2,9-Dichloro-1,10-phenanthroline is a chemical compound widely used in laboratory settings, particularly in catalysis and inorganic chemistry. As a nitrogen-donor ligand, it plays a crucial role in the formation of metal complexes, which are essential in various chemical reactions. This compound is commonly utilized in synthetic processes involving both organic and inorganic materials, making it a versatile reagent in modern chemical research. Its stability and reactivity make it a valuable tool for researchers working on complex chemical systems.
The compound’s unique molecular structure, featuring two chlorine atoms at positions 2 and 9, contributes to its high reactivity, especially at the nitrogen atoms located at positions 1 and 10. These structural features enhance its ability to participate in substitution, oxidation, and reduction reactions. The compound’s stability under various reaction conditions further supports its use in a wide range of experimental setups. Its reliability and consistent performance make it a preferred choice for laboratory applications requiring precise chemical interactions.
In Indonesian laboratories, 2,9-Dichloro-1,10-phenanthroline is a key reagent for research in catalysis and the synthesis of complex compounds. It is frequently used in academic and industrial research settings to support chemical processes that require nitrogen-donor ligands. Its availability and effectiveness make it a standard component in many chemical experiments conducted in Indonesian research institutions.
- Catalytic reactions benefit from this compound due to its ability to form stable metal complexes, enhancing reaction efficiency and selectivity.
- Inorganic synthesis relies on its nitrogen-donor properties to create coordination compounds with various metal ions.
- Organic synthesis applications utilize its reactivity to facilitate substitution and oxidation processes in complex molecule formation.
- Reductive processes in chemical synthesis take advantage of its structural stability and reactivity for controlled electron transfer.
- Analytical chemistry uses it as a reference standard for identifying and quantifying nitrogen-containing compounds in various samples.
| Brand | TCI |
|---|---|
| CAS number | 29176-55-4 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Catalysis and Inorganic Chemistry > Nitrogen-Donor Ligands [Catalysis] |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. While it is not classified as hazardous under standard conditions, it is important to follow standard chemical handling protocols to minimize any potential risks. Proper storage and handling ensure its effectiveness and safety in laboratory applications.
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