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Triclosan

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Identification
Molecular formula
C12H7Cl3O2
CAS number
3380-34-5
IUPAC name
3,4,5-trichloro-2,6-dimethoxy-phenol
State
State

At room temperature, triclosan is in a solid state.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.15
Boiling point (Celsius)
120.00
Boiling point (Kelvin)
393.15
General information
Molecular weight
289.55g/mol
Molar mass
289.5450g/mol
Density
1.4920g/cm3
Appearence

Triclosan appears as a white crystalline powder. It is slightly soluble in water but soluble in organic solvents like ethanol and diethyl ether.

Comment on solubility

Solubility of 3,4,5-trichloro-2,6-dimethoxy-phenol

3,4,5-trichloro-2,6-dimethoxy-phenol, often referred to for its numerous applications, exhibits interesting solubility characteristics:

  • Polar Solvents: This compound tends to be more soluble in polar solvents such as water, largely due to its phenolic group which can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, it shows lower solubility in non-polar solvents, aligning with the principle that "like dissolves like." This is reflective of its molecular structure which possesses both polar and non-polar characteristics.
  • Effect of Temperature: The solubility can be significantly affected by temperature; generally, increased temperature enhances solubility for many organic compounds.

Overall, the solubility of 3,4,5-trichloro-2,6-dimethoxy-phenol can be summarized with the quote: "Understanding solubility is key to unlocking the potential of chemical compounds!" Its unique structure contributes to its behavior in various solvents, making it a subject of interest in both research and application.

Interesting facts

Interesting Facts about 3,4,5-Trichloro-2,6-dimethoxy-phenol

3,4,5-Trichloro-2,6-dimethoxy-phenol is a fascinating compound known for its significant applications and rich chemistry. Here's what makes it stand out:

  • Key Industry Application: This compound is primarily used as a herbicide. Due to its ability to control unwanted vegetation, it plays a crucial role in agricultural practices.
  • Environmental Perspective: As a chlorinated phenol, it raises interesting discussions about environmental impacts and persistence. Its chemical stability can lead to concerns regarding soil and water contamination.
  • Mechanism of Action: 3,4,5-Trichloro-2,6-dimethoxy-phenol inhibits the activity of specific enzymes within plants, effectively interfering with their growth and metabolic processes.
  • Research Interest: The compound's unique composition has attracted researchers looking to explore its potential as a starting point for the synthesis of other compounds, especially in the field of agrochemicals.
  • Toxicity and Safety: Like many chlorinated compounds, safety measures are essential during handling. Understanding the toxicological profiles helps in mitigating risks associated with its use.
  • Structure and Stability: The presence of both chlorine and methoxy groups in its structure contributes to the compound's stability and reactivity, making it a prime example for studies in organochlorine chemistry.

In conclusion, 3,4,5-trichloro-2,6-dimethoxy-phenol is more than just a chemical compound; it is a significant player in the agricultural sector and a valuable research subject. Its unique chemical characteristics open avenues for innovation and caution alike.

Synonyms
Trichlorosyringol
3,4,5-Trichloro-2,6-dimethoxyphenol
3,4,5-Trichlorosyringol
CCRIS 4060
Phenol, 3,4,5-trichloro-2,6-dimethoxy-
DTXSID7074246
DTXCID9037292
2539-26-6
SCHEMBL9188444
ZZCSBXFJFLSDRR-UHFFFAOYSA-N
AKOS040757843
DA-69861
HY-133606
CS-0128383