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Merck
CN

V000656

1-Naphthylamine

p.a., 99.0%

Synonym(s):

α-Naphthylamine, 1-Aminonaphthalene

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About This Item

Linear Formula:
C10H7NH2
CAS Number:
134-32-7
Molecular Weight:
143.19
PubChem Substance ID:
329828155
Beilstein/REAXYS Number:
386133
MDL number:
MFCD00004016

Key Documents

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assay

99.0%

InChI key

RUFPHBVGCFYCNW-UHFFFAOYSA-N

SMILES string

Nc1cccc2ccccc12

InChI

1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2

grade

p.a.

bp

301 °C (lit.)

mp

47-50 °C (lit.)

density

1.114 g/mL at 25 °C (lit.)

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1A

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

314.6 °F - closed cup

flash_point_c

157 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
DCBD7579V
DCBD5457V

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Cüneyt Türkeş et al.
Journal of enzyme inhibition and medicinal chemistry, 30(4), 622-628 (2014-12-19)
In this study, we investigated the effects of antibacterial drugs (moxifloxacin hydrochloride, levofloxacin hemihidrate, cefepime hydrochloride, cefotaxime sodium and ceftizoxime sodium) on human serum paraoxonase-1 (hPON1) enzyme activity from human serum in vitro conditions. For this purpose, hPON1 enzyme was
Susanta Adhikari et al.
Dalton transactions (Cambridge, England : 2003), 44(32), 14388-14393 (2015-07-23)
The X-ray structurally characterized naphthalene appended diformyl-p-cresol derivative () selectively detects Sn(2+) by both colorimetric and fluorescence methods. In the presence of Sn(2+), exhibits a monomer emission at 420 nm along with a strong red excimer emission at 582 nm
F F Kadlubar et al.
Cancer research, 38(11 Pt 1), 3628-3638 (1978-11-01)
The carcinogen N-hydroxy-1-naphthylamine reacted with nucleic acids and protein under slightly acidic conditions (pH 5) to form covalently bound derivatives with 3 to 20 naphthyl residues/1000 monomer units. The level of binding was in the following order: DNA greater than
Andrew R Korte et al.
Analytical and bioanalytical chemistry, 407(8), 2301-2309 (2015-01-27)
A significant limiting factor in achieving high spatial resolution for matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS) imaging is the size of the laser spot at the sample surface. Here, we present modifications to the beam-delivery optics of a commercial MALDI-linear
Jayita Dutta et al.
Dalton transactions (Cambridge, England : 2003), 44(30), 13615-13632 (2015-07-07)
N-(Naphthyl)-4-R-salicylaldimines (R = OCH(3), H and Cl; H(2L)(1)-H(2)L(3)) and 2-hydroxy-N-(naphthyl)naphthaldimine (H(2)L(4)) readily undergo, upon reaction with Na(2)[PdCl(4)] in the presence of triphenylphosphine, cyclopalladation via C-H bond activation at the peri-position to afford complexes of type [Pd(L)(PPh(3))] (L = L(1)-L(4)). The
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