CAS 825-90-1
:Sodio 4-hidroxibenzenosulfonato
- 4-Hydroxybenzenesulfonic acid sodium salt
- 4-Hydroxybenzenesulphonic acid sodium salt
- 4-Phenolsulphonic acid sodium salt
- Benzenesulfonic acid, 4-hydroxy-, monosodium salt
- Benzenesulfonic acid, 4-hydroxy-, sodium salt (1:1)
- Benzenesulfonic acid, p-hydroxy-, monosodium salt
- Sodium 4-Hydroxybenzenesulfonate
- Sodium 4-Hydroxybenzenesulphonate
- Sodium Sulfophenylic Acid
- Sodium p-hydroxybenzenesulfonate
- Sodium p-hydroxyphenylsulfonate
- Sodium p-phenolsulfonate
- p-Hydroxybenzenesulfonic acid monosodium salt
- p-Hydroxybenzenesulfonic acid sodium salt
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Sodium 4-Hydroxybenzenesulfonate
CAS:Fórmula:C6H5NaO4SPureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:196.15Sodium 4-Hydroxybenzenesulfonate
CAS:Fórmula:C6H5NaO4SPureza:98%Forma y color:SolidPeso molecular:196.1563Sodium p-Hydroxybenzenesulfonate
CAS:Sodium p-HydroxybenzenesulfonatePureza:98%Peso molecular:196.16g/mol4-Hydroxybenzenesulfonic Acid Sodium Salt
CAS:Producto controladoApplications 4-Hydroxybenzenesulfonic Acid is a useful synthetic intermediate. It is used in the synthesis of difluoromethyl sulfonates. It can be also used to prepare Famphur Oxon (F102330) which is a metabolite of Famphur (F102325), an organophosphate insecticide and pesticide.
References Eisler, R.: US Dept. Int. Nat. Biol. Surv., 20, No pp. given (1994); Henny, C., et al.: J. Wild. Manag., No vol. given, 648 (1985); Loomis, E. & Schock, R.: J. Med. Entomol., 14, 649 (1978); Wright, J., & Schwarz, M.: J. Econ. Entomol., 65, 1644 (1972)Fórmula:C6H5NaO4SForma y color:NeatPeso molecular:196.16Sodium 4-hydroxybenzenesulfonate
CAS:Sodium 4-hydroxybenzenesulfonate is a chemical compound that is the sodium salt of 4-hydroxybenzenesulfonic acid. It has an inhibitory effect on sucrase activity and can be used as an antidiabetic drug. Sodium 4-hydroxybenzenesulfonate is synthesized by reacting sodium carbonate with 4-hydroxybenzene sulfonyl chloride in the presence of a proton, usually generated from an acid or base. The reaction mechanism for this process is nucleophilic substitution at the carbonyl group. This product has been shown to have optical properties that are sensitive to changes in pH and chloride concentration. Sodium 4-hydoxybenzenesulfonate has been immobilized onto a glassy carbon electrode surface using electrochemical immobilization techniques and then characterized using electrochemical impedance spectroscopy (EIS).
Fórmula:C6H6O4S•NaPureza:Min. 95%Forma y color:PowderPeso molecular:197.17 g/molSodium 4-hydroxybenzenesulfonate
CAS:Fórmula:C6H5NaO4SPureza:98%Forma y color:White to very pale yellow powderPeso molecular:196.15





