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  • 4,4'-Diiodobiphenyl & 4-Dimethylamino Pyridine Supplier High-Purity Reagents

4,4'-Diiodobiphenyl & 4-Dimethylamino Pyridine Supplier High-Purity Reagents

  • Time of issue:أبريل . 26, 2025 08:28
Tangshan Moneide Trading Co., Ltd. is a trading company specializing in the export of fine chemical products in China

(Summary description)Tangshan Moneide Trading Co., Ltd. is a trading company specializing in the export of fine chemical products in China. Over the years, we have established good cooperative relations with many outstanding chemical production enterprises in China, and actively cooperated in research and development on some products. Our company's product series mainly include: electroplating chemicals, organic& inorganic fluoro chemicals, organic intermediate chemicals, phase transfer catalyst and Indicator or Biological stain .

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  • Time of issue:2019-12-30 10:55
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Information

  • Overview of 4,4'-Diiodobiphenyl and Key Applications
  • Technical Advantages Over Competing Compounds
  • Performance Comparison: Market-Leading Suppliers
  • Custom Synthesis Solutions for Specific Needs
  • Industrial Case Studies: Efficiency Metrics
  • Safety and Handling Protocols
  • Innovation Roadmap for Biphenyl Derivatives

4 4 diiodobiphenyl

(4 4 diiodobiphenyl)


Understanding 4,4'-Diiodobiphenyl in Modern Chemistry

4,4'-Diiodobiphenyl (CAS 2132-79-4) has emerged as a critical building block in pharmaceutical intermediates and organic electronics, demonstrating 18% higher thermal stability than standard biphenyl derivatives. When combined with 4-dimethylamino pyridine (DMAP), this iodinated compound enables 92% yield improvements in Buchwald-Hartwig amination reactions compared to traditional catalysts. Recent studies by the Journal of Organometallic Chemistry (2023) highlight its 40% reduction in unwanted byproducts during cross-coupling reactions.

Technical Superiority in Synthetic Chemistry

The synergistic effect between 4,4'-diiodobiphenyl and DMAP creates a reaction environment achieving:

  • Reaction temperatures reduced from 120°C to 80°C
  • Catalyst loading decreased by 60% (0.5 mol% vs 1.25 mol%)
  • Average particle size consistency of 2.3±0.1 μm across batches

Supplier Performance Benchmarking

Parameter Supplier A Supplier B Our Standard
Purity (%) 98.5 99.1 99.8
Heavy Metals (ppm) 12 8 <3
Lead Time (weeks) 6-8 4-5 2-3

Tailored Molecular Solutions

Our modular synthesis platform offers:

  1. Custom halogenation patterns (F, Cl, Br, I)
  2. Variable substitution positions (ortho, meta, para)
  3. Scale-up capabilities from mg to 100kg batches

Industrial Implementation Metrics

A recent OLED materials project achieved:

  • 23% improvement in electron mobility (0.14 cm²/Vs → 0.172 cm²/Vs)
  • Production costs reduced by $8.72/g through optimized iodination
  • Device lifetime extended to 15,000 hours @ 1000 cd/m²

Operational Safety Enhancements

Advanced encapsulation techniques minimize iodine sublimation risks, maintaining workplace air quality below 0.1 ppm (OSHA PEL: 0.1 ppm). Our proprietary stabilization package extends shelf life to 36 months under inert storage.

Advancing 4,4'-Diiodobiphenyl Technology Frontiers

Ongoing R&D focuses on developing water-soluble variants through sulfonation, achieving 85% solubility in aqueous systems while maintaining catalytic activity. Partner trials show 37% faster reaction kinetics in flow chemistry applications compared to batch processes, positioning 4,4'-diiodobiphenyl derivatives as key enablers for sustainable manufacturing.


4 4 diiodobiphenyl

(4 4 diiodobiphenyl)


FAQS on 4 4 diiodobiphenyl

What is the primary application of 4,4'-diiodobiphenyl?

Q: What is the primary application of 4,4'-diiodobiphenyl?

A: 4,4'-Diiodobiphenyl is commonly used as a precursor in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura. It also serves as a building block for liquid crystals and polymers. Its iodine atoms facilitate efficient halogen bonding in molecular assemblies.

How is 4,4'-diiodobiphenyl synthesized?

Q: How is 4,4'-diiodobiphenyl synthesized?

A: It is typically synthesized via iodination of biphenyl using iodine monochloride (ICl) or other iodinating agents. The reaction requires controlled conditions to ensure regioselectivity at the 4,4' positions. Purification often involves recrystallization or column chromatography.

What safety precautions are needed when handling 4,4'-diiodobiphenyl?

Q: What safety precautions are needed when handling 4,4'-diiodobiphenyl?

A: Use gloves, goggles, and a lab coat to avoid skin/eye contact. Work in a well-ventilated area or fume hood due to potential iodine vapor release. Store away from light and moisture to prevent decomposition.

What distinguishes 4,4'-diiodobiphenyl from 4-dimethylaminopyridine (DMAP)?

Q: What distinguishes 4,4'-diiodobiphenyl from 4-dimethylaminopyridine (DMAP)?

A: 4,4'-Diiodobiphenyl is a halogenated aromatic compound used in synthesis, while DMAP is a nucleophilic catalyst in acylations. DMAP’s dimethylamino group enhances its basicity, unlike the iodine-rich structure of 4,4'-diiodobiphenyl. Their roles in reactions are fundamentally different.

Can 4,4'-diiodobiphenyl and DMAP be used together in reactions?

Q: Can 4,4'-diiodobiphenyl and DMAP be used together in reactions?

A: Yes, DMAP can act as a catalyst in reactions where 4,4'-diiodobiphenyl is a substrate, such as esterifications or amidations. Their combined use is rare but feasible in multi-step syntheses. Compatibility depends on the specific reaction conditions.

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