Basic information Safety Supplier Related

2-ETHYLNAPHTHALENE

Basic information Safety Supplier Related

2-ETHYLNAPHTHALENE Basic information

Product Name:
2-ETHYLNAPHTHALENE
Synonyms:
  • 2-ETHYLNAPHTHALENE
  • naphthylethane
  • 2-ethyl-naphthalen
  • beta-Ethylnaphthalene
  • -Ethylnaphthalene
  • 2-ETHYLNAPHTHALENE, 99+%
  • 2-ETHYLNAPHTHALENE 99% (GC)
  • 2-ETHYLNAPHTHALENE, FOR FLUORESCENCE
CAS:
939-27-5
MF:
C12H12
MW:
156.22
EINECS:
213-360-0
Product Categories:
  • Arenes
  • Building Blocks
  • Organic Building Blocks
  • Bioactive Small Molecules
  • Biochemicals and Reagents
  • Building Blocks
  • Naphthalene derivatives
  • Cell Biology
  • Chemical Synthesis
  • E
  • Luminescent Compounds/Detection
  • Organic Building Blocks
  • Wavelength Index
Mol File:
939-27-5.mol
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2-ETHYLNAPHTHALENE Chemical Properties

Melting point:
-70 °C (lit.)
Boiling point:
251-252 °C (lit.)
Density 
0.992 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.599(lit.)
Flash point:
104 °C
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
Water Solubility 
8mg/L(25 ºC)
BRN 
1903545
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey
RJTJVVYSTUQWNI-UHFFFAOYSA-N
LogP
4.380
CAS DataBase Reference
939-27-5(CAS DataBase Reference)
EPA Substance Registry System
2-Ethylnaphthalene (939-27-5)
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Safety Information

Safety Statements 
23-24/25
WGK Germany 
3
RTECS 
QJ6960000
HS Code 
2902.90.9000

MSDS

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2-ETHYLNAPHTHALENE Usage And Synthesis

Chemical Properties

colourless liquid

Uses

2-Ethylnaphthalene is a commonly used organic substance in the laboratory for hydrodealkylation reactions, energy transfer studies under varying concentrations of donor conditions and its vapour pressure in phase equilibrium cells.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as C2-ETHYLNAPHTHALENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction.

2-ETHYLNAPHTHALENESupplier

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