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(4-Pyrazol-1-Ylphenyl)Methanol

    • Product Name (4-Pyrazol-1-Ylphenyl)Methanol
    • Alias 4-(1H-Pyrazol-1-yl)benzyl alcohol
    • Einecs 661-131-3
    • 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
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    Specifications

    HS Code

    309872

    Iupac Name (4-pyrazol-1-ylphenyl)methanol
    Molecular Formula C10H10N2O
    Molecular Weight 174.20 g/mol
    Cas Number 41624-92-6
    Appearance White to off-white solid
    Melting Point 118-122°C
    Boiling Point Decomposes before boiling
    Solubility In Water Slightly soluble
    Density 1.21 g/cm³ (estimated)
    Smiles C1=CN(N=C1)C2=CC=C(CO)C=C2
    Inchi InChI=1S/C10H10N2O/c13-8-9-2-4-10(5-3-9)12-7-1-6-11-12/h1-7,13H,8H2
    Pubchem Cid 2889731

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

    Packing & Storage
    Packing 250g of (4-Pyrazol-1-Ylphenyl)Methanol supplied in a sealed, amber glass bottle with tamper-evident cap and detailed labeling.
    Shipping (4-Pyrazol-1-ylphenyl)methanol is shipped in tightly sealed containers to prevent moisture and contamination. The chemical should be handled in accordance with relevant safety regulations. It may require labeling as a laboratory chemical and transported under ambient temperature unless specified otherwise. Ensure proper documentation and compliance with local and international shipping guidelines.
    Storage (4-Pyrazol-1-ylphenyl)methanol should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizing agents. Proper labeling and storage in accordance with safety regulations are essential. Use in a laboratory equipped with appropriate chemical handling protocols and personal protective equipment.
    Application of (4-Pyrazol-1-Ylphenyl)Methanol

    Applications of (4-Pyrazol-1-Ylphenyl)Methanol in Industrial Manufacturing

    (4-Pyrazol-1-ylphenyl)methanol finds application in advanced synthetic pathways across pharmaceutical, agrochemical, specialty pigment, and polymer additive manufacturing sectors. As the original producer, we supply this raw material to firms implementing precise synthesis protocols and demanding regulatory adherence. Below, we detail core downstream applications with technical integration notes, compliance requirements, industry-specific usage ratios, and typical finished goods.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this compound as a key starting material or intermediate when building heterocyclic frameworks in antihypertensive and anti-inflammatory drug development. The unique pyrazole-phenyl structure facilitates selective derivatizations, enabling robust lead optimization in small molecule APIs. Our large-scale shipments fit solid-phase and solution-phase synthesis routes, integrating readily in multi-step manufacturing lines for regulated healthcare end-products.

    Industry compliance standards

    • ICH Q7 GMP Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <1078> Good Storage and Shipping Practices
    • 21 CFR Part 210/211 (U.S. FDA regulations)
    • EDQM CEP Certificate of Suitability (as applicable to route)

    Typical usage ratio

    • Used at 0.2–1.5 molar equivalents depending on the specific API scaffold
    • Adjusted for step yield and pharmacophore modification needs
    • Integration rate optimized based on impurity control and final batch yield

    Downstream process integration

    • Introduced at key cyclization or N-alkylation step in heterocycle synthesis
    • Used in both batch and flow reactor schemes
    • Purified by crystallization or chromatography prior to further conversion

    Final product types

    • Antihypertensive small molecule APIs
    • Anti-inflammatory pharmaceutical actives
    • Experimental CNS (central nervous system) drug candidates for clinical trials
    • Pyrazole-based medicinal chemistry screening compounds

    2. Agrochemical Synthesis Building Block

    Leading agrochemical producers rely on this material for constructing selective fungicide and herbicide intermediates requiring the pyrazole motif. Its high reactivity and defined substituents facilitate functional group conversions under mild to moderate catalytic conditions. Manufacturer data supports safe, reproducible usage across pilot and commercial production lines targeting active plant protection agents.

    Industry compliance standards

    • FAO/WHO JMPR specifications for active substances
    • EU REACH Annex VII-VIII Data Requirements
    • ISO 9001:2015 certified quality management systems
    • Regulation (EC) No 1107/2009 (placing plant protection products on the market)

    Typical usage ratio

    • Applied at 0.7–1.3 equivalents relative to key acyl or aryl halide reactants
    • Adjusted for catalyst loading and target impurity profile
    • Ratio fixed per downstream bioactivity trial route

    Downstream process integration

    • Fed into stepwise condensation or arylation unit operations
    • Processed in closed systems with automated metering
    • Monitored via in-process HPLC/GC to ensure conversion and purity prior to formulation

    Final product types

    • Pyrazole-containing fungicide active ingredients (e.g., SDHI class)
    • Systemic herbicide intermediates for cereal crop protection
    • Finished agrochemical actives for granules and emulsifiable concentrates
    • Intermediate formulations for pilot-scale biological evaluation

    3. High-Performance Pigment Synthesis

    Specialty pigment manufacturers utilize this compound to engineer high-stability azo and heteroaromatic colorants, offering excellent thermal and weather resistance for industrial coatings and printing inks. Its aromatic hydroxymethyl group enhances reactivity in diazotization and coupling chemistries. Production uses strictly controlled conditions to meet end-use safety and color fastness standards required by OEM automotive, textile, and industrial ink clients.

    Industry compliance standards

    • EN 71-3 Toy Safety Standard for migration of certain elements
    • REACH Regulation (EC) No 1907/2006 Annex XVII (restricted substances)
    • ISO 18451-1:2019 Pigments and extenders – Terminology
    • AP89:1 (BfR Safety Assessment for printing inks)

    Typical usage ratio

    • Adopted at 1.0 equivalent in diazotization and azo-coupling reactions
    • Adjustment performed for shade strength and tinctorial yield
    • Final usage typically between 2–6% of total pigment input mass

    Downstream process integration

    • Charged into batch pigment reactors after primary diazonium salt synthesis
    • Integrated in wet synthesis routes with temperature/time profile controls
    • Filtered and milled post-coupling for particle size uniformity

    Final product types

    • High-stability azo pigments for automotive OEM coatings
    • Lightfast pigments in high-precision textile dyeing
    • Industrial printing ink pigments
    • Plastisol pigment masterbatches

    4. Functional Polymer Additives

    Polymer compounding specialists introduce this material as a functional monomer or reactive modifier during the synthesis of engineered plastics and elastomers. The compound’s alcohol moiety reacts efficiently with isocyanate or epoxy monomers, supporting the fabrication of polymers with enhanced impact resistance, UV stability, and processability, especially for advanced electronics and automotive interior components.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems for polymer production
    • UL 94 Flammability Standards for plastics
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Annex XVII chemical restrictions

    Typical usage ratio

    • Incorporated at 0.5–2.0 wt% relative to main polymer feed
    • Ratio optimized for targeted crosslinking density and mechanical properties
    • Dosing dependent on melt index and final polymer structure

    Downstream process integration

    • Fed into twin-screw extruders during reactive extrusion
    • Used in bulk polymerization or solution casting
    • Pre-mixed with initiators or chain-transfer agents for uniform dispersion

    Final product types

    • UV-stabilized engineering plastics (e.g., polyurethanes, polyesters)
    • Electronics-grade encapsulation resins
    • Impact-modified interior automotive parts
    • Specialty elastomers for technical sealing applications
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    Certification & Compliance
    More Introduction

    Introducing (4-Pyrazol-1-Ylphenyl)Methanol: A Chemist’s Perspective

    A Chemist’s Year-Round Companion

    Chemistry labs run on certainty, yet discovery steps in every day. After working through thousands of synthesis batches and development projects, I’ve spent more hours than I can count measuring, purifying, and applying (4-Pyrazol-1-ylphenyl)methanol. This is one of those niche intermediates that rarely makes the front page, but it shapes a lot of what modern chemistry can achieve behind the scenes. From the first multi-gram scale up to tonnage in our plant, this compound has carved out a unique role for itself.

    Everyday Utility in Research and Industry

    Let’s talk about where this product excels. The core structure — a pyrazole ring fused to a phenyl backbone, with a methanol group attached — gives it just the right balance for a range of building-block applications. It enables access to substituted pyrazole chemistry without dragging in the complexity or instability found with more aggressive intermediates. Years of trial and error taught us that (4-Pyrazol-1-ylphenyl)methanol holds up, stays stable, and reacts predictably in both high-temperature and sensitive catalytic environments.

    Many clients start with exploratory projects and expansion into method development. Medicinal chemists and agrochemical developers put their trust in this molecule for the preparation of advanced intermediates, especially when the final targets contain heterocycles or need precise functionalization next to an aromatic ring. It’s earned its place by being tolerant of the conditions those teams throw at it, whether coupling reactions, protection-deprotection schemes, or direct modifications.

    Model and Specifications

    We manufacture several models to serve both research and industrial needs, but our most-requested grade features high above 98% purity, white to off-white solid appearance, and minimal contaminant profile. We keep residual solvents and byproduct levels tight—every synthetic batch goes through rigorous HPLC and NMR analysis, so no surprises derail downstream workflows.

    What really counts in manufacturing is batch consistency and traceability. One overlooked error in material handling — moisture, oxidants, impurities — can cascade into all kinds of further headaches at scale. What I’ve learned is there is no substitute for methodical isolation, vacuum drying, and proper packaging. Tanks, reactors, dryers, and final product drums all play a role in guaranteeing a batch of (4-Pyrazol-1-ylphenyl)methanol meets the needs it was manufactured for.

    Standing Apart from Similar Building Blocks

    A natural question arises: why pick this specific compound rather than one of the many similar pyrazole derivatives? From my own lab work before moving to plant operations, I remember the headaches posed by isomeric products or those with unstable leaving groups. Clients often complain that some building blocks with halogenated phenyl groups or reactive aldehydes force compromises — yield problems, safety flags, downstream reactivity issues.

    (4-Pyrazol-1-ylphenyl)methanol hasn’t caused those sorts of bottlenecks. The methanol moiety brings a degree of synthetic flexibility; it opens up protection and activation pathways without becoming a liability in the reactor. That means you can apply straightforward oxidation, esterification, or coupling chemistry as projects demand. In our facility, we’ve consistently seen higher conversion rates and less fouling than with many other phenyl substituted pyrazoles. Minor differences in solubility and handling might seem trivial, but they add up in kilo-lab and pilot-scale settings.

    Direct Experience with Usage

    Few things teach as much as hands-on experience. In my years scaling up this product, I’ve taken part in both column chromatography purifications for research-grade material and continuous crystallization for bulk runs. I’m always struck by the ease with which it dissolves in most common polar organic solvents — ethanol, acetonitrile, ethyl acetate — making reaction optimization smoother compared to bulkier or more hydrophobic analogues.

    Our technical support team gets questions ranging from gram-level research runs to 200-liter reactor protocols. No matter the scale, this molecule tolerates both acidic and basic conditions and remains manageable under the inert gas blanketing that customers often request. We’ve shaved hours off workup steps by optimizing the product for filtration and drying, a detail that matters for any operation trying to improve scheduling and throughput. One of my colleagues who runs the kilo-lab has repeatedly commented that it’s rare to see such straightforward filtration and consistent crystal morphology on scale.

    Ideal for Synthesis and Scale-Up

    This compound enjoys a unique place, striking a balance between reactivity and manageability. For process chemists, each added functional group tends to bring extra risk—instability, sensitivity, unexpected side reactions, or troublesome byproducts. Here, you get consistent behavior batch after batch. I’ve looked back at years of stability studies; this molecule holds up to transport, long-term storage, and doesn’t degrade or discolor quickly like some others in the same class.

    As manufacturers, keeping a clean product profile is critical for downstream hydrogenations, C–N couplings, or oxidation reactions common in the pharmaceutical sector. Compared to aldehyde-containing pyrazole intermediates, you won’t face polymerization or degradation during work-up. Teams also leverage this molecule in boronic acid or Suzuki coupling precursor synthesis, where the primary alcohol group cleans up easily after functionalization.

    Minimizing Process Variability

    Any production manager will vouch for the importance of minimizing variables, especially when working with building blocks that might trace their impact through several production stages. For us, (4-Pyrazol-1-ylphenyl)methanol’s lack of unstable functional groups not only streamlines compliance around hazardous materials rules but means less risk during both shipping and process design. Simple alcohol handling procedures and standard containment approaches get the job done safely.

    When customers scale up routes from bench to bulk, repeatability is everything. We’ve supported process validation studies where every lot of (4-Pyrazol-1-ylphenyl)methanol delivered matched prior analytical profiles over months, giving production and QA teams more breathing room. This reliability means untold man-hours saved and a better working relationship between our teams and the chemists working toward project deadlines.

    A Role in Specialty Synthesis

    Over the years, the shift in custom synthesis has moved more toward functional complexity, not just volume. Projects involving antibody-drug conjugates, new crop protection active ingredients, or targeted catalysts often depend on specialized intermediates. Here, pyrazole chemistry shines, especially when substituted in a manner that supports varied downstream reactivity.

    Having firsthand experience working with contract research organizations, I can say (4-Pyrazol-1-ylphenyl)methanol is prized for its ability to act as a plug-and-play moiety. You don’t run into purification headaches or unpredictable instability midstream. Its solid-state stability, reasonable melting point, and compatibility with most common process solvents keep both the chemists and the plant team out of trouble.

    Problems Users Face and How We Address Them

    Quality control and material traceability get mentioned most often in calls from users. Even tiny deviations in purity or residual solvent content can grind campaigns to a halt. We’ve developed closed-loop feedback with our analytics lab to detect even small impurities before they reach a drum or bottle. Several times we’ve caught polymorph transitions or unexpected byproduct formation in time to keep a client’s project on track.

    Another common concern comes during upscaling. A material that handles well in a glovebox may not behave the same in a larger reactor. We learned early on to optimize crystallization and drying to reduce fines formation — nothing slows down a plant more than slow filtration or failure to reach a proper specification on particle size. Walking the plant floor and watching how operators handle each drum, scoop, or lot gives perspective that’s hard to find in a book.

    Color change or instability under storage has flagged trouble for other intermediates. By switching to inert-atmosphere packing and controlling moisture exposure, we’ve kept (4-Pyrazol-1-ylphenyl)methanol bright, free-moving, and ready for use even over extended storage.

    Supporting Advanced Chemistry with Practical Know-How

    The chemical industry may love big breakthroughs, but progress often hangs on the quiet reliability of intermediates like (4-Pyrazol-1-ylphenyl)methanol. I’ve collaborated with process development teams optimizing C–H activation, cross-coupling reactions, and heterocycle expansion — all areas needing intermediates that behave the same, week after week. Our batch records run deep; nothing gets approved without a complete trail from raw input tracking to release testing.

    Instead of just promising flexibility, we enable our customers’ teams to focus on what matters—rational design, smart scale-up, and rapid troubleshooting. Both our production managers and R&D liaisons visit client sites, supporting their process improvements and training new chemists to get the most value from this building block. Whether talking shop over video call or troubleshooting on the plant floor, we approach each request as a chance to keep chemistry moving forward.

    Differences from Other Solutions: What Experience Has Taught Us

    Within the broad pool of pyrazole derivatives, every structural modification changes a compound’s handling and downstream value. Some analogs come with bulky substituents or halogen groups, raising flags over solubility, environmental impact, or regulatory handling. Direct competitors often struggle to match our lots on purity, reproducibility, or downstream reactivity. Whenever we’ve benchmarked against these, our analytical teams found cleaner spectral profiles, less need for reprocessing, and quicker process turnaround using our (4-Pyrazol-1-ylphenyl)methanol.

    Process efficiency matters just as much. The methanol group offers chemists an entry point for further derivatizations — oxidation to aldehydes or carboxylic acids, protection as silyl ethers, or direct arylation — without undue risk of side reactions. More reactive intermediates tend toward instability or regulatory scrutiny; less reactive ones slow down campaigns, burning time and budget. In practice, we enable a balanced route to downstream derivatives without saddling end-users with extra purification or process controls.

    Collaborative Problem Solving in Action

    From the earliest projects to the present, we’ve partnered with clients to troubleshoot new reaction schemes and scale-up pathways. This may look as simple as adjusting solvent options for more efficient dissolution or supporting bespoke drying protocols to meet unique regulatory standards. Sometimes it involves developing a completely new isolation protocol to support a client’s unique particle size distribution.

    Experience also taught us the value of sharing data—spectral, chromatographic, and stability profiles—with both academic and production partners. Whether supporting a doctoral student’s exploration of novel cyclization chemistry or partnering with an industrial innovation team, we believe in transparent, data-driven support. It’s the small, practical steps that allow our customers to blaze new trails without legacy problems from unstable or unpredictable building blocks.

    Looking at the Horizon: The Evolution of Use Cases

    We’re seeing new applications for (4-Pyrazol-1-ylphenyl)methanol each year. Some involve greener synthesis—switching away from more toxic or persistent building blocks — others grow from the speed with which this material adapts to bioconjugation, polymer modification, or electronic material innovation. Our decades in the plant and on the bench made it clear: today’s chemical landscape moves quickly, and the right building block can still make or break a campaign.

    There’s no magic bullet, but I’ve watched how this molecule fits into a flexible, modern chemical toolkit. It’s gone into kilogram-scale pilot projects, high-throughput synthesis, and late-stage process optimizations. Each time, the lessons carry forward, keeping chemistry safer, more predictable, and adaptable to changing project needs.

    Value Grows from Experience, Not Just from Purity

    Some manufacturers focus solely on the certificate of analysis — the numbers that show up on paper. That matters, but it’s only part of the equation. Learning from real-world feedback, seeing where products perform under fire (and where they don’t), and responding quickly to both routine and oddball issues built our reputation with users of (4-Pyrazol-1-ylphenyl)methanol.

    We’ve fielded urgent calls from client plants dealing with process slowdowns, debris buildup in reactors, or batch discolorations. Each time, direct support made the difference. Sometimes the answer came from a tweak to a process variable; sometimes it called for shipping a fresh lot with tighter moisture control or consulting on a purification step. Gaining this firsthand knowledge only comes from standing behind your material, not just shipping out drums.

    The Quiet Backbone of Reliable Chemistry

    (4-Pyrazol-1-ylphenyl)methanol doesn’t make headlines, yet workhorses like it keep large-scale and high-value syntheses feasible, efficient, and cost-effective. The pride in manufacturing stems not just from an on-spec product, but from knowing, after years of feedback, collaboration, and improvement, that the material solves more problems than it creates. That’s the real measure of value in this business — the ability to adapt, troubleshoot, and deliver where it counts.

    Every batch stands as the result of lessons learned, process improvements, operator experience, and a relentless focus on end-user needs. For those searching for a dependable pyrazole building block, one that gives room for creative chemistry without sacrificing control, (4-Pyrazol-1-ylphenyl)methanol has proven its worth over decades of real-world use. My career has been shaped through countless projects, tight schedules, and daily problem solving. Feedback and results from real chemists and process engineers drive every improvement we make, shaping the product you find today.