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5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid

    • Product Name 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid
    • Alias Compound 47
    • 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

    958650

    Chemical Name 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid
    Molecular Formula C13H13F3N2O2
    Molecular Weight 286.25 g/mol
    Cas Number 1433901-91-1
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, sparingly soluble in water
    Storage Temperature 2-8°C (Refrigerated)
    Synonyms None reported
    Iupac Name 4-[5-(Trifluoromethyl)-3,4,5,6-tetrahydro-2H-pyridin-2-yl]pyridine-3-carboxylic acid
    Smiles C1CCNC(C1)C2=CN=CC(=C2)C(=O)O
    Inchi InChI=1S/C13H13F3N2O2/c14-13(15,16)10-6-17-7-9(8-10)11-3-1-2-4-12(11)18(19)20/h6-8H,1-4H2,(H,19,20)

    As an accredited 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in an amber glass bottle containing 1 gram, sealed with a screw cap and labeled with product and safety information.
    Shipping The chemical **5'-Trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid** is shipped in secure, airtight containers, typically under ambient or cooled conditions to preserve stability. Packaging complies with all relevant safety regulations for transport of laboratory chemicals and includes appropriate hazard labeling and documentation for safe, compliant delivery.
    Storage Store 5'-Trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid in a tightly sealed container, protected from moisture and light. Keep at room temperature (15–25°C) in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Properly label the storage area and implement safety measures to avoid inhalation, ingestion, or skin contact.
    Application of 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid

    Applications of 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid in Industrial Manufacturing

    This specialized bipyridinyl acid serves as a key synthetic intermediate in regulated chemical sectors. Our manufacturing quality ensures suitability for advanced industrial requirements across several precise downstream fields. We outline key application scenarios below with industry-specific compliance, dosage, integration, and final product guidance.

    1. Active Pharmaceutical Ingredient Intermediate for CNS Drug Synthesis

    Originating in our GMP facility, this raw material is leveraged during the multi-step synthesis of select central nervous system (CNS) pharmaceuticals. The scaffold supports structure-activity modification in the development process of pyridine-based drugs, notably in the creation of small-molecule antagonists. Precise carboxylation and trifluoromethyl groups enable chemical transformations as mandated by global pharmaceutical regulatory frameworks.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211: cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia Monographs (as applicable for APIs and intermediates)
    • USP General Chapters for residual solvents and impurity profiling

    Typical usage ratio

    • 50–200 g per mol basis as a key intermediate, adjusted by synthesis scale and batch reaction yield optimization

    Downstream process integration

    • Feeding into catalytic heterocyclic condensation
    • Employed at the carboxylation or reduction step
    • Purification via preparative chromatography before final API assembly
    • Control of impurity profiles during each synthesis stage

    Final product types

    • CNS-focused pharmaceutical compounds (e.g., anticonvulsants, anxiolytics under development)
    • Small-molecule research actives for clinical trials
    • API pre-final intermediates delivered to licensed drug manufacturers
    • Reference standards for pharmaceutical QC labs

    2. Agrochemical Intermediate for Pyridine-Based Herbicides

    Our raw material enters the synthetic processes of advanced herbicides built on bipyridinyl scaffolds. Formulators use this acid to introduce trifluoromethyl and carboxylic functionalities, critical for weed-selective activity. Tight control of purity supports compliance with agricultural product safety standards globally.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • Regulation (EC) No 1107/2009: EU Plant Protection Products
    • U.S. EPA 40 CFR Part 158: Data requirements for pesticide registration
    • ISO 17025: Testing for residue limit validation

    Typical usage ratio

    • 5–20% in pre-herbicide syntheses, tailored by active molecule synthesis route and target selectivity spectrum

    Downstream process integration

    • Enters amidation or halogenation steps during technical ingredient synthesis
    • Incorporation prior to ring-closing for active material assembly
    • QC at each intermediate to comply with persistent organic pollutant limits
    • Dilution and formulation blending before packaging for end-use

    Final product types

    • Broadleaf-selective herbicide technical concentrates
    • Pre-emergent weed control actives distributed to agri-input refiners
    • Analytical standards for environmental residue testing
    • Bioactive analogs for regulatory submission dossiers

    3. Specialty Chemical for OLED Display Synthesis

    Display manufacturers require fluorinated bipyridinyl acids as building blocks for OLED emitter and electron transport compounds. This intermediate provides both electronic properties and process compatibility required for downstream organic semiconductors. Quality-controlled batches support integration into proprietary material development under electronics compliance protocols.

    Industry compliance standards

    • IEC 62321: Determination of certain substances in electronic equipment
    • RoHS 2011/65/EU: Restriction of Hazardous Substances
    • JEDEC JESD24-1: Reliability Test Methods for Organic Semiconductors
    • ISO 9001:2015 for total process traceability

    Typical usage ratio

    • 0.1–1% by weight in emitter or electron transporting layer formulations; proportion depends on layer thickness and device architecture

    Downstream process integration

    • Chemical precursor in Suzuki coupling or cyclization step for light-emitting molecules
    • Purification prior to vacuum deposition onto ITO-glass substrates
    • Quality screening for fluorine content and residual solvents before device fabrication
    • Batch-to-batch tracing in the product history for OEM contracts

    Final product types

    • OLED emission layer materials for panel production
    • Electron injection/transport films sold to display module assemblers
    • Prototype organic semiconductors for R&D in electronic companies
    • Performance evaluation kits for display technologists

    4. Intermediate for Specialty Coating Resins

    Producers of high-performance coatings source this carboxyl-functionalized bipyridinyl for the synthesis of specialty acrylate or polyurethane systems. The fluorinated structure enables resistance to solvents, UV degradation, and aggressive chemicals in end-use environments. Precise process integration ensures reproducible physical film properties as required by industrial coating regulations.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006: Registration and Evaluation of Chemicals
    • ASTM D01.23: Organic Coatings, Subcommittee on Polymers
    • ISO 12944: Corrosion protection of steel structures by protective paint systems
    • UL 2818: GREENGUARD Certification for low chemical emissions

    Typical usage ratio

    • 0.5–3% by mass in coating resin synthesis, adjusted for specific end-use performance such as hydrophobicity or anti-graffiti functionality

    Downstream process integration

    • Introduced during pre-polymer chain extension or crosslinking steps
    • Reaction monitored for free acid content and copolymer incorporation
    • In-line QC verifies dispersibility and compatibility with pigments or solvents
    • Lot release analysis for shelf-life stability and application performance

    Final product types

    • Industrial protective coatings for infrastructure and marine equipment
    • UV- and chemical-resistant architectural paints
    • Specialty finishes for automotive or aerospace applications
    • Functional powder coatings for electronics enclosures
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    Certification & Compliance
    More Introduction

    5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']Bipyridinyl-4-Carboxylic Acid: Practical Insights from the Manufacturer

    Real-World Experience with a Precision Tool for Complex Synthesis

    Over the years, chemical innovation has matured through the steady demand for more functionalized and labor-saving intermediates. In that spirit, 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid has emerged as a helpful building block for researchers aiming to build complexity and precision into their synthesis work. From our production floor to R&D benches, our hands-on experience tells a clearer story about its practical role and key differences.

    One Step Ahead for Specialty Synthesis

    Standing behind the reactor vessels day after day teaches respect for reagents that let you advance a project with consistency, purity, and efficiency. This specific bipyridinyl carboxylic acid packs a trifluoromethyl group—added not by chance, but for chemists who want more than just a simple pyridine scaffold. Trifluoromethyl substitution doesn’t just tweak electronic effects; it reshapes reactivity, solubility, and how the molecule fits into downstream transformations. Such a feature delivers more than a substitution gimmick. Our partners in pharmaceutical research trust it for steps where small differences in electronegativity or molecular shape can make or break a project.

    Specifications that Matter on the Factory Floor

    From the first kilogram we synthesized, our commitment to reproducible, clean output shaped our process. Our batches pass close quality control with purity that meets demanding pharma and agrochemical requirements. Chromatographic methods confirm low residual solvents and controlled isomeric ratios. We avoid using unsustainable solvents and heavy metals in the process, making downstream purification easier for formulators.

    Engineering this molecule involves more than following the recipe. Bipyridinyl rings are sensitive under harsh conditions, and introducing trifluoromethyl causes a shift in the reactivity window. Our process avoids excessive temperatures and stoichiometric waste. The result? Robust production, solid yields, and a level of confidence that lets customers formulate or modify as their science demands.

    Usage Shaped by Real Laboratory Needs

    Applications for this compound extend far beyond just being a chemical name on a drum. Medicinal chemistry teams ask for such bipyridinyl scaffolds due to their role in ligand design, kinase inhibition, charged catalytic cycles, and the growing trend to incorporate fluorinated motifs in lead optimization. At this stage of the industry, a non-fluorinated analog often falls short in metabolic stability, binding affinity, or simply fails to survive the high-throughput screening grind.

    Customers often share their frustrations with non-fluorinated carboxylic acids. Many tell us about issues with regioselectivity, solubility, and metabolic lability in animal testing. By introducing the trifluoromethyl at the 5'-position, chemists report measurable improvements. The electron-withdrawing nature stabilizes reactive positions, and tweaks lipophilicity—both critical for reaching new levels in drug discovery.

    Besides drug discovery, agrochemical developers lean on this building block for crop-protection research. Structure-activity exploration frequently calls for new scaffolds with altered field persistence and environmental fate—needs that the trifluoromethyl group addresses.

    No Substitute for Consistency and Trust

    Years in manufacture are not just about being able to produce a kilogram today or a ton tomorrow. Our production approach emphasizes avoiding cross-contamination, minimizing trace impurities, and ensuring reproducibility batch to batch. Maintaining quality means strict raw material selection, regular cleaning validation, and investment in analytics that detect even low-level byproducts. We don’t cut corners on drying, storage, or packaging because we know our partners need as much assurance as data. It’s not just about purity—it’s about reliable reactivity and no surprises on the bench.

    How Real-World Feedback Shapes Our Manufacturing

    Customers in advanced materials and medicinal chemistry often relay stories from the lab. Early on, some struggled with side reactions or purification headaches when using generic or poorly controlled bipyridinyl carboxylates. Based on such direct feedback, we refined our crystallization and drying sequence, moving away from older techniques that risked hydration or polymorphic shifts. Storage conditions matter: tightly sealed, moisture-free, and ambient transport proved best for stability.

    From these practical lessons, we now offer clear stability profiles, recommend storage in tight drums, and have improved our on-site packaging to avoid product caking or density variation. These changes have reduced customer complaints and improved reaction outcome predictability for new users.

    The Big Picture: Demanding Structures in Modern Chemistry

    Advanced synthesis needs aren’t met with the same old building blocks. Over the past two decades, the rise of combinatorial chemistry, high-throughput screening, and personalized medicine has shifted what researchers ask from their suppliers. Versatility, high reactivity, and functional group tolerance—these aren’t just buzzwords, they drive success or delay across R&D programs. At the intersection of these needs stands our 5'-trifluoromethyl-substituted bipyridinyl acid.

    Our team has seen the push for more fluorinated intermediates from companies seeking novel bioactivity. While simple fluorinated aromatics saturate catalogs, the specificity of a bipyridinyl with defined regioselectivity and coupled carboxylic acid functionality is much rarer—and more valuable—to a seasoned synthetic chemist.

    Why This Product Delivers Where Others Fall Short

    Chemists in the field share frustrations about inconsistent performance when switching between similar-looking building blocks. Not every bipyridinyl carboxylic acid is interchangeable, especially when moving between fluorinated and non-fluorinated analogs. The presence of the trifluoromethyl group at the 5'-position impacts not only the electronic environment but also how the molecule behaves under both nucleophilic aromatic substitution and palladium-catalyzed coupling reactions.

    Sometimes teams try generic or off-the-shelf bipyridinyl acids as a shortcut, expecting similar outcomes. Instead, much time and resource get spent troubleshooting process inconsistencies or chasing after minor byproducts. Our direct control over raw materials and process analytics gives the product a tighter specification—which in real terms leads to higher confidence in scale-up and downstream modifications. Users can extend it into various derivatives, attach pharmacophores, or weave it into polymer structures with less troubleshooting.

    Production Insights: Doing Things Differently

    It’s tempting to believe any generic manufacturer can churn out a sufficiently pure compound, but close involvement in the workflow tells a more complicated story. The introduction of the trifluoromethyl group isn’t trivial; it changes solubility, handling, and even purification. Trace contaminants can derail downstream reactions or skew analytical data. Early in our manufacturing, we noticed unexpected signals on NMR, which turned out to be trifluoromethyl positional isomers from poorly controlled reaction steps. Fixing these “minor” variations actually made a difference in customers’ SAR campaigns and increased reproducibility.

    We invested in fine-tuning temperature ramps and solvent choices, and added extra QC checkpoints to catch every deviation. Scale-up doesn’t come from magic, but from persistent optimization—solving the real issues surfaced by in-lab and in-plant troubleshooting. That’s what ensures not just a product, but a consistently performing part of critical research.

    Guiding Principles: Scientific Integrity and Long-Term Partnership

    Reliable supply underpins every successful R&D program. We’ve watched customers struggle with fluctuating quality from unproven sources, leading to wasted time on purity assessment and failed syntheses. We believe in forthright communication; we won’t overpromise on what the material can do, and we won’t understate the challenges of handling advanced chemistries.

    Every batch leaves the plant after rigorous chromatographic, spectroscopic, and elemental analysis. Stability testing and shelf-life prediction are routine, not afterthoughts. As users tackle challenging target molecules, our technical teams regularly answer questions on solvent compatibility, reactivity patterns, or optimal storage. We’ve even taken hard feedback about unwanted side reactions or suboptimal crystallization and fed it back into new process runs—benefiting everyone down the line.

    Comparing With Traditional Pyridine and Bipyridine Carboxylic Acids

    Many projects start with commodity chemicals—simple pyridine or bipyridine frameworks, sometimes decorated with methyl or carboxyl groups. Such building blocks have powered decades of pharmaceutical discovery and industrial development. Yet, as needs progress, these core skeletons fall short in tackling new challenges in bioavailability, metabolic resistance, or new target engagement.

    By contrast, the inclusion of trifluoromethyl brings the ability to modulate pKa, increase resistance to metabolic oxidation, and improve membrane penetration. From formulators to synthetic chemists, users working with our 5'-trifluoromethyl variant confirm that minor changes on the scaffold can have outsized impacts on both the ease of synthesis and the performance of final molecules.

    Many users shared before and after results showing higher selectivity in ligand binding or more robust crystallization for x-ray studies—integral benefits driven by the trifluoromethyl moiety, not achievable with older, less functionalized starting materials.

    Supporting Users With Application Guidance

    Beyond simple supply, we see a responsibility to help users navigate this increasingly complex compound landscape. Our technical support addresses not just grade and spec questions but practical advice on solvent selection, handling, and derivatization paths. We have had cases where crystallization failed due to water uptake—simple tweaks like switching to a drier transfer and sealed containers made a material improvement in yield and product usability. That learning gets passed on to new customers, so future projects don’t hit old snags.

    Safety, Scalability, and the Push Toward Sustainability

    Our manufacturing emphasizes process safety—trifluoromethylation carries an extra level of hazard, and we strictly control exotherms and waste generation. Operators have direct experience with the practicalities of managing fluorinated intermediates, from secondary containment to precise temperature control. In scaling from bench to commercial volumes, our team prioritizes containment and exhaustive analytics, ensuring user safety further downstream.

    Sustainability counts—a topic taken seriously both internally and by our partners. Waste minimization and solvent recovery are not optional add-ons; they are integrated into regular process reviews. We keep fluorinated waste out of regular streams and work with specialty handlers for responsible disposal. Constant reviews look for ways to cut down on energy or reagent usage, driven by the knowledge that modern customers expect not just a product, but a responsible manufacturing pedigree.

    Real-World Innovations Driven by the Compound

    We’ve seen academic groups publish new ligands and small-molecule drugs built on the bipyridinyl core, with our compound serving as a springboard into new therapeutic areas. Agrochemical users have shown us data pointing to improved pest resistance or reduced runoff compared with traditional chemistries. Material scientists send detailed reports on the improved stability of coordination complexes derived from our intermediate—evidence that structural innovation pays dividends in field performance and patentability.

    It’s not unusual for users to ask for documentary evidence of origin and quality. We support these needs with clear documentation, trusted analytical data, and a willingness to undergo third-party audits and validation requests. Such openness builds confidence far exceeding any claims made in a product description.

    Staying Ahead: How Our Operation Adapts

    We treat manufacturing as continuous improvement, not a static pipeline. Any supply disruption, customer quality alert, or novel application request triggers internal review. We meet regularly with supply chain and R&D partners for early warning on coming market need shifts. Batch records and analytic data flow straight to technical leads who interpret trends and flag emerging issues.

    This way of working means we catch problems before they grow; adjust for raw material shifts; and fine-tune cycle times for quicker, scalable response. The real world rarely stands still, and we match the pace so users don’t face delays waiting for a classic intermediate repurposed for a new challenge.

    Contributing to Industry Benchmarks

    A focus on data quality and factual reporting supports both our customers and the broader industry. We participate in round-table discussions and present cumulative insights into bipyridinyl derivative handling—always backed up by real observations, not marketing claims. Lessons learned in controlling hydrate levels, minimizing trace organofluorine byproducts, and optimizing carboxylate protection strategies enrich the best practices that customers and peers rely upon.

    Sometimes researchers ask for alternate grades, higher purity, or specific packaging. We accommodate these requests directly, based on clear communication rather than generic promises. Fielding these special requests reminds us that a direct link between manufacturer and user fosters flexibility and faster turnaround—key advantages that distant brokers or traders can struggle to deliver.

    Looking Forward with Confidence

    Our engagement with new users always aims to foster a sense of partnership. Technology transfer visits, process troubleshooting calls, or custom batch requests see our team maintaining an active role in customers’ project success, rather than simply pushing inventory out the door. This approach not only sharpens our competitive edge, but also aligns with industry direction toward closer manufacturer-user collaboration and supply transparency.

    As markets push further into complex synthesis, narrower structural requirements, and ever-closer tolerance limits, suppliers must evolve. Our long-term focus remains clear: deliver advanced chemical building blocks with a foundation of real-world data, technical depth, and a network of support that matches today’s ambitious projects. That’s what gives our 5'-Trifluoromethyl-3,4,5,6-Tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid its unique position in the world of modern synthesis—not just as a point of differentiation, but as a trusted partner in advancing chemical progress.