16011-90-8

Basic information

• Product Name: 4-aminobutyronitrile monohydrochloride
• Synonyms: 4-aminobutyronitrile monohydrochloride;Butanenitrile, 4-aMino-, hydrochloride;Butanenitrile, 4-aMino-, Monohydrochloride;4-Aminobutanenitrile hydrochloride;4-Aminobutyronitrile hydrochloride
• CAS NO: 16011-90-8
• Molecular Formula: C₄H₈N₂*ClH
• Molecular Weight: 120.58066
• EINECS: 240-145-9
• Mol File: 16011-90-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 201.2°Cat760mmHg
• Flash Point: 75.5°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.312mmHg at 25°C
• CAS DataBase Reference: 4-aminobutyronitrile monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-aminobutyronitrile monohydrochloride(16011-90-8)
• EPA Substance Registry System: 4-aminobutyronitrile monohydrochloride(16011-90-8)

Safety Data

• Hazardous Substances Data: 16011-90-8(Hazardous Substances Data)

Usage

General Description

4-aminobutyronitrile monohydrochloride, also known as γ-Aminobutyronitrile hydrochloride, is a chemical compound with the molecular formula C4H9N2·HCl. It is a white crystalline powder that is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 4-aminobutyronitrile monohydrochloride is a versatile intermediate in the production of various drugs and has applications in the pharmaceutical industry for the treatment of diseases such as cancer and hypertension. It is also utilized in the synthesis of pesticides and other agricultural chemicals. This chemical is an important building block in the manufacture of a wide range of products, making it a valuable compound in the chemical industry.

InChI:InChI=1/C4H8N2.ClH/c5-3-1-2-4-6;/h1-3,5H2;1H

Upstream product

• 5332-06-9 4-bromobutanenitrile 
• 110-61-2 butanedinitrile 
• 32754-99-7 4-aminobutyronitrile 
• 146952-04-7 5-Amino-2-(hydroxyimino)pentansaeure 

Downstream Products

• 32039-00-2 4-(Benzoylamino)butansaeurenitril 
• 150671-79-7 4-(Phenylacetylamino)butansaeurenitril 

Relevant articles and documents

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The 1,7-bis(trimethylsilyl)hepta-2,5-diyne reacts with iminium ions generated in situ from primary alkyl- or primary functional amines by a double aminomethylation-desilylation process leading to N-substituted 3,5-divinylidenepiperidines.

Copper-catalyzed ring-opening C(sp3)-N coupling of cycloketone oxime esters: Access to 1°, 2° and 3° alkyl amines

A novel copper-catalyzed C(sp3)-N coupling of cycloketone oxime esters with nitrogen nucleophiles has been realized. All of the N-aryl/alkylanilines, anilines and benzophenone imine could be employed in this protocol to produce a variety of 1°, 2° and 3° alkyl amines in one or two steps. These resultant cyano-containing alkyl amines were proven to be versatile synthetic building blocks in a variety of chemical transformations.

Novel aromatic compounds and poly(oxyalkylene) containing aromatic compounds possessing antibacterial, antifungal or antitumor activity

The present invention provides novel compounds possessing one or more of the following activities: antibacterial, antifungal and antitumor activity. The compounds are of Formula (I): Pharmaceutical compositions containing these compounds, methods of making and methods for using these compounds are also provided.