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Merck
CN

127035

1-Naphthylmethylamine

97%

Synonym(s):

1-(Aminomethyl)naphthalene, 1-Naphthalenemethylamine

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About This Item

Linear Formula:
C10H7CH2NH2
CAS Number:
Molecular Weight:
157.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-244-0
Beilstein/REAXYS Number:
2206459
MDL number:
Assay:
97%
Form:
liquid
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Product Name

1-Naphthylmethylamine, 97%

InChI key

NVSYANRBXPURRQ-UHFFFAOYSA-N

InChI

1S/C11H11N/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8,12H2

SMILES string

NCc1cccc2ccccc12

assay

97%

form

liquid

refractive index

n20/D 1.643 (lit.)

bp

290-293 °C (lit.)

density

1.073 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

Gene Information

rat ... Adra2a(25083)

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Application

  • Photoluminescence Modulation: A study demonstrates the modulation of photoluminescence in Ruddlesden-Popper perovskite using phase distribution regulation, revealing potential applications in optoelectronic devices. 1-Naphthylmethylamine plays a critical role in enhancing the material properties for improved device performance (Zhao et al., 2023).
  • Perovskite Light-Emitting Diodes: Research highlights the dimensional tailoring of quantum wells through ultrahigh vacuum annealing to enhance the efficiency of perovskite light-emitting diodes. This process utilizes 1-Naphthylmethylamine to improve the interlayer electronic properties and device stability, contributing significantly to advancements in LED technology (Yu et al., 2020).

General description

1-Naphthylmethylamine is used as a building block in organic synthesis to produce dyes, pigments, and pharmaceuticals.

1-Naphthylmethylamine increases the induced circular dichroism (ICD) magnitude exhibited by Poly[(4-carboxyphenyl)acetylene]. It forms carbamate by reacting with monomethoxypoly(ethylene glycol) succinimido carbonate (mPEG-SC).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Kazuhide Morino et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(19), 4703-4707 (2004-09-17)
Poly[(4-carboxyphenyl)acetylene] (poly-1) exhibits an intense induced circular dichroism (ICD) in the UV-visible region upon complexation with excess (R)-1-(1-naphthyl)ethylamine ((R)-2), owing to the formation of a predominantly single-handed helical conformation of the polymer backbone. In the presence of a small amount
Susan D Van Arnum et al.
Journal of pharmaceutical and biomedical analysis, 50(2), 138-143 (2009-05-12)
An UV-HPLC method for the determination of the potency of mPEG-SC, 5 kDa (1) has been developed and validated. Validation acceptance criteria that is typical of small molecule method validation was successfully applied for this method. The method relies on

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