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(R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid

    • Product Name (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid
    • Alias (R)-TFH
    • Einecs 416-130-7
    • 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

    465188

    Product Name (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid
    Cas Number 75134-93-1
    Molecular Formula C4H5F3O3
    Molecular Weight 158.08 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 50-54°C
    Optical Rotation [α]D20 +12° to +16° (c=1, MeOH)
    Solubility Soluble in water and methanol
    Synonyms (R)-2-Hydroxy-2-methyl-3,3,3-trifluoropropanoic acid
    Structure CC(C(=O)O)(O)C(F)(F)F
    Storage Keep tightly closed in a cool, dry place

    As an accredited (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid supplied in an amber glass bottle with a tamper-evident sealed cap.
    Shipping **Shipping Description:** (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid is shipped in sealed, chemical-resistant containers under ambient conditions. It should be handled with care, avoiding exposure to moisture and direct sunlight. Ensure compliance with local and international regulations regarding transport of chemicals and provide appropriate hazard identification and documentation during shipping.
    Storage (R)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizing agents. Store in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator), and protect from light. Proper labeling and secondary containment are recommended to prevent leaks and accidental contact.
    Application of (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid

    Applications of (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid to support advanced chemical synthesis across several precision downstream sectors. Below, we outline key, real-world industrial application scenarios with specific attention to genuine industry standards, formulated inclusion levels, integration points, and resulting end-products for manufacturers.

    1. Chiral Pharmaceutical Intermediate for Antidiabetic Drug APIs

    This raw acid serves as a core chiral building block for synthesizing certain active pharmaceutical ingredients (APIs), particularly for DPP-4 inhibitor drugs. Its enantiomeric purity and trifluoromethyl functionality enable stereoselective construction, supporting complex molecule assembly in new antidiabetic medications. Manufacturers must maintain strict control throughout both chiral resolution and subsequent coupling phases to ensure regulatory-grade purity.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • US FDA cGMP regulations (21 CFR Part 211)
    • ISO 9001:2015 for Quality Management Systems

    Typical usage ratio

    • Stoichiometric levels in API synthesis routes (molar-equivalent to coupling partner), generally 1.0–1.2 molar equivalents depending on the cross-coupling stage and target molecule scale; ratio adjusts based on impurity specifications.

    Downstream process integration

    • Incorporated in the chiral alcohol coupling step, following optically active separation, and fed into organofluorine route for heterocycle construction.

    Final product types

    • Pharmaceutical APIs for antidiabetic drug formulations (e.g., sitagliptin intermediates)
    • Research-grade reference compounds for clinical development
    • Regulatory submission samples and pilot plant scale intermediates

    2. Fluorinated Agrochemical Synthesis

    Synthetic crop protection research relies on this acid for producing key fluorinated alcohol and ester motifs in next-generation herbicide actives. Its unique trifluoro group increases target binding efficiency and metabolic stability in agrochemical molecules during field trials and scale-up, requiring rigorous quality monitoring through synthesis.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Active Substances (JMPR)
    • ISO 9001:2015 Quality Management
    • REACH (EC No. 1907/2006) registration for raw materials
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.2–0.5 molar equivalents per target molecule, adjusted to synthetic yield, scalability, and cost limitations in novel agrochemical discovery.

    Downstream process integration

    • Enters fluorinated esterification or amidation as a substrate precursor during the late-stage synthesis of herbicide or pesticide actives.

    Final product types

    • Registered agrochemical active substances (e.g., fluorinated pyrazoles)
    • New herbicide molecular candidates for development pipelines
    • Field trial sample batches for regulatory submission

    3. Advanced Material Monomer: Fluoropolymer Additive Manufacture

    Materials science and specialty plastic formulators employ this acid to introduce defined fluorinated side chains into architectural monomers. Direct copolymerization or esterification imparts enhanced hydrophobicity, chemical resistance, and dielectric performance, especially in engineered surface coating formulations and microelectronic barrier films.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in chemical manufacturing
    • RoHS 2 Directive (2011/65/EU) for electronic polymer applications
    • REACH (EC No. 1907/2006) for substance registration and tracking
    • ASTM D2116 test methods for fluoropolymer resins

    Typical usage ratio

    • 1–8 wt% as a functional monomer component in specialty copolymers; precise loading set by target material properties, end-use standards, and formulation viscosity.

    Downstream process integration

    • Dosed into prepolymer mix for controlled radical, condensation, or ring-opening reactions; often added with initiator in batch or continuous polymerization lines for electronics or industrial coatings.

    Final product types

    • Hydrophobic/oleophobic protective films for microelectronics
    • Engineered fluorinated coatings for industrial pipelines and valves
    • Functionalized polymer additives for membrane and barrier films

    4. Specialty Chemical Synthesis for Organofluorine Intermediates

    Fine chemical manufacturers leverage this acid in the stepwise assembly of organofluorine building blocks used across life science and specialty additive sectors. Its high purity facilitates nucleophilic substitution and asymmetric catalysis, where maintaining trace-level impurity profiles is critical for downstream isolation and certification.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (EC No. 1907/2006) for specialty chemicals
    • Chemical Weapons Convention (CWC Annex on Chemicals) screening
    • Responsible Care® global management standards

    Typical usage ratio

    • 0.1–1.0 molar equivalents, calibrated to reaction scale, catalyst system, and desired enantiomeric excess in industrial synthesis processes.

    Downstream process integration

    • Supplied as a reaction intermediate for electrophilic trifluoromethylation, then isolated and purified as downstream specialty building blocks for use in catalog chemicals or further transformations.

    Final product types

    • Precursor chemicals for further modification in pharmaceutical and agrochemical pipelines
    • Chiral reference standards for analytical laboratories
    • Organofluorine moiety intermediates in advanced reaction libraries
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    Competitive (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid: Driving Advancement in Synthetic Chemistry

    A Look at Our Manufacturing Commitment

    At our facility, day after day, the core lies in the meticulous crafting of specialty intermediates. (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid stands out among the reagents that demand precision, repeatability, and a steadfast approach to process safety. Our team has spent years developing pathways that consistently yield high-purity (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid, with strict control over stereochemistry and trace impurity content, because nobody wants unpredictability in a scale-up that underpins a clinical candidate or a new materials application.

    The requests from partners often come with challenges—enantiomeric purity thresholds in excess of 99%, impurity benchmarks below 0.1%. Our in-house production model uses chiral catalysts and tailored crystallization methods to stay ahead of these demands, and we regularly tweak our processes to account for batch-to-batch feedback.

    What Sets This Molecule Apart

    This acid opens doors that many other hydroxy acids can’t. Add the trifluoromethyl group, and the landscape changes entirely. In our daily work, we hear from medicinal chemists racing to fine-tune metabolic stability in new drug scaffolds. The introduction of a trifluoromethyl group, especially at the alpha position, gives a sharp boost to oxidative resistance. Our (R)-enantiomer proves far more suitable for insertion into enantioselective probes and chiral ligands. Unlike its racemic or (S)-counterparts, this particular configuration speeds up SAR cycles by removing ambiguities in downstream biological data. The users who collaborate with us run less risk running into issues with unwanted side-products during later-stage functionalization, thanks to the clean separation we consistently achieve.

    Others on the market attempt to approximate these results, but real-world dialogues with end-users reveal persistent headaches: surfacing minor diastereomers, broad LC peaks, gaps in NMR spectra from impurities below detection that still trip up regulatory submissions. We respond by verifying optical purity and rigorously monitoring trace metal content, not because regulations demand it, but because downstream failures ripple back up the chain at astonishing speed. Clients in high-throughput screening hit bottlenecks when small impurities skew readouts, and it’s here that our manufacturing discipline pays off.

    Specifications Powered by Experience

    Every kilo of (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid rolling off our line shows tight adherence to the trusted specification model:

    The analytical work does not stop at release. Each lot faces a rigorous QC panel that includes multidimensional NMR, chiral HPLC analysis, and ICP-MS for trace elemental analysis. The feedback from global clients—laboratories striving for consistency—pushes us to exceed, not just meet, expected thresholds.

    End Uses Guided by Custom Synthesis Demands

    (Chemists looking for an edge in their next project bring us their toughest roadblocks.) This acid finds its strongest foothold in drug development, particularly for making fluorinated analogs where improved in vivo stability matters most. It serves as a chiral building block for non-natural amino acid synthesis, bridged fluorinated esters, and specialized ligands for asymmetric catalysis. Many partners need the (R)-enantiomer for constructing APIs targeting novel metabolic and CNS pathways. Its utility shows up regularly in peptide modifications, where the trifluoromethyl group retunes physicochemical behavior without sacrificing bioactivity.

    Environmental chemists have also come knocking. The robust C–F bond resists breakdown, and our acid supports development of agrochemicals designed for controlled environmental persistence. In materials science labs, researchers deploy our product to design polymers or coatings demanding hydrophobicity combined with site-selective reactivity. Industrial feedback points to better yield, purer final formulation, and less reliance on post-reaction scrubbing.

    Comparative Advantages: Not All Reagents Deliver Equally

    Peers sometimes argue that purchasing generic alpha-hydroxy acids or even lower-purity, bulk-market trifluorinated acids is cost-effective. Our hands-on experience proves otherwise. Workups using bulk-grade material show clogging in advanced columns, more failed batches in high-throughput settings, or variable yields from step to step. Our end-users want assurance that each batch behaves as expected—for both scale-up batches and tightly monitored pharmaceutical routes.

    The (R)-enantiomer, specifically our optimized form, brings notable improvements in enantioselective synthesis. Peptide chemists have reported sharper resolution in chiral separations, and multistep syntheses face fewer sequence deletions. These reports do not always make their way into journals; they show up in the time saved, the lower waste disposal bills, and the reduction in reprocessing. Materials scientists note uniformity in their end‐products, giving reproducible properties in coating or polymer systems. These practical wins build our confidence in the material we make.

    Why Source from an Actual Manufacturer Matters

    The chemical trade, flooded with resellers and distributors, can obscure the true origin of critical intermediates. End users are often blind to the number of hands their order passes through—each step amplifies risks of mislabeling, improper storage, and accidental racemization. Our clients demand traceability right down to the lot and, in some cases, right to reactor charge records. Working directly with us, they reach the team running the reactors, the chemists tweaking the work-up, and the people verifying the data.

    Prompt feedback on order status, technical support during scale-up troubleshooting, and direct access to production documentation are part of our daily routine. Project managers returning for repeat material often ask for slight modifications—lower residual solvents, a finer powder, a different packaging format—so we do not outsource this process. These iterative improvements happen through daily dialogue between our engineers and our customers’ project teams, many of whom are tackling aggressive timelines in pharmaceutical or advanced materials development.

    Supporting Safe Handling, Storage, and Regulatory Confidence

    Every chemist who has run into unanticipated exotherms or dissolution hiccups with hydroxy acids knows the critical nature of clear, transparent documentation and robust manufacturing controls. (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid, by nature, stays stable under dry, cool, and dark storage conditions. Our operational protocols, honed over years, minimize cross-contamination risk, degradation, and moisture absorption. Our warehouse keeps the temperature and humidity consistent, monitored digitally and checked by staff throughout every day.

    Documentation prepared for each batch, reviewed and signed off by our analytical chemists, tracks not only critical points like synthesis date and shelf life, but also ensures we detect the subtlest signs of decompositions, such as discoloration or changes in purity. We provide detailed COA packages with full analytical data. Regulatory teams receiving our material know what to expect, and regulatory authorities trust our documentation. This consistent transparency matters more now, as controls tighten on fluorinated organic acids and their derivatives.

    Pursuing Continuous Improvement in Chemical Manufacturing

    Each year sees new challenges. Shifts in global regulatory requirements for trace impurities, volatility in raw material markets, and emerging demand for ever greater purity and batch-to-batch consistency keep us vigilant. We review feedback from dozens of pharmaceutical and materials science partners seeking changes in specification ranges, new certificate formats, and sometimes, urgent improvement in cycle times. Internally, we invest in equipment upgrades—a new HPLC column here, a solvent recycling system there—to hold down costs and boost environmental responsibility.

    In dialogue with partners working towards “greener” syntheses, we invest heavily in solvent management and waste minimization. Our continuous efforts to reduce the carbon footprint for each product batch highlight decades of experience in balancing technical performance with sustainability targets. The trifluoromethyl group, as many customers know, holds both promise and responsibility. Responsible manufacturing means more than using certified raw materials; it means optimizing reaction thermodynamics, streamlining work-ups, and sharply minimizing solvent load.

    Our team takes pride in the efficiency we bring to each stage of synthesis. From raw material selection to filtration and packaging, we constantly refine and adjust, ensuring our manufacturing route both maximizes atom economy and supports end-user compliance with environmental and quality standards. Our on-site analytical personnel run sample checks on all critical steps, from reaction mixture work-up to final drying. Each small change, sometimes as minor as adjusting the rate of addition of a catalyst, can make a profound difference in the final product, a lesson learned from years on the plant floor.

    Staying Ahead: The Next Generation of Trifluoromethylated Building Blocks

    The drive toward fine-tuned molecular performance in both pharmaceuticals and new materials feeds a demand for specialty acids that can stand up to scrutiny. We tap into our decades of process development expertise to continually support those on the frontier—chemists in biotech firms making libraries of enantiopure compounds, researchers in advanced polymer testing looking for materials with high environmental resilience, and agrochemical designers searching for building blocks that resist breakdown yet allow downstream modification.

    Sourcing directly from our facility, partners benefit from a transparent supply chain, rapid and clear communication, and the assurance that every batch reflects shared experience and a commitment to technical excellence. This is not just about moving volume—it is about understanding the subtleties that can mean the success or delay of a crucial project. We speak the same language as the chemists and engineers who rely on us, and years of feedback continue to shape the way we do business.

    In our daily work, we are reminded by each order and every sample request: seemingly small differences in chiral purity, trace impurity levels, or batch homogeneity can cast long shadows in downstream synthesis and testing. Our job is to anticipate those complications and meet them head-on, saving time and safeguarding our partners’ investments.

    What the Future Holds

    Expectations never stand still, and neither do we. Research grows more complex, with discovery cycles demanding faster turnaround, higher purity, and more robust documentation. The trend toward tighter control of fluorinated intermediates across the US, EU, and Asia also pushes us to maintain clean audit trails and hold ourselves to voluntary standards beyond the bare minimum. We respond not by simply ticking off paperwork but by investing in our key strength: the expertise of people who understand chemistry, who see the impact of every process change, and who know what it means to deliver reliability.

    Markets shift, regulations evolve, but the fundamental recipe stays the same: attention to every kilogram, respect for every detail in the analytic printout, and collaboration with customers who need timely, predictable, tailored supply. In our experience, shortcuts come with hidden costs. We have built our business, reputation, and technical processes around getting this right every time. For those looking to push boundaries with fluorinated chiral acids, we listen, we adapt, and we deliver—not from a catalog, but from the synthesis bench up.

    Let’s Move Chemistry Forward Together

    (R)-3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic Acid has earned its place as an essential tool for chemists developing next-generation molecules. We have seen firsthand the challenges that come with sourcing, the rewards of investing in tight quality control, and the satisfaction that comes with supporting projects from concept to final batch. Every inquiry, every order, and every project brings its own lessons and shapes the next improvements in our process. In our hands, this acid is not just a molecule on a shelf, but a commitment to partnership, progress, and continual scientific growth.