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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 is primarily converted to formaldehyde, which is widely used in many areas, especially polymers. The conversion entails oxidation: 2 CH 3 OH + O 2 → 2 CH 2 O + 2 H 2 O. Acetic acid can be produced from methanol. The Cativa process converts methanol into acetic acid. [35] Methanol and isobutene are combined to give methyl tert-butyl ...

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

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

    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 ...

  5. Sigma-Aldrich - Wikipedia

    en.wikipedia.org/wiki/Sigma-Aldrich

    1975 – Merger of Sigma Chemical and Aldrich Chemical to created Sigma-Aldrich. [13] Their first year earned $43 million in sales. [14] 1999 – Sigma-Aldrich reaches $1 billion in sales; 2005 – Announced membership in The RNAi Consortium [15] 2014 – Merck KGaA announced that it would purchase Sigma-Aldrich for approx. $17 billion (€13.1 ...

  6. Tetramethylammonium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Tetramethylammonium_hydroxide

    One of the earliest preparations is that of Walker and Johnston, [4] who made it by the salt metathesis reaction of tetramethylammonium chloride and potassium hydroxide in dry methanol, in which TMAH is soluble, but potassium chloride is not: NMe 4 + Cl − + KOH → NMe 4 + OH − + KCl. Where Me stands for the methyl group, –CH 3.

  7. 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.

  8. Risk and Safety Statements - Wikipedia

    en.wikipedia.org/wiki/Risk_and_Safety_Statements

    Risk and Safety Statements, also known as R/S statements, R/S numbers, R/S phrases, and R/S sentences, is a system of hazard codes and phrases for labeling dangerous chemicals and compounds.

  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.