4-Amino-1-naphthalenesulfonic Acid - >98.0%(HPLC), high purity , CAS No.84-86-6

  • ≥98%(HPLC)
Item Number
A151594
Grouped product items
SKUSizeAvailabilityPrice Qty
A151594-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$74.90

Basic Description

SynonymsSCHEMBL150853 | 4-AMINO-1-NAPHTHALENESULFONIC ACID | 4-amino-naphthalene-1-sulfonic acid | 4-Aminonaphthalene-1-sulfonic acid | .alpha.-Naphthylamine-p-sulfonic acid | 1-Amino-4-naphthalenesulfonic acid | 1-Naphthalenesulfonic acid, 4-amino- | 1-Naphthyla
Specifications & Purity≥98%(HPLC)
Shipped InNormal

Associated Targets(Human)

NT5E Tchem 5'-nucleotidase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NCI-H157 (619 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCEC (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NT5E Tchem 5'-nucleotidase (622 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

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
Canonical SMILES C1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)O)N
Isomeric SMILES C1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)O)N
WGK Germany 3
RTECS QK1270000
PubChem CID 6790
Molecular Weight 223.25
Beilstein 1971300
Reaxy-Rn 1971299

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

SensitivityLight Sensitive,Air Sensitive

Safety and Hazards(GHS)

Pictogram(s) GHS05
Signal Danger
Hazard Statements

H314:Causes severe skin burns and eye damage

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P363:Wash contaminated clothing before reuse.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes.

P316:Get emergency medical help immediately.

WGK Germany 3
RTECS QK1270000
Reaxy-Rn 1971299
Merck Index 6403

Related Documents

References

1. R F Willes,B Stavric,J C Craig,J A Ruddick.  (1980-06-30)  Circulating naphthionic acid in nonpregnant and pregnant rats after feeding amaranth..  Toxicology and applied pharmacology,  54  ((2)): (276-284).  [PMID:7423494]
2. M Y Osman,I A Sharaf,H M Y Osman,Z A El-Khouly,E I Ahmed.  (2004-10-07)  Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases..  British journal of biomedical science,  61  ((3)): (128-132).  [PMID:15462257]
3. Yinggang Luo,Shuangjun Lin,Jian Zhang,Heather A Cooke,Steven D Bruner,Ben Shen.  (2008-04-05)  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,  283  ((21)): (14694-14702).  [PMID:18387946]
4. C Juárez-Ramírez,R Velázquez-García,N Ruiz-Ordaz,J Galíndez-Mayer,O Ramos Monroy.  (2012-04-12)  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,  39  ((8)): (1169-1177).  [PMID:22492166]
5. David E Lefebvre,Nikia Ross,Andrea L Kocmarek,Simon Cowell,Shelley Dai,Cunye Qiao,Ivan Curran,Terry Koerner,Genevieve S Bondy,Jason H Fine.  (2017-11-07)  In vitro immunomodulation of splenocytes from DO11.10 mice by the food colouring agent amaranth..  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,  110  (395-401).  [PMID:29107027]
6. A S Rodrigues,M J Nunes,A Lopes,J N Silva,L Ciríaco,M J Pacheco.  (2018-05-01)  Electrodegradation of naphthalenic amines: Influence of the relative position of the substituent groups, anode material and electrolyte on the degradation products and kinetics..  Chemosphere,  205  (433-442).  [PMID:29705634]
7. E Tragni,M Marinovich,P Ciuffreda,M Anastasia,A Ferrari,C L Galli.  (1990-01-01)  Identification of [14C]carmoisine metabolites in bacterial suspension of rat faeces..  Food additives and contaminants,  ((1)): (1-7).  [PMID:2307258]
8. I Lindh,W J Griffiths,T Bergman,J Sjövall.  (1994-10-01)  Charge-remote fragmentation of peptides derivatized with 4-aminonaphthalenesulphonic acid..  Rapid communications in mass spectrometry : RCM,  ((10)): (797-803).  [PMID:8000077]
9. Sebastian Günther,Daniel Deredge,Amanda L Bowers,Alessandra Luchini,Daniel A Bonsor,Robert Beadenkopf,Lance Liotta,Patrick L Wintrode,Eric J Sundberg.  (2017-09-21)  IL-1 Family Cytokines Use Distinct Molecular Mechanisms to Signal through Their Shared Co-receptor..  Immunity,  47  ((3)): (510-523).  [PMID:28930661]

Solution Calculators