1.0 2016-05-22 03:46:19 UTC 2026-08-18 17:50:02 UTC Sulfadimethoxine SmallMolecule Sulfadimethoxine is an organic compound with the chemical formula C12H14N4O4S and an average molecular weight of 310.33 g/mol. Sulfadimethoxine belongs to the benzenesulfonamides, a subclass of benzene and substituted derivatives within the organic compounds. This compound is identified as being found in or released from 13 recorded sources. Within healthcare, pharmaceuticals, and veterinary products, it is used as an antibiotic. Other sources include drinking water and water supply systems. In the context of food, food processing, and cookware, it is associated with food preservation and the processing of meats. It is also linked to building and construction materials, specifically ceilings. Furthermore, it is found in household cleaning and consumer products, such as ash trays and non-electric simulated smoking devices. Recorded sources related to electrical and electronic equipment include electrodes, discharge lamps, electric switches, electrically stimulated smoking devices, and conductors or conductive bodies characterised by the conductive materials. Recorded exposure routes for this substance include oral and inhalation. Sulphadimethoxine C12H14N4O4S 310.329 310.073575646 4-amino-N-(2,6-dimethoxypyrimidin-4-yl)benzene-1-sulfonamide sulfadimethoxine 122-11-2 COC1=NC(OC)=NC(NS(=O)(=O)C2=CC=C(N)C=C2)=C1 InChI=1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16) ZZORFUFYDOWNEF-UHFFFAOYSA-N Organic compounds Benzenoids Benzene and substituted derivatives Benzenesulfonamides Aminobenzenesulfonamides Alkyl aryl ethers Aminosulfonyl compounds Aniline and substituted anilines Azacyclic compounds Benzenesulfonyl compounds Heteroaromatic compounds Hydrocarbon derivatives Imidolactams Organic oxides Organopnictogen compounds Organosulfonamides Primary amines Pyrimidines and pyrimidine derivatives Alkyl aryl ether Amine Aminobenzenesulfonamide Aminosulfonyl compound Aniline or substituted anilines Aromatic heteromonocyclic compound Azacycle Benzenesulfonyl group Ether Heteroaromatic compound Hydrocarbon derivative Imidolactam Organic nitrogen compound Organic oxide Organic oxygen compound Organic sulfonic acid or derivatives Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Organosulfonic acid amide Organosulfonic acid or derivatives Organosulfur compound Primary amine Pyrimidine Sulfonyl Aromatic heteromonocyclic compounds aromatic ether pyrimidines substituted aniline sulfonamide sulfonamide antibiotic Detected and Not Quantified Sulfadimethoxine Drug Metabolism Action Pathway SMP0143994 Sulfadimethoxine Predicted Metabolism Pathway SMP0174678 logp 1.26 logp 1.08 ALOGPS logs -3.05 ALOGPS solubility 2.78e-01 g/l ALOGPS logp 1.26 ChemAxon pka_strongest_acidic 6.91 ChemAxon pka_strongest_basic 1.95 ChemAxon iupac 4-amino-N-(2,6-dimethoxypyrimidin-4-yl)benzene-1-sulfonamide ChemAxon average_mass 310.329 ChemAxon mono_mass 310.073575646 ChemAxon smiles COC1=NC(OC)=NC(NS(=O)(=O)C2=CC=C(N)C=C2)=C1 ChemAxon formula C12H14N4O4S ChemAxon inchi InChI=1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16) ChemAxon inchikey ZZORFUFYDOWNEF-UHFFFAOYSA-N ChemAxon polar_surface_area 116.43 ChemAxon refractivity 77.75 ChemAxon polarizability 29.6 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 7 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon #<HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f7225f4ea68> DB06150 5323 5132