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4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid

    • Product Name 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid
    • Alias 4-Bromo-3,5-dimethylpyrazole-5-carboxylic acid
    • Einecs 696-195-8
    • 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

    498608

    Productname 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid
    Casnumber 1040725-94-7
    Molecularformula C6H7BrN2O2
    Molecularweight 219.04
    Appearance White to off-white powder
    Purity Typically ≥98%
    Meltingpoint Approx. 215-220°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Boilingpoint Decomposes before boiling
    Synonyms 4-Bromo-1,3-dimethylpyrazole-5-carboxylic acid
    Storagecondition Store at 2-8°C, protected from light and moisture

    As an accredited 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid is packaged in a sealed amber glass bottle with labeling.
    Shipping 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is typically transported at ambient temperature with standard chemical handling precautions. Appropriate labeling and documentation, conforming to local and international regulations, are required. Avoid exposure to direct sunlight and incompatible substances during shipment.
    Storage **4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Store away from incompatible substances such as strong oxidizing agents. Label the container clearly, and avoid exposure to heat or direct sunlight. Ensure access is restricted to trained personnel using appropriate safety precautions.
    Application of 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid

    Applications of 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid in Industrial Manufacturing

    4-Bromo-1,3-dimethyl-1H-pyrazole-5-carboxylic acid serves as a critical building block in multiple advanced chemical synthesis routes. As a direct manufacturer, we support a variety of industries with consistent quality and traceable supply for large-scale production requirements. The following applications detail precise industry utilization and integration specifics.

    1. Agrochemical Intermediate for Fungicide Synthesis

    Leading agrochemical producers use our material as a core intermediate in triazole-based fungicide active ingredient synthesis, where controlled halogen incorporation is essential for target-specific molecular scaffolds. Its stable brominated pyrazole backbone allows selective reactivity under closed reactor conditions with anhydrous solvent systems. Downstream partners in crop protection achieve yield quality by maintaining defined impurity profiles and scalability across tonnage.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Residues Code
    • Global GAP input approval protocols
    • EU REACH Registration and agricultural intermediates safety dossier
    • ISO 9001:2015 production traceability for large-scale synthesis

    Typical usage ratio

    • Employed at 0.15–0.35 molar equivalents based on batch scale, adjusted according to desired fungicidal entity and crop-residue limits

    Downstream process integration

    • Introduced after initial amide condensation, often before final triazole ring closure and subsequent purification by crystallization

    Final product types

    • Penthiopyrad synthetics
    • Brominated triazole fungicides for cereals and oilseeds
    • Custom crop protection actives for Asian and EU markets
    • Seed treatment formulation ingredients

    2. Pharmaceutical Intermediate in Antitumor Drug APIs

    API facilities employ this compound as a brominated heterocycle scaffold in preclinical and clinical route selection for anticancer drug leads featuring modified pyrazole frameworks. GMP manufacturers value strict batch reproducibility to support process validation and regulatory submissions, with each batch accompanied by structural confirmation and full impurity control in the downstream ring-system elaboration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (FDA cGMP)
    • European Pharmacopoeia (Ph. Eur.) reference testing
    • DMF requirements for advanced intermediates

    Typical usage ratio

    • Ranges from 0.05 to 0.20 molar equivalents per API synthesis, depending on scale and target impurity specifications

    Downstream process integration

    • Added post-initial core coupling as a precursor before late-stage halogen exchange and amide functionalization

    Final product types

    • Small-molecule kinase inhibitor APIs
    • Experimental oncology research compounds
    • Highly regulated GMP pharmaceutical intermediates
    • Custom reference standards for preclinical studies

    3. Specialty Chemical for Electronics Material Synthesis

    In advanced materials manufacturing, this brominated pyrazole carboxylic acid is utilized for synthesizing custom organic semiconductors and functional dyes tailored to high-durability electronic components. Its precise monomer purity and controlled bromine content allow for reproducible polymerization and downstream integration in optoelectronic and sensor device systems.

    Industry compliance standards

    • RoHS Directive compliance for restricted substances
    • UL94 V0 material flame retardance certification
    • IEC 61249 for halogen-free electronics testing
    • ISO 14001 for environmental management in electronics production

    Typical usage ratio

    • Dosage between 0.2–2.0 wt% in pre-polymer feed, fine-tuned per dye/semiconductor load and end-product electrical tolerance requirements

    Downstream process integration

    • Charged during oligomeric stage blending before the final co-polymerization and spin-coating for thin-film manufacture

    Final product types

    • Organic photoconductor layers in laser printers
    • High-stability sensor housings
    • Flexible printed electronic circuit substrates
    • Optical thin film coatings

    4. Fine Chemical Intermediate in Azo Dye Manufacture

    Dye producers employ our brominated pyrazole derivative in the controlled synthesis of high-performance azo dyes, enabling intense color saturation and halogen stability for demanding fibers and plastics. Its molecular structure enhances electron affinity during diazotization, supporting robust pigment formation consistent with textile and plastics regulatory requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 textile chemical safety
    • REACH Annex XVII for dye chemicals
    • EN 71-3 (Toy Safety) for pigment residues in coloring agents
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • Used at 0.5–2.5% by weight of target pigment, adjusted to color fastness and compatibility with end substrate

    Downstream process integration

    • Integrated during diazonium salt coupling, typically before final pigment isolation and washing

    Final product types

    • Synthetic fiber-compatible azo pigments
    • Masterbatch colorants for plastics
    • Textile fiber dye formulations
    • High-saturation print ink additives

    5. Building Block in Custom Catalyst Development

    Homogeneous catalyst manufacturers utilize this carboxylated pyrazole as a ligand precursor for assembling bespoke palladium and platinum complex catalysts for specialty hydrogenation and coupling reactions. The structure directs selectivity and stability for high-value fine chemical transformations. Clients require traceable supply and analytical batch validation to support reproducibility in engineered catalyst systems.

    Industry compliance standards

    • ISO 9001:2015 certified catalyst production QC
    • Responsible Care Initiative for chemical handling
    • Relevant regional chemical registration (e.g., US TSCA, EU REACH)
    • GHS Safety Data Sheet alignment for catalyst ingredients

    Typical usage ratio

    • Typically 1:1 molar ratio as core chelating ligand in complex, with adjustments per customer catalyst design and targeted turnover frequency

    Downstream process integration

    • Employed in metal salt pre-complexation step, before neutralization and supported catalyst immobilization

    Final product types

    • Custom palladium catalysts for Suzuki-Miyaura reactions
    • High-purity platinum hydrogenation catalysts
    • Ligand libraries for R&D screening projects
    • Industrial fine chemical process catalysts
    Free Quote

    Competitive 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid: Manufacturer’s Insight

    Understanding the Molecule at the Factory Floor

    Standing on the production floor, handling 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid is a daily part of our routine. Over years of practice, it becomes clear—the real value in this molecule comes from the steady demand from research labs, pharmaceutical innovators, and specialty chemical developers. There’s nothing abstract about the way it’s produced or shipped; our team manages each batch as an exacting process rather than an assembly of interchangeable goods. The structure of this compound comes from a calculated sequence of reactions, starting with the selection of quality raw materials, progressing through strict temperature controls, and ending in precise purification that meets the industry’s rising standards.

    Model and Specifications Born from Experience

    For us, 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid represents more than a name or formula. The work starts long before the synthesis. Raw material choice changes the outcome, and that’s been proven in hundreds of internal tests. Each time we run a batch, our goal reaches beyond meeting a specification; it’s about achieving reproducibility at scale. Our model reflects a crystalline, white to off-white powder, usually with a purity above 98% by HPLC after final drying and filtration. Moisture control is central, so our analysts check Karl Fischer moisture levels batch by batch. Melting range, color, solubility in organic solvents, and trace heavy metals—each quality test gets logged and tracked across every production lot.

    Large volumes, especially multi-kilo productions, sometimes reveal details missed in gram-scale methods. Sometimes an unexpected impurity pops up, forcing tweaks in recrystallization or solvent removal. Over time, our improvements have meant lower impurity levels, consistent melting points, and easier downstream reactions for our customers. We stick with certain brands of filtration media or crystallization solvents because our records show reduced batch failure rates when we use these. This level of process attention keeps us honest—if a quality parameter flags as out of line, it gets traced quickly to a root cause.

    Practical Uses: Insights from the Source

    Usage trends tell much of the story. The number-one application for 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid is definitely as an intermediate in agricultural chemicals and pharmaceutical research. No marketing spin—customers come to us with concrete synthesis plans, often centered around halogen-substituted pyrazole rings or specific carboxylic acid functionalities. Quite a few custom synthesis orders focus on further modification through amide or ester formation at the carboxyl group, or coupling reactions that swap out the bromo group. We see steady demand from medicinal chemistry projects testing new kinase inhibitors, anti-inflammatory leads, or enzyme-targeted ligands.

    This compound allows for effective entry into heterocyclic compound development due to its robust core and orthogonal functional groups. Direct bromine coupling and dimethyl substitution make for efficient synthetic handles—customers get flexibility to attach various groups without elaborate protecting group schemes. The carboxylic acid is a trusty anchor for peptide or bioconjugation work, which our partners say helps streamline early-phase biological screening. We frequently support teams working on patent-protected scaffolds who require this specific substitution pattern and purity level to meet stringent test protocols.

    Unlike standard pyrazole-5-carboxylic acid, the dual methyl substitution changes solubility and makes the core more lipophilic. This property often shows up in the solubility tests we run; it dissolves more readily in polar aprotic solvents, offering advantages for parallel synthesis campaigns and high-throughput screening. Many researchers prefer the bromo version over the iodo or chloro analogs due to smoother cross-coupling performance, which becomes evident in hands-on Suzuki or Buchwald-Hartwig reactions. Synthetic yields climb noticeably when trace impurities, especially unreacted starting materials or residual catalysts, remain at a minimum—our QC data consistently show this on certificate of analysis reports we share.

    Manufacturing Challenges: Real-World Lessons

    Producing this molecule at factory scale isn’t a matter of transferring a literature procedure and hoping for the best. We’ve learned hard lessons around moisture sensitivity during the bromo addition—the intermediate stages can hydrolyze if ambient humidity spikes, so we control air flow and dehumidification religiously. That means regular investment in climate controls in storerooms and process areas. Reaction exotherms require accurate dosing rates and jacketed reactors, otherwise, by-product formation shoots up and batch clean-up drags. Each step, from bromination to carboxylation and on to methylation, runs on carefully controlled timelines; a few hours’ deviation, and you spot impurity profiles drifting from the norm.

    Filtration presents its own challenge. Because the product can form fine, sticky crystals, standard filter media can clog, risking product loss or extended drying. We monitor particle size through sieving and laser scatter measurements, tweaking agitation speed to shape ideal crystal morphology. Packing the material for shipment involves moisture barrier liners and nitrogen purging, especially for clients working in high-purity synthetic applications. Over years, this attention to the link between small habits—operator training, equipment cleaning, regular calibration—pays off through minimal batch rejection and consistent client praise.

    Differences from Other Pyrazole Derivatives: Direct Comparison from the Manufacturer’s Bench

    Having produced dozens of pyrazole derivatives, the unique features of 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid stand out on the lab table and in the plant. The methyl groups at the 1 and 3 positions stabilize the molecule against hydrolysis in aqueous work-ups, a regular issue with non-methylated versions. The bromo at the 4 is more reactive in cross-coupling chemistry than a chloro or methyl substituent, but does not release the same level of environmental halide burden as iodinated compounds, which appeals to sustainability programs.

    Compared to 1,3-dimethyl pyrazole or the parent pyrazole-5-carboxylic acid, the bromo version delivers greater selectivity during ring-forming reactions that demand high yields, especially in automated or continuous flow reactors. This reduces waste, improves energy efficiency, and opens up error margins for less experienced operators. From a storage and shipping perspective, the bromo derivative resists caking and clumping if humidity is kept under control, unlike some ammonium or sodium pyrazole carboxylates which form hard crusts after a few weeks on the shelf.

    Feedback from our regular clients confirms—during method development or scale-up, 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid presents fewer surprises than other pyrazole rings with more labile functionalities. Its melting point remains stable batch after batch, and analytical signatures line up with reference standards in NMR and HPLC. That consistency only comes from close factory control, aggressive root cause tracking, and open lines with client chemists.

    Supporting Research and Innovation

    We regularly field requests for custom derivatives and tailored syntheses, always rooted in our experience with this core molecule. Academic partners approach us for isotope-labeled versions, while pharmaceutical companies want detailed impurity profiles or DMF-ready documentation to speed regulatory submissions. It’s often these conversations—about a process bottleneck, trace impurity, or scale-up snag—that push us to hone reaction conditions further.

    Supporting innovation means giving clients not just a material, but insights from other users and feedback from dozens of completed projects. Common success stories include medicinal chemists reporting better-than-expected yields for late-stage C–N coupling, or synthetic biologists using the carboxylic acid group as a modular linker for new biomolecule conjugates. By acting as an extension of our clients’ research teams, we help anticipate issues before they appear—suggesting alternative solvents, advising on purification, or troubleshooting reactivity questions. Our own analytical chemists share data from pilot lots to reassure first-time users, providing transparency about lot variation, residual solvents, and stability under storage.

    Technical partnerships matter too. We keep lines open with glassware suppliers, chromatography resin vendors, and process automation engineers to upgrade our plant as new demands come in. If a new analytical method offers faster impurity detection, we test and implement it. This approach keeps our data package up-to-date and our product positioned at the forefront for strict research settings.

    Quality Control and Traceability: The Day-to-Day Reality

    Quality assurance isn’t a line in a brochure; it’s daily routines and long-term memory. For every package of 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid that leaves our warehouse, there’s a paper trail—batch processing notes, chromatograms, moisture readings, and cross-checked QA signatures. Our team documents deviations, tracebacks, and corrective actions. The benefit shows up in lower product recalls, more repeat orders, and trust among demanding clients.

    Routine sampling of in-process material catches process drift early. Sometimes a hotplate reads a few degrees off, or a filter cake dries a bit too fast; years in the business mean we recognize these signs before they cause trouble. Any batch not passing our internal release criteria gets held, reworked, or scrapped—costly, but key for our reputation. Long-term stability studies inform clients how to store the chemical for maximum shelf life, avoiding surprises after long ocean shipments or customs holds.

    Each bottle gets labeled with lot data, purity figures, and a full certificate of analysis. For regulatory-focused clients, we assemble spectral scans and impurity tables on request. Legal compliance matters, too—we’ve adapted processes to comply with changing rules on waste streams, employee safety, and permitted emissions.

    Industry Trends: Changing Demands and New Opportunities

    Demands shift each year. At first, requests came mostly from medicinal chemists exploring new lead candidates. Increased agricultural R&D led to more bulk orders. Lately, environmental and process safety concerns dominate—clients need assurance that manufacturing minimizes hazardous by-products and waste. These pressures drive us to invest in greener solvents, more efficient filtration recovery, and better emission controls. Each adjustment, even if it starts as a small tweak, tends to generate less environmental impact and helps our partners maintain compliance, especially where product pedigree plays into national or regional regulations.

    Price pressures matter, too. This drives continuous improvement in yield and throughput, so we’ve automated feeding systems and digitalized our batch records for cleaner data. Our operators run in-depth training on every process change, minimizing errors and upholding batch-to-batch reliability. Some larger clients even visit our site for audits before long-term contracts, and we’re always ready to demonstrate procedures because the story behind the product matters just as much as its analytical data.

    Challenges and Practical Solutions

    Even the most robust process can face a curveball. Raw material delays or quality shifts force contingency planning. We maintain solid supplier relationships and test every shipment before it hits our tanks. If we spot issues, we act fast to redirect, blend, or, if needed, halt production. Equipment failure—pump leaks, filter gaskets, or heater glitches—demands quick, coordinated maintenance. Our technical teams keep a close eye on wear and tear, and process engineers keep redundant systems on standby for critical operations.

    Training stands as the buffer against most human error. Operators must understand why every step matters—how fast to add reagents, what reaction color or smell indicates trouble, when to call an engineer. Training programs combine classroom instruction with hands-on mentoring, usually by senior staff who've solved hundreds of scale-up puzzles. This helps catch unusual problems quickly.

    Digital process controls help, too. We’ve invested in real-time monitoring—temperature curves, pH readings, agitation speed, and atmospheric conditions—so trends or anomalies pop up faster. Each deviation gets logged, reviewed, and discussed daily. This level of vigilance makes compliance checks smoother, not to mention easier for clients to audit our processes in detail.

    Future Outlook: Evolving Alongside Customers

    As new markets grow, the molecule’s story keeps evolving. Biotech applications, such as targeted molecular linkers for drug conjugates or DNA modifiers, open doors for tailored syntheses. Industry moves toward stricter sustainability targets influence our raw material choices and process improvements. Regulators expect traceability, and research teams need speed—so every part of production, from order intake through delivery, gets measured and improved wherever possible.

    Feedback from clients inspires new projects. One pharmaceutical partner requested an enantiopure variant for asymmetric synthesis; another needed custom packaging for robotic sampling. Meeting these requests isn’t just about retaining business; it’s about advancing the science behind what we do. Modifying a workflow, scaling up a side reaction, or improving purification feeds directly into making 4-Bromo-1,3-Dimethyl-1H-Pyrazole-5-Carboxylic Acid more reliable and accessible for future generations of researchers.

    The real work of a chemical manufacturer is in the details—the hands-on commitment to quality, safety, and innovation. Every day spent at the plant, every batch record signed, every challenge solved, shapes the way our partners create, test, and deliver the next wave of discoveries built on this backbone molecule.