p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals
p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals
p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals
p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals

CAS: 6192-52-5 | C7H10O4S | 190.21 g/mol
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Catalog number ALFA14119.0B
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Chemical Identifiers
CAS39394-84-8
IUPAC Namediphosphooxidane; methanesulfonic acid
Molecular FormulaCH4O8P2S
InChI KeyJHNLZOVBAQWGQU-UHFFFAOYSA-N
SMILESCS(O)(=O)=O.O=P(=O)OP(=O)=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Form)Solution
Titration with NaOH6.5 to 10.0 % (P2O5)
Appearance (Color)Clear colorless to yellow to orange
AppearanceMay contain precipitate, re-dissolves on warming
Appearance (Color)to light brown or pale pink
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p-Toluenesulfonic acid monohydrate is used as a catalyst in the synthesis of resveratrol, in oxane derivatives as an antimalarial agent, as substituted piperidine and unsymmetrical benzyl. It acts as a catalyst in the preparation of 1,3,5-trisubstituted pyrazoles derivatives, selenated ketene dithioacetals, triazoloquinazolinone and benzimidazoquinazolinone derivatives. It also serves as an intermediate in the esterification and in reductive amination reactions.

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
p-Toluenesulfonic acid monohydrate is used as a catalyst in the synthesis of resveratrol, in oxane derivatives as an antimalarial agent, as substituted piperidine and unsymmetrical benzyl. It acts as a catalyst in the preparation of 1,3,5-trisubstituted pyrazoles derivatives, selenated ketene dithioacetals, triazoloquinazolinone and benzimidazoquinazolinone derivatives. It also serves as an intermediate in the esterification and in reductive amination reactions.

Notes
Hygroscopic. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only