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  2. Methanol (data page) - Wikipedia

    en.wikipedia.org/wiki/Methanol_(data_page)

    Here is a similar formula from the 67th edition of the CRC handbook. Note that the form of this formula as given is a fit to the Clausius–Clapeyron equation, which is a good theoretical starting point for calculating saturation vapor pressures:

  3. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol and its vapours are flammable. Moderately toxic for small animals – Highly toxic to large animals and humans (in high concentrations) – May be fatal/lethal or cause blindness and damage to the liver, kidneys, and heart if swallowed – Toxicity effects from repeated over exposure have an accumulative effect on the central nervous system, especially the optic nerve – Symptoms may ...

  4. File:Cr-Ac-OH-MSDS SigmaAldrich.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Cr-Ac-OH-MSDS_Sigma...

    This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

  5. Tetramethylammonium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Tetramethylammonium_hydroxide

    It is commonly encountered in form of concentrated solutions in water or methanol. TMAH in solid state and its aqueous solutions are all colorless, but may be yellowish if impure. Although TMAH has virtually no odor when pure, samples often have a strong fishy smell due to presence of trimethylamine which is a common impurity. TMAH has several ...

  6. Sodium bis (2-methoxyethoxy)aluminium hydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_bis(2-methoxyethoxy...

    At low temperatures (below -60°C), the solution solidifies to a glassy pulverizable substance with no sharp melting point. SMEAH is a versatile hydride reducing agent. It readily converts epoxides , aldehydes , ketones , carboxylic acids , esters , acyl halides , and anhydrides to the corresponding alcohols .

  7. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    The required methanol is obtained from synthesis gas . [7] Other possible improvements call for a dual catalyst system that permits both methanol synthesis and dehydration in the same process unit, with no methanol isolation and purification. [7] [8] Both the one-step and two-step processes above are commercially available. The two-step process ...

  8. Methyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Methyl_chloroformate

    Methyl chloroformate hydrolyzes in water to form methanol, hydrochloric acid, and carbon dioxide. [3] This decomposition happens violently in the presence of steam, causing foaming. The compound decomposes in heat, which can liberate hydrogen chloride, phosgene, chlorine, or other toxic gases.

  9. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.