133477
1-氨基-2-萘酚 盐酸盐
technical grade, 90%
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线性分子式:
H2NC10H6OH · HCl
化学文摘社编号:
分子量:
195.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-830-8
MDL number:
产品名称
1-氨基-2-萘酚 盐酸盐, technical grade, 90%
InChI key
DEKREBCFNLUULC-UHFFFAOYSA-N
InChI
1S/C10H9NO.ClH/c11-10-8-4-2-1-3-7(8)5-6-9(10)12;/h1-6,12H,11H2;1H
SMILES string
Cl.Nc1c(O)ccc2ccccc12
grade
technical grade
assay
90%
form
crystals
mp
250 °C (dec.) (lit.)
Application
1-Amino-2-naphthol hydrochloride was used in a study on degradation of the azo dye Acid Orange 7 in batch anaerobic unstirred assay.
General description
1-Amino-2-naphthol undergoes condensation with methylene-substituted azaheterocycles in presence of an oxidizing agent to yield photochromic spirooxazines.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Anita Sztojkov-Ivanov et al.
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
Yang Mu et al.
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
Synthesis of photochromic spirooxazines from 1-amino-2-naphthols
Lokshin V, et al.
Tetrahedron, 53(28), 9669-9678 (1997)
Anaerobic treatment of azo dye Acid Orange 7 under batch conditions.
Mendez-Paz D, et al.
Enzyme and Microbial Technology, 36(2), 264-272 (2005)
D Dillon et al.
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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