Butan-1-amine

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Butan-1-amine

This colourless liquid is one of the four isomeric amines of butane , the others being sec -butylamine , tert -butylamine , and isobutylamine. It is a liquid having the fishy, ammonia-like odor common to amines. The liquid acquires a yellow color upon storage in air. It is soluble in all organic solvents. Its vapours are heavier than air and it produces toxic oxides of nitrogen during combustion. It is produced by the reaction of ammonia and alcohols over alumina :. This compound is used as an ingredient in the manufacture of pesticides such as thiocarbazides , pharmaceuticals , and emulsifiers. It is used in the synthesis of fengabine , the fungicide benomyl , and butamoxane , and the antidiabetic tolbutamide. Contents move to sidebar hide. Article Talk. Read Edit View history. Tools Tools. Download as PDF Printable version.

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Butan-1-amine

Amines are the derivatives of ammonia remember NH 3 from General chemistry. Replacing one hydrogen of ammonia with an alkyl group forms an amine with a general formula of R-NH 2 :. Depending on the number of alkyl groups are connected to the nitrogen, we have primary, secondary, and tertiary amines :. In general, amines can be named either by systematic or common names. Naming amines by the systematic nomenclature follows the same rules we discussed earlier for the IUPAC nomenclature rules for alkanes. Step 4. Put everything together having the substituents in alphabetical order.

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Read Edit View history. This compound is used as an ingredient in the manufacture of pesticides such as thiocarbazides , pharmaceuticals , and emulsifiers. Check here for automatic Y scaling 3. I'm looking to find general data on compound availability. Work e-mail. N verify what is Y N? REL Recommended. Please see the following for information about the library and its accompanying search program. If none of these solutions worked, please contact our technical service at customerservice molport. Hall, Jr.