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HS Code |
878097 |
| Product Name | 4,5-Diphenyl-2-Imidazolethiol |
| Cas Number | 1194-82-7 |
| Molecular Formula | C15H12N2S |
| Molecular Weight | 252.33 g/mol |
| Appearance | Light yellow to beige powder |
| Melting Point | 222-225 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at room temperature, away from light and moisture |
As an accredited 4,5-Diphenyl-2-Imidazolethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, clearly labeled "4,5-Diphenyl-2-Imidazolethiol, 10g," chemical hazard symbols and batch number. |
| Shipping | 4,5-Diphenyl-2-Imidazolethiol is shipped in tightly sealed containers to prevent moisture and light exposure. It is classified as a laboratory chemical, so transport complies with relevant local and international regulations. The package includes proper labeling, safety data sheets, and appropriate hazard warnings, ensuring safe handling and delivery during transit. |
| Storage | Store 4,5-Diphenyl-2-Imidazolethiol in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from moisture and direct sunlight. Use appropriate safety precautions, including gloves and eye protection, when handling. Store according to all applicable regulations and safety guidelines. |
Applications of 4,5-Diphenyl-2-Imidazolethiol in Industrial Manufacturing4,5-Diphenyl-2-Imidazolethiol is a specialty intermediate that supports advanced performance in critical industrial sectors, including photopolymer technology, flame retardants, electrochemical devices, and high-performance coatings. Below we present verified, targeted downstream implementation scenarios drawn from active market adoption. 1. Photoinitiators for UV-Curable SystemsThe imidazole-thiol structure makes this raw material an effective building block for synthesizing Type II photoinitiators. End users in inkjet and offset printing formulations exploit its reactivity to achieve high pattern precision and fast cure rates in UV-initiated polymerization. Integrators typically use it to improve depth of cure and image sharpness in free radical-based photoresists, particularly for fine electronics and packaging applications where reduced migration and low-odor profiles are critical. Industry compliance standards
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2. Sulfur-Based Flame Retardant FormulationsProducers of specialty polycarbonate, polyurethane, and polyester engineering plastics utilize this compound as a reactive sulfur donor in halogen-free flame retardant systems. Its thiol group enables synergistic charring and radical quenching when combined with phosphorus or nitrogen co-additives, helping manufacturers achieve reduced smoke generation and compliance with stringent fire safety codes in electronic components and mass transit interiors. Industry compliance standards
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3. Corrosion Inhibitor Packages for Acidic MediaChemical processors in petroleum extraction and metal finishing sectors deploy the unique thiol-imidazole moiety as a film-forming booster in custom corrosion inhibitor blends. This material provides strong adsorption onto steel and copper alloys in hydrochloric acid, minimizing uniform and pitting corrosion during acid pickling, cleaning, and downhole acidizing without introducing chlorinated byproducts or sulfur gas. Industry compliance standards
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4. Electrolytic Additive for Silver Plating BathsTechnical silver-plating lines require specialized grain refiners and brightening agents to achieve uniform deposit morphology and reduce microcracking. The imidazolethiol molecule provides dual action: promoting even nucleation during electrodeposition and reducing hydrogen embrittlement for high-reliability connectors and conductor components in electronics and telecommunication equipment manufacturing. Industry compliance standards
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5. Precursor Intermediate in Pharmaceutical API SynthesisManufacturers of benzothiazole-based pharmaceuticals utilize this compound in controlled synthesis of antibiotic and antifungal drug precursors. Its specific ring system and thiol functionality allow for esterification, cyclization, and alkylation steps targeting high-purity bioactive intermediates under tight GMP regulation, especially in European and North American cGMP facilities. Industry compliance standards
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6. Additive for High-Performance Anticorrosion CoatingsThe advanced heterocyclic structure delivers consistent performance as a secondary corrosion inhibitor in water-based or solventborne primer systems. Protective coatings manufacturers for offshore, automotive chassis, and industrial plant equipment use this material to reinforce adhesion and boost resistance to salt spray, especially where exposure to cyclic wet/dry environments requires extended coating lifetimes beyond conventional standards. Industry compliance standards
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