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4-(Trifluoromethyl)Mandelic Acid

    • Product Name 4-(Trifluoromethyl)Mandelic Acid
    • Alias TFMMA
    • Einecs 243-743-3
    • 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
    VTB
    Specifications

    HS Code

    858875

    Chemical Name 4-(Trifluoromethyl)mandelic acid
    Cas Number 808-52-4
    Molecular Formula C9H7F3O3
    Molecular Weight 220.15
    Appearance White to off-white solid
    Melting Point 108-112°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.43 g/cm³
    Purity Typically ≥98%
    Synonyms α-Hydroxy-4-(trifluoromethyl)benzeneacetic acid
    Storage Temperature Store at 2-8°C
    Smiles C1=CC(=CC=C1C(C(=O)O)O)C(F)(F)F
    Inchi Key GAYLMRMWHDJIMG-UHFFFAOYSA-N
    Pka 3.33

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with screw cap, featuring hazard symbols and product labeling for 4-(Trifluoromethyl)Mandelic Acid.
    Shipping 4-(Trifluoromethyl)Mandelic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is typically handled as a hazardous material, requiring appropriate labeling and documentation. Shipping may be subject to local and international chemical regulations, and it is often sent via trusted carriers specializing in chemical transport.
    Storage 4-(Trifluoromethyl)mandelic acid should be stored in a cool, dry, and well-ventilated area, away from moisture and sources of ignition. Keep the container tightly closed and protected from direct sunlight. Store separately from incompatible substances such as strong oxidizing agents and bases. Use appropriate, labeled chemical containers to prevent contamination and ensure safe handling and retrieval.
    Application of 4-(Trifluoromethyl)Mandelic Acid

    Applications of 4-(Trifluoromethyl)Mandelic Acid in Industrial Manufacturing

    As a direct producer of 4-(Trifluoromethyl)Mandelic Acid, we deliver this specialized intermediate to critical sectors relying on advanced organic synthesis, API manufacturing, and complex fine chemical formulations. The following application scenarios reflect actual use cases in established industrial workflows, each supported by industry-specific compliance, technical usage details, process integration context, and end product examples.

    1. Pharmaceutical Active Ingredient Synthesis

    API manufacturers incorporate our material as a key enantioselective building block in the multi-step synthesis of β-blockers and advanced intermediates used for antihypertensive compounds. Its trifluoromethyl group contributes to high metabolic stability in the final molecules, which is critical for many novel small-molecule drug candidates. The addition typically occurs during early-stage condensation or amidation reactions, ensuring retention of the chiral center throughout further transformations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU-GMP EudraLex Volume 4
    • United States Pharmacopeia (USP) for impurity and residual solvent control
    • Regulations (EC) No 1907/2006 (REACH) for chemical safety

    Typical usage ratio

    • 5%–18% of total reaction mass depending on route and molecular target; chemists adjust based on stoichiometry and desired enantiomeric excess

    Downstream process integration

    • Charged during chiral condensation, amidation, or coupling phases, preceding further derivatization or ring closure steps

    Final product types

    • β-blocker APIs (e.g., nebivolol intermediates)
    • Atypical antidepressant intermediates
    • Prodrug intermediates for oncology pipelines

    2. Agrochemical Intermediate Manufacturing

    Producers of advanced agrochemical actives use this compound as a fluorinated mandelic acid analog in synthesis strategies for specialty herbicides and fungicides. The molecule enters synthetic routes engineered to introduce enhanced bioactivity and environmental persistence by leveraging its electron-withdrawing properties, often in side-chain elaboration steps for heterocyclic crop protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for Agrochemical Manufacturing
    • Good Laboratory Practice (GLP) for synthesis testing
    • EU Regulation (EC) No 1107/2009 for plant protection product approval

    Typical usage ratio

    • 2%–8% by weight of precursor mixture; varies by crop protection agent formula and target efficacy

    Downstream process integration

    • Fed into initial functionalization or nitration stages, followed by esterification or halogen exchange for final active ingredient assembly

    Final product types

    • Trifluoromethylated fungicidal actives
    • Pre-emergent herbicide intermediates
    • Custom pesticide analog compounds for contract R&D synthesis

    3. Chiral Ligand and Catalyst Development

    Specialty chemical suppliers and research divisions utilize our raw material for the tailored synthesis of chiral ligands and transition metal catalysts. The electron-deficient mandelic structure serves as a precursor during asymmetric catalysis research aimed at improving both stereoselectivity and turnover frequency in industrial-scale hydrogenation and cross-coupling reactions.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 17025 Analytical Lab Accreditation
    • Responsible Care® Management System for industrial chemicals
    • REACH registration for chiral intermediates

    Typical usage ratio

    • 0.4–2.5% of total ligand or catalyst reaction batch, calculated to balance catalytic efficiency with availability; optimizations rely on structure-activity profiling

    Downstream process integration

    • Introduced in the initial chiral scaffold assembly before metal complexation and functional group installation

    Final product types

    • Asymmetric hydrogenation catalysts for pharmaceutical manufacture
    • Organometallic ligand libraries
    • Research chemicals for chiral selectivity improvement in synthetic process development

    4. Specialty Coating Additive Synthesis

    Producers of high-performance fluorinated coatings and surface modification agents include our product as a synthesis intermediate to create unique hydrophobic and anti-fouling additives for electronics and optical substrates. Its fluorinated aromatic backbone delivers a persistent non-stick effect and improves abrasion resistance when functionalized for integration into polymer matrix resins or silane crosslinkers.

    Industry compliance standards

    • ISO 12944 for Protective Paint Systems
    • Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU
    • ISO 14001 Environmental Management for chemical processing
    • ASTM D3359 for coating adhesion testing

    Typical usage ratio

    • 0.3%–1.7% of total formulation mass; proportion chosen based on polymer compatibility and target surface energy values

    Downstream process integration

    • Converted in a dedicated pre-polymerization step to yield functionalized coating monomers or resin additives; subsequent blending into masterbatches

    Final product types

    • Anti-smudge coatings for glass touchscreens
    • Hardcoat additives for technical optical lenses
    • Fluorinated resins for specialty industrial films

    5. High-Purity Analytical Reference Material Preparation

    Producers of analytical standards use this compound for the preparation of certified reference materials for chromatographic quality control in pharmaceutical and agrochemical labs. Its stability and well-defined fluorinated structure provide a reliable standard for LC-MS and GC-MS method calibration, impurity profiling, and quantitative residue analysis in regulated testing environments.

    Industry compliance standards

    • ISO 17034 General Requirements for Reference Material Producers
    • Good Manufacturing Practice (GMP) for Reference Substances
    • US EPA SW-846 for Test Methods in Chemical Analysis
    • ICH Q2(R1) Validation of Analytical Procedures

    Typical usage ratio

    • Reference standard batches typically are prepared at a 50–100 mg per vial concentration for dilution and direct injection, adjusted per analytical protocol

    Downstream process integration

    • Purified using preparative HPLC and crystalline isolation; distributed as certified single-component reference standards for QC laboratories

    Final product types

    • Chromatographic calibration standards for QA/QC in drug and pesticide labs
    • Trace analysis reference substances for compliance routine monitoring
    • External standards for stability and degradation studies
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    Certification & Compliance
    More Introduction

    4-(Trifluoromethyl)Mandelic Acid: Bringing Precision and Reliability to Your Synthesis

    An Introduction From the Chemists Who Make It

    For decades, we have specialized in making high-purity building blocks for the life sciences. Among our standout products for demanding synthetic chemistry workloads, 4-(Trifluoromethyl)mandelic acid often finds itself in a leading role. Bringing both the subtlety of a mandelic acid scaffold and the strong electron-withdrawing power of a trifluoromethyl group, this compound provides key advantages for medicinal and process chemists. Only manufacturers with rigorous preparation and quality control can meet the narrow requirements for both research and full-scale production. We’ve faced and overcome the real-life challenges that crop up at every step, and have spent years refining our processes to serve innovators and established formulators alike.

    Pushing for Purity—Not Just on Paper

    From batch to batch, our focus stays fixed on consistency. Purer starting acids avoid unnecessary headaches, so we control every step from raw material procurement to final crystallization. We check the fluorination step closely—since the trifluoromethyl group sometimes lags in reactivity with substituted aromatics, sloppy work leads to incomplete reactions or troublesome byproducts that not every downstream process will tolerate. By investing in specialized distillation and analytical chromatography, we hit 99% minimum purity for both small and large lots. Quality in, quality out: crystal-clear melting point, reliable solubility profile, and NMR signatures that satisfy the most skeptical specialists. Many of the chemists in our team use these metrics in their own R&D, so our standards never slip out of familiarity.

    Applications From Project Ideas to Production Yields

    The practical uses of 4-(Trifluoromethyl)mandelic acid reach far beyond textbook examples. Custom synthesis firms come to us for selective coupling agents. Medicinal chemists often reach for it to introduce chirality and increased metabolic stability in advanced intermediates. The carboxylic acid group opens routes to esters, amides, and other derivatives; the alpha-hydroxyl group welcomes further manipulation; the electron-deficient trifluoromethyl group adjusts lipophilicity and impacts biological half-life—a trio hardly matched by other mandelic acid analogues.

    Not every structural variant hits the same sweet spot between aqueous solubility, chemical robustness, and predictable downstream reactivity. In the world of advanced intermediates and final APIs, minor impurities or batch variability can put entire projects at risk. Skipping corners in production means someone downstream—sometimes at the kilo or ton scale—will be forced to troubleshoot delays or contamination. We’ve worked with contract manufacturers who share feedback directly, and more than once, resolving issues in their routes started with examining the details in our own purification. That collaborative spirit means we support open communication about specs, and we’re not afraid to recommend a competing molecule if something else will suit a route better.

    What Sets 4-(Trifluoromethyl)mandelic Acid Apart

    A synthetic organic chemist or process engineer tends to compare closely related molecules side by side—straight mandelic acid, 4-chloromandelic acid, and the trifluoromethyl variant. Regular mandelic acid boasts versatility but lacks the fluorine "edge" that often tunes absorption and potency in pharmaceutical scaffolds. The 4-chloro modification brings different reactivity, but its steric and electronic features rarely match the triple-fluorine effect. By adding the trifluoromethyl group to the para-position, the acid tips the balance toward higher metabolic resistance, increased hydrophobicity, and sometimes sharper selectivity for target enzymes or channels.

    As a bulk manufacturer, we manage the nuanced preparation of the trifluoromethyl variant. Direct substitution with CF3 at the 4-position—done carelessly—can generate incomplete products, over-halogenation, or oligomerization, all of which complicate isolation or scale-up. Over the years, careful control of molar ratios, real-time monitoring, and sensitive post-reaction workups has let us drive impurity levels down to the low parts per million. Scale brings new technical demands: 10-gram sample preps require different crystallization parameters than a multi-kilo campaign, and subtle tweaks make the difference between a chunky solid that clogs filtration systems and a fine powder that dissolves smoothly in DMF or DCM.

    Inside the Production Shop—How Experience Shapes Each Lot

    Every operator on our plant floor has seen how easy it is for a single missed wash or slightly out-of-range temperature to produce off-spec material. Early on, we saw that slightly impure batches clouded reaction mixtures in acylation or reduction steps done by our clients. Fluctuations in melting point signal more than just a paperwork headache—they mean real-world variability in shelf-life or performance. Our standard practice goes beyond batch recordkeeping. We keep detailed logs of every raw material lot, downtime, and deviation, then trace each back to yield, purity, and color. There are mornings where a gentle change in solvent grade or wash temperature can make or break purity, so we’ve learned to listen to operators who catch small oddities before they snowball.

    Operators regularly consult with analytical chemists stationed at our plant’s QC labs, not just those who sit in offices miles away. Early-morning GC and HPLC runs often spark lively debate, especially if an unfamiliar secondary peak surfaces. Asking the hard questions—at what ppm level will that unknown start causing trouble for coupling partners?—keeps everyone invested in the chain from plant to customer. We’ve found that open QC feedback beats a hands-off approach every time, both for the plant and for the end user.

    Why Customers Choose Us—Not Just a Label, But a Partnership

    Buyers in our space, particularly those developing new syntheses, will often call to ask about a lot’s actual handling, stability under ambient shipping, or even true shelf life under humid lab benches. We encourage these questions. Over years of commercialization, our clients have pointed out how many failures trace to inconsistent quality from less-invested producers. Anecdotes from the field have kept us humble—especially cases where downstream scale-ups tanked because a competitor’s material carried subtly different isomeric content. That’s led us to double down on secondary testing—sadly, not every flask of “99% pure” material, if bought on the open market, holds up to detailed scrutiny, and we’ve run our competitor’s brands through our own labs more times than we can count, simply to avoid our projects suffering from someone else’s shortcuts.

    Kilo-scale or larger synthesis often demands both technical performance and practical handling. Some research teams want a free-flowing crystalline powder; others focus on stability during long transport. Our feedback loop with end users allows us to adjust packaging, drying conditions, or even the frequency of stability testing during long-term storage. Everyone benefits when information flows both ways—one recent collaboration resulted in a modified drying method that reduced caking inside bulk containers, saving an entire pilot plant project several hours of wasted effort.

    Supporting Complex Chemistry—Applications in the Real World

    Project managers and lead researchers order 4-(Trifluoromethyl)mandelic acid to launch medchem campaigns, explore structure–activity relationships, or scale a new route toward a clinical API. The molecule’s structure allows it to serve as a template for advanced fragment libraries or as a source of chiral centers during asymmetric synthesis. The trifluoromethyl substitution draws significant attention in preclinical programs aiming to increase blood–brain barrier penetration or disrupt traditional metabolic clearance. Environmental scientists working on advanced analytical standards have also chosen our acid as a calibration reference.

    We’ve watched the compound support industrial researchers working in pesticides and next-generation surface coatings—anywhere chemists want to outpace the oxidative power of the environment or achieve hard-to-break molecular architectures. The majority of our product heads for life sciences, but the flexibility shown by customers in battery and new electronics applications has prompted us to finish extra characterization, especially when dealing with low-level metals content or minimizing any trace halide contamination picked up in earlier synthetic steps.

    Field-Driven Solutions to Real Problems

    Troubleshooting in specialty chemicals emerges fast and often. Years ago, we occasionally saw sulfonation byproduct creeping into lots made at slightly higher acid strengths, which led us to upgrade reactor material and vent controls. A few clients reported that subtly yellowed material reacted sluggishly in their own O-methylation steps. Detailed solvent screening and revised washing cycles restored batch reproducibility, and we circulated those fixes as best practices both in our own protocol and in client-facing documentation. One team in the northeast flagged minor variability in crystal size between winter and summer deliveries, a challenge we overcame through double-jacketed cooling tanks and calibrated air-knife drying.

    We’ve always found that multilayered transparency with users pays off. Honest conversations about non-conforming batches—delays, contaminant spikes, or unavoidable shortfalls—help avoid rushed fixes that only breed bigger problems. A frank phone call with a partner beats a series of abstract emails every time, and long-term relationships thrive on mutual technical accountability. As a result, many of our long-term users stick with us not just for paperwork but for direct technical assurance: if they run into process trouble, our own chemists can visit, analyze samples, and help implement solutions that stick.

    Improving the Future—Sustainability and Compliance

    Manufacturing 4-(Trifluoromethyl)mandelic acid means answering to evolving demands, not only technical but regulatory and environmental. The fluorinated intermediates industry faces scrutiny over volatility, occupational exposure, and downstream product safety. Our team applies both in-plant environment monitoring and regular operator training to limit exposure and waste. Chemical plant audits—from both customer teams and regulatory agencies—happen frequently, and we’ve welcomed them. Transparency beats compliance theater. We keep material safety data current and immediately accessible, and share new toxicology or handling findings with our community of buyers and researchers as soon as they arise.

    Responsible process management also reduces actual waste. Minor process tweaks—swap-outs for less hazardous solvents, improvements to catalyst recovery—can save thousands of liters of solvent and kilowatt-hours of energy every year. A single small improvement, such as optimizing pH-controlled workups, sometimes makes a significant difference after all. We support customers seeking to meet sustainability benchmarks and welcome technical challenges that help us reduce our own footprint. If a route can be adjusted for greener chemistry without sacrificing quality, we dig in alongside our customers and test the best alternatives in-house before adding them to our established processes.

    Market Trends and the Way Forward

    Over the last decade, requests for 4-(Trifluoromethyl)mandelic acid have moved steadily from gram-scale research to commercial projects that measure lots in the hundreds of kilograms. Each jump in demand stretches a plant’s flexibility: procurement, equipment, and logistics all need agile response. Early adopters helped iron out the wrinkles in shelf life, storage, and shipping. Now, as patents on key intermediates expire or start to run out, we’re shipping more acid for process-scale work in generics production and custom APIs.

    We see clear differences between customers ordering for early-stage studies and those prepping for regulatory filings or market launches. Researchers may want flexible lot sizes, expedited shipping, or ongoing analytical support. Bulk-scale buyers ask pointed questions about impurity profiles, document control, and delivery traceability. We keep both needs in mind, delivering what fits the purpose, not just a shipment but an ongoing collaboration. Our lab benches are covered with notes from customers: tweaks for smoother bottle openings, non-static packaging, or preferred delivery days, because experience shows the biggest wins often come from solving small, persistent headaches.

    Continuous Improvement and Shared Responsibility

    After every major order, our technical team meets to review outcomes. Real improvement comes from listening: frontline packaging staff point out recurring problems with foil wraps; senior chemists identify whether lots from different reactors show minor variations. Not long ago, we learned from a client’s in-house NMR analysis that trace residuals picked up through a shared distillation line affected their catalyst’s turnover in a high-value coupling step. By adapting our cleaning schedule and verifying its effectiveness with additional GC-MS and ICP-OES runs, we resolved the issue and kept future projects on track.

    Our methods and philosophy keep us invested well after a shipment arrives. We’ve driven overnight to fix a problem on-site, sent staff to help with downstream purification, and supplied extra reference standards even for lots made elsewhere, simply to maintain trust. By approaching each production challenge as if it affected our own synthesis pathway, we aim to set a higher bar in the industry—avoiding shortcuts, sharing hard-earned knowledge, and acknowledging our own learning curve.

    Summary—Why 4-(Trifluoromethyl)mandelic Acid Remains in Demand

    Few synthetic intermediates match the performance, reliability, and flexibility required by innovative industries and researchers as 4-(Trifluoromethyl)mandelic acid. The careful design—rooted in both synthetic tradition and modern needs—allows this molecule to play a part in drug discovery, advanced materials, and analytical science. Our long-standing experience not only as a manufacturer but as technical partners to our clients gives us the perspective needed to refine, troubleshoot, and adjust both product and service.

    At every step, trust is earned not by flashy claims, but by repeated, transparent action—batch to batch, barrel to barrel. We look forward to supporting the next generation of research and commercial breakthroughs as both a reliable supplier and an invested member of our community.