Methyltriphenylphosphonium iodide
Inhibitors/Agonists
Methyltriphenylphosphonium iodide (MePh3PI) is a quaternary ammonium salt that has gained significant attention in the scientific community due to its diverse applications in various fields. It is a white crystalline powder that is soluble in polar solvents such as water, ethanol, and methanol. MePh3PI has been extensively studied for its biological activity, potential therapeutic effects, and industrial applications.
404.2 g/mol
404.2 g/mol
Formulation:
404.2 g/mol
Source:
Usage:
Methyltriphenylphosphonium iodide
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-321319
CAS Number: 2065-66-9
Molecular Formula: C19H18IP
Molecular Weight: 404.2 g/mol
Purity: ≥ 98%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 5g | bt-321319-5g | $297.23 | |
| 25g | bt-321319-25g | $1,055.54 | |
| 100g | bt-321319-100g | $3,177.23 | |
| 250g | bt-321319-250g | $4,499.38 | |
| 500g | bt-321319-500g | $9,542.00 |
| CAS Number | 2065-66-9 |
|---|---|
| Product Name | Methyltriphenylphosphonium iodide |
| Molecular Formula | C19H18IP |
| Molecular Weight | 404.2 g/mol |
| InChI | InChI=1S/C19H18P.HI/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19;/h2-16H,1H3;1H/q+1;/p-1 |
| InChI Key | JNMIXMFEVJHFNY-UHFFFAOYSA-M |
| IUPAC Name | methyl(triphenyl)phosphanium;iodide |
| Canonical SMILES | C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[I-] |
| Description | Methyltriphenylphosphonium iodide (MePh3PI) is a quaternary ammonium salt that has gained significant attention in the scientific community due to its diverse applications in various fields. It is a white crystalline powder that is soluble in polar solvents such as water, ethanol, and methanol. MePh3PI has been extensively studied for its biological activity, potential therapeutic effects, and industrial applications. |
| Method of Synthesis or Extraction | Methyltriphenylphosphonium iodide can be synthesized by various methods, including the reaction of triphenylphosphine with methyl iodide in the presence of a base such as potassium carbonate. Another method involves the reaction of triphenylphosphine with methyl iodide in the presence of iodine. The efficiency and yield of each method depend on the reaction conditions, such as temperature, pressure, and reaction time. The yield of Methyltriphenylphosphonium iodide can range from 60% to 90%. Environmental and safety considerations must be taken into account during the synthesis process, as Methyltriphenylphosphonium iodide is a toxic substance that can cause skin and eye irritation. |
| Chemical Structure and Biological Activity | Methyltriphenylphosphonium iodide has a quaternary ammonium structure, with a positively charged methyl group attached to a triphenylphosphine group and an iodide ion. The positively charged methyl group allows Methyltriphenylphosphonium iodide to interact with negatively charged biological molecules, such as DNA and proteins. Methyltriphenylphosphonium iodide has been shown to have biological activity against various microorganisms, including bacteria, fungi, and viruses. It has also been studied for its potential therapeutic effects, such as anti-cancer and anti-inflammatory properties. |
| Biological Effects | Methyltriphenylphosphonium iodide has been shown to affect cell function and signal transduction pathways. It can inhibit the growth of cancer cells by inducing apoptosis and inhibiting cell proliferation. Methyltriphenylphosphonium iodide has also been shown to modulate the immune response by inhibiting the production of pro-inflammatory cytokines. However, Methyltriphenylphosphonium iodide can also have toxic effects on cells, such as inducing oxidative stress and DNA damage. |
| Applications | Methyltriphenylphosphonium iodide has various applications in medical, environmental, and industrial research. In medical research, Methyltriphenylphosphonium iodide has been studied for its role in drug development, particularly in the development of anti-cancer and anti-inflammatory drugs. Clinical trials have shown promising results in the use of Methyltriphenylphosphonium iodide as a therapeutic agent. However, potential side effects, such as toxicity and immunosuppression, must be carefully considered. In environmental research, Methyltriphenylphosphonium iodide has been studied for its effects on ecosystems and its role in pollution management. Methyltriphenylphosphonium iodide has been shown to have potential as a sustainable and environmentally friendly alternative to traditional pesticides. In industrial research, Methyltriphenylphosphonium iodide has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations must be taken into account when using Methyltriphenylphosphonium iodide in industrial settings. |
| Future Perspectives and Challenges | Despite the promising applications of Methyltriphenylphosphonium iodide, there are still limitations in its use and study. The toxicity and potential side effects of Methyltriphenylphosphonium iodide must be carefully considered in future research. Possible solutions and improvements include the development of more selective and less toxic derivatives of Methyltriphenylphosphonium iodide. Future trends and prospects in the application of Methyltriphenylphosphonium iodide in scientific research include the development of new therapeutic agents and the use of Methyltriphenylphosphonium iodide in sustainable and environmentally friendly technologies. Conclusion: Methyltriphenylphosphonium iodide is a versatile compound with diverse applications in various fields. Its chemical structure and biological activity make it a promising candidate for drug development and environmental management. However, careful consideration must be given to its toxicity and potential side effects. Future research should focus on developing more selective and less toxic derivatives of Methyltriphenylphosphonium iodide and exploring its potential in sustainable technologies. |
| Other CAS Number | 1560-52-7 2065-66-9 20667-19-0 |
| Pictograms | Acute Toxic;Irritant |
| SMILES | C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[I-] |
| Synonyms | Triphenylmethylphosphinium Iodide; Methyltriphenylphosphonium iodide |
| PubChem Compound | Methyltriphenylphosphonium iodide |
| Last Modified | May 29 2023 |