15753-35-2

Basic information

• Product Name: N-BUTYLHEXAMETHYLENEIMINE 97
• Synonyms: N-BUTYLHEXAMETHYLENEIMINE 97
• CAS NO: 15753-35-2
• Molecular Formula: C₁₀H₂₁N
• Molecular Weight: 155.283
• Product Categories: Heterocyclic Compounds;Building Blocks;Heterocyclic Building Blocks;Homopiperidines;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks
• Mol File: 15753-35-2.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 197.8 °C at 760 mmHg
• Flash Point: 145 °F
• Appearance: /
• Density: 0.836 g/mL at 25 °C
• Vapor Pressure: 0.371mmHg at 25°C
• Refractive Index: n20/D 1.456
• CAS DataBase Reference: N-BUTYLHEXAMETHYLENEIMINE 97(CAS DataBase Reference)
• NIST Chemistry Reference: N-BUTYLHEXAMETHYLENEIMINE 97(15753-35-2)
• EPA Substance Registry System: N-BUTYLHEXAMETHYLENEIMINE 97(15753-35-2)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 2735 8/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 15753-35-2(Hazardous Substances Data)

Usage

General Description

N-BUTYLHEXAMETHYLENEIMINE 97 is a chemical compound with the molecular formula C12H25N. It is a colorless liquid with a molar mass of 187.33 g/mol. N-BUTYLHEXAMETHYLENEIMINE 97 is primarily used as a chemical intermediate in the production of surfactants, detergents, and specialty chemicals. It is also employed in the manufacture of corrosion inhibitors, lubricants, and oilfield chemicals. Additionally, this compound is utilized as a raw material in the synthesis of quaternary ammonium compounds, which are widely used as disinfectants, fabric softeners, and antistatic agents. N-BUTYLHEXAMETHYLENEIMINE 97 is a versatile chemical with diverse applications in the industrial sector.

InChI:InChI=1/C10H21N/c1-2-3-8-11-9-6-4-5-7-10-11/h2-10H2,1H3

Upstream product

• 111-49-9 hexamethylene imine 
• 109-65-9 1-bromo-butane 
• 123-72-8 butyraldehyde 
• 129885-51-4 1-<(butyl(5-hexenyl)carbamoyl)oxy>-2(1H)-pyridinethione 
• 25170-82-5 6-n-butylamino-1-hexanol 

Relevant articles and documents

Effect of cation structure on the oxygen solubility and diffusivity in a range of bis{(trifluoromethyl)sulfonyl}imide anion based ionic liquids for lithium-air battery electrolytes

This paper reports on the solubility and diffusivity of dissolved oxygen in a series of ionic liquids (ILs) based on the bis{(trifluoromethyl)sulfonyl}imide anion with a range of related alkyl and ether functionalised cyclic alkylammonium cations. Cyclic voltammetry has been used to observe the reduction of oxygen in ILs at a microdisk electrode and chronoamperometric measurements have then been applied to simultaneously determine both the concentration and the diffusion coefficient of oxygen in different ILs. The viscosity of the ILs and the calculated molar volume and free volume are also reported. It is found that, within this class of ILs, the oxygen diffusivity generally increases with decreasing viscosity of the neat IL. An inverse relationship between oxygen solubility and IL free volume is reported for the two IL families implying that oxygen is not simply occupying the available empty space. In addition, it is reported that the introduction of an ether-group into the IL cation structure promotes the diffusivity of dissolved oxygen but reduces the solubility of the gas.

Nanosized MCM-22 zeolite using simple non-surfactant organic growth modifiers: Synthesis and catalytic applications

Non surfactant cyclic alkylammonium can selectively decrease the rate of crystal growth along the x-y crystal axes during the synthesis of MWW zeolite. This results in an ～60 nm nanocrystalline zeolite that shows remarkable catalytic properties for the production of cumene.

Colloidal and Nanosized Catalysts in Organic Synthesis: XXIII. Reductive Amination of Carbonyl Compounds Catalyzed by Nickel Nanoparticles in a Plug-Flow Reactor

Reductive amination of aldehydes and ketones with primary and secondary amines under catalysis with nickel nanoparticles supported on zeolite X, MgO, or activated carbon in the gas phase or in the gas-liquid system in a plug-flow reactor proceeds at atmospheric pressure of hydrogen with the formation of secondary or tertiary amines in high yield.