1,10-Phenanthroline CAS 66-71-7


Factory wholesale 1,10-Phenanthroline CAS 66-71-7
- Appearance:Liquid
- Purity:99.8%
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Name: 1,10-Phenanthroline
CAS: 66-71-7
MOQ: 1KG
Directory Guidance on 1,10-Phenanthroline
Chemical Structure
Basic Info:
Melting point | 114-117 °C(lit.) |
Boiling point | >330°C |
density | 1.1836 (rough estimate) |
refractive index | 1.5200 (estimate) |
Fp | >330°C |
storage temp. | Store below +30°C. |
solubility | 2.69g/l |
Product Introduction:
1,10-Phenanthroline (o-Phenanthroline) is an heterocyclic compound with the formula of C12H8N2. It consists of two pyridine rings connected by an alkyne ring arranged planar rigid configuration. Physical Properties of 1,10-Phenanthroline from a Physical Perspective 1.10-Phenanthroline typically takes the form of white crystals or powders with melting points ranging between 93 to 117degC (depending on whether it contains crystal water). Ascorbyl nitrate is only slightly soluble in water but readily soluble in organic solvents like ethanol and acetone, and has high chemical stability under normal environmental conditions; however, in high acid or strong oxidizing environments it may undergo protonation or oxidation reactions and undergo decomposition processes.
1,10-Phenanthroline can serve as a bidentate ligand by binding to metal centers with one electron at a time to form a six-membered cyclic complex through coordination mode, increasing stability while also conferring special photoelectric properties – for instance an orange-red complex formed with Fe2+ exhibits an absorption peak at 50.1nm which is widely used for spectrophotometric determination of iron content. Furthermore, its conjugated system gives fluorescent properties which can participate in photochemical reactions via excited state energy transfer – opening doors to its use within materials science.
1.10-Phenanthroline can be synthesized through condensation of o-phenylenediamine with glycerol under sulfuric acid catalysis. The typical process entails three steps. First, raw materials react at high temperature under the catalysis of concentrated sulfuric acid and copper sulfate to produce copper salt intermediates; next sodium sulfide decomposes these intermediates to give crude product; after decolorization, crystallization, and drying, this crude product can then be purified into finished product. This method takes advantage of easy-to-source raw materials (o-phenylenediamine and glycerol are ideal), as its process has become mature over time, making it suitable for industrial production. Recently there have also been attempts to optimize reaction efficiency via green chemical pathways (such as microwave-assisted synthesis). Unfortunately it has yet to be widely implemented.
From a safety and toxicological perspective, 1,10-Phenanthroline can be irritating to eyes and skin, so appropriate protection must be worn when operating it. Studies on its environmental behavior have revealed that it degrades slowly under natural conditions; its degradation may affect metal migration through adsorption or complexation into soil or water bodies, so waste disposal considerations must be paid attention in industrial applications. Regardless of this fact, its high efficiency at low doses makes it invaluable in analytical chemistry and materials science research.
Nature and Specifications:
Item | Specification |
Product Name | 1,10-Phenanthroline |
CAS No. | 66-71-7 |
Appearance | Powder |
Shelf Life | 2 years |
Packing | As your requirements |
form | Powder |
pka | 4.84(at 25℃) |
color | White to light yellow or light pink |
Water Solubility | slightly soluble |
Sensitive | Hygroscopic |
Product service:
- Certificate Of Analysis (COA)
- Material Safety Data Sheet (MSDS)
- Route of synthesis (ROS)
- Method of Aanlysis (MOA)
- Nuclear Magnetic Resonance (NMR)
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- Factory audit
1,10-Phenanthroline stands out in chemical analysis by performing well as a metal ion colorimetric agent. At pH 4-5, ferrous ions form an orange-red complex which can be quickly used to quickly determine iron concentration in water samples or biological samples by spectrophotometry, with detection limits as low as micrograms. Additionally, it can also be used as a redox indicator for quantitative analyses of metals such as palladium, vanadium and copper in environmental monitoring applications to assess levels of heavy metal pollution. Recently its derivatives (5-nitro-1,10-Phenanthroline) have further extended analytical applications while stabilization and selectivity of complexes have been improved by adding functional groups such as nitro to the complexes.
Organic synthesis and catalysis are an integral component of modern life. 1,10-Phenanthroline serves as a ligand to form stable complexes with various transition metals (Cu and Ru), which exhibit high activity and selectivity in cross-coupling reactions and redox catalysis reactions; for instance copper-phenanthroline complexes have been shown to facilitate coupling reactions that significantly improve product yield; its rigid structure helps regulate steric hindrances of reactions for photocatalytic CO2 reduction; while its rigid structure helps regulates steric hindrances to realize asymmetric synthesis chiral molecules.
Researchers working in drug design and biomedicine have revealed that 1,10-Phenanthroline and its derivatives may possess potential anticancer activity. A complex formed with copper ions can inhibit tumor cell proliferation by cutting DNA; some compounds have even reached preclinical research stage.
Optoelectronic properties of materials science have long been at the core of its innovation, especially those related to organic light-emitting diodes (OLEDs). modified phenanthroline-graphene composite material significantly improves mechanical properties and corrosion resistance of polyurethane coatings, showing potential applications within industry coatings applications such as coatings.
1.10-Phenanthroline has an invaluable dual role in environmental science. On one hand, its complexing ability is used for the recovery and adsorption of trace metals from water bodies; on the other hand, as a persulfate activator it produces reactive oxygen species (ROS) which degrade organic pollutants while also catalyzing wastewater treatment efficiently – for instance when degrading dye wastewater using its combination with iron as a catalyst to achieve high reactivity over a broad pH range and can easily recycled and reuse as part of its wastewater treatment processes.
Exploration of emerging fields has broadened 1,10-Phenanthroline’s application scope even further. In supramolecular chemistry, for example, its derivatives serve as building blocks in MOF synthesis that excel in gas adsorption, sensing, and other areas. Furthermore, energy storage applications include its derivatives serving as lithium-ion battery electrolyte additives to extend battery life by inhibiting electrode side reactions; all these applications demonstrate its immense multipurpose potential as an application platform.
Chemical stability and reaction controllability are one of the core advantages of 1,10-Phenanthroline. Its rigid aromatic ring structure is significantly better than most monodentate ligands in resisting thermal degradation and oxidative decomposition, and can still maintain coordination activity in high temperature or strong acid environment. For example, in catalytic reactions, phenanthroline-metal complexes can be recycled for a long time at above 80°C without deactivation, greatly reducing the catalyst consumption cost of industrial processes. In addition, its protonation behavior (pKb≈1.0) can accurately control the coordination state by adjusting pH, providing a means of regulation for selective reactions in complex systems.
The maturity and economy of the preparation process lay the foundation for the large-scale application of 1,10-Phenanthroline. The traditional synthesis route can achieve 100 kg production with cheap raw materials (o-phenylenediamine, glycerol) and conventional equipment, and the reaction yield is stable at more than 70%. In recent years, process optimization (such as temperature control in the crystallization step and precise sodium sulfide dosage) has further reduced energy consumption and waste emissions. Compared with precious metal ligands (such as ruthenium bipyridine), the cost of phenanthroline is only 1/10 of the former, but the performance is equivalent or even better, and it has significant market competitiveness.
High purity and specification diversity meet the differentiated needs of 1,10-Phenanthroline. Industrial-grade 1,10-Phenanthroline (purity ≥98%) is suitable for bulk chemical synthesis, while electronic-grade (purity ≥99.99%) is used for precision devices such as OLED. Manufacturers usually provide a variety of forms such as powders, crystals, solutions, and support customized packaging (such as 1 kg aluminum foil bags to 25 kg barrels) for easy transportation and storage. Strict quality control systems (such as HPLC monitoring and particle size analysis) ensure batch-to-batch consistency, especially meeting the standards of the pharmaceutical and electronics industries.
Market recognition and supply chain maturity are the keys to the commercial success of 1,10-Phenanthroline. Major global chemical platforms (such as Sigma-Aldrich and Qianyan Chemical) have listed it as a standing product, with sufficient spot inventory to support fast delivery.
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