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Toluene chemical
50.00 - 150.00 USD ($)/Metric Ton
Product Details:
- Chemical Name methylbenzene
- Other Names Phenyl methane
- Classification Other
- CAS No 108-88-3
- Type Other
- Application paints
- Raw Material industrial
- Supply Ability : 25 Metric Ton Per Month
- Click to view more
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Price And Quantity
- 50.00 - 150.00 USD ($)/Metric Ton
- 25 Metric Ton
Product Specifications
- Other
- solvent
- 99%
- years Years
- industrial
- Other
- Liquid Coating
- Phenyl methane
- methylbenzene
- 108-88-3
- paints
Trade Information
- FOB MUNDRA PORT
- Cash Advance (CA)
- 25 Metric Ton Per Month
- 7 Week
- Yes
- Free samples are available
- Africa, Middle East, Western Europe, Eastern Europe, South America, North America, Central America, Australia, Asia
- All India
Product Description
Toluene reacts as a normal aromatic hydrocarbon in electrophilic aromatic substitution.[14][15][16] Because the methyl group has greater electron-releasing properties than a hydrogen atom in the same position, toluene is more reactive than benzene toward electrophiles. It undergoes sulfonation to give p-toluenesulfonic acid, and chlorination by Cl2 in the presence of FeCl3 to give ortho and para isomers of chlorotoluene.
Importantly, the methyl side chain in toluene is susceptible to oxidation. Toluene reacts with Potassium permanganate to yield benzoic acid, and with chromyl chloride to yield benzaldehyde (Étard reaction).
The methyl group undergoes halogenation under free radical conditions. For example, N-bromosuccinimide (NBS) heated with toluene in the presence of AIBN leads to benzyl bromide. The same conversion can be effected with elemental bromine in the presence of UV light or even sunlight. Toluene may also be brominated by treating it with HBr and H2O2 in the presence of light.[1
Importantly, the methyl side chain in toluene is susceptible to oxidation. Toluene reacts with Potassium permanganate to yield benzoic acid, and with chromyl chloride to yield benzaldehyde (Étard reaction).
The methyl group undergoes halogenation under free radical conditions. For example, N-bromosuccinimide (NBS) heated with toluene in the presence of AIBN leads to benzyl bromide. The same conversion can be effected with elemental bromine in the presence of UV light or even sunlight. Toluene may also be brominated by treating it with HBr and H2O2 in the presence of light.[1
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Contact Details
- Plot No. F-11, R-16 Square, Opp. Dominos Pizza, Kapodara Patiya, Ankleshwar - 393002, Gujarat, India
- Mr. Sandeep (Export Manager)
- Send Inquiry
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