enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.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. 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. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    It has a fishy odor and is miscible with water. Like other amines, it is a weak base , compared to strong bases such as NaOH , but it is a stronger base than its aromatic analog, aniline . It is a useful intermediate in the production of many other organic compounds (e.g. cyclamate )

  5. 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]

  6. 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 ...

  7. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    nh 3 + 3 c 2 h 5 oh → n(c 2 h 5) 3 + 3 h 2 o The pK a of protonated triethylamine is 10.75, [ 4 ] and it can be used to prepare buffer solutions at that pH. The hydrochloride salt , triethylamine hydrochloride (triethylammonium chloride), is a colorless, odorless, and hygroscopic powder, which decomposes when heated to 261 °C.

  8. This Much Exercise May Be Enough to Lower Your Dementia Risk

    www.aol.com/much-exercise-may-enough-lower...

    Researchers followed 21 people with an average age of 60 who also had prediabetes, a condition where blood sugar levels are higher than normal but not high enough to be diagnosed with type 2 diabetes.

  9. 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.