Chlorhexidine
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- Molecular formula
- C12H16Cl2O2
- CAS Number
- 88-04-0
- IUPAC Name
- 4,6-dichloro-2-hexyl-benzene-1,3-diol
- Molecular Weight
- 285.15g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2400g/cm3
- Synonyms
- 4, 6-DICHLORO-2-HEXYLRESORCINOL
Identification
Interesting facts
Exploring 4,6-Dichloro-2-hexyl-benzene-1,3-diol
4,6-Dichloro-2-hexyl-benzene-1,3-diol is a fascinating chemical compound with a variety of intriguing characteristics and applications. Here are some noteworthy points that highlight its significance in the field of chemistry:
- Structure and Composition: This compound features a benzene ring that is substituted with two chlorine atoms and a hexyl group, making it structurally unique. The presence of the diol functional groups, specifically at the 1 and 3 positions, indicates that it contains two hydroxyl (–OH) groups that contribute to its reactivity and solubility properties.
- Biological Importance: Compounds like 4,6-dichloro-2-hexyl-benzene-1,3-diol are often studied for their potential biological activity, including antimicrobial properties. Such compounds can serve as important lead substances for developing new pharmaceuticals or agricultural products.
- Environmental Impact: Being a chlorinated compound, it is essential to study its environmental behavior. Understanding its degradation pathways and persistence in nature is critical for assessing its potential ecological implications.
- Applications: This compound may find applications in various fields including:
- Pesticide or herbicide formulation due to its active properties.
- Synthesis of more complex organic compounds in the pharmaceutical industry.
- Research studies targeting chlorinated organic compounds to understand their effects on human health and the environment.
- Research Potential: Scientists continue to explore the use of compounds like this for innovative applications, such as in materials science or as intermediates in organic synthesis.
In summary, 4,6-dichloro-2-hexyl-benzene-1,3-diol exemplifies the intricate connections between chemical structure, biological activity, and environmental considerations. Its multifaceted nature makes it a compound of interest for ongoing research and development in the scientific community.