31897-98-0

Basic information

• Product Name: 1-(3-Aminopropyl)adamantane hydrochloride
• Synonyms: 1-(3-Aminopropyl)adamantane hydrochloride;3-(adamantan-1-yl)propan-1-amine hydrochloride
• CAS NO: 31897-98-0
• Molecular Formula: C₁₃H₂₃N*ClH
• Molecular Weight: 229.83
• Mol File: 31897-98-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 265.8°Cat760mmHg
• Flash Point: 110.4°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.00896mmHg at 25°C
• CAS DataBase Reference: 1-(3-Aminopropyl)adamantane hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-Aminopropyl)adamantane hydrochloride(31897-98-0)
• EPA Substance Registry System: 1-(3-Aminopropyl)adamantane hydrochloride(31897-98-0)

Safety Data

• Hazardous Substances Data: 31897-98-0(Hazardous Substances Data)

Usage

Safety Profile

Poison by intraperitoneal route.Moderately toxic by ingestion. When heated todecomposition it emits very toxic fumes of HCl and NOx.

InChI:InChI=1/C13H23N.ClH/c14-3-1-2-13-7-10-4-11(8-13)6-12(5-10)9-13;/h10-12H,1-9,14H2;1H

Upstream product

• 31897-96-8 3-(adamant-1-yl)propanamide 
• 52582-89-5 3-((3r,5r,7r)-adamantan-1-yl)propanenitrile 

Downstream Products

• 1305348-96-2 methyl (4-{[3(adamant-1-ylpropyl)amino]methyl}phenyI)acetate 

Relevant articles and documents

Effect of adamantyl compounds on dynamics of spin labelled multilamellar liposomes

Interactions of two adamantyl molecules: 3-(adamantan-1-yl)propan-1-aminium chloride (compound A) and 1-hydroxyadamantan (compound B) with multilayer liposomes composed of L-a-phosphatidylcholine, cholesterol and dicetylphosphate, spin labelled with n-doxylstearic acids (n = 5, 7, 10, 12, 16) were investigated. In the presence of aminium salt (A) or alcohol (B) the increased dynamics of 5-doxylstearic acids and 16-doxylstearic acids in the multilamellar liposomes were determined in the temperature range from 250 K to 295 K. The increased dynamics of 5-doxylstearic acids suggested that both adamantyl compounds influenced molecular motions in the interfacial region of the liposome. The increased motional properties of 16-doxylstearic acids, located in the core of the multilamellar liposomes, suggested that both adamantyl compounds induced the structural changes in the hydrophobic core as well.