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  2. Acetaldehyde (data page) - Wikipedia

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

    This page provides supplementary chemical data on acetaldehyde. ... 22.3 dyn/cm at 10 °C ... log 10 of Acetaldehyde vapor pressure.

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  4. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    The equilibrium constant is 6 × 10 −7 at room temperature, thus that the relative amount of the enol form in a sample of acetaldehyde is very small. [27] At room temperature, acetaldehyde ( CH 3 CH=O ) is more stable than vinyl alcohol ( CH 2 =CHOH ) by 42.7 kJ/mol: [ 28 ] Overall the keto-enol tautomerization occurs slowly but is catalyzed ...

  5. Chloral - Wikipedia

    en.wikipedia.org/wiki/Chloral

    Chloral is produced commercially by the chlorination of acetaldehyde in the presence of hydrochloric acid, producing chloral hydrate. Ethanol can also be used as a feedstock. This reaction is catalyzed by antimony trichloride: H 3 CCHO + 3 Cl 2 + H 2 O → Cl 3 CCH(OH) 2 + 3 HCl. The chloral hydrate is distilled from the reaction mixture.

  6. Phenylacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Phenylacetaldehyde

    Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an alpha-CH2-containing aldehyde and a member of ...

  7. Acetaldoxime - Wikipedia

    en.wikipedia.org/wiki/Acetaldoxime

    Acetaldoxime can be prepared by combining pure acetaldehyde and hydroxylamine under heating in the presence of a base. [3] Preparation of acetaldoxime from acetaldehyde and hydroxylamine. The use of CaO as a base in the preparation of oximes from various types of ketones and aldehydes under mild conditions also gave quantitative yields. [4]

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  9. 4-Hydroxyphenylacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxyphenylacetaldehyde

    4-Hydroxyphenylacetaldehyde, also known as p-hydroxyphenylacetaldehyde, is a natural product with the formula HOC 6 H 4 CH 2 CHO. It is a derivative of phenylacetaldehyde and occurs as a white solid at room temperature. [1]