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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. Sodium dodecyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_dodecyl_sulfate

    For instance, SDS is a component, along with other chain-length amphiphiles, when produced from coconut oil, and is known as sodium coco sulfate (SCS). [26] SDS is available commercially in powder, pellet, and other forms (each differing in rates of dissolution), as well as in aqueous solutions of varying concentrations. [citation needed]

  5. 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.

  6. Methanethiol - Wikipedia

    en.wikipedia.org/wiki/Methanethiol

    The molecule is tetrahedral at the carbon atom, like methanol. It is a weak acid, ... The safety data sheet (SDS) lists methanethiol as a colorless, flammable gas ...

  7. 2-Methoxyethanol - Wikipedia

    en.wikipedia.org/wiki/2-Methoxyethanol

    It can be formed by the nucleophilic attack of methanol on protonated ethylene oxide followed by proton transfer: C 2 H 5 O + + CH 3 OH → C 3 H 8 O 2 + H + 2-Methoxyethanol is used as a solvent for many different purposes such as varnishes, dyes, and resins. It is also used as an additive in airplane deicing solutions.

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