-2-ol: 2-Methyl-2-propanol (2M2P), tert-Butyl alcohol ((TBA), tert-butanol), t-BuOH Tertiary 75-65-0 2-Phenylethan-1-ol Phenethyl alcohol, 2-Phenylethanol Primary 60-12-8 3-Methylbutan-1-ol