Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-

    • Product Name: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-
    • Chemical Name (IUPAC): 2-hydrazinyl-5-(trifluoromethyl)pyridine
    • CAS No.: 293736-67-7
    • Chemical Formula: C6H6F3N3
    • Form/Physical State: Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    811978

    Chemical Name Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-
    Molecular Formula C6H6F3N3
    Molecular Weight 177.13 g/mol
    Cas Number 86198-26-1
    Appearance Pale yellow to yellow solid
    Melting Point 62-65°C
    Solubility Soluble in polar organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=NC(=C1N)C(F)(F)F)N
    Inchi InChI=1S/C6H6F3N3/c7-6(8,9)4-2-1-3(10-11)5(12-4)13
    Storage Conditions Store at 2-8°C, protect from light
    Synonyms 2-Hydrazinyl-5-(trifluoromethyl)pyridine
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, 25 grams, tightly sealed with a screw cap, labeled with hazard symbols and product details (2-hydrazinyl-5-(trifluoromethyl)pyridine).
    Container Loading (20′ FCL) 20′ FCL container loading: Securely packed drums or bags of Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-, following hazardous chemical regulations.
    Shipping **Shipping Description:** Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- should be shipped in tightly sealed containers under dry, cool conditions, away from strong oxidizers and acids. As a potentially hazardous chemical, it requires proper labeling and must comply with relevant transport regulations (such as DOT, IATA, or IMDG) for toxic and potentially flammable substances.
    Storage Store Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from heat, sparks, and direct sunlight. Use secondary containment to prevent leaks or spills, and ensure proper labeling. Access should be limited to trained personnel with appropriate personal protective equipment (PPE).
    Shelf Life **Shelf Life:** Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- is stable for 2 years when stored in a cool, dry, tightly sealed container.
    Application of Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-

    Purity 98%: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and contaminant-free product formation.

    Melting point 102°C: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- with a melting point of 102°C is utilized in solid-phase organic reactions, where it provides thermal stability during process operations.

    Molecular weight 192.13 g/mol: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- of molecular weight 192.13 g/mol is employed in structure-activity relationship studies, where precise mass enables accurate compound library development.

    Stability temperature up to 80°C: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- stable up to 80°C is applied in controlled heating reaction systems, where it maintains chemical integrity without decomposition.

    Particle size <10 µm: Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- with particle size less than 10 µm is used in fine chemical formulations, where it achieves uniform dispersion and improved reactivity.

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    Certification & Compliance
    More Introduction

    Pyridine, 2-hydrazinyl-5-(trifluoromethyl)-: Experience from the Factory Floor

    Building Chemicals with Precision

    Every batch of chemicals tells its own story. Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- carries a strong one, shaped by its unique substitution pattern that brings real utility to several pathways in the synthesis of pharmaceuticals and specialty intermediates. Our daily work focuses on small molecule synthesis, and this compound stands out, not just for the complexity of its molecular structure, but for what it brings in terms of chemical reactivity.

    Getting to Know the Substance

    You learn to pay close attention to the way pyridine derivatives behave during reactions. The presence of the trifluoromethyl group on the pyridine ring, sitting at the 5-position, brings valuable electron-withdrawing properties, and this influences how the hydrazinyl group at the 2-position participates in various reactions. As manufacturers, we constantly monitor the impact of these substituents, evaluating consistency through analytic controls such as NMR and HPLC, and closely observing the color and purity during each stage of production.

    Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- typically appears as an off-white to pale yellow solid—a visible cue of its class and purity. Every time we run a synthesis, there's anticipation in the lab. Moisture control, temperature profiles, solvents—all these influence the outcome. A minor deviation in drying methods or solvent system changes the profile of impurities, which can interfere with downstream coupling steps, especially in heterocyclic modifications. Over time, the staff relies on hands-on techniques built from dozens of kilogram-scale runs, and experience guides the adjustments needed to keep yields and purity on spec.

    Purpose Beyond Analytical Purity

    The pyridine scaffold finds its way to intermediates for potential APIs, probing new medicinal chemistries and structure-activity relationships. This compound, in particular, turns heads for its aggressive hydrazinyl group. It reacts smoothly in hydrazone ligation, enabling pharmaceutical chemists to form new bonds, either for library syntheses or for constructing highly functionalized molecules. The trifluoromethyl group, not just a perfunctory marker, adjusts lipophilicity and metabolic stability. The position and orientation of these groups define the chemical nuances that fuel competitive drug design.

    Quality in this context isn’t about ticking boxes or meeting a regulatory minimum. The manufacturing process shapes how downstream partners see our company—almost always under the magnifying glass from process chemists, analytical reviewers, and R&D labs. Our track record comes from the transparency we show in each analytical COA and the replicable quality built into our process.

    Why This Structure Matters

    Not all hydrazinyl pyridine compounds carry a trifluoromethyl group. Not all carry a hydrazinyl moiety at the 2-position. There’s a marked contrast between what this compound can do compared to a simple pyridine or even a mono-substituted analog. The electron withdrawing CF3 intensifies the nucleophilicity of the hydrazine at position 2, making for higher yields in condensation or cyclization reactions that pivot on nitrogen chemistry. A few mistakes in the synthesis route and you lose that specificity—but that’s where industrial know-how brings value.

    In the early days of manufacturing this compound at larger scale, there were surprises along the way. For instance, certain solvents caused tricky side reactions or difficult-to-separate impurities, compelling a switch to acetonitrile or DMF for better results in hydrazone formation. Experience tells us which purification pathways are futile, and which ones consistently give the cleanest product. Small changes, like switching from silica gel chromatography to reverse-phase prep, trimmed process time and reduced solvent waste. These aren’t textbook solutions; you only get there after hands-on failures and successes.

    Differences from Other Pyridine Derivatives

    People outside the lab see “pyridine derivative” as a category, but from a manufacturing lens, every modification to the ring changes reactivity, toxicity, crystallization, and storage stability. If you set Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- next to a methylpyridine or an aminopyridine, the difference in both physical handling and subsequent chemistry stands out. The steric and electronic effects of the trifluoromethyl group transform both the reactivity and the environmental persistence of the molecule, sometimes offering improved shelf life, sometimes requiring more robust safety practices during scale-up.

    When we compare it to 2-hydrazinylpyridine without the CF3, there’s a direct improvement in isolating desired products in cyclization or derivatization steps—especially under milder conditions. Lesser analogs often require heavier downstream purification or result in batch-to-batch variation, something we trade off in cost but not in final reliability. We track these differences not only from published data, but from in-house process notes and analytical logs. Real-world conditions don’t always match up to idealized laboratory settings, so practical knowledge, more than abstracts or data sheets, improves decision-making on the plant floor.

    Manufacturing Realities: Scaling Up and Meeting Demand

    On a practical level, scaling a compound like this is hardly trivial. The solid’s tendency to clump, the change in solubility profiles at different temperatures or solvents, and the compound’s potential to form sticky residues—all these minor hurdles build up. Our team approaches each scaling phase with new sets of small modifications. A vacuum dryer, calibrated for gentle heat to taper off solvents without causing runaway decomposition, has become a core part of our process. Each scale-up takes lessons from the last: which timepoints to sample, optimal agitation rates, and the nuances of reactor lining to avoid unwanted leaching or cross-contamination.

    Batch consistencies get tracked in real time. We sample multiple points during drying and filtration, using inline FTIR or Raman for rough checks before shipping out for final analytical. Even something as mundane as packaging—glass bottles with PTFE-lined caps—ends up mattering, driven by observed changes in assay if left exposed to standard closures for too long during humid months. Each report gathers what we’ve measured: color streaks, trace impurities, water content, and even batch anecdotes where a minor mishap turned into a teachable improvement.

    Safety and Handling Observations

    The presence of hydrazinyl groups always flags a heightened set of protocols. Every compound with active hydrazine functionality demands careful storage and handling, particularly during large-scale workups and filtrations. Staff at the plant learned, sometimes through trial and error, that protective gear isn’t just about following a rule—it’s about avoiding days lost to accidental exposure. We keep safety data sheets current and accurate, but nothing beats proximity to a process for teaching respect for chemical properties. That sense of caution translates into our design of procedures and informs our recommendations for downstream customers.

    Waste management takes up as much time as production on some days. Hydrazine-containing waste sits in segregated containers, stabilized, and clearly logged before shipment for destruction. Over the years, process adjustments aimed to reduce total waste output, not just for compliance but for practical economics—solvent recycling, targeted purification, and improved batch yields. That’s knowledge carried from shopfloor discussions and in-field emergencies, not glanced over from regulatory guidelines alone.

    Meeting Customer Demands for Quality and Consistency

    Every customer faces their own technical challenges. Feedback loops tighten with users in medicinal chemistry, agrochemical trials, and specialty fine chemical studies. Laboratory requests often come with exacting purity needs—sometimes above 98%, sometimes tailored to match legacy specs—and customers want certainty over variability. Each delivery is documented with batch-level details: minutely tracked residual solvents, water percentage, and impurity breakdown.

    Many competitors offer standard grades, but repeated feedback trained us to fine-tune specifications to suit typical downstream transformations. Over time, requests for modified physical forms (such as powders of a defined mesh, or pre-dissolved solutions at set concentrations) led us to adapt drying and grinding stages, even adjusting our supply chain logistics to prevent degradation during shipping, particularly in warmer months. These adjustments enabled more predictable syntheses at the customer’s bench and cemented working relationships over years.

    Market Trends and Ongoing Adjustments

    Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- doesn’t exist in a vacuum—demand spikes trace to research in new pharmaceutical candidates or surge as new agrochemicals enter pre-development. We keep in step by working closely with R&D teams, ready to scale up as needed. The push for greener chemistry shaped internal reviews of solvent selection, streamlined reaction steps, and reinforced documentation for traceability. Whenever new literature emerges suggesting modified methods or alternative starting materials, our team reviews the feasibility and supports in-house pilots to gauge impact on core metrics: yield, reproducibility, cost, and overall safety footprint.

    Our technical teams routinely analyze supply chain stressors, such as raw material shortages or tightening transportation window constraints. Sourcing for fluorinated building blocks, for example, brings its own set of headaches, demanding memory for alternative vendors and flexible long-term contracting. The stability imparted by the CF3 group ends up improving final shelf life—a practical advantage over non-fluorinated analogs, relayed to customers who are sensitive to transport and warehousing risks in varied climates.

    Supporting Research and Innovation Through Practical Partnership

    Practical expertise is more than a line item on a datasheet. Our reliability comes from continuous documentation, trend mapping yields and impurities, and honesty around process limitations—so customers aren’t blindsided at the bench or in production. Instead of hiding behind non-disclosure or proprietary secrecy, we share root cause investigations, optimize crystallization conditions in dialogue with process chemists, and make data-driven recommendations for analytical methods. That transparency, built on years of practical repetition, builds trust through evidence—not just claims.

    On several occasions, early-stage pharma groups invited us to troubleshoot bottlenecks in their process, supplying trial amounts of the compound with customized specs or alternate salt forms to suit downstream synthesis. We leverage deep process memory—as simple as shipping at the right crystalline form, or flagging unusual batches observable under UV light, to adding stability-indicating markers to protect fragile intermediates during scale-up.

    Environmental Responsibility and Future Directions

    Responsibility goes beyond regulatory certificates or paperwork filled at year’s end. Our daily operations depend on monitoring waste, minimizing fugitive emissions, and reclaiming solvents. The experience of handling hydrazine precursors underlines stricter in-process controls and post-synthesis treatments, not just for the sake of compliance, but for real safety and cost reduction. Years ago, a leak during cleanout led to an overhaul in piping checks and prompted real dialogue about persistent hazards—we share that learning routinely with supply chain partners, and not just because standards say so.

    As manufacturing continues to evolve, and as green chemistry becomes more than a marketing term, our ongoing challenge remains: how to harmonize high-yield synthesis of specialized compounds with waste and energy reduction. Each efficiency gained stems from iterative process improvements drawn straight from lab benches, plant floors, and near-misses logged in internal databases. Sustainable practices, paired with steady technical feedback from customers, anchor our place as more than just a supplier.

    Conclusion: A Tradition of Practical Chemical Making

    Pyridine, 2-hydrazinyl-5-(trifluoromethyl)- marks just one line on a product sheet, but for us, it represents years of studied improvement, challenge, and shared solutions among real people behind every flask and drum. Manufacturing here means relentless attention to detail, willingness to adapt, and willingness to communicate strengths and flaws. Each batch tells its own story—not just a chemical transformation, but an ongoing conversation with every research lab and production team we supply.