2-Amino-6-(trifluoromethyl)pyridine

    • Product Name: 2-Amino-6-(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 2-Amino-6-(trifluoromethyl)pyridine
    • CAS No.: 22233-78-5
    • Chemical Formula: C6H5F3N2
    • Form/Physical State: Solid
    • 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

    901445

    Cas Number 22233-90-9
    Molecular Formula C6H5F3N2
    Molecular Weight 162.12
    Iupac Name 2-amino-6-(trifluoromethyl)pyridine
    Appearance White to off-white solid
    Melting Point 41-45°C
    Boiling Point 215-217°C
    Density 1.38 g/cm3
    Solubility Soluble in organic solvents like DMSO, methanol
    Smiles C1=CC(=NC(=C1)N)C(F)(F)F
    Refractive Index 1.487
    Synonyms 6-(Trifluoromethyl)pyridin-2-amine

    As an accredited 2-Amino-6-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 2-Amino-6-(trifluoromethyl)pyridine is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Container Loading (20′ FCL) 20′ FCL container loading for 2-Amino-6-(trifluoromethyl)pyridine ensures secure, bulk shipment, compliant with safety and chemical transport regulations.
    Shipping 2-Amino-6-(trifluoromethyl)pyridine is shipped in tightly sealed containers under dry, cool conditions to prevent moisture absorption and degradation. It is classified as a hazardous chemical, so packaging complies with relevant regulations, including labeling and documentation. Handle with care during transport, avoiding exposure to heat, open flames, or incompatible substances.
    Storage Store 2-Amino-6-(trifluoromethyl)pyridine in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Ensure proper labeling and use appropriate personal protective equipment when handling. Keep away from heat and store at ambient temperature unless otherwise specified by the supplier.
    Shelf Life 2-Amino-6-(trifluoromethyl)pyridine is stable under recommended storage conditions; shelf life is typically 2–3 years in cool, dry environments.
    Application of 2-Amino-6-(trifluoromethyl)pyridine

    Purity 98%: 2-Amino-6-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product integrity.

    Melting point 40–44°C: 2-Amino-6-(trifluoromethyl)pyridine with melting point 40–44°C is used in agrochemical formulation, where consistent melting aids homogeneous blending.

    Stability temperature up to 120°C: 2-Amino-6-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in high-temperature reactions, where it maintains structural integrity during processing.

    Particle size <50 μm: 2-Amino-6-(trifluoromethyl)pyridine with particle size <50 μm is used in fine chemical manufacture, where rapid dissolution improves reaction rates.

    Water content <0.2%: 2-Amino-6-(trifluoromethyl)pyridine with water content <0.2% is used in electronic chemical synthesis, where low moisture prevents unwanted hydrolysis.

    Molecular weight 164.12 g/mol: 2-Amino-6-(trifluoromethyl)pyridine with molecular weight 164.12 g/mol is used in heterocyclic compound production, where precise stoichiometry ensures reproducibility.

    Monitored by HPLC assay: 2-Amino-6-(trifluoromethyl)pyridine with quality monitored by HPLC assay is used in custom synthesis services, where analytical verification assures product reliability.

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    Certification & Compliance
    More Introduction

    2-Amino-6-(trifluoromethyl)pyridine: Value in Modern Synthesis

    Building Versatility into Every Molecule

    In our field, we deal with a wide variety of pyridine derivatives, but 2-Amino-6-(trifluoromethyl)pyridine stands out. Its structure – a trifluoromethyl group attached to the 6-position, paired with an amine at the 2-position – opens the door for significant reactivity. This basic framework delivers more than just a starting block, thanks to the unique interaction between the electron-withdrawing influence of the CF3 group and the nucleophilicity enabled by the amino moiety. That interplay changes the course of downstream modifications in ways that other substituted pyridines don’t offer.

    Through years of scale-up and R&D, it's clear that this compound adds value at multiple stages, particularly for those working in the pharmaceutical and agrochemical industries. The specificity of the meta-substitution means our teams have seen consistent, clean results in a range of cross-coupling reactions and heterocycle construction processes. We’ve supplied this chemical to researchers testing options for kinase inhibitor scaffolds as well as partners investigating new crop protection candidates, and in both cases, the molecule’s stability and selectivity have been key.

    Our View on Purity, Quality, and Tailoring to Process Demands

    Lab requirements aren’t uniform, and we prefer not to think about manufacturing as just “producing a molecule” but about guiding the product into its optimal form for its next use. Over time, we’ve noticed critical differences between what, say, a drug discovery lab values versus a company in pigment development. We typically prepare 2-Amino-6-(trifluoromethyl)pyridine with a purity above 98% (HPLC), providing batches with moisture content and residual solvent data on request. From multiple recrystallization cycles to controlled drying conditions, the routines for ensuring batch consistency have been shaped by direct feedback from customers who’ve tried to run late-stage functionalization reactions or need reliable data for regulatory filings.

    We take pride in running in-house analytical checks, especially NMR and GC-MS, beyond spot tests. Even a tiny deviation can ripple forward, affecting catalytic reactivity or leading to downstream purification headaches. What we've found is that most off-the-shelf pyridines, often produced in bulk for the fine chemicals market, rarely manage such tight controls – and complaints usually follow. Our repeat customers cite fewer delays from residue traces or subpar color, which matter when you’re aiming for high-value downstream applications like API intermediates or diagnostic probes.

    Handling and Processing Experience Counts

    Spend enough years in chemical manufacturing and you start spotting nuances in how fine specialty compounds behave. For example, 2-Amino-6-(trifluoromethyl)pyridine exhibits strong chemical stability, with no real tendency to hydrolyze in ambient conditions, unlike some other aminopyridines. Its relatively low melting range makes it straightforward to work with during synthesis or formulation – the substance stays manageable at room temperature, and on occasion, we've advised clients to avoid high-speed stirring since that can hasten unwanted dust formation. Knowing these quirks defines the difference between industrial chemistry as theory and chemistry as practiced day after day.

    Every stage of handling reflects lessons learned from real setbacks: clogged filters, batch cross-contamination, recrystallization hiccups. By tracing these back to sources as small as trace metal content or solvent carryover, our team draws on actual production runs instead of blanket manufacturing “rules.” It’s this blend of diligence and hard-won know-how that moves a specialty chemical from check-box purity to genuine reliability.

    Real-World Usage: Where This Molecule Makes a Difference

    The trifluoromethylated pyridine isn’t for bulk, undemanding usage. It finds its niche when a project calls for fine control over electronic effects on the ring, or resilience during demanding synthetic steps. Medicinal chemists often gravitate toward this compound because introducing the CF3 group not only changes hydrogen bonding patterns but also changes metabolic stability of final products. Our partners in drug discovery routinely incorporate it as a core piece in kinase inhibitor libraries or anti-inflammatory agent analogues.

    We’ve watched the molecule’s use expand. Agricultural chemical clients utilize it for next-generation herbicide scaffolds, basing much of their design on the ability to modulate biological activity through both the electron-rich amino function and the electron-deficient CF3 on the same aromatic ring. This duality gives molecular designers a chance to fine-tune activity in a way that other substituted pyridines can’t manage. We've supported several multi-kilogram campaigns based on the client’s need for both high-purity and scalable output.

    Comparing with Other Pyridine Derivatives

    It’s tempting to think of pyridine chemistry as a series of minor tweaks to the same base structure, but our production experience say otherwise. Introducing a CF3 group affects both volatility and solubility, which redefines safe handling parameters and even changes scaling strategy for larger campaigns. We routinely provide straight 2-aminopyridine as well, and those who switch to its trifluoromethylated cousin notice the direct impact: improved acidity of adjacent protons, distinct NMR shifts, and a marked resistance to oxidative degradation in storage.

    On the other hand, similar products like 2-Amino-4-(trifluoromethyl)pyridine or 3-Amino-6-(trifluoromethyl)pyridine don’t show the same combination of electron demand and ring activation. We have seen different hydrogenation profiles and variable yields in Suzuki and Buchwald-type couplings. It often boils down to the specific position of the substituents – a seemingly small change but one that we see amplified in project-by-project feedback.

    Organic synthesis doesn’t tolerate mediocre input. For those running high-throughput screening, signal clarity in LC-MS traces or yield reliability during scale-up matter more than catalog page entries. Handling hundreds of kilograms per year forces you to watch for supplier shortcuts like incomplete purification or improper solvent stripping, common issues with lower-grade imports. Years ago, a client pointed out troublesome by-product profiles in a competing batch; after in-house analytical work, we found the origin in downstream halide contamination due to lack of distillation steps. That sort of outcome stays with you and drives how we operate.

    Supporting New Research Directions

    Our manufacturing group supports customers leading research in targeted therapies and modern crop sciences. The pace of innovation means our role extends from batch supply to joint evaluation of synthetic feasibility. Recently, we collaborated on crafting new functionalized conjugates built from a 2-amino-6-(trifluoromethyl)pyridine core. The structure’s bias toward both nucleophilic attack and stabilized aromatic substitution allowed previously unexplored reactivity that older scaffolds couldn’t deliver.

    Feedback from the field tells us there’s more to value than specification in a data sheet. Positive client experiences often stem from the reality that our batches turn into publication-ready reactions, not “troubleshooting sessions” for grad students. We see repeated orders from synthetic teams who need reliable lot-to-lot consistency, since even minor variation can lead to wasted time during screening or SAR cycles.

    Troubleshooting and Real-World Chemical Practice

    Problems can show up anywhere in the value chain, and tight margins mean a misstep can easily tank an entire production run. Our plant directs significant effort into minimizing downtime from solvent incompatibility or crystallization faults – issues commonly triggered by minor formulation differences from batch to batch. For 2-Amino-6-(trifluoromethyl)pyridine, we’ve learned not to overlook pH and ionic strength in post-synthetic washing steps, since improper workup leads to trace acid impurities that later complicate analytical characterization.

    Over the years, we’ve fine-tuned our approach based on customer feedback and our own scale-up failures. Managing finely tuned temperature ramps, working up to controlled cooling, and finishing with rigorous filtration with low-extractables equipment all help avoid downstream hassle. Customers hoping to skip steps to save on operating costs usually end up learning that shortcuts only compound headaches later.

    Environmental Considerations

    Beyond the four walls of the plant, global regulations and green chemistry mandates shape how we work. Trifluoromethylated aromatics receive close scrutiny, and production demands environmental controls not always present in older facilities. Our engineers designed collection and scrubbing systems for fluorinated off-gassing, and solvent recycling programs help us manage VOC exposure and raw material costs. The push for green manufacturing isn’t just rhetoric; it’s reflected in our waste water analyses, permitting documentation, and even our choice of process chemistries to reduce hazardous by-products.

    This mindful approach also benefits customers down the supply chain. Substantial time goes into helping them anticipate environmental hazards or compliance issues in markets with emerging fluorochemical regulations. Upfront solvent selection, batch record transparency, and lifecycle reporting aren’t extras. For us, these are essential for traceability and maintaining business relationships that span years, not just quarters.

    Encouraging Collaboration and Process Transparency

    After years in chemical manufacturing, we value clear, honest communication above all else. Past partnerships have taught us that long-term business relies on openness about process challenges, not just successes. With 2-Amino-6-(trifluoromethyl)pyridine, more than a few projects prospered because both sides were willing to discuss limits and potential. This attitude applies from initial samples to full-scale deliveries.

    We maintain batch records and supply analytical data in forms that suit regulatory and R&D expectations alike. If a project calls for a custom intermediate based on this core scaffold, we engage clients to offer realistic timelines, feasibility checks, and process safety evaluation. This practice stemmed from hard-earned lessons – one costly incident in which late-stage data gaps forced an international shipment recall continues to shape our emphasis on transparency today.

    Future Developments in Pyridine Chemistry

    The significance of fluorinated building blocks in medicinal and materials chemistry keeps growing. More research teams ask for complex substituted pyridines than ever before, driving us to refine our routes and analytical routines. Some projects focus on making new imaging agents; others chase hybrid agrochemical scaffolds resistant to both oxidative and enzymatic breakdown. Our hands-on role in pilot runs lets us spot shifts in downstream requirements, for example tweaking reaction stoichiometry or adjusting purification steps as new impurity profiles emerge.

    We also see a trend toward replacing more hazardous halogenated reagents, which shapes how we supply input chemicals. Teams value a route that avoids specialized or tightly controlled solvents, and reduces exposure risks at both the lab and plant scales. 2-Amino-6-(trifluoromethyl)pyridine plays well in these scenarios, matching both reactivity and compliance needs.

    The Crucial Role of Experience

    It’s easy to read about specialty chemicals in textbooks or databases. Daily production tells a much deeper story – one shaped by troubleshooting, repeated improvement, and decades spent supporting customers with very specific project goals. This background forms the backbone of how we approach every batch we make.

    As a manufacturer, we don’t just deliver molecules; we offer a record of accumulated problem-solving that underpins every shipment of 2-Amino-6-(trifluoromethyl)pyridine that leaves our facility. Every subtlety in the compound’s production and application reflects not just what works in the lab for one test, but what succeeds again and again in the real world of advanced chemistry.