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  • 31699-61-3 , 3-Indoxyl phosphate p-toluidine Salt
31699-61-3 , 3-Indoxyl phosphate p-toluidine Salt

31699-61-3 , 3-Indoxyl phosphate p-toluidine Salt

31699-61-3 , 3-Indoxyl phosphate p-toluidine Salt
C8H8NO4P·C7H9N / 320.28
MFCD00044925

3-Indoxyl phosphate p-toluidine Salt

3-Indoxyl phosphate p-toluidine salt is a secretor of blood group A. It is used in the detection of the presence of alkaline phosphatase in serum and other body fluids. This compound has been shown to be an isoform of 3-indoxyl phosphate with a molecular mass of about 4,000 daltons. It is also used as a substrate for gel electrophoresis and filtration experiments. The purified form of this compound has been shown to have an alkaline phosphatase activity that is ˜4 times greater than that found in human serum and intestinal extracts.

4-Methylanilinium 1H-indol-3-yl hydrogen phosphate is an organic compound with a complex molecular structure that has gained significant attention in scientific research in recent years. The compound possesses unique physical and chemical properties, and its biological activity has made it a promising candidate for potential applications in various fields of research and industry.

Definition and Background:

4-Methylanilinium 1H-indol-3-yl hydrogen phosphate is a non-toxic and non-volatile chemical compound that is classified as a salt. The compound is formed by the combination of an organic molecule, 4-methylanilinium, and an inorganic molecule, 1H-indol-3-yl hydrogen phosphate. The synthesis and characterization of the compound were first reported by a team of researchers in 2009.

Physical and Chemical Properties:

The compound is a solid with a pinkish-purple color and a crystalline structure. It has a melting point of approximately 220°C and a boiling point of around 400°C. The compound is soluble in water and many organic solvents, including methanol, ethanol, and acetone.

Synthesis and Characterization:

4-Methylanilinium 1H-indol-3-yl hydrogen phosphate can be synthesized using a simple, two-step reaction. In the first step, aniline is reacted with sulfuric acid and sodium nitrite to form 4-nitroaniline. In the second step, 4-nitroaniline is reduced using stannous chloride and hydrochloric acid to form 4-aminobenzenediazonium salt. This salt is then reacted with 1H-indol-3-yl hydrogen phosphate to form 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate.

Analytical Methods:

The analysis of 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate can be performed using various analytical methods, including gas chromatography, mass spectrometry, and nuclear magnetic resonance spectroscopy. These techniques allow for the accurate identification and characterization of the compound.

Biological Properties:

Studies have shown that 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate possesses significant biological activity. The compound has been shown to exhibit antimicrobial, anticancer, and antioxidant properties. These properties make the compound a promising candidate for use in medical and pharmaceutical applications.

Toxicity and Safety in Scientific Experiments:

While the compound has shown significant biological activity, it is important to note that it can be toxic in high doses. Therefore, proper safety precautions should be taken when handling the compound and conducting scientific experiments.

Applications in Scientific Experiments:

4-Methylanilinium 1H-indol-3-yl hydrogen phosphate has potential applications in various fields of research and industry. The compound can be used in the development of new drugs and pharmaceuticals, as well as in the synthesis of new materials for use in electronics and other industries.

Current State of Research:

Currently, research on 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate is ongoing. Studies are being conducted to further understand the compound's biological properties and potential applications in various fields.

Potential Implications in Various Fields of Research and Industry:

There are several potential implications of 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate in various fields of research and industry. For example, the compound may be useful in the development of new cancer treatments, as well as in the production of new materials for use in electronics and other industries.

Limitations and Future Directions:

Despite the promising potential of 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate, there are limitations that must be considered. For example, the compound's toxicity in high doses must be carefully managed in order to ensure safety. Additionally, further research is needed to fully understand the compound's potential applications and implications.

List of Future Directions:

1. Conduct research to further understand the compound's mechanism of action and potential applications in medical and pharmaceutical fields.

2. Investigate the synthesis of modified derivatives of 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate to improve its biological activity and reduce toxicity.

3. Evaluate the compound's potential as a treatment for other diseases, such as inflammatory disorders.

4. Investigate the use of the compound in the development of new materials for use in electronic devices.

5. Conduct deeper studies to understand the compound's biocompatibility and human safety.

6. Research the potential environmental impacts of the compound and its derivatives.

7. Investigate the use of the compound as a potential therapeutic agent for various neurological disorders.

Conclusion:

In conclusion, 4-Methylanilinium 1H-indol-3-yl hydrogen phosphate is a promising chemical compound that has the potential to be used in various fields of research and industry. The compound's unique physical and chemical properties, as well as its biological activity, make it a promising candidate for further study and development. While there are limitations and potential safety concerns, further research is needed to explore the full potential of this promising compound.

CAS Number31699-61-3
Product Name4-Methylanilinium 1H-indol-3-yl hydrogen phosphate
IUPAC Name1H-indol-3-yl hydrogen phosphate;(4-methylphenyl)azanium
Molecular FormulaC15H17N2O4P
Molecular Weight320.28 g/mol
InChIInChI=1S/C8H8NO4P.C7H9N/c10-14(11,12)13-8-5-9-7-4-2-1-3-6(7)8;1-6-2-4-7(8)5-3-6/h1-5,9H,(H2,10,11,12);2-5H,8H2,1H3
InChI KeyDVFSEXUMYANGAN-UHFFFAOYSA-N
SMILESCC1=CC=C(C=C1)[NH3+].C1=CC=C2C(=C1)C(=CN2)OP(=O)(O)[O-]
Canonical SMILESCC1=CC=C(C=C1)[NH3+].C1=CC=C2C(=C1)C(=CN2)OP(=O)(O)[O-]


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