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4-Bromo-1-Isopropyl-1H-Pyrazole

    • Product Name 4-Bromo-1-Isopropyl-1H-Pyrazole
    • Alias 4-Bromo-3-(propan-2-yl)-1H-pyrazole
    • Einecs 629-518-0
    • 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
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    Specifications

    HS Code

    938643

    Productname 4-Bromo-1-Isopropyl-1H-Pyrazole
    Casnumber 120739-96-8
    Molecularformula C6H9BrN2
    Molecularweight 189.05 g/mol
    Appearance White to off-white solid
    Meltingpoint 57-61°C
    Purity Typically ≥97%
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Smiles CC(C)n1cc(cn1)Br
    Inchikey XPXLJMRIPMBLHT-UHFFFAOYSA-N
    Synonyms 1-Isopropyl-4-bromo-1H-pyrazole
    Storageconditions Store in a cool, dry place; keep container tightly closed

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

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    Application of 4-Bromo-1-Isopropyl-1H-Pyrazole

    Applications of 4-Bromo-1-Isopropyl-1H-Pyrazole in Industrial Manufacturing

    Our facility manufactures 4-Bromo-1-Isopropyl-1H-Pyrazole to meet the requirements of pharmaceutical and agrochemical intermediates production. Below, we highlight several applied downstream scenarios where this material demonstrates value based on regulatory, technical, and process-based industry realities.

    1. Pharmaceutical Intermediate for Pyrazole Derivative Drug Synthesis

    Pharmaceutical manufacturers incorporate 4-Bromo-1-Isopropyl-1H-Pyrazole during multi-step synthesis of active pharmaceutical ingredients (APIs) relating to pyrazole core drug molecules. This compound acts as a critical building block enabling selective bromination and functionalization during heterocycle assembly, supplying backbone structure for selective serotonin receptor modulators, kinase inhibitors, and anti-inflammatory therapies.

    Industry compliance standards

    • EU Good Manufacturing Practice (GMP) Part II for active substance production
    • ICH Q7 guidelines for API intermediates
    • Chinese Pharmacopoeia (2020 Edition, for raw material synthesis)
    • U.S. FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.3 molar equivalents per API target batch; adjusted according to desired yield and reaction pathway selectivity

    Downstream process integration

    • Introduced during stagewise condensation and ring transformation reactions after initial pyrazole cyclization, typically in the derivatization or halogenation step prior to final API refinement

    Final product types

    • Novel anti-inflammatory drugs based on pyrazole scaffold
    • Central nervous system (CNS) agents such as selective serotonin receptor ligands
    • Pyridazinone and indazole-based kinase inhibitor precursors

    2. Agrochemical Intermediate for Pyrazole-based Pesticide Synthesis

    Major agrochemical producers utilize 4-Bromo-1-Isopropyl-1H-Pyrazole in the multi-step creation of innovative pyrazole pesticides, including fungicides and herbicides. The compound's isopropyl and bromo-substituted pyrazole scaffold allows downstream synthetic chemists to access new ring substitutions, aiding resistance management against plant pathogens and weeds.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP) for agrochemical intermediate synthesis
    • ISO 9001:2015 certified production systems for crop protection chemicals
    • REACH Regulation (EC) No 1907/2006 Registration for European markets

    Typical usage ratio

    • 0.6–1.1 molar equivalents per target pesticide batch based on bromination stage yield; increased for pilot reactions requiring higher conversion rates

    Downstream process integration

    • Added after initial pyrazole core synthesis during bromination and alkylation steps to give functionalized intermediates for downstream coupling, oxime formation, or esterification

    Final product types

    • Pyrazole-based broad-spectrum fungicides
    • Selective herbicides containing substituted pyrazole motifs
    • Seed treatment active materials for improved crop vigor

    3. Intermediate in Custom Synthesis of Specialty Fine Chemicals

    Chemical processors producing specialty fine chemicals for electronics, analytical, and specialty polymer segments employ this material as a pyrazole-brominated intermediate. Its precise positioning facilitates the synthesis of tailored ligands, diagnostic reagents, and advanced monomers, supporting proprietary molecular designs and controlled reactivity in targeted applications.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • Responsible Care® Management System
    • National Institute of Metrology (China) standards for analytical grade precursors

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target compound batch; process chemists select precise ratios based on intended downstream modifications

    Downstream process integration

    • Used as a primary functionalizing intermediate after pyrazole ring construction; commonly incorporated in Grignard coupling, Suzuki cross-coupling, or nucleophilic substitution to prepare downstream functional groups

    Final product types

    • Bifunctional ligands for transition metal complexation
    • Analytical detection reagents containing pyrazole moieties
    • Reactive monomers for advanced polymer materials

    4. Intermediate for Veterinary Drug Synthesis

    Producers of veterinary actives leverage the unique substitution pattern of this intermediate to develop molecules with targeted pharmacokinetic properties for animal health. Its use allows synthesis of pyrazole-based anti-parasitic agents and growth promotors with optimized structure-activity relationships through precise halogenation steps validated by regulatory frameworks for animal-use drugs.

    Industry compliance standards

    • Veterinary International Cooperation on Harmonisation (VICH) Guidelines
    • EU GMP for veterinary medicinal product active substances
    • US FDA 21 CFR 514 New Animal Drug Application (NADA) standards

    Typical usage ratio

    • 0.8–1.0 molar equivalents per batch, with adjustments in early-phase synthesis or for impurities management in animal-use APIs

    Downstream process integration

    • Incorporated in the heterocycle decoration step after initial condensation, facilitating late-stage bromination prior to final purification and API formulation

    Final product types

    • Pyrazole-based anti-parasitic drugs
    • Feed additive actives for animal growth support
    • Veterinary injectable and oral formulations

    5. Intermediate for Synthesis of Research Chemical Libraries

    Specialty laboratories and CROs use this compound during parallel synthesis campaigns to build diverse pyrazole-derived scaffolds for screening and structure–activity relationship exploration. Its bromopyrazole structure streamlines pathway modification, essential for SAR libraries in medicinal chemistry and agrochemical discovery research under validated analytical and purification protocols.

    Industry compliance standards

    • ISO/IEC 17025:2017 accreditation for analytical laboratories
    • OECD Principles of Good Laboratory Practice (GLP)
    • GMP-like documentation for advanced intermediates where required by project sponsors

    Typical usage ratio

    • 0.7–1.3 molar equivalents per reaction, modulated by target diversity and yield targets for multi-parallel synthesis

    Downstream process integration

    • Serves as a halogenated pyrazole source in combinatorial chemistry, coupled in initial diversification rounds including Suzuki, Buchwald–Hartwig, or Sonogashira coupling

    Final product types

    • Pyrazole-based chemical libraries for pharmaceutical and agrochemical lead identification
    • Tool compounds for functional genomics studies
    • Reference standards for regulatory and patent filings
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    More Introduction

    4-Bromo-1-Isopropyl-1H-Pyrazole: Unpacking Its Role in Modern Chemistry

    Reimagining Synthesis: Not Just Another Pyrazole

    Researchers and developers keep reaching for new tools to push chemistry forward, especially those tackling life’s big problems—from cleaner energy to new medicines. 4-Bromo-1-Isopropyl-1H-Pyrazole stands out for people looking to innovate on that front. With the model title built right into its name, this compound offers a fresh take on what a halogenated pyrazole can deliver, especially for those exploring cross-coupling, heterocycle modifications, or next-generation pharmaceutical candidates.

    Material Matters: Purity, Structure, and Key Specs

    Quality shapes outcomes right from the start. This compound, built on the pyrazole ring, features a bromine at the fourth position and an isopropyl group at the first. You don’t have to dig deep to appreciate what this does for reactivity—this structure helps organic chemists go after Suzuki or Buchwald-Hartwig coupling reactions without running into extra purification headaches or unwanted byproducts. High-purity batches running above 98% keep side reactions to a minimum. From a practical lab point of view, having fewer impure compounds means less rework and more reliable downstream yields.

    Why the Substitution Pattern Changes the Game

    Chemists rarely just swap out substituents for fun; the addition of bromine on this scaffold brings unique properties. On one hand, bromine allows for targeted substitution—a favorite move in drug discovery teams chasing bioactive molecules. On the other hand, the isopropyl at the nitrogen gives the molecule enough bulk to tune solubility and reactivity. Pairing both, chemists find more handles for further derivatization. It doesn’t sound revolutionary until you notice how often bottlenecks in synthetic projects boil down to the lack of easy, modular starting points.

    From the Bench: Why This Matters in Day-to-Day Research

    I’ve watched teams spend weeks troubleshooting reactions that struggle with poorly designed starting materials. Choose something with the wrong substitution, and you’re fighting solubility and selectivity from start to finish. This compound, simple as it might look, saves time for those building custom pyrazole cores for agrochemical or medicinal leads. Synthetic teams rely on intermediates like this one, which behave predictably and open the door to safe, scalable reactions—especially when stakes run high, such as developing crops resistant to disease or targeting tough-to-treat infections. It’s easy to underestimate how much one relatively obscure molecule can steer a whole research direction, but those in the lab know every shortcut helps.

    Where It Stands Out: The Comparative Picture

    Stack up 4-Bromo-1-Isopropyl-1H-Pyrazole against the standard entries in the pyrazole lineup, and the differences show up quickly. Compare it with its non-brominated cousin: you’ll see far fewer options for direct functionalization, making downstream synthesis more labor-intensive. Switching the isopropyl for a methyl or ethyl, users often see less structural selectivity, which can be a dealbreaker in pharmaceutical pipelines that demand precise effects. While other derivatives offer intriguing profiles, this compound’s balance—bulky enough for effect, reactive enough for modification, clean enough for reproducibility—keeps showing up in studies published across chemical and pharmaceutical journals.

    Everyday Utility in Research and Innovation

    Out in the world, industries often focus on the headline-grabbing big molecules, but progress leans on intermediate building blocks. The ease with which this compound enters cross-coupling reactions lets synthetic chemists experiment, knowing their centerpiece won’t get in the way. Anyone who’s spent long hours scaling up knows the pain of intermediary steps that just won’t cooperate; a compound like this, that reliably takes part in established palladium- and copper-catalyzed reactions, means less troubleshooting, fewer surprises, and a swifter path from concept to workable prototype.

    Why Structure Drives Value: Insights from Practice

    Take the structure into the field—literally. Researchers working on crop protection agents or antifungals see the direct impact of slight changes in pyrazole derivatives. Adding a bromine and isopropyl doesn’t just tweak the reaction outcomes, it can strongly alter the biological activity. As someone who’s worked shoulder-to-shoulder with applied chemistry teams, I’ve watched them grab for this type of intermediate when a new lead gets flagged in screening, precisely because small structural shifts often spell the difference between a dud and a breakthrough. The right molecular tweaks keep today’s R&D machines humming, especially in areas where the cost of stalling is high.

    Stability, Storage, and Handling: Lab Realities

    Chemical stability factors into every research plan. This compound holds up well under typical lab conditions, with shelf stability that reduces the risk of last-minute setbacks. Colleagues have shared stories where similar pyrazoles broke down before reactions could even start—costing time, materials, and morale. There’s no substitute for a compound that resists moisture or air degradation, especially in busy academic or industrial workflows. Less spoilage and more predictable performance go a long way toward making sure breakthroughs aren’t lost to sheer logistics.

    Delivering Value in Pharmaceutical Development

    Every few months, another paper emerges reporting the use of pyrazole derivatives as key components in kinase inhibitors or as ligands in transition-metal complexes. The value of 4-Bromo-1-Isopropyl-1H-Pyrazole comes out strongest in these contexts—offering a starting point for adding new moieties, guiding SAR studies, or optimizing pharmacokinetic properties. Medicinal chemists keep cycling through libraries of derivatives to boost selectivity or reduce toxicity, and they reach for intermediates that prove consistent not just in theory but in practice.

    Known Limitations and Everyday Trade-offs

    No compound solves every problem. For projects that require absolute minimal steric bulk, other pyrazole derivatives can fit better. Some catalytic processes also show more sensitivity to the bromine placement, occasionally making alternatives more attractive. Those balancing reactivity and downstream handling learn to weigh each intermediate against the needs of the final application. Only experience with full synthetic routes clarifies when this structure’s trade-offs work in your favor, and that’s knowledge teams only build over time and with repeated use.

    Towards Sustainable Practice

    Modern labs face mounting pressure to cut waste and choose greener processes. Compounds that slot into shorter, cleaner syntheses lower the overall impact of research. 4-Bromo-1-Isopropyl-1H-Pyrazole features in several published protocols that highlight both high yields and mild conditions—a draw for those aiming to use less hazardous solvents or bring energy costs down. In my own experience, steps that skip unnecessary purification or hazards get rapid buy-in from both safety officers and finance directors alike.

    Beyond the Lab: Translational Potential

    Industry moves fast when a new intermediate shows promise—not just for immediate applications, but for what it enables further down the line. Pyrazole derivatives have found a home in everything from paints to specialty polymers, and those innovations hinge on building blocks that are reliable, easy to ship, and amenable to both small- and large-scale preparation. The business end of research doesn’t want surprises; they want quality, consistency, and versatility, especially with supply chains under strain. I’ve sat in meetings where small but well-chosen changes to sourcing intermediates like this one ended up being the tipping point for project timelines and budgets.

    Demystifying the Details: Addressing Misconceptions

    Some newer chemists dismiss halogenated compounds as mere stepping stones, forgetting they anchor some of the field’s most important innovations. Adding a 4-bromo substitution isn’t just a way station—it’s a strategic move to open up a pathway for systematic modification. Every synthetic lab has stories of late-stage discoveries rooted not in headline molecules, but in plain, robust intermediates selected with an eye to what comes next. 4-Bromo-1-Isopropyl-1H-Pyrazole keeps making the cut for teams who want options on hand rather than simply shuttling through whatever’s on the shelf.

    What the Future Holds

    Already, chemical research is trending towards automation and high-throughput screening. Having a library of well-characterized, unique building blocks is no longer a luxury—it’s a necessity. Even outside the pharma space, materials science and electronics have shown new roles for pyrazole derivatives, using smart functionalization and late-stage modification. Those who invest in reliable intermediates now will be positioned to adapt to shifting research needs, whether that’s stretchier electronics, more targeted therapies, or safer, more effective crop protection.

    What Actually Sets It Apart: Hands-On Perspectives

    The days of hunting for exotic compounds just to force a synthetic route are over. Labs are choosing intermediates like 4-Bromo-1-Isopropyl-1H-Pyrazole for their ease-of-use and scalable performance. Reliability earns trust, and seasoned researchers keep returning to what delivers. In conversations over the years, peers have praised such compounds not just for their chemistry, but for reducing the guesswork that plagues exploratory research. Risk goes down, throughput goes up, and team morale follows.

    Potential Solutions for Improving Usability and Reach

    There’s always room for improvement. Transparent supply chains and up-to-date testing help end-users pick the right batch for their project, cutting down on mismatched expectations. Producers can help by investing in robust production protocols—all the way from raw material sourcing to final product verification. At the same time, sharing real-world performance data, rather than relying on legacy standards, keeps labs from running into unexpected snags.

    A second approach involves ongoing communication between makers and users. Many issues stem from misaligned specifications or a lack of clarity about application details. Regular feedback loops not only spot and solve production hiccups, they also drive the kind of iterative improvement that keeps industrial partners loyal.

    Supporting Collaborative Progress in Chemistry

    By prioritizing clear labeling, accessible documentation, and routinely tested batches, suppliers give buyers better control over their own synthesis work. Streamlined returns or replacement policies ease worries about outlier performance. Everyone from research assistants to principal investigators appreciates fewer headaches when benchwork goes awry—especially at scale.

    Looking for the Next Breakthrough

    No one molecule makes the world go round, but pick the right building blocks, and the path to new discoveries gets easier. In a field marked by tough challenges and fierce competition, 4-Bromo-1-Isopropyl-1H-Pyrazole delivers practical value by making sure each stage of research runs smoother. Its popularity among chemists isn’t just about one property or another; it’s about the cumulative effect of reliable, clean, and adaptable chemistry. The next wave of innovation may not lean solely on this compound, but those prepared to work with well-chosen intermediates will always have options others can’t match.