2183-17-7, 磷酸萘酯二钠盐,
a-Naphthyl phosphate disodium salt hydrate;
1-Naphthalenol dihydrogen phosphate disodium salt; 1-Naphthyl disodium orthophosphate,
Cas:2183-17-7
C10H7O4PNa2 / 268.11(as anhydrous)
MFCD00041007
1-Naphthalenol dihydrogen phosphate disodium salt; 1-Naphthyl disodium orthophosphate
磷酸萘酯二钠盐,
Sodium naphthalen-1-yl phosphate is a chemical compound that has been shown to have antioxidant properties. It has been found to be a potent inhibitor of phosphatase, an enzyme that participates in the degradation of amino acids and nucleotide metabolism. This compound also inhibits the activity of enzymes such as catalase, lipoxygenase, and glutathione peroxidase. Sodium naphthalen-1-yl phosphate is used as a component in some toothpastes and mouthwashes. In addition, this substance has been used for the treatment of liver diseases.
Disodium naphthyl phosphate (DNPP) is a compound that belongs to the family of naphthalene derivatives. It has a white crystalline appearance and is soluble in water. In this paper, we will discuss the definition and background of DNPP, its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, and applications in scientific experiments.
Definition and Background:
DNPP is a compound used as a phosphorus source in dye chemistry. It is also used in the manufacture of pigments for coloring plastics, textiles, and other materials. DNPP has been used as an ingredient in the production of chemiluminescent substances, as well as in industrial water treatment processes.
Synthesis and Characterization:
DNPP is synthesized by reacting naphthalene with phosphorus oxychloride, which produces a mixture of products. The mixture is then neutralized with sodium hydroxide to yield DNPP. The purity and identity of DNPP can be confirmed using various characterization techniques such as nuclear magnetic resonance (NMR), infrared spectroscopy (IR), and mass spectrometry (MS).
Analytical Methods:
The quantitative analysis of DNPP can be performed using different analytical methods such as gas chromatography (GC), high-performance liquid chromatography (HPLC), and capillary electrophoresis (CE). These methods can be used to determine the purity, composition, and concentration of DNPP in different matrices.
Biological Properties:
Research has shown that DNPP has anti-inflammatory and antibacterial properties. It has been shown to inhibit the growth of Escherichia coli and Staphylococcus aureus. DNPP has also been found to increase the production of cytokines and chemokines in human bronchial epithelial cells.
Toxicity and Safety in Scientific Experiments:
DNPP is considered to be a low toxicity compound. However, it can cause irritation to the skin and eyes upon contact. Ingestion of DNPP can cause irritation to the digestive system. In scientific experiments, proper safety measures should be taken to avoid exposure to DNPP.
Applications in Scientific Experiments:
DNPP is used as a substrate in the enzyme-catalyzed chemiluminescence reaction for the detection of enzymes such as peroxidase and alkaline phosphatase. It is also used as a dyeing auxiliary and surfactant in the textile industry. DNPP has been used as a phosphorus source in the synthesis of nanostructures such as zinc oxide nanoparticles.
Current State of Research:
Research on DNPP is ongoing in various fields such as materials science, chemistry, and microbiology. There has been an increasing interest in the use of DNPP as a substrate for enzyme-catalyzed chemiluminescence reactions. Researchers have also investigated the synthesis of DNPP-based nanoparticles for various applications.
Potential Implications in Various Fields of Research and Industry:
DNPP has potential implications in various fields such as materials science, textile industry, and enzyme detection. It can also be used in the synthesis of nanomaterials for various applications such as drug delivery and sensing.
Limitations and Future Directions:
One of the limitations of DNPP is its limited solubility in organic solvents. Future research can focus on improving the solubility of DNPP in organic solvents to expand its applications. Other future directions can include the development of DNPP-based materials with unique properties and the investigation of the use of DNPP in biological applications.
In conclusion, DNPP is a compound with various applications in scientific experiments and industry. Its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety, and potential implications have been discussed in this paper. The current state of research and future directions for DNPP have also been highlighted.
CAS Number | 2183-17-7 |
Product Name | Disodium naphthyl phosphate |
IUPAC Name | disodium;naphthalen-1-yl phosphate |
Molecular Formula | C10H7Na2O4P |
Molecular Weight | 268.11 g/mol |
InChI | InChI=1S/C10H9O4P.2Na/c11-15(12,13)14-10-7-3-5-8-4-1-2-6-9(8)10;;/h1-7H,(H2,11,12,13);;/q;2*+1/p-2 |
InChI Key | QYURIFWAOPAPAJ-UHFFFAOYSA-L |
SMILES | C1=CC=C2C(=C1)C=CC=C2OP(=O)([O-])[O-].[Na+].[Na+] |
Canonical SMILES | C1=CC=C2C(=C1)C=CC=C2OP(=O)([O-])[O-].[Na+].[Na+] |
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