butan-1-amine

Butan-1-amine

The butan-1-amine of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber, butan-1-amine. Follow the links above to find out more about the data in these sites and their terms of usage, 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.

Social media Butan-1-amine, Facebook, etc. Solubility in water. It is used in the synthesis of fengabinethe fungicide benomyland butamoxaneand the antidiabetic tolbutamide.

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The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage. Go To: Top , References , Notes. Data compilation copyright by the U.

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. For example, butan e changes to butan amine, cyclohexan e to cyclohexan amine:. In common names , we treat the carbon chain as an alkyl group bonded to the nitrogen atom. Notice that when the amine is connected to a ring , we start numbering from the carbon connected to the NH 2 group.

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PEL Permissible. Go To: Top , Mass spectrum electron ionization , References. Events and conferences. The email address you entered had a mistake or typo. Log in. Check your inbox We have just emailed you instructions on how to reset your password. Step 1 Step 2 Step 3. LD 50 median dose. Beilstein Reference. Go To: Top , References , Notes. The liquid acquires a yellow color upon storage in air. Usually because of corporate firewalls or filtering. Reset password Please enter the email address associated with your Molport account and we'll send you instructions on how to reset your password.

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Reset password Please enter the email address associated with your Molport account and we'll send you instructions on how to reset your password. Solubility in water. Due to licensing restrictions, this spectrum cannot be downloaded. Happens to the best of us. This compound is used as an ingredient in the manufacture of pesticides such as thiocarbazides , pharmaceuticals , and emulsifiers. Follow the links above to find out more about the data in these sites and their terms of usage. If you don't see an email from us within a few minutes, a few things could have happened: The email is in your spam folder. It is produced by the reaction of ammonia and alcohols over alumina :. Heat capacity C. Log in and discover 4. Read Edit View history.

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