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HS Code |
610441 |
| Cas Number | 1194-98-5 |
| Molecular Formula | C26H19Br |
| Molecular Weight | 411.33 g/mol |
| Iupac Name | 1-bromo-1,2-diphenyl-2-(4-phenylphenyl)ethene |
| Synonyms | Triphenylbromoethylene; BTE; Bromotriphenylethene |
| Appearance | White to off-white crystalline powder |
| Melting Point | 174-176°C |
| Solubility | Insoluble in water; soluble in organic solvents |
| Chemical Class | Nonsteroidal selective estrogen receptor modulator (SERM) |
| Pubchem Cid | 19513 |
As an accredited Bromotriphenylethylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Bromotriphenylethylene, 25g, is packaged in a sealed amber glass bottle with a secure cap, labeled with hazard symbols and product information. |
| Shipping | Bromotriphenylethylene should be shipped in tightly sealed containers, protected from light and moisture. Handle as a hazardous organic chemical. Comply with relevant regulations for transport, including appropriate labeling and documentation. Use cushioning and absorbent material to prevent leaks or breakage during transit. Suitable for ground, air, or sea freight as permitted by local laws. |
| Storage | Bromotriphenylethylene should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. It should be kept away from incompatible materials such as strong oxidizing agents. Proper labeling and secure storage are essential to prevent accidental exposure. Use appropriate safety precautions, including personal protective equipment, when handling and storing this chemical. |
Applications of Bromotriphenylethylene in Industrial ManufacturingBromotriphenylethylene plays a specialized role in targeted chemical and pharmaceutical manufacturing sectors where precise synthetic intermediates are essential. We supply this compound directly to industrial clients who require high-grade materials for advanced process integration in regulated production environments. Explore the following application scenarios to understand how this material functions within real downstream industries. 1. Pharmaceutical API Synthesis: Selective Estrogen Receptor Modulator (SERM) IntermediatesLeading pharmaceutical companies employ Bromotriphenylethylene as a critical intermediate in synthesizing non-steroidal selective estrogen receptor modulators (SERMs) such as clomiphene for the treatment of ovulatory dysfunction and hormone-responsive cancers. This compound’s halogenated structure supports key C–C coupling and substitution reactions, enabling control over stereochemistry at a late stage in multi-step synthesis. Consistent purity and traceability are crucial for compliance; active pharmaceutical ingredient (API) departments introduce this material during the penultimate step, often coupling with substituted benzaldehydes or other electron-rich aryl reagents. Industry compliance standards
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2. Fine Chemical Intermediates for Advanced Organic SynthesisContract manufacturers and custom synthesis providers utilize Bromotriphenylethylene as an advanced halogenated intermediate in preparing specialty aryl compounds. Its controlled reactivity—particularly in Suzuki, Heck, and Ullmann reactions—makes it ideal for producing custom ligands, specialty polymers, and novel building blocks that are not commercially available in bulk. Chemical process development teams implement rigorous process analytical technologies (PAT) to maintain batch reproducibility and impurity profiles within custom product specifications. Industry compliance standards
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3. Synthesis of Advanced Liquid Crystal MaterialsHigh-tech electronic and display manufacturers source Bromotriphenylethylene for its unique triphenylethylene motif, which serves as a precursor to custom mesomorphic compounds. The halogen substituent increases molecular rigidity and electronic effects, resulting in enhanced anisotropy required for liquid crystalline alignment and phase stability. Liquid crystal formulation teams demand precise control of halogen content as it directly influences electro-optical responsiveness in finished displays and device sub-assemblies. Industry compliance standards
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4. Synthesis of Photoinitiators for UV-Curable CoatingsSpecialty chemical manufacturers leverage Bromotriphenylethylene in producing customized aryl-based photoinitiators that support polymerization of UV-curable resins in coatings and printing inks. The brominated aromatic motif increases photoinitiator absorption in the UV-A/UV-B spectrum, enhancing cure speed and depth for high-performance formulations. Product stewardship incorporates batch-wise NMR and photometric analysis at every stage to guarantee compliance with regulatory and client-specific performance benchmarks. Industry compliance standards
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