Butan-1-amine

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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.

Butan-1-amine

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We are working on a new version of ChemSpider — if you want to try the new interface go to beta. Simple Structure Advanced History. Comment on this record. Featured data source. Butanamin [German]. Butylamine [ISO] [Wiki].

Butan-1-amine

The relative density was 0. Boiling point Melting Point Refractive index The vapor pressure was 9. Can be miscible with water, ethanol, ether.

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Log in Didn't get an email? Secretary of Commerce on behalf of the U. It is produced by the reaction of ammonia and alcohols over alumina :. Data compilation copyright by the U. Read Edit View history. Related compounds. Go To: Top , Mass spectrum electron ionization , Notes. Use or mention of technologies or programs in this web site is not intended to imply recommendation or endorsement by the National Institute of Standards and Technology, nor is it intended to imply that these items are necessarily the best available for the purpose. Create an account or log in Sign up and discover 4. Word of mouth. All rights reserved. Infobox references. Chemical compound.

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 :.

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