|
HS Code |
185139 |
| Chemical Name | 2-hydrazino-4-trifluoromethylpyridine |
| Molecular Formula | C6H6F3N3 |
| Molecular Weight | 177.13 g/mol |
| Cas Number | 107295-10-9 |
| Appearance | Light yellow solid |
| Melting Point | 77-80°C |
| Boiling Point | No data available |
| Solubility | Soluble in organic solvents like DMSO and DMF |
| Density | No data available |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Purity | Typically ≥98% |
| Synonyms | 2-Hydrazinyl-4-(trifluoromethyl)pyridine |
| Smiles | NNc1nccc(C(F)(F)F)c1 |
| Inchi | InChI=1S/C6H6F3N3/c7-6(8,9)4-1-2-5(11-10)12-3-4/h1-3H,10H2,(H,11,12) |
As an accredited 2-hydrazino-4-trifluoromethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2-hydrazino-4-trifluoromethylpyridine is packaged in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | 20′ FCL container loading: 2-hydrazino-4-trifluoromethylpyridine packed in sealed drums, pallets, labeled securely for safe international transport. |
| Shipping | **Shipping Description:** 2-Hydrazino-4-trifluoromethylpyridine should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be clearly labeled, handled as a hazardous chemical, and transported in accordance with relevant international and local regulations (e.g., DOT, IATA). Use appropriate cushioning and secondary containment to prevent leaks or spills. |
| Storage | Store 2-hydrazino-4-trifluoromethylpyridine in a cool, dry, and well-ventilated area, tightly sealed in a chemically compatible container. Keep away from heat, ignition sources, and incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Label the storage container clearly, and restrict access to trained personnel only. Follow all relevant safety and local regulatory requirements. |
| Shelf Life | 2-hydrazino-4-trifluoromethylpyridine should be stored cool, dry, and tightly closed; shelf life is typically 2-3 years under proper conditions. |
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Purity 99%: 2-hydrazino-4-trifluoromethylpyridine with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized byproducts. Melting Point 105°C: 2-hydrazino-4-trifluoromethylpyridine with a melting point of 105°C is used in organic synthesis reactions, where it allows for precise thermal control during processing. Molecular Weight 178.12 g/mol: 2-hydrazino-4-trifluoromethylpyridine at a molecular weight of 178.12 g/mol is used in agrochemical research, where accurate dosing and formula optimization are achieved. Stability Temperature up to 120°C: 2-hydrazino-4-trifluoromethylpyridine with stability up to 120°C is used in high-temperature coupling reactions, where it maintains structural integrity and reactivity. Particle Size <10 µm: 2-hydrazino-4-trifluoromethylpyridine with particle size below 10 µm is used in catalysis applications, where enhanced surface area accelerates reaction kinetics. Water Solubility 8 mg/mL: 2-hydrazino-4-trifluoromethylpyridine with water solubility of 8 mg/mL is used in aqueous formulation development, where it improves homogeneity and processibility. UV Absorption Max 310 nm: 2-hydrazino-4-trifluoromethylpyridine with a UV absorption maximum at 310 nm is used in analytical standard applications, where it provides reliable detection and quantification. Residual Solvent <0.1%: 2-hydrazino-4-trifluoromethylpyridine with residual solvent below 0.1% is used in fine chemical manufacturing, where it supports compliance with stringent regulatory requirements. |
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In the world of organic synthesis, progress hinges on consistency, purity, and a willingness to push boundaries. Over the years, we’ve spent countless hours refining our approach to producing 2-hydrazino-4-trifluoromethylpyridine, a compound that has earned the trust of chemists in demanding applications. Our journey with this material didn’t begin in a catalog; it started with persistent questions in the lab: “How can we introduce the trifluoromethyl group into a pyridine ring and offer a hydrazino functionality without sacrificing stability or scalability?” The outcome is a product that reflects the experiences of bench chemists and the feedback of researchers who know the difference between an adequate reagent and a reliable workhorse.
The batch-to-batch consistency of our 2-hydrazino-4-trifluoromethylpyridine is not just a promise; it’s a result of careful process control and traceable sourcing of precursors. Specifying for modern laboratory use, we target a purity above 98 percent by HPLC. Each lot presents as a pale solid, crystallizing well under carefully controlled temperature and humidity to maintain physical integrity during shipping and long-term storage. You won’t find odd tints or unexpected odors—these are signs we watch for, as even minor deviations can signal issues upstream.
One lesson we learned early on: hydrazino compounds demand strict exclusion of moisture through every synthesis step. Residual water has a knack for introducing side reactions, and catching these is not just about hitting a spec sheet value. Every deviation potentially impacts customers’ yields, selectivity, and sometimes the entire validity of a medicinal chemistry screening. We employ a vacuum drying regimen post-synthesis that runs longer than most commercial producers consider necessary. In our own hands, this step means less time troubleshooting in downstream reactions, and researchers have reported fewer surprises during scale-up trials.
Handling 2-hydrazino-4-trifluoromethylpyridine in the lab reveals a lot about its properties. The compound holds up well during standard transfer and weighing, with minimal static and no tendency to cake like some other hydrazines. This stability reflects on the way it’s packed—airtight, with sufficient headspace to guard against pressure shifts during climate fluctuations in transit. Storage out of direct sunlight and under inert gas best preserves its reactivity; these are methods we apply ourselves before delivery. Some competitors overlook these basics and ship in sub-optimal containers that allow for subtle degradation, a risk multiplied in sensitive catalytic studies.
Most buyers initially seek out this compound for its reputation in cyclization and condensation reactions, targeting heterocycle formation or as a key building block for pharmaceutically relevant scaffolds. The presence of the trifluoromethyl group is far from cosmetic; it’s well-documented in expanding metabolic stability and introducing distinctive electronic influences, which shift reactivity in desirable ways. Our customers tell us the hydrazino group unlocks flexibility for follow-on chemistry—particularly in regioselective transformations and as a source for N-N bond construction. We learned through joint projects with academic collaborators that small shifts in purity or isomeric content change the outcome of multi-step syntheses.
You’ll find our 2-hydrazino-4-trifluoromethylpyridine blending smoothly into established procedures for the synthesis of pyridazine, pyrazolopyridine, and other fused-ring systems. Experienced chemists value how quickly this compound dissolves in polar aprotic solvents, cutting prep time. We’ve observed that using inferior grades introduces chromatographic artifacts and purification headaches; it’s an area where dollars saved upfront become productivity lost later on.
The risk of trace impurities sneaking past a superficial check is always present, especially with hydrazines. Our team uses a methodical approach, combining HPLC, NMR, and trace-level metallic analysis for every lot. On one occasion, a routine audit caught micrograms of organotin residue, likely from imported raw materials. Rather than discounting the batch, we uncovered the root in supplier pipeline changes and rebuilt our screening procedures. This kind of diligence means greater peace of mind for process development chemists who must maintain strict regulatory compliance.
A well-defined impurity profile matters most in medicinal chemistry, where regulatory filings demand more than a statement of percentage purity. We actively share analytic files with researchers performing preclinical work, reinforcing transparency at every step. Years of experience have shown us that building trust through open data fosters long-term partnership instead of single-transaction sales. Chemists on tight timelines appreciate fast access to answer sheets, not evasions or evasive customer service.
2-hydrazino-4-trifluoromethylpyridine distinguishes itself sharply from classic hydrazinyl pyridines and trifluoromethyl pyridines without hydrazino substitution. Hydrazino-pyridines lacking the trifluoromethyl group offer weaker electronic pushing effects and can prove less selective in some cyclization protocols. Classic trifluoromethylpyridines, while robust as electron-deficient scaffolds, miss out on the reactive handle required for advanced heterocyclic assembly. We’ve supported teams who initially opted for less expensive hydrazine alternatives, only to find yield and product profile fell short during crucial steps.
Mechanistically, the presence of the CF3 group alters not just electron distribution, but also downstream handling—the product is more shelf-stable and less prone to spontaneous decomposition, as verified by accelerated stability studies we’ve made standard procedure. The hydrazino function complements this with reliable nucleophilicity, broadening the range of acylations, sulfonylations, and condensations possible.
Some users assume the distinction between 2-hydrazino-4-trifluoromethylpyridine and isomeric materials doesn’t impact their end syntheses. This is often disproved by their own results, where unwanted side products or drops in selectivity force a return to the drawing board. Having worked shoulder-to-shoulder with R&D teams troubleshooting these bottlenecks, we stress that our process minimizes formation of regioisomeric impurities from the earliest stages of synthesis.
There’s an argument in some circles that “chemicals are chemicals”—so long as the purity reads high, source doesn’t count for much. Our years of making and using 2-hydrazino-4-trifluoromethylpyridine day after day challenge that mindset. Direct evidence comes from collaborative projects where switching from distributor-supplied material to ours cut the chromatographic baseline drift or eliminated trace artifact peaks previously unexplained. We take these field reports seriously because, at scale, unnoticed contaminants or minor stability differences can become show-stoppers.
Our staff chemists still spend time at the bench, not just in front of procurement spreadsheets. We hear the daily feedback from academic and industrial users, adapting our own QA protocols in real-time to reflect what’s actually happening downstream, not just what ought to happen on paper. Years of accumulated feedback drive the improvements in both purity and reliability.
Transparency doesn’t begin and end with a certificate of analysis. For 2-hydrazino-4-trifluoromethylpyridine, we openly share full NMR traces, chromatograms, and impurity benchmarks with those who need them. Some users require assurance of lot-to-lot reproducibility beyond the usual numbers, and we stand ready to provide supporting evidence. During scale-up runs, even tiny shifts—like residual solvent traces or colorimetric discrepancies—require scrutiny; we include both digital and physical reference standards for verification.
Researchers with experience in the medicinal chemistry field ask questions that go beyond spec sheets. They request data on long-term storage, batch aging, and even photostability under bright laboratory lighting. Over the years, we’ve maintained stability testing in-house, running parallel shelf-life trials to catch problems that would only show up months down the line. What comes out of this process is a product that doesn’t just pass a one-off test; it consistently lives up to its role during hit-to-lead and beyond.
Bringing a compound into a synthetic pipeline always carries risk. Our effort has gone toward neutralizing avoidable risks: batch inconsistency, supplier change-blindness, and unreliable documentation. The biggest headaches often stem from inconsistent wetting properties, unpredictable hygroscopicity, or the need for excessive purification. Years of direct manufacturing have allowed us to fine-tune not just synthesis and drying, but also packaging systems. These adjustments translate to faster reaction set-up, fewer unplanned deviations during product work-up, and more reliable data from finished API or intermediate screens.
We also recognize the importance of communication, especially when unexpected observations arise. Our technical team maintains open lines with user labs to help troubleshoot synthetic problems in real time. For example, a recent customer flagged lower-than-expected reactivity; after a rapid look through our shipping logs and process sheets, we identified that a brief customs hold during an overseas shipment introduced an unusual temperature excursion. We provided follow-up testing and a replacement shipment at no extra cost, and our own documentation made explaining the anomaly straightforward.
Close work with academic and industrial collaborators has shown us how important an agile supplier relationship is for modern research. We’ve provided this compound for projects ranging from new fluorinated medicinal candidates to advanced materials development, and each scientific challenge teaches us something new. Some research teams have handed us back their full synthetic sequences for review, asking us to spot possible bottlenecks. This open feedback allows us to tune both the impurity limits and the packaging sizes to best match actual laboratory workflows, an approach that simply isn’t possible through a distributor who doesn’t touch production.
This culture of cooperation has led to iterative improvements in both physical and data-handling characteristics. Chemists now demand robust digital documentation, compatibility cross-checks, and assurance on trace impurity carryover—needs that we take seriously as a manufacturer. We know firsthand that breakthrough molecules rarely originate in the isolation of a metrics-obsessed procurement office. They grow out of close dialogue, the exchange of actual data, and a willingness to tweak production in response to evolving scientific needs.
With the rise of online chemical marketplaces, the danger of traceability loss only increases. We hear regularly from chemists frustrated by opaque supply chains and unexplained anomalies in their reaction outcomes. Bringing manufacturing in-house means full transparency in every intermediate, solvent, and even inert gas used during processing. If an issue occurs, the root cause can be traced in hours, not weeks. Traders and resellers may promise price advantage, but too often the cost is uncertainty—an expense that reveals itself only in critical failure runs.
We support direct research collaborations, open test protocols, and reference material exchange so all parties stay aligned. There are no surprises about what goes into each batch. Our lot tracking goes back to every precursor shipment, and this logistical clarity frees customer chemists from tracing dead-ends when publishing or scaling up. At the end of the day, our responsibility as a direct producer is not just shipping a reagent at spec—it's in making sure each user achieves target results reliably and without costly re-dos.
Years of manufacturing 2-hydrazino-4-trifluoromethylpyridine has shaped our philosophy that excellence isn’t a one-off project, but the result of constant improvement. Each batch reflects the accumulated insights of chemists who believe better starting materials translate directly to better finished chemistry. By rooting decision-making in open data, rigorous process control, and honest collaboration, we do more than supply a compound—we give researchers a crucial edge. This edge isn’t always evident on a spec sheet, but becomes obvious in bench results where reproducibility, yield, and confidence matter most.
Every technical obstacle encountered has refined both our process and our understanding. We see ourselves as allies to scientific progress, able to troubleshoot, adjust outputs, and share detailed data whenever necessary. This hands-on involvement means chemists can rely on the material they receive, reducing variables in multi-step routes and supporting ambitious goals from hit-discovery to advanced process development.
Working directly in chemical manufacturing has revealed that success hinges on reliable processes and active dialogue with the field. 2-hydrazino-4-trifluoromethylpyridine stands as an example of the value that emerges from focused production: not just high purity, but uniform handling, transparent analytics, and data-backed customer support. We see ourselves on the same side as our customers, working toward predictability in each synthesis. Choosing material from a dedicated manufacturer means fewer surprises and smoother progress, project after project.