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2,2'-Bipyridine CAS 366-18-7

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  • Appearance: White powder
  • Assay: 99. 0%min
  • Stock: In stock
  • Sample: Available
  • Zhishang Chemical: 2,2′-Bipyridine Supplement
366-18-7

Basic Info of 2,2'-Bipyridine

What is 2,2'-Bipyridine?

2,2′-Bipyridyl, a symmetrical bipyridyl, is usually used as a neutral ligand for complexing with metal ions. The molecule is a plane with trans conformation and crystallizes in monoclinic system.

2,2′- Bipyridine is a natural compound with the molecular formula C 10 h 8 N 2. This anemic solid is a vital isomer of bipyridine household. It is a bidentate chelating ligand, which creates complicateds with numerous transition steels. The ruthenium as well as platinum complexes of bipy show strong luminescence, which may have useful applications.

2,2'-Bipyridine Uses

  • 2,2′- Bipyridine is a bipyridine in which 2 pyridine parts are attached by a bond in between settings C-2 and C-2 ‘. It works as an iron death inhibitor as well as chelator.
  • 2,2′-Bipyridine is an analytical reagent for the determination of ferrous, silver, cadmium, molybdenum, and also as a redox indicator.
  • 2,2′-Bipyridine for shift metal-catalyzed as well as aluminum-initiated polymerizations; as a metalloproteinase inhibitor and also a high-affinity iron chelator.
  • As a bidentate chelating ligand, 2,2′- bipyridine develops a facility with change steel ions and also has antifungal, anti-bacterial as well as antiviral tasks. It is made use of for colorimetric decision of iron as well as redox sign to confirm the presence of ferrous ion in dirt. It develops facilities with ruthenium and also platinum and shows solid luminescence, which may have functional applications. Copper (I) bipyridyl complicateds associated with alcohol oxidation under cardio problems.

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Preparation of 2,2'-Bipyridine

2,2′-bipyridine is manufactured by the response of pyridine with ferric chloride. Mix 70 g of anhydrous pyridine with 13 g of anhydrous ferric chloride, as well as warmth and react in a sealed tube at 300 ° C. for around 35 hours. After cooling down, the reactant solidified right into red-black crystals, the sealed tube was opened, as well as the solid red-black remedy was washed out with a small amount of warm water. Oily pollutants were eliminated by removal with ether. After neutralization with sodium bicarbonate, excess pyridine was eliminated by home heating with vapor. The mixture was then made highly basic and the 2,2′-bipyridine was distilled off with vapor.

Reference

Quality Control of 2,2'-Bipyridine

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