4-phenyl-1H-1,2,4-triazole-5-thione
95%
- Product Code: 196336
CAS:
5373-72-8
| Molecular Weight: | 177.23 g./mol | Molecular Formula: | C₈H₇N₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00227514 | |
| Melting Point: | Boiling Point: | 260.4 °C at 760 mmHg | |
| Density: | 1.33 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a corrosion inhibitor for metals, especially in acidic environments. It forms a protective layer on metal surfaces, reducing the rate of corrosion in industrial cleaning and oil well acidizing processes.
Acts as a ligand in coordination chemistry, forming stable complexes with transition metals such as copper, zinc, and nickel. These complexes are studied for catalytic activity and potential use in material science.
Investigated for biological applications due to its structural similarity to nucleic acid components. Shows antimicrobial and antifungal properties in laboratory studies, making it a candidate for pharmaceutical development.
Serves as a building block in organic synthesis, particularly in the preparation of heterocyclic compounds with potential medicinal properties. Its thione group allows for easy modification and incorporation into larger molecules.
Also explored in the development of sensors and electronic materials because of its electron-donating ability and metal-binding characteristics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿3,900.00 |
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| 250mg | 10-20 days | ฿6,610.00 |
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| 1g | 10-20 days | ฿21,840.00 |
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4-phenyl-1H-1,2,4-triazole-5-thione
Used as a corrosion inhibitor for metals, especially in acidic environments. It forms a protective layer on metal surfaces, reducing the rate of corrosion in industrial cleaning and oil well acidizing processes.
Acts as a ligand in coordination chemistry, forming stable complexes with transition metals such as copper, zinc, and nickel. These complexes are studied for catalytic activity and potential use in material science.
Investigated for biological applications due to its structural similarity to nucleic acid components. Shows antimicrobial and antifungal properties in laboratory studies, making it a candidate for pharmaceutical development.
Serves as a building block in organic synthesis, particularly in the preparation of heterocyclic compounds with potential medicinal properties. Its thione group allows for easy modification and incorporation into larger molecules.
Also explored in the development of sensors and electronic materials because of its electron-donating ability and metal-binding characteristics.
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