Skip to Content
Merck
CN

P24152

N-Phenylethylenediamine

98%

Synonym(s):

N-(2-Aminoethyl)aniline

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C6H5NHCH2CH2NH2
CAS Number:
1664-40-0
Molecular Weight:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24898326
EC Number:
216-773-4
Beilstein/REAXYS Number:
508205
MDL number:
MFCD00008162

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

N-Phenylethylenediamine, 98%

InChI key

OCIDXARMXNJACB-UHFFFAOYSA-N

InChI

1S/C8H12N2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,10H,6-7,9H2

SMILES string

NCCNc1ccccc1

assay

98%

refractive index

n20/D 1.587 (lit.)

bp

262-264 °C (lit.)

density

1.041 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000482105
0000482105
0000339263
0000339263
0000246903

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

Babli Kumari et al.
Dalton transactions (Cambridge, England : 2003), 47(39), 14008-14016 (2018-09-20)
Structurally characterised two polymeric complexes of Cu(ii) (3) and Mn(iii) (4) of the ligand L (2-(((2-(phenylamino)ethyl)imino)methyl)phenol) have been explored for catecholase-like activity, fluorescence recognition of histidine and catalytic activity towards coupling of aryl iodides with benzamide, leading to N-arylbenzamides. CuO
Yue Fan et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(1), 1801368-1801368 (2019-01-16)
Disperse reactive dyes with appropriate chemical structure are key for the coloration of natural fibers in the water-free environmentally friendly medium of supercritical carbon dioxide with various advantages. The objective of this work is to design and synthesize a novel
Sakthi Raje et al.
Chemistry, an Asian journal, 13(11), 1458-1466 (2018-04-01)
Koneramines (LR OR', R=Ph or Ts; R'=Me, iPr) and their complexes were found to emerge from the system of pyridine-2-carboxaldehyde and N-phenyl/tosylethylenediamine when a primary or secondary alcohol was used as solvent. Imidazolidinylpyridines (LR , R=Ph or Ts) became major
Leslie S Hamachi et al.
Chemical science, 10(26), 6539-6552 (2019-08-02)
We report a method to control the composition and microstructure of CdSe1-x S x
Abhijit Ghosh et al.
Dalton transactions (Cambridge, England : 2003), 44(26), 11797-11804 (2015-06-09)
A very simple molecule derived from salicylaldehyde and N-phenyl ethylenediamine (L1) functions as dual-mode ratiometric fluorescence "turn on" sensors for Zn(2+) and Al(3+) at two different wavelengths. The sensing is based on the combined effect of inhibition of excited-state intra-molecular

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service