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1,2,4-Trimethylbenzene
[CAS# 95-63-6]

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Complete supplier list of 1,2,4-Trimethylbenzene
Identification
Classification Organic raw materials >> Hydrocarbon compounds and their derivatives >> Aromatic hydrocarbon
Name 1,2,4-Trimethylbenzene
Synonyms 1,3,4-Trimethylbenzene
Molecular Structure CAS # 95-63-6, 1,2,4-Trimethylbenzene, 1,3,4-Trimethylbenzene
Molecular Formula C9H12
Molecular Weight 120.19
CAS Registry Number 95-63-6
EC Number 202-436-9
SMILES CC1=CC(=C(C=C1)C)C
Properties
Solubiity 0.006 g/100g
Density 0.876
Melting point -44 ºC
Boiling point 168 ºC
Refractive index 1.504
Flash point 48 ºC
Safety Data
Hazard Symbols symbol symbol symbol   GHS02;GHS07;GHS09 Warning    Details
Hazard Statements H226-H332-H335-H315-H319-H411    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P264-P264+P265-P271-P273-P280-P301+P316-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P317-P319-P321-P331-P332+P317-P337+P317-P362+P364-P370+P378-P391-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Flammable liquidsFlam. Liq.3H226
Acute toxicityAcute Tox.4H332
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Aspiration hazardAsp. Tox.1H304
Skin corrosionSkin Corr.1BH314
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Specific target organ toxicity - single exposureSTOT SE3H370
Specific target organ toxicity - single exposureSTOT SE3H336
Specific target organ toxicity - repeated exposureSTOT RE2H373
Specific target organ toxicity - repeated exposureSTOT RE1H372
Transport Information UN 3295
SDS Available
up Discovory and Applicatios
1,2,4-Trimethylbenzene, commonly known as mesitylene, is a valuable aromatic hydrocarbon with a wide range of industrial applications. It was discovered in the mid-19th century and its unique properties make it a key compound in a variety of fields.

1,2,4-Trimethylbenzene was first isolated in 1866 by German chemist August Kekulé, who also played an important role in the development of chemical structural theory. Kekulé discovered that mesitylene is one of three isomers of trimethylbenzene, which also include 1,3,5-trimethylbenzene (hemicetylene) and 1,2,3-trimethylbenzene (pseudocetylene). The compound is a colorless liquid with a characteristic aromatic odor.

Mesitylene is a clear, colorless liquid with a boiling point of 163°C and a melting point of -40°C. It is relatively nonpolar and insoluble in water, but miscible with many organic solvents. Its chemical formula C₁₀H₁₂ indicates that it is a derivative of benzene with three methyl groups attached at the 1, 2, and 4 positions, giving it unique electronic and stereogenic properties.

Mesitylene is widely used as a solvent and intermediate in organic synthesis. It is used as a solvent in the preparation of various chemical reactions and as an ingredient in the production of other chemicals such as trimellitic anhydride, which is used to make high-performance resins and plastics.

Due to its low reactivity and ability to dissolve a wide range of organic substances, mesitylene is used as a solvent in the paints, coatings, and adhesives industries. It is used in formulations that require high purity and stability.

In the field of catalysis, mesitylene is used as a ligand in certain catalytic processes. It helps stabilize metal catalysts and improve their efficiency in chemical conversions. Its role in catalysis is essential in the production of various industrial chemicals and pharmaceuticals.

Mesitylene is used in the production of polymers, particularly in the manufacture of polyimides and other high-performance materials. These polymers are valued for their thermal stability and mechanical properties, making them suitable for use in aerospace and electronics.

The compound is also explored for environmental applications such as the removal of pollutants from water and soil. Its ability to act as a solvent and carrier for other substances makes it very useful in cleanup and remediation processes.

Research on mesitylene continues to focus on enhancing its applications and discovering new uses. Advances in chemical synthesis and environmental technologies are expected to expand its role in various industries and improve their sustainability.
Market Analysis Reports
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