Cas no 24731-81-5 (1,6-Hexanediamine,hydrobromide (1:2))

1,6-Hexanediamine,hydrobromide (1:2) structure
24731-81-5 structure
Product Name:1,6-Hexanediamine,hydrobromide (1:2)
CAS No:24731-81-5
MF:C6H18Br2N2
MW:278.028520107269
CID:281971
PubChem ID:53436643
Update Time:2025-07-30

1,6-Hexanediamine,hydrobromide (1:2) Chemical and Physical Properties

Names and Identifiers

    • 1,6-Hexanediamine,hydrobromide (1:2)
    • 6-azaniumylhexylazanium,dibromide
    • Hexamethylenediammonium dibromide
    • hexane-1,6-diamine dihydrobromide
    • Hexamethylenediammonium dihydrobromide
    • 24731-81-5
    • Hexane-1,6-diammonium bromide
    • hexane-1,6-diaminium bromide
    • EINECS 246-439-3
    • 6-azaniumylhexylazanium;dibromide
    • hexane-1,6-diammonium dibromide
    • SCHEMBL21293918
    • 1,6 CHexanediammonium dibromide
    • Inchi: 1S/C6H16N2.2BrH/c7-5-3-1-2-4-6-8;;/h1-8H2;2*1H
    • InChI Key: XSYPBULLQGGYPJ-UHFFFAOYSA-N
    • SMILES: [Br-].[Br-].[NH3+]CCCCCC[NH3+]

Computed Properties

  • Exact Mass: 257.8428
  • Monoisotopic Mass: 275.984
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 5
  • Complexity: 31.5
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 55.3A^2

Experimental Properties

  • Boiling Point: 293.7°C at 760 mmHg
  • Flash Point: 131.4°C
  • PSA: 44.6

1,6-Hexanediamine,hydrobromide (1:2) Pricemore >>

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Additional information on 1,6-Hexanediamine,hydrobromide (1:2)

1,6-Hexanediamine Hydrobromide (1:2) - A Comprehensive Overview

Introduction to 1,6-Hexanediamine Hydrobromide (CAS No. 24731-81-5)

1,6-Hexanediamine hydrobromide (1:2) is a versatile chemical compound with the CAS registry number 24731-81-5. This compound is widely recognized in the chemical industry for its role as an intermediate in the synthesis of various polymers and materials. The hydrobromide salt form of 1,6-hexanediamine is particularly valuable due to its enhanced solubility and reactivity compared to its free base counterpart. Recent advancements in polymer chemistry have further highlighted the importance of this compound in the development of high-performance materials.

Chemical Structure and Properties

The molecular structure of 1,6-hexanediamine hydrobromide (1:2) consists of a six-carbon chain with two amine groups (-NH?) at each end and two bromide ions (Br?) as counterions. This arrangement not only enhances its stability but also contributes to its unique chemical reactivity. The compound exhibits a melting point of approximately 230°C and is soluble in water and common organic solvents such as ethanol and methanol.

Recent studies have explored the influence of steric and electronic effects on the reactivity of hexanediamines in various polymerization reactions. These findings underscore the importance of understanding the molecular interactions that govern the behavior of this compound in different chemical environments.

Synthesis and Production Methods

The synthesis of 1,6-hexanediamine hydrobromide (1:2) typically involves the reaction of hexamethylenediamine with hydrobromic acid (HBr). This process is highly efficient and ensures the formation of a stable salt structure. Researchers have recently investigated alternative methods to improve yield and reduce production costs, including the use of catalytic systems and optimized reaction conditions.

One notable advancement is the development of green chemistry approaches for synthesizing this compound. By utilizing renewable feedstocks and minimizing waste generation, these methods align with global sustainability goals while maintaining product quality.

Applications in Polymer Chemistry

Hexanediamines, including their hydrobromide salts, are critical components in the production of polyamides, polyurethanes, and other high-performance polymers. For instance, hexanediamine-based polyamides are widely used in textiles, automotive components, and industrial fibers due to their excellent mechanical properties and thermal stability.

Recent research has focused on expanding the applications of hexanediamines into emerging fields such as biodegradable polymers and smart materials. For example, studies have demonstrated the potential of hexanediamine derivatives in creating stimuli-responsive polymers that can adapt to environmental changes such as temperature or pH levels.

Additionally, hexanediamines are employed as crosslinking agents in epoxy resins and adhesives, enhancing their mechanical strength and durability. The use of hydrobromide salts in these applications has been shown to improve reaction kinetics and overall performance.

Biological Applications and Toxicology

Beyond its industrial applications, hexanediamine hydrobromide (CAS No. 24731-81-5) has shown promise in biological systems. Recent studies have explored its potential as a chelating agent for heavy metals, offering a novel approach to detoxification processes.

In terms of toxicity, research indicates that hexanediamines exhibit moderate toxicity when exposed to aquatic organisms. However, their biodegradability under specific environmental conditions suggests that proper waste management practices can mitigate ecological risks.

Efforts are ongoing to develop safer alternatives or modifications to reduce potential health hazards associated with handling this compound.

Market Trends and Future Prospects

The demand for hexanediamine hydrobromides (CAS No. 24731-81-5) continues to grow driven by increasing applications in advanced materials and specialty chemicals markets. The Asia-Pacific region has emerged as a key market due to rapid industrialization and rising demand for high-performance polymers.

Futuristic trends suggest that innovations in polymer chemistry will further expand the utility of this compound across diverse industries such as aerospace electronics textiles and biomedical engineering.

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