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4-(1H-Pyrazol-1-Yl)Benzoic Acid

    • Product Name 4-(1H-Pyrazol-1-Yl)Benzoic Acid
    • Alias 4-(Pyrazol-1-yl)benzoic acid
    • Einecs 607-257-2
    • 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

    311716

    Product Name 4-(1H-Pyrazol-1-Yl)Benzoic Acid
    Cas Number 51862-12-3
    Molecular Formula C10H8N2O2
    Molecular Weight 188.18
    Appearance White to off-white solid
    Melting Point 255-258°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Smiles C1=CN(N=C1)C2=CC=C(C=C2)C(=O)O

    As an accredited 4-(1H-Pyrazol-1-Yl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-(1H-Pyrazol-1-Yl)benzoic acid is packaged in a 25-gram amber glass bottle with a secure screw cap.
    Shipping 4-(1H-Pyrazol-1-yl)benzoic acid is shipped in tightly sealed containers, protected from moisture, heat, and light. It is packed according to standard chemical safety regulations, with appropriate labeling for transport. Material Safety Data Sheets (MSDS) accompany the shipment to ensure safe handling during transit and upon arrival.
    Storage 4-(1H-Pyrazol-1-yl)benzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and moisture. Keep away from incompatible materials such as strong oxidizing agents. Store at room temperature, and ensure proper labeling. Follow all safety protocols for handling organic acids and pyrazole derivatives.
    Application of 4-(1H-Pyrazol-1-Yl)Benzoic Acid

    Applications of 4-(1H-Pyrazol-1-Yl)Benzoic Acid in Industrial Manufacturing

    As a specialized manufacturer of 4-(1H-Pyrazol-1-Yl)Benzoic Acid, we serve key downstream sectors where this intermediate is required for advanced synthesis and precise formulation. Below, we outline verified industrial applications and their specific process details, covering pharmaceutical intermediates, agricultural chemicals, specialty dyes, and advanced polymer additives.

    1. Pharmaceutical Intermediate for Anti-Inflammatory Agents

    Major pharmaceutical producers rely on this intermediate during the multi-step synthesis of anti-inflammatory and analgesic medications in the pyrazole family. It enters the route delivering pyrazolyl-benzoic derivative structures, which act as core scaffolds for APIs targeting COX-2 inhibition. End-users conduct stringent validation and traceability throughout their synthesis workflow to ensure quality consistency and regulatory alignment in finished API batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 (GMP guidelines)
    • USP/NF and Ph. Eur. compendial monographs for final API checks
    • Regulatory audits (FDA/EMA) for traceability and impurity profiling

    Typical usage ratio

    • Utilization ranges from 12–18% molar equivalent based on specific target compound; the exact ratio is controlled per synthetic route and is adjusted depending on the substitution pattern required in the final API.

    Downstream process integration

    • Charged at the initial heterocycle coupling stage within multi-step synthesis of pyrazolyl-benzoic derivatives
    • Subject to controlled addition under inert atmosphere conditions in high-purity reactors
    • Monitored for residual unreacted precursor at every stage to comply with impurity limits

    Final product types

    • COX-2 selective anti-inflammatory APIs
    • Non-steroidal analgesics (pyrazolyl-benzoic acid derivatives)
    • Related intermediate reference standards for pharmaceutical QC

    2. Advanced Agrochemical Synthesis (Herbicide & Pesticide Intermediates)

    Producers of next-generation crop protection products use this pyrazole-functional aromatic acid for creating core intermediates in the synthesis of novel selective herbicides and systemic pesticides. Integration at key coupling and condensation steps ensures proper structural assembly, meeting modern requirements for environmental safety and residue control.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for agrochemical manufacturing
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals – EU) compliance, including safety and toxicological data
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 5–10%, depending on the synthetic route for the targeted herbicide or pesticide active; adjusted for the number of coupling steps and overall molecular yield requirements.

    Downstream process integration

    • Added during either Suzuki or Buchwald-Hartwig type cross-coupling reactions to introduce the pyrzole-benzoic structure
    • Careful dosing during condensation with amines or heterocycles to ensure active site formation
    • Enters purification stages to meet final product purity required for agrochemical registration

    Final product types

    • Pyrazole-carboxylic herbicide active intermediates
    • Systemic pesticide precursor compounds
    • Degradate standards for environmental fate studies

    3. Dye & Pigment Intermediate for High-Fastness Applications

    Material scientists in specialty colorants select 4-(1H-Pyrazol-1-Yl)Benzoic Acid as a coupling component for producing advanced azo and heterocyclic dyes with superior color fastness on cellulose fibers and synthetic textiles. The pyrazole ring strengthens chromophore stability and enhances solubility modulation for eco-compliancy in coloration processes.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile-related articles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Annex XVII (Azo dye restrictions for European textile market)
    • GOTS (Global Organic Textile Standard) for pigment additives

    Typical usage ratio

    • 3.5–7.0% within the dye synthesis reaction mass, based on target dye class and batch scale; ratio amendments made based on molarity and intensity of desired shade.

    Downstream process integration

    • Feeds into diazotization or direct coupling reactions with primary amines or phenols
    • Utilized in closed reaction vessels to avoid contamination of high-value pigment fractions
    • Monitored for residual aromatic acid via HPLC at each post-synthesis step

    Final product types

    • Reactive and acid dyes for textile and paper markets
    • High-purity pigments for industrial coatings
    • Masterbatch colorants for synthetic fibers (polyamide, polyester)

    4. Functional Monomer Component in High-Performance Polymers

    R&D and scale manufacturers in the specialty polymers sector incorporate this molecule as a functional monomer or chain modulator for engineering resins that demand specific polar functionality or heterocyclic integration. These applications may include the manufacturing of copolymers for electronics, filtration membranes, or surface-active films, where stability and chemical compatibility remain essential.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems – Polymer Synthesis)
    • UL 94 (Flammability Safety for finished polymer materials)
    • RoHS Compliance for electrical and electronic equipment parts
    • REACH Full Registration for monomer use in polymerizations above 1t/y

    Typical usage ratio

    • 0.5–2.5% in copolymerization batch, typically adjusted depending on the target polarity and chain architecture of the resulting polymer; R&D batches may screen up to 5% for property optimization pre-scale-up.

    Downstream process integration

    • Added as a comonomer or chain-end functionalizing agent in solution or melt-phase polymerization reactors
    • Directly incorporated at initiation or propagation stages with monitoring of molecular weight distribution
    • Quality control checks for residual unreacted monomer and compatibility with target additives

    Final product types

    • Functional engineering polymers with enhanced polar compatibility
    • Membrane materials for water and organic filtration systems
    • Specialty films and coatings for electronic circuit protection
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    Certification & Compliance
    More Introduction

    4-(1H-Pyrazol-1-Yl)Benzoic Acid: Lessons from the Shop Floor

    Our Experience in Synthesizing Quality

    Years on the production line and in the lab teach a person to respect the difference between a promising molecule on paper and a substance fit for real research or application. 4-(1H-Pyrazol-1-Yl)benzoic acid has earned its place as a staple among benzoic acid derivatives. In our plant, each batch starts with scrupulous selection of raw materials, and we never cut corners on solvent purity or glassware cleanliness. This discipline undergirds not just our yield but the reproducibility that research clients quietly rely on.

    We manufacture this compound under controlled temperatures and a closely monitored pH environment. Using high-performance liquid chromatography, our technicians watch for every impurity, and we pull samples every hour, not just at batch start and finish. Over time, these routines turn into reliable habits, and our lot records show tight, predictable purity — typically exceeding 98% by HPLC. Impurities tend toward trace amounts, and our experience tells us not to relax vigilance even when a hundred batches pass without issue.

    Understanding the Chemical — From Synthesis Bench to Bottle

    The molecular structure of 4-(1H-pyrazol-1-yl)benzoic acid brings together aromatic strength with the distinctive reactivity of a pyrazole ring. It is the benzoic acid moiety that gives it anchor and durability; the pyrazole functionality brings options for custom synthesis. Our product presents as an off-white to light tan solid at room temperature. It doesn’t clump under normal storage, and customers tell us they rarely see handling issues — the powder flows easily, so losses during weighing stay minimal.

    Over dozens of production campaigns, we realized careful control during the pyrazole coupling step matters more than solvent grade alone. Precipitation can introduce microscopic occlusions of mother liquor. We extended our drying step after observations during scale-up, and the result is a compound with consistent loss on drying values below 0.50%. Batch-to-batch reproducibility isn’t a marketing claim; regular validation with FTIR and NMR confirms the expected spectral signatures and silences guesswork.

    Our Standard Specifications

    After years of listening to customers, we understood that a stated specification matters less than whether that value reflects reality. Ours hold up in the real world. Our 4-(1H-pyrazol-1-yl)benzoic acid model ships at a minimum 98% purity by HPLC, with water content and residual solvents far beneath ICH Q3C thresholds. It exhibits a sharp melting range, usually within 4 degrees Celsius between onset and completion, which fits the demands of both analytical and synthetic chemists.

    Crystallinity, particle size, and appearance distinguish our batches. Visual checks and sieving make sure that fines and oversized particles don’t find their way into finished containers. Subtleties like color come from years standing over the drying oven — a flaw here often signals unseen process drift. Every new operator trains under senior staff for at least a year on these subtleties.

    Why Chemists Keep Coming Back

    Many synthetic chemists prize 4-(1H-pyrazol-1-yl)benzoic acid as an intermediate for heterocyclic compound development. In our own labs, we tested reactivity with a range of aryl halides in Suzuki couplings, and found the compound retains stability through multiple reaction cycles, even after prolonged bench exposure. The acid function allows for straightforward condensation and modification. Our product typically dissolves easily in DMF, DMSO, and light polar organic solvents, which matches the expectations of most synthesis workflows.

    Academic clients often mention that our material avoids the yellow tint seen in some commercial samples — a warning sign of decomposition or incomplete purification. We attribute this to our staged crystallization and early interception of off-spec fractions. It’s easier to discard a suspect crystallization than face emails about failed reactions later.

    Scaling up from gram to kilo lots, we have learned to navigate the hazards associated with higher thermal loads and exotherms during pyrazole formation. Our temperature probes and real-time tracking help catch these events before runaway reactions can threaten quality or safety. By keeping each vessel cleaned and pre-flushed, cross-contamination issues shrink to near zero — an experience-driven policy, not a regulatory checkbox.

    How Our Product Stands Out in Real Practice

    The world offers dozens of ways to make 4-(1H-pyrazol-1-yl)benzoic acid, but years in the industry reveal that routes using cheaper intermediates typically leave behind higher levels of process-related impurities. We decided early to invest in purer pyrazole and benzoic acid sources. The payoff shows up in purity and stability, not just on certificates, but in weeks-long real storage trials. Client feedback often points to shelf-life as a difference-maker — our product keeps its appearance and melting point over extended storage at ambient conditions, if kept dry and tightly sealed.

    Other manufacturers sometimes try to cut synthesis steps for speed. This practice can trap low-level impurities between reaction layers and spoil downstream applications. Among clients working in drug discovery, reactivity trends and failed purifications matter more than textbook yields or theoretical purity. That’s why our extra diligence in the purification and filtration stages matters. Clients report no surprises in later stages, so process development timelines stay on track.

    We refrain from adding anti-caking agents or extra stabilizers, since properly controlled crystallization ensures the natural stability of our powder. Adding anything artificial could introduce new unknowns in sensitive synthetic routes. After observing some batches of competitor material clump or yellow with time, we doubled down on maintaining low residual moisture and rapid drying after final isolation.

    Applications That Demand Reliability

    In the hands of experienced chemists, this compound finds broad application well beyond initial catalyst screening. Our pharmaceutical clients use it as a scaffold in the search for new kinase or protease inhibitors, and our academic contacts rely on its reactivity in coupling studies. Over time, we’ve received detailed feedback about downstream product purity and ease of purification, which speaks as much to the base material as to the synthetic plan.

    Quality matters most where reaction yields can hinge on starting material purity. For those synthesizing custom pyrazole derivatives, a rogue contaminant can create side-products that not only sap time but cast doubt over otherwise solid experimental work. Because we manufacture and analyze everything in-house, each lot includes an attached NMR and HPLC trace with the shipped item, so clients know precisely what enters their processes.

    For anyone pursuing scale-up or regulatory chemistry, batch homogeneity and traceability become real concerns. Our tightly controlled production parameters have enabled several clients to submit regulatory filings or scale their explorations to pilot scale without surprises. Scalability is not a feature but a practice — each scale jump starts with a process safety review, and our documentation covers every tweak or modification since our first batch.

    Typical User Feedback — And What We Learn From It

    Many of our repeat customers have commented on the lot-to-lot reproducibility. A customer synthesizing analogs for preclinical studies wanted the assurance that materials ordered months apart would behave identically. Over several seasons, we shipped over a dozen lots to the same group and have tracked their feedback. The only product-related change came from a minor temperature ramp adjustment in the crystallization step, adopted after analysis revealed a slightly narrower melting range could help cut purification steps downstream.

    Another client flagging trace yellowing in early shipments led us to implement periodic, not only batch-end, UV-VIS purity checks. Simple changes, like adjusting storage protocol in summer months, made a measurable difference in the color and shelf-life of subsequent batches. The learning goes both ways; open discussion with the research community helps us change and improve faster than closed-loop manufacturers absorbing only their own metrics.

    Over time, we noticed that requests for custom particle sizing or alternate grading grew as our customers’ methods evolved. Rather than treat these as one-off requests, we adapted our process to offer fractional sieving — splitting production into several particle size bands. Our default grade fits 99% of users, but specialty requests don’t face long lead times because we set aside time during bulk production for parallel size cuts.

    Supporting Advanced Research and Development

    Our relationship with cutting-edge research groups gave us early warning about growing interest in pyrazole-based ligands and advanced materials. Several research consortia now use our 4-(1H-pyrazol-1-yl)benzoic acid as a base unit in coordination chemistry, organic electronics, or next-generation functional materials. For catalytic work, the purity of the starting acid plays an outsized role in ligand-metal attachment, as residual benzoic acid or other byproducts can alter reactivity profiles and block desired transformations.

    Experiments with in situ CO2 capture and derivatization have turned up new uses. Some energy storage groups prefer this molecule for its sturdy benzoic acid anchor and the reactivity window offered by the attached pyrazole. Our QC and applications teams regularly dialogue with these customers to exchange stability data covering several climate zones. The product stands up not just in the lab, but in trade show demos and multi-month shipping—an outcome of real-world scrutiny.

    Recently, we supported a group working on photoresponsive materials who required documentation of photostability under extended UV lamp exposure. Our response blended historic batch performance data, full spectra, and practical advice on storage in amber bottles. Years of maintaining a consistent record across these metrics opened doors for new applications where lesser-known impurities could skew testing or performance.

    Differences That Matter in Your Lab and Ours

    The marketplace often focuses on price, but long-term chemists recognize that quality assurance brings real value, especially for demanding syntheses. 4-(1H-pyrazol-1-yl)benzoic acid from our facility avoids the variable crystallinity and color seen in some third-party offerings. While a casual glance may miss these subtleties, experienced users benefit from lower rates of solid-state variability: no unpredictable solubility, no hidden batch-to-batch surprises. That difference emerges, not just from analyses but also from stubborn adherence to cleanroom habits and batch logs with no skipped entries.

    Many alternative products rely on nonstandard isolation procedures or skip secondary recrystallization, a practice that saves time and paperwork but leaves the end-user dealing with side reactions and purification headaches. Because we run every step in-house — from raw material inspection to packaging — traceability becomes natural. Each bottle traces back to a batch date, operator, and validated instrument runs. Few complaints means our technical staff spend their time improving process steps, not troubleshooting external issues.

    Some customers compare analytical traces before placing bulk orders. Our transparency policy means we share not just summary sheets, but the full spectra: raw HPLC, NMR overlays, UV-VIS curves, and if needed, XRD patterns for crystallinity analysis. That approach came from hard-won trust, built over years of learning that a clean certificate doesn’t always tell the whole story.

    Solutions to Common Industry Challenges

    Many synthetic shops run into bottlenecks when lower-quality intermediates gum up a downstream pipeline. Early in our production, we dealt with issues from variable pyrazole supply, sometimes yielding excess residues during acidification. Our fix involved dual sourcing and a pretreatment protocol — the lessons from that challenge keep our batches within tight impurity specs, and our records show a noticeable drop in corrective actions.

    For large-scale users, storage and handling remain persistent pain points. Moisture ingress, ozone exposure, and photodegradation subtly chip away at purity, especially in humid climates. We worked with clients to refine packaging, introducing high-barrier inner liners and full light-blocking outer containers. Clients report improved stability even during months-long overseas transport.

    Communication closes gaps, especially when handling needs don’t match textbook conditions. Some labs require nitrogen blanketing; others blend immediately from stock into reactor lines. By discussing these practical setups, we have tailored not just documentation but delivery options, including nitrogen-filled packs or pre-scored easy-open bottles for glovebox entry.

    The Impact of Consistency on Research Outcomes

    Chemists running serial syntheses or multi-step processes know how a small difference in an intermediate can ripple through final product characteristics. Inconsistent raw materials waste more than time; they cast doubt over discovery claims. We see our job as protecting researcher time, reducing the number of confounding variables, and safeguarding against batch drift that might otherwise derail studies or process validations.

    Among users mining structure-activity relationships or scaling up for animal studies, the feedback rings clear: lots that behave the same way, regardless of ship date, are rare and valuable. This expectation informs every process adjustment we make. When a parameter change brings an unexpected melting point shift, we halt production, revisit SOPs, and rerun validation instead of releasing potentially unstable stock.

    Over time, these small disciplines bring higher yields, more reliable processes, and genuine cost savings for end users — fewer purification cycles, more predictable reactivity, and, ultimately, faster progress in development programs.

    Looking Forward — Continuous Improvement, Transparent Processes

    Improvement never stops at our plant. New analytical technologies, better environmental controls, and training protocols mean every year brings incremental gains. We pay attention to real feedback — whether about handling, application, or shelf-life — and fold it into regular reviews. Documentation matches lived experience; procedural updates come from practical observations, not distant offices.

    The result carries forward in every order: a compound with reliable purity, consistent reactivity, and full documentation from raw material through finished lot. We recognize each new batch is only as good as the care put into every production and inspection. Real competency comes from standing ready to answer detailed questions, share test results, and trace every bottle back to a verifiable history of diligence.

    We draw confidence from the hands-on work done daily in labs and production spaces. The lessons of the past decades reinforce a simple truth: for those relying on precise chemical building blocks, nothing replaces the rigor of process, the clarity of documentation, and openness to change — values that make our 4-(1H-pyrazol-1-yl)benzoic acid a trusted choice for those prioritizing both current application and future discovery.