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  2. Acetic acid (data page) - Wikipedia

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

    1 Material Safety Data Sheet. 2 Structure and properties. ... Vapor-liquid Equilibrium for Acetic acid/Water [3] P = 760 mm Hg BP Temp. °C mole % water liquid vapor

  3. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

  4. Template:Chembox - Wikipedia

    en.wikipedia.org/wiki/Template:Chembox

    An infobox for chemicals. It has a large number of options to add relevant data and images. The Chembox has a modular design. After the general information like the chemical name and images, it can be built from multiple sections, each covering a group of information (like "pharmacology"). Depending on the compound, sections can be added or left out, and within a section parameters can be ...

  5. Molybdenum(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Molybdenum(II)_acetate

    Safety data sheet (SDS) External MSDS: ... acetate is an iconic example of a compound with a metal-metal quadruple bond. [2] ... with acetic acid.

  6. Acetate - Wikipedia

    en.wikipedia.org/wiki/Acetate

    An acetate is a salt formed by the combination of acetic acid with a base (e.g. alkaline, earthy, metallic, nonmetallic or radical base). "Acetate" also describes the conjugate base or ion (specifically, the negatively charged ion called an anion) typically found in aqueous solution and written with the chemical formula C

  7. Propyl acetate - Wikipedia

    en.wikipedia.org/wiki/Propyl_acetate

    This colorless liquid is known by its characteristic odor of pears. Due to this fact, it is commonly used in fragrances and as a flavor additive. It is formed by the esterification of acetic acid and propan-1-ol, often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct. [6]

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  9. Isopropyl acetate - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_acetate

    Isopropyl acetate decomposes slowly on contact with steel in the presence of air, producing acetic acid and isopropanol. It reacts violently with oxidizing materials and it attacks many plastics. [5] Isopropyl acetate is quite flammable in both its liquid and vapor forms, and it may be harmful if swallowed or inhaled. [6]