U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H7NO3S
Molecular Weight 173.19
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFANILIC ACID

SMILES

NC1=CC=C(C=C1)S(O)(=O)=O

InChI

InChIKey=HVBSAKJJOYLTQU-UHFFFAOYSA-N
InChI=1S/C6H7NO3S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H,8,9,10)

HIDE SMILES / InChI

Molecular Formula C6H7NO3S
Molecular Weight 173.19
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sodium sulfanilate is a salt of sulphanilic acid and has been used to monitor the degree of renal dysfunction in dogs.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Nitrate and nitrite content in potatoes from ecological and conventional farms].
2001
Spectrophotometric determination of certain vicinal dihydroxybenzene derivatives in pharmaceutical preparations.
2001 Apr
Voltammetric studies of 2-hydroxy-5-[(4-sulfophenyl)azo]benzoic acid as a novel prodrug of 5-aminosalicylic acid.
2001 Dec
[Color reactions for identification of sodium cromoglycate].
2001 May
Biological activity of secondary metabolites produced by a strain of Pseudomonas fluorescens.
2002
Replacement of cyanogen bromide solution PH. EUR. with 1,3-dibromo-5,5-dimethylhydantoin (DBH). Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 13.
2002 Apr
Novel hydrogen-bonded three-dimensional networks encapsulating one-dimensional covalent chains: [M(4,4'-bipy)(H2O)(4)](4-abs)(2).nH2O (4,4'-bipy = 4,4'-bipyridine; 4-abs = 4-aminobenzenesulfonate) (M = Co, n = 1; M = Mn, n = 2).
2002 Dec 2
Degradation of acid orange 7 in an aerobic biofilm.
2002 Jan
Diaquabis(1,3-propanediamine-kappa(2)N,N')nickel(II) bis(sulfanilate).
2002 Jul
Zero-valent iron pretreatment for enhancing the biodegradability of Azo dyes.
2002 May-Jun
Kinetic-spectrophotometric determination of theophylline, dyphylline, and proxyphylline by use of partial least-squares regression.
2002 Sep
Study of tropaeolin degradation by iron--proposition of a reaction mechanism.
2003 Dec
The hydrogen-bonded adduct 7,16-diazonia-18-crown-6-4-aminobenzenesulfonate-water (1/2/2).
2003 Feb
High performance degradation of azo dye Acid Orange 7 and sulfanilic acid in a laboratory scale reactor after seeding with cultured bacterial strains.
2003 Jun
[Evaluation of a colorimetric method for studying the interaction between microorganisms and intestinal epithelial cells].
2003 Oct-Dec
Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases.
2004
Micellar electrokinetic chromatographic screening method for common sexual assault drugs administered in beverages.
2004 Apr 20
Mer-(4-aminobenzenesulfonato-kappa N)triaqua(1,10-phenanthroline-kappa 2N,N')cobalt(II) chloride.
2004 Jan
Photochemical fate of sulfa drugs in the aquatic environment: sulfa drugs containing five-membered heterocyclic groups.
2004 Jul 15
Hepatopulmonary syndrome induced by common bile duct ligation in a rabbit model: correlation between pulmonary vascular dilatation on thin-section CT and angiography and serum nitrite concentration or endothelial nitric oxide synthase (eNOS)1 expression.
2004 Jul-Sep
[Preparation and FTIR properties of amino compounds modified glutaraldehyde crosslinked chitosan resin activated with cyanuric chloride].
2004 Nov
Decolorization and partial degradation of selected azo dyes by methanogenic sludge.
2004 Oct
Arylsulfonates as sole source of sulfur for Clostridium pasteurianum DSM 12136.
2005
Triggered release of proteins from emulsan-alginate beads.
2005 Dec 5
Removal of acetaldehyde vapor with impregnated activated carbons: effects of steric structure on impregnant and acidity.
2005 Jul 15
Electroenzymatic degradation of azo dye using an immobilized peroxidase enzyme.
2005 Nov 11
Evaluation of tumour necrosis factor alpha, interleukin-2 soluble receptor, nitric oxide metabolites, and lipids as inflammatory markers in type 2 diabetes mellitus.
2006
Microbial conversion of selected azo dyes and their breakdown products.
2006
Mineralization of 4-aminobenzenesulfonate (4-ABS) by Agrobacterium sp. strain PNS-1.
2006 Dec
Enhanced biodegradation of azo dyes using an integrated elemental iron-activated sludge system: I. Evaluation of system performance.
2006 Jan
Optical fiber reflectance sensor coupled to a multisyringe flow injection system for preconcentration and determination of 1-naphthylamine in water samples.
2006 Jul 28
Nucleotide-mimetic synthetic ligands for DNA-recognizing enzymes One-step purification of Pfu DNA polymerase.
2006 Jul 28
Liquid chromatographic determination of maleic hydrazide in technical and formulated products: collaborative study.
2006 Jul-Aug
Aerobic degradation of acid orange 7 in a vertical-flow constructed wetland.
2006 Jun
Spectrophotometric determination of peptide transport with chromogenic peptide mimetics.
2007 Aug 15
Decolorization and partial degradation of monoazo dyes in sequential fixed-film anaerobic batch reactor (SFABR).
2007 Jul
Free-radical-induced oxidative and reductive degradation of sulfa drugs in water: absolute kinetics and efficiencies of hydroxyl radical and hydrated electron reactions.
2007 Sep 20
Nitrergic response to cyclophosphamide treatment in blood and bone marrow.
2008
Electrochemical synthesis of polyaniline nano-networks on p-aminobenzene sulfonic acid functionalized glassy carbon electrode Its use for the simultaneous determination of ascorbic acid and uric acid.
2008 Dec 1
A coupled reagent of o-phthalaldehyde and sulfanilic acid for protein detection based on the measurements of light scattering signals with a common spectrofluorometer.
2008 May 30
Role of vitamins C and e in regulating antioxidant and pro-oxidant markers in preeclampsia.
2008 Nov
Oxidation of sulfamethoxazole by UVA radiation and modified Fenton reagent: toxicity and biodegradability of by-products.
2009
Lack of genotoxic effect of food dyes amaranth, sunset yellow and tartrazine and their metabolites in the gut micronucleus assay in mice.
2009 Feb
Species distribution and antimicrobial susceptibility of gram-negative aerobic bacteria in hospitalized cancer patients.
2009 Feb 19
[Kinetics and mechanism of 4-aminobenzenesulphonate biodegradation].
2009 Jul 15
Reductive reaction mechanisms of the azo dye Orange II in aqueous solution and in cellulose: from radical intermediates to products.
2009 May 28
Effect of a sulfonated azo dye and sulfanilic acid on nitrogen transformation processes in soil.
2009 Oct 30
Oxidative stress and S-100B protein in children with bacterial meningitis.
2009 Oct 8
New room temperature ionic liquids with interesting ecotoxicological and antimicrobial properties.
2009 Sep
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Thu Jul 06 02:01:12 UTC 2023
Edited
by admin
on Thu Jul 06 02:01:12 UTC 2023
Record UNII
434Z8C2635
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFANILIC ACID
HSDB   MI   USP-RS  
Systematic Name English
SULFADIMETHOXINE SODIUM FOR VETERINARY USE IMPURITY D [EP IMPURITY]
Common Name English
ANILINE-4-SULFONIC ACID
Common Name English
P-SULFOANILINE
Common Name English
1-AMINOBENZENE-4-SULFONIC ACID
Systematic Name English
P-AMINOBENZENESULFONIC ACID
Common Name English
SULFADIMETHOXINE IMPURITY D [EP IMPURITY]
Common Name English
P-AMINOPHENYLSULFONIC ACID
Common Name English
BENZENESULFONIC ACID, 4-AMINO-
Systematic Name English
4-SULFOANILINE
Systematic Name English
ANILINE-P-SULFONIC ACID
Common Name English
SULFADIMIDINE IMPURITY F [EP IMPURITY]
Common Name English
4-AMINOBENZENESULFONIC ACID
Systematic Name English
SULFADIAZINE IMPURITY B [EP IMPURITY]
Common Name English
SULPHANILIC ACID
Common Name English
SULFANILIC ACID [MI]
Common Name English
4-AMINOPHENYLSULFONIC ACID
Systematic Name English
NSC-7170
Code English
MESALAZINE IMPURITY O [EP IMPURITY]
Systematic Name English
SULFANILIC ACID [HSDB]
Common Name English
SULFAMETHOXAZOLE IMPURITY D [EP IMPURITY]
Common Name English
P-ANILINESULFONIC ACID
Common Name English
SULFANILIC ACID [USP-RS]
Common Name English
Code System Code Type Description
MESH
C100016
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
EPA CompTox
DTXSID6024464
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
WIKIPEDIA
SULFANILIC ACID
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
RS_ITEM_NUM
1633506
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
CHEBI
27500
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
PUBCHEM
8479
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
FDA UNII
434Z8C2635
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
CAS
121-57-3
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
HSDB
5590
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
NSC
7170
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-482-5
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY
MERCK INDEX
M10328
Created by admin on Thu Jul 06 02:01:12 UTC 2023 , Edited by admin on Thu Jul 06 02:01:12 UTC 2023
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
Correction factors: for the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
FOR VETERINARY USE
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY