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trimethylbenzene

Base Information Edit
  • Chemical Name:trimethylbenzene
  • CAS No.:25551-13-7
  • Molecular Formula:C9H12
  • Molecular Weight:120.21
  • Hs Code.:2902909090
  • Mol file:25551-13-7.mol
trimethylbenzene

Synonyms:Aromosol H;Methylxylene; Trimethylbenzene

Suppliers and Price of trimethylbenzene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 29 raw suppliers
Chemical Property of trimethylbenzene Edit
Chemical Property:
  • Vapor Pressure:1.45mmHg at 25°C 
  • Melting Point:-68.52°C (estimate) 
  • Refractive Index:1.5000 (estimate) 
  • Boiling Point:176.8°Cat760mmHg 
  • Flash Point:53.1°C 
  • PSA:0.00000 
  • Density:0.869g/cm3 
  • LogP:2.61180 
Purity/Quality:

99.9% *data from raw suppliers

Safty Information:
  • Pictogram(s): TLV: 25 ppm. 
  • Hazard Codes:TLV: 25 ppm. 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Uses Raw material for chemical synthesis. As a raw material in chemical syntheses; as ultraviolet stabilizers in plastics; found in solvents and as a constituent of gasoline.
Refernces Edit

Structural elucidation of an oxidation product of sedimentary porphyrins by one-pot synthesis of 3-methylphthalimide

10.1246/bcsj.74.1975

Shinya Nomoto et al. report the development of a one-pot synthesis method for 3-methylphthalimide starting from 1,2,3-trimethylbenzene. The process involves multiple steps, including bromination, nitric acid oxidation, conversion to an anhydride, and a thermal reaction with urea. The synthesized 3-methylphthalimide was confirmed to be identical to an oxidation product of sedimentary porphyrins previously identified by Barwise and Whitehead. Sedimentary porphyrins, which are complex mixtures resulting from the diagenetic modification of chlorophylls, have substitution patterns that can be determined after decomposition to maleimides. The study's findings provide a practical method for synthesizing 3-methylphthalimide, which is not commercially available, and offer insights into the precursors of benzoporphyrins in geological samples.

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