enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Acetic acid (data page) - Wikipedia

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

    1 Material Safety Data Sheet. ... Print/export Download as PDF; ... Vapor-liquid Equilibrium for Acetic acid/Water [3] P = 760 mm Hg BP Temp.

  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. Hazardous Materials Identification System - Wikipedia

    en.wikipedia.org/wiki/Hazardous_Materials...

    In the NFPA system, the white area is used to convey special hazards whereas HMIS uses the white section to indicate which personal protective equipment (PPE) should be used when working with the material. [6] [13] X. ask supervisor or safety specialist for handling instructions, or refer to the MSDS sheet for specific directions

  5. Acetyl bromide - Wikipedia

    en.wikipedia.org/wiki/Acetyl_bromide

    As is expected, it may be prepared by reaction between phosphorus tribromide and acetic acid: [2] 3 CH 3 COOH + PBr 3 → 3 CH 3 COBr + H 3 PO 3. As usual for an acid halide, acetyl bromide hydrolyzes rapidly in water, forming acetic acid and hydrobromic acid. It also reacts with alcohols and amines to produce acetate esters and acetamides ...

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  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]

  8. Sodium diacetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_diacetate

    It can be viewed as the result of homoassociation, an effect that enhances the acidity of acetic acid in concentrated solution: 2 CH 3 CO 2 H + NaOH → Na + [(CH 3 CO 2) 2 H] − + H 2 O. Also described as the sodium acid salt of acetic acid, it is best described as the sodium salt of the hydrogen-bonded anion (CH 3 CO 2) 2 H −.

  9. Isoamyl acetate - Wikipedia

    en.wikipedia.org/wiki/Isoamyl_acetate

    Isoamyl acetate, also known as isopentyl acetate, is an ester formed from isoamyl alcohol and acetic acid, with the molecular formula C 7 H 14 O 2. It is a colorless liquid that is only slightly soluble in water, but very soluble in most organic solvents. Isoamyl acetate has a strong odor which is described as similar to both banana and pear. [3]