6-Amino-2-naphthalenesulfonic Acid - ≥98%(HPLC) , CAS No.93-00-5

CAS: 93-00-5 Cat. No.: A139448 Peso molecular: 223.252 Número EC: 202-208-9
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)
Synonyms
Bronner's acid | ethyl N-(26-Amino-2-naphthalenesulfonic Acid,3,5,6-tetramethylphenyl)carbamate | 2-amino-naphthalene-6-sulfonic acid | 2-Aminonaphthalene-6-sulfonic acid | EN300-1666592 | (6Or7)-aminonaphthalene-2-sulphonic acid | 6-Amino-2-naphthalenesu
Storage
Protected from light,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
A139448-25g
3

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
100g
A139448-100g
3

29,90US$

44,90US$
Guardar 15,00 US$ (33.41%)
250g
A139448-250g
2

65,90US$

98,90US$
Guardar 33,00 US$ (33.37%)
500g
A139448-500g
1

118,90US$

178,90US$
Guardar 60,00 US$ (33.54%)
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Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

6-Amino-2-naphthalenesulfonic Acid is used in the synthesis of diaryl urea derivatives bearing sulfonamide moiety with an in vitro antitumor activity.

Specifications

Sinónimos
Bronner's acid | ethyl N-(26-Amino-2-naphthalenesulfonic Acid, 3, 5, 6-tetramethylphenyl)carbamate | 2-amino-naphthalene-6-sulfonic acid | 2-Aminonaphthalene-6-sulfonic acid | EN300-1666592 | (6Or7)-aminonaphthalene-2-sulphonic acid | 6-Amino-2-naphthalenesu
Especificaciones y pureza
≥98%(HPLC)
Condiciones de almacenamiento de almacenamiento
Protected from light, Room temperature
Enviado en
Normal
Pureza
≥98%(HPLC)
Nombres e identificadores
Pubchem Sid488180299
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180299
Sonrisas canónicasC1=CC2=C(C=CC(=C2)S(=O)(=O)O)C=C1N
IUPAC Name6-aminonaphthalene-2-sulfonic acid
InChIKeySEMRCUIXRUXGJX-UHFFFAOYSA-N
INCHI1S/C10H9NO3S/c11-9-3-1-8-6-10(15(12,13)14)4-2-7(8)5-9/h1-6H,11H2,(H,12,13,14)
Isómeros SMILES C1=CC2=C(C=CC(=C2)S(=O)(=O)O)C=C1N
CAS alternativo 52365-47-6
Peso molecular 223.252
Reaxy-Rn 647859
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=647859&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseNaphthalenes
SubclassNaphthalene sulfonic acids and derivatives
Intermediate Tree Nodes Naphthalene sulfonates
Direct Parent2-naphthalene sulfonates
Alternative Parents 2-naphthalene sulfonic acids and derivatives  1-sulfo,2-unsubstituted aromatic compounds  Sulfonyls  Organosulfonic acids  Primary amines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 2-naphthalene sulfonate - 2-naphthalene sulfonic acid or derivatives - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organic nitrogen compound - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 2-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 2-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors aminonaphthalenesulfonic acid
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeFechaArticulo
J2217076Certificate of AnalysisMay 11, 2026 A139448
J2217077Certificate of AnalysisMay 11, 2026 A139448
J2217122Certificate of AnalysisMay 11, 2026 A139448
J2217144Certificate of AnalysisMay 11, 2026 A139448
C2306665Certificate of AnalysisDec 09, 2024 A139448
L2411036Certificate of AnalysisNov 20, 2024 A139448
L2411037Certificate of AnalysisNov 20, 2024 A139448
L2411039Certificate of AnalysisNov 20, 2024 A139448
J2120459Certificate of AnalysisAug 18, 2023 A139448
J2120458Certificate of AnalysisAug 18, 2023 A139448
H1520040Certificate of AnalysisMar 15, 2023 A139448

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Propiedades químicas y físicas
SensibilidadLight sensitive.
Peso molecular223.250 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass223.03 Da
Monoisotopic Mass223.03 Da
Topological Polar Surface Area88.800 Ų
Heavy Atom Count15
Formal Charge0
Complexity322.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Jiang Jinhui, Pan Yiwen, Zhao Jingyi, Zhang Siwei, Ma Fulong, Zhang Zicong, Liu Mengli, Qiu Zijie, Zhao Zheng, Sun Jianwei, Kwok Ryan T. K., Xiong Yu, Lam Jacky W. Y., Han Wei, Tang Ben Zhong.  (2026)  Poly(vinyl alcohol) induced chirality inversion and amplification of circularly polarized room-temperature phosphorescence in homopolypeptide aggregates.  Nature Communications,      [PMID:41708632] [10.1038/s41467-026-69707-3]
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