1,2,4,5-Tetramethylbenzene Cas:95-93-2

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1,2,4,5-Tetramethylbenzene

Product name:

CAS NO. 95-93-2 1,2,4,5-Tetramethylbenzene

CAS NO.:

95-93-2

Structure:

Synonyms:

1,2,4,5-tetramethyl-benzen;2,5-dimethyl-p-xylen;benzene,1,2,4,5-tetramethyl-;I,i,4,5-Tetramcthylben~oiaG;sym-Tetramethylbenzene;1.2.4.5-TetraM;1,2,4,5-TETRAMETHYLBENZENE;LABOTEST-BB LT00852111

MF:

C10H14

EINECS:

202-465-7

Chemical Properties:

white to brown semi-transparent crystals

Purity

98%

Capacity:

1000KG /month

Package

In paper drums /Fluoride drums /plastic drums/IBC Tank ,etc.

Shipment method :

By Sea,Air,Courier door to door,etc.

Storeage:

Under room temperature ,keep away from direct sun light

Loading Port :

China any port,Beijing,Shanghai,Hongkong

Transportation condition:

Shipped as non- dangerous chemicals

Product Categories

Highly Purified Reagents;Other Categories;Zone Refined Products;Arenes;Building Blocks;Chemical Synthesis;Organic Building Blocks

Information of CAS NO. 95-93-2 1,2,4,5-Tetramethylbenzene

CAS NO. 95-93-2 1,2,4,5-Tetramethylbenzene is an organic compound with the formula C6H2(CH3)4. It is a colourless solid with a sweet odor. The compound is classified as an alkylbenzene. It is one of three isomers of tetramethylbenzene, the other two being prehnitene (1,2,3,4-tetramethylbenzene, m.p. −6.2 °C) and isodurene (1,2,3,5-tetramethylbenzene, m.p. −23.7 °C). Durene has an unusually high melting point (79.2 °C), reflecting its high molecular symmetry.

CAS NO. 95-93-2 1,2,4,5-Tetramethylbenzene is an electron-rich arene, exhibiting nucleophilicity comparable to that of phenol.It is readily halogenated on the ring for example. Nitration gives the dinitro derivative, a precursor to duroquinone. In industry, it is the precursor to pyromellitic dianhydride, which is used for manufacturing curing agents, adhesives, coating materials. It is used in the manufacture of some raw materials for engineering plastics (polyimides) and cross-linking agent for alkyd resins.It is also a suitable starting material for the synthesis of hexamethylbenzene



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