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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. 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.

  7. tert-Butylamine - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylamine

    tert-Butylamine (also erbumine and other names) is an organic chemical compound with the formula (CH 3) 3 CNH 2.It is a colorless liquid with a typical amine-like odor. tert-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and isobutylamine.

  8. 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.

  9. MiPT - Wikipedia

    en.wikipedia.org/wiki/MiPT

    MiPT is the N-isopropyl analog of DMT and the N-methyl analog of DiPT. MiPT base, unlike many other tryptamines in their freebase form, does not decompose rapidly in the presence of light or oxygen.

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