Skip to Content
Merck
All Photos(2)

Key Documents

More Documents

D35201

Sigma-Aldrich

N,N′-Dibenzylethylenediamine

97%

Synonym(s):

DBED

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C6H5CH2NHCH2CH2NHCH2C6H5
CAS Number:
140-28-3
Molecular Weight:
240.34
EC Number:
205-408-4
MDL number:
MFCD00004771
UNSPSC Code:
12352100
PubChem Substance ID:
24893762
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.565 (lit.)

bp

195 °C/4 mmHg (lit.)

density

1.02 g/mL at 25 °C (lit.)

SMILES string

C(CNCc1ccccc1)NCc2ccccc2

InChI

1S/C16H20N2/c1-3-7-15(8-4-1)13-17-11-12-18-14-16-9-5-2-6-10-16/h1-10,17-18H,11-14H2

InChI key

JUHORIMYRDESRB-UHFFFAOYSA-N

Related Categories

General description

N,N′-Dibenzylethylenediamine, also known as DBED, is a donor ligand often used in the synthesis of coordination compounds and in the formation of stable metal complexes such as nickel (II) carboxylate complex.

Application


  • Ring-Opening Polymerization of rac-Lactide Catalyzed by Octahedral Nickel Carboxylate Complexes: Focuses on a complex involving N,N′-dibenzylethylenediamine as a syndioselective catalyst in polymer synthesis (A Nikiforov et al., 2023).

  • Synthesis, Crystal Structures and Catalytic Activities of Two Copper Coordination Compounds Bearing an N, N′-Dibenzylethylenediamine Ligand: Examines copper coordination compounds that incorporate N,N′-dibenzylethylenediamine and their structural and catalytic properties (C Liu et al., 2020).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Benzathine interference in the EMIT-st urine amphetamine assay.
N R Badcock et al.
Clinical chemistry, 33(6), 1080-1080 (1987-06-01)
[High pressure liquid chromatography of dibenzylethylenediamine in benzathine penicillin].
B Stuber
Pharmaceutica acta Helvetiae, 57(10-11), 293-294 (1982-01-01)
Muran Zhou et al.
Scientific reports, 9(1), 6035-6035 (2019-04-17)
Tissue engineering is a promising technology used as an alternative to organ/tissue transplantation which is often limited by donor shortage. The construction of large-sized engineered tissue requires a fast and sufficient vascularization process. Previous studies have shown that hypoxia-inducible factor
Peter M Grace et al.
Anesthesia and analgesia, 128(1), 161-167 (2018-03-30)
Opioids are effective postoperative analgesics. Disturbingly, we have previously reported that opioids such as morphine can worsen inflammatory pain and peripheral and central neuropathic pain. These deleterious effects are mediated by immune mediators that promote neuronal hyperexcitability in the spinal
Michael H Augenbraun
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 35(Suppl 2), S187-S190 (2002-09-28)
After a precipitous increase in the incidence of infectious syphilis in the United States during the late 1980s and early 1990s, the rate of new cases has declined so dramatically that a program initiated by the Centers for Disease Control
View All Related Papers

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