Skip to main content

1,4-Dibromobutan-2-ol

ADVERTISEMENT
Identification
Molecular formula
C4H8Br2O
CAS number
5430-71-9
IUPAC name
1,4-dibromobutan-2-ol
State
State

1,4-Dibromobutan-2-ol is usually found in a liquid state at room temperature, owing to its relatively high melting point and significant boiling point. It should be stored in a cool, dry place, away from any sources of ignition due to its flammability.

Melting point (Celsius)
21.00
Melting point (Kelvin)
294.15
Boiling point (Celsius)
257.60
Boiling point (Kelvin)
530.75
General information
Molecular weight
243.91g/mol
Molar mass
243.8960g/mol
Density
2.2703g/cm3
Appearence

1,4-Dibromobutan-2-ol typically appears as a colorless to pale-yellow liquid. It may seem somewhat viscous and has a slightly sweet, alcohol-like odor. The compound should be handled while observing standard safety precautions as it can be irritating to the skin and eyes.

Comment on solubility

Solubility of 1,4-Dibromobutan-2-ol

1,4-dibromobutan-2-ol, with the chemical formula C4H8Br2O, exhibits notable solubility characteristics that can be understood through the examination of its molecular structure and the polar nature of its functional groups.

Factors Influencing Solubility

The solubility of this compound can be influenced by several key factors:

  • Polarity: The presence of the hydroxyl group (-OH) contributes to hydrophilicity, allowing the compound to interact favorably with water.
  • Halogen Atoms: The Br atoms increase the molecular weight but also add to the overall polarity of the compound, affecting solubility in organic solvents.
  • Chain Length: With a three-carbon aliphatic chain, the compound is likely to be less soluble in nonpolar solvents but can dissolve reasonably well in polar solvents.

General Solubility Trends

It can be summarized that:

  • 1,4-dibromobutan-2-ol is moderately soluble in water.
  • It shows higher solubility in alcohols and other polar solvents.
  • It is likely to have limited solubility in nonpolar solvents due to the presence of polar functional groups.

In conclusion, the solubility of 1,4-dibromobutan-2-ol is chiefly dictated by its polar hydroxyl group juxtaposed against its hydrocarbon skeleton, resulting in its behavior as a compound that is more soluble in polar environments, making it of particular interest in organic synthesis and formulation chemistry.

Interesting facts

Interesting Facts About 1,4-Dibromobutan-2-ol

1,4-Dibromobutan-2-ol is a fascinating organic compound that offers intriguing insights into both chemical behavior and applications. Here are some interesting aspects of this compound:

  • Structure and Stability: The presence of bromine atoms in its structure contributes to the unique reactivity of 1,4-dibromobutan-2-ol. Typically, compounds with halogens are known for their diverse reactivity, which can be harnessed in organic synthesis.
  • Synthetic Applications: This compound can serve as an important intermediate in the synthesis of various other chemical products, including pharmaceuticals and agrochemicals. Due to the bromine substituents, chemical reactions like nucleophilic substitution become viable pathways to create new substances.
  • Research Potential: 1,4-Dibromobutan-2-ol can be explored in academic research settings for studying mechanisms of halogenation reactions and the behavior of alcohols containing halogen substituents.
  • Chiral Considerations: While 1,4-dibromobutan-2-ol itself may not exhibit chirality, its derivatives can lead to chiral compounds, which are crucial in the field of asymmetric synthesis for creating enantiomerically pure substances.
  • Biological Significance: As a brominated alcohol, 1,4-dibromobutan-2-ol can provide insights into biological activities. Brominated compounds are often investigated for their potential pharmaceutical applications and their roles in biological systems.

In conclusion, 1,4-dibromobutan-2-ol is not just a simple chemical compound; it embodies the intricate relationships between structure, reactivity, and utility in the broader field of chemistry. Its exploration opens doors to various synthetic methods and potential applications in research and industry.

Synonyms
1,4-Dibromo-2-butanol
19398-47-1
2-BUTANOL, 1,4-DIBROMO-
EINECS 243-029-6
NSC 84192
BRN 1733831
4-01-00-01581 (Beilstein Handbook Reference)
PSSRAPMBSMSACN-UHFFFAOYSA-N
RefChem:73207
1,4-Dibromobutan-2-ol
MFCD00000252
1,4-Dibromo-butan-2-ol
2-Butanol,1,4-dibromo-
NSC84192
1 4-DIBROMO-2-HYDROXYBUTANE
2-Butanol,4-dibromo-
WLN: E2YQ1E
SCHEMBL422142
SCHEMBL6238640
racemic 1,4-dibromobutan-2-ol
SCHEMBL29239828
DTXSID201319034
BR1637
NSC-84192
SBB007842
AKOS008901277
SB49402
AS-47602
SY051432
DB-073428
DB-080841
CS-0449071
D1743
NS00053825
1,4-Dibromo-2-butanol, 85%, technical grade
EN300-207506
F14612