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Merck

133477

Sigma-Aldrich

1-氨基-2-萘酚 盐酸盐

technical grade, 90%

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About This Item

线性分子式:
H2NC10H6OH · HCl
CAS号:
分子量:
195.65
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

technical grade

化驗

90%

形狀

crystals

mp

250 °C (dec.) (lit.)

SMILES 字串

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

InChI 密鑰

DEKREBCFNLUULC-UHFFFAOYSA-N

一般說明

1-Amino-2-naphthol undergoes condensation with methylene-substituted azaheterocycles in presence of an oxidizing agent to yield photochromic spirooxazines.

應用

1-Amino-2-naphthol hydrochloride was used in a study on degradation of the azo dye Acid Orange 7 in batch anaerobic unstirred assay.

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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
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
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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