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3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde

    • Product Name 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde
    • Alias DMAPPC
    • Einecs 629-435-9
    • 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

    578743

    Iupac Name 3,5-Dimethyl-1-phenyl-1H-pyrazole-4-carbaldehyde
    Molecular Formula C12H12N2O
    Molecular Weight 200.24 g/mol
    Cas Number 27143-01-9
    Appearance White to off-white solid
    Melting Point 106-109 °C
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Smiles CC1=NN(C(=C1C=O)C)c2ccccc2
    Purity Typically ≥ 97%
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Synonyms 4-Formyl-3,5-dimethyl-1-phenylpyrazole
    Inchi Key BKJQIQNKUBJPQS-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Brown glass bottle with a secure cap, 25 grams, labeled with chemical name, hazard symbols, batch number, and safety information.
    Shipping 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde is shipped in tightly sealed containers, protected from light, moisture, and heat. It is handled as a laboratory chemical and transported according to relevant chemical safety regulations, typically under ambient temperature, with safety documentation and labeling in compliance with local and international shipping guidelines.
    Storage **Storage Description for 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde:** Store in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature. Label the container appropriately, and ensure access is restricted to authorized personnel. Handle under a fume hood and follow standard laboratory chemical storage protocols.
    Application of 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde

    Applications of 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde in Industrial Manufacturing

    As the original producer of 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde, we deliver consistent material direct to specialized industries where this advanced intermediate enables targeted synthesis. Our customers integrate this raw material through established protocols across pharmaceutical manufacturing, agrochemical synthesis, pigment formulation, polymer modification, and advanced material research—each requiring strict adherence to sector-specific processes and compliance systems. Below is a focused overview of real industrial application scenarios based on customer downstream workflows.

    1. Pharmaceutical Intermediate for Pyrazole-Based Drug Synthesis

    Leading pharmaceutical companies employ this raw material in multi-step syntheses of pyrazole-derivative APIs, harnessing its reactive aldehyde group for precision coupling. As a key intermediate, it enters the process during the heterocyclic core construction to attach functional side chains required in targeted therapies. Its stability, purity, and defined impurity profile enable reproducible scale-up and ease of analytical control, meeting the stringency of commercial drug API production, particularly for anti-inflammatory and CNS candidate compounds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and EP monograph reference for applicable intermediates
    • FDA and EMA registration dossier requirements (DMF, CEP)
    • ISO 9001:2015 certified Quality Management System for raw material traceability

    Typical usage ratio

    • Applied at 0.8–1.2 molar equivalents relative to the targeted pyrazole core in stepwise batch or continuous reactor systems; varies based on desired API complexity and route optimization

    Downstream process integration

    • Introduced post-nucleophilic aromatic substitution as a coupling partner in closed vessel reactors, with real-time in-process HPLC monitoring to ensure completion of condensation and subsequent cyclization

    Final product types

    • Small molecule APIs for anti-inflammatory, analgesic, and central nervous system therapies (e.g., celecoxib analogues, research-stage kinase inhibitors)

    2. Agrochemical Synthesis for Fungicidal and Herbicidal Actives

    Large-scale agrochemical manufacturers utilize this pyrazolecarbaldehyde as a precursor for assembling heterocyclic frameworks of next-generation fungicides and herbicides. It joins multi-component reactions with hydrazines and amines to construct potent crop protection agents that address resistance concerns. Trace-metals management and precise stoichiometry are required to maintain regulatory compliance and downstream environmental safety.

    Industry compliance standards

    • FAO/WHO specifications for active ingredient purity and impurity profiling
    • Regulation (EC) No. 1107/2009 on Plant Protection Products (EU)
    • ISO 17025-controlled analytical validation for batch release
    • OECD GLP guidelines for intermediate material handling and process documentation

    Typical usage ratio

    • 1.0–1.3 equivalents as building block, with process adaptation depending on downstream substitution pattern and desired ring substitution

    Downstream process integration

    • Reacted with hydrazine compounds under controlled temperature, followed by oxidative cyclization; employed at the initial formation stage for active ingredient synthesis, then removed after further derivatization

    Final product types

    • Pyrazole-based fungicidal AIs (e.g., analogues of fenpyrazamine, isopyrazam)
    • Herbicidal intermediates with enhanced selectivity for cereal and vegetable crops

    3. Organic Pigment and Dye Intermediates

    Specialty pigment producers rely on this compound to craft colorants with high tinctorial strength and solvent fastness. By integrating the aldehyde into condensation reactions with anilines or hydrazones, it defines color shade, chromatic purity, and pigment particle morphology. Consistent particle size and crystal phase control are achieved during the pigment synthesis, supporting high-performance coatings and plastics coloration.

    Industry compliance standards

    • ISO 787 general methods for pigment testing and consistency
    • REACH Registration and SVHC (Substances of Very High Concern) restrictions
    • EN 71-3:2019 (toy safety – migration of certain elements)
    • ISO 14001 Environmental Management for pigment manufacturing

    Typical usage ratio

    • 5–15% (w/w) as intermediate input in pigment precursor reactions, ratio tailored for color intensity and crystal structure targeted during synthesis

    Downstream process integration

    • Introduced as a reactant during azo or hydrazone condensation, before milling/refining and surface treatment for dispersibility; critical for color-trend matching applications

    Final product types

    • High-performance organic pigments for automotive, coil coatings, and plastics
    • Specialty dyes for plastics compounding and printing inks

    4. Advanced Polymer Modification Additive

    Polymer additive formulators incorporate this pyrazolecarbaldehyde at the pre-polymerization stage to introduce reactive sites for crosslinking, thermal stabilization, and UV resistance in engineering resins. By forming covalent linkages within copolymer matrices, it enhances mechanical durability for demanding end-use environments such as electrical housings and automotive interiors. Only precisely formulated additions meet the spectral and mechanical property targets without negatively impacting processability.

    Industry compliance standards

    • UL 94 and IEC 60695 for flammability classification of finished polymers
    • FDA 21 CFR 177 for food-contact compliance where required
    • IEC 60216 for thermal endurance and stability in electrical applications
    • RoHS Directive 2011/65/EU for restricted substance content in electronics

    Typical usage ratio

    • 0.2–1.0% w/w as a polymer modulator; optimized based on the degree of crosslinking and balance of mechanical versus chemical resistance

    Downstream process integration

    • Added to the monomer or oligomer melt prior to curing; reacts via the aldehyde with compatible functional groups during extrusion or in situ cure, with FTIR monitoring of incorporation efficiency

    Final product types

    • Modified polyamides and polyesters for automotive and E&E housings
    • Crosslinked resins for high-durability powder coatings

    5. Fine Chemical Intermediate for Specialty Aroma and Flavor Compounds

    Producers of specialty aroma chemicals implement this compound in targeted syntheses for heterocyclic notes in perfumery and complex flavor bases. Employed in laboratory-scale and scaled-up flavor additive manufacturing, the pyrazolecarbaldehyde enables nuanced top notes and heat-resistant olfactory characteristics when condensed with alkyl amines or further derivatized into ketones and acids. The process demands food-grade compliance and in-house analytical validation for safety and migration limits.

    Industry compliance standards

    • FEMA GRAS status for approved derivative aroma compounds
    • EU Regulation (EC) No 1334/2008 on flavorings and food ingredients
    • ISO 22000 Food Safety Management System
    • FCC (Food Chemicals Codex) for purity requirements in food-grade materials

    Typical usage ratio

    • Typically 0.1–0.5% as a precursor in formulated flavor bases; adjusted according to desired aroma intensity and compatibility with other reactive components

    Downstream process integration

    • Condensed with specific amines or ketones under mild acid catalysis; introduced in the blending stage prior to purification and micro-encapsulation for shelf-stability

    Final product types

    • Flavors for baked goods and savory products
    • Heterocyclic notes for high-temperature-stable fragrances
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    Certification & Compliance
    More Introduction

    3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde: An Inside Look at a Key Intermediate

    Working with 3,5-Dimethyl-1-Phenyl-1H-Pyrazole-4-Carbaldehyde over many production cycles provides a certain appreciation for its role in a modern lab or factory setting. The compound stands out as a versatile aromatic aldehyde, built around a pyrazole core that brings both chemical stability and the capacity for tailored reactivity. We’ve refined its synthesis and quality—seeing firsthand how tighter control over each processing stage gives consistently better outcomes and more satisfaction in the finished product.

    Our Approach to Synthesis

    Producing a chemical like this becomes much more than chasing purity on a spec sheet. The synthetic pathway involves selective methylation and precise protection steps, demanding both patience and a willingness to scrutinize each batch—impurity trends, color shifts, yield nuances. We start with selected phenylhydrazines for better lot-to-lot consistency. Our teams learned early that any minor shift in solvent quality or reaction times can create side-products, which, if ignored, reduce the value of every subsequent reaction the aldehyde supports. This hands-on attention draws a clear line between well-executed batches and those that need reworking or, in rare cases, full disposal.

    Knowledge gained from earlier decades’ limitations—manual separations, inconsistent heat transfer—helps us defend against avoidable variability. Over the years, investments in batch reactor controls eliminated many of the temperature and agitation issues common to small- and medium-scale operations. We validate with each run that the crystalline aldehyde looks as it should—typically off-white to pale yellow—signaling a clean formation and minimal degradation.

    Why the Aldehyde Matters to Our Customers

    From our end, supply to pharmaceuticals and specialty materials researchers tops the usage charts, but stories from customers matter most. Teams engaged in heterocyclic chemistry, searching for novel drug candidates, describe how other aldehydes fall short. The unique electronic bias conferred by the methyl groups eliminates certain unwanted background reactions, which veteran chemists quickly learn to appreciate. The phenyl ring, introduced early in production, works as a scaffold for further derivatization—especially for those aiming to modify the pyrazole for new biological targets.

    In the real world, a research cycle’s value can hinge on a single step going as planned. We hear from scientists who had to scrap months of work due to contaminated or impure lots of pyrazole aldehyde from less rigorous suppliers. Our tighter purity profiles—regularly reaching 98% or higher by HPLC—mean downstream steps suffer fewer surprises: fewer unknowns by NMR, less color in final products, and easier interpretations at every stage of scale-up.

    Specifications That Reflect Real-World Use

    We manufacture this aldehyde under specifications that reflect actual lab requirements, not some generic or export-focused standard detached from practice. Trace metal content remains closely monitored, since even low parts-per-million iron or copper can poison downstream catalytic processes. Water content—always under 0.5%—addresses the reactivity needs of those working in air- and moisture-sensitive routes. Melting point inspections keep us truthful about batch quality; our lots almost always fall within the narrow 154-158°C range documented in major literature—a small window, but a useful measure of successful synthesis.

    We avoid unnecessary fillers or byproducts. You won’t find stabilizers or unknown adducts in our material. Each gram sent to a customer represents decisions made in the plant: extra filtration, dried glassware, even careful lot segregation when any anomaly surfaces. That matters both for those in scale-up—where unused material may have to sit in inventory for weeks—and for high-throughput screening groups who demand the same reactivity profile with every weighing.

    Comparing with Similar Aromatic Pyrazole Aldehydes

    Some pyrazole aldehydes find application as academic curiosities, others as workhorse intermediates. Our specific compound, with methyl groups at the 3 and 5 positions and a phenyl on nitrogen, walks a line between selectivity and versatility. Compared to less substituted pyrazole-4-carbaldehydes, this one typically offers fewer side reactions with strong nucleophiles: the added methyls twist the electronic profile just enough to favor selective reactions, something colleagues in custom synthesis have noted while optimizing fragment reactions or Suzuki couplings.

    For those exploring combinatorial libraries, the steric and electronic tuning available via the methyl substituents provides differentiation from more basic, unsubstituted pyrazoles and from competitors like indazole or imidazole aldehydes. Feedback from process chemists often points to improved yields in formation of hydrazones, Schiff bases, and heterocyclic rings due to this molecular balance—an advantage for anyone weary of ambiguous melting points or broad NMR peaks from lower-quality aromatic aldehydes.

    Handling and Storage Observations from Production

    Longer experience with storage and shipment highlights some differences vs. simpler aromatic aldehydes. A well-crafted batch of 3,5-dimethyl-1-phenyl-1H-pyrazole-4-carbaldehyde stands up better to temperature cycling; the structure resists oxidation and polymerization, issues that plague benzaldehyde derivatives in damp or warm conditions. Even so, we keep batches vacuum-sealed and away from sunlight and air—not just for shelf life, but because we know neglected storage can spoil even the best original batch. This may seem like small detail, but those working in fast-paced discovery environments depend daily on such material consistency.

    Feedback helped us realize that laboratory staff too often struggle with pyrazole-based compounds that degrade or change color in storage. Implementing nitrogen-flushed packing and transparent batch dating let us cut down on spoilage and minimize inquiries related to reactivity drops—a win both for lab staff and for our production oversight. Nothing builds confidence like a container that opens with no odd smell, no trapped condensation, no hint of decomposition.

    Supporting Advanced Synthesis

    Beyond simply filling orders, we keep in close contact with scientists who push reaction development or scale-up boundaries. Projects in regulated sectors, from antifungal agents to agrochemical intermediates, depend on both the physical integrity and verified origin of their aldehyde stocks. Our records show repeated requests for rapid re-verification of lots long after dispatch, often during audits or patent filings. That reporting trail—every sample tracked, every storage condition documented in detail—forms a bedrock for regulatory workflows impossible to shortcut or ignore.

    Users working in asymmetric synthesis or who face frequent reaction troubleshooting also report advantages with this compound. Its rigid, substituted core helps lower chances for side-reactions or byproduct cascades. Our technical staff now routinely field feedback sessions with these teams, offering both insight on handling and willingness to adjust crystal particle size or packing density to make process integration easier. As adoption of automated dosing systems grows, such details prove as valuable as purity or analytical traceability.

    Challenges Facing Consistent Quality

    Keeping up the highest material standard in the face of market and supply chain pressures brings its own set of hurdles. For instance, fluctuations in supply of high-quality methylating agents or protection group reagents can slow timelines, but accepting subpar input risks ending up with a batch that could cause headaches across dozens of customer projects. Our in-house analytical lab techs have become skilled at flagging even subtle profile changes in starting materials, sometimes persuading upstream suppliers to raise their own game or, in rare cases, prompting us to bring crucial raw materials production in-house.

    During shipping, atmospheric moisture presents a persistent threat. While the molecule resists direct hydration, repeated opening and closing of user containers draws water inside, especially in humid climates. This risk increased during recent years’ global logistics disruptions, with warehouses relying on stopgap packaging. Custom-sized, pre-measured containers helped cut this exposure; delivering smaller, precisely filled bottles lets end-users minimize oxygen and water ingress, safeguarding the aldehyde for the long reaction cycles that lead to meaningful new molecules.

    Developing for Environmental and Safety Commitments

    We have seen industry evolve from casual chemical manufacturing to a place where environmental assurances and workplace safety take a central role. Our facility implements vapor capture and advanced waste solvent treatment, limiting exposure both for our teams and for the communities nearby. This compound, with its moderate reactivity and manageable volatility, fits well within our broader goal: deliver advanced building blocks without creating unnecessary risks or accumulating waste. Real improvement began with process redesign—optimized reagent concentrations, shorter cycle times, and energy-efficient heating setups.

    On the safety front, we work proactively with partners to provide direct insights on dusting, safe weighing, and correct response to accidental spills. Hard-won experience in the plant shows that simple habits—like using glove-box transfers for multi-kilo lots or always checking seals before storing—bear more fruit than relying on printed guidance. In-house training incorporates learnings from both near-misses and seamless campaigns, all aimed at keeping downstream users out of harm’s way and in compliance with both local and global regulations.

    Continuous Improvement Through Open Dialogue

    What keeps this business fulfilling is the constant feedback loop with users. We invite suggestions on solubility, ease of handling, or direct reports of unexpected behavior in scale-up work. Not every tip leads to an immediate process change, but the cumulative effect—practical, ground-level insights from those at the bench—shapes our future batches as much as any internal SOP.

    Customers who once struggled with poor re-dissolution or unexpected side reactions inform our adjustments in drying times, carton selection, or even label design. These aren’t decisions taken lightly; each tweak can ripple through stock control or even affect regulatory filings for bigger users. In the long run, a manufacturer’s reputation rests on fine details, day-to-day conversations, and the reliability that comes from listening as carefully as producing.

    Future Prospects: Learning and Adapting

    Demand patterns for 3,5-dimethyl-1-phenyl-1H-pyrazole-4-carbaldehyde keep changing as new pharmaceutical scaffolds and organic electronic materials continue to evolve. Each emerging application brings its own nuances, sometimes calling for extra analytical runs, sometimes for shifts in crystal properties. We’re preparing by cross-training operators and investing in next-gen analytics to double down on fast, accurate detection of even rare impurities. With technical partnerships across academia and industry, new routes to the pyrazole core, greener methylation methods, and improved aldehyde isolation are already in pilot scale review.

    It’s become clear that one-size-fits-all intermediates no longer serve a sophisticated research and production landscape. The feedback we receive turns quickly into applied change. We make this compound not as a commodity, but as an enabling ingredient—a small molecule with a major impact for those who know its value. Every batch offers us a new chance to refine, to learn from others, and to help support the next scientific breakthrough. That’s what turns a simple aldehyde into an object of genuine craft for those on both sides of the supply chain.