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4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde

    • Product Name 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde
    • Alias 4-Chloro-1-methyl-1H-pyrazole-3-carboxaldehyde
    • Einecs EINECS 695-764-7
    • 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

    430640

    Product Name 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde
    Cas Number 941714-57-0
    Molecular Formula C5H5ClN2O
    Molecular Weight 144.56
    Appearance White to off-white solid
    Melting Point N/A
    Boiling Point N/A
    Purity Typically ≥98%
    Solubility Soluble in common organic solvents (e.g. DMSO, methanol)
    Smiles Cn1cc(c(n1)Cl)C=O
    Inchi InChI=1S/C5H5ClN2O/c1-8-2-4(3-9)5(6)7-8/h2-3H,1H3
    Density N/A
    Storage Temperature Store at 2-8°C
    Synonyms 4-Chloro-1-methylpyrazole-3-carboxaldehyde
    Refractive Index N/A

    As an accredited 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle, screw-capped, with a chemical-resistant label stating "4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde, 25g, for laboratory use only."
    Shipping 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde is shipped in tightly sealed containers, protected from moisture, light, and incompatible materials. The package complies with relevant hazardous materials regulations and includes clear labeling. Handling and transport are conducted by trained personnel, ensuring safe delivery at ambient temperature under standard shipping conditions, unless specific requirements are stated.
    Storage Store **4-Chloro-1-methyl-1H-pyrazole-3-carbaldehyde** in a tightly sealed container, in a cool, dry, and well-ventilated area away from light and sources of ignition. Keep separate from strong oxidizing agents and bases. Use appropriate chemical-resistant gloves and eyewear when handling. Ensure all containers are clearly labeled and avoid prolonged exposure to air to prevent degradation.
    Application of 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde

    Applications of 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde in Industrial Manufacturing

    4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde serves as a key intermediate in multiple industrial synthesis routes, supporting high-value sector production through controlled integration in regulated workflow environments.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical producers incorporate this raw material primarily for the generation of heterocyclic scaffolds in modern pesticide and fungicide active ingredients. The aldehyde functionality reacts selectively with various amines and hydrazines by condensation, ensuring precise construction of target molecules. Facility chemists carefully monitor impurity profiles and stepwise yields according to crop protection compound registration guidelines. Typical integration takes place in the core intermediate stage before final formulation with solvents, additives, and adjuvants required for field performance.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • OECD Harmonized Templates for Pesticide Chemistry
    • GB/T 1604-2001 (Agrochemical Intermediate Quality)
    • China Pesticide Registration Requirements (ICAMA/NICMA)

    Typical usage ratio

    • 0.2–1.5 mol per mol of backbone hydrazine or amine, dependent on targeted scaffold and desired selectivity in condensation or cyclization steps. Chemists optimize ratio via pilot batch scaleouts.

    Downstream process integration

    • Integrated in the heterocyclic ring forming step as a limiting reactant. Purification via crystallization or extraction follows to ensure minimal carryover of unreacted aldehyde.

    Final product types

    • Systemic fungicides (e.g., pyrazole-based active molecules)
    • Pesticide intermediates used in further modification steps
    • Seed treatment agents
    • Herbicide precursor materials

    2. Pharmaceutical API Intermediate Manufacturing

    Pharmaceutical process chemists utilize 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde in the selective synthesis of fused pyrazole ring systems, which function as privileged scaffolds in innovative small molecule active pharmaceutical ingredients (APIs), especially in central nervous system and oncology drug research. Production lines require strict trace impurity management and documentation under cGMP to meet regulatory submission standards. Aldehyde handling operators dose the material into Buchwald–Hartwig and Suzuki–Miyaura cross-coupling reactions or as the key aldehyde moiety in multistep buildouts.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • USP-NF Monographs (where specified)
    • 21 CFR Parts 210/211 (FDA cGMP)
    • EDQM TSE Guidelines

    Typical usage ratio

    • Typically 1.0 mol per mol of amine or arylboronic acid partner in coupling reactions. Adjustment possible based on scale and impurity profile, usually set by process validation studies.

    Downstream process integration

    • Fed into the API intermediate synthesis stage, combining with protected amines, anilines, or catalyst systems. Purification steps include chromatographic separation and impurity tracing for DMF filings.

    Final product types

    • CNS-targeted small molecule drug candidates
    • Oncology therapy intermediates
    • Antiviral agent precursors
    • Registration-grade pharmaceutical intermediates

    3. Fine Chemical Synthesis for Specialty Dyestuffs

    Advanced dye and pigment manufacturers employ the aromatic aldehyde for constructing extended conjugated systems in the synthesis of heat-stable, lightfast specialty dyes. Its controlled reactivity allows for the tailored introduction of substituted pyrazole cores, supporting chromophore extension and bathochromic shifts. These processes require consistent batch quality and precision monitoring to meet international textile or plastic coloration specifications. Reactions often include Vilsmeier–Haack or Knoevenagel condensation steps in multi-kilogram production settings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Dyestuff Environmental Certification)
    • EN 71-3:2019 (Toy Safety, Element Migration for Pigments)
    • ISO 105-B02:2014 (Lightfastness of Colored Textiles)
    • REACH Annex XVII (Azo Dyes Restrictions)

    Typical usage ratio

    • Generally 0.3–1.2 equivalents relative to dye-forming nucleophile, based on desired chromophore extension degree and production batch size.

    Downstream process integration

    • Charged directly in condensation reaction kettle prior to further dye coupling, sulfonation, or azo development. Post-synthesis, process includes phase separation and granular pigment conversion.

    Final product types

    • Disperse textile dyes
    • High-temperature plastic colorants
    • Solvent-based inkjet dyes
    • Industrial coating pigments

    4. Advanced Material Research and Electronic Chemical Production

    Material science laboratories and commercial electronics chemical suppliers adopt this building block for synthesizing specialized heterocycles used in organic electronic devices, such as OLEDs and sensors. The chemical structure supports custom functionalizations that enhance charge carrier mobility and molecular orientation in thin film deposition. Quality control teams enforce rigorous specifications on water content, trace residue, and particle size to ensure reproducible device yield during scale-up or prototyping. Integration occurs in the early design of precursor molecules.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Electronic Materials Substances Restriction)
    • IPC-4101 (Base Materials for Printed Boards)
    • ISO 14001:2015 (Environmental Management for Chemical Manufacturing)
    • TSCA Inventory Listing (U.S. Advanced Material Chemical Approval)

    Typical usage ratio

    • 0.1–0.7 mole per mole of co-monomer or linker in oligomer/polymer synthesis, adjusted for preferred band gap properties. Lab to pilot scale-up requires batch-specific optimization.

    Downstream process integration

    • Incorporated at the pre-polymerization stage of functional material synthesis, followed by film-forming, spin coating, or vacuum deposition for device assembly.

    Final product types

    • Organic light emitting diode (OLED) precursor compounds
    • Photonic sensor intermediates
    • Semiconductive additives for thin films
    • Smart coating material bases

    5. Crop Protection Analytical Reagent Manufacturing

    Certified analytical laboratories and industrial standards manufacturers use 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde for producing calibration and reference materials, which are critical for quantifying pesticide residue in agricultural exports. The compound’s distinct chemical signature aids in rapid development of reliable spiking solutions needed for LC-MS/MS and HPLC systems. Quality assurance teams validate every lot for purity, stability, and trace-specific impurities according to international residue analysis protocols, supporting food safety monitoring programs.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratory Standards)
    • Codex Alimentarius Residue Analysis Protocols
    • EU Regulation (EC) No 396/2005 (MRL Compliance for Pesticides)
    • EPA Guidelines for Pesticide Residue Methods

    Typical usage ratio

    • High-purity standards produced at 0.01–1.0 mg/mL in validation solvents for final solution preparation, based on instrument sensitivity requirements and matrix effect studies.

    Downstream process integration

    • Weighing and precise dilution by mass, followed by bottling in inert-atmosphere vials. Integration with certified method batch runs before shipment to laboratories or regulatory agencies.

    Final product types

    • LC-MS/MS pesticide reference standards
    • Quality control spiking solutions for residue monitoring
    • HPLC working standards for multiresidue screening
    • Certified reference material kits
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    Certification & Compliance
    More Introduction

    Introducing Our 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde

    Crafting Novel Building Blocks for Chemical Synthesis

    Every time a batch of 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde leaves our reactors, we are reminded of its versatility as a building block in the world of organic chemistry. Our team has spent years perfecting both the consistency and purity of this compound, so researchers and industry partners can count on a reliable foundation for further synthesis. The aldehyde and pyrazole ring structures work together in ways that open up synthesis routes often closed to simpler compounds.

    Our model for this product centers on a rigorous process control during chlorination and methylation steps, followed by controlled oxidation. Through experience, we’ve learned how minor shifts in temperature or solvent composition impact yield, color, and shelf stability. Walk through our production areas and you’ll see batch records marked with timing details and analytics data—testament to a process born from decades of cumulative knowledge.

    Features Driven by Chemistry and Real-World Demand

    Specifications for 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde are meant to serve practical needs, not just tick boxes on a data sheet. We keep purity at a minimum of 98% by HPLC to prevent side reactions when used in pharmaceutical intermediate synthesis. Moisture control matters for protecting the aldehyde group, so our final drying step uses vacuum ovens with proven temperature profiles that avoid decomposition while fully removing solvents. The product appears as an off-white to pale yellow crystalline solid, and every batch gets NMR and mass spectrometry confirmation before packaging.

    Our own labs run this compound in both gram-scale pilot syntheses and multi-ton industrial projects. One day might see it used for aryl hydrazone formation; the next, as a precursor for agrochemical actives; and then a research group stops by to share NMR spectra for a new triazole ring system formed by cyclization. That back-and-forth helps us understand what matters to end-users: not just that the aldehyde reacts, but that it survives storage, melts repeatably, and resists oxidative color change.

    Packaged in double-layer polyethylene liners and HDPE containers, our 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde arrives ready to fit right into gloveboxes or fume hoods. No dusty flasks, no sticky residues—just free-flowing product that scoops and measures cleanly.

    Usage Reflects Deep Industry Integration

    We’ve supplied this compound to pharmaceutical process groups developing active pharmaceutical ingredients, with it serving as a key intermediate for pyrazole ring construction and aldehyde functionality that enables coupling reactions. Several crop protection projects use it to build selective herbicide scaffolds, where substitution patterns on the pyrazole ring pull electronic effects in the ideal direction. The aldehyde can be elaborated into oximes, hydrazones, or even reduced to corresponding alcohols—the choices reflect what researchers find in their screens, not just what looks elegant on paper.

    Over the years, conversations with synthetic chemists revealed an appetite for small-molecule diversity without excessive protection-deprotection steps. This compound suits that need. Because the methyl group sits on the pyrazole nitrogen, downstream chemistry avoids N-deprotection issues so common in polynuclear heterocyclic synthesis. The chloro substituent enables variant regioselective couplings, a prized advantage in medicinal chemistry where small structure differences yield large changes in biological activity.

    Process engineers appreciate our product’s traceability. Each lot links back to raw material sources, reaction logs, and finished goods analytics. End-users tell us they rarely experience batch-to-batch reactivity shifts, which matters more than any claim about “high purity”—real value flows from reactivity that matches across kilograms and years.

    How Our Variant Stands Apart

    We chose not to chase the lowest-cost route—quality and dependability matter too much for our customers’ applications. Each incoming raw material gets screened for trace impurities, since our experience shows poor-quality starting materials quickly lead to off-spec or decomposed aldehyde. Outgassing protocols after chlorination remove residual volatiles that could otherwise cause storage container pressure build-up. Our operators track these details because they’ve seen what happens if a minor deviation slips through; careful process design prevents downstream headaches.

    Competing products from other countries sometimes skip steps in purification or offer “technical” grade as standard. In contrast, we maintain pharmaceutical intermediate-grade material, running finished product through preparative chromatography if analytics suggest even a hint of unexpected peaks. In bulk, this means higher upfront costs, but time and time again, feedback from clients confirms that downstream purification and lost runs cost much more in aggregate.

    We aim for transparency in reporting heavy metal content and residual solvents. Pyrazole chemistry can concentrate trace elements, and we police these levels to satisfy our own internal guidelines—often more stringent than the market minimums. Shelf-life testing under controlled humidity and moderate light conditions shows our packaging decisions keep color and composition stable well past standard storage windows.

    Feedback from contract research organizations guided us toward multi-kilo pack sizes and barcoded tracking, simplifying inventory audits for sites juggling hundreds of small-batch intermediates. We cannot count the number of colleagues who’ve told us, “We switched because every time we opened yours, it looked and worked just like the last one.”

    Facing Challenges from New Synthetic Needs

    The chemical industry always searches for the next molecule or synthetic pathway. Lately, growing interest in green chemistry and continuous-flow production raises new questions about how robustly a compound like 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde performs under these conditions. We now test it in microreactors, exploring whether exposure to high shear rates or non-traditional solvents changes its behavior. Our analytical teams track stability and conversion in flow just as closely as in batch. Initial results look strong; our solid-state purification tends to exclude microcontaminants that would otherwise foul flow systems.

    There’s also attention on regulatory matters. Given new scrutiny over solvent residues, we switched to azeotropic drying and maintain validated cleaning cycles for reactors and glassware. We regularly submit samples for third-party evaluation, not just for show, but to verify our in-house metrics and meet emerging customer documentation requirements.

    As the world moves toward digital supply chains, traceability and data integrity grew in importance. We now attach encrypted batch analytics summaries and keep digital twins of each batch record so no detail gets lost from order to delivery. Some may consider that overkill, but from our vantage, it supports everyone’s peace of mind about regulatory audits and product recalls.

    Learning from Industry Partnerships

    Nearly every successful project involving our 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde traces back to real-world collaboration. Pharmaceutical firms sometimes need shorter lead times for development batches. We built a flexible production schedule and extra isolation capacity to handle just-in-time orders. Agrochemical developers require detailed impurity profiles for regulatory dossiers; we dedicated extra resources for long-term storage studies and trace contaminants analysis, drawing on worldwide best practices. Our lab teams keep in touch with academic researchers exploring new coupling partners or reaction cascades, and these conversations feed back into our continuous improvement cycles.

    One example comes from a university group who reported inconsistent aldehyde group reactivity during a multi-step synthesis. Working together, we traced an impurity back to a trace siloxane introduced during an older distillation process. Updated filtration and distillation protocols eliminated the issue, and their project progressed without delay. We shared the details with other partners facing similar reactivity hiccups, adding a “lessons learned” note to our internal technical forum.

    We see our role not just as manufacturers, but as contributors to the broader chemical knowledge pool. Many of our team members speak at industry conferences and share anonymized insights about process optimization, impurity control, and regulatory compliance. These efforts help elevate quality standards across our field, not just in our own factory.

    Potential Solutions to Emerging Challenges

    Adapting to regulatory demands finishes high on our priority list. As more countries implement controls over trace contaminants, we routinely scan for nitrosamines, heavy metals, and persistent organic pollutants, setting benchmarks tied to upcoming global standards rather than waiting for enforcement action.

    The laboratory effect on downstream process design cannot be overstated. Early input about reactivity or physical stability lets us tweak isolation or drying steps long before a new variant sees kilogram-scale production. Once, a process partner warned about melamine-forming side reactions during scale-up. Our team assembled a cross-functional working group, ran micro-scale simulations, and adjusted catalytic ratios to block byproduct formation—a fix implemented within a production cycle.

    Environmental teams on our site push for greener processes every year. Solvent recycling programs now reclaim over 70% of used solvents for reprocessing, cutting both cost and ecological footprint. On-site wastewater pre-treatment removes persistent halogenated organics, backing up regulatory compliance with real-world data from independent testing facilities.

    Customers working at the frontiers of chemical biology and materials science need fresh sets of documentation. We respond by generating full spectral libraries across solvent systems, supporting method development for rapid chromatography and mass spec quantification. The science keeps moving, and we invest to match those new analytical demands—sometimes ahead of client requests.

    Outlook and Ongoing Commitment

    For those working in R&D, plant scale-up, or regulatory affairs, a strong supplier brings more than just molecules. We view every batch of 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde as a test of our commitment to quality, transparency, and continual improvement. Today’s production lines reflect yesterday’s feedback—a product of shared knowledge and real-world trial.

    We expect to see new demands for custom specifications, alternative solvents, and packaging solutions as industries evolve. Our process improvement team stays nimble, constantly refining methods and exploring new characterization technologies. The needs of pharmaceutical chemists may overlap with those of agrochemical formulators, but each group brings distinct requirements for documentation, particle size, and even handling protocols. By staying close to each project, we anticipate—and meet—those needs rather than waiting for a problem to surface.

    Supply chain security has become part of every conversation. We invest in raw material verification and supplier audits, so uncertainties around precursor quality never translate into lost batches or inefficiencies at the user end. Recent global disruptions only reinforced the value of close connections with upstream vendors and logistics providers.

    As digitalization expands across laboratories and manufacturing plants, traceability and data accessibility set new standards. We deploy ERP integrations for customer order histories and analytics reports, and our technical staff support customer method development with detailed usage histories from previous lots. These efforts create an open channel between manufacturers and consumers of chemical intermediates—a feedback loop embedded in each drum we ship.

    Our promise: keep listening, keep learning, and keep improving the product. Every batch represents not just chemistry, but trust. Years in the field, deep partnerships with scientists and engineers, and a willingness to adapt make our 4-Chloro-1-Methyl-1H-Pyrazole-3-Carbaldehyde not just another entry in a catalog but a true foundation for future synthesis.