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1-Benzyl-4-Iodo-1H-Pyrazole

    • Product Name 1-Benzyl-4-Iodo-1H-Pyrazole
    • Alias MFCD18252238
    • Einecs 822-346-1
    • 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

    534478

    Product Name 1-Benzyl-4-Iodo-1H-Pyrazole
    Cas Number 612841-59-9
    Molecular Formula C10H9IN2
    Molecular Weight 284.10 g/mol
    Appearance Off-white to light yellow solid
    Smiles C1=CC=C(C=C1)CN2C=CN=C2I
    Inchikey IBQPAHABSUNVIG-UHFFFAOYSA-N
    Solubility Soluble in DMSO and methanol
    Purity Typically >98%
    Storage Temperature 2-8°C
    Synonyms 4-Iodo-1-benzylpyrazole
    Mdl Number MFCD11226163

    As an accredited 1-Benzyl-4-Iodo-1H-Pyrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial, labeled "1-Benzyl-4-Iodo-1H-Pyrazole, 5g," tightly sealed with a screw cap, desiccant included, hazard warnings displayed.
    Shipping 1-Benzyl-4-Iodo-1H-Pyrazole is shipped in tightly sealed, chemical-resistant containers to ensure safety and stability during transit. Packaging complies with all relevant hazardous material regulations. The shipment includes proper labeling, documentation, and handling instructions. Temperature and protection from light are maintained as required to preserve compound integrity.
    Storage Store 1-Benzyl-4-Iodo-1H-Pyrazole in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of heat, ignition, and incompatible substances such as strong oxidizers. Ensure proper labeling and use secondary containment if possible. Access should be restricted to trained personnel, and personal protective equipment should be available when handling.
    Application of 1-Benzyl-4-Iodo-1H-Pyrazole

    Applications of 1-Benzyl-4-Iodo-1H-Pyrazole in Industrial Manufacturing

    1-Benzyl-4-Iodo-1H-Pyrazole serves as a specialized intermediate in the development and production of advanced chemical compounds across multiple high-value industrial sectors. As the original manufacturer, we collaborate with downstream formulators and processors to ensure our material meets the rigorous demands of each specific application. Below, we detail specialized use cases with technical integration points, regulatory compliance, and typical formulation guidance for industrial partners.

    1. Pharmaceutical Intermediate for Pyrazole-Based Drug Synthesis

    Pharmaceutical companies employ 1-Benzyl-4-Iodo-1H-Pyrazole as a pivotal intermediate in the synthesis of innovative pyrazole core pharmaceuticals, such as kinase inhibitors and anti-inflammatory drugs. The compound enters targeted Suzuki, Sonogashira, or N-alkylation reactions, providing a functionalized backbone crucial for scaffolding and downstream molecule diversification. Process batch records and analytics focus on managing halogen content and impurity profiles to meet strict pharmacopoeial monograph requirements required for active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP <1092>: Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs relevant to finished APIs
    • 21 CFR Part 211 – US Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Employed at 1.0–1.4 molar equivalents versus starting aryl halide in cross-coupling; precise stoichiometry dictated by target API synthetic route and impurity allowance

    Downstream process integration

    • Charged during early or mid-step fragment coupling under inert atmosphere with palladium or copper catalysts before hydrogenation or derivatization

    Final product types

    • Small molecule kinase inhibitors
    • Anti-inflammatory agents incorporating pyrazole derivatives
    • API precursors for CNS and oncology drug candidates

    2. Agrochemical Intermediate for Heterocyclic Crop Protection Agents

    The crop protection industry integrates this compound in the multi-stage synthesis of selective herbicides and fungicides featuring pyrazole structural motifs. Due to the iodo functional group, it provides a reactive site for further aryl or alkynyl substitution in late-stage active ingredient (AI) building, supporting stringent control over side product formation and residue limits in downstream technical materials.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems in agrochemical production plants
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)
    • EPA 40 CFR Part 158: Data Requirements for Pesticide Registration (US)

    Typical usage ratio

    • Applied at 0.9–1.2 molar equivalents relative to coupling reactants; formula adjusted per technical specification sheets of target AI

    Downstream process integration

    • Fed into closed reactor vessels for halogen exchange and Suzuki couplings prior to functionalization with amine or alkoxy groups

    Final product types

    • Pre-emergent and post-emergent pyrazole-based herbicides
    • Systemic fungicide actives for cereals and vegetables
    • Technical concentrations for micro-encapsulated pesticide formulations

    3. Fine Chemical Intermediate for OLED and Photonic Materials

    Manufacturers of specialty fine chemicals use 1-Benzyl-4-Iodo-1H-Pyrazole in the assembly of donor-acceptor frameworks required for high-performance organic light-emitting diodes (OLEDs) and photoactive compounds. Its iodo-activated pyrazole ring is exploited for selective palladium-catalyzed cross-coupling with arylboronic acids and alkynes. Applications demand rigorous purity and batch consistency to ensure end-use electronic performance and yield in device-scale processes.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance in functional material manufacturing
    • IEC 60068: Environmental Testing for Electronic Components
    • RoHS Directive (Restriction of Hazardous Substances) for electronic materials (EU)
    • Internal optical grade purity specifications defined by downstream device producers

    Typical usage ratio

    • Loaded at 1.05–1.20 molar equivalents based on designer molecule protocol; purity adjusted to photonic-grade (≥99.5%) for minimal electronic noise

    Downstream process integration

    • Introduced as a functionalized precursor in cross-coupling set-ups prior to purification, vacuum deposition, or thin film fabrication

    Final product types

    • Electroluminescent monomers and emitters for OLEDs
    • Pyrazole-containing charge transport materials
    • Photoactive compounds for organic electronics

    4. Chemical Building Block for Advanced Research Chemicals

    In research chemical supply, university labs and corporate R&D units employ this compound as a modular, iodo-activated core for the rapid assembly of novel heterocycles, kinase probe libraries, and tagged molecules for assay development. The reactivity of both the pyrazole and benzyl functionalities enables targeted elaborations in high-throughput organic synthesis and combinatorial chemistry workflows. Batch provenance, traceability, and analytical validation are routinely required to satisfy institutional QA/QC protocols and safety oversight.

    Industry compliance standards

    • ISO 13485:2016 (where used in development of diagnostic chemicals)
    • GHS (Globally Harmonized System) for chemical classification and labeling
    • Relevant university or corporate research safety committees and documentation
    • OECD Principles of Good Laboratory Practice (GLP) for analytical validation

    Typical usage ratio

    • Utilized at variable equivalents (0.5–2.0) depending on synthetic goal; often adjusted for library scale, screening needs, or probe sensitivity

    Downstream process integration

    • Employed directly in solution-phase synthesis (manual or automated), or arrayed for solid phase/fragment-based combinatorial assembly

    Final product types

    • Small molecule chemical probes
    • Reference standards for analytical assay calibration
    • Heterocyclic fragments for medicinal chemistry lead generation
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    Certification & Compliance
    More Introduction

    Introducing 1-Benzyl-4-Iodo-1H-Pyrazole: A Key Intermediate Forged in Our Own Reactors

    A Chemist’s Perspective on 1-Benzyl-4-Iodo-1H-Pyrazole

    Over the years, our plant floor has seen countless molecules cross its reactors, but 1-Benzyl-4-Iodo-1H-Pyrazole has stood out as a steady performer among specialty heterocycles. We dedicate tank space, time, and significant research to this compound, as demand has noticeably grown from labs scaling up research as well as firms expanding into targeted drug discovery. This material’s distinctive iodo substituent and benzyl group on the pyrazole ring provide a rare starting point for synthesizing highly functionalized pyrazole derivatives, helping medicinal chemists and material innovators achieve progress with fewer synthetic steps.

    The physical and chemical realities of this compound make it distinct from generic pyrazoles and standard halogenated heterocycles. In-process, the iodo substitution pattern increases the complexity of purification, especially when compared with brominated or chlorinated analogs. We tune reactions continuously and work closely with our analytical staff during every campaign. Each batch achieves high consistency, and we confirm purity and identity using advanced chromatographic techniques and NMR analysis performed in-house. There is no reliance on outside contract labs for final confirmation: we operate full-suite analytical capabilities within arm’s reach of synthesis.

    Our Process and Quality Insights

    The pathway to 1-Benzyl-4-Iodo-1H-Pyrazole requires careful control of both reagents and conditions, especially since iodo compounds often face stability and handling challenges. We invested in inert handling lines and strictly segregated work-up areas for products containing heavy halogens. Scaling this molecule from kilo to multi-kilo required rethinking purification steps; pack column chromatography doesn’t transition easily to the dozens-of-kilograms scale, so we designed custom crystallization processes that allow for repeatable batch-to-batch consistency.

    Our operators have encountered the full spectrum of batch behaviors—from sticking points during crystallization to temporary discolorations during reaction work-up. These experiential learnings inform our processing SOPs, ensuring that we avoid known pitfalls. There is no shortcut for incremental improvement, and we refuse to compromise on key checks for halide content and cross-contaminants which can make or break downstream synthetic success. Blind trust in generic raw materials does not have a place in our workflow. Since so many of our clients operate in regulated or IP-sensitive arenas, we commit to transparency in traceability from raw input to finished output.

    Specifications and Product Confidence

    We manufacture 1-Benzyl-4-Iodo-1H-Pyrazole as a high-purity crystalline solid, with a well-defined melting point that we validate against every production lot. Rigorous HPLC and GC analysis verify low-level impurity thresholds. As a team immersed directly in chemical synthesis—not trading or drop-shipping—we take pride in the subtleties of solid handling, temperature requirements, and even the particle size that downstream formulation chemists request.

    Each inquiry prompts us to share COA and spectral records, not just because it’s a client expectation, but because it forms the backbone of reliability for those building complex molecules or prototypes. Sourcing from us, customers skip the unpredictability and variable lead-times that can accompany generic procurement. Every sample and batch carries the weight of our operational reputation, and over repeated production runs, we have refined a supply route that works for gram-scale requests from startup labs as well as multi-kilogram orders for advanced applications.

    Differences from Other Compounds

    Whereas standard pyrazoles offer a blank template for functionalization, 1-Benzyl-4-Iodo-1H-Pyrazole delivers a much more reactive chemical handle. Iodine on a heterocycle creates new activation possibilities for coupling reactions—Suzuki, Sonogashira, or Stille—at positions that might otherwise require elaborate synthetic detours. The benzyl group’s specific electronic and steric properties further tune the overall molecule, making it more than just a halogenated heterocycle. This has led to direct feedback from research groups who have reached new chemical space in kinase inhibitor work or agrochemical scaffold development, attributed directly to the accessibility of this compound. Our technical team follows these advancements, exchanging notes with clients on reaction outcomes, sharing insights gained during scale-up, and troubleshooting both in our lab and through direct customer support.

    Compared to brominated or chlorinated pyrazoles, which saturate SMS stock lists but often underdeliver in coupling efficiency, the iodo variant offers greater reactivity under milder conditions. This advantage does come with drawbacks—higher cost of iodine, greater oxidation sensitivity, and sometimes lower shelf stability. These realities push us to invest in best-in-class containment and packaging, so that every shipment keeps its integrity intact. Current orders include advanced vapor-barrier liners and inert gas-purged containers, all based on direct experience with real-world transit and storage challenges.

    Field Experiences and Customer Collaboration

    The partnership between manufacturer and research team always unfolds in iterative steps. Early on, some clients received lots that responded differently under high-purity photochemical screens. Instead of sending away feedback as academic theory, our own technical service chemists re-created the conditions, compared results, and found minute trace side products below threshold—remnants undetectable by outdated test panels. After updating our procedures and investing in more sensitive detection, we turned this experience into a technical win, offering finer specifications tailored to both pharma and crop-science collaborators.

    The value of this collaborative approach rings especially true at the pilot plant scale, where minute changes in column temperature or stirring speed can tip yields by whole percentage points. With each new production run, our process engineers update live records, running risk assessments on every change, and our scheduling accounts for unexpected delays to avoid compromising product quality in the rush to meet deadlines. The result is a high bar in both process stability and shipment reliability. If we spot emerging trends in user demand—such as requests for form-specific pyrazoles, or feedback about handling—we feed this back into next-batch planning, adjusting grinding, sieving, or packaging as required.

    Direct Impact and Real-World Benefits

    The scientific impact of 1-Benzyl-4-Iodo-1H-Pyrazole now extends beyond early-stage drug and ag-chem screening. Chemical biology groups have sourced material tailored for linker development, using the iodinated position to graft photoreactive groups. Materials science teams solicit this product for crosslinking pathways inaccessible using lighter halogens. Such requests drive us to stay nimble with new application notes and real-case technical guides, drawn from both in-house synthesis runs and trusted client feedback. As the user landscape shifts, we stand ready to respond—sometimes developing process route variations or testing alternate salt forms if standard product no longer fits a new application window.

    Reports continue to show that raw access to reactive iodo-pyrazole intermediates accelerates overall R&D cycle time; the alternative route—building these motifs from scratch—costs chemists extra weeks and more extensive hazardous handling, especially where selective halogenation is unreliable at scale. By investing years into refining safe, scalable iodo chemistry and robust QA, we help project teams focus where value is created: on final product innovation, not basic building block synthesis. And as the pressure grows to make every campaign count, such advantages become more than marginal.

    Long-Term View: Sustainability, Safety, and Future Investment

    Manufacturers bear direct responsibility for upstream safety and sustainability. We evaluated solvent choices, waste stream minimization, and iodine recovery processes as core elements from the earliest days of scale-up. Heavy halide chemistry cannot rely on disposable protocols, and each iodo-containing mother liquor undergoes reclamation and neutralization cycles designed by our own environmental team. Operators receive full hazard training, PPE protocols, and waste logs are reviewed with every campaign for process improvement. Despite the higher up-front cost and effort, this discipline has proven itself repeatedly: process bottlenecks shrink, and we sustain regulatory confidence as markets and compliance demands shift.

    Over the past year, we launched a new process control platform that allows real-time tracking of critical parameters during batch progression. Sensors and automated logging catch deviations fast, reducing the chances of out-of-spec product or wasted material needing costly rework. Senior chemists lead route evaluation projects, looking for ways to cut energy and water usage, particularly in the work-up phase. Batch records, environmental monitoring, and safety audits all come from the people who actually run the plant, not faceless back-end teams. Direct engagement drives higher commitment and greater responsiveness, ensuring each lot of 1-Benzyl-4-Iodo-1H-Pyrazole reaches end users exactly as specified.

    Ongoing Innovation and Response to Market Pressure

    Markets always demand new levels of efficiency; innovation in pyrazole chemistry is no exception. Demand for selectively functionalized heterocycles has doubled in some segments, leading to greater scrutiny on lead times, batch size flexibility, and documentation depth. Unlike warehouse traders or generic listing websites, our response begins at the synthesis bench and lab notebook, evaluating process stoppers and running direct pilot batches to test new concepts. When biotechs need small custom lots, our R&D team steps up to adapt synthetic routes; when a staple client signals a major scale-up, operations leverages previous campaign data to gear up seamlessly.

    As regulatory controls increase, documentation must be as robust as the product itself. We prepare dossiers and full traceability records, ensuring every lot can be traced back to the exact supplier and timestamp for primary reagents. Quality isn’t a single department; it is every person’s job—whether running glassware through QA checks, logging work-up logs, or finalizing shipments. Maintaining this culture gives our partners the confidence that their supply chain holds steady under all circumstances, whether they’re sourcing grams or dozens of kilograms.

    Distinctiveness Born of Real-World Practice

    Direct experience from synthesis and purification has colored everything about how we approach 1-Benzyl-4-Iodo-1H-Pyrazole. From the early trial-and-error days to the now-routinized multistep campaigns, our knowledge deepened every time a flask misbehaved or a chromatography column performed better than prediction. Practical learnings still drive improvements in crystal habit, drying protocols, and long-term shelf life in varying humidity. These are lessons only the group performing primary synthesis can draw, not a third-party or batch aggregator. Every improvement, every troubleshooting cycle and client dialogue loop back into daily operations, deepening our knowledge base.

    Feedback trends suggest future customers look for even greater customizability—whether in salt form, particle size, or solvent inclusion—within their heterocyclic intermediates. Several colleagues are pursuing alternate synthetic approaches, evaluating if non-hazardous oxidants or greener halogenation methods can match the precision of traditional chemistry without trade-offs in purity or price. While bench trials continue, our reassurance to users remains grounded in decades of experience: it is the manufacturer’s own process learning and ongoing commitment to openness that delivers not just a compound, but a solution to real laboratory and process plant challenges.

    Meeting Today’s Demand, Ready for Tomorrow’s Challenge

    Today, 1-Benzyl-4-Iodo-1H-Pyrazole spins out of our reactors for entities ranging from agile biotech startups to established global formulators. We do not see this as a commodity—but as a solution tailored on the back of active research, production experience, and direct conversation between producer and user. We invite practitioners—those at the bench, on the plant floor, or in project management—to challenge us with new requirements, unusual analytic requests, or questions about sourcing. Our story as a manufacturer continues, batch by batch, driven by the trust earned through practical knowledge and technical improvement at each stage of the journey.