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4-Difluoromethoxy-3-Hydroxybenzaldehyde

    • Product Name 4-Difluoromethoxy-3-Hydroxybenzaldehyde
    • Alias 4-DFM-3-HBA
    • Einecs 697-698-8
    • 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

    997322

    Productname 4-Difluoromethoxy-3-Hydroxybenzaldehyde
    Casnumber 886762-55-2
    Molecularformula C8H6F2O3
    Molecularweight 188.13
    Appearance White to off-white solid
    Meltingpoint 85-89°C
    Boilingpoint No data available
    Solubility Soluble in DMSO, moderately soluble in methanol
    Purity Typically ≥ 98%
    Smiles OC1=CC(OC(F)F)=CC=C1C=O
    Inchi InChI=1S/C8H6F2O3/c9-8(10)13-7-2-1-5(4-11)6(12)3-7/h1-4,12H
    Density No data available
    Synonyms 4-(Difluoromethoxy)-3-hydroxybenzaldehyde

    As an accredited 4-Difluoromethoxy-3-Hydroxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 4-Difluoromethoxy-3-Hydroxybenzaldehyde, labeled with hazard warnings and product details.
    Shipping **4-Difluoromethoxy-3-Hydroxybenzaldehyde** is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical is packaged according to international regulations for safe transport, labeled with hazard information, and typically shipped via ground or air freight, ensuring controlled temperatures and secure handling to prevent damage or contamination.
    Storage 4-Difluoromethoxy-3-hydroxybenzaldehyde should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat, and incompatible substances such as strong oxidizers and acids. Store at room temperature and protect from moisture. Use appropriate labeling, and ensure access is restricted to trained personnel. Handle under a chemical fume hood when dispensing or using.
    Application of 4-Difluoromethoxy-3-Hydroxybenzaldehyde

    Applications of 4-Difluoromethoxy-3-Hydroxybenzaldehyde in Industrial Manufacturing

    As a specialist producer of 4-Difluoromethoxy-3-Hydroxybenzaldehyde, we supply this key chemical intermediate for technically advanced manufacturing sectors that require stringent process control and traceable quality compliance. The following application segments illustrate established industrial deployment in line with international standards and the latest downstream integration trends.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This compound supports synthesis of select APIs within regulated environments where aromatic aldehyde units enhance molecular design. Its fluorinated and hydroxy functional groups support custom condensation or cyclization steps during non-steroidal anti-inflammatory drug (NSAID) and CNS-active therapeutics development. QC teams specify its use based on analytical traceability and process yield requirements for high-value small-molecule APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (API)
    • USP-NF and Ph. Eur. monographs (where applicable to finished APIs)
    • FDA DMF and EMEA CEP submission guidelines

    Typical usage ratio

    • 0.5–5.0% w/w as a key building block; precise loading adjusted based on route, target stage yield, and impurity control in multistep syntheses

    Downstream process integration

    • Charged directly to reaction vessels during stagewise synthesis—often in Mannich, Henry, or custom condensation reactions prior to crystallization/purification of the target API intermediate

    Final product types

    • High-purity pharmaceutical intermediates
    • Final stage APIs such as CNS modulators and advanced pain therapeutics
    • Reference standards for pharmaceutical QC

    2. Advanced Agrochemical Synthesis

    Chemical formulators in the agrochemical industry utilize this material in the development of advanced crop protection agents, particularly for specific fungicide scaffolds and novel herbicidal leads. The difluoromethoxy and aldehyde functions facilitate selective coupling or cyclization, enabling regulatory-compliant synthesis for high-performance agroactive compounds with improved metabolic stability.

    Industry compliance standards

    • FAO/WHO specifications for pesticide manufacturing
    • ISO 9001:2015 Quality Management System (ingredient traceability)
    • REACH registration (EU) where applicable as a chemical intermediate
    • Chinese National Standard GB2763 for maximum residue limits in food crops

    Typical usage ratio

    • 0.2–2.0% w/w in target fungicide or herbicide synthetic chains, fine-tuned by structure–activity demands, reactivity, and downstream tolerance studies

    Downstream process integration

    • Fed into flow or batch reactors during heterocyclic compound assembly, frequently as an early-stage fragment or for final aldehyde introduction before formulation and technical purification

    Final product types

    • Systemic fungicide actives
    • Herbicide technical concentrates for post-emergent weed control
    • Analytical reference substances for agrochemical QC

    3. Development of High-Performance Liquid Crystals

    In specialty materials manufacturing, integration of difluoromethoxy-functionalized aromatic aldehydes provides specific orientation properties critical for high-performance liquid crystal mixtures. Chemical engineers incorporate it as a precursor to enhance dielectric anisotropy and temperature response for thin-film transistor LCDs, relying on its unique electronic properties to diversify molecular design in proprietary nematic and smectic phase mixtures.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic materials
    • IEC 61249-2-21 (materials for printed wiring boards and electronic assemblies)
    • ISO 9001:2015 with full lot traceability for materials entering display production
    • Internal corporate supplier audits (Samsung, LG Display, BOE Technology)

    Typical usage ratio

    • 0.1–1.0% w/w as a liquid crystal precursor; effect screens and electrooptic curves dictate final loading per display technology generation

    Downstream process integration

    • Blended with other aromatic and fluorinated intermediates during advanced organic synthesis, introduced in early phase to design specific birefringence and viscosity properties prior to eutectic mixture formulation

    Final product types

    • High-resolution TFT-LCD and OLED display compounds
    • LC mixture components in television screen and mobile device assemblies
    • Product platform samples for electronics OEM qualification

    4. Fragrance and Aroma Intermediate Production

    The aromatic aldehyde structure, coupled with unique fluorine-substitution, positions this compound in the synthesis of modern aroma chemicals, especially for fragrance houses seeking new notes in floral and woody blends. Downstream manufacturers leverage its impact odor unit (IOU) enhancements via targeted condensation with alcohols or cyclic ketones, creating long-lasting scent molecules for fine fragrance and functional consumer products.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009
    • REACH registration (as intermediate)
    • ISO 9235 (Aromatic Natural Raw Materials for Fragrance Use)

    Typical usage ratio

    • 0.05–0.5% w/w in targeted aroma chemical syntheses; perfumers calibrate input based on reaction yield and olfactory evaluation protocols

    Downstream process integration

    • Introduced during stepwise fragrance chemical synthesis, particularly via acetalization or aldol-type reactions, followed by purification and QC according to analytical and sensory benchmarks

    Final product types

    • Fine fragrance intermediates for luxury perfumes
    • Aroma additives for personal care and home care brands
    • Stabilized synthetic flavors for food-safe applications (non-direct food additive; strictly as an ingredient for further processing)

    5. Materials for Specialty Polymer Additives

    Polymer manufacturers adopt this aromatic moiety in the development of functionalized additives, especially where chain transfer or side group modification imparts unique anti-fouling or durability properties. Its introduction supports the design of performance-enhanced polyesters, polyamides, or specialty resins used in coatings, membranes, and engineering plastics with tunable surface characteristics.

    Industry compliance standards

    • ISO 9001:2015 (polymer additive manufacturing)
    • REACH compliant for manufacturing and use as an intermediate
    • ASTM D256 (Standard Test Methods for Plastic Impact Resistance)
    • EPA TSCA Inventory (tracking U.S. commercial polymer ingredients)

    Typical usage ratio

    • 0.05–0.3% w/w in masterbatch or direct copolymerization feeds; technical teams optimize level for final polymer mechanical and chemical properties

    Downstream process integration

    • Added at oligomerization or functionalization stages—often during melt-phase extrusion or solution-phase backbone modification, before downstream compounding and molding

    Final product types

    • Anti-static engineering plastics
    • Specialty surface coatings for medical or filtration devices
    • Performance resin masterbatches for technical film and fiber
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    Certification & Compliance
    More Introduction

    4-Difluoromethoxy-3-Hydroxybenzaldehyde: Meeting High Standards in Chemical Synthesis

    Our Direct Approach to Quality and Consistency

    The day often starts with a review of our reactors, a double-check of parameter logs, and a look at the critical line for 4-Difluoromethoxy-3-Hydroxybenzaldehyde production. Every chemical manufacturer knows true consistency comes from hands-on attention and careful process control. At our production plant, pride runs deep in our direct oversight, not only in synthesis but across every purification and packaging step.

    This compound, commonly called by its full name or sometimes abbreviated for internal efficiency, holds a distinct presence in portfolios focused on building block chemistry. With the structure featuring a difluoromethoxy group at the para position and a hydroxyl group ortho to the formyl, its value emerges from the versatility these substitutions grant, especially in the context of pharmaceutical intermediate production.

    Characteristics Derived from Rigorous Synthesis

    Our units produce this item under exacting reaction controls. Production routes rely on decades-honed formylation and alkoxy substitution, yielding high purity batches that have withstood rigorous spectroscopic and chromatographic inspection. The product presents as a crystalline solid under ambient conditions, demonstrating stability over standard storage times. We set physical specs that hold up in the field: melting points hover within a tight range, and moisture content falls well below the threshold often triggering downstream issues.

    Supply lots often measure in the tens or hundreds of kilograms, with batch records reviewed alongside in-house NMR, HPLC, and GC data. Our spectra show clear, expected peaks—proving that no corners were cut in the wash steps or vacuum stripping. Each kilogram arises from repeated, continuous improvement cycles: pressure adjustments, filtration tweaks, and tailored drying protocols based on real-world observations, not generic guidance.

    Intended Uses: Designed with Practice in Mind

    Customers often ask what sets our 4-Difluoromethoxy-3-Hydroxybenzaldehyde apart. It starts with concrete supply to research-driven and pilot-scale drug manufacturers searching for a phenolic aldehyde that stands up through multiple synthetic steps. The major application lands squarely in the preparation of active pharmaceutical ingredient (API) building blocks, especially where electron-withdrawing difluoro groups and the reactivity of the hydroxy and formyl functionalities play unique roles.

    Some partners capitalize on the precise balance between the aldehyde’s reactivity and the electronic effects tuned by the difluoromethoxy group. This balance has driven demand for libraries targeting kinase inhibition, improved solubility in final candidates, and metabolic stability enhancements. The feedback cycle remains open: new process chemists supply queries about solubility, reactivity in oxidative conditions, or possible downstream protection strategies. Our technical team does not respond from arm’s length. We synthesize analogs, trial coupling reactions, and routinely perform custom purification runs to meet diverse needs while documenting process data for each adjustment.

    Academic groups have also reached out, focusing on its reactivity profile and suitability for method development. The ortho-hydroxyl enables route flexibility impossible with many other benzaldehydes. One team used our material in a novel condensation that succeeded where standard trifluoromethoxy derivatives failed due to steric clashes.

    What Matters in a Specialty Benzaldehyde

    Other aldehydes in the market, especially single-substituted fluorinated variants, tend to either break down during isolation or suffer from lingering side products caused by incomplete reactions at the methoxy group. Consistency across batches is critical. Even a minor change in impurity profile can alter a catalyst’s selectivity in downstream routes. We have reviewed competitor material where trace acids or halide contamination complicated hydrogenation or Grignard steps. Sourcing directly from our reactors connects users to a feedback loop where observed issues become improvements in the very next production lot.

    We often take calls from process chemists commenting on color variations in purchased intermediates. Off-tint batches—from competitors or small re-packagers—often trigger concern. We associate high purity with a bright, near-white appearance paired with unambiguous NMR and GC results that speak for themselves. This matters when every batch is earmarked for multi-step organic synthesis or scale-up to production intermediates.

    Our process avoids the use of acidic catalysts known to generate trace by-products. We run additional plate counts on chromatography columns to eliminate ambiguous co-elution. These steps might seem excessive, but our experience shows that even one poorly resolved impurity can disrupt a week’s worth of optimization work on the customer side. Reliable color, clean spectra, and minimal moisture aren’t just checkboxes; they’re the difference between wasted hours and productive synthesis.

    Differences from Competing Benzaldehyde Products

    Our experience showcases tangible differences in both product and support. Competing products arriving from purchased traders often vary from shipment to shipment, whether due to differences in precursor quality, inconsistent drying cycles, or bulk repackaging in suboptimal environments. Shipments arriving from our facility reflect a closed supply loop: raw material audits, calibrated reaction conditions, direct sampling, and air-tight post-purification transfer.

    Many in the field have encountered benzaldehydes that look fine on delivery yet degrade within weeks. Our packaging line operates under constant humidity monitoring. We choose non-reactive liners and dedicate containers for this compound alone. This prevents cross-contamination customers sometimes spot when third-party packers handle multiple open-bottle-fill lines. We regularly conduct stress tests, leaving reference samples open in controlled humidity chambers and tracking both visual and analytical parameters.

    Customers bring up trace residual solvents as a recurring concern with generic sources. Our purification techniques utilize tailored vacuum stripping protocols, confirmed by post-process headspace and residue analysis, to bring residual solvents down to far below pharmacopeial requirements. This direct approach eliminates the lingering solvent signals in NMR, which could mask close-lying product resonances or introduce baseline drift in LC analyses.

    Dealing with Real-World Ups and Downs in Production

    Production does not always go as planned in chemical manufacturing. Fluorinated benzaldehydes require careful control at every thermostat, every pH checkpoint, and every atmospheric transfer. Our team reviews every batch record detailing temperature excursions, agitation rates, and wash solvent turnover. We have encountered and solved issues like the formation of colored by-products during rapid quenching—a problem eliminated by reclaiming reaction mixture through stepwise cooling under nitrogen sweep. The ability to detect, diagnose, and correct subtle issues comes from daily hands-on engagement with the entire process.

    Once, during a particularly humid summer, we identified a problem with trace moisture causing caking in drummed product. Not content to add generic drying, we re-engineered the post-drying step to include in-line moisture monitoring, then adapted storage protocols to further minimize exposure from packing to warehouse loading. The effort paid off: recent supply runs have arrived overseas, passing customer fingerprinting tests for both physical and chemical specs on the first try.

    Supporting Advanced Development and Process Optimization

    Process development labs often approach us for support that extends beyond product delivery. We’ve provided reference samples, offered spectral assignments, and supplied detailed impurity profiles for project-specific route screening. One customer, exploring an oxidative coupling, struggled with over-reaction due to an unknown minor impurity found in material sourced elsewhere. Upon switching to our product—with documented ultra-low contaminant profiles—the group reported a sudden rise in target yield and resolution.

    Another testament comes from a long-time materials science collaborator, who required precise stoichiometry in polymer synthesis. Slight variability in the starting aldehyde led to irregular polymer weight distribution. After switching supply, those variations disappeared in successive trials, enabling cleaner, reproducible materials for downstream electronic studies.

    Feedback from such partnerships cycles directly into process improvement. If an academic group stumbles across an unusual impurity under certain reaction environments, they send us the findings, and we tweak our purification to address it at source. Listening pays off, and our repeat clients value this hands-on, cyclical relationship built on practical details, not marketing claims.

    Insights from Long-Term Operation: Earning Trust through Technical Depth

    It takes years, not months, to gain the experience necessary to anticipate challenges with fine chemicals like 4-Difluoromethoxy-3-Hydroxybenzaldehyde. Each structure has quirks revealed only through repeated synthesis, failed runs, customer feedback, and real-world process refinement. For this compound, the dual impact of the difluoromethoxy and hydroxy substituents complicates both the synthesis and the downstream chemistry.

    We remember lessons from regulatory and process audits where tiny deviations in impurity control forced last-minute batch reprocessing. Instead of minimum-spec shipments, we adopted ongoing training and analytical back-ups. Our operating staff understand both the chemistry and the reasons behind it. They know that a missed endpoint titration or sluggish agitation could cascade into downstream customer issues days or weeks later.

    Over the years, incoming regulatory demands have shaped our documentation and batch traceability. Every outgoing batch can be linked back to starting materials, analytical runs, and even environmental controls during storage and logistics. When regulators check cleaning validation protocols or documentation chains, our data stands up to scrutiny not as a favor, but as the expected level of diligence built into every shift.

    Facing Future Challenges in Benzaldehyde Manufacturing

    Growing environmental and safety scrutiny places extra burdens on chemical operations. For this compound, that means close monitoring of solvent emissions, adherence to updated handling protocols, and pre-emptive safety reviews with every process iteration. Our plant modified exhaust management after identifying an uptick in formyl-related VOCs during scale-up; scrubber efficiency improved, and community concerns eased. On the worker safety side, enhanced PPE and updated exposure monitoring now form standard practice for all operators handling fluorinated reagents.

    We also confront global sourcing challenges, from raw material price spikes to regulatory shifts impacting certain reagents. By investing directly in raw material audits and sustaining relationships with core upstream suppliers, we guard against abrupt cost surges or forced last-minute reformulation. This direct engagement with both chemical process and supply market has proven essential.

    Supply chain resilience often becomes an abstract talking point elsewhere, but for us it plays out in physical buffers, backup sourcing plans, and on-site pre-blending where applicable. On several occasions, these measures have kept product arriving at customer sites even as industry-wide bottlenecks slowed competitors.

    Building Confidence, One Batch at a Time

    Trust comes only with repeated, problem-free experience. End users return to our supply not just for a compound specification, but for predictability and technical follow-up. We do not see ourselves as mere suppliers. We take pride in being manufacturing partners who offer direct, factory-rooted support at every stage—a value growing ever more important as the demands for reliability, documentation, and adaptability rise across the specialty chemicals sector.

    Facility staff recognize that a quality aldehyde goes beyond dry numbers. The invisible factors—the smooth pour from the drum, the texture after storage, the clarity of the solid fraction, the absence of lagging extraneous aroma—speak volumes. Every improvement earned in-house translates to a smoother process for those relying on our output. That depth of engagement and willingness to adapt according to practical user feedback sets our 4-Difluoromethoxy-3-Hydroxybenzaldehyde apart.

    Summary: Real Manufacturing Experience, Real Solutions

    From direct synthesis oversight and careful purification, our 4-Difluoromethoxy-3-Hydroxybenzaldehyde offers a tool that chemists and process engineers can rely on for high-value, research, and commercial-scale operations. It supports discovery, accelerates optimization, and withstands the scrutiny of both end-users and regulators. Through every order, we commit to keeping batches consistent, open to improvement, and responsive to challenges that arise not in theory, but in the heat of actual process work.

    Chemistry keeps evolving. The foundation remains the same: attentive people, a willingness to learn from each batch, and the discipline to apply those lessons without compromise. Our pride in this approach runs through every kilogram of 4-Difluoromethoxy-3-Hydroxybenzaldehyde that leaves our site, destined for those who expect not just a product, but a partner invested in their process success.