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HS Code |
842189 |
| Chemical Name | 3-Amino-2-chloro-5-(trifluoromethyl)pyridine |
| Cas Number | 84371-65-3 |
| Molecular Formula | C6H4ClF3N2 |
| Molecular Weight | 196.56 |
| Appearance | White to light yellow solid |
| Melting Point | 56-59°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Structure | Pyridine ring with amino at position 3, chloro at position 2, and trifluoromethyl at position 5 |
| Synonyms | 2-Chloro-3-amino-5-(trifluoromethyl)pyridine |
| Smiles | C1=CC(=NC(=C1N)Cl)C(F)(F)F |
| Inchi | InChI=1S/C6H4ClF3N2/c7-5-4(6(8,9)10)1-2-11-3(5)12/h1-2H,12H2 |
As an accredited 3-Amino-2-chloro-5-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-Amino-2-chloro-5-(trifluoromethyl)pyridine, sealed with a screw cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packed drums/bags of 3-Amino-2-chloro-5-(trifluoromethyl)pyridine, ensuring safe, efficient chemical transport. |
| Shipping | 3-Amino-2-chloro-5-(trifluoromethyl)pyridine is securely packaged in air-tight, chemical-resistant containers and shipped in compliance with all relevant safety regulations. The package includes proper labeling and documentation, and is handled by authorized carriers specializing in hazardous materials to ensure safe, prompt delivery while minimizing risk of leakage, exposure, or damage. |
| Storage | Store 3-Amino-2-chloro-5-(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. Protect from moisture and direct sunlight. Ensure that storage is in accordance with local, state, and federal regulations. Use appropriate personal protective equipment when handling the compound. |
| Shelf Life | 3-Amino-2-chloro-5-(trifluoromethyl)pyridine typically has a shelf life of 2 years if stored properly in cool, dry conditions. |
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Purity 98%: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in target molecules. Melting Point 78°C: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine featuring a melting point of 78°C is used in agrochemical development, where it provides precise control during formulation processing. Particle Size <50 μm: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine with a particle size below 50 μm is used in catalyst preparation, where it enhances dispersion and reactivity in catalytic systems. Stability Temperature up to 180°C: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine stable up to 180°C is used in high-temperature material research, where it maintains integrity and effective reactivity. Moisture Content <0.2%: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine with moisture content less than 0.2% is used in electronics chemical synthesis, where it prevents hydrolysis and increases shelf-life. Color Index ≤10 APHA: 3-Amino-2-chloro-5-(trifluoromethyl)pyridine with color index not exceeding 10 APHA is used in fine chemical manufacturing, where it provides product color consistency and improved optical clarity. |
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Manufacturing 3-Amino-2-chloro-5-(trifluoromethyl)pyridine demands an eye for operational consistency and a strong understanding of its value in real-world chemistry. Years spent refining our process taught us that not all pyridine derivatives behave the same in syntheses, especially with multiple functional groups at play. This particular compound, with its unique arrangement of amino, chloro, and trifluoromethyl groups, consistently provides advantages for clients in the pharmaceutical, agrochemical, and material science sectors.
Each batch of 3-Amino-2-chloro-5-(trifluoromethyl)pyridine leaves our reactor under stringent controls. We maintain purity levels that typically reach or exceed 98%, measured by HPLC, and water content that rarely crosses 0.2%. These numbers do more than fill in a specification form—they result from hard-won experience. A single percentage point can make the difference between a downstream reaction working or stalling, so we monitor every variable from raw material quality to drying conditions. Keeping our own engineers on the production line means decisions are made quickly and problems are solved without waiting for instructions from a distant office.
Fluorinated pyridines stand apart thanks to their stability and unique electronic properties, and 3-Amino-2-chloro-5-(trifluoromethyl)pyridine finds repeated use as a building block in synthetic cycles where other intermediates falter. Medicinal chemists frequently select this compound for its combination of electron-withdrawing and donating groups, which fine-tunes molecular reactivity. The amino group activates specific aromatic substitutions, the chloro enables further coupling or displacement under milder conditions, and the trifluoromethyl group frequently increases metabolic stability in drug design. This particular substitution pattern doesn’t happen by accident—it answers specific synthetic challenges that simpler analogues cannot.
Work on this molecule hasn’t always been smooth. Pyridine handling, especially when you stack halogens and amines onto the same ring, can lead to unpleasant surprises during scale-up. Exotherms, unanticipated side products, and impurities such as isomers or over-chlorinated derivatives kept us troubleshooting for months on our earliest runs. Adjusting the sequence of functional group installation, improving the quality of trifluoromethylating agents, and regular training for operators all contributed to building a robust process. We don’t outsource any reaction steps to third parties, so every improvement in our procedure reflects directly in our product.
Chemists ask us about the differences between 3-Amino-2-chloro-5-(trifluoromethyl)pyridine and other pyridine derivatives, such as 2-chloro-5-(trifluoromethyl)pyridine or 3-amino-5-trifluoromethylpyridine. Here, the presence of the chloro next to the amino group does more than create an additional functional handle: it enables selectivity in subsequent reactions that can be difficult to achieve with other substitution patterns. For example, in Suzuki or Buchwald-Hartwig couplings, the ortho relationship between amino and chloro affects both rate and product selectivity. Our clients in medicinal chemistry report fewer byproducts and higher yields when optimizing conditions with this specific molecule, especially compared to cases where the amino group is meta or para to the chlorine.
Our facilities in the manufacturing zone allow us to handle large quantities of 3-Amino-2-chloro-5-(trifluoromethyl)pyridine. The crystalline solid remains stable at ambient temperatures, but exposure to moisture can lead to hydrolysis or loss of purity. Standard packaging involves high-barrier, internally lined drums that block out humidity during overseas transit. We recommend keeping containers tightly sealed and storing only in dry areas—this isn’t just a precaution written on a label, it reflects years of experience tracking product stability in real logistics chains. Every batch is tracked with dedicated lot numbers, and our QMS handles full traceability from raw material to shipment.
When this molecule first left the lab bench and entered multi-kilo production, process scale-up involved more than spinning a knob on a larger reactor. We invested in in-line sensors and real-time analytics to monitor impurity profiles and reaction exotherms. By integrating these controls, we cut batch failures and improved output consistency. Building reliable plant-level experience with these controls reduced downtime and rework, letting us provide more predictable lead times to clients under tight development deadlines.
3-Amino-2-chloro-5-(trifluoromethyl)pyridine rarely ends up in a final consumer product, but its true value emerges in the hands of downstream researchers. Our teams regularly support clients developing kinase inhibitors, anti-infective compounds, or new crop protection agents. Direct conversations with application chemists shape both our product quality standards and our technical documentation. If a client reports an unexpected impurity interfering with detection in their analytical HPLC, our support teams pull retention time data, run parallel analysis on retained samples, and suggest possible trace contaminants for monitoring. These incremental improvements stack up to make downstream development smoother for everyone.
Regulatory compliance for intermediates such as 3-Amino-2-chloro-5-(trifluoromethyl)pyridine is never one-size-fits-all. Every region brings different expectations, from REACH registration in Europe to required documentation in North America and Asia. Our regulatory teams devote substantial hours preparing submission files, validating analytical methods, and providing impurity dossiers. Over time, this documentation base allows us to support client filings with greater speed and confidence. We don’t just hand over a COA—we supply full analytical packages and are prepared to answer authorities’ queries about synthesis routes, trace metal content, or residual solvents.
Chemical manufacturing runs at its best when waste generation is minimized and resource use kept to a minimum. Early on, our pyridine synthesis routes generated higher volumes of solvent waste and unreacted halogenated byproducts. Implementing solvent recycling and refining our workup protocols dropped this waste by over 25%. In addition, installing fume scrubbing and water treatment in our plant ensured that air emissions and wastewater releases consistently meet or exceed local environmental standards. We continually collaborate with technology partners and regulatory specialists to audit and improve our sustainability performance, aware that cleaner production doesn’t just preserve reputation—it keeps our site running and neighbors happy.
Some projects require tweaks to the standard 3-Amino-2-chloro-5-(trifluoromethyl)pyridine material. Over the years, we’ve run custom purifications for clients seeking tighter salt profiles or specific particle sizes for solid handling. Our process flexibility means we adjust crystallization steps, solvent washes, or downstream drying to slot into specialized workflows. Academic partners sometimes need isotopically labeled versions, while high-throughput screening groups want volumes divided into pre-weighed vials. Collaborating directly with end-users benefits our plant by uncovering process optimizations that improve the general product line for everyone.
Once a molecule like this enters commercial production, the learning doesn’t stop. Batch-to-batch consistency only stays high through ongoing investment in both people and equipment. We hold regular troubleshooting sessions with synthesis operators and maintenance teams, using ‘lessons learned’ logs to patch up process weak spots as production ramps up or equipment ages. In cases where a customer’s process uncovers a rare impurity or unexpected reactivity, we track those observations and study root causes—sometimes leading to tweaks in our own process parameters or raw material suppliers. Each feedback cycle makes us a little faster, a little more reliable, and much more focused on delivering value where it counts.
Unlike simple pyridines or those bearing only chloro or amino groups, the simultaneous presence of both plus a trifluoromethyl group changes chemical reactivity and physical handling. Some intermediates lack functional handles for further derivatization, requiring extra synthetic steps or harsher conditions. Here, 3-Amino-2-chloro-5-(trifluoromethyl)pyridine streamlines synthetic planning by offering a ‘multi-tool’ structure for rapid construction of complex architectures. We’ve seen medicinal chemists save several weeks during SAR studies by starting from this intermediate rather than lower-substituted analogues. Its role as a ‘plug-and-play’ unit is well established across medicinal, agrochemical, and specialty chemical projects.
Shipping to global destinations demands resilience in packing and clarity in documentation. Moisture-proof packaging, full batch traceability, and rapid re-issuance of analytical data support customs clearance and downstream acceptance. Logistics failures—like a drum delayed by port inspection or a typo on a shipment notice—have real costs for everyone downstream. We have built redundancies into our shipping and tracking systems, so material arrives on time, in specification, and ready for immediate use. Your timelines become ours, underpinned by in-plant agility and direct communication lines.
Every molecule faces the test of time and changing technology. Process improvements in catalyst selection, greener solvents, and inline reaction monitoring continue to raise the ceiling for achievable quality. Our R&D team works closely with the production floor to trial new ideas on pilot scales before implementing at full capacity. Changes that bring measurable gains, like a recent adjustment to the trifluoromethylation step that improved yield by nearly 7%, don’t stay theoretical—they enter daily operation after validation. Every gain compounds over thousands of kilos, benefitting all users down the value chain.
Problems don’t always show up on the specification sheet. Sometimes a batch that passes every QC metric generates unexpected coloration during a customer’s coupling reaction. In such cases, our technical support doesn’t end with a data sheet—we review archived samples, cross-reference operator logs, and recreate the conditions in our own pilot plant. These follow-ups help us close the loop on recurring issues and, where possible, share learnings across our whole customer base. We believe every unsolved problem hides an opportunity to improve the molecule or the way it’s supplied.
The core strength of 3-Amino-2-chloro-5-(trifluoromethyl)pyridine surfaces at the bench where researchers need to unlock biotech, medical, or agrochemical value. It works as a precursor for pharmaceutical actives, boosting synthetic accessibility for both heterocycle construction and fragment-based drug discovery. Its reactivity profile lends itself to diverse reactions, including N-arylation, amide bond formation, and nucleophilic substitutions. Material scientists recognize the stability of the trifluoromethyl group and the advantageous electronics for advanced polymers or specialty coatings. Since each application has its technical demands, we’re tuned to listen and respond—adjusting how we sample and package to fit, not frustrate, R&D timelines.
Chemical manufacturing operates on trust built through consistency, clarity, and transparency—not just on price or specification. Many partners return to us because each new requirement, technical hurdle, or regulatory ask finds an answer grounded by time spent on the production floor. We’ve seen how a single intermediate can serve as the backbone of multiple commercial launches, and recognize that reliability at the commodity level enables invention at the application level. Our ongoing investment in people, plant, and customer service reinforces every kilogram of product shipped.
Supplying advanced intermediates means anticipating change—whether stricter environmental expectations, pandemic-level supply disruptions, or the rise of new synthetic methods. We regularly assess our feedstock sources, adapt to global logistical fluctuations, and stay up to date with upcoming regulations. By keeping all production steps in-house, and owning every layer from raw material receipt to outbound logistics, we reduce risk for ourselves and our partners. We advocate for honest communication if new technical, environmental, or regulatory hurdles rise. Together, we solve them, building robust, long-lasting supply networks for current and next-generation projects.
Experience teaches the value of molecules like 3-Amino-2-chloro-5-(trifluoromethyl)pyridine in high-stakes syntheses and new discoveries. Our daily work focuses on making every batch steadily, safely, and with an open channel for feedback. Collaboration between in-plant teams and users nurtures improvement, while never losing sight of why this molecule matters: as a key enabler in the search for tomorrow’s medicines and advanced materials. We invite ongoing conversation, confident that each shared experience creates better science, smoother development, and a more resilient global chemical supply chain.