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1H-Pyrazole-4-Carboxaldehyde

    • Product Name 1H-Pyrazole-4-Carboxaldehyde
    • Alias 4-Formylpyrazole
    • Einecs 664-207-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    631859

    Cas Number 15862-38-1
    Molecular Formula C4H4N2O
    Molecular Weight 96.09
    Iupac Name 1H-pyrazole-4-carbaldehyde
    Appearance White to light yellow solid
    Melting Point 140-144°C
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Chemical Class Pyrazole derivative

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

    Packing & Storage
    Packing White, screw-capped glass vial containing 5 grams of 1H-Pyrazole-4-Carboxaldehyde, labeled with product name, CAS number, and hazard information.
    Shipping **Shipping Description:** 1H-Pyrazole-4-Carboxaldehyde is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be packed according to chemical safety regulations, with appropriate labeling for hazardous organic compounds. Handle with care, and ensure the shipment includes all relevant safety documentation and material safety data sheets (MSDS).
    Storage 1H-Pyrazole-4-carboxaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizers. Ensure the storage area is clearly labeled and follow applicable safety protocols, including the use of secondary containment to prevent spills or leaks.
    Application of 1H-Pyrazole-4-Carboxaldehyde

    Applications of 1H-Pyrazole-4-Carboxaldehyde in Industrial Manufacturing

    1H-Pyrazole-4-Carboxaldehyde is an essential intermediate manufactured to support specialized chemical synthesis for various industrial sectors. Our consistent quality control and process management enable downstream industries to integrate this material efficiently into their established production environments. Below we present the principal application scenarios based on real industrial demand, covering compliance, formulation guidelines, process roles, and main end products.

    1. Pharmaceutical Intermediate for Pyrazole-Based APIs

    Global pharmaceutical companies utilize 1H-Pyrazole-4-Carboxaldehyde primarily as a core intermediate in the multi-step synthesis of pyrazole derivative active pharmaceutical ingredients, including anti-inflammatory and anticancer agents. This building block’s unique aldehyde functionality is crucial for achieving selective bond formations under stringent cGMP controls, making it indispensable for finished API production involving heterocyclic frameworks.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia intermediate requirements
    • U.S. FDA cGMP, 21 CFR Parts 210/211
    • Chinese Pharmacopoeia ChP standards for intermediates

    Typical usage ratio

    • Applied at 0.8–1.2 molar equivalents relative to pyrazole API core, adjusted according to specific synthesis pathways and yield optimization in pilot or commercial-scale API manufacturing.

    Downstream process integration

    • Added during the early condensation or cyclization step, followed by condensation with hydrazines, Grignard reagents, or aryl halides depending on the target API structure. Incorporated inline with solvent and catalyst systems adhering to validated batch records for GMP compliance.

    Final product types

    • COX-2 inhibitor APIs (e.g., celecoxib intermediates)
    • Anti-tumor pyrazole derivatives
    • Agro-pharmaceutical active intermediates with pyrazole motifs
    • Custom contract-manufactured APIs incorporating heterocyclic aldehyde subunits

    2. Crop Protection Synthesis: Selective Herbicide and Fungicide Intermediates

    Major agrochemical formulators employ 1H-Pyrazole-4-Carboxaldehyde for the synthesis of selective pyrazole-based herbicides and fungicides, capitalizing on its ability to introduce reactive heterocyclic scaffolds into lead compound libraries. This function supports scalable development routes that require precise integration of the aldehyde group to achieve targeted weed and fungal selectivity.

    Industry compliance standards

    • ISO 9001:2015 quality management for agrochemical active ingredient production
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • U.S. Environmental Protection Agency (EPA) registration standards for technical grade active ingredients
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)

    Typical usage ratio

    • Blended at 3–10% by weight in precursor formulation stages, specific proportioning determined by the synthetic route, desired substitution pattern, and efficiency in downstream oxidation or reduction processes.

    Downstream process integration

    • Engaged during initial alkylation, halogenation, or condensation reaction sequences to build pyrazole rings, often directly coupled with ketones or hydrazide reagents before catalytic conversion to the final pesticide backbone.

    Final product types

    • Selective herbicide technical concentrates (e.g., pyrazole-substituted amides)
    • Systemic fungicide actives with pyrazole rings
    • Pesticidal intermediates for subsequent formulation into EC/SC/WG products
    • Patented crop protection molecules incorporating pyrazole moieties

    3. Fine Chemical Synthesis for Dye and Pigment Manufacture

    Manufacturers in the colorant and pigment sector use 1H-Pyrazole-4-Carboxaldehyde as a chelating and color-tuning intermediate within the synthesis of specialty azo, diazo, and pyrazole-based dyes. The functionalization enabled by this aldehyde group impacts the wavelength absorption properties, thermal stability, and metal-complexing activity of the final products.

    Industry compliance standards

    • REACH (EC No. 1907/2006) registration for dye raw materials
    • ETAD Code of Practice for colorant manufacturers
    • CFR Title 21 – Subchapter B for food-contact dye components, where applicable
    • ISO 9001 and ISO 14001 for environmental and quality management in pigment synthesis plants

    Typical usage ratio

    • Utilized between 1–5% by weight in the reaction matrix, with precise dosing governed by the target chromophore type, desired color intensity, and downstream compatibility with metal ion additives for chelation.

    Downstream process integration

    • Introduced as a nucleophile or electrophile during key coupling steps, especially in synthesis of metal-complexed pigments or during diazotization and azo coupling stages, closely monitored under closed reactor conditions to ensure high chromophore yield.

    Final product types

    • Pyrazole-based azo dyes for textile applications
    • Specialty pigments for plastics and coatings
    • Colorfast dye intermediates for inkjet and printing inks
    • Metal-complexed dyes for automotive finish and architectural coatings

    4. Development of Specialty Heterocyclic Building Blocks in R&D and Custom Synthesis

    Custom synthesis organizations and research laboratories depend on 1H-Pyrazole-4-Carboxaldehyde to generate unique pyrazole derivatives required for exploratory drug and agrochemical development. Its key role as a skeleton-building aldehyde allows for rapid assembly and SAR expansion in high-throughput screening or lead optimization workflows.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for non-clinical health and environmental safety studies
    • ISO 17025 laboratory competence, where custom synthesis chemistry supports regulatory filings
    • REACH Annex XVII for substances used in chemical R&D screening
    • Company-specific SOPs for raw material handling and documentation

    Typical usage ratio

    • Dosed from 0.05–1.0 mmol scale for screening reactions in laboratory synthesis, up to 2–10 g per batch for kilo-lab and pilot-scale custom projects depending on complexity and reaction pathway.

    Downstream process integration

    • Initiates the construction of substituted pyrazole rings or fused-ring systems in building block libraries; often reacts with amines, hydrazines, or other functionalized aldehydes and is directly incorporated into iterative parallel synthesis protocols or multi-step scale-up, tracked by LC-MS and NMR for structural verification.

    Final product types

    • Reference compound libraries for pharmaceutical R&D
    • Structural motifs for combinatorial chemistry sets
    • Specialty chemical intermediates for academic or government-funded research
    • Lead optimization candidates for agrochemical or material science innovation

    5. API Impurity Profiling and Analytical Standards Preparation

    Certified analytical laboratories and QC departments in both chemical and pharmaceutical industries utilize 1H-Pyrazole-4-Carboxaldehyde as a known impurity marker or retention standard within method development for high-precision HPLC, LC-MS, and GC-MS analysis. Its chemical distinctiveness allows accurate quantification of process impurities, supporting regulatory submissions and lot release specifications.

    Industry compliance standards

    • ICH Q3A (R2) – Impurities in New Drug Substances
    • USP General Chapter <621> Chromatography
    • ISO/IEC 17025:2017 for accredited laboratories
    • FDA analytical validation guidelines for pharmaceuticals

    Typical usage ratio

    • Prepared as analytical reference solutions at 0.1–100 ppm, specific concentration guided by system sensitivity, target API concentration, and method detection limits.

    Downstream process integration

    • Dissolved or spiked into test matrices prior to chromatographic analysis; incorporated as certified reference material or as part of forced degradation studies. Employed for impurity marker co-elution and stability assessments during QC and release testing.

    Final product types

    • Analytical reference standards
    • Certified impurity markers for ICH-defined API profiling
    • QC calibration mixes for bulk pharmaceutical manufacturing
    • Validation kits for accredited analytical laboratories
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    Certification & Compliance
    More Introduction

    Introducing 1H-Pyrazole-4-Carboxaldehyde: Practical Experience From the Manufacturer’s Bench

    What Sets 1H-Pyrazole-4-Carboxaldehyde Apart

    At our facility, the real work begins in the laboratory, not a boardroom. We have spent years refining the process to produce 1H-Pyrazole-4-Carboxaldehyde with tightly controlled parameters. This compound, known for its molecular structure featuring a reactive aldehyde group at the fourth position on the pyrazole ring, often carries the CAS number 31245-56-4. Handling and producing this molecule requires skill—it's not something you mix up with casual ease. The fine distinction between practical synthesis and textbook chemistry only gets sharper with experience. Some batches demand patience, others call out for more targeted analytical support, and each variance in input can alter the nuances of the final material.

    Chemists with hands stained from years of reactions know that aldehyde-substituted heterocycles carry subtle behavioral differences from their relatives. In practice, the aldehyde function on the ring offers a chemical handle for fine modifications. This isn’t a product made for sitting on a storage shelf; customers use it directly for further synthesis, especially in pharma and agrochemical research. We’ve watched teams trial countless intermediates, only to circle back to 1H-Pyrazole-4-Carboxaldehyde for its reliability in cyclocondensation and alkylation reactions where more labile positional isomers fall short.

    Purity, Form, and Real-World Consistency

    Researchers depend on clean compounds. Over the years, we set tighter targets for purity than the basic trade threshold. Typical specification for our prime batches is a minimum of 98%, based on HPLC analysis we validate for every production lot. Achieving this level repeatedly isn’t a matter of cranking up machines. Consistency comes from careful control—choosing the right raw materials, employing a workup that doesn’t leave behind irritating side impurities, planning for detection of subtle hydrolysis or ring-opened byproducts, and keeping the production line honest by confirming results through analytical checks, not assumptions.

    The white to slightly pale crystalline powder people receive is the outcome of several crystallization and drying steps, not just an end product shaken from a flask. Moisture absorption, a nagging factor with aldehydes, gets managed at every point. Our experienced crew knows what to watch for during bottle filling and packing. You’d be surprised at the difference these precautions make when the compound is applied in real process environments, especially in scale-up where batch repeatability isn’t negotiable.

    Practical Utility in Modern Laboratories

    Lab chemists bring us unusual demands. 1H-Pyrazole-4-Carboxaldehyde rarely gets used for a single, simple transformation. The aldehyde group invites attachment in fragment-based drug design and constructs where molecular complexity grows from the pyrazole core—true especially in kinase inhibitor research. Some customers screen dozens of related rings each month looking for meaningful biological activity. Our product finds its way into research projects aimed at finding new antiparasitic leads, sometimes as the rigid backbone for advanced small molecule construction. Others push it through multistep routes where a less stable N-unsubstituted pyrazole would disintegrate.

    In our own benchmarking, carboxaldehyde functionality on pyrazole reacts with amines and hydrazines under milder conditions than several other heterocyclic aldehydes, such as pyridine-carboxaldehydes, which sometimes resist condensation without harsh acid catalysis or extended heat. The 1H-pyrazole substitution means our product stays in solution longer, doesn’t precipitate out unexpectedly, and resists oxidation when processed with reasonable care. Scale-up staff report lower losses to decomposition compared to related structures, which minimizes costly recovery and redistillation steps. This translates directly into time saved for end users.

    Differences From Similar Chemicals

    You have options in the pyrazole world, but not all give you the same control or outcome. 1H-Pyrazole-4-carboxylic acid (the acid analog) lacks the reactive aldehyde moiety and goes sluggish in condensation routes. 3- or 5-substituted pyrazole carboxaldehydes introduce different steric hindrance; we have watched them yield unexpected regioisomers or demand longer reaction times in model syntheses. In essence, the position and nature of the aldehyde substituent matter more than most realize—small structural changes bring large impacts in both reactivity and downstream functionalization.

    There is another persistent issue that chemists new to heterocyclic chemistry often encounter: the confusion between the unsubstituted N1-hydrogen and the N1-methyl or N1-phenyl substituted analogs. Substitution alters electron density far more than textbooks imply. For example, N-methyl pyrazole-4-carboxaldehyde—a product we’ve tested on request—shows higher volatility and different polarity, leading to separation challenges in downstream processing. Our N-unsubstituted variant, in contrast, displays predictable solubility and crystalline properties, which translate into cleaner analytical profiles and better-controlled purification, especially by column chromatography or preparative HPLC.

    Handling and Packaging Insights From the Shop Floor

    Too many specialty manufacturers overlook packaging details that affect the day-to-day work in the user’s lab. We take extra steps because we’ve seen the impact: heatsealed aluminum bags keep the powder stable during shipping, but those with brittle liners crack when squeezed by global carriers. Secure double-layer packs and carefully chosen desiccants keep the product from clumping before it arrives; the less time a chemist spends breaking up lumps or worrying about humidity, the better.

    Shipping logistics aren’t just about regulations. We coordinate batch dispatch closely to minimize time in transit. Experience has shown that even trace exposure to atmospheric moisture can alter physical handling properties enough to frustrate someone who paid for a premium research compound.

    Environmental and Safety Observations on Practical Use

    Aldehyde-functionalized heterocycles demand more attention during handling than simple ring structures. The workers in our plant learn right away to keep sources of oxidants and contaminants away from carboxaldehyde stocks and intermediates. Waste stream planning runs alongside synthesis for each batch, since nobody wins if nitrogenous, aldehyde-laden effluents end up untreated. We run dedicated lines for minimally contaminated waste, and routinely test for escape of volatile organics to stay below regulatory thresholds. These steps didn’t come from compliance efforts alone; they result from years of on-the-ground experience seeing how quickly a lack of control can snowball.

    As with many nitrogen-rich chemistries, trace contaminants sometimes arise if storage vials or lines are reused without thorough verification. The team remains vigilant for cross-contamination. Fermenters, solvent handling tanks, and glassware each get tracked with a lot-based QA system. It’s a discipline that comes from ruined batches, not a memo in a manual. Cleanliness reflects in the high quality of the final product and lower complaint rates from downstream researchers. We learned these lessons the hard way so that our customers avoid the same.

    Instrumentation, Analysis, and the Role of Human Judgement

    We rely on more than numbers on a readout. Running LC-MS and NMR on every major production lot tells us what’s there, but understanding why a slight peak persists, or knowing how much to adjust for residual moisture, comes from long practice. For this type of pyrazole, careful titration of solvents, attention to glassware, and a watchful eye on batch color during evaporation serve as the first defense against invisible losses or overreaction.

    Plant staff have built up a sixth sense—years of seeing both the mistakes and the successes show up as small deviations. A crisp white powder usually means a well-run batch, but small dark flecks hint at unnoticed thermal decomposition, calling for a run through a tighter filter or an extra recrystallization. We have watched new hires learn that the subtle phenolic odor of some side products is a sign to double-check HPLC traces.

    Supporting Advanced Synthetic Projects

    Research groups want predictability. Our clients in medicinal chemistry, combinatorial synthesis, and early-stage pharmaceutical labs consistently return to our 1H-Pyrazole-4-Carboxaldehyde because it standardizes results in routes for pyrazole-derived scaffolds. It takes out the guesswork over whether a slow Staudinger or Pictet-Spengler reaction failed from starting material impurity or a hidden sidegroup. Over time, we have supplied benchmark samples to contract research organizations looking for well-behaved building blocks.

    Synthetic targets change, but the underlying chemical demands stay consistent. As new classes of kinase inhibitors, antifungals, or agrochemical actives are sought, the utility of our compound persists because it accommodates iterative transformations without drifting out of specification. That reliability does not emerge from marketing—it's a result of lived experience, close process control, and direct dialogue with chemists who feedback outcomes of success or failure so we can adapt.

    Reliability Through Long-Term Production

    Some intermediates appear, fade, and vanish from the catalog as trends shift, but 1H-Pyrazole-4-Carboxaldehyde has held a steady demand profile at our plant for years. This stability reflects not only its core use in medicinal and agricultural research, but an adaptability to projects ranging from small exploratory routes to pilot production. Our team revisits key process steps every few cycles, updating filtration media, solvent ratios, and drying protocols as tools and knowledge evolve in the field.

    Throughout these years, what stands out isn’t a formula on paper, but the thousands of individual process decisions—from choosing tubing and joint grease resistant to aldehyde corrosion, to selecting analytics that catch even faint secondary peaks. These decisions gave us product batches with longer shelf life and fewer customer complaints about reactivity or purity. Mistakes never vanish entirely, but their frequency and impact drop as experience grows. Consistent quality earns trust, and in our business, word-of-mouth weighs more than flashy advertising.

    Research Applications From Real Requests

    At the bench, the diversity of transformations enabled by pyrazole-4-carboxaldehyde continues to surprise us. One biotech customer used it to launch a library of pyrazole-imine conjugates for enzyme inhibition profiling. In another collaboration, a team developed new ligand frameworks for copper and ruthenium catalysis, specifically valuing the compound’s ease of complexation and predictable purity. The feedback loop has expanded our understanding of how small details in starting material drive whole research programs forward.

    A notable application involves the use of the aldehyde for direct reductive amination. Where comparable heterocycles sometimes require pre-activation or bring along contaminating byproducts, this material reacts cleanly with primary amines to give target amines in high yield—a trick that saves days in the synthesis of advanced pharmaceutical intermediates. Academic researchers share examples of rapid fragment attachment, while agricultural chemists leverage the pyrazole ring for bioactive lead design, counting on reliable supply and minimal variability.

    Continuous Improvement Grounded in Reality

    Quality comes from iteration, not aspiration. Each round of batch production includes a review of yields, impurity profiles, downtime events, and even minor equipment anomalies. Over the years, we have replaced filtration screens, changed out solvent tanks, and adopted new analytical standards after small discoveries in process break-points. Chemists at the intake points value these small improvements, reporting fewer batch delays and less time resolving minor variances. Where we once lost product to hydrolysis on humid days, we switched to temperature and humidity-controlled environments, reducing annual wastage by a measurable margin.

    Our plant’s team language remains rooted in practicalities, not abstractions. We debate the significance of microimpurities, study every sequenced step in the workup, and make changes after collective reflection—not only boardroom decrees. This process-led, craft-driven approach forms the backbone of our 1H-Pyrazole-4-Carboxaldehyde. It means customers see not just a chemical compound, but a support network built through practice, tough days, failed batches, and hands-on learning.

    Why Customers Return Again and Again

    Buyers who scale up their work do not simply shop based on paper specs. They look for material that will react the same day after day, allowing them to plan projects without hedging for surprises. Teams in charge of large combinatorial screens, or those charting out series of analogs for patent applications, depend on this regularity. Many of our long-term users started with small trial packs, moved to kilogram quantities, and later received custom lots or adjusted purities tuned for their routes. Reliability at this level cannot be faked. Our most loyal customers spot shortcuts instantly and provide direct feedback if a batch underperforms, which helps us maintain the high standards the market expects.

    We seldom discuss “market differentiation” or “added value”—our clients inform us plainly on what works and what blocks their research. It is this grounded, results-focused relationship that shapes our production philosophy. In the end, the compound isn’t just a bottle on a shelf; it’s the outcome of resolved issues, honed experience, and day-after-day attention from people who understand its role as a critical research tool.

    Looking Ahead: Supporting New Scientific Directions

    Innovation in fields like medicinal chemistry, advanced materials, and crop science keeps generating fresh requirements. Our work with 1H-Pyrazole-4-Carboxaldehyde keeps pace, leveraging feedback from the front lines of science. Production methods adapt, analytical windows broaden, and packaging protocols get reexamined to anticipate where research might go next. Actions we take on the shop floor set the standard. These improvements come from collaboration with our clients, reviewing their latest routes, learning from their wins and setbacks, and incorporating small but crucial upgrades into our workflow.

    Above all, it takes humility to acknowledge the unending pursuit of betterments—no batch ever seems completely “finished” in the eyes of an experienced team. Every new collaboration unveils a tweak, a new analytical insight, or a shipping solution. Through this ongoing dialogue and the hands-on skills of chemists who trust the process, our 1H-Pyrazole-4-Carboxaldehyde continues as a reliable foundation in fast-moving scientific arenas. While some view it as a technical commodity, every bottle stands as the output of integrated effort and persistent fine-tuning, shaped by real lab and plant experience.