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HS Code |
243176 |
| Product Name | 2-Aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride |
| Molecular Formula | C7H6ClF3N2·HCl |
| Molecular Weight | 247.05 g/mol (free base) / 282.52 g/mol (hydrochloride salt) |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and polar organic solvents |
| Melting Point | No data widely available; check specific supplier documentation |
| Purity | Typically ≥98% (varies by manufacturer) |
| Storage Conditions | Store at room temperature, keep container tightly closed, protect from light and moisture |
| Synonyms | 2-(Aminomethyl)-3-chloro-5-(trifluoromethyl)pyridine hydrochloride |
| Smiles | C1=CC(=C(N=C1CCl)C(F)(F)F)CN.Cl |
| Usage | Chemical intermediate, pharmaceutical research |
| Hazard Classification | May cause irritation; handle with care |
As an accredited 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 2-Aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride, labeled and tamper-evident. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 6 MT packed in 200 kg UN-approved HDPE drums, securely palletized, suitable for export shipping. |
| Shipping | **Shipping Description:** 2-Aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride is shipped in tightly sealed containers under dry, cool conditions. It is classified as a laboratory chemical, with packaging compliant to safety and regulatory standards. Proper labeling, MSDS documentation, and protection from moisture and light are ensured throughout transit to maintain product integrity. |
| Storage | Store 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature, and handle under inert atmosphere if necessary, to minimize degradation or contamination. Ensure appropriate labeling and follow standard laboratory chemical storage protocols. |
| Shelf Life | 2-Aminomethyl-3-chloro-5-(trifluoromethyl)-pyridine hydrochloride typically has a shelf life of 2-3 years when properly stored. |
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Purity 98%: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures reproducible reaction yields and consistent product quality. Melting point 186°C: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with melting point 186°C is used in medicinal chemistry research, where its well-defined phase transition enables precise compound handling and formulation. Stability temperature 50°C: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with stability temperature 50°C is used in bulk storage and transportation, where this property minimizes degradation and maintains active compound integrity. Molecular weight 263.06 g/mol: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with molecular weight 263.06 g/mol is used in agrochemical development, where defined molar mass facilitates accurate dosing and formulation. Particle size <100 µm: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with particle size <100 µm is used in solid-phase synthesis applications, where fine particle size improves reaction kinetics and dispersion. Residual solvent <0.1%: 2-AMINOMETHYL-3-CHLORO-5-(TRIFLUOROMETHYL) - PYRIDINE HYDROCHLORIDE with residual solvent <0.1% is used in GMP-compliant manufacturing processes, where low solvent content enhances product safety and regulatory compliance. |
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In our daily production schedule, 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride stands out as one of those compounds that hold their value across several high-stakes sectors. Taking a closer look at the compound, you’ll notice the difference next to simpler pyridine derivatives. The introduction of the trifluoromethyl group and the hydrochloride salt formation does more than just tweak its name; both alter properties crucial for modern synthesis. Our experience on the line tells an interesting story—products like this start as chemical equations, but their importance only shows in the plant, the lab, and out in the field.
We stay practical on production floors. Let’s talk about what makes this compound so remarkable, starting with the trifluoromethyl group at the 5-position. Chemists chase these fluorinated motifs for a reason: they impact electron density, stability, and bioisosteric character, which makes a difference to medchem researchers looking for something lasting. The presence of a chlorine at the 3-position and the aminomethyl at the 2-position marks the backbone for late-stage modification or direct use in drug intermediates, agrochemicals, and specialty applications. It’s a piece of the toolkit for those chasing performance in tough regulatory climates.
Many of our team members have spent years developing robust batches of trifluoromethylated pyridines. With each cycle, attention to consistency makes a measurable difference. We monitor purity as though delivering active pharmaceutical ingredients, though in many cases the compound acts as a building block. Differences between lots can mean hours lost to troubleshooting in downstream syntheses. That is why each crystalline batch is checked for melting point, trace halide levels, and amine content. Impurity carries a cost—not just for us, but for every chemist downstream. Our technique relies on batchwise crystallization under nitrogen. In our experience, open vessels in older plants almost always pick up extra chloride contamination or water, reducing shelf-life and increasing the tendency toward clumping.
Even in crowded catalogs of multi-substituted pyridines, the 2-aminomethyl-3-chloro-5-(trifluoromethyl) variant has a clear identity. Pyridines with only one or two substitutions—say, a methyl or a single chloro group—don’t offer the polarity profile, the resistance to nucleophilic attack, or the pronounced lipophilicity this compound brings. The hydrochloride salt provides stability during shipping and storage, allowing handlers to avoid dusting associated with free-bases. Many who use alternatives with unsubstituted backbone or different salt forms have reported handling issues and variable performance in scale-up. Our customers in pharma and crop sciences seem to prefer the simple, consistent hydrochloride salt for these reasons.
Making derivatives or coupling on the aminomethyl position is also less challenging with this compound. The electron-withdrawing effects help control reactivity—something we learned the hard way scaling up for a European client. Simple aminopyridines, or those lacking the chloro trifluoromethyl arrangement, present a different reactivity profile, often giving more side products or requiring laborious purification. In several pharmaceutical specialties, the starting material dictates half the struggle. Because of its balanced reactivity, we’ve seen this one reduce total process time for customers.
Through collaborations, pilot programs, and feedback cycles, we hear about the successes and challenges from end-users first hand. In the pharmaceutical world, the compound frequently enters as a key intermediate in the synthesis of biologically active molecules. Many modern pharmaceutical design strategies need positions for late-stage functionalization—what our R&D colleagues call “synthetic handles”—and 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride provides that. A typical example: a customer working with kinase inhibitor scaffolds found that incorporating our pyridine intermediate cut their hydrogenation steps by nearly half. The time and cost savings went straight into further development cycles. With the move toward more selective, less toxic active substances, our product’s unique combination of stability and reactivity has proven its worth in this application.
The agricultural market also values this compound for its role in the synthesis of new-generation crop protection agents. In this space, consistent batch purity translates to reduced variability when producing pilot lots of actives needed for field trials. Even minor off-spec batches can affect formulation performance, causing ripple effects throughout a growing season—something that only becomes apparent at scale. Our plant runs regular process validation and traceability checks, because without these, unpredictable batches can halt new registrations or cause waste that cuts already thin development timelines short.
We keep an eye on shifting trends in environmental controls and industrial hygiene. In the field of trifluoromethyl pyridines, regulatory scrutiny has increased. From our perspective, quality now matters more than ever, not just for downstream compliance but for acceptance into wider global markets. Whether destined for EU, North American, or Asia-Pacific clients, batch records must allow full backward trace. We audit our supply of fluoro intermediates and chlorinating agents. For a product derived in part from halogenated chemistry, transparency in the origins of the reagents and the final batch record has become a company hallmark. Our compliance teams collaborate directly with production, and no lot leaves the plant without a clear traceability record.
We’ve also noticed the market demand for greener production routes. Several clients have asked about solvent recovery, effluent minimization, and energy usage. There’s pressure, rightly so, from authorities and local communities around plants like ours. Over the last decade, the plant adopted improvements in mother liquor recycling, distillation energy savings, and replacement of older, more toxic co-solvents. Whenever downstream clients show us their own green chemistry targets, we compare notes. Sometimes demand aligns with what is technically possible—sometimes not. But each year we move incrementally toward integrating cleaner, safer, and less wasteful production methods across all pyridine derivatives, this one included.
The real-world difference between good and bad hydrohalide salts becomes obvious on the drying line and at the packaging bench. Some salts, especially those prepared under humid or uncontrolled conditions, cake together, pick up water from the air, and clog feeders during downstream formulation. Through years of process learning, we invested in controlled drying environments, giving the hydrochloride salt less chance to absorb atmospheric water or produce unwanted agglomerates. In several test shipments to global partners, we found packaging inertness plays a critical role. Thin-layer polyethylene liners handle the task better than thicker but less chemically compatible materials; residual leachables sometimes show up in projects where organic lining hasn’t had enough R&D behind it.
On the analytical side, reliable assay and impurity profiling shape our understanding of what end users actually need. For years, washed samples off competitor materials revealed outliers in trace chloride, variable amine concentrations, or the presence of unwanted organics from unpurged solvents. Not every user checks these variables—some rely on spec sheets, but those working at process scale see the variation in API conversion or agricultural actives solidify. Based on direct conversations, users switching from other salt forms often share that hydrochloride consistently outperforms tosylate, mesylate, or even free base, especially in long-term storage or when handling needs strict dust control.
Bringing a pyridine derivative from the custom project phase to full production isn’t routine. Several years ago, as custom orders for this particular compound grew, we faced and solved issues scaling the selectivity of the trifluoromethylation step. In small flasks, temperature stability remains easy. The challenge lies in repeating those tight conditions at hundreds of liters. Overcooling, inconsistent mixing, or poor raw material feed can swing purity up or down, impacting the downstream hydrochloride salt formation step.
In the years since, we implemented automated dosing systems for key steps, allowing us to react within tighter tolerance and reduce the frequency of out-of-spec batches. Investments in process analytical technology (PAT) let us monitor reaction rates and impurity profiles in real time, rather than waiting for offline analysis. These improvements expanded what we could guarantee—not only to our own QA teams but to increasingly data-driven customers. Data from past production cycles fed into our decision-making, eliminating guesswork with each successive batch.
We encounter customers who often compare our product’s hydrochloride salt form to others like tosylate or free base. Most notice improved storage, easier handling, and better throughput during downstream chemistry when they switch. The hydrochloride counterion imparts stability, curbs static build-up, and prevents product migration out of sealed containers, which cuts down on waste. In free base form, especially in humid environments, users report caking and even chemical shifts after prolonged storage. Our feedback suggests that for those synthesizing active intermediates under strict regulatory oversight, the shift to hydrochloride gave measurable improvements in monthly yields and simplified process controls.
For users working with automated solid feeders, especially in agriculture or continuous manufacturing setups, this product’s granularity matters. Our team learned that small fluctuations in milling speed or a shift in dryer temperature presents in how material flows and suspends. Fine-tuning our blend of drying conditions and particle size control kept feeders moving well over long production runs, a lesson that came only after field support visits and troubleshooting on-site with partners. Customers who value low dust environments or who handle material at scale have a clear preference for batches with tighter particle size distribution, based on our shared results and incident logs from process lines.
Quality in chemical manufacturing doesn’t show only on an assay certificate—differences appear in customer returns, rework rates, and process efficiencies. Since switching to this product several years ago, a major client in the pharmaceutical sector reported a 20% drop in batch failures of an advanced intermediate. In deeper review, the outgoing impurity profile from the hydrochloride salt outperformed previous sources, reducing unwanted side products downstream. On the agricultural side, one partner observed that uniform flow in granulation led to fewer line stoppages and improved product throughput.
The role of hands-on quality assurance comes into focus as projects scale. Every shipment carries a record linking back to equipment logs, operator sign-offs, and a snapshot of intermediate chance-of-success. Unlike minimal spec approaches from distributive sources, the direct-from-manufacturer route gives users two advantages: a direct pipeline into in-plant knowledge and the ability to quickly resolve unique challenges. In our experience, being able to respond to special requirements—or rapidly adjust production in response to new findings—makes this product a consistent choice. We don't just observe, we adapt with each customer story.
With regulations tightening, raw material costs fluctuating, and the industrial world shifting toward sustainability, manufacturers like us have to proactively address the approaching challenges. In the case of 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride, ongoing process improvement matters. Upcoming investments focus on energy optimization, solvent recovery, and zero-discharge effluent. Collaborations with supply partners aim to strengthen the traceability chain from raw fluoro chemicals to final product. Time and again, such traceability supports smoother market registration, faster customer approvals, and reduces risk from regulatory changes.
Feedback-driven production—where customer experience shapes research priorities—continues to drive better versions of this compound. For several application streams, we’re piloting tweaks in impurity control, optimizing drying to limit residual water, and even adjusting packaging methods to resist variable climates during global shipping. Suggestions from formulators or process chemists who use our product on the front lines carry more weight than what a specification sheet alone might signal. As these recommendations feed back to the plant, improvements roll into the next round of batches.
In high-stakes industries, technical support makes the difference between smooth operation and costly rework. Each new project starts with direct dialogue between technical leads on both sides. We share technical bulletins, encourage regular handling training, and run remote troubleshooting sessions. Over time, these activities led to fewer mistakes in scale-up or handling. User success stories often carry a common theme: joint training up front prevents misunderstandings that otherwise invade the middle of expensive development cycles. In cases where process teams encounter unexpected handling or flow interruptions, our in-house team responds with site visits or real-time video troubleshooting to resolve bottlenecks without halting the process for days.
For newer chemists and formulators, we recommend handling this hydrochloride salt in well-ventilated spaces, using gloves and common lab PPE. Although it lacks the volatility or acute toxicity of some alternatives, respect for all synthetic intermediates underpins plant safety culture. Over the years, near-miss analyses revealed dust control and secondary containment prevent costly cleanups and health risks, especially as demand pushes upward and site turnover grows.
Looking to the future, our focus stays on reliability, data-driven improvement, and environmental integration. Growth in biologics and more sophisticated synthetic actives continues pushing demand for robust, high-purity intermediates. We continue to invest in better production monitoring, digital tracking of process parameters, and cross-company knowledge exchanges to ensure each lot meets ever-tighter standards. As new crop technology companies and pharmaceutical innovators bring forward tougher spec profiles, our goal remains consistent—providing a product that removes barriers, not creates new ones.
In short, what started as a specialized building block has evolved into a mainstay, recognized by users who value reliability, manageability, and transparent lineage through every processing step. Supporting the most innovative work in pharmaceutical, agricultural, and specialty chemical sectors, 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride continues to earn its keep—not only by structure, but by the lived experience of all who work with it.