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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
Biological activity of secondary metabolites produced by a strain of Pseudomonas fluorescens.
2002
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
Kinetic-spectrophotometric determination of theophylline, dyphylline, and proxyphylline by use of partial least-squares regression.
2002 Sep
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
Decolorization and partial degradation of selected azo dyes by methanogenic sludge.
2004 Oct
Triggered release of proteins from emulsan-alginate beads.
2005 Dec 5
Degradation of 4-aminobenzenesulfonate by alginate encapsulated cells of Agrobacterium sp. PNS-1.
2006 Sep
Enhancement of intracellular gamma-tocopherol levels in cytokine-stimulated C3H 10T1/2 fibroblasts: relation to NO synthesis, isoprostane formation, and tocopherol oxidation.
2007 Jul 3
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
Bioprotective properties of seaweeds: in vitro evaluation of antioxidant activity and antimicrobial activity against food borne bacteria in relation to polyphenolic content.
2008 Jul 10
Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges.
2008 Oct 21
Mutagenicity and genotoxicity of acid yellow 17 and its biodegradation products.
2009
Phytochemical screening and polyphenolic antioxidant activity of aqueous crude leaf extract of Helichrysum pedunculatum.
2009 Nov 13
Hybrid UASFB-aerobic bioreactor for biodegradation of acid yellow-36 in wastewater.
2010 May
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 Mon Mar 31 19:22:12 GMT 2025
Edited
by admin
on Mon Mar 31 19:22:12 GMT 2025
Record UNII
434Z8C2635
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFANILIC ACID
HSDB   MI   USP-RS  
Systematic Name English
NSC-7170
Preferred 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
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 Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID6024464
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
WIKIPEDIA
SULFANILIC ACID
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
RS_ITEM_NUM
1633506
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
CHEBI
27500
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
PUBCHEM
8479
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
FDA UNII
434Z8C2635
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
CAS
121-57-3
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
HSDB
5590
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
NSC
7170
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-482-5
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
PRIMARY
MERCK INDEX
m10328
Created by admin on Mon Mar 31 19:22:12 GMT 2025 , Edited by admin on Mon Mar 31 19:22:12 GMT 2025
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