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  2. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    An infrared spectroscopy correlation table (or table of infrared absorption frequencies) is a list of absorption peaks and frequencies, typically reported in wavenumber, for common types of molecular bonds and functional groups.

  3. Butyl propionate - Wikipedia

    en.wikipedia.org/wiki/Butyl_propionate

    Butyl propionate is used to make fragrances, perfumes and as a flavoring.It is also used in paints and primers for auto body or engine, appliance coatings (paints designed specifically for painting household items and vehicles like microwave ovens, refrigerators and automobiles), enamels, lacquers, and printing inks, as a solvent for adhesives and nitrocellulose, and in polymerization ...

  4. C7H14O2 - Wikipedia

    en.wikipedia.org/wiki/C7H14O2

    n-Butyl propionate; sec-Butyl propionate; Isobutyl propionate; tert-Butyl propionate; Ethyl isovalerate; Ethyl pentanoate; Heptanoic acid; Isoamyl acetate; Methyl ...

  5. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:

  6. Infrared spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy

    Infrared spectroscopy (IR spectroscopy or vibrational spectroscopy) is the measurement of the interaction of infrared radiation with matter by absorption, emission, or reflection. It is used to study and identify chemical substances or functional groups in solid, liquid, or gaseous forms. It can be used to characterize new materials or identify ...

  7. Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate ...

    en.wikipedia.org/wiki/Octadecyl_3-(3,5-di-tert...

    Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate is significantly less volatile than simpler phenolic antioxidants such as butylhydroxytoluene (BHT). This makes it more suitable to stabilising plastics, as it is not driven out by the high temperatures experienced during plastic extrusion and moulding, [2] when they are heated to 150-320 °C (300–600 °F). [3]

  8. Mass spectral interpretation - Wikipedia

    en.wikipedia.org/wiki/Mass_spectral_interpretation

    For example, hexane fragmentation patterns. The m/z=57 butyl cation is the base peak, and other most abundant peaks in the spectrum are alkyl carbocations at m/z=15, 29, 43 Da. [6] [2] [11] The possible mechanisms for EI ionization spectra of hexane. Branched alkanes have somewhat weaker molecular ion peaks in the spectra.

  9. 2,6-Di-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,6-Di-tert-butylphenol

    Of particular note is methyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate (CAS# 6386-38-5), which is formed by the Michael addition of methyl acrylate. This compound is used as a feedstock in the synthesis of more complex antioxidants such as Irganox 1098 . 2,6-Di- tert -butylphenol is also used in the synthesis of CGP-7930 , probucol , and ...