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1,2,3-Tribromopropane

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Identification
Molecular formula
C3H5Br3
CAS number
96-11-7
IUPAC name
1,2,3-tribromopropane
State
State

At room temperature, 1,2,3-tribromopropane is in a liquid state.

Melting point (Celsius)
-16.00
Melting point (Kelvin)
257.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
280.78g/mol
Molar mass
280.7760g/mol
Density
2.4930g/cm3
Appearence

1,2,3-Tribromopropane is a colorless to pale yellow liquid under standard conditions.

Comment on solubility

Solubility of 1,2,3-Tribromopropane

1,2,3-Tribromopropane (C3H6Br3) is a halogenated hydrocarbon that exhibits unique solubility properties. When exploring its solubility in various solvents, several factors come into play:

  • Polarity: The presence of three bromine atoms makes this compound more polar compared to non-halogenated hydrocarbons, influencing its solubility.
  • Solvent Compatibility: 1,2,3-Tribromopropane tends to dissolve well in polar organic solvents, such as:
    • Alcohols
    • Aromatic hydrocarbons
    • Chlorinated solvents
    • Certain ethers
  • Water Solubility: This compound is generally insoluble in water due to its hydrophobic nature, leading to a tendency to separate from aqueous environments.

The solubility behavior can lead to intriguing applications in organic synthesis and extraction processes. As a practical consideration, understanding the solubility of 1,2,3-tribromopropane helps in optimizing its use in chemical reactions and formulations. Remember, "like dissolves like"; thus, the solubility characteristics can help predict compatibility with various media in chemical applications.

Interesting facts

Interesting Facts About 1,2,3-Tribromopropane

1,2,3-Tribromopropane is a fascinating chemical compound that belongs to the family of halogenated organic compounds. As a synthetic derivative of propane, it has captured the interest of chemists and industrial practitioners alike due to its unique properties and applications. Here are some intriguing facts:

  • Halogenation Hero: This compound is formed by the bromination of propane, where each carbon atom in the propyl chain is substituted with bromine atoms. The process showcases the reactivity of alkanes when subjected to halogenation.
  • Explosive Potential: 1,2,3-Tribromopropane has been investigated for its potential use in explosive formulations, particularly because of its ability to release significant amounts of energy when decomposed.
  • Solvent Insights: It serves as a solvent in various organic reactions, often employed in the laboratory setting for dissolving certain organic substrates.
  • Biological Activity: Studies have suggested that halogenated compounds, such as this one, can exhibit various biological activities. Understanding these effects can open pathways in pharmacological research, although safety precautions are pivotal given their toxicity.
  • Trace Environmental Impact: As a brominated compound, it is essential to consider its environmental footprint. Compounds like 1,2,3-tribromopropane are monitored for their persistence and potential impact on ecosystems.

In summary, 1,2,3-tribromopropane stands as a compelling subject of study within the field of chemistry. Its unique characteristics and implications in industrial applications and biological research reflect the ever-evolving landscape of organic chemistry. Remember: Every molecule tells a story!

Synonyms
1,2,3-TRIBROMOPROPANE
96-11-7
s-Tribromopropane
Propane, 1,2,3-tribromo-
Glycerol tribromohydrin
Glyceryl tribromohydrin
sym-Tribromopropane
NSC 78932
CCRIS 6706
UNII-D2R8L96TOV
EINECS 202-478-8
D2R8L96TOV
BRN 1732082
AI3-18135
1,2,3-tribromo-propane
NSC-78932
DTXSID9059129
CHEBI:18859
TRIBROMOPROPANE, 1,2,3-
4-01-00-00221 (Beilstein Handbook Reference)
1,2,3-TRIBROMOPROPANE [MI]
Tribromohydrin
sTribromopropane
symTribromopropane
MFCD00017884
1,3-Tribromopropane
1.2.3-Tribromopropane
Propane,2,3-tribromo-
Propane, 1,2,3tribromo
NCIOpen2_004459
SCHEMBL66165
DTXCID0048979
1,2,3-Tribromopropane, 97%
NSC78932
AKOS000120060
FT43734
AS-58199
DB-057620
NS00040473
T0355
EN300-19787
E78688
Q4545647
F0001-2288
202-478-8