133477
1-Amino-2-naphthol hydrochloride
technical grade, 90%
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About This Item
Produtos recomendados
grau
technical grade
Ensaio
90%
Formulário
crystals
pf
250 °C (dec.) (lit.)
cadeia de caracteres SMILES
Cl.Nc1c(O)ccc2ccccc12
InChI
1S/C10H9NO.ClH/c11-10-8-4-2-1-3-7(8)5-6-9(10)12;/h1-6,12H,11H2;1H
chave InChI
DEKREBCFNLUULC-UHFFFAOYSA-N
Descrição geral
1-Amino-2-naphthol undergoes condensation with methylene-substituted azaheterocycles in presence of an oxidizing agent to yield photochromic spirooxazines.
Aplicação
1-Amino-2-naphthol hydrochloride was used in a study on degradation of the azo dye Acid Orange 7 in batch anaerobic unstirred assay.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Journal of separation science, 28(18), 2505-2510 (2006-01-13)
The enantiomers of 1-(alpha-aminobenzyl)-2-naphthol and 2-(alpha-aminobenzyl)-1-naphthol analogs were separated isothermally on a cellulose-tris-3,5-dimethylphenyl carbamate-based chiral stationary phase (Chiralcel OD-H), at 10 degrees C increments in the range of 5-35 degrees C, using n-hexane/2-propanol/diethylamine as mobile phase. The mobile phase composition
Synthesis of photochromic spirooxazines from 1-amino-2-naphthols
Tetrahedron, 53(28), 9669-9678 (1997)
Anaerobic treatment of azo dye Acid Orange 7 under batch conditions.
Enzyme and Microbial Technology, 36(2), 264-272 (2005)
Environmental science & technology, 43(13), 5137-5143 (2009-08-14)
Azo dyes are ubiquitously used in the textile industry. These dyes need to be removed from the effluent prior to discharge to sewage due to their intense color and toxicity. In this study we investigated the use of a bioelectrochemical
Mutagenesis, 9(4), 295-299 (1994-07-01)
D & C Red No. 9 is a monoazo dye used for manufacturing printing inks, rubber and plastics, and as an additive in cosmetics and drugs. In an NTP carcinogenicity study in rats and mice it induced splenic sarcomas and
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