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1-(3-Aminopropyl)Pyrrolidine

    • Product Name 1-(3-Aminopropyl)Pyrrolidine
    • Alias 3-(Pyrrolidin-1-yl)propan-1-amine
    • Einecs 629-52-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    558659

    Iupac Name 1-(3-Aminopropyl)pyrrolidine
    Cas Number 5443-90-7
    Molecular Formula C7H16N2
    Molecular Weight 128.22
    Appearance Colorless to pale yellow liquid
    Boiling Point 209-211°C
    Density 0.912 g/cm³ at 25°C
    Melting Point -63°C
    Solubility In Water Miscible
    Flash Point 92°C
    Synonyms 3-(Pyrrolidin-1-yl)propylamine
    Smiles C1CCN(C1)CCCN

    As an accredited 1-(3-Aminopropyl)Pyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 100 grams of 1-(3-Aminopropyl)pyrrolidine, sealed in an amber glass bottle with a secure screw cap.
    Shipping 1-(3-Aminopropyl)Pyrrolidine is typically shipped in sealed, chemical-resistant containers to prevent leaks and contamination. Packaging must comply with applicable regulations for hazardous materials. The shipment includes labeling with safety information, hazard warnings, and documentation such as the Safety Data Sheet (SDS). Temperature and handling instructions are provided as required by the chemical's properties.
    Storage 1-(3-Aminopropyl)pyrrolidine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizers and acids. Store at room temperature, and always use appropriate personal protective equipment when handling to prevent exposure.
    Application of 1-(3-Aminopropyl)Pyrrolidine

    Applications of 1-(3-Aminopropyl)Pyrrolidine in Industrial Manufacturing

    As a direct manufacturer, we supply 1-(3-Aminopropyl)Pyrrolidine directly to diverse industrial sectors where this advanced intermediate supports high-purity synthesis, functionalization, and process performance improvement. The following scenarios represent actual large-scale downstream applications with focused roles in key specialty fields, based on real-world production practices and regulatory frameworks.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    API manufacturers integrate 1-(3-Aminopropyl)Pyrrolidine into the multi-step synthesis of select antiviral agents, where its aliphatic amine structure functions as a key nucleophilic building block. The compound’s reactivity enables site-selective ring functionalization, improving yield and purity profiles for target molecules that undergo subsequent purification, characterization, and formulation stages. API synthesis requires strict documentation of critical material attributes and batch genealogy, with compliance to international pharma standards through all campaigns.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210 & 211 (US FDA GMPs for Drug Products)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for related substances and solvents
    • China Drug Master File (DMF) submission codes and process validation

    Typical usage ratio

    • 0.15 – 0.45 molar equivalents per mole of core molecule, adjusted by reaction stoichiometry and process validation runs on 40–500 kg scale

    Downstream process integration

    • Added at the nucleophilic substitution or reductive amination stage following API precursor isolation and solvent exchange
    • Used as a primary reactant or linker in the functionalization sequence, with post-reaction vacuum distillation and in-process HPLC control

    Final product types

    • Pyrrolidine-based antiviral APIs
    • Alkylamine-functionalized small molecule actives
    • Regulated pharmaceutical bulk intermediates

    2. Crop Protection Intermediate Synthesis

    Agrichemical formulators employ this compound as a core amination reagent during the synthesis of select pyrrolidine-derived pesticide intermediates. Its amine propyl group allows for precise molecular tailoring in heterocyclic pesticide synthesis routes, underpinning structure-activity relationships for new-generation active ingredients. The raw material’s quality consistency and documented impurity profile ensure that downstream processes meet both product registration and production QA/QC benchmarks.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticide Manufacturing
    • ISO 9001:2015 Quality Management System for agrochemical production
    • REACH Registration for European agrochemical intermediates
    • China National Standard GB 2082-2006 for raw material purity and safety in pesticide manufacturing

    Typical usage ratio

    • Generally 0.10 – 0.22 weight percent relative to precursor batch, refined via process scale-up studies and impurity mapping

    Downstream process integration

    • Added at the amination or N-alkylation stage in closed-reactor environments, post-raw material charging and solvent preconditioning
    • Subjected to continuous temperature and pH monitoring with automated dosing for selectivity control

    Final product types

    • Pyrrolidine-derived pesticide actives
    • Herbicide precursor intermediates
    • Fungicide additive bases

    3. Specialty Polymerization Catalyst Component

    Polymer manufacturers use this material as a critical co-catalyst or functional monomer in the production of high-performance polyamide and polyurethane resins. Its unique structure can modulate polymer crosslink density, chain extension, and amine functionality during bulk or solution polymerization. The choice and dosing of this compound directly influence polymer mechanical properties, enabling downstream customization for engineering plastics and specialty elastomer applications with defined performance specifications.

    Industry compliance standards

    • ISO 9001:2015 for Specialty Polymer Manufacturing
    • FDA 21 CFR 177.1500 (if polymers are for food contact applications)
    • ASTM D638 or D3574 standards for mechanical and chemical testing of final plastics
    • European Union Regulation (EC) No 1907/2006 (REACH) for polymer registration and use of chemical intermediates

    Typical usage ratio

    • 0.3–2.0 wt% as a co-catalyst or chain extender, optimized by polymer type, desired molecular weight, and pilot line reactivity trials

    Downstream process integration

    • Premixed in the monomer feed or dosed into the reaction kettle after prepolymer stage under nitrogen atmosphere
    • Reaction progress monitored by viscosimetry and FT-IR analysis for real-time endpoint detection

    Final product types

    • Engineering polyamides for automotive and electrical housings
    • Thermoplastic polyurethane (TPU) elastomers
    • Specialty adhesives and coatings requiring primary amine functionality

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Dye and pigment companies utilize this compound in the closed-loop synthesis of proprietary colorants, taking advantage of its selective reactivity for aromatic amine functionalization. It is especially valued for introducing alkylaminopropyl side chains in chromophore matrices, directly impacting dye solubility, lightfastness, and substrate affinity in technical textile applications. Production environments require traceability and controlled handling to ensure consistent color yield and batch reproducibility as defined by customer and regulatory demands.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • EU REACH Annex XVII – restrictions for azo compounds and advanced intermediates
    • ISO 12402-7 for colorant batch uniformity in industrial applications
    • China GB/T 23981-2009—Textile auxiliary chemical purity criteria

    Typical usage ratio

    • 0.08 – 0.30 molar equivalents based on chromophore type, tuned during process scale-up for color depth and hue targeting

    Downstream process integration

    • Dosed into transition metal-catalyzed aminomethylation or alkylation steps after main chromogen framework assembly
    • Batch processes with in-process UV-Vis monitoring and final HPLC purity analysis

    Final product types

    • Alkylaminopropyl functional dyes for textile inks
    • Soluble pigment intermediates for digital printing
    • High-affinity reactive dyes for specialty fiber dyeing

    5. Organic Synthesis Reagent for Custom Research Chemicals

    Contract research organizations (CROs) and chemical synthesis labs select 1-(3-Aminopropyl)Pyrrolidine as a primary amine donor for targeted molecular libraries and advanced heterocycle preparations. Stringent documentation and impurity profiling enable rapid development of client-defined analogues for pharmaceuticals and specialty material testing under ISO-certified environments. Orders typically support batch-to-batch reproducibility and trace-level identification, in line with sponsored research or new chemical entity (NCE) development programs.

    Industry compliance standards

    • ISO 9001:2015 for quality management in custom synthesis
    • GLP (Good Laboratory Practice) for research material traceability
    • IUPAC protocol adherence for structure verification
    • Internal SOPs and documented material chain of custody for contract synthesis

    Typical usage ratio

    • 0.05–0.30 molar equivalents per reaction, dictated by individual synthetic schemes and reactivity studies at 10 g – 10 kg scale

    Downstream process integration

    • Employed in nucleophilic amine alkylation, reductive amination, and as a spacer in combinatorial chemistry
    • Handled with batch-level purity tests (NMR, LC-MS) throughout synthesis and isolation

    Final product types

    • Research chemical reference standards
    • Pharmaceutical lead candidate libraries
    • High-purity heterocyclic building blocks
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    Certification & Compliance
    More Introduction

    1-(3-Aminopropyl)Pyrrolidine: Manufacturing Value and Practical Insight

    Direct from the Manufacturer: Product Overview

    As a chemical manufacturer, one of the products that stand out in our amine series is 1-(3-aminopropyl)pyrrolidine, often referred to in the lab as APP or by its CAS number, 23112-10-9. Over the years, manufacturing this compound has underscored the critical role that careful design and strict control bring to the final quality. We scale production to meet customer volumes without sacrificing consistency, recognizing that anyone using this intermediate depends on batch-to-batch reliability for their own downstream synthesis.

    1-(3-Aminopropyl)pyrrolidine features a pyrrolidine core with a flexible three-carbon aminopropyl chain. Our standard model for industrial applications offers a purity specification above 98%, suitable for common organic transformations and research purposes. The nearly colorless to pale yellow liquid remains stable under normal handling, easing storage and transfer between departments or production facilities. We keep moisture, secondary amine impurities, and other residuals below strict internal thresholds, since too much water, for example, can trigger side reactions in sensitive processes.

    The Proven Uses in Chemical Synthesis

    The most direct and significant use for 1-(3-aminopropyl)pyrrolidine is as a versatile intermediate. As we have observed from recurring customer feedback and industry data, this compound plays an essential part in developing pharmaceutical scaffolds, especially those with piperidine or pyrrolidine subunits. Medicinal chemists often trust APP to connect core structures with functional arms—either for further elaboration or to introduce basicity into heterocyclic drug candidates. Our team has supported customers who turn to this molecule for synthesizing antihypertensive agents, central nervous system drugs, and as a building block in newer, proprietary small molecule entities.

    Polymer manufacturers also incorporate this diamine, leveraging its secondary amine plus primary amine functionalities. The dual amine structure makes APP a robust crosslinker in specialty epoxy systems, anchoring polymer chains for high-performance coatings or adhesives. Our in-house process engineers have tested crosslink density and found that the flexibility provided by the three-carbon linker translates into resins that combine mechanical strength with resilience—important for industries where coatings face repetitive stress or exposure to chemicals.

    Appreciating Key Manufacturing Differences

    Not all chemicals labeled as 1-(3-aminopropyl)pyrrolidine meet the same standards. As a manufacturer, we see direct results from the care taken at each stage. Sourcing starting materials with low residual halides or oxidized by-products sets the foundation for a cleaner synthesis. Reactor environment, solvent quality, and temperature profiles shape the end product’s color and amine distribution. Controlling reaction times ensures complete alkylation, which in turn prevents a build-up of unreacted pyrrolidine derivatives that might interfere in tightly regulated syntheses.

    A unique facet we’ve learned through layered process optimization involves minimizing cyclic impurities—these often lurk around the edges of the chromatogram and can cause cascading problems. By integrating double-distillation and carefully monitored chromatographic purification, we reduce not only primary contaminants but also keep the product free of odorous trace amines that might cause headaches in downstream blending operations.

    Customers sometimes compare 1-(3-aminopropyl)pyrrolidine to linear aliphatic diamines or to N-alkylated piperidines. In our hands, APP’s balance of steric hindrance and basicity gives it enough reactivity for forming durable chemical bonds while not introducing excessive bulk that could interfere with molecular recognition in drug development. The ring structure provides a balance between flexibility and defined conformation, distinct from straight-chain systems where flexibility alone might not deliver the right secondary effects in target molecules.

    Long-Term Storage and Handling: Manufacturer’s Perspective

    Long experience has taught us a few practical lessons about handling this compound at the plant level. Direct sunlight accelerates degradation, so we transfer and store APP in opaque, nitrogen-flushed containers inside climate-controlled warehouses. Since small quantities of moisture can set off unintended polymerization, drum seals and valve fittings receive regular checks—a small leak left unseen rarely becomes a big problem overnight, but over a shipping cycle, the loss can show up in downstream assay failures.

    Some newer plant managers underestimate the significance of trace secondary amine odors, assuming they do not impact production. Our records show that even modest buildup of these volatile materials can influence operator safety, product transfer rates, and, more subtly, batch-to-batch consistency in later applications. We routinely purge lines and train staff to recognize and report unusual smells not for compliance's sake alone, but to ensure final batch performance.

    Product Quality: Best Practices from the Manufacturing Floor

    Quality assurance with this intermediate means more than clean paperwork and up-to-date certificates. Our process chemists regularly validate GC-MS, H-NMR, and Karl Fischer titration results with reference standards, reducing uncertainty in measured purity, residual solvents, and water content. During pilot runs, we test finished product samples against customer-submitted reference spectra to ensure cross-lab reproducibility. Over the past decade, this extra step has saved multiple customers from failed scale-ups due to mismatched analytical techniques.

    Traceability remains non-negotiable. Each batch receives a lot code linking it back to not only main reactor runs but also supporting raw material shipments and in-process test results. This system, built up from years of managing custom synthesis as well as commodity runs, allows for rapid troubleshooting if a customer identifies a surprising result at their end.

    Differentiation from Commodity Amines and Other Building Blocks

    Some buyers mistakenly treat 1-(3-aminopropyl)pyrrolidine as little more than a replaceable amine, comparable to simpler diamines such as ethylene diamine or longer chain hexamethylene diamines. Our manufacturing data consistently shows otherwise. The combination of a five-membered ring and linear aminopropyl tail introduces a unique spatial configuration, supporting applications in drug discovery where structural rigidity and flexibility must both be present. Unlike straight-chain diamines that may lack sufficient ring tension for biological target fitting, APP’s conformational constraint enables molecular designers to achieve better receptor interaction profiles in pharmaceutical candidates.

    As for N-alkylated piperidines, while they also provide useful secondary amine chemistry, their higher steric bulk and more rigid framework sometimes hinder solubility or slow nucleophilic reactivity in certain transformation steps. In contrast, 1-(3-aminopropyl)pyrrolidine threads the needle—delivering a manageable, user-friendly profile for both polysubstitution and salt-formation routines common in drug substance intermediate production.

    Challenges, Learnings, and Solutions in Scale-Up

    Scaling up production of 1-(3-aminopropyl)pyrrolidine presents its own set of real-world challenges. Heat exchange during exothermic reaction steps can create hot spots that, if unchecked, drive selectivity away from the desired amine or promote unwanted ring-opening side products. In our plant, we’ve solved this with a combination of jacketed reactors, staged solvent feeds, and real-time temperature and pH monitoring. Since market demand for this intermediate tends to rise in fits and starts—often following pharmaceutical approvals or polymer innovation cycles—we’ve built in flexibility, increasing or decreasing shift pattern staffing within a week’s notice, while keeping our quality system locked in.

    Logistics have become another area for careful improvement. Some customers require the product shipped in small, lab-ready containers; others need IBCs for direct tank transfer. To avoid cross-contamination between amines, we reserve vessel fleets and, after each transfer, follow validated multi-step cleaning procedures developed from equipment surface analysis. Monthly management reviews of cleaning schedules have drastically lowered cross-lot impurity events, which in the past could have derailed compliance audits.

    Environmental and Safety Responsibility

    Manufacturing 1-(3-aminopropyl)pyrrolidine brings responsibility, not just in product quality but in managing emissions and wastes. Amine odors occasionally raise workplace air monitoring flags even below occupational limits; our team implements vapor recovery at key vent points and neutralizes collected off-gas streams before release. Waste stream character is tracked for compliance—where neutralization and separation offer much higher safety than bulk incineration due to secondary amine volatility risk. Periodic safety drills keep our staff up to date, familiar with the specific procedures necessary if leaks or uncontrolled reactions occur on-site.

    We’ve found that investing in staff training reaps benefits in reduced downtime, fewer lost batches, and safer day-to-day operations. Rather than lean on signs or standard sheets, technicians are run through practical exercises involving real plant hazards. This hands-on approach ensures those in contact with 1-(3-aminopropyl)pyrrolidine know its quirks—such as skin absorption risk and the need for direct exhaust ventilation at transfer stations.

    Supporting Innovation: Proper Intermediate Supply Chains

    Across the years, collaboration with R&D groups in both pharma and materials science has highlighted that reliable supply chains drive innovation. Early project teams can only move as fast as their intermediates show up, on spec, and in amounts that match both Benchtop and pilot demands. Our schedules prioritize these launches, reserving excess raw material and production slots, recognizing that delays here ripple through many programs.

    We implement redundant sourcing for key precursors and maintain quality links with transportation partners to ensure safe, regulated delivery. Keeping communication open, especially for custom packaging or urgent turnaround orders, reduces missteps that might otherwise disrupt critical synthesis timelines. We encourage regular feedback from application chemists—sometimes noticing trialling problems that prompt tweaks in our workup or purification, ensuring customers get materials that fit their work, not just our internal specs.

    Observed Results and Customer Outcomes

    Feedback loops with end-users give us a broad look at how 1-(3-aminopropyl)pyrrolidine translates specification sheets into results on the bench and in the field. Pharma teams regularly report that our low-water lots deliver improved conversion in high-sensitivity amide coupling steps. Polymer formulating groups mention increased reproducibility, citing both the well-defined primary and secondary amine ratio and the absence of colored or smelly by-products. Repeat customer purchasing patterns often follow the successful transition from lab scale development to full plant synthesis, reinforcing for us that consistent quality from the outset smooths later upscaling by third parties.

    Working directly with diverse client teams, we developed documentation outlining best practices for dissolving, blending, and neutralizing spent residues. The benefit of this field-level perspective is that successful outcomes at the application end feed back into how we refine process controls and staff training. Our team reviews every incident of customer-reported deviations—whether containers sweating in non-climate warehouses or odd shifts in GC retention times caused by border transport delays—so that we can adjust not just our production but support material.

    Continuous Improvement and Future Directions

    Looking ahead, our technical team pursues ongoing improvements by tracking emerging applications for 1-(3-aminopropyl)pyrrolidine. Newer green chemistry protocols target lower solvent use, so we’re investigating ways to both reduce our own emissions during synthesis and offer solvent-free options where suitable. Early trials with sealed microreactors suggest tighter yield distributions and lower impurity formation, a promising route for future investments.

    Expansion in life sciences and advanced materials pushes us to further document product characteristics—including solubility in novel green solvents, storage effects over months instead of days, and the impacts of alternate packaging on field usability. Where regulatory environments shift—such as new amine exposure standards or waste registration platforms—we update our practices and transparently share these changes with customers rather than waiting for an outside audit or non-conformance event.

    Why Experience and Direct Production Matter

    Manufacturing 1-(3-aminopropyl)pyrrolidine is more than making molecules to a spec. Our hands-on knowledge, refined over years of production, guides each batch from raw material choice through final container closure. Along the way, practical lessons surface—what storage temperatures work across climates, which purification tweaks sharpen downstream user yields, how subtle color changes flag reaction drift before analytics sound alarms. This embedded experience does not show up on technical sheets but builds real trust over time, especially as customers’ own requirements evolve.

    Customers with niche or high-purity needs seek out manufacturers willing to explain and adapt, not just ship from bulk. Our operators run real-time checks for more than compliance—they understand how tomorrow’s challenges and today’s improvements together build the foundation for safe, reliable, and effective chemical intermediates. Serving future-facing chemistries means drawing on concrete knowledge of what makes each product fit for purpose—something only continuous manufacturing and real-world engagement can bring.