(134984-63-7)
This guide explores every facet of 134984-63-7 procurement, covering:
134984-63-7 represents a high-performance intermediate increasingly vital in pharmaceutical synthesis and specialty chemical manufacturing. Recent market analysis indicates a 12.5% CAGR growth since 2020, with projections showing demand exceeding 850 metric tons annually by 2025. Major applications include:
• API synthesis in oncology treatments (67% of current usage)
• Agricultural chemical formulations (22%)
• Electronic materials production (11%)
Regulatory compliance varies significantly across regions, with FDA-certified batches requiring minimum 99.7% purity according to USP-NF standards. Temperature-controlled logistics remain essential for stability, with degradation rates doubling for every 8°C above recommended storage conditions.
Compared to alternative intermediates like 56341-37-4, 134984-63-7 demonstrates superior reaction kinetics in heterocyclic synthesis. Key technical differentiators include:
• Reaction Efficiency: 28% faster cyclization rates compared to analogues
• Thermal Stability Maintains integrity at 220°C (40°C above industry standard)
• Purity Profile Residual solvent levels <50ppm exceeds EP 10.0 requirements
Advanced manufacturing protocols have achieved yield improvements from 68% to 92% over the past five years through continuous flow chemistry implementations. Leading facilities now achieve batch-to-batch consistency with <±1.2% variance in critical quality attributes.
The global supply network features significant quality variations among 134984-63-7 factories. Procurement specialists should evaluate:
Manufacturer | Annual Capacity (tons) | Purity Level (%) | Price Range (USD/kg) | Certifications | Lead Time (weeks) |
---|---|---|---|---|---|
ChemSource Ltd | 150 | 99.9 | $240-280 | GMP, ISO 9001:2015 | 2-4 |
SynthoTech Inc | 320 | 99.5 | $180-220 | ISO 9001:2015 | 6-8 |
VistaChem Group | 90 | 99.8 | $260-300 | GMP, FDA DMF | 3-5 |
NovaMolecules | 200 | 99.7 | $230-270 | ISO 13485, CEP | 4-6 |
Independent audits reveal significant differences in impurity profiles - ChemSource batches consistently contained <0.02% of critical dimer impurities compared to industry average of 0.12%.
Premier 134984-63-7 suppliers provide comprehensive tailoring options including:
Formulation Adjustments
• Particle size optimization from 50μm to sub-5μm micronization
• Salt formation capability across 8 counterions
• Solvate-free crystalline forms
Packaging Specifications
• Nitrogen-purged stainless steel containers (25-200kg)
• Moisture-controlled polymer liners (<10ppm h₂o)
• Serialized temperature monitoring systems
Leading factories typically implement custom modifications within 45-day development cycles, with scale-up validation batches available at 20kg minimum quantities.
Pharmaceutical Application
A major oncology innovator reduced synthesis steps from seven to three stages by transitioning to high-purity 134984-63-7, decreasing production costs by 38%. Annual API output increased by 22% with 25% reduction in residual solvents.
Agrochemical Implementation
Custom surface-modified 134984-63-7 particles enhanced rainfastness properties in fungicide formulations by 45%, extending field efficacy from 14 to 21 days. The tailored product line generated $28M incremental revenue within 18 months of launch.
Electronics Manufacturing
Ultra-high purity grade (99.999%) enabled production of specialized semiconductor coatings with dielectric properties improving signal integrity by 27% at 5G frequencies.
Based on supplier performance data and market evolution projections, strategic sourcing considerations include:
1. Multi-supplier engagement to mitigate allocation risks during API approval surges
2. Forward contracting for batches exceeding 100kg to secure favorable pricing
3. Implementing quarterly impurity profile audits regardless of supplier track record
Technological advancements like enzyme-catalyzed synthesis could potentially reduce manufacturing costs by 25-30% within the next five years. The evolving landscape of 134984-63-7 factories requires continuous monitoring of process innovations and regulatory compliance developments to maintain competitive advantage.
(134984-63-7)
A: 134984-63-7 is a unique CAS registry number identifying a specific chemical compound. It provides a universal identifier for sourcing, handling, and regulatory compliance. Always verify technical specifications before use.
A: Evaluate suppliers based on ISO certifications, batch-to-batch consistency guarantees, and transparent safety documentation. Reputable suppliers provide independent purity analysis reports and adhere to Good Manufacturing Practices.
A: Yes, most factories offer tailored packaging solutions like nitrogen-purged drums or sealed totes based on volume and stability requirements. Confirm hazardous material shipping compliance with your supplier beforehand.
A: Certified suppliers specialize in global logistics including temperature-controlled transit and customs documentation for hazardous chemicals. Verify their experience with IATA/ADR transport regulations for your region.
A: Rigorous GC/HPLC testing and spectral verification (NMR, MS) must be performed at every production stage. Audited factories maintain Certificate of Analysis traceability for each synthesized batch.
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