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  2. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine has a low acute toxicity with LD 50 (rat; p.o.) = 0.71 ml/kg [6] Like other amines, it is corrosive. Cyclohexylamine is listed as an extremely hazardous substance as defined by Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act .

  3. 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.

  4. 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and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. Chloroethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroethyl_chloroformate

    Chloroethyl chloroformates (chemical formula: C 3 H 4 Cl 2 O 2) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents. [1] They are listed as extremely hazardous substances. [2]

  7. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  8. HN1 (nitrogen mustard) - Wikipedia

    en.wikipedia.org/wiki/HN1_(nitrogen_mustard)

    Bis(2-chloroethyl)ethylamine is the organic compound with the formula C 2 H 5 N(CH 2 CH 2 Cl) 2.Often abbreviated HN1, it is a powerful vesicant and a nitrogen mustard gas. HN1 was developed in the 1920s and 1930s to remove warts and later as a military agent.

  9. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    CH 3 CHO + NH 3 + H 2 → CH 3 CH 2 NH 2 + H 2 O. Ethylamine can be prepared by several other routes, but these are not economical. Ethylene and ammonia combine to give ethylamine in the presence of a sodium amide or related basic catalysts. [5] H 2 C=CH 2 + NH 3 → CH 3 CH 2 NH 2. Hydrogenation of acetonitrile, acetamide, and nitroethane ...