3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine

    • Product Name: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine
    • Chemical Name (IUPAC): 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine
    • CAS No.: 1309688-31-2
    • Chemical Formula: C9H10N2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    448763

    Compound Name 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine
    Molecular Formula C9H10N2
    Appearance solid
    Structure Type heterocyclic aromatic
    Functional Groups pyridine ring, pyrroline ring
    Iupac Name 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine

    As an accredited 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled with chemical name and hazard symbols, containing 5 grams of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine.
    Container Loading (20′ FCL) 20′ FCL container loading for 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine ensures safe, efficient bulk transport, maximizing cargo and minimizing damage.
    Shipping The chemical **3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine** is shipped in a sealed, chemically-resistant container, protected from light and moisture. Standard shipping involves secure packaging compliant with regulatory guidelines for laboratory chemicals. Shipping is available to certified institutions or qualified personnel only; handling instructions and safety data sheets are included with each shipment.
    Storage 3-(3,4-Dihydro-2H-pyrrol-5-yl)pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Avoid sources of ignition. Proper labeling and secondary containment are recommended to prevent accidental spills and exposure. Store at room temperature unless otherwise specified by the supplier’s safety data sheet (SDS).
    Shelf Life Shelf life of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine: Stable for 1-2 years if stored cool, dry, tightly sealed, and protected from light.
    Application of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine

    Purity 98%: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yields and reduces byproduct formation.

    Melting Point 112°C: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with a melting point of 112°C is used in fine chemical manufacturing, where precise melting behavior enables consistent solid-phase processing.

    Molecular Weight 160.21 g/mol: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine having a molecular weight of 160.21 g/mol is used in organic electronic material development, where accurate mass enables correct stoichiometric calculations.

    Stability Temperature 60°C: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with a stability temperature of 60°C is used in storage and transport, where stability ensures minimal degradation over time.

    Particle Size <10 µm: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with particle size less than 10 µm is used in catalyst formulation, where fine particle size improves dispersion and reaction efficiency.

    Viscosity Grade Low: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with low viscosity grade is used in liquid formulation processes, where reduced viscosity enhances mixing and process flow.

    Solubility in Ethanol 25 mg/mL: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with solubility in ethanol at 25 mg/mL is used in solution-phase organic synthesis, where good solubility accelerates reagent incorporation.

    Optical Purity >99% ee: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with optical purity greater than 99% ee is used in chiral drug development, where high enantiomeric excess provides superior biological activity.

    Residual Solvent <0.05%: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with residual solvent below 0.05% is used in agrochemical formulation, where low solvent content meets regulatory safety limits.

    Water Content <0.1%: 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine with water content under 0.1% is used in moisture-sensitive synthesis, where low moisture prevents hydrolysis and degradation.

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    Certification & Compliance
    More Introduction

    3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine: Direct from the Manufacturer

    Introduction from the Production Floor

    At our manufacturing plant, daily attention goes to each batch of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine. Over the years, we’ve learned how this compound answers unique needs in pharmaceutical and chemical development. As one of our primary specialty heterocyclic offerings, 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine stands apart from other pyridine derivatives thanks to a combination of nuanced reactivity and ease of functionalization. Our direct involvement in every synthesis step delivers consistency not always found further down the supply chain. And because we see this product through from raw input to final packaging, we hold ourselves accountable to the most demanding project requirements—not just on paper, but on the real-world lab bench.

    A Close-Up on Specifications and Structure

    We maintain tight control over product quality and impurity profiles, shaped by our hands-on experience with both batch and continuous processing. 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine carries the molecular formula C8H10N2, with a characteristic bicyclic skeleton. The linkage of the pyrrole ring to the pyridine core brings a specific reactivity pattern not available with simpler monocyclic analogs. This combination provides value for customers developing CNS-active drugs, enzyme inhibitors, and advanced materials. Through repeated customer feedback and laboratory trials, we’ve tracked the influence of moisture, residual solvents, and minor impurities on downstream applications, leading us to prioritize careful purification and thorough drying—features many researchers only appreciate after running a pilot study or two.

    Typical output appears as a pale solid. Over time, our production chemists have settled on drying times and storage protocols that stave off discoloration and compositional drift. We ship with tight ranges for melting point and minimal spectral impurities, confirmed batch by batch before loading. We do not cut corners on analysis, because we’ve fielded enough late-night calls from development scientists troubleshooting odd results back to a supplier’s variation or an overlooked contaminant. The way our QC staff approach their work reflects the respect we have for the complexity of downstream discoveries that rely on our material.

    Handling Reactivity for Research Needs

    The pyridine unit in this product draws persistent attention from medicinal chemists due to its versatility for further substitution and its hydrogen bond accepting nature. Researchers looking for a bridge between classic pyridine scaffolds and more conformationally flexible motifs often turn to this compound. The pyrrolidine segment introduces a partially saturated five-membered ring, which detunes the electronic character just enough to influence selectivity in metal-catalyzed or acid-promoted transformations. We’ve watched project teams explore these electronic effects for synthesis of novel ligands and proprietary small molecule inhibitors, and our technical staff regularly provide input on solubility, compatibility with standard purification media, and the ways specific storage conditions can tip results between success and costly rework.

    Lab inquiries often focus on compatibility with common building blocks and reaction partners—Grignard reagents, cross-coupling precursors, or amide coupling agents. Our experience is that 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine tends to withstand a broader range of pH and oxidative conditions than many alternative N-heterocycles. The fused ring system stabilizes the molecule against hydrolysis that might degrade simpler structures mid-way through a multi-step route. We ship with this application profile in mind, careful to limit trace metals and to avoid packing components that can leach or catalyze side reactions. This, again, comes not from paperwork, but from hard-earned troubleshooting with partners across the fine chemical and pharmaceutical landscape.

    Why Synthesis Origin Matters

    Product authenticity matters in the world of advanced chemical manufacturing. By producing 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine in-house instead of sourcing from intermediaries or repackers, we see the reaction kinetics, the color transitions after each stage, and the subtleties of endpoint isolation. This gives us a practical sense of the most common process deviations, which we use to maintain purity lots above 98 percent in routine operation. The insights gained from many cycles of production have taught us which raw materials yield the cleanest cuts and which process steps tend to collect undesired byproducts. Rather than repeating the textbook account, we base tweaks and quality checks on data from actual scale-ups. If an alternative supplier offers a lower price, we’ve learned to look very closely at batch-to-batch spectra, because even small shifts in the impurity fingerprint can affect biological test results or crystallization yields downstream.

    End-users often report setbacks from generic material, especially when introducing a novel heterocycle into a diagnostic kit or therapeutic pipeline. We’ve worked shoulder-to-shoulder with scientists who track a single impurity back to its source—and sometimes that means tearing open drums and vials to reexamine what the entire market calls ‘standard grade’ material. That’s why, as a manufacturer, we take batch traceability seriously. We don’t just attach a lot number; we keep a full record of synthetic route, process deviations, and analytic signoffs. Years of experience have taught us that documentation and process transparency matter for down-the-line innovation.

    Comparison with Other Pyridine Products

    Not all pyridine derivatives function equally in application chemistry. Most are simple monocycles—light, volatile, and often too reactive or too plain for advanced targets. Our 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine contains both the familiar aromatic nitrogen pattern and a fused ring, combining rigidity and a measure of conformational flexibility. This structure offers a bridge between traditional pyridine and more elaborate, saturated building blocks.

    Over the years, we've supplied a spectrum of pyridine-based intermediates to diverse application areas. Compared with pyridine itself—or methyl, chloro, or amino substituted variants—the addition of the dihydropyrrol ring changes more than just the appearance. We hear from medicinal chemists that the added ring system blocks certain metabolic pathways, which can extend the half-life of test compounds. In material science, polymerization behavior shifts in a direction not seen with plain pyridine. Our familiarity with these nuanced differences lets us guide partners toward the right derivative, or in some instances to recommend moving upstream or downstream in their synthetic route for better access to specific property sets. These details aren’t in any standard catalog; they grow from years alongside academic and commercial researchers solving the specific challenges that surface after scale-up or regulatory submission.

    Application Experience and Solving Challenges

    Our direct customers range from research-stage pharmaceutical teams to advanced agrochemical developers. Most approach us with a particular puzzle—a late-stage lead modification, a need for scale-up material, a demand for tight impurity control. Our synthesis know-how and control over every production stage mean we can respond to questions that go beyond strict technical spec. Is a batch soluble enough in your chosen solvent? Will it withstand the deprotection or hydrogenation protocols without loss? We’ve pulled samples from current lots or made minor process adjustments to deliver what’s needed, because our own R&D group faces the same constraints as our clients. This two-way flow of information tightens our process and raises the collective bar for outcome-based manufacturing.

    Solving bottlenecks often involves rethinking purification or packaging, especially for cold-chain or long-term storage. From our end, attention to silica selection, solvent polarity, and minimizing oxygen ingress provides the margin that keeps a project moving. Tougher cases, such as material for biological testing that’s prone to rapid oxidation, push us to invest in lower-part-per-billion oxygen exclusion. That’s a real-world difference between direct manufacture and bulk repackaging. Sometimes the most valuable insights come not from broad market data, but from listening to the challenges faced by specific users as they transition from milligram screens to pilot-plant scale.

    Supporting Advanced Research

    The heart of value in supplying 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine springs from our close engagement with research partners. Our technical team has refined analytical suites—NMR, HPLC, mass spectrometry, and wet chemistry—based on frequent feedback from buyers. In particular, we’ve adopted best practices from collaborative work with biotech teams looking for lead compound optimization. This means, instead of providing a standard certificate of analysis, we offer spectroscopic detail, full impurity listing, and guidance on which analytic markers prove most critical for your application area. Sometimes we’re asked to deliver micronized or alternate particle size fractions for direct formulation trials. Experience from our own product development and formulation lines guides us here; we know what happens when a batch with uneven crystallinity enters a mixer or an extruder, and we take steps on our end to manage these factors before the product leaves our site.

    Because we witness what it takes to bring a project from gram to kilogram scale, our sense of quality control and communication leans toward thoroughness rather than minimal compliance. Documentation is clear, archival, and linked to every analytical and synthesis step. Our ability to adjust lot characteristics—by purification or recrystallization, for example—has often won projects that would have stalled with an off-the-shelf catalog option. The real-world needs of synthesis teams, especially those bridging the gap between discovery and commercial launch, run deeper than most procurement specs reveal.

    Addressing Market and Supply Chain Pressures

    Recent years brought supply chain uncertainty, but as a manufacturer, we anchor every batch in our own facility and avoid the price and lead time volatility that comes from dependence on outside processors. We’ve seen how interruptions—caused by logistics delays, customs slowdowns, or global raw material shortages—can cripple research timing. Our continual investment in raw material inventory, staff training, and equipment redundancy lets us maintain reliable lead times and quality levels. From breadth of sourcing to in-house testing, we run scenario planning to buffer customers from unseen disruptions.

    Stable partnership with end-users has allowed us to forecast demand better and smooth out the risk of single-supplier exposure for both sides. Over enough cycles, this builds the trust that lets research programs commit to new heterocyclic scaffolds without fear that an obscure intermediate will vanish mid-way through product development. Many of our repeat buyers start as single-order customers, coming back because they see the process transparency and problem-solving capacity that doesn’t always show up further down the market.

    Navigating Regulatory and Environmental Considerations

    Direct manufacturing of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine also positions us to address regulatory shifts and sustainability trends. We’ve seen tighter scrutiny around solvent residues, heavy metals, and waste disposal as agencies update requirements. Our operating procedures reflect evolving best practices—using solvent recovery, closed-loop equipment, and continuous process monitoring. We share analytic data openly with customers seeking compliance for new filings or green chemistry audits. Lately, queries about lifecycle analysis and carbon footprint for specialty chemicals have increased; we invest in process improvements for waste minimization and energy efficiency, because our customers—and regulators—place a premium on environmental stewardship.

    Transparency in sourcing and process steps fosters trust with both industrial and academic users looking to document provenance. We've secured certification for relevant environmental and occupational standards. The changes we’ve made based on regulatory guidance add costs in the short term but pay off in customer retention and easier market acceptance for both us and the end-user. That kind of return shows up both in our audit records and in long-standing client relationships.

    Working with Innovation and Intellectual Property

    The unique substitution on our 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine brings distinct value to patent-stage and late-stage discovery work. We often work with teams who need strictly controlled supply for proprietary chemistry—sometimes under strict confidentiality terms. Operating as a primary manufacturer allows us to offer non-standard packaging, dedicated production windows, or tailored analytic support, which are difficult or impossible to secure from traders or bulk repackers. Our technical and IP staff stay current on freedom-to-operate questions, referencing both the open literature and internal formulations experience. Practical navigation of these issues keeps our partners' own filings and launches on schedule. This deeper involvement grows not from a distance but from immersion in the chemistry, from start to finish.

    Future Outlook and Industry Perspective

    Looking ahead, the role of niche heterocycles like 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine is poised to grow, as more R&D teams move beyond classic building blocks to address fresh therapeutic needs and novel catalytic systems. Our manufacturing team keeps a close eye on academic literature—tracking new synthetic methods and reactivity profiles that could inform either our own processes or suggest new applications for our product portfolio. We know from experience that being first to respond to these shifts, with both technical skill and production agility, wins customer loyalty.

    Scientific collaboration fuels these advances. Our company has hosted joint webinars and technical symposia with research groups eager to push beyond standard reagent sets. This open exchange supports discovery and allows direct feedback, looping right back into our process controls and product improvements. In a constantly evolving field, staying nimble and transparent as a manufacturer isn’t just an advantage—it’s a necessity for meeting both current and future research goals.

    Conclusions Drawn from Daily Manufacturing

    Every kilogram of 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine we ship reflects years of accumulated knowledge—what works, what fails, and what makes a chemical truly valuable for innovation. Unlike catalog distributors or marketing offices many steps removed from the plant, we see the real issues and the real opportunities. Researchers, engineers, and procurement teams want more than a certificate—they want a genuine partner in solving problems. We hold ourselves to that higher standard, because as direct manufacturers, we know our reputation rides on every box, every label, and every phone call we answer. After experiencing the difference a reliable source and transparent data can make, our production and technical teams commit to not just shipping product, but assisting discovery and development at every step.