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4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde

    • Product Name 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde
    • Alias 4-Hydroxy-3-(trifluoromethyl)salicylaldehyde
    • Einecs 241-266-5
    • 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

    678564

    Chemical Name 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde
    Cas Number 402-28-0
    Molecular Formula C8H5F3O2
    Molecular Weight 190.12
    Appearance White to off-white solid
    Melting Point 96-99°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC1=CC(=C(C=C1C=O)O)C(F)(F)F
    Storage Conditions Store in a cool, dry, well-ventilated place away from incompatible substances
    Synonyms 3-(Trifluoromethyl)-4-hydroxybenzaldehyde

    As an accredited 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde 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 25 grams of 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde, sealed with a screw cap and labeled with hazard information.
    Shipping 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled according to regulatory standards. During transit, the chemical is stored away from incompatible substances, heat, and direct sunlight. Shipments comply with relevant chemical transportation regulations to ensure safety and product integrity.
    Storage Store **4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde** in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizers. Keep in a cool, dry, well-ventilated area. Handle under inert atmosphere if possible to prevent oxidation. Clearly label the container and ensure it is stored in accordance with all local regulations and safety guidelines for hazardous chemicals.
    Application of 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde

    Applications of 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde to a range of downstream industrial sectors requiring high-purity aromatic intermediates. Below, we detail key application channels, processing requirements, compliance standards, and final product types informed by our supply experience to fine chemical, pharmaceutical, agrochemical, and specialty material markets.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical producers incorporate this material as a building block during multi-step synthesis of APIs, particularly in the manufacturing of drugs that require trifluoromethyl-substituted phenolic frameworks. The aldehyde group provides a reactive position for condensation, coupling, or cyclization, enabling construction of advanced molecular scaffolds. Our quality control ensures batch-to-batch consistency to meet stringent pharma requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Regulation (EC) No 1907/2006 (REACH) Registration
    • USP/EP monograph adherence in downstream applications
    • ISO 9001 certified production system

    Typical usage ratio

    • 0.1–1.5 molar equivalents based on targeted condensation or Grignard steps
    • Adjustment according to purity and molecular yield targets set in process validation

    Downstream process integration

    • Enters at the intermediate synthesis stage after preparation of substituted benzene rings
    • Reacted with amines or hydrazines for API precursor formation
    • Used in subsequent cyclization under acidic or neutral conditions

    Final product types

    • Central nervous system drug intermediates
    • Fluorinated anti-inflammatory agent precursors
    • Anti-infective bulk actives
    • Experimental oncology molecules

    2. Agrochemical Synthesis Intermediate

    Crop protection manufacturers leverage this trifluoromethylated aldehyde for the design of herbicides and fungicides, as its electron-withdrawing nature enhances biological activity in fluorine-containing agrochemicals. Used in key coupling reactions and ring-forming steps, it allows downstream producers to introduce fluorinated building blocks in final molecules that must pass regulatory residue and stability requirements.

    Industry compliance standards

    • FAO/WHO specifications for pesticide ingredients
    • OECD Principles of Good Laboratory Practice (GLP)
    • China’s GB 2763 Maximum Residue Limits for Pesticides
    • ISO 17025 qualified analytical compliance

    Typical usage ratio

    • 1.0–2.0 molar equivalents per target molecule depending on synthesis needs
    • Ratio adjusted in scale-up to minimize unreacted starting material in waste streams

    Downstream process integration

    • Utilized in aromatic nucleophilic substitution to introduce CF3 groups
    • Acts as a coupling partner in Suzuki or Wittig reactions with heterocycles
    • Integrated late in process before formulation of technical-grade products

    Final product types

    • Trifluoromethylated azole fungicides
    • Systemic herbicide active ingredients
    • Seed-treatment micro-ingredients
    • Specialty plant growth regulator precursors

    3. Advanced Polymer and Resin Modifier

    High-performance polymer manufacturers use this aromatic aldehyde as a modifier to enhance chemical resistance, UV stability, and processability in specialty polyesters, epoxies, and resin formulations. Its trifluoromethyl substituent imparts hydrophobicity and dimensional stability, which is critical in demanding electronic and protective coating materials. In this scenario, accurate stoichiometry and compatibility testing are key to successful integration with the polymer matrix.

    Industry compliance standards

    • RoHS Directive (EU) 2011/65/EU heavy metals and halogen content
    • UL 94 fire safety standards for plastics
    • ISO 14001 environmental management in production
    • ASTM D638 for mechanical testing of plastics

    Typical usage ratio

    • 0.5–5.0 wt% as a functional monomer or chain modifier
    • Adjustment based on desired level of hydrophobicity and material compatibility studies

    Downstream process integration

    • Added during pre-polymerization blending prior to monomer conversion
    • Introduced to resin kettle with other additives, under controlled temperature and pH
    • Reacted through aldehyde or phenol group with polymer backbone via condensation or addition reactions

    Final product types

    • High-end electrical insulation films
    • Anticorrosive epoxy floor coatings
    • Optically clear polymer films
    • Adhesion promoters in electronics encapsulants

    4. Fine Fragrance and Aroma Chemical Intermediate

    Producers of aroma chemicals choose this compound as an intermediate for the synthesis of high-value fragrance ingredients, especially in developing novel aldehydic and phenolic notes for perfumery. The presence of the trifluoromethyl group enables stability and unique olfactory characteristics, which are essential in complex fragrance blends and specialty aroma offerings.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Guidelines
    • EU Regulation 1223/2009 on cosmetic safety
    • REACH registration for ingredient traceability
    • ISO 9001 traceable supply chain management

    Typical usage ratio

    • 0.2–2.0 wt% as an intermediate in multi-step fragrance synthesis
    • Adjusted according to target aroma profile and shelf-life requirements

    Downstream process integration

    • Subjected to reduction, oxidative or condensation reactions to produce fragrance aldehydes or ketones
    • Blended with other functional intermediates before fragrance compounding
    • Processed in controlled environments to safeguard olfactory purity

    Final product types

    • High-stability perfume base notes
    • Specialty aldehyde aroma chemicals for fine fragrances
    • Flavor and fragrance intermediates for compounded products
    • Scented home care formulations
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    Certification & Compliance
    More Introduction

    4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde: A Manufacturer’s Perspective

    Understanding the Material and How We Produce It

    4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde ranks high among our specialty aromatic aldehydes. Over the years, we’ve refined our process to deliver this compound with tight control over purity and moisture levels, avoiding contamination from related byproducts. The distinct presence of both a trifluoromethyl and hydroxy group on the benzene ring brings unique reactivity, making the molecule indispensable in several fine chemical applications.

    Our plant’s production lines focus on consistently delivering high assay levels. The material emerges from a multi-step synthesis, where careful reagent selection and controlled conditions help suppress impurities. After the main reaction, our purification process — painstakingly tuned — removes side products common in aromatic aldehyde chemistry, including residual starting aromatic acids and tri-substituted phenols. Filtration and drying steps are engineered for stability, so the product arrives with minimal moisture content, supporting longer shelf life and faster downstream integration.

    Model and Specifications That Matter in Daily Manufacturing

    Across our output, the main specification we target is purity above 99%. Each batch runs through both GC-MS analysis and wet chemistry verification to confirm low levels of common side substances. The crystalline powder typically presents a pale color—an indicator that oxidation and degradation have remained in check. Melting point lies consistently between 108°C and 111°C.

    Moisture, although a minor concern for stable aldehydes, can pose issues in longer storage or when clients require absolute dryness. We keep water content below 0.2% by employing vacuum drying and specialized packaging. Particle size is controlled through sieving and milling but is usually a secondary concern unless customers require rapid solubilization. Bulk density lands within predictable limits, supporting easy input to reactor feed systems. Our packaging team handles filling in a dedicated low-humidity zone to block atmospheric moisture and airborne contaminants, an aspect that makes a difference for users running sensitive transformations.

    Why Chemists Seek Out This Benzaldehyde

    Our experience shows that 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde finds its strongest demand from pharmaceutical and agrochemical sectors. The compound’s core structure provides both electron-donating (hydroxy) and electron-withdrawing (trifluoromethyl) effects, enabling selective transformations and building highly functionalized intermediates. Medicinal chemists routinely pick this aldehyde for synthesizing target molecules where a strong lipophilic group coupled with an activated aldehyde function is required. It’s not rare for research teams to request custom runs if their route needs extra regulatory scrutiny or enhanced traceability in the supply line.

    Beyond drug discovery and crop science, research labs push the product’s utility in new directions such as materials science and specialty dyes. The interplay of the trifluoromethyl and hydroxy functionalities opens doors in constructing ligands and tuning electronic behavior in polymer scaffolds. We follow developments from academic groups, adapting our process when new research demands even tighter impurity control.

    Comparing With Standard Aromatic Aldehydes

    Having worked with a range of aromatic aldehydes, the distinctions become clear both on paper and in practice. Common variants like plain 4-hydroxybenzaldehyde lack the fluorine-driven effects seen in the trifluoromethyl model. When a synthetic route requires resistance to metabolic oxidation, or reactivity modulation, the trifluoromethyl group’s presence makes an obvious difference. Chemists who’ve tested regular para-hydroxybenzaldehyde often run into issues with over-reactivity or solubility mismatches in nonpolar media. Our product handles those hurdles by altering both hydrophobic and electronic characteristics, permitting reactions in a broader series of solvents and offering more robust intermediate stability.

    From a production standpoint, introducing a trifluoromethyl group makes manufacturing more complex. The step requires specialized handling of fluorinated reagents and demands corrosion-resistant equipment, especially in the presence of acids generated during synthesis. Attention to safety and continuous training is non-negotiable in our plant, since these reagents don’t forgive procedural drift. These realities also affect cost and supply timelines, and clients with experience in the material’s chemistry understand why this benzaldehyde stands apart on both pricing and reactivity.

    Market Drivers and Application Demands: First-Hand Observations

    Market shifts in pharmaceutical building blocks influence our planning. Just a few years back, supply disruptions for fluorinated starting materials sent ripples through global supply chains, catching many fine chemical firms off guard. We invested in backward integration and long-term contracts for precursor supply, protecting both our production and client projects from unexpected bottlenecks. Our team not only monitors market price movements but also maintains an active dialogue with end-users, learning which application processes put the most stress on product quality.

    In process development discussions, formulation teams often raise questions about substitution effects on reaction mechanisms. We support these teams with technical documentation, and if needed, direct batch-testing in collaborative settings. The hydroxy group’s placement impacts reactivity in key transformations like nucleophilic additions, condensations, and acylation. Our process chemists test reaction outcomes using our product under various conditions—neutral, acidic, or basic environments. This allows us to recommend specific grades or offer advice on pre-treatment steps for maximum synthetic flexibility.

    Technical Challenges and Solutions

    Synthesis of 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde brings a distinctive set of hurdles. Maintaining high chemical purity while controlling byproduct formation requires agile process optimization. Batch reactors are optimized with in-situ monitoring tools that pick up shifts in concentration profiles, letting us adjust temperature and feed rates in real time. Experienced operators know small deviations at this stage, left unchecked, can lead to colored impurities or lower yields.

    Filtration presents a challenge due to the fine particulate matter sometimes generated during crystallization. Mechanical agitation and decanting must strike a delicate balance to keep filter clogging at bay. Years spent perfecting filter media choices now let us achieve consistent cake filtration, minimizing downtime and material loss. Washing with select solvents ensures surface residues disappear, ensuring the delivered product fits the rigorous demands of both analytical and process-scale clients.

    Another technical issue arises from the hygroscopic nature of many aromatic aldehydes. Oxygen exclusion becomes vital, both in bulk storage and in sampling zones. Our investment in nitrogen-blanketed drums and antistatic packaging gives extra protection. Routine shelf stability testing, freshly performed on every batch, tracks both moisture pickup and chemical integrity over six to twelve months. Test data feed directly back into raw material acceptance criteria and packaging upgrades.

    Supporting Sustainable Chemistry and Downstream Security

    Environmental and safety compliance walk hand-in-hand with advanced chemical manufacture. Our process design stresses closed-system operation and solvent recovery at every feasible step. Most waste streams get chemical treatment and recycling, sharply reducing need for incineration. Responsible fluorinated reagent handling is tightly audited, and every employee receives frequent training on safe handling, both for personal and environmental protection.

    We work with downstream users to optimize their own environmental footprint. Several pharmaceutical clients insist on life-cycle analyses, so they can demonstrate to regulators where every atom ends up. Our documentation and supply-chain tracking satisfy these requirements, providing backward traceability for every delivered package. We invest in process data sharing and collaborative troubleshooting, accelerating time-to-market for new drug candidates and advanced materials.

    Feedback Loops and Continuous Process Improvement

    Customer feedback isn’t just a metric for us—it shapes process improvement. Technical sales engineers keep in touch with R&D teams and production chemists at buying firms, taking every performance note seriously. When a specific batch returns feedback about a minor impurity peak or unexpected color shift, we track it to the root cause and review the entire workflow. Small iterative changes—whether in feedstock pre-treatment, temperature ramp speed, or additive choice—build up to measurable improvements over time.

    Our R&D group pushes ongoing improvements not just for cost but for batch-to-batch stability. Insights from failed scale-ups or subpar runs help us tweak procedures for both robustness and sustainability. The chemistry involved in attaching and protecting trifluoromethyl groups to an aromatic core demands this kind of vigilance. We’ve adjusted conditions to enhance selectivity, cut down waste, and extend catalyst lifetimes. All these steps benefit the end users with more predictable performance and less troubleshooting on their part.

    Collaboration extends beyond chemistry. Packaging innovation, for example, came after repeated feedback from formulation chemists who wanted both easy access and moisture control. Our current sealed, resealable packaging grew out of brainstorming with key accounts who needed flexibility for both small-scale experiments and larger runs.

    Lessons Learned from Decades in Specialty Aromatic Chemistry

    No production run happens in a vacuum. Each batch’s performance in a client’s reactor or lab is shaped by thousands of hours on our end. Common lessons recur: Don’t underestimate the impact of trace water on reactivity, even when spec sheets list “dry” numbers. Expect the unexpected with fluorinated intermediates—trace acids, oddball side products, and accelerated degradation from small impurities can upend timelines fast.

    We’ve come to recognize the value of in-process controls not just for yield, but for making life easier for the next chemist using the material. Ultrafine attention to particle size, evenness of color, and material flowability can head off downstream mixing challenges and blockages. Even with proven processes, our team reviews the latest research and acts quickly if superior reagents or extraction systems emerge.

    The greatest challenge in this sector remains keeping ahead of regulatory demands and emerging application trends. As new synthetic targets emerge globally, fresh demand can surface suddenly. We keep capacity available for spur-of-the-moment scale-ups, holding raw materials in reserve and investing in modular plant additions when necessary. This flexibility means rapid response for innovative clients chasing new molecules, while still safeguarding consistent deliveries for established projects.

    The Road Ahead: Opportunities and Industry Impact

    Demand for sophisticated building blocks such as 4-Hydroxy-3-(Trifluoromethyl)Benzaldehyde continues to expand. Teams in drug discovery, agricultural chemistry, and functional materials depend on reliable, high-quality supplies. Continuous dialogue between suppliers and end users spurs process refinement, encourages adoption of greener practices, and supports faster scaling from research to commercial production.

    As the only manufacturer in direct conversation with large global buyers, we see how application-driven specifications change expectations for the product. Medicinal chemists may demand ever-lower impurity levels for new API syntheses; materials scientists seek tighter control over electron-donating and withdrawing balance. Farmers, through agrochemical research, press forward in seeking higher efficacy with less environmental impact. The answer isn’t a one-size-fits-all product, but more agile, collaborative manufacturing.

    Our ongoing commitment remains simple: make each batch more consistent, each run more sustainable, and each delivery more reliable. That effort benefits both seasoned chemists who know aromatic aldehydes inside-out and newcomers exploring new chemical territory. The lessons from hundreds of successful campaigns and the few stumbles along the way keep us striving for steady improvements—never losing sight of the hands-on realities of chemical manufacture in the global supply chain.