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  2. 1-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/1-aminopentane

    1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2.It is used as a solvent, as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers, and pharmaceutical products, [1] and as a flavoring agent.

  3. Pentylamine - Wikipedia

    en.wikipedia.org/?title=Pentylamine&redirect=no

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  4. Phentolamine - Wikipedia

    en.wikipedia.org/wiki/Phentolamine

    The primary application for phentolamine is for the control of hypertensive emergencies, most notably due to pheochromocytoma. [5]It also has usefulness in the treatment of cocaine-induced cardiovascular complications, where one would generally avoid β-blockers (e.g. metoprolol), as they can cause unopposed α-adrenergic mediated coronary vasoconstriction, worsening myocardial ischemia and ...

  5. Pentamine - Wikipedia

    en.wikipedia.org/wiki/Pentamine

    This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.

  6. Primene amines - Wikipedia

    en.wikipedia.org/wiki/Primene_amines

    In chemistry, primene amines are mixtures of long-chain branched primary amines.One member of this class of amine is tert-octylamine, H 2 NC(CH 3) 2 (CH 2) 4 CH 3. [1] These compounds have a faint ammonia-like odor.

  7. Pentyl group - Wikipedia

    en.wikipedia.org/wiki/Pentyl_group

    Pentyl is a five-carbon alkyl group or substituent with chemical formula-C 5 H 11.It is the substituent form of the alkane pentane.. In older literature, the common non-systematic name amyl was often used for the pentyl group.

  8. 5-Amino-1-pentanol - Wikipedia

    en.wikipedia.org/wiki/5-Amino-1-pentanol

    5-Amino-1-pentanol is an amino alcohol with a primary amino group and a primary hydroxy group at the ends of a linear C 5-alkanes.As a derivative of the platform chemical furfural (that is easily accessible from pentoses), 5-amino-1-pentanol may become increasingly important in the future as a building block for biodegradable polyesteramides and as a starting material for valerolactam — the ...

  9. n-Butylamine - Wikipedia

    en.wikipedia.org/wiki/N-Butylamine

    The LD 50 to rats through the oral exposure route is 366 mg/kg. [ 7 ] In regards to occupational exposures to n -butylamine, the Occupational Safety and Health Administration and National Institute for Occupational Safety and Health have set occupational exposure limits at a ceiling of 5 ppm (15 mg/m 3 ) for dermal exposure.

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