14302-46-6

Basic information

• Product Name: 3-AMINO-1-PROPANOL HYDROCHLORIDE
• Synonyms: 3-AMINO-1-PROPANOL HYDROCHLORIDE;PROPANOLAMINE HYDROCHLORIDE;Aminopropanolhydrochloride;3-aminopropan-1-ol hydrochloride;3-Amino-1-propanolHCl;3-AMINO-1-PROPANOL HYDROCHLORIDE 95+%;n-Propanolamine hydrochloride
• CAS NO: 14302-46-6
• Molecular Formula: C3H10ClNO
• Molecular Weight: 111.57
• EINECS: 238-240-5
• Product Categories: omega-Aminoalkanols;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
• Mol File: 14302-46-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 187.5 °C at 760 mmHg
• Flash Point: 79.4 °C
• Appearance: /
• Water Solubility: almost transparency
• CAS DataBase Reference: 3-AMINO-1-PROPANOL HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-1-PROPANOL HYDROCHLORIDE(14302-46-6)
• EPA Substance Registry System: 3-AMINO-1-PROPANOL HYDROCHLORIDE(14302-46-6)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-41-22
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 14302-46-6(Hazardous Substances Data)

Usage

General Description

3-AMINO-1-PROPANOL HYDROCHLORIDE is a chemical compound that consists of an amino group and an alcohol group attached to a three-carbon chain, with a hydrochloride salt. It is commonly used in the production of pharmaceuticals and agrochemicals, as well as in the synthesis of chiral ligands and catalysts. 3-AMINO-1-PROPANOL HYDROCHLORIDE is also used as a buffer solution in biochemical and molecular biology applications, and as an intermediate in the manufacturing of dyes and pigments. Additionally, 3-AMINO-1-PROPANOL HYDROCHLORIDE is used in the production of surfactants, lubricants, and corrosion inhibitors due to its amphiphilic nature.

Upstream product

• 109-78-4 3-Hydroxypropionitrile 

Relevant articles and documents

Synthesis of 13C-dilabeled 4-coumaroylspermidines

Five 13C-dilabeled constitution isomers of 4-coumaroylspermidines were prepared in nine to eleven steps: N1,4-di[(E)-4-coumaroyl]-(5,8- 13C2)spermidine (13b), N1-[(E)-4-coumaroyl]-(5,8-13C2)spermidine (17b), N1,8-di[(E)-4-coumaroyl]-(1,4-13C2)spermidine (20b), N4-[(E)-4- coumaroyl]-(1,4-13C2)spermidine (24b) and N1,4,8-tri[(E)-4-coumaroyl]- (5,8-13C2)spermidine (26). The two 13C-atoms were subsequently introduced using labeled potassium cyanide. The synthesis proceeds through stepwise construction of the polyamine backbone including protection and deprotection steps of the amino functions. Based on 1H-1H NOE interactions, the preliminary study of their binding reveals that 20b binds to tRNA in the same way as spermidine does, whereas 24b and 26 do not show any NOE effects with the tRNA protons.