Molecular structure of 4,4′-Diamino-2,2′-bipyridine, CAS Number: 18511-69-8
4,4′-Diamino-2,2′-bipyridine (CAS 18511-69-8)
Application:
4,4′-Diamino-2,2′-bipyridine is a bidendate chelator
CAS Number:
18511-69-8
Purity:
≥95%
Molecular Weight:
186.21
Molecular Formula:
C10H10N4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
4,4′-Diamino-2,2′-bipyridine is an organic compound that is soluble in water and transparent. Acting as a ligand, it serves as a key component in the synthesis of coordination complexes. Additionally, it functions as a catalyst in organic reactions, enhancing their efficiency and rate of occurrence. Moreover, it serves as a fundamental building block for synthesizing an array of organic compounds. In the formation of coordination complexes, 4,4′-Diamino-2,2′-bipyridine acts as a ligand, binding to metal ions and creating a complex wherein the metal ion resides at the core. This complex subsequently assumes the role of a catalyst, facilitating a range of organic reactions and expediting their progress with heightened efficiency.
4,4′-Diamino-2,2′-bipyridine (CAS 18511-69-8) References
- Bipyridine: the most widely used ligand. A review of molecules comprising at least two 2,2'-bipyridine units. | Kaes, C., et al. 2000. Chem Rev. 100: 3553-90. PMID: 11749322
- DNA sensor with a dipyridophenazine complex of osmium(lI) as an electrochemical probe. | Maruyama, K., et al. 2002. Anal Chem. 74: 3698-703. PMID: 12175156
- Ruthenium bisbipyridine complexes of horse heart cytochrome c: characterization and comparative intramolecular electron-transfer rates determined by pulse radiolysis and flash photolysis. | Luo, J., et al. 2000. Inorg Chem. 39: 2321-9. PMID: 12526492
- DNA electrochemical sensor using osmium complex. | Maruyama, K., et al. 2001. Nucleic Acids Res Suppl. 161-2. PMID: 12836314
- Mitochondrial ultrastructure study with the new cytochrome c binding agent 4,4'-diamino-2,2'-bipyridyl ferrous chelate. | Tsou, KC., et al. 1976. J Ultrastruct Res. 54: 235-42. PMID: 175172
- Synthesis, characterisation and biological properties of gold(III) compounds with modified bipyridine and bipyridylamine ligands. | Casini, A., et al. 2010. Dalton Trans. 39: 2239-45. PMID: 20162197
- Aquaporin inhibition by gold(III) compounds: new insights. | Martins, AP., et al. 2013. ChemMedChem. 8: 1086-92. PMID: 23653381
- Ambient-Temperature Spin-State Switching Achieved by Protonation of the Amino Group in [Fe(H2Bpz2)2(bipy-NH2)]. | Luo, YH., et al. 2016. Inorg Chem. 55: 8147-52. PMID: 27472267
- Binding CO2 from Air by a Bulky Organometallic Cation Containing Primary Amines. | Luo, YH., et al. 2018. ACS Appl Mater Interfaces. 10: 9495-9502. PMID: 29513512
- An Ir(III) complex capable of discriminating homocysteine from cysteine and glutathione with luminescent signal and imaging studies. | Wang, H., et al. 2021. Talanta. 221: 121428. PMID: 33076061
- Synthesis and properties of polyimides containing 2, 2′‐bipyridine derivatives | Sun, X., Yang, Y. K., & Lu, F. 1997. Macromolecular Chemistry and Physics. 198(3): 833-841.
- Enhancing the glass‐transition temperature of polyimide copolymers containing 2, 2′‐bipyridine units by the coordination of nickel malenonitriledithiolate | Chen, C. T., Hsu, T. S., Jeng, R. J., & Yeh, H. C. 2000. Journal of Polymer Science Part A: Polymer Chemistry. 38(3): 498-503.
- Improved synthesis of 4,4′-diamino-2,2′-bipyridine from 4,4′-dinitro-2,2′-bipyridine-N,N′-dioxide | Kavanagh, P., & Leech, D. 2004. Tetrahedron Letters. 45(1): 121-123.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4,4′-Diamino-2,2′-bipyridine, 1 g | sc-277685 | 1 g | $166.00 |