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What is N butylamine used for?

What is N butylamine used for?

Uses. This compound is used as an ingredient in the manufacture of pesticides (such as thiocarbazides), pharmaceuticals, and emulsifiers. It is also a precursor for the manufacture of N,N′-dibutylthiourea, a rubber vulcanization accelerator, and n-butylbenzenesulfonamide, a plasticizer of nylon.

Is butylamine a primary amine?

Tert-butylamine is a primary aliphatic amine that is ethylamine substituted by two methyl groups at position 1. It is a conjugate base of a tert-butylammonium.

Is butylamine polar?

Information on this page: Kovats’ RI, non-polar column, isothermal.

What is the boiling point of n butylamine?

172.4°F (78°C)n-Butylamine / Boiling point

What products contain butylamine?

Butylamine is used to produce agricultural chemicals (e.g. benomyl), rubber chemicals (e.g. di-n-butylthiourea), nylon plasticers (e.g. n-butylbenzenesulphonamide), alkyl alkanol amines (Butyldiethanolamine) as well as fuel and oil additives.

How do you make butylamine?

Butylamine can also be prepared in a two-step synthesis starting from 1-bromopropane, CH3CH2CH2Br. Write an equation for each of the two steps in this synthesis. Butylamine can also be prepared in a two-step synthesis starting from 1-bromopropane, CH3CH2CH2Br.

Is butylamine a secondary amine?

Sec-butylamine is a primary aliphatic amine that is butane in which one hydrogen at position 2 is replaced by an amino group.

Is tertiary butylamine is tertiary amine?

A primary aliphatic amine that is ethylamine substituted by two methyl groups at position 1.

What intermolecular forces are in butylamine?

Butylamine does not exhibit H-bonding between each other, where as alcohols do. This added force from the hydrogen bond makes the boiling point of alcohols higher than those of most other ORGANIC molecules. Ionic bonds have the most strength.

What is the structure of butylamine?


PubChem CID 8007
Structure Find Similar Structures
Chemical Safety Laboratory Chemical Safety Summary (LCSS) Datasheet
Molecular Formula C4H11N or CH3(CH2)3NH2
Synonyms Butylamine N-BUTYLAMINE butan-1-amine 109-73-9 1-Butanamine More…

Why is butylamine stronger than ammonia?

Alkylamines (like butylamine) are stronger bases than ammonia, as there is a higher electron density on the nitrogen atom. This is because the alkyl group is electron releasing.

What is the name of ch3ch2ch2ch2nh2?

The name of the compound is butanamine.

What is the structure of tert-Butylamine?

C4H11Ntert-Butylamine / Formula

Which of the following is a tertiary amine?

CH3N(CH3)2 and N(CH3)3 are tertiary amines tertiary amines have no hydrogen atom and three alkyl or aryl groups attached to the nitrogen.

Is butylamine a stronger or weaker base than ammonia?

Why is phenylamine a weaker base?

The availability of a lone pair of electrons on a base determines its strength as it is these electrons that will “mop up” H+ ions in solution and hence increase pH towards more alkaline conditions. Therefore, phenylamine is a weaker base than ethylamine because its lone pair is less available.

What is the name for CH3CH2CH2CH2CH2CH2CH2CH3?

Octane – CH3CH2CH2CH2CH2CH2CH2CH3. Nonane – CH3CH2CH2CH2CH2CH2CH2CH2CH3. Decane – CH3CH2CH2CH2CH2CH2CH2CH2CH2CH3. Alkenes. unsaturated hydrocarbons (at least one double bond) CnH2n.

What is the Iupac name of tert-Butylamine?


Preferred IUPAC name 2-Methylpropan-2-amine
Other names 2-Aminoisobutane 2-Amino-2-methylpropane Dimethylethylamine 2-Methyl-2-aminopropane 2-Methyl-2-propylamine Trimethylaminomethane Erbumine (INN)
CAS Number 75-64-9

What is the Iupac name of sec-butylamine?


Preferred IUPAC name Butan-2-amine
Other names 2-Aminobutane 2-Butanamine (±)-sec-Butylamine DL-sec-Butylamine 1-Methylpropylamine Mono-sec-butylamine
CAS Number 13952-84-6 13250-12-9 (R) 513-49-5 (S)