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D216402

2,2′-Dipyridylamine

Name: 2,2′-Dipyridylamine
Brand: ALDRICH

98%

Synonym(s):

bipyam

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₉N₃

CAS Number:

1202-34-2

Molecular Weight:

171.20

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893648

EC Number:

214-864-3

Beilstein/REAXYS Number:

127131

MDL number:

MFCD00006247

Assay:

98%

Form:

solid

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Properties

Quality Level

200

assay

98%

form

solid

bp

222 °C/50 mmHg (lit.)

mp

90-92 °C (lit.)

SMILES string

N(c1ccccn1)c2ccccn2

InChI

1S/C10H9N3/c1-3-7-11-9(5-1)13-10-6-2-4-8-12-10/h1-8H,(H,11,12,13)

InChI key

HMMPCBAWTWYFLR-UHFFFAOYSA-N

Description

Application

2,2′-Dipyridylamine (bipyam) can be used:

As a bidentate N-donor ligand in the synthesis of various metal complexes.
To synthesize Pd-polyoxovanadates, heterogeneous catalyst for the oxidation of benzylic hydrocarbons.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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N2-functionalized blue luminescent guanosines by 2,2'-dipyridylamino and 2-(2'-pyridyl)benzimidazolyl chelate groups and their interactions with Zn(II) ions.

Sanela Martić et al.

Inorganic chemistry, 47(18), 8315-8323 (2008-08-20)

The syntheses of new blue luminescent N(2)-modified guanosine derivatives with chromophores p-4,4'-biphenyl-NPh2 (1a), p-4,4'-biphenyl-N(2-py)2 (1b), and p-4,4'-biphenyl-2-(2'-pyridyl)benzimidazolyl (1c), respectively, have been achieved. These new N(2)-guanosines are moderate blue emitters with lambda(max) = 395 nm (1a), 370 nm (1b), and 403

Third generation fluoroquinolones antibacterial drug based mixed-ligand Cu(II) complexes: structure, antibacterial activity, superoxide dismutase activity and DNA-interaction approach.

Mohan N Patel et al.

Journal of enzyme inhibition and medicinal chemistry, 26(2), 188-197 (2010-06-30)

The copper(II) complexes of the type [Cu(SPF)(A(n))Cl]/[Cu(PFL)(A(n))Cl] (where SPF is sparfloxacin, PFL is pefloxacin and A(n) is 2,2'-dipyridylamine/pyridine-2-carboxalehyde/thiophene-2-carboxaldehyde) were synthesised and were found to have a pyramidal geometry with a square base. The superoxide dismutase (SOD) like activity of the

Synthesis and structural characterization of ternary Cu (II) complexes of glycine with 2,2'-bipyridine and 2,2'-dipyridylamine. The DNA-binding studies and biological activity.

Mervat S Mohamed et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 86, 562-570 (2011-12-14)

In this study two new complexes [Cu(bpy)(Gly)Cl]·2H(2)O (1) and [Cu(dpa)(Gly)Cl]·2H(2)O (2) (bpy=2,2'-bipyridine; dpa=2,2'-dipyridylamine, Gly=glycine) have been synthesized and characterized by elemental analysis, IR, TGA, UV-vis and magnetic susceptibility measurements. The binding properties of the complexes with CT-DNA were investigated by

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Global Trade Item Number

SKU	GTIN
D216402-5G	04061833561829
D216402-25G	04061833561812