Chemodex

4,4'-Dimethyl-2,2'-dipyridyl

Product Code:
 
CDX-B0213
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+20°C
1 / 1
Chemical Structure

Chemical Structure

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CDX-B0213-G0055 g£114.00
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CDX-B0213-G02525 g£426.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
2,2'-Bi(gamma-picoline); 4,4'-Dimethyl-2,2'-bipyridine; DMB; NSC3261
Appearance:
White to off-white powder.
CAS:
1134-35-6
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C12H12N2/c1-9-3-5-13-11(7-9)12-8-10(2)4-6-14-12/h3-8H,1-2H3
InChiKey:
NBPGPQJFYXNFKN-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 1134-35-6. Formula: C12H12N2. MW: 184.2. Synthetic. Building block and intermediate for synthesis. Used in the synthesis of a series of o-phenanthroline-substituted ruthenium(II) complexes and luminescent molecules.
MDL:
MFCD00006441
Molecular Formula:
C12H12N2
Molecular Weight:
184.2
Package Type:
Vial
Precautions:
P261, P305, P351, P338
Product Description:
Building block and intermediate for synthesis. Used in the synthesis of a series of o-phenanthroline-substituted ruthenium(II) complexes and luminescent molecules.
Purity:
>98%
Signal word:
Warning
SMILES:
CC1=CC=NC(C2=NC=CC(C)=C2)=C1
Solubility Chemicals:
Soluble in ethanol, acetic acid, benzene, toluene or water (at pH < 2).
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +20°C.

References

(1) N.H. Damrauer & J.K. McCusker; J. Phys. Chem. A 103, 8440 (1999) | (2) G.A. van Albada; Inorg. Chim. Acta. 331, 208 (2002) | (3) B.H. Kim, et al.; Talanta 62, 595 (2004) | (4) K.L. Reddy, et al.; Nucleos. Nucleot. Nucleic Acids 28, 204 (2009) | (5) Y.J. Liu, et al.; DNA Cell Biol. 30, 829 (2011) | (6) G.J. Lin, et al.; J. Biol. Inorg. Chem. 18, 873 (2013) | (7) A. Srishailam, et al.; J. Photochem. Photobiol. B. 141, 47 (2014) | (8) A. Draksharapu, et al.; Dalton Trans. 44, 3647 (2015)