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Catalog Number:
49224
CAS Number:
109-64-8
1,3-Dibromopropane
Purity:
≥ 99% (GC)
Synonym(s):
Trimethylene dibromide
Hazmat
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Product Information

It may be used in the preparation of chiral geminal dicationic ionic liquid and 1,3-bis(1-7?-chloro-4-quinolyl-4- piperazinyl)propane

Synonyms
Trimethylene dibromide
CAS Number
109-64-8
Purity
≥ 99% (GC)
Molecular Formula
C3H6Br2
Molecular Weight
0
MDL Number
MFCD00000255
Melting Point
-34 °C
Density
1.98
Appearance
Colorless to light yellow liquid
Boiling Point
167 °C
Refractive Index
1.523
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Trimethylene dibromide
CAS Number
109-64-8
Purity
≥ 99% (GC)
Molecular Formula
C3H6Br2
Molecular Weight
0
MDL Number
MFCD00000255
Melting Point
-34 °C
Density
1.98
Appearance
Colorless to light yellow liquid
Boiling Point
167 °C
Refractive Index
1.523
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,3-Dibromopropane is widely utilized in research focused on:

  • Synthesis of Organic Compounds: This chemical serves as a versatile building block in organic synthesis, allowing chemists to create a variety of brominated compounds, which are important in pharmaceuticals and agrochemicals.
  • Solvent Applications: It is used as a solvent in various chemical reactions, providing a medium that can dissolve both polar and non-polar substances, which is crucial for reaction efficiency.
  • Intermediate in Chemical Manufacturing: 1,3-Dibromopropane acts as an intermediate in the production of specialty chemicals, including flame retardants and surfactants, thus playing a key role in the chemical industry.
  • Research in Material Science: Its properties make it useful in the development of new materials, such as polymers, where it can enhance thermal stability and chemical resistance.
  • Laboratory Reagent: Frequently employed as a reagent in laboratories for various analytical techniques, it aids in the identification and quantification of other compounds, streamlining research processes.

Citations