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  2. Methylhexanamine - Wikipedia

    en.wikipedia.org/wiki/Methylhexanamine

    Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.

  3. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    C 6 H 5 NH 2 + 3 H 2 → C 6 H 11 NH 2. It is also prepared by alkylation of ammonia using cyclohexanol. Applications ... (40 mg/m 3) over an eight-hour workshift. [2

  4. Hexylamine - Wikipedia

    en.wikipedia.org/wiki/Hexylamine

    Hexylamine or n-hexylamine is a chemical compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 NH 2. This colorless liquid is one of the isomeric amines of hexane. At standard temperature and pressure, it has the ammonia/bleach odor common to amines and is soluble in almost all organic solvents.

  5. Fluazinam - Wikipedia

    en.wikipedia.org/wiki/Fluazinam

    Its chemical name is 3-chloro-N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-2-pyridinamine. [1] The mode of action involves the compound being an extremely potent uncoupler of oxidative phosphorylation in mitochondria [ 2 ] and also having high reactivity with thiols . [ 1 ]

  6. 3-Chloromethcathinone - Wikipedia

    en.wikipedia.org/wiki/3-Chloromethcathinone

    The chemical name of 3-chloromethcathinone (3-CMC) is 1-(3-chlorophenyl)-2-(methylamino)-1-propanone. It is a N-alkylated and ring-substituted cathinone derivative. The drug is the analogue of bupropion in which its N - tert -butyl group has been replaced with an N - methyl group .

  7. Ethylmethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylmethylamine

    C 3 H 9 N: Molar mass: 59.112 g·mol −1 Appearance Colorless liquid Density: 688 kg m −3 (at 25 °C) Boiling point: 33 to 34 °C (91 to 93 °F; 306 to 307 K) Hazards

  8. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    4-methylpent-2-yne; 3,3-dimethylbut-1-yne This page was last edited on 22 May 2021, at 18:45 (UTC). Text is available under the Creative Commons Attribution ...

  9. Novaluron - Wikipedia

    en.wikipedia.org/wiki/Novaluron

    The absorbed novaluron was metabolized and 14 and 15 components were detected in the urine and bile respectively. The main metabolic pathway was cleavage of the urea bridge between the chlorophenyl- and difluorophenylgroups. The products of this reaction are 2,6-difluorobenzoic acid and 3-chloro-4-(1,1,2-trifluoro-2-trifluoromethoxyethoxy) aniline.