291137
2-Amino-1-naphthalenesulfonic acid
98%
Sinonimo/i:
2-Naphthylamine-1-sulfonic acid, Tobias acid
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About This Item
Formula condensata:
H2NC10H6SO3H
Numero CAS:
Peso molecolare:
223.25
Beilstein:
613084
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
98%
Stato
solid
Stringa SMILE
Nc1ccc2ccccc2c1S(O)(=O)=O
InChI
1S/C10H9NO3S/c11-9-6-5-7-3-1-2-4-8(7)10(9)15(12,13)14/h1-6H,11H2,(H,12,13,14)
GWIAAIUASRVOIA-UHFFFAOYSA-N
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Descrizione generale
2-Amino-1-naphthalenesulfonic acid is a manufacturing intermediate in the monosulfo monoazo color additive D&C Red No. 34 and its lakes[1].
Applicazioni
2-Amino-1-naphthalenesulfonic acid has been used in the preparation of 2-(2-naphthylamino)benzoxazole by reacting with 2-chlorobenzoxazole[2].
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
S Kumar et al.
British journal of industrial medicine, 38(2), 167-169 (1981-05-01)
Immunological studies have shown an increased lymphocyte reactivity in patients with early stage bladder cancer and individuals with pre-stage T1 exposed to bladder carcinogens (2-naphthylamine and industrial 1-naphthylamine containing 4-8% 2-naphthylamine) before 1952-that is, those at high risk of developing
Bhakti Petigara Harp et al.
Journal of AOAC International, 92(6), 1639-1643 (2010-02-20)
A reversed-phase LC method was developed to determine two manufacturing intermediates in the monosulfo monoazo color additive D&C Red No. 34 and its lakes. The analytes are 2-amino-1-naphthalenesulfonic acid (Tobias acid) and 3-hydroxy-2-naphthalenecarboxylic acid (3-hydroxy-2-naphthoic acid). This method can be
Ayman Ayoub Abdel-Shafi
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(4-5), 1228-1236 (2006-09-05)
The photophysical characteristics of the ground and excited states of 2-naphthylamine-6-sulfonate (2-NA-6-S) were investigated in different solvents and in beta-cyclodextrin (beta-CD). The spectral shifts are well correlated with Kamlet-Taft relationship. Multiple linear regression analysis indicated that both non-specific dipolar interaction
Non-carcinogenicity in mice of a sulfonic acid derivative of 2-naphthylamine.
G Della Porta et al.
Carcinogenesis, 3(6), 647-649 (1982-01-01)
Jolanta Polak et al.
International journal of molecular sciences, 21(6) (2020-03-21)
Novel sustainable processes involving oxidative enzymatic catalysts are considered as an alternative for classical organic chemistry. The unique physicochemical and bioactive properties of novel bio-products can be obtained using fungal laccase as catalyst. Among them are textile biodyes synthesised during
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