4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide

    • Product Name: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide
    • Chemical Name (IUPAC): 4-[2-(tert-butylcarbonyl)hydrazinylidene]pyridine 1-oxide
    • CAS No.: 1416573-86-6
    • Chemical Formula: C11H15N3O3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    715529

    Product Name 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide
    Molecular Formula C11H15N3O3
    Molecular Weight 237.26 g/mol
    Appearance Solid (typically powder or crystalline)
    Solubility Soluble in common organic solvents (e.g., DMSO, methanol)
    Purity Varies by supplier; typically >95%
    Storage Conditions Store in a cool, dry place; protect from light
    Structure Features Pyridine N-oxide ring, tert-butylcarbonyl substituent, formylhydrazyl group
    Application Intermediate for organic synthesis and chemical research
    Safety Handle with appropriate protective equipment; avoid inhalation and contact with skin

    As an accredited 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine-N-oxide, labeled with hazard and handling information.
    Container Loading (20′ FCL) 20′ FCL container securely packed with 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide in sealed, labeled drums or cartons, ensuring safe transport.
    Shipping This chemical, 4-(2-(tert-butylcarbonyl)formylhydrazyl) pyridine-N-oxide, is shipped in tightly sealed containers, under ambient or recommended controlled temperatures, with appropriate labeling for hazardous materials. Packaging complies with safety regulations for chemicals, minimizing exposure to moisture and light, and is accompanied by relevant safety data documentation during transit.
    Storage Store **4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide** in a tightly sealed container at 2–8 °C (refrigerator). Protect from light, moisture, heat, and incompatible substances. Store in a well-ventilated, dry place, and use only with appropriate chemical-resistant gloves and protective eyewear. Follow all standard laboratory safety protocols for handling potentially hazardous organic compounds.
    Shelf Life Shelf life: Store at 2-8°C, dry and tightly closed. Stable for at least 2 years under recommended storage conditions.
    Application of 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide

    Purity 98%: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal side impurities.

    Melting Point 145°C: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide with a melting point of 145°C is used in fine chemical manufacturing, where it allows precise process temperature control and consistency.

    Molecular Weight 250.3 g/mol: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide of molecular weight 250.3 g/mol is used in organic reaction optimization, where it provides predictable stoichiometry and reproducible results.

    Particle Size <10 µm: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide with particle size below 10 µm is used in advanced material coatings, where it improves surface homogeneity and dispersion.

    Stability Temperature up to 120°C: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide stable up to 120°C is used in catalytic process development, where it maintains structural integrity during thermal cycling.

    Solubility in DMSO 50 mg/mL: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide with solubility in DMSO at 50 mg/mL is used in high-throughput screening assays, where it guarantees uniform solution preparation and accurate dosing.

    UV Absorption Maximum 285 nm: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide with UV absorption maximum at 285 nm is used in analytical chemistry applications, where it enables sensitive detection and quantification.

    Storage Condition 2–8°C: 4-(2-(tert-butylcarbonyl) formylhydrazyl) pyridine -N-oxide requiring storage at 2–8°C is used in chemical inventory management, where it preserves chemical stability and extends shelf life.

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    Certification & Compliance
    More Introduction

    Introducing 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide: Real Insights from a Chemical Manufacturer

    Understanding Our Commitment to Purity and Consistency

    Our direct experience in synthesizing 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide has shown us that reliability matters at every batch level. We produce this compound using precise stoichiometric controls and tight temperature monitoring. Years of refining the crystalline separation process have brought down the trace byproducts to negligible levels, letting us deliver material that meets both lab-scale research and scale-up runs in advanced applications.

    The typical batch comes as a pale yellow crystalline solid, and over time we have found that vacuum drying at moderate heat stabilizes the product for long-term storage. Impurity profiles are confirmed by NMR and HPLC in-house; we have learned these extra controls save our clients from having to re-verify the identity or run extra purifications downstream. Experience tells us that one missed step in workup—letting inert atmosphere slip, missing a single wash—can throw off both yield and composition. Reliable, repeatable output can only come from established habit and technical discipline, and we've learned to value each of those highly.

    Why Customers Turn to 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide

    This molecule’s utility lies in the axis of selectivity and reactivity. In our work with both large and small molecule groups, its value becomes apparent for those who need a balance between steric bulk and tunable reactivity in hydrazone coupling strategies. Chemists working on next-generation nitrogen- or oxygen-containing heterocycles often tell us how this hydrazyl derivative helps them avoid side reactions common with smaller, less hindered analogues.

    We have seen increased interest from the pharmaceutical development sector and medicinal chemistry teams exploring the design of enzyme inhibitors. The pyridine-N-oxide framework brings both polarity and electronic tuning; the sterically protected hydrazyl group limits unwanted decomposition in solution, a benefit cited by several of our partners. Where smaller hydrazyls might hydrolyze early in a route, this compound consistently remains intact through more diverse conditions—something you only find out after losing precious time to failed runs.

    Model, Specifications, and Batch Traceability

    Our primary offering aligns with a minimum content of 98.5% as measured by both HPLC and qNMR. Most runs surpass this value, and our clients routinely request certificates of analysis that detail exact composition, residual solvents, and trace metals. We keep every lot traceable to its raw material sources, synthesis records, and QA reports. This comes from recognizing just how much time we lose as a manufacturer tracking down issues in outsourced materials, and from deciding years ago to keep audits and final release tightly under our direct supervision.

    All packaging uses chemically compatible, low-particulate liners and containers. In our own reactions in the lab, we learned how easily a plasticizer or environmental impurity creeps into a sensitive synthetic step if careless containment is used. So every package gets sealed under nitrogen with tamper-evident closures. Shelf stability holds up over 18 months, owing to both solid-state purity and controlled hydration conditions.

    Differentiation from Similar Compounds

    We’ve produced several hydrazyl-pyridine derivatives across different alkyl and aryl side chains. From a manufacturer’s vantage point, the tert-butylcarbonyl group makes a clear difference. Less hindered analogues, such as acetyl variants, tend to offer higher reactivity but at the cost of lower thermal and hydrolytic stability. Aromatic carbonyl groups, like benzoyl, make products more lipophilic and can hinder solubility or limit compatibility with polar solvents. In direct trials with research partners, the tert-butylcarbonyl group on this compound provides distinctive steric shielding; it resists unwanted side reactions in multistep syntheses, and remains less prone to elimination or rearrangement during workups.

    Pyridine-N-oxides themselves offer a unique entry to modulate hydrogen bonding and Lewis base interactions; this specific substitution pattern aligns with groups seeking finer control of electron density for catalysis. Several comparative trials with related hydrazyls show this product stands out for maintaining reversible imine formation even under crowded conditions, where less hindered hydrazyls had already degraded.

    Manufacturing Considerations: From Scale-Up to Robustness

    Scaling this compound required addressing a few specific challenges. The tert-butylcarbonyl group reacts efficiently under batch conditions when using careful addition and controlled temperature ramps. Too rapid addition, or minor temperature overshoot, permits undesired byproducts that take extra time to remove. Through a dozen pilot runs, we identified both a solvent system and agitation protocol that reliably keeps the hydrazyl group free from oxidation and decomposition. We adopted in-line monitoring to ensure every stage is on track, a decision shaped by several interrupted pilot batches early in our production history.

    In practical terms, these decisions translate into repeat orders and longer-term partnerships with end-users. Research chemists often underestimate the role of batch reproducibility at the manufacturing scale; our hands-on work illustrates this every production cycle. We have learned that feedback from customers—about clumping, static, inconsistent flow, or issues in large (>1kg) synthesis—pays off when we trace it back to micron-size variations or subtle residual acidity. Every process tweak, from filtration timing to drying kinetics, affects the final quality.

    User Feedback and Real-World Problem Solving

    Seasoned process chemists who have trialed our 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide cite fewer purification steps downstream. One client, who scaled their flow chemistry run from tens of grams to multi-kilo, reported significant time savings in both workup and isolation, thanks to our narrow impurity window. This reflects our decision to control rather than outsource each critical step of the synthesis.

    End-users in medicinal chemistry circles shared another advantage: improved batch-to-batch reproducibility compared to material from general catalog suppliers. Our direct customer feedback loops, which we set up after initial pilot runs exposed some variability in melting point and trace organics, helped us standardize the washing and drying stages.

    Other hydrazyl derivatives in the marketplace often require further grindings or washes before use, but we have found most clients use our product as delivered, with only routine pre-use drying in their own environment. Controlling particle size and dusting also minimized losses during transfer and mixing, a detail we only fully appreciated after standing at the bench ourselves and seeing measured mass drop due to static or clumping. Little operational improvements add up after observing repeated failures on the production line.

    Industry Uses and Case Stories

    Much of the installed base for this hydrazyl derivative fits R&D and technology development. Synthetic chemists most often use it in solution phase modifications or as a precursor to other heterocyclic scaffolds. Our product finds roles in both combinatorial library assembly and synthesis of intermediates for bioactive small molecules—tasks that cannot afford unpredictable reactivity or instability between stocks.

    A process developer told us about successfully integrating this molecule into a continuous flow operation, attributing ease of handling and consistent crystallization behavior post-quench to our tight specifications. In a dozen other instances, clients working on new materials for advanced coatings valued this derivative’s unique blend of solubility and stability, which allowed their teams to work in mixed solvent systems without losing integrity to hydrolysis or oxidation.

    Some of our most innovative feedback came from an academic collaborator who used this product to explore new cross-coupling methodologies. They achieved higher yields by capitalizing on both the electronic and steric contribution of the tert-butylcarbonyl group—a lesson later adopted in related solid phase applications by industry partners. Through sharing both positive and less-than-perfect outcomes, we have refined post-synthesis QA and improved our dehydration protocol, which keeps error margins low and gives research teams peace of mind over final purity.

    Challenges We Overcame in Regular Production

    Scaling any hydrazyl-pyridine-N-oxide product taught us real lessons about process sensitivity. Repeated thermal cycling or exposure to atmospheric moisture tends to degrade the N-oxide group—something we addressed by switching to continuous nitrogen and implementing moisture sensors for storage. We have found, through real losses and batch-holds, that minor process deviations magnify downstream. Our in-process analytics now include online gas chromatography to check for subtle decomposition before final isolation.

    Shipping hydrazyl derivatives overseas brings up worries about transit temperature and integrity. For several shipments, we developed protocols to monitor temperature throughout transport and upgraded our insulation packaging after real-world feedback showed materials arriving with variable appearance. These small investments have paid off, with fewer customer queries and no reported product loss across the last five years.

    Why Our Direct Manufacturing Approach Delivers Distinct Value

    Continuing to keep every major step in-house—from raw material qualification through final material release—lets us deliver quality that distributors and traders often cannot match. Our test lab sits adjacent to the synthesis floor, so both QA staff and process operators catch potential deviations quickly. For any buyer, the benefit often surfaces as shortened timelines, clear answers to technical questions, and reliable availability. We’ve learned, over decades, that open technical exchange with research partners drives continuous improvements in both process and product.

    Direct manufacturing offers another advantage: the ability to troubleshoot in real time. Sustaining relationships with both routine and first-time buyers keeps us sharp—no batch ships without full traceability and supporting documentation. In the rare case of a customer concern, our production and technical team respond with root-cause analysis instead of passing the buck. This hands-on approach comes from years spent in both R&D and production bays, and from a real respect for the stakes involved in chemical research and manufacturing.

    Environmental and Safety Priorities

    Handling 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide at production scale raises distinct safety challenges. We prioritize containment—using closed systems and in-line venting—because subtle skin or inhalation exposure to hydrazyls can lead to health concerns, learned from real near-misses early in development. Process improvements include smartvent filtration and redundant monitoring of workspace air. On the environmental side, we neutralize spent reaction streams and reclaim solvents wherever possible, a practice adopted after discovering both cost savings and regulatory advantages.

    Regular team training, both for synthesis and for handling unexpected spills or exposures, became our norm after seeing the difference in response time and confidence across varying shift teams. Safe, efficient production of advanced intermediates goes hand-in-hand with ongoing education and a willingness to adapt as new safety insights are published.

    Solutions to Persistent Challenges

    Over time, feedback loops with our customers and internal review boards revealed the shortcomings of early manual batching, inconsistent crystallization scale, and solvent carryover. We adopted semi-automated batch control, laser particle sizing, and end-point moisture determinations to counter these. Archiving batch histories, including each process deviation and corrective action, enables us to backtrack any quality blip, learning new ways to deliver reliable supply.

    Several clients encountered trouble using material from secondary sources—ranging from poor lot-to-lot consistency to subpar flow properties—so we began including more detailed supporting data, covering batch rheology and recommended handling protocol based on our direct observations. These technical additions may sound detailed, but they remove guesswork for formulators and chemists pressed for time.

    Supply chain disruptions—from raw material shortages to new transportation rules—prompted us to invest in both local sourcing and redundant logistics. An early lesson came during a regional shortage, when we kept supplying long-term partners due to our reserve stock and real-time supplier outreach, while others went without. These policies make a difference not only in routine business, but in crisis mode.

    Supporting Data Transparency and Scientific Dialogue

    Our philosophy values open data. Clients frequently request spectral archives and trace impurity information not only for regulatory review, but also for adjusting downstream process parameters. We learned the hard way that sharing too little invites technical setbacks for both sides; our present model includes spectral data, impurity breakdowns, and technical notes led by those who have run both the synthesis and the analytics. This approach helps prime collaborative projects, especially where complex chemistry meets tight regulatory windows.

    As a manufacturer, we support direct technical discussions with customers and research collaborators, avoiding the “black box” experience so common in generic sourcing routes. This mentality flows from firsthand lab problems, nights troubleshooting a puzzling side band on spectra, and endless technical emails until every ambiguity is resolved. Science moves forward when data moves forward.

    Looking Forward: Supporting Research with Consistent Materials

    With the growing interest in novel hydrazone chemistry, we see applications stretching into new fields—from enzyme probe development to materials science. Continued dialogue with academic and industrial groups keeps our process direction relevant, and challenges us to improve as research priorities shift.

    We’ve learned something useful from every batch, every out-of-spec result, and every client demand for fresh technical data. Making and delivering 4-(2-(tert-butylcarbonyl)formylhydrazyl)pyridine-N-oxide is more than a routine; it's a real collaboration with researchers worldwide, shaped by practical manufacturing insight and the persistent pursuit of better, more reliable chemistry.