142-95-0

Basic information

• Product Name: OCTYLAMINE HYDROCHLORIDE
• Synonyms: 1-AMINOOCTANE HYDROCHLORIDE;OCTYLAMINE HYDROCHLORIDE;N-OCTYLAMINE HYDROCHLORIDE;1-octanamine,hydrochloride;octylammoniumchloride;TIMTEC-BB SBB003900;OctylamineHCl;Octylamine hydrochloride,99%
• CAS NO: 142-95-0
• Molecular Formula: C₈H₂₀N*Cl
• Molecular Weight: 165.7
• EINECS: 205-574-8
• Mol File: 142-95-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 198°C(lit.)
• Boiling Point: 179.4 °C at 760 mmHg
• Flash Point: 62.8 °C
• Appearance: /
• Water Solubility: Soluble in water
• CAS DataBase Reference: OCTYLAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: OCTYLAMINE HYDROCHLORIDE(142-95-0)
• EPA Substance Registry System: OCTYLAMINE HYDROCHLORIDE(142-95-0)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-22
• Safety Statements: 36/37/39-26
• Hazardous Substances Data: 142-95-0(Hazardous Substances Data)

Usage

Chemical Properties

white to almost white crystalline powder

InChI:InChI=1/C8H19N.ClH/c1-2-3-4-5-6-7-8-9;/h2-9H2,1H3;1H

Upstream product

• 629-01-6 n-octanamide 
• 629-37-8 1-nitrooctane 
• 111-86-4 n-Octylamine 
• 111-83-1 1-bromo-octane 
• 57368-74-8 isopropylidene-octyl-amine 
• 33735-29-4 N,N-Bis(phenylmethyl)octanamine 
• 7438-05-3 1-azidooctane 
• 124-12-9 caprylnitrile 
• 1150-31-8 N-octyl-4-methylbenzenesulfonamide 

Downstream Products

• 70775-75-6 octenidine dihydrochloride 
• 64690-19-3 4-(octylamino)pyridine 
• 5006-92-8 1-(p-Chlor-phenyl)-3-n-octyl-harnstoff 
• 137872-94-7 4-n-Octylamino-6-(2'-chloro-trans-cinnamoyl)amino-2-methyl-quinoline 
• 732984-48-4 1,5-dioctyl-biguanide 
• 60852-95-1 N-octyl-N'-cyanoguanidine 
• 17968-75-1 1,5-bis(3,4-dichlorobenzyl)biguanide 
• 146510-58-9 1-(3,4-dichlorobenzyl)-3-cyanoguanidine 
• 13281-03-3 1-n-octyl-2-thiourea 

Relevant articles and documents

Compositional introduction of lithium ions into conductive polyoxovanadate-surfactant hybrid crystals

Polyoxovanadate-surfactant hybrid layered crystals were successfully synthesized as single crystals by employing a primary alkylammonium cation, octylammonium ([C8H17NH3]+, C8NH3). Two types of hybrid crystals with the formulae [C8H17NH3]6[V10O28]·2H2O (C8NH3-V10) and [C8H17NH3]4Li2[V10O28]·4C2H5OH??6H2O (C8NH3-Li-V10) were obtained by different synthetic procedures. Changing the synthetic conditions enabled the precise introduction of lithium cations into the polyoxovanadate-surfactant hybrid crystals according to compositional control. C8NH3-V10 contained a discrete [V10O28]6- anion, while C8NH3-Li-V10 was composed of a [V10O28]6- anion associated with two lithium cations formulated as {[Li(H2O)3]2[V10O28]}4-. The conductivities of C8NH3-V10 and C8NH3-Li-V10 were investigated under anhydrous conditions at intermediate temperatures.

Micelle and oligomer kinetics in aqueous solutions of n-octylammonium chloride: Monomer exchange, protrusion and chain isomerization

Based on measurements of ultrasonic spectra in the frequency range between 0.1 and 2000 MHz the ultrasonic relaxation properties of solutions of the short-chain cationic surfactant n-octylammonium chloride in water are reported at solute concentrations be

Hydrosilane Reduction of Nitriles to Primary Amines by Cobalt-Isocyanide Catalysts

Reduction of nitriles to silylated primary amines was achieved by combination of 1,1,3,3-tetramethyldisiloxane (TMDS) as the hydrosilane and a catalytic amount of Co(OPIV)2 (PIV = COtBu) associated with isocyanide ligands. The resulting silylated amines were subjected to acid hydrolysis or treatment with acid chlorides to give the corresponding primary amines or imides in good yields. One-pot synthesis of primary amides to primary amines with hydrosilanes was also achieved by iron-cobalt dual catalyst systems.

Synthesis of cobalt nanoparticles by pyrolysis of Vitamin B12: A non-noble-metal catalyst for efficient hydrogenation of nitriles

A facile preparation of vitamin B12-derived carbonaceous cobalt particles supported on ceria is reported. The resulting composite material is obtained upon wet impregnation of ceria with natural cyanocobalamin and consecutive pyrolysis under inert conditions. The novel catalyst shows good to excellent performance in the industrially relevant heterogeneous hydrogenation of nitriles to the corresponding primary amines.