35161-67-2

Basic information

• Product Name: 2-(N-PENTYLAMINO)ETHANOL
• Synonyms: 2-(Amylamino)ethanol;2-(pentylamino)-ethano;Ethanol, 2-(pentylamino)-;n-Pentylaminoethanol;N-Pentylethanolamine;LABOTEST-BB LTBB000631;2-(N-AMYLAMINO)ETHANOL;2-(N-PENTYLAMINO)ETHANOL
• CAS NO: 35161-67-2
• Molecular Formula: C₇H₁₇NO
• Molecular Weight: 131.22
• EINECS: 252-409-0
• Mol File: 35161-67-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 63-65°C 0,2mm
• Flash Point: 79.3°C
• Appearance: /
• Density: 0.872g/cm³
• Vapor Pressure: 0.0261mmHg at 25°C
• Refractive Index: 1.439
• PKA: 14.83±0.10(Predicted)
• CAS DataBase Reference: 2-(N-PENTYLAMINO)ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(N-PENTYLAMINO)ETHANOL(35161-67-2)
• EPA Substance Registry System: 2-(N-PENTYLAMINO)ETHANOL(35161-67-2)

Safety Data

• Statements: 34-36
• Safety Statements: 26-36/37/39-45
• RIDADR: 2735
• Hazardous Substances Data: 35161-67-2(Hazardous Substances Data)

Usage

General Description

2-(N-Pentylamino)ethanol is a chemical compound with the molecular formula C7H17NO. It belongs to the class of chemical entities known as amino alcohols, which contain both an amine and an alcohol group. It is used in the manufacturing of pharmaceuticals, surfactants, corrosion inhibitors, emulsifiers, and chemical intermediates. 2-(N-PENTYLAMINO)ETHANOL is a potential skin and eye irritant, thus safety precautions are recommended when handling it. The structure of 2-(N-Pentylamino)ethanol features a hydrophilic hydroxyl group and an amine group, and a hydrophobic hydrocarbon chain in the molecule, making it a versatile chemical reagent.

InChI:InChI=1/C7H17NO/c1-2-3-4-5-8-6-7-9/h8-9H,2-7H2,1H3

Upstream product

• 75-21-8 oxirane 
• 110-58-7 n-Pentylamine 
• 141-43-5 ethanolamine 
• 71-41-0 pentan-1-ol 
• 107-07-3 2-chloro-ethanol 
• 110-53-2 1-Bromopentane 
• 110-62-3 pentanal 

Downstream Products

• 1204408-35-4 2-((2,6-dinitro-4-trifluoromethyl-phenyl)-pentylamino)-ethanol 

Relevant articles and documents

N-Alkylation of Alkylolamines with Alcohols Over Mesoporous Solid Acid–Base Cs–B–Zr Catalyst

Abstract: The mesoporous solid acid–base Cs–B–Zr mixed oxides were synthesized using the co-precipitation method followed by a subsequent thermal treatment. The catalytic activity of solid Cs–B–Zr mixed oxide was tested for solvent free acid–base catalysed direct alkylolamines with alcohols as green alkylating agent. The effects of Cs/B/Zr ratio, calcination temperature, reaction conditions, and reaction substrate on the catalytic performance of the catalysts were investigated. The XRD, N2 adsorption–desorption, ICP-OES, FT-IR and NH3/CO2-TPD results showed that the mesoporous structure and acid–base properties of the catalysts play important roles in the reaction. A suitable number of acid and basic sites on the catalyst lead to a high activity for the N-alkylation reaction. Graphical Abstract: A direct N-alkylation of amino alcohol with alcohols has been developed using mixed oxide Cs–B–Zr as an acid–base bifunctionalized catalyst.[Figure not available: see fulltext.]

Syntheses of N-alkyl-N-(hydroxy- or oxo-alkyl)nitrosamines related to N-butyl-N-(4-hydroxybutyl)nitroamine, a potent bladder carcinogen

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