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Methyl benzenesulfonate, 98%, Thermo Scientific Chemicals
CAS: 80-18-2 | C7H8O3S | 172.20 g/mol
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Catalog number ALFB24515.22
Price (MYR)
555.00
Quantity:
100 g
Price (MYR)
555.00
Specifications
Chemical Name or MaterialMethyl benzenesulfonate
CAS80-18-2
Health Hazard 1H302-H314-H317-H335
Health Hazard 2GHS H Statement
H314-H341-H302
Causes severe skin burns and eye damage.
Suspected of causing genetic defects.
Harmful if swallowed.
H314-H341-H302
Causes severe skin burns and eye damage.
Suspected of causing genetic defects.
Harmful if swallowed.
Health Hazard 3P260-P264b-P270-P271-P272-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P333+P313-P363-P501c
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Methyl benzenesulfonate is a sulfonate ester which acts as a potential genotoxic impurity in drug substances. Further, it exerts genotoxic effects in bacterial and mammalian cell systems.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl benzenesulfonate is a sulfonate ester which acts as a potential genotoxic impurity in drug substances. Further, it exerts genotoxic effects in bacterial and mammalian cell systems.
Solubility
Miscible with chloroform, methanol, ethanol and ether. Immiscible with water.
Notes
Incompatible with strong oxidizing agents, strong acids and strong bases.
Methyl benzenesulfonate is a sulfonate ester which acts as a potential genotoxic impurity in drug substances. Further, it exerts genotoxic effects in bacterial and mammalian cell systems.
Solubility
Miscible with chloroform, methanol, ethanol and ether. Immiscible with water.
Notes
Incompatible with strong oxidizing agents, strong acids and strong bases.
RUO – Research Use Only
General References:
- Alkylating agent.
- Giricheva, N. I.; Fedorov, M. S.; Girichev, G. V. Conformations of methylbenzenesulfonate and its substituted derivatives: gas-phase electron diffraction versus vibrational spectroscopy. Struct. Chem. 2015, 26 (5), 1543-1553.
- Zhang, X.; Jiang, X.; Li, Y.; Lin, Z.; Zhang, G.; Wu, Y. Synthesis, crystal structures and properties of new quinolinium derivatives. Chem. Phys. Lett. 2015, 641, 141-145.