CAS 825-90-1
:Sodium 4-hydroxybenzènesulfonate
- 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
- Voir plus de synonymes
Sodium 4-Hydroxybenzenesulfonate
CAS :Formule :C6H5NaO4SDegré de pureté :>98.0%(T)(HPLC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :196.15Sodium 4-Hydroxybenzenesulfonate
CAS :Formule :C6H5NaO4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :196.1563Sodium p-Hydroxybenzenesulfonate
CAS :Sodium p-HydroxybenzenesulfonateDegré de pureté :98%Masse moléculaire :196.16g/mol4-Hydroxybenzenesulfonic Acid Sodium Salt
CAS :Produit contrôléApplications 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)Formule :C6H5NaO4SCouleur et forme :NeatMasse moléculaire :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).
Formule :C6H6O4S•NaDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :197.17 g/molSodium 4-hydroxybenzenesulfonate
CAS :Formule :C6H5NaO4SDegré de pureté :98%Couleur et forme :White to very pale yellow powderMasse moléculaire :196.15





