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Naphthionic acid

CAS No.:
84-86-6
Catalog Number:
AG0033WP
Molecular Formula:
C10H9NO3S
Molecular Weight:
223.2484
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$60
- +
5g
97%
In Stock USA
United States
$115
- +
25g
97%
In Stock USA
United States
$248
- +
Product Description
Catalog Number:
AG0033WP
Chemical Name:
Naphthionic acid
CAS Number:
84-86-6
Molecular Formula:
C10H9NO3S
Molecular Weight:
223.2484
MDL Number:
MFCD00004027
IUPAC Name:
4-aminonaphthalene-1-sulfonic acid
InChI:
InChI=1S/C10H9NO3S/c11-9-5-6-10(15(12,13)14)8-4-2-1-3-7(8)9/h1-6H,11H2,(H,12,13,14)
InChI Key:
NRZRRZAVMCAKEP-UHFFFAOYSA-N
SMILES:
Nc1ccc(c2c1cccc2)S(=O)(=O)O
EC Number:
201-567-9
UNII:
8ZIK65C5CD
NSC Number:
4155
Properties
Complexity:
322  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
223.03g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
223.246g/mol
Monoisotopic Mass:
223.03g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
88.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Degradation kinetics of 4-amino naphthalene-1-sulfonic acid by a biofilm-forming bacterial consortium under carbon and nitrogen limitations. Journal of industrial microbiology & biotechnology 20120801
Post-treatment of anaerobically degraded azo dye Acid Red 18 using aerobic moving bed biofilm process: enhanced removal of aromatic amines. Journal of hazardous materials 20111115
Lack of genotoxic effect of food dyes amaranth, sunset yellow and tartrazine and their metabolites in the gut micronucleus assay in mice. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20090201
Preparation of a library of EDTA amide x-aminenaphthalene-y-sulfonic acid derivatives on solid phase and their fluorescence behavior toward transition metals. Journal of combinatorial chemistry 20090101
Detection of conformational changes in immunoglobulin G using isothermal titration calorimetry with low-molecular-weight probes. Analytical biochemistry 20080915
Two novel mixed-ligand complexes containing organosulfonate ligands. Acta crystallographica. Section C, Crystal structure communications 20080701
Regiospecific O-methylation of naphthoic acids catalyzed by NcsB1, an O-methyltransferase involved in the biosynthesis of the enediyne antitumor antibiotic neocarzinostatin. The Journal of biological chemistry 20080523
5-Aminonaphthalene-1-sulfonic acid and its manganese, nickel and cobalt salts. Acta crystallographica. Section C, Crystal structure communications 20071201
Diaquabis(ethylenediamine)cadmium(II) bis(4-aminonaphthalene-1-sulfonate) dihydrate. Acta crystallographica. Section C, Crystal structure communications 20060901
Recognition-induced supramolecular porous nanosphere formation from cyclodextrin conjugated by cholic acid. Langmuir : the ACS journal of surfaces and colloids 20060328
Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases. British journal of biomedical science 20040101
Synthesis of naphthalenesulfonic acid small molecules as selective inhibitors of the DNA polymerase and ribonuclease H activities of HIV-1 reverse transcriptase. Journal of medicinal chemistry 19940805
Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. Journal of medicinal chemistry 19930709
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound. Life sciences 19900101
Properties