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Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate

    • Product Name Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate
    • Alias AKOS024960693
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    909289

    Product Name Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate
    Cas Number 1445731-94-7
    Molecular Formula C17H22N4O2
    Molecular Weight 314.39
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, methanol
    Storage Temperature 2-8°C (refrigerated)
    Smiles CC(C)(C)OC(=O)NNCC1=CC=C(C2=NC=CC=N2)C=C1
    Iupac Name tert-butyl 2-[[4-(pyridin-2-yl)phenyl]methyl]hydrazine-1-carboxylate
    Synonyms N-Boc-4-(2-pyridyl)benzylhydrazine
    Inchi InChI=1S/C17H22N4O2/c1-17(2,3)23-16(22)20-21-12-13-6-8-14(9-7-13)15-5-4-10-18-11-15/h4-11,20-21H,12H2,1-3H3

    As an accredited Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, 5 grams, labeled with chemical name, CAS number, hazard pictograms, batch number, and storage conditions.
    Shipping This chemical, Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate, is shipped in tightly sealed containers under ambient temperature. It should be packaged according to safety regulations, avoiding moisture and direct sunlight. The shipment must comply with relevant chemical transportation guidelines, ensuring proper labeling and documentation for secure and compliant delivery.
    Storage Store Tert-Butyl 2-(4-(Pyridin-2-yl)benzyl)hydrazinecarboxylate in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from strong acids, bases, and oxidizing agents. Recommended storage temperature is 2–8°C (refrigerated). Ensure proper labeling and restrict access to trained personnel. Handle in accordance with standard laboratory safety protocols.
    Application of Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate

    Applications of Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate in Industrial Manufacturing

    As the original manufacturer, we supply Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate to professional industries undertaking advanced synthesis, especially in pharmaceuticals, fine chemicals, crop protection, and diagnostics. Our product integrates into critical process steps, supporting high levels of regulatory compliance and traceability.

    1. Pharmaceutical Intermediates for Novel API Synthesis

    This compound serves in multi-step synthesis routes for advanced pharmaceutical intermediates, notably within the assembly of heterocyclic and hydrazine-functionalized molecules. Its protected hydrazine group allows selective deprotection at late-stage transformations, reducing side reactions and improving yields in scale-up settings. Customers optimize coupling and cyclization steps under GMP manufacturing, applying strict impurity control aligned with registration-dossier requirements for small-molecule APIs. Our long-term supply supports reliable submission timelines in regulated markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • EMA Guideline on the Chemistry of Active Substances
    • USP and EP Monographs for relevant starting/intermediate substances

    Typical usage ratio

    • Intermediate typically charged at 1.0–1.2 molar equivalents relative to target core scaffold; exact ratio adjusted for route-specific stoichiometry and impurity formation risk.

    Downstream process integration

    • Material enters post-halogenation step, providing protected hydrazine functionality required for regulated C-N bond formation in key intermediates; final deprotection often performed under acidic or hydrogenolysis conditions prior to API isolation.

    Final product types

    • Small-molecule oncology drugs
    • Anti-infective compounds
    • Neuroactive agents in clinical development
    • Intermediates for peptide-hydrazones

    2. Advanced Ligand Precursor in Catalysis Development

    Chemical process engineers incorporate this hydrazinecarboxylate derivative as a precursor in ligand design for homogeneous catalytic systems, particularly for asymmetric hydrogenation or cross-coupling. Its structural motif improves metal-chelation and fine-tunes selectivity, supporting robust scale-up for catalyst batch manufacture. Professional R&D labs and process intensification teams procure this raw material due to its consistent purity and low trace-metal content, both crucial for stringent QC in catalyst production.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Systems for Industrial Manufacturing
    • REACH Registration (EC No. 1907/2006) for Speciality Chemicals
    • Internal Corporate EHS Protocols for Metal-Complex Ligand Production

    Typical usage ratio

    • Ligand precursor typically added at 1.0 molar equivalent per target ligand species; ratio may increase to 1.05–1.1 under multi-step modification sequences to compensate for side product formation.

    Downstream process integration

    • Raw material charged into ligand-assembly reactors alongside base and metal salt precursors for direct condensation or cross-coupling; product integrated into catalyst blending or immobilization steps for downstream chemical process development.

    Final product types

    • Organometallic catalysts for fine chemical synthesis
    • Stereoselective hydrogenation catalysts
    • Bulk chemical production process catalysts
    • Speciality ligand sets for R&D screening

    3. Building Block for Agrochemical Active Ingredient Synthesis

    Leading crop protection companies use this hydrazinecarboxylate as a specialty reagent to construct novel active ingredient cores, particularly for new-generation fungicides or insecticides with pyridinyl/benzyl motifs. Controlled protection and deprotection enable precise substitution patterns, essential for patent-protected molecules. We maintain supply stability and batch traceability to meet agrochemical pre-registration requirements and to facilitate pilot-to-commercial transfer programs with robust data support for regulatory submissions worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Technical Grade Active Ingredients
    • EPA 40 CFR Part 158 Data Requirements for Pesticides
    • China’s ICAMA Registration Guidelines
    • OECD Good Laboratory Practice requirements (for pre-market studies)

    Typical usage ratio

    • Reagent dosed at 1.05–1.15 molar equivalents relative to the corresponding aryl halide or heterocycle central ring scaffold; excess neutralized and removed to minimize final formulation residues.

    Downstream process integration

    • Material added during late-stage heterocycle assembly and functional group introduction in batch or semi-continuous synthesis of new agrochemical actives; final purification done before formulation into technical concentrates.

    Final product types

    • Pyridinyl-benzyl type fungicides (e.g., SDHI inhibitors)
    • Novel insecticide actives
    • Seed treatment technicals
    • Active ingredient intermediates for pesticide cocktails

    4. Hydrazine-Based Probe Synthesis in Analytical Diagnostics

    Diagnostic reagent manufacturers utilize this compound as a core intermediate when assembling hydrazine- and benzyl-functionalized molecular probes. The tert-butyl protecting group enhances stability, crucial for controlled release or activation within target assay systems. Synthesis teams employ this intermediate in conjugation steps with dyes or reporter molecules, where reliability in protection group removal yields reproducible probe batches, critical for trace analytical applications and clinical diagnostics validation.

    Industry compliance standards

    • ISO 13485 Quality Management Systems for Medical Devices (Including Diagnostic Reagents)
    • CLSI Guidelines (Clinical and Laboratory Standards Institute)
    • FDA 21 CFR Part 820 for In Vitro Diagnostic Device Manufacturing
    • EU IVDR (Regulation (EU) 2017/746) for Clinical Diagnostics

    Typical usage ratio

    • Intermediate introduced at 0.9–1.1 molar equivalents against probe scaffold, with minor adjustments for different labeling chemistries or probe designs.

    Downstream process integration

    • Introduced during coupling stage with linker or dye; subsequent deprotection and functionalization steps produce the active probe ready for formulation into diagnostic test kits.

    Final product types

    • Chemiluminescence and fluorescence-based molecular probes
    • Enzyme substrate markers for clinical biochemistry
    • Diagnostic kit raw materials
    • Affinity labeling reagents for proteomics
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    Certification & Compliance
    More Introduction

    Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate: Practical Insights from the Manufacturer

    Crafting Molecules with Purpose

    From the factory floor, shaping specialty intermediates draws more from actual experience than any catalog entry could capture. Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate reflects thousands of hours spent tuning method parameters, managing scale-up, and collecting feedback from teams who work with these molecules every day. This compound isn’t mass-produced for basic commodity use—it deserves a closer look at what it brings to the table in real-world applications.

    Model and Specifications: A Closer Look at the Details

    We always begin with the fundamentals: proper molecular identity and batch repeatability. Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate is not just another hydrazinecarboxylate. For every batch, purity targets regularly stay above 98% by HPLC, monitored by both in-process and final QC checkpoints. Consistent appearance, correct melting point range, and LC-MS confirmation contribute to more predictable outcomes once this material reaches your synthesis plan. While it offers a tert-butyl protecting group on the hydrazine function, we enforce close control of water content and packing conditions. Small changes in environmental moisture can impact downstream deprotection success—something that only repeated handling at scale truly reveals.

    Visually, the product arrives as a fine off-white solid, easy to weigh without caking in normal humidity environments. Flow characteristics in jars or drums matter on the line; we avoid over-packing and choose container sizes based on feedback from bench chemists and production users. By sticking to practical package volumes, the risk of product bridging or waste drops, especially during repeat weigh-outs.

    Purpose and Use Cases: What This Intermediate Delivers

    The main value of Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate lies in offering a reliably masked hydrazine for targeted, stepwise synthesis involving pyridine-containing sidechains. Our partners—especially in drug development labs—report smoother coupling reactions and fewer failed runs when switching from earlier unprotected hydrazines to this tert-butyl form.

    Direct experience makes clear that deprotection profiles stay reproducible, even after shipment over long distances. Teams working with harsh deprotecting agents, like TFA or other strong acids, note high recovery of the free hydrazine because this protecting group copes better with moisture than other, less stable groups used on similar intermediates. Building up nucleoside analogs, negotiating multi-step syntheses, or refining agricultural research molecules—many workflows benefit from the solubility and selectivity built into this specific intermediate.

    Production Insights: Reliable Scale-Up and Consistency

    Overseeing actual production lines highlights realities that spec sheets rarely mention. The hydrazine edge group, attached to a benzylic linker with a pyridyl substituent, throws some curveballs at the person scaling up the process. Early trials showed that rate of addition and solvent choice could influence both yield and impurity profile—details only uncovered by running dozens of pilot batches and watching for microcontaminant buildup.

    To meet steady demand, we've assigned this product a permanent position on multi-purpose reactors with full cleaning validation between campaigns. In practice, this means we can jump from pilot to full batch within weeks, without losing yield or running into regulatory headaches. Consistency grows out of training teams to spot handling issues and catch subtle shifts in crystallization or solid handling before they cause bigger problems.

    Among manufacturers, a common complaint gets raised about losing yield to “cleaning losses” or product getting lost in transfer. Our solution stemmed from adapting transfer protocols to minimize air exposure—reducing loss and maintaining batch integrity even when pushing production volume. The lessons learned from repeat production now shape how we offer guidance to users attempting scale-up on their end.

    Comparing with Similar Hydrazinecarboxylates

    There's no shortage of protected hydrazine intermediates, most with subtle changes to the aromatic or alkyl backbone. In our own hands, we’ve compared tert-butyl-protected hydrazinecarboxylates bearing tolyl, phenyl, quinoline, and pyridine groups at the benzylic position. The pyridinyl-benzyl hybrid—specific to this compound—offers the broadest compatibility in coupling reactions, thanks to that nitrogen atom triggering less side reactivity. Other derivatives sometimes run into side reactions with strong nucleophiles, while this compound’s backbone delivers cleaner transitions in Suzuki, Mizoroki-Heck, or Buchwald-type conditions.

    Another reality surfaces in the warehouse. Other forms using alternative protecting groups, like Boc, Fmoc, or benzyl, may show product “sweating” or discoloration under less-than-ideal storage. Tert-butyl brings better storage stability, evidenced by year-long sample retention tests under both ambient and refrigerated conditions. Distinctive odors sometimes present in closely related hydrazine specialties don’t occur here, improving workplace acceptability and lowering user aversion compared to nitrosyl or acyl-substituted cousins.

    Feedback from Users and Adjustments Over Time

    Beyond the lab, industrial users taught us where the real risks lie in handling. A single misplaced drum or a batch exposed for too long to air can undermine quality. Tips from experienced research chemists have changed how we qualify drums, set retest periods, and train staff. In response, we now coordinate real-time batch tracking and regularly update users on best practices. Reports of airborne dust spillage led us to switch over to antistatic-lined liners and more robust jar seals.

    End users care about reliability, not just technical specs. Drug discovery labs especially want every batch to behave like the last—no surprises in yield or unexpected LC peaks. In the process sector, losses at just one stage can mean scrapping days of work; that's why we profile every new lot against long-term stability data, even before shipping. In thirty years of specialty manufacturing, direct calls about “soft lumps” or “product cake” taught us to tune the drying stage closely. The balance comes from drying long enough to cut residual moisture but not so long that thermal decomposition starts. There’s no shortcut—it comes from experience and countless production tunings.

    Supporting Cleaner Chemistry

    Handling nitric or acyl protecting groups often means running extra wash cycles or specialty incinerators on the cleanup line—a hassle not seen with this tert-butyl version. Teams working in compliance-heavy fields, like regulated pharmaceutical manufacturing, appreciate having fewer residual byproducts to track or neutralize in their spent streams. Our internal data confirm residual levels stay comfortably below regulatory concern, making downstream filtration or extraction steps simpler.

    Lab teams frequently highlight the friendliness of this product in solution-handling steps. While benchwork with alternative hydrazine derivatives sometimes generates emulsions during workup, this compound allows smoother separation phases. These insights don’t surface in generic data sheets; they come up in production scale conversations and after actual user trials.

    We also note that the tert-butyl group resists over-alkylation or decomposition under mild base conditions, which gives more synthetic flexibility. In actual operational runs, this translates to fewer retries and a longer service life for stock solutions.

    Real-World Handling Tips and Lessons

    Over the years, repeated questions about stability, flow, and shelf-life steered improvements not only in how the product is prepared but also in how it is shipped. Keeping the material in double-lined containers and away from the plant’s more reactive inventories stops cross-contamination before it begins. Pallet stacking on the warehouse floor is staggered to avoid pressure caking at the bottom; this detail, picked up during regular operator training sessions, translates to easier unsealing at customer sites.

    On the shop floor, accurate weighing saves hours downstream. The current packing format comes directly from watching chemists struggle with bulkier containers and looking for ways to cut down time spent scraping material from edges. Feedback on powder size encouraged refining the final milling step—leading to a product that pours evenly and clumps less.

    Some projects require urgent material needs. To answer this, we maintain rolling batch logs, allowing for a quick ship from reserved stock for repeat customers. The direct connection between operations and logistics cut typical lead times, helping teams avoid costly delays from waiting on specialty intermediates. No imported stock, no third-hand transfer—just uninterrupted production cycles.

    Quality, Compliance, and Traceability on the Line

    Any chemical company claims to track quality, but as the original producer, we live and die by data integrity. Each outgoing package traces to retained samples and batch QA runs. Reporting results from independent labs helps clear regulatory reviews, but our strongest quality insights come from in-house trend records. When small drifts in byproduct profile show up, adjustments in starting material purity, solvent profile, or temperature ramps follow almost immediately.

    Routine audits by major life sciences firms bring extra scrutiny, but also improve our process. Auditors taught us to tighten in-process checks and reinforce contamination controls in all warehouse and loading areas. We keep detailed batch genealogy, so finished product data can always be linked to process conditions, raw material suppliers, and even operator signatures for each step. This kind of transparency grows only after years of producing for the most demanding sectors, where a single slip can break a partnership.

    Environmental and Safety Considerations

    Safe handling runs deeper than just meeting regulations. Real incidents drive home how quickly a spill can halt operations, or how subtle operator fatigue can creep into late-shift weigh-outs. We emphasize regular hands-on safety drills, using lessons learned from actual near-misses. This focus helps us reduce real-world risks, not just check boxes on a form.

    From an environmental angle, the steps taken to lower solvent footprints and cut waste discharge aren’t optional—they’re a function of survival in an industry facing new scrutiny every year. Recovery and recirculation of non-chlorinated solvents used in final purification set a standard for reducing hazardous waste generation per kilogram of output. By reducing the number of intermediate handling and transfer steps, unplanned exposure events and fugitive emissions also shrink, benefitting both staff and the wider community.

    Incorporating closed-loop sampling heads and modular packaging lines minimizes both material waste and operator exposure. This practice started in response to feedback, not from a spreadsheet but from people actually working in PPE in hot, enclosed plants.

    Market and Supply Chain Observations

    Global logistics shifts, tighter regulatory landscapes, and rising feedstock prices make direct manufacturing relationships increasingly valuable. Over the past decade, we've observed disruptions in generic intermediate supply chains, stemming from over-reliance on offshore or bulk aggregators. Manufacturing hydrazinecarboxylates in-house, under direct process oversight, brings not only predictability but also the capacity for process improvements based on evolving regulatory expectations.

    Customer retention, in the end, reflects more than pricing. Teams choosing to source directly from us report lower returns, faster investigation resolution, and greater confidence during their audits. Facing down tough delivery timelines or last-minute spec questions, direct lines between user and manufacturer limit communication breakdowns. This model benefits everyone, keeping synthesis timelines on track and reducing administrative overhead.

    Another advantage emerges during regulatory filings, where the need for supporting analytical, impurity, and batch history data intensifies. This is where direct manufacturer engagement matters most. With retained batch data, ongoing impurity trend monitoring, and long-standing ties to the analytical labs doing the actual testing, our users move through approval processes with fewer regulatory snags.

    Collaborative Improvement and Looking Forward

    Manufacturing specialty intermediates like Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate means listening more than dictating. Every new campaign introduces fresh learning; whether improving powder handling, using a more robust QC marker, or recalibrating drying targets based on user feedback, we let hands-on data guide decisions. Volume users with recurring projects receive lot-stability summaries, and any handling suggestion returns to our production SOP for serious review.

    Even now, as research pushes into more complex small molecule targets and stricter regulations roll in, the need for well-behaved, traceable intermediates only grows. Our internal teams track submission requirements for emerging pharmaceutical registration and compliance. Each improvement, born in the plant or suggested from the lab, feeds back to offer users better results and fewer surprises.

    Tert-Butyl 2-(4-(Pyridin-2-Yl)Benzyl)Hydrazinecarboxylate didn’t become a mainstay overnight, nor did it evolve in isolation. Feedback loops from real users, on production lines and in R&D centers, carve out its strengths. Its place on the shelf stems from concrete service in processes demanding fewer unknowns and more repeatable progress.