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HS Code |
916431 |
| Iupac Name | tert-butyl 2-(4-(pyridin-2-yl)benzyl)hydrazinecarboxylate |
| Molecular Formula | C17H23N3O2 |
| Molecular Weight | 301.39 g/mol |
| Cas Number | 1264011-97-5 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 98-102°C |
| Solubility | Soluble in DMSO, DMF, dichloromethane |
| Storage Conditions | Store at 2–8°C, protect from light and moisture |
| Smiles | CC(C)(C)OC(=O)NNCC1=CC=C(C2=NC=CC=N2)C=C1 |
As an accredited t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram portion of t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate is supplied in a sealed amber glass bottle. |
| Container Loading (20′ FCL) | Packed in 20′ FCL, securely contained in sealed HDPE drums or fiber drums, lined bags, compliant with chemical transport regulations. |
| Shipping | The chemical *t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate* is shipped in a tightly sealed container, protected from light and moisture. It is handled as a laboratory chemical, often shipped according to regulations for non-hazardous organic compounds, and packaged with cushioning material to prevent breakage or exposure during transit. |
| Storage | Store t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate in a tightly sealed container under an inert atmosphere (e.g., nitrogen or argon) in a cool, dry place, away from direct sunlight and moisture. Keep it at 2–8°C (refrigerator) and avoid sources of ignition. Handle under a chemical fume hood and segregate from oxidizing agents and strong acids for safety. |
| Shelf Life | Shelf life: Store t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate at 2–8°C; stable for at least 2 years when unopened. |
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Purity 98%: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal by-product formation. Melting Point 122°C: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate at melting point 122°C is used in organic ligand preparation, where it provides thermal stability during reaction processes. Molecular Weight 314.40 g/mol: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with molecular weight 314.40 g/mol is used in medicinal chemistry research, where it allows for precise molar calculations and accurate dosing. Stability Temperature 90°C: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with stability temperature 90°C is used in catalyst development, where it maintains structural integrity under elevated reaction conditions. Hydrazine Functionality: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with hydrazine functionality is used in heterocycle formation, where it enables efficient ring-closing steps and increases synthetic versatility. Particle Size <25 μm: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with particle size <25 μm is used in solution-phase synthesis, where it promotes rapid and uniform dissolution in organic solvents. Solubility in DMSO >20 mg/mL: t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate with solubility in DMSO >20 mg/mL is used in screening assays, where it delivers high assay reliability and minimal precipitation. |
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T-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate has found a niche in modern synthesis. In our experience on the production line, we’ve seen the requests for this molecule rise with the boom in pharmaceutical and advanced material development. Its structure—anchoring a t-butyl hydrazinecarboxylate scaffold to a benzyl-pyridine core—delivers the flexibility and specificity researchers need for target molecule development.
On our plant floor, precise steps are essential. T-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate is not a common intermediate that rolls out with standard reagents. The synthesis involves handling air- and moisture-sensitive reagents, requiring close process monitoring and careful isolation at every stage. The final product must meet purity benchmarks, as slight impurities can throw off kinetic studies or bioassay results for the end-user.
Over the years, we noticed that no two requests look the same. Some clients need small lots for research, others want kilogram batches for pilot studies. The backbone of the molecule—the hydrazinecarboxylate group—opens reaction pathways, and the pyridyl-benzyl part makes it a key intermediate for more than one target class. On a busy day, tanks and reactors dedicated to this product turn over rapidly, with continuous sampling for quality control and an experienced crew monitoring each batch to hit requested specifications.
From a synthetic perspective, few intermediates offer the same kind of reactivity and scope as t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate. The t-butyl group provides significant steric support and protection in multi-step syntheses—a property that synthetic chemists recognize and rely on. We know from our service records that more clients are asking for finely tuned hydrazinecarboxylate intermediates. Compared to the standard phenyl- or methyl-based compounds, adding a benzyl-pyridine group has opened up selectivity for heterocycle-rich targets.
Experience on the manufacturing side tells us that customers working on next-generation kinase inhibitors or nitrogen heterocycle frameworks get the most out of this compound. The substituted hydrazine fragment allows clean transformation—and the stability of the t-butyl group means less degradation or side-product formation during downstream processing steps. Small inefficiencies at the intermediate stage often snowball into bigger problems as synthesis continues. We’ve found that minimizing residual inorganic content and protecting against unwanted hydrolysis helps clients scale up with fewer surprises.
In chemical manufacturing, repeatability relies on practice as much as on analytical instrumentation. Each batch begins with rigorous in-house raw material testing. Even temperature deviations of a degree or two during condensation or hydrogenation steps can affect the outcome. Bright, off-white crystalline solids signal correct formation; discoloration or off-odors reveal something has gone awry.
Quality goes further than HPLC purity figures. We calibrate each batch against in-house reference standards and double-check critical impurity profiles using NMR and LC-MS. Many of our research-focused customers request detailed COAs with spectral data, not just purity percentage. Our feedback loop with clients has shown that even subtle shifting in melting point or solubility betrays chemical instability. The production team incorporates these findings to plan each future synthesis.
Our process design draws from both textbook chemistry and hard-won onsite experience. We continually work on solvent recovery and optimized crystallization to ensure that specifications for melting point, water content, and mineral residue meet regulatory and research expectations. The most challenging aspect in scale-up involves removing trace metals and byproducts without affecting yield, since purification methods must remain consistent from 10-gram to multi-kilogram scale.
Customers often ask why our t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate has fewer batch-to-batch differences than competitors. We’ve tailored our process over many cycles to account for the product’s sensitivities. Unlike standard benzhydrazines or simple hydrazinecarboxylates, this molecule demands both steric and electronic precision. Impurities tend to cling in difficult-to-separate byproducts, requiring more refined column purification and multiple recrystallizations. The t-butyl group, while conferring stability, can also challenge some isolation processes, as incomplete removal of byproduct tert-butanol tends to affect downstream use.
From the operator’s perspective, controlling the introduction rate for the pyridine-containing intermediate curbs side-reactions. We learned the hard way that speeding up this portion of the process invites tarring or polymerization. Our operators intervene as soon as NMR monitoring hints at the wrong chemical shifts. Visual inspection rounds out our day-to-day check-list. Even as we automate more, nothing replaces experienced eyes following each step.
Most requests for t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate come from research chemists driving new molecule development—often anti-infective or oncology candidates. Our product structure, defined by its protected hydrazine functionality, creates a robust stepping stone for subsequent cyclizations and cross-coupling reactions. Real-world feedback tells us that researchers value how efficiently t-butyl protection can be removed under mild acid, without eroding sensitive functional groups elsewhere in their molecules.
Industry partners value purity and reproducibility over purely theoretical specs. For example, a common customer scenario involves wanting hydrazine incorporation with minimal residual metallic catalyst—often a pain point for downstream medicinal chemistry assays. Because the downstream product’s performance often depends on unseen batch-to-batch nuances, precise repeatability becomes more than a talking point—it determines years of discovery work.
The refined design also keeps competing nucleophiles at bay. In contrast, hydrazines based on simpler alkyl or aryl scaffolds often scramble or decompose during functionalization, especially at larger scales. Teams working on high-throughput library formations have written to us about faster purification and lower batch rejection rates after switching to our product.
A manufacturer’s responsibility extends beyond simply providing a compound. We must anticipate likely problems at the process level and from our customer’s experiments. Tightening our analytical process, introducing more robust drying steps, and reducing exposure to atmospheric oxygen stand out as improvements we implemented from client feedback. By reducing product trace moisture and fine-tuning the removal of reaction solvents, we open up new uses—such as in water-sensitive transformations or microwave-assisted syntheses.
From the perspective of a plant operator, ensuring chemical homogeneity at scale prevents costly rework. Our approach includes step-wise seeding during crystallization, which leads to more uniform crystal habits. Allowing product batches to mature under controlled temperature cycles produces material that dissolves more consistently in common solvents. These practical tweaks pay off, sparing chemists from scale-up dead-ends.
Trust earns itself quietly on the manufacturing floor. Chemists and chemical engineers who rely on our t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate depend on strict adherence to good manufacturing practices. Regulatory changes in chemical control have pushed us to check documentation at every turn. Every tank, filter, and dryer receives regular validation. Announcing that a batch conforms to specification means a real investment in time and analysis—not just ticking a box but working through potential outliers and scrutinizing data integrity.
Rather than standardizing specs for every customer, we collaborate at the quotation stage to understand what will give the best result in the end-use reaction. Sometimes that requires extra analytical data, sometimes different pack sizes, or even a new drying technique. Flexibility driven by experience saves both time and resources over a project’s lifetime.
Data tracking runs deep, from raw material lot origins to in-house product stability timepoints. There’s no shortcut around careful record keeping. Scientists appreciate when they get prompt answers to their questions—especially when timelines matter. Being able to reference precise cumulative production figures or to pull historical impurity reports from our records gives customers confidence, rooted in real production runs rather than sales promises.
Compliance is not just an obligation but a solved puzzle. Over years of adjusting to global changes in chemical control—for example, the shift in European customs on imported intermediates or the requirement for product traceability in life sciences—we adjusted internal policies, rolled out staff training, and adopted new analytical tools. As a manufacturer, seeing challenges not as hurdles but as invitations to do better sets us apart.
Hydrazinecarboxylate chemistry offers a range of tools for synthetic chemists. We produce several such compounds, and every variant brings something new to the bench. T-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate, with its benzyl-pyridine mark, uniquely combines aromatic reactivity and nitrogen-rich functionality. In contrast, less substituted analogs falter during alkylation or aromatic substitution, leading to bottlenecks or inferior product yields downstream.
Our technicians sometimes run parallel syntheses between this compound and related entries in the catalog. Consistently, the t-butyl-protected variant stands out for longer shelf stability and greater chemical selectivity. The pyridyl substituent not only guides desired reactivity but also steers clear of byproduct formation that afflicted older hydrazine chemistries. Results from our in-house process scale-ups show that modern t-butyl hydrazinecarboxylates dramatically streamline isolation, saving time at every production step—advantages echoed by feedback from custom synthesis groups outside our labs.
From the loading docks to the reaction vessels, production teams see firsthand how demand ebbs and flows. We have updated forecasting tools and maintain strategic inventory of sensitive raw materials to buffer sudden spikes in orders. Every kilogram of dry ice, every box of specialty solvent counts; shortages ripple through research timelines. Close partnerships with specialty logistics outfits keep our product fresh through customs checks and long hauls, which is critical since hydrazinecarboxylates do not forgive careless transport or storage.
We also run pilot programs to tweak particle size distribution or solvent content based on particular client workflows. If a new purification technique saves customers a day, we bring it into full production. Requests from academic labs often spark these practical innovations before they take hold in commercial settings.
On the manufacturing side, we have seen machinery upgrades—such as automated feeding pumps or sealed vacuum filtration—play a significant role in consistent throughput. It eliminates many of the edge-case complications that plagued older batch records. The investment in real-time monitoring means fewer surprises and less material loss during unforeseen upsets.
Scaling t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate production raises classic chemistry questions: how to keep product moisture low, how to prevent trace impurity buildup, and how to gently remove protection groups for high-value derivatives. Factory staff work closely with QC teams to troubleshoot issues like variable endpoint crystallization—a problem that used to cause downtime and waste. We’ve learned to adjust filtration speed, tweak pH, and control cooling rates, all in pursuit of that perfect product batch.
In dealing with customer returns, the most frequent complaint relates to minor product discoloration or off-odors. Responding, we revised some of our post-processing purification, incorporated additional wash stages, and found the root cause in a side-reaction triggered by trace aldehydes in a raw material. Fielding these problems directly strengthens customer loyalty and lessens tension between the discovery and manufacturing ends.
Growing reliance on controlled environments and sealed packaging led us to overwrap products in inert atmospheres for long-haul deliveries, so researchers receive the same solid, whether in the wet spring of Boston or the dry winter of Beijing. This attention to detail comes from first-hand experience—lost batches and misapplied packaging taught us what works and what fails.
Every year brings new applications for t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate. Our production team stays alert to changes in research priorities and end-to-end process improvements. We learn from chemists pushing the limits of what's possible and apply those lessons to batch production, packaging, and delivery.
Years spent running reactors, maintaining instruments, and collaborating with analytical labs culminate in more than just another batch of product. They build a deep understanding of what makes a good chemical and how it helps drive new discoveries. Feedback from our clients is never an afterthought, but a crucial part of process innovation—from raw materials selection, drying techniques, reactor cleaning, to final sample vials. The partnership between the production floor and the end-customer keeps us evolving, ensuring t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate meets the changing landscape of modern chemical research.
The chemistry may seem routine by now, but every new customer request brings an opportunity to refine our approach. From hands-on control over every stage of synthesis, robust and transparent documentation, rapid troubleshooting, and meaningful communication with users, we strive for more than just commodity supply. We commit to providing not just a chemical, but a solution drawn from deep manufacturing knowledge, solid scientific principles, and years on the ground, crafting every shipment with both precision and pride.