Dytek® HMI Hexamethyleneimine

Product Information

Molecular Structure
IUPAC Name Azepane
CAS Number
  • 111-49-9
Other Names
  • Azepane
  • 1H-Azepine, Hexahydro-,Homopiperidine
  • Hexahydro-1H-azepine
  • Hexahydroazepine, DYTEK® HMI
Molecular Formula C6H13N
Molecular Weight 99.177 g/mol
Description Clear, colorless liquid with an ammonia-like odor
Typical Composition
(wt %)
Hexamethyleneimine 99.5
Cyclohexylamine 0.38
n-Hexylamine 0.02
Water 0.07
Hexamethylenediamine 0.02
Chemical & Physical Properties

Chemical & Physical Properties

Property Name Value
Boiling Point (760 mm Hg), °C (°F) 138
Melting Point, °C (°F) –37 (-34.6)
Flash Point (Closed Cup), °C (°F) 22 (71.6)
Specific Gravity, 25°C (77°F) 0.88
Vapor Pressure (mm Hg, 20°C) 9 (48)
Refractive Index, D, 20°C (68°F) 1.463
Amine Value, mg KOH/g 560
Heat of Vaporization, kcal/mol 9.3
Applications & Uses

Applications & Uses

  • Pharmaceuticals
  • Textile Chemicals
  • Dyes
  • Agricultural chemicals
  • Corrosion Inhibitor
  • Inks
  • Zeolite manufacture
  • Ore Flotation
  • Rubber Chemicals
References in Literature

References in Literature

Showing most recent 1 to 5 of 491

Title Journal or Book Year
Analysis of US FDA-Approved Drugs Containing Sulfur Atoms Topics in Current Chemistry 2018
Recent Approaches Toward the Generation of Molecular Diversity Based on β-Lactam Structures Beta-Lactams 2017
Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity Chemistry of Heterocyclic Compounds 2017
Synthesis of seven-membered nitrogen heterocycles through the Ugi multicomponent reaction Chemistry of Heterocyclic Compounds 2017
Infrared spectroscopy as an effective tool in ring-opening metathesis polymerization: monitoring the polymerization kinetics of norbornene with amine-based Ru catalysts in real time Reaction Kinetics, Mechanisms and Catalysis 2017


Source: Springer Nature

Description: Literature references related to scientific contents from Springer Nature journals and books.



Showing most recent 1 to 5 of 491


Source: PubChem

Description: Data deposited in or computed by PubChem