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Trimethyl 1,2,4-benzenetricarboxylate

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Identification
Molecular formula
C12H14O6
CAS number
2108-61-8
IUPAC name
trimethyl benzene-1,2,4-tricarboxylate
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
81.00
Melting point (Kelvin)
354.00
Boiling point (Celsius)
288.00
Boiling point (Kelvin)
561.00
General information
Molecular weight
264.24g/mol
Molar mass
264.2410g/mol
Density
1.2690g/cm3
Appearence

Trimethyl 1,2,4-benzenetricarboxylate appears as a white crystalline solid or powder. It is often odorless and may exhibit a slight sheen or glisten when in the powdered form.

Comment on solubility

Solubility of Trimethyl Benzene-1,2,4-tricarboxylate

The solubility of Trimethyl Benzene-1,2,4-tricarboxylate is influenced by several factors, including its molecular structure and the nature of the solvent. This compound, characterized by the presence of multiple carboxylate groups, can exhibit varied solubility in different environments.

Key Factors Affecting Solubility:

  • Molecular Structure: The bulky trimethyl groups can hinder the compound's ability to interact with polar solvents, potentially leading to lower solubility in water.
  • Polarity: As a tricarboxylate, its acidic groups can ionize, increasing solubility in basic solutions.
  • Temperature: As with many organic compounds, elevated temperatures may enhance solubility by reducing intermolecular forces.
  • Solvent Choice: Trimethyl Benzene-1,2,4-tricarboxylate tends to be more soluble in organic solvents such as dichloromethane or ethanol compared to water.

In summary, while Trimethyl Benzene-1,2,4-tricarboxylate may show limited solubility in polar solvents, its solubility can increase significantly in organic solvents and under specific conditions. A thorough understanding of these properties is crucial for applications involving this compound.

Interesting facts

Interesting Facts about Trimethyl Benzene-1,2,4-tricarboxylate

Trimethyl benzene-1,2,4-tricarboxylate, commonly known in scientific circles for its unique structure and functionality, is an intriguing compound with several noteworthy characteristics:

  • Versatile Applications: This compound is widely utilized in the field of organic synthesis. Its derivatives serve important roles in the manufacture of polymers, fragrances, and food additives.
  • Synthetic Pathways: The synthesis of trimethyl benzene-1,2,4-tricarboxylate often involves multistep chemical reactions, showcasing the complexity and creativity in organic chemistry.
  • Structural Significance: The presence of three carboxylate groups on the benzene ring offers multiple points of reactivity, paving the way for the formation of various derivatives that can find applications in diverse chemical systems.
  • Environmental Impact: Studies on this compound also delve into its ecological footprint, emphasizing the importance of assessing the environmental implications of chemical production and usage.
  • Ongoing Research: Researchers are exploring innovative ways to utilize trimethyl benzene-1,2,4-tricarboxylate in green chemistry, working towards sustainable practices in chemical manufacturing.

As *George J. Hatfield* famously said, "The beauty of chemistry is in its ability to create new materials through the combination of existing structures." Trimethyl benzene-1,2,4-tricarboxylate is a prime example of this creative potential in the world of chemical science.

In summary, trimethyl benzene-1,2,4-tricarboxylate stands out not only for its diverse applications but also for the rich tapestry of reactions and syntheses it inspires, making it a subject of considerable interest in both academic and industrial settings.

Synonyms
Trimethyl trimellitate
2459-10-1
Trimethyl benzene-1,2,4-tricarboxylate
TRIMETHYL 1,2,4-BENZENETRICARBOXYLATE
1,2,4-Benzenetricarboxylic acid, 1,2,4-trimethyl ester
Methyl trimellitate
Trimellitic acid trimethyl ester
1,2,4-Benzenetricarboxylic acid, trimethyl ester
DTXSID8044620
16O7DT5N66
DTXCID6024620
HSDB 5880
EINECS 219-547-3
AI3-08219
1,2,4-BENZENETRICARBOXYLIC ACID, TRIMETHYL
TRIMETHYL 1,2,4-BENZENETRICARBOXYLATE [HSDB]
Trimethyl benzene1,2,4tricarboxylate
1,2,4Benzenetricarboxylic acid, trimethyl ester
1,2,4Benzenetricarboxylic acid, 1,2,4trimethyl ester
219-547-3
TRIMETHYL1,2,4-BENZENETRICARBOXYLATE
1,2,4-Benzenetricarboxylic Acid Trimethyl Ester
1,2,4-trimethyl benzene-1,2,4-tricarboxylate
MFCD00043629
SCHEMBL126043
UNII-16O7DT5N66
CHEMBL3183850
1,2,4-Tris(methoxycarbonyl)benzene
Tox21_302449
AKOS025116660
NCGC00256621-01
AS-69579
CAS-2459-10-1
CS-0204614
NS00046154
T1229
Trimethyl 1,2,4-benzenetricarboxylate, 98%
benzene-1,2,4-tricarboxylic acid trimethyl ester
Q27251833
InChI=1/C12H12O6/c1-16-10(13)7-4-5-8(11(14)17-2)9(6-7)12(15)18-3/h4-6H,1-3H