Key Documents

View All Documentation

376469

5-Amino-1-naphthol

Name: 5-Amino-1-naphthol
Brand: ALDRICH

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

Select a Size

Change View

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

Assay:

95%

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

95%

mp

190 °C (dec.) (lit.)

SMILES string

Nc1cccc2c(O)cccc12

InChI

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

InChI key

ZBIBQNVRTVLOHQ-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)

Characterization of the urinary metabolites of 5-amino-1-naphthol in the rat.

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

Synthesis and beta 1-, beta 2-adrenergic receptor binding studies of 4-acylamino-substituted phenoxypropanolamine and 5-acylamino-substituted naphthyloxypropanolamine derivatives.

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

View All Related Papers

Global Trade Item Number

SKU	GTIN
376469-25G	04061832279978
376469-100G	04061832279961