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Bromotriphenylethylene

    • Product Name Bromotriphenylethylene
    • Alias Triphenylbromoethylene
    • Einecs 204-365-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Bromotriphenylethylene

    Applications of Bromotriphenylethylene in Industrial Manufacturing

    Bromotriphenylethylene 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) Intermediates

    Leading 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) substance monographs for intermediate controls
    • US FDA CFR Title 21, Part 210/211
    • ISO 9001:2015 for quality management systems

    Typical usage ratio

    • Pharmaceutical synthesis integrates 1.0–1.2 molar equivalents relative to the core substrate; specific ratios depend on reaction scale-up yields and stoichiometric efficiency.

    Downstream process integration

    • Introduced during penultimate or antepenultimate coupling steps in multi-stage reactor sequences. Purification typically follows via crystallization or preparative chromatography to meet GMP impurity thresholds.

    Final product types

    • Active pharmaceutical ingredients for fertility treatments (e.g., clomiphene citrate tablets)
    • Research-grade SERMs
    • Bulk intermediates shipped for contract manufacturing organizations (CMOs)

    2. Fine Chemical Intermediates for Advanced Organic Synthesis

    Contract 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

    • REACH (Regulation (EC) No 1907/2006) for substance registration and safe handling
    • ISO 9001:2015 for quality assurance procedures
    • Internal client-specific batch documentation (multinational chemical groups)

    Typical usage ratio

    • Commonly used at 0.5–2.0 equivalents depending on desired coupling efficiency and side reaction suppression; stoichiometry adjusted based on catalyst and substrate availability.

    Downstream process integration

    • Added to stirred-tank reactors with controlled addition rates; often forms aryl coupling partners in cross-coupling or functionalization stages before final purification by column chromatography or HPLC.

    Final product types

    • High-purity aryl intermediates for further custom synthesis
    • Novel ligands for homogeneous catalysis systems
    • Specialty organic building blocks for academic and industrial R&D

    3. Synthesis of Advanced Liquid Crystal Materials

    High-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

    • RoHS (Restriction of Hazardous Substances Directive) for electronic components
    • ISO 14001 for environmental management in specialty chemicals
    • Client-validated analytical validated method protocols

    Typical usage ratio

    • Typically incorporated at 2–10% by mole in precursor blends, optimized based on target birefringence and phase transition temperature requirements.

    Downstream process integration

    • Enters liquid crystal precursor synthesis via controlled halogen exchange, followed by multi-stage condensation and purification steps. Downstream integration occurs in small-batch reactors under inert atmosphere.

    Final product types

    • Custom liquid crystal compounds for display panels
    • Electro-optical assembly materials
    • Mesogenic intermediates for fine-tuned molecular design

    4. Synthesis of Photoinitiators for UV-Curable Coatings

    Specialty 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

    • Regulation (EC) No 1935/2004 on materials intended to come into contact with food (for food packaging coatings)
    • ASTM D7767 / D7869 for photoinitiator and UV-coating performance testing
    • ISO 9001:2015 for chemical manufacturing management

    Typical usage ratio

    • Used at 0.2–5.0% by mass in precursor blends, based on absorption efficiency and targeted crosslinking rate; optimization guided by end-use performance in UV testing.

    Downstream process integration

    • Introduced during early stages of photoinitiator synthesis, typically before aryl functionalization and purification. Incorporated into pilot batch reactors, followed by distillation and drying prior to blending into final photoinitiator formulations.

    Final product types

    • Photoinitiators for UV-cured wood and industrial coatings
    • Photoinitiators used in UV inkjet printing ink formulations
    • Specialty curing agents for electronics encapsulation
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