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1-Benzyl-2,5-Dihydro-1H-Pyrrole

    • Product Name 1-Benzyl-2,5-Dihydro-1H-Pyrrole
    • Alias N-Benzylpyrroline
    • Einecs 630-736-8
    • 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
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    Specifications

    HS Code

    267815

    Productname 1-Benzyl-2,5-Dihydro-1H-Pyrrole
    Casnumber 13612-65-6
    Molecularformula C11H13N
    Molecularweight 159.23
    Appearance Colorless to pale yellow liquid
    Boilingpoint 285-287 °C
    Density 1.03 g/cm3
    Flashpoint 115 °C
    Purity Typically ≥97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractiveindex 1.573

    As an accredited 1-Benzyl-2,5-Dihydro-1H-Pyrrole 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 25 grams of 1-Benzyl-2,5-dihydro-1H-pyrrole, sealed with a screw cap and labeled for laboratory use.
    Shipping 1-Benzyl-2,5-Dihydro-1H-Pyrrole is shipped in securely sealed containers, compliant with chemical safety regulations. Packaging ensures protection from moisture, light, and physical damage. Accompanied by proper labeling and safety documentation (SDS), the product is transported using appropriate carriers to prevent leaks or exposure, in accordance with international and local shipping guidelines.
    Storage **1-Benzyl-2,5-Dihydro-1H-Pyrrole** should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Properly label the container and avoid prolonged exposure to air to prevent degradation. Store in accordance with local regulations and chemical safety guidelines.
    Application of 1-Benzyl-2,5-Dihydro-1H-Pyrrole

    Applications of 1-Benzyl-2,5-Dihydro-1H-Pyrrole in Industrial Manufacturing

    As a dedicated manufacturer, we supply 1-Benzyl-2,5-Dihydro-1H-Pyrrole to critical downstream industries requiring consistent quality and manufacturing-grade specification. Below, we detail its core applications, compliance guidelines, technical integration, and final product end-uses within real industrial sectors.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies employ 1-Benzyl-2,5-Dihydro-1H-Pyrrole as a building block for heterocyclic APIs, especially in the preparation of pyrrolidine-containing compounds for CNS and cardiovascular drug classes. Our material enters early-stage synthesis where controlled purity, traceability, and validated impurity profiles are essential for compliance. It participates in N-alkylation and cyclization steps under GMP documentation policies. Leading formulators adjust usage between 0.25 and 2.5 equivalents depending on the target molecule, impurity acceptance criteria, and process step yield controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US FDA cGMP for finished pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) guidelines for API intermediates
    • ISO 9001:2015 quality management systems

    Typical usage ratio

    • 0.25–2.5 equivalents, set based on stoichiometry and process optimization studies
    • Adjusted according to impurity limits and byproduct control in multi-step syntheses

    Downstream process integration

    • Added as a core intermediate in small molecule API multi-step synthesis
    • Utilized during heterocycle-forming reactions under nitrogen or inert atmosphere
    • Tracked by in-process analytical methods (HPLC/GC for residuals and by-products)

    Final product types

    • Pyrrolidine-based CNS therapeutics
    • Cardiovascular drug intermediates
    • Custom small-molecule building blocks for lead optimization
    • Specialty active pharmaceutical ingredients

    2. Agrochemical Active Ingredient Precursor

    Crop protection formulators incorporate our material as a precursor in manufacturing substituted pyrrole and pyrrolidine agrochemicals, particularly for selective herbicides and insecticides. The chemical's reactivity enables direct introduction into condensation and cyclization reactions, typically under controlled temperature and catalyst-guided conditions. Compliance follows agrochemical APIs’ strict regulatory tracks regarding purity and trace solvent contents. Usage typically ranges from 5 to 20% relative to total batch mass, determined by crop safety studies and downstream process requirements.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • OECD principles of Good Laboratory Practice (GLP) for manufacturing trials
    • ISO 17025 certified analytical testing

    Typical usage ratio

    • 5–20% by mass of synthetic batch, depending on final molecule design
    • Varied based on targeted biological activity and environmental fate studies

    Downstream process integration

    • Fed into base-catalyzed coupling and ring-forming reactions under closed system
    • Monitored by mass balance and GC-MS to ensure trace contaminant compliance
    • Straight addition to in-situ reaction vessels with real-time parameter logging

    Final product types

    • Selective pyrrolidine herbicides (e.g., broadleaf weed control)
    • Functionalized pyrrole insecticides
    • Intermediates for fungicidal actives
    • Stabilized active ingredient concentrates

    3. Fine Fragrance and Aroma Chemical Manufacturing

    Aroma chemical producers value the compound in producing specialty musky and amber notes in fine fragrance bases. It acts as a tailored heterocyclic intermediate entering reductive amination, acylation, and further ring modification reactions. Industrial usage ratio is typically between 1 and 5% on a formulation mass-balance, optimized for olfactory profile and base stability. Producers adhere to IFRA standards and international cosmetic regulatory guidelines, validating key impurity profiles with comprehensive GC-MS testing.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9235 criteria for aromatic raw materials
    • REACH Regulation (EC) No 1907/2006 for substance registration

    Typical usage ratio

    • 1–5% within aroma formulation, adjusted based on target note intensity
    • Precise level established by GC-olfactometry trials and customer sensory panels

    Downstream process integration

    • Introduced during synthesis of pyrrole-based aroma building blocks
    • Processed via stepwise transformation before final fragrance compounding
    • Quality control covers both trace residual screening and odor purity validation

    Final product types

    • Fine fragrance base oils
    • Premium eau de parfum compositions
    • Luxury-grade aroma modifier intermediates
    • Scented personal care actives

    4. Specialty Polymer and Advanced Material Synthesis

    Research and advanced materials sectors use the compound as a monomeric unit or specialist modifier in conductive polymer preparations and functional coatings. It participates in controlled polymerization via oxidative or catalytic mechanisms, contributing nitrogen-based functionalities to the final matrix. Industrial practitioners directly feed it into pre-polymerization blends in concentrations of 0.5 to 4 wt%, determined by the target electronic property and polymer backbone type. Full traceability, purity reports, and documentation for each lot are provided to meet end-use quality protocols.

    Industry compliance standards

    • ISO 14001:2015 for environmental management systems in chemical processes
    • ASTM D638 and D882 for physical property validation of polymers
    • RoHS Directive 2011/65/EU for hazardous substance thresholds
    • Global Chemical Inventory Registration (TSCA, REACH)

    Typical usage ratio

    • 0.5–4 wt% of total polymer batch, tailored for conductivity and surface energy
    • Adjusted by lab-scale screening and scale-up for specific film thickness or device application

    Downstream process integration

    • Added to polymerization reactor prior to oxidant or co-monomer introduction
    • Monitored for conversion efficiency and residuals using NMR and GPC analysis
    • Included in formulation logs and end-use performance documentation

    Final product types

    • Conductive coatings and inks for electronics
    • Functionalized polymer films for sensors
    • Specialty resin additives for high-durability coatings
    • Advanced membrane materials for energy applications
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    Certification & Compliance
    More Introduction

    Introducing 1-Benzyl-2,5-Dihydro-1H-Pyrrole: Our Approach to Quality in Fine Chemicals

    Understanding 1-Benzyl-2,5-Dihydro-1H-Pyrrole

    Working in chemical synthesis every day, I’ve seen researchers and process chemists gravitate toward specialty intermediates that help unlock new molecular spaces. Among the unique building blocks we manufacture, 1-Benzyl-2,5-dihydro-1H-pyrrole stands out for its versatility and stability. This compound—model BDHP125M—finds recurrent use in advanced organic synthesis and comes to us as a colorless to pale yellow liquid, typically manufactured at the 99% purity threshold.

    This product results from a rigorous synthetic process conducted in controlled conditions. Years of refining the hydrogenation of benzylpyrrole, careful distillation, and robust analytical checks have helped us maintain a strong track record for both purity and consistency. Every batch gets verified by GC and NMR, with full documentation. Over time, organic and medicinal chemists have come to trust this approach.

    Characteristics and Hands-On Experience

    Chemical intermediates aren’t created equal. Sourcing 1-Benzyl-2,5-dihydro-1H-pyrrole directly from the manufacturing line, I’ve watched as process engineers balance reaction temperature, pressure, and stoichiometry to avoid residual starting materials or heavy byproducts. The resulting compound demonstrates a clear benzyl-saturated pyrrole ring, offering both the structural rigidness and flexibility needed for downstream reactions.

    On the bench, customers notice the difference. Low water content helps maintain reactivity, especially in condensation, cyclization, and coupling reactions with sensitive reagents. A tight control of color and odor reflects the minimal presence of non-volatile contaminants. Chemists working on lead molecule development offer direct feedback—less time spent purifying and fewer batch-to-batch surprises make a difference over extended multi-step syntheses.

    The molecular weight sits just over 173 g/mol, and careful distillation ensures no tails or heads make it into the collection flask. Over my career, I’ve learned that a clear, narrow fraction translates to reproducibility in downstream chemistry. The liquid form lends itself well to accurate measurement and mixing.

    Working with the Compound: Real-World Applications

    Our partners use 1-Benzyl-2,5-dihydro-1H-pyrrole as a key intermediate when constructing nitrogen heterocycles, often the cornerstone of novel pharmaceuticals. Some employ it in the synthesis of targeting ligand scaffolds for imaging agents or as a step in the creation of alkaloid-inspired molecules.

    I remember discussions with medicinal chemistry teams working on small molecule libraries for central nervous system targets. Their priorities: scalability, low impurity profile, and predictable reactivity. It’s rewarding to hear that this pyrrole derivative slots reliably into diverse transformations—N-alkylation, metal catalyzed cross-couplings, or as a precursor to more complex fused ring systems.

    Compatibility stands out: the benzylic nitrogen allows varied substitution while the dihydro structure moderates aromaticity, giving chemists options for both further reduction and selective oxidation. Some have told us the benzyl group offers tractable points for deprotection under mild hydrogenolysis, liberating the parent amine cleanly in good yield.

    The versatility isn’t limited to pharma work. Teams in specialty materials turn to this compound when designing monomers with heterocyclic backbones. Its electron-rich nature fits well in fine-tuning charge transfer properties of organic electronics or as a functional modifier in polymer science, especially when handleability and defined structure are essential.

    How Our 1-Benzyl-2,5-Dihydro-1H-Pyrrole Differs from Other Sources

    I’ve watched the market for pyrrole intermediates for over a decade. Traders and resellers sometimes circulate off-spec lots, but as primary manufacturers we track every synthesis back to the raw starting materials. This results in a narrower impurity spectrum and detailed batch histories. We rely on automated fraction collection and inline IR to monitor each critical control point, limiting the risk of cross-contamination or residual byproducts.

    Some laboratories purchase this compound from brokered stocks, only to face inconsistent purity or stability. We deliver within stable glass packaging, shielded from light and air exposure. Each shipment is sealed with tamper-proof crimp tops, and we supply batch-specific chromatograms so customers know what’s in their flask—something difficult to verify with repackaged bulk stocks.

    Beyond purity, handling properties differ. Our direct-from-plant lots demonstrate a uniform viscosity profile and minimal peroxide content. Electrochemical applications, for instance, require low background currents and well-defined voltammetry, achievable only with minimal trace metals and peroxides—attributes best achieved at source.

    Rather than relying on bulk market speculation, we invest in maintenance and calibration. Our technicians follow a validated protocol for every production run. Analytical packages include reference standards, and we maintain reserve retention samples for customer confirmation. We back this up with technical support from our own chemists, not just sales representatives—my colleagues and I routinely join project review meetings to troubleshoot or optimize user conditions.

    We receive repeat orders from teams who’ve worked with both types of supply chains—the difference in performance outcomes can be measured directly in project timelines and reproducibility. Direct feedback often points to fewer side reactions, more robust yields, and greater confidence integrating the compound into final regulatory filings.

    Supporting Innovation in Applied Chemistry

    I’ve always believed that manufacturers can be more than suppliers; we’re partners in innovation. This product was born from requests in the late 1990s, as chemists grew frustrated by inconsistent quality and inconvenient customs delays from offshore brokers. Working alongside our own R&D team, we established a continuous synthesis route based around local, audited raw materials. This has given us years of control over trace elements, minimization of residual solvents, and the optimization of the final purification step.

    Customer-driven feedback shaped every step. Early adopters sent in feedback about solubility in acetonitrile and toluene, and suggestions to tighten water spec below 250 ppm for catalysis applications. Our engineers responded by introducing molecular sieve drying directly in the final product vessel. Others requested traceability—so every bottle that leaves our fulfillment center carries a unique identifier with batch-level analytical data, including ^1H and ^13C NMR spectra.

    Even during global supply fluctuations, we work with redundant upstream contracts for our benzylamine and 1-pyrroline starting materials, minimizing risk for our customers. Technical issues come up—occasional foaming in scale-up, or increased humidity exposure on rainy days—but real-time monitoring and a culture of process improvement keep our lead times stable. When bottlenecks occur, we keep our communication lines open. When a client’s reaction sequence required a modified specification, we accommodated with special runs, and relayed stability test data upfront.

    People expect reliability, and that’s earned batch by batch. This means more than just ticking boxes for official certifications; our GMP-compliant site conducts full environmental monitoring, and our QA team manages both supplier audits and end-use support for pharmaceutical partners. Site visits from client quality teams are welcomed—tours of the plant often lead directly to process improvements benefiting both sides.

    Continuous Improvement: Safety, Sustainability, and Regulatory Compliance

    Any manufacturer serious about long-term success needs to invest in safety and sustainability. Over the last twenty years, we’ve adopted closed-system transfer for hazardous intermediates and vapor recovery at every key vent point. This not only improves yields but also reduces solvent consumption and emissions. Waste minimization features into both the technical and economic calculation: regular audits have identified areas to reclaim more mother liquor and recover solvents without compromising purity.

    Our compliance team monitors changing regulatory standards: ICH, REACH, and domestic workplace exposure guidelines drive ongoing updates in storage, packaging, and labeling. Annual internal reviews confirm material control and training, especially for shipping under ADR and DOT guidelines. As a direct producer, full traceability is a must—outgoing product never commingles with third-party intermediates.

    Safety on the plant floor matters just as much as documentation. I’ve seen accidental spills halted quickly due to well-drilled staff, and regular walk-throughs capture and fix small issues before they escalate. Our on-site safety committee includes both chemists and operators, so concerns get addressed with practical, hands-on approaches.

    Sustainability goes beyond process chemistry. We invest in community outreach, energy-saving retrofits on the plant floor, and responsible sourcing for packaging supplies. These steps make a difference for partners facing their own corporate responsibility audits. It isn’t a distant or abstract challenge: unless every batch meets both performance and sustainability criteria, customer trust dissolves faster than any chemical we produce.

    On the documentation side, our data integrity plan uses both paper and digital records—the latter gets archived for at least ten years. This guarantees that customer audits, registration dossiers, or problem-solving requests get answered swiftly and accurately.

    Collaboration with Research and Industry

    Chemistry is driven by collaboration. Many projects begin as a simple inquiry—a small pilot order for 1-Benzyl-2,5-dihydro-1H-pyrrole, a few discussions about solvent compatibility, or a question about scalability to multi-ton volumes. Over time, these exchanges lead to joint development: one client requested batch-controlled material for a phase II drug candidate; another needed kilogram-scale lots for new catalyst R&D. We offered not just catalog quantities but custom synthesis, modified packaging, and even stability testing tailored to novel end-use conditions.

    Some clients later share preprints or publications citing our material—proof that scientific advances depend on reliable access to high-quality starting points. Novel coupling reactions, photochemically driven processes, or scale-up demonstrations often cite the need for a consistently pure pyrrole intermediate. We view these successes not just as endorsements but as feedback loops, fueling further process optimization on our side.

    Research consortia and industrial pilot plants require close consultation on everything from documentation to supply schedules. We coordinate with technical teams to align release specs, batch numbering, and impurity threshold controls, keeping projects moving smoothly from lab to plant. When regulatory filings require full impurity profiling, we work hand-in-hand with project staff to deliver all needed analytical records and validation runs.

    Forward-thinking clients sometimes share unpublished results on novel transformations or byproduct minimization using unique conditions. We routinely take these insights back into our production review meetings. Several process changes in our own synthesis flow were inspired directly by partner-chemist feedback. It’s a two-way street: their results drive our own developments, ensuring both sides benefit.

    Product Handling and Lifecycle Support

    Purchasing a fine chemical is hardly the end of the relationship—long-term users depend on accessible technical support and responsive service. Our team engages directly with customers post-delivery; we record all feedback on handling, storage, and compatibility. Some universities require specialized packaging to meet tight storage guidelines, so we engineered custom ampoules with pre-scored necks for safer transfer in glove boxes.

    Industrial customers focus on rapid unpacking and usage. We standardized inner seals for repeat access under nitrogen blanket, and introduced QR-coded labels that link directly to batch certificates and safety information. Real-world feedback prompted these upgrades, and every new lot launch is reviewed for ways to further simplify and safeguard user experience.

    Troubleshooting sometimes reveals challenges—maybe a previously robust reduction route now shows sluggish yield, or a different coupling catalyst exposes a byproduct below the usual detection threshold. We stay directly involved, running bench-scale test syntheses using actual customer protocols, confirming or troubleshooting reported issues. If necessary, we revise our own processes to replicate and solve unexpected performance drifts.

    For customers facing regulatory registration, our documentation team compiles dossiers with full analytical data, MSDS, and traceability documentation suitable for both internal and external audits. We participate in supplier qualification audits and offer access to archived batch records on request. Every order, large or small, includes post-delivery check-ins to confirm safe arrival, product condition, and application feedback.

    Conclusion: Value in Direct Manufacture

    Direct involvement in the production and ongoing customer engagement sets our 1-Benzyl-2,5-dihydro-1H-pyrrole apart. Over the last twenty years, I’ve watched consistent quality, tight analytical controls, and customer-focused technical support turn a simple chemical intermediate into a trusted tool for research and manufacturing teams worldwide.

    Improvement never stops—each project, batch, and new user provides lessons for refining our own approach. For those engineering the next generation of pharmaceuticals, specialty materials, or advanced intermediates, direct partnership makes all the difference. Providing not just a chemical, but a foundation for successful discovery and innovation, drives our work daily.