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Merck
CN

376469

5-Amino-1-naphthol

95%

Synonym(s):

1-Amino-5-hydroxynaphthalene, 1-Amino-5-naphthol, 5-Amino-α-naphthol, 5-Amino-1-naphthalenol, 5-Hydroxy-1-naphthalenamine, 5-Hydroxy-1-naphthylamine

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About This Item

Linear Formula:
H2NC10H6OH
CAS Number:
83-55-6
Molecular Weight:
159.18
NACRES:
NA.22
PubChem Substance ID:
24863445
UNSPSC Code:
12352100
EC Number:
201-486-9
MDL number:
MFCD00041826

Key Documents

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Product Name

5-Amino-1-naphthol, 95%

InChI key

ZBIBQNVRTVLOHQ-UHFFFAOYSA-N

InChI

1S/C10H9NO/c11-9-5-1-4-8-7(9)3-2-6-10(8)12/h1-6,12H,11H2

SMILES string

Nc1cccc2c(O)cccc12

assay

95%

mp

190 °C (dec.) (lit.)

Quality Level

100

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ9540
MKCK0038
MKCK0037
MKCK0039
MKBQ6058V

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Study of a heteropolyanion-doped poly (5-amino-1-naphthol) film electrode and its catalytic activity.
Pham M-C, et al.
Electrochimica Acta, 42(3), 439-447 (1997)
Ewa Rozycka-Sokolowska et al.
Acta crystallographica. Section C, Crystal structure communications, 65(Pt 11), o565-o568 (2009-11-07)
The crystal structure of the title compound, C(10)H(9)NO, (I), contains intermolecular O-H...N and N-H...O hydrogen bonds which together form sheets parallel to the (001) plane containing rings with an unusual R(4)(4)(18) motif. These rings are additionally stabilized by an intermolecular
Electrochemical synthesis and study of poly (5-amino 1-naphthol) film in aqueous and organic media.
Pham M-C, et al.
Synthetic Metals, 63(1), 7-15 (1994)
Dharam Paul Jindal et al.
Arzneimittel-Forschung, 52(9), 654-663 (2002-10-31)
The object of this study was to investigate the beta-adrenergic receptor binding affinity of 4-acylaminophenoxypropanolamine (10-15) and 5-acylaminonaphthyloxypropanolamine (21-24) derivatives, which were prepared from 4-aminophenol (5) and 5-amino-1-naphthol (16), respectively. The in vitro beta 1- and beta 2-adrenergic receptor binding
P M Enriquez et al.
Toxicology, 29(4), 337-343 (1984-02-01)
The metabolic fate of [14C]5-amino-1-naphthol (5A1N) was investigated in Sprague-Dawley rats. [14C]5A1N was administered by gastric intubation to male rats at doses 1, 37 and 135 mg/kg body weight. In a separate experiment the rats were also dosed with 150
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