35161-67-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(N-Pentylamino)ethanol is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to act as a building block in the development of new drugs, contributing to the creation of molecules with specific therapeutic properties.
Used in Surfactant Production:
In the manufacturing of surfactants, 2-(N-Pentylamino)ethanol serves as a key component. Its amphiphilic nature, with both hydrophilic and hydrophobic elements, makes it suitable for creating surfactants that can reduce surface tension in solutions and are used in a variety of cleaning and personal care products.
Used in Corrosion Inhibitor Formulation:
2-(N-Pentylamino)ethanol is utilized as a corrosion inhibitor in various industrial applications. Its ability to form protective films on metal surfaces helps prevent corrosion, making it a valuable additive in formulations designed to protect metal infrastructure and equipment.
Used in Emulsifier Creation:
As an emulsifier, 2-(N-Pentylamino)ethanol is used to stabilize mixtures of immiscible liquids, such as oil and water. Its dual hydrophilic and hydrophobic characteristics enable it to act as a bridge between different phases, facilitating the formation of stable emulsions in applications like food processing, cosmetics, and pharmaceuticals.
Used in Chemical Intermediates:
2-(N-Pentylamino)ethanol also serves as a versatile chemical intermediate in the synthesis of a range of organic compounds. Its reactivity and functional groups make it a useful precursor in the production of various specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 35161-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,6 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35161-67:
(7*3)+(6*5)+(5*1)+(4*6)+(3*1)+(2*6)+(1*7)=102
102 % 10 = 2
So 35161-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H17NO/c1-2-3-4-5-8-6-7-9/h8-9H,2-7H2,1H3
35161-67-2Relevant academic research and scientific papers
N-Alkylation of Alkylolamines with Alcohols Over Mesoporous Solid Acid–Base Cs–B–Zr Catalyst
Chen, Aimin,Wang, Houyong,Liu, Rui,Bo, Yingying,Hu, Jun
, p. 1182 - 1193 (2016/07/06)
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.]
Synthesis and properties of pentane amino derivatives
Talybov,Mamedbeili,Abbasov,Kochetkov
experimental part, p. 2455 - 2459 (2011/04/16)
Synthesis of pentane amino derivatives by the reaction of the corresponding amines with 1-bromopentanes of n-and iso-structure by environmentally safe methods in water medium was carried out. The structure of the compounds obtained was confirmed by elemental analysis, IR, 1H and 13C NMR spectroscopy. The products synthesized were tested as reagents for the suppression of growth of the sulfate-reducing bacteria and as the anticorrosive substances. It was found that they are effective bactericides for the sulfate-reducing bacteria and exhibit high anticorrosive properties. Pleiades Publishing, Ltd., 2010.
