2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1)

    • Product Name: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1)
    • Chemical Name (IUPAC): 3-chloro-5-(trifluoromethyl)pyridin-2-ylmethanamine hydrochloride
    • CAS No.: 107875-07-0
    • Chemical Formula: C7H6ClF3N2·HCl
    • 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

    335363

    Iupac Name 2-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)ethan-1-amine hydrochloride
    Cas Number 1229556-79-3
    Molecular Formula C7H6ClF3N2 · HCl
    Molecular Weight 248.59 g/mol (free base), 284.05 g/mol (hydrochloride salt)
    Synonyms 3-Chloro-5-(trifluoromethyl)-2-pyridinemethanamine hydrochloride
    Appearance White to off-white solid
    Solubility Soluble in water
    Purity Typically ≥98% (as specified by suppliers)
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, 25 grams, with tamper-evident cap, labeled with chemical name, hazard symbols, and handling instructions.
    Container Loading (20′ FCL) 20′ FCL container loaded with securely packed `2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1)` in sealed drums, ensuring safe transport.
    Shipping **Shipping Description:** 2-Pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) is shipped in tightly sealed containers, protected from moisture and light. Transport complies with relevant chemical safety regulations, including proper labeling and hazard documentation. Ensure temperature control if specified in the material safety data sheet, and handle as a potentially hazardous laboratory chemical.
    Storage **2-Pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1)** should be stored in a tightly sealed container, protected from moisture and light. Keep at room temperature (15–25°C) in a well-ventilated area, away from incompatible substances such as strong oxidizers. Avoid humidity and direct sunlight. Ensure the storage area is equipped for safe handling of chemicals and labeled in accordance with regulatory requirements.
    Shelf Life Shelf life: Store at 2-8°C, tightly sealed, protected from light and moisture; typically stable for 2 years under proper conditions.
    Application of 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1)

    Purity 98%: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation.

    Melting Point 185°C: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) with melting point 185°C is used in solid formulation processes, where it provides enhanced handling stability.

    Particle Size D90 <10 µm: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) of particle size D90 <10 µm is used in fine chemical manufacturing, where it allows for efficient dissolution and uniform mixing.

    Moisture Content <0.5%: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) with moisture content below 0.5% is used in moisture-sensitive synthesis routes, where it prevents hydrolytic degradation of reactants.

    Stability Temperature up to 110°C: 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride (1:1) with stability temperature up to 110°C is used in high-temperature reaction systems, where it maintains chemical integrity under processing conditions.

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    Certification & Compliance
    More Introduction

    2-Pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, Hydrochloride: A Chemist’s Perspective

    What Makes 2-Pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, Hydrochloride Distinct?

    Over a decade of handling aromatic amines has taught us to pay close attention to every atom and every substituent. The compound 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride brings together three key groups: a pyridine aromatic ring, a methanamine side arm, and a pairing of electron-withdrawing chlorine and trifluoromethyl substituents. These features not only alter its reactivity, but also define its profile among intermediates used in pharmaceutical and agrochemical projects.

    We do not regard this molecule as just “another pyridine-based building block.” Our years in synthesis have repeatedly shown that the position and identity of each ring substituent make or break each batch’s subsequent steps. The only way to prove reliability is batch-after-batch reproducibility, which comes from technical control, careful purification, and awareness of what downstream applications expect out of this hydrochloride salt.

    Product Model and Physical Characteristics

    Most users recognize this compound visually before they ever reach for a reference: pale, off-white or a faintly yellowish crystalline powder. Every lot is carefully monitored for color, as hints of brown or strong yellow often signal side products or incomplete reactions—an issue we address with process adjustments or further purification. Our standard product matches molecular formula C7H7ClF3N2·HCl and typically records a melting point close to 210°C, with decarboxylation or decomposition setting in shortly above that. Moisture control in storage and handling always gets top priority, since the hydrochloride salt readily picks up water from the air, risking caking or slow hydrolysis if left uncapped or exposed.

    Packing and delivery format matter a great deal to end-users who need dust-free handling for their automated lines. For kilogram to multi-kilogram orders, we favor HDPE drums with inner polyethylene linings. This keeps particles free-flowing and contamination out. End-users requesting analytical purity find our in-house HPLC methods distinguishing this amine hydrochloride from other isomers or ring-substituted analogues, with a purity assay not less than 98.5% on dry basis unless specialty requirements dictate otherwise. Moisture content is monitored at or below 0.5% w/w using Karl Fischer titration.

    Keys to Downstream Performance: Molecular Structure, Purity, and Solubility

    It’s easy to overlook the subtle impact of ring substituents on synthetic progress. In our hands, the trifluoromethyl and chlorine groups on the pyridine ring do two important things. The trifluoromethyl group at the 5-position draws electrons out of the ring, lowering basicity and altering nucleophilic character. In parallel, the 3-chloro group introduces both a steric block and further electronic withdrawal. This changes how the amine group engages in coupling or activation reactions—crucial for chemists designing heterocyclic scaffolds for pharmaceutical targets or advanced agrochemicals.

    We observed that solubility trends shift from more typical pyridinemethanamines. The hydrochloride salt dissolves efficiently in water and polar protic solvents, yet precipitation occurs rapidly in less polar mixtures. This characteristic influences both extraction and crystallization procedures at scale. Teams working on peptide or amide couplings regularly report that salt form not only ensures longer stability, but prevents evaporation or volatilization compared to free amine.

    Application Insights: Where Function Meets Performance

    Every year our product supports dozens of projects advancing a range of active pharmaceutical ingredients (API) and crop protection agents. Among synthetic chemists, this amine hydrochloride is sometimes selected at the earliest stage of drug development, when candidates with high metabolic stability and strong activity are being screened. The electron-poor nature of the trifluoromethyl-pyridine ring acts as a foundation for coupling with acid chlorides, activated esters, or various aldehydes in reductive amination, leading to uniquely substituted scaffolds.

    Other industries draw from similar features, tapping into this molecule’s resistance to metabolic breakdown and its ability to support fine-tuned molecular design. Agrochemical research often exploits the stability and electronic characteristics conferred by both chlorine and trifluoromethyl groups—a foundation for building blocks leading to herbicides or fungicides with extended field performance. We see that pharmaceutical intermediates made from this compound often show improved bioavailability or metabolic characteristics, precisely because of the balancing act between hydrophobic and hydrophilic features introduced.

    We regularly field questions from drug discovery teams about differences with other related pyridinemethanamine salts and are honest about both the opportunities and limitations. This molecule stands out for its lower nucleophilicity on the amine—owing directly to the electron-withdrawing ring substituents—which makes it less likely to participate in unwanted side reactions, especially under basic or oxidative conditions.

    Comparisons and Distinctions: Going Beyond Standard Pyridinemethanamines

    The difference between 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride and other methanamine derivatives is not just a matter of catalog numbers. The interplay between chlorine and trifluoromethyl sets this product apart from both simple methyl- and ethyl- analogues and from other multifluorinated pyridines. Chemists quickly learn that most simple pyridinemethanamine analogues show greater amine basicity and higher nucleophilicity, but react less selectively in challenging transformations.

    By experience, this trifluoromethyl-chloro compound resists overreaction with typical acylating agents, leading to cleaner product profiles and higher yields in demanding multistep syntheses. The hydrochloride salt, besides improving shelf-life and handling, avoids the volatility and odor issues often present in the free base. No matter how advanced laboratory ventilation has become, minimizing exposure to pungent amines remains an important part of safety and daily comfort.

    Colleagues working in formulation development also cite this compound’s crystalline nature as an advantage compared to oilier, more hydrophobic analogues. The powder’s manageable particle size helps keep dosing and weighing precise in both small-batch R&D and scale-up production. Chemists exploring new libraries appreciate the stable reactivity profile, which provides more predictable conversion in combinatorial synthesis arrays.

    Production Controls and Quality Assurance: Lessons from the Plant Floor

    We committed years ago to tightening each step of our manufacturing process, having seen the tough downstream effects that even minor impurities or process drift can cause. Each production batch begins with high-purity pyridine feedstock and carefully timed halogenation. Every reactor run prompts immediate in-process analytics, not just at the end. Chlorination and trifluoromethylation require monitored temperature and dose control to avoid unwanted polysubstitution, which in our experience remains a risk for less rigorous operations.

    Our purification stages rely on liquid-liquid extraction, followed by recrystallization steps tuned for salt formation. Dissolved gases, particularly HCl, are measured and controlled so that the hydrochloride form remains in the desired stoichiometry. Finished product undergoes batch-specific HPLC and NMR analysis, not only for identity, but for the profile of isomeric impurities below the 0.1% level. We have found, on more than one occasion, that neglecting this subthreshold level invites unpredictable outcomes in catalytic or condensation reactions downstream.

    Moisture monitoring during packaging and storage cannot be left to end users. We inspect water content before shipping and seal containers promptly with desiccants for longer logistics chains. A product that absorbs too much water invites not only caking, but creates the groundwork for hydrolysis or altered solubility, frustrating our partners at the most crucial moments in their synthesis runs.

    Safe Handling and Environmental Awareness

    Safe manufacture and distribution of this compound draw on both lived experience and regulatory developments. Our production teams use closed system transfer and engineered local exhaust, reducing risk from fine powder and vapor generation. Old habits relied on batchwise open transfers, but risk assessments and process audits drove us to upgrade to powder transfer in containment, addressing both worker safety and product cleanliness.

    Environmental responsibility figures strongly in our daily conversations. We recover process solvents and reactants—acetonitrile, toluene, dichloromethane—using vacuum distillation or phase separations, looping them back into subsequent production wherever possible. Waste brine and spent extraction streams are held for characterization and approved disposal, as traces of chlorinated organics or fluorinated compounds in effluent never pass unnoticed by regulatory bodies. Our environmental records and audits remain open to our customers, reflecting a hard-earned trust.

    Worker training and continuous safety review cut accident rates sharply in recent years. New staff receive in-depth instruction not just on hazard communication, but actual hands-on defense against spills, inhalation, or environmental discharge. Regular simulation of emergency procedures keeps both product and personnel safeguarded, even in peak production seasons.

    Supporting Innovation in Research and Scale-Up

    This hydrochloride salt finds its way into the research notebooks of some of the most accomplished synthetic chemists worldwide. We support collaborative work with universities, small biotech startups, and multinational pharma alike. Our technical team stays plugged in to customer development updates, providing real-time feedback on reactivity differences between this compound and simpler analogues. We have advised on process modifications to accommodate its lower amine reactivity, helping formulate milder acylation or alkylation conditions, and tuning solvent selection for rapid isolation or downstream purification.

    We participate in project troubleshooting, working alongside R&D teams to chase down root causes for stalled reactions or unexpected byproducts. Quite often, the clues trace back to subtle differences in purity, moisture, or byproduct profile—which our in-house analytics teams work to resolve at source. Our role extends beyond supply: we routinely help scale up pilot studies for kilogram to multi-ton lots, adjusting synthesis plans to accommodate larger reactors, mixing speeds, or filtration steps.

    Academic researchers value not only the consistent material quality, but our openness about potential impurities and process challenges. The “warts and all” approach, learned through direct manufacturing experience, means avoiding overpromising or supplying data that does not match practical outcomes. In return, our partners share feedback from compound evaluation runs, pointing out unexpected behaviors or application-specific quirks. This feedback loop directly improves the next round of manufacturing and speeds up the time from discovery to production.

    Regulatory Expectations and Product Traceability

    Modern chemical distribution must align with regional and global regulatory expectations. Our production, analysis, and shipment records remain accessible for customer audits and regulatory review as needed. Each batch is tracked from raw material intake to final shipment, including retention samples stored in controlled-access conditions. In case of process deviations or customer complaints, we commit to rapid trace-back and root cause analysis.

    Where regulatory compliance dictates, we support certificate requests and safety data preparation. Any differences in synthetic route, starting materials, or impurity profile are clearly documented and communicated. Our customers, especially in pharma and crop protection, look for this transparency as part of their own risk management programs. In one noteworthy case, a seemingly minor change in a third-party supplier’s halogen source led to altered trace impurity levels—a lesson reinforcing the importance of full supply chain vigilance.

    Continuous Process Improvement: Lessons from Repeated Production

    Reliability comes as much from listening to customer feedback as from internal technical review. Our pilot plant teams meet quarterly with both analytical and process chemists to review yield, impurity levels, and downstream performance trends. Every feedback loop, from small-scale bench runs to industrial-scale reactors, leads to process refinement. One such adjustment—switching to finer filtration immediately after initial salt precipitation—helped reduce trace solid carryover into isolated product, which in turn reduced color variability in final batches.

    Process engineers work closely with chemists to examine solvent and reagent consumption, minimizing waste and cost while ensuring product purity. Each kilo saved lowers both environmental impact and operational overhead. This lean management approach, rooted in direct plant experience, has proven more effective than top-down directives alone.

    Periodic review of analytical methodologies stays just as important. Advances in HPLC, NMR, and GC-MS analysis assist in quick identification of off-specification lots and tracing subtle impurities before they reach end users. By integrating control points and technical updates into every production campaign, we spot opportunities for excellence and detect risks before they escalate.

    Operational Challenges: What We Have Learned

    Our years of producing 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride have not been without challenges. We see strong batch-to-batch variability in certain raw materials, notably trifluoromethylating agents, sometimes leading to off-target substitution that must be caught quickly to avoid cascading issues. Some supply disruptions in starting materials, frequent in global trade, obligate contingency planning to keep commitments on lead time and product quality.

    Handling and safety practices continually evolve. Improvements in packaging, dust control, and product tracking stem from lessons learned during real events—including accidental dust emissions, clumping from moisture ingress, and tracing product batches through complex logistics. Every new lesson transpires into revised protocols and improved responsiveness to both customers and regulators.

    The Path Forward: Focus on Scientific Advancement and Dependable Manufacturing

    Research teams and production chemists depend on reliable, consistent supply of building blocks like 2-pyridinemethanamine, 3-chloro-5-(trifluoromethyl)-, hydrochloride to sustain project momentum. We see this material not as a generic commodity, but as a linchpin for innovation in molecular discovery and product improvement.

    Continual investment in both analytical infrastructure and manufacturing flexibility reinforces our ability to meet tight specifications and respond quickly to shifting research priorities. By holding fast to high standards in every batch and keeping a practical, hands-on sensibility, we have strengthened partnerships across the value chain—from the lab bench to final product development.

    We believe the real-world value of this compound lies not just in its molecular structure, but in our experience and daily practices. Supporting global innovation with confidence comes from understanding practical needs, solving problems collaboratively, and maintaining the willingness to adapt—or reinvent—processes as new challenges arise.