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HS Code |
574881 |
| Chemicalname | 5-Amino-3-(trifluoromethyl)2-cyanopyridine |
| Molecularformula | C7H4F3N3 |
| Molecularweight | 187.12 |
| Casnumber | 89719-55-1 |
| Appearance | Off-white to light yellow crystalline powder |
| Purity | Typically ≥98% |
| Meltingpoint | 105-109°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storageconditions | Store at 2-8°C, tightly closed, in a dry place |
| Synonyms | 5-Amino-3-(trifluoromethyl)pyridine-2-carbonitrile |
| Smiles | C1=CC(=NC(=C1N)C(F)(F)F)C#N |
| Inchi | InChI=1S/C7H4F3N3/c8-7(9,10)5-2-1-4(11)13-6(5)3-12/h1-2H,(H2,11,13) |
As an accredited 5-Amino-3-(trifluoromethyl)2-cyanopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed with a screw cap, features a hazard label and printed product details for 5-Amino-3-(trifluoromethyl)-2-cyanopyridine. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Amino-3-(trifluoromethyl)2-cyanopyridine involves bulk packing in secure, sealed chemical-grade drums. |
| Shipping | 5-Amino-3-(trifluoromethyl)-2-cyanopyridine is shipped in sealed containers and packed to prevent moisture and light exposure. It is handled in compliance with chemical safety regulations and transported as a non-hazardous solid, typically via courier or freight services, ensuring protection against contamination and physical damage during transit. |
| Storage | Store **5-Amino-3-(trifluoromethyl)-2-cyanopyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents. Use appropriate chemical storage cabinets and clearly label the container. Handle under inert atmosphere if sensitive to moisture. Follow all relevant safety protocols. |
| Shelf Life | 5-Amino-3-(trifluoromethyl)-2-cyanopyridine has a typical shelf life of 2 years when stored cool, dry, and tightly sealed. |
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Purity 98%: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yields and minimal impurity formation. Melting point 122°C: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with a melting point of 122°C is used in crystallization studies for novel compounds, where predictable solid-state properties enhance reproducibility. Particle size <50 μm: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with particle size below 50 micrometers is used in micronized formulations, where improved dissolution rates in organic solvents are achieved. Stability at 80°C: 5-Amino-3-(trifluoromethyl)2-cyanopyridine stable at 80°C is used in high-temperature reaction processes, where product integrity is maintained without thermal degradation. Low moisture content <0.2%: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with low moisture content under 0.2% is used in moisture-sensitive syntheses, where side reactions due to water are significantly reduced. High solubility in DMSO: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with high DMSO solubility is used in medicinal chemistry screening libraries, where rapid compound dissolution enables efficient screening workflows. Molecular weight 185.12 g/mol: 5-Amino-3-(trifluoromethyl)2-cyanopyridine of molecular weight 185.12 g/mol is used in analytical method development, where precise mass accuracy improves quantitative analysis. Assay ≥99%: 5-Amino-3-(trifluoromethyl)2-cyanopyridine with an assay of at least 99% is used in reference standard preparation, where analytical reliability and consistency are assured. |
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After spending years refining our pyridine chemistry, we have learned that every upgrade in intermediate design comes from addressing customer feedback and laboratory hurdles. 5-Amino-3-(trifluoromethyl)2-cyanopyridine, sometimes called by its model identifier as 3-(trifluoromethyl)-5-aminopyridine-2-carbonitrile, steps out from the crowd of substituted pyridines in both its utility and process flexibility. We synthesize this compound under strict conditions to maintain consistency. Judging by our daily lab notes and plant logs, this intermediate demonstrates dependable batch integrity, which is often missing from more generic stocks.
The introduction of the trifluoromethyl group onto the pyridine ring, combined with a cyano and amino group at specific positions, delivers a nuanced reactivity profile. Many newer synthetic routes require unique halide or amine substitution patterns. With this configuration, customers bypass some tedious protection/deprotection steps, directly creating linkages that typically stall in earlier, less advanced analogs.
Trifluoromethyl-substituted pyridines have become essential for pharmaceutical developers seeking new scaffolds. Adding the CN and NH2 groups at the right positions gives medicinal chemists a more direct route to pharmacophores that exhibit enhanced metabolic stability, altered polarity, or specific targeting abilities. The molecule’s three major groups interact cleanly with modern transition metal catalysts, so cross-coupling applications move ahead with higher yields, even in scale-up.
From an agrochemical standpoint, the combination of electron-withdrawing and -donating groups on a single pyridine moiety opens the door for formulating crop protection products with greater environmental resilience and improved bioactivity. Over the last few seasons, conversations with field researchers showed us a growing interest in these tailored structures as starting points for next-generation herbicides.
Speaking to R&D teams struggling with cumbersome multi-step routes, we recognized that the dual functionality packed inside this product enables direct amide couplings, Suzuki reactions, and selective nucleophilic substitutions, all without introducing downstream purification headaches or problematic byproducts. Compared to more symmetrical or less densely substituted pyridines, working with 5-Amino-3-(trifluoromethyl)2-cyanopyridine shortens pilot plant timelines and lets process engineers experiment without fearing loss of product integrity.
Bench chemists in our network remarked on the molecule’s solubility in standard organic solvents. They see solid handling and easy extraction—two features that save time during work-up and isolation. While many other trifluoromethylpyridines either complicate crystallization or call for specialized storage, this one proves robust in drums and containers for extended periods.
Our QC lab runs high-performance liquid chromatography and NMR analyses to keep each lot within consistent purity and moisture content targets. The light yellow to off-white crystalline powder form travels well and reads clear under UV, so handlers can carry out routine inspections with confidence. Throughout our production chain, plant operators value the consistency and predictable melting point, which eliminates batch-to-batch variability and unexpected reprocessing steps.
We avoid overengineering: the melting temperature, solubility profile, and shelf stability all align with practical process needs. Any changes in crystal habit or impurity level register early in our on-site analytics. Because of this, end-users in the pharmaceutical, crop protection, and specialty materials spaces rarely see downstream failures or reruns attributable to off-spec intermediate feeds.
Looking at the commercial landscape for substituted pyridines, we’ve worked with many 2-cyano, 3-amino, or 5-trifluoromethyl variants as single substitutions. None show the same versatility that this trio of functional groups delivers together. The 3-(trifluoromethyl) positioning, in particular, confers a unique balance of lipophilicity and reactivity, making downstream functionalization much more predictable. Lesser-known analogs sometimes offer either reactivity or ease of handling—but seldom both.
Where customers previously tried simple amino-cyanopyridines or alternative mono/trisubstituted pyridines, they often reported needing additional protecting groups, special catalysts, or more aggressive purification. Each adjustment cost them time and material. Blending the power of all three groups in precise locations, our product outperforms these alternatives, especially in scalable laboratory and continuous-flow settings.
There’s no shortcut for on-the-ground manufacturing experience. We’ve witnessed pilot lines stall because a batch of poorly crystalline intermediate clogs the filters. We’ve heard complaints when customers tried analogs sourced from labs with less stringent process control, leading to poor conversion rates and high impurity burdens. Our focus stays on uniform process conditions, repeatable product behavior, and open feedback loops with end-users to quickly address actual bottlenecks.
Many raw material buyers want an intermediate that behaves the same way in the bench lab, the pilot plant, and full production. This isn’t a luxury. It’s a baseline requirement. The more complex the synthetic route, the more critical it becomes to avoid surprises mid-run. Our on-site teams know this from years of personally investigating every moving part in the chain—from pressure ratings on reactors to drying times and storage stability.
One of the biggest variables in chemical manufacturing comes from supplier inconsistencies. To avoid surprises, we invested in a process pipeline that scrutinizes not just purity, but also flowability, pack density, and batch morphology. In feedback from long-term partners, we hear how this attention to physical characteristics pays back in hours of saved troubleshooting and less waste during scale-up.
We have seen synthetic research teams demand higher-throughput screening and faster route optimization. The presence of the trifluoromethyl, amino, and cyano groups within a single scaffold lets chemists adjust their reaction setups with fewer preliminary runs. Instead of spending days sifting through feeble analogs or troubleshooting unstable intermediates, our clients move right into functionalization experiments and bioactivity assays.
Compared to older intermediates that can degrade during storage or require specialized inert handling, our product shows stable reactivity profiles even after transport across continents. This has allowed formulators working in global development centers to count on batch performance without special shipping and handling logistics.
Instead of being boxed into a narrow set of reaction pathways, project chemists are able to test a wide range of catalysts, solvents, and coupling partners. Reviews of data sets from client pilot facilities point to strong conversion rates and fewer failed reactions. This is not just chance: we track heat and mass balances at every stage, learning directly from every kilolab and metric ton produced.
Waste reduction is no longer an abstract sustainability goal—it's now built into procurement KPIs for every major customer. Our long collaboration with green chemistry advisors taught us that minor impurities in starting materials can cascade into downstream rework, solvent washing, and offcuts. By producing 5-Amino-3-(trifluoromethyl)2-cyanopyridine under controlled conditions, we push impurity profiles far below the limits that cause scale-up failures.
On real production lines, less sidestream production and fewer batch-to-batch corrections mean greater output and happier procurement managers. Better impurity control lets companies run their purification trains at higher throughput and reduces solvent burdens across the plant. Over a year, this translates to kilograms saved and reductions in landfill and regulatory disposal costs.
Modern chemical development doesn’t operate in a vacuum. Customers must answer to aggressive internal and external audit standards, manage traceability for every input, and comply with REACH, TSCA, and local environmental oversight. By basing our documentation and batch release processes around traceability and transparency, we remove pain points before shipments leave the gate.
Our verification records include certificate of analysis with every consignment, direct access to batch histories, and pre-audit reviews for flagged impurities or outlier data. By giving customers clear, traceable lot backgrounds and open communication from our staff chemists, procurement teams streamline their own compliance processes—no more time wasted tracking down answers or rerunning data.
Material safety is not a paper protocol; it shapes every phase of manufacturing. Production teams working with substituted pyridines report concerns about dusting, hygroscopicity, and contact sensitivity. Our technical advances lowered airborne particulates during handling by improving grain size distribution and bulk density. Long-term storage in warehouse conditions confirms no caking, pooling, or cross-contamination between lots.
Compared to earlier generations of pyridine intermediates, operators and lab staff face fewer handling hazards and avoid unnecessary exposure incidents. Smoother dispensing and monitored packaging reduce worker fatigue. All these improvements feed directly back into faster, less error-prone workflows at customer facilities.
With the rise of automation and digital batch records, many labs and plants shifted to seamless process data integration. By supplying 5-Amino-3-(trifluoromethyl)2-cyanopyridine with machine-readable barcodes and full digital trace files, supply teams keep their documentation fully synced. Audits become quicker and every production event links back to original inventory records. Customers avoid bottlenecks at incoming QC because all relevant information is present from the start.
Such digital traceability lets project managers monitor trends, spot recurring variances, and connect synthesis outcomes to supply chain records. Problems never stay hidden; improvements from our plant translate directly to customer returns on their own data dashboards.
We believe that an intermediate should fit evolving synthesis strategies, not restrict them. Thanks to ongoing collaboration with medical chemists, agricultural formulators, and materials scientists, our formulation of 5-Amino-3-(trifluoromethyl)2-cyanopyridine meets real-world demands, not only today’s catalogs. During regular project meetings and technical site visits, end-users have described how the molecule’s robust performance minimizes switching costs and lets them tackle new projects with fewer changes to existing workflow.
This compound powers up screening campaigns in pharma R&D, opens streamlined coupling options in pesticide innovation, and enables novel polymer architectures. Our own pilot site, equipped with continuous feedback from its technical advisory board, acts as a testbed for customer-driven process refinements.
Rarely do chemicals exist in a vacuum. The best structure in the world means little if it fails to deliver at scale, in application, or in the hands of a stressed overnight shift. Most of our innovations stem from real, sometimes blunt, customer feedback—sometimes joyous, sometimes filled with line stoppage and the search for answers.
One recent example: an agricultural chemistry partner ran stress tests on several structural analogs. Their report highlighted that our intermediate enabled an entire downstream coupling step to proceed under milder conditions, with higher isolation yield and less need for reprocessing. Such incremental improvements, resting on proper functionalization and real-world process knowledge, deliver major upside to tight project budgets and aggressive market timelines.
The past several years have shown that global chains for specialty chemicals must work with a mix of robustness and flexibility. Even a small disruption in intermediate delivery kicks off headaches stretching from laboratory to field trials. Because we control the process and track every production run, we can reroute sourcing, respond to urgent batches, and offer technical backup when new regulations or sudden scale-up projects surface.
Chemical manufacturing never stands still. As regulatory barriers rise and market appetites shift toward high-performance, low-impurity intermediates, we stay committed to direct customer engagement, transparent quality assurance, and quick-response formulation adjustments. The lesson: resilience and reliability go hand-in-hand with deep technical expertise and an unswerving focus on the problems customers actually face, not abstract priorities dreamed up in conference rooms.
Making intermediates like 5-Amino-3-(trifluoromethyl)2-cyanopyridine goes beyond running a process sheet or publishing a spec. It requires immersion in the realities of plant and laboratory demands: the pinch points, time sinks, and breakthrough needs that shape every project timeline. Our track record with this product comes not from marketing talk, but from grounded experience earned over years of hands-on operation, troubleshooting, and dialogue with every strata of the industry.
Anyone driving chemical innovation faces an ever-wider range of challenges—from squeezing more performance out of known scaffolds to managing exhaustive regulatory reporting. Our experience proves that a well-designed, consistent, versatile intermediate sets the groundwork for every downstream success.