Sulfonic aromatic compounds are widely used in the textile industry for the synthesis of azo dyes. The presence of the sulfonic group endows these compounds with high water-solubility and resistance to biological treatment. The present work analysed the efficacy of oxidation with ozone in the treatment of waters containing naphthalene-1-sulfonic acid, naphthalene-1,5-disulfonic acid and naphtha...

The title compound, C(26)H(25)NO, was obtained via a one-pot synthesis from the reaction of 2-naphthol, 1-(p-tol-yl)ethyl-amine, p-toluene-sulfonic acid and benzaldehyde. There are three mol-ecules per asymmetric unit, all having similar conformations. There are intra-molecular O-H⋯N and C-H⋯O hydrogen bonds, with only van der Waals forces found between mol-ecules.

In the crystal structure of the title compound, C(14)H(17)NO(4), obtained by the reaction of N-benzoxycarbonyl-l-valine, paraformaldehyde and 4-methyl-benzene-sulfonic acid, mol-ecules are linked by C-H⋯O hydrogen bonds, generating linear chains parallel to the a axis. C-H⋯π inter-actions of stacked benzene rings also provide stability for the crystal structure.

The asymmetric unit of the title compound, C(5)H(7)N(5) (2+)·2C(7)H(7)O(3)S(-)·H(2)O, consists of one diprotonated adeninium cation, two p-toluene-sulfonic acid anions and one water mol-ecule. In the crystal, the cations and anions are connected through N-H⋯O hydrogen bonds forming R(2) (2)(8) and R(2) (2)(9) graph-set motifs. The solvent water mol-ecule links cations and anions through O-H⋯O a...

The title mononuclear complex, [Zn(C(8)H(11)N(2)O(3)S)(2)], is a zinc salt of 2-(2-pyridylmethyl-amino)ethane-sulfonic acid (Hpmt). The Zn(II) ion is located on an inversion centre and is octahedrally surrounded by four N and two O atoms. The deprotonated pmt(-) anion coordinates in a facial arrangement through its two N atoms and one of the sulfonate O atoms. The crystal packing is determined ...

Human peroxiredoxins serve dual roles as anti-oxidants and regulators of H(2)O(2)-mediated cell signaling. The functional versatility of peroxiredoxins depends on progressive oxidation of key cysteine residues. The sulfinic or sulfonic forms of peroxiredoxin lose their peroxidase activity, which allows cells to accumulate H(2)O(2) for signaling or pathogenesis in inflammation, cancer, and other...

IN THE TITLE COMPOUND [SYSTEMATIC NAME: 5-(5,7-dihydr-oxy-4-oxo-4H-chromen-yl)-2-hydroxy-benzene-sulfonic acid dihydrate], C(15)H(10)O(8)S·2H(2)O, the benzopyran-one ring is not coplanar with the phenyl ring, the dihedral angle between them being 41.35 (3)°. No H atom was placed on the sulphonic acid group because it was not possible to distinguish between the two S=O bonds and the S-O bond. In...