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2-(4-Chlorophenyl)Pyrrolidine

    • Product Name 2-(4-Chlorophenyl)Pyrrolidine
    • Alias 4-chlorodex
    • Einecs 629-822-9
    • 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

    860918

    Chemical Name 2-(4-Chlorophenyl)Pyrrolidine
    Molecular Formula C10H12ClN
    Cas Number 113305-88-1
    Appearance White to off-white solid
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1CC(NC1)C2=CC=C(C=C2)Cl
    Inchi InChI=1S/C10H12ClN/c11-9-3-1-8(2-4-9)10-5-6-12-7-10/h1-4,10,12H,5-7H2
    Pubchem Cid 70083

    As an accredited 2-(4-Chlorophenyl)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 50 grams of 2-(4-Chlorophenyl)Pyrrolidine, securely sealed in an amber glass bottle with a tamper-evident cap.
    Shipping Shipping for 2-(4-Chlorophenyl)pyrrolidine is handled in compliance with chemical transport regulations. The compound is packaged securely in sealed containers to prevent leakage or contamination. It is transported by authorized carriers, accompanied by proper documentation, and labeled according to hazard classification to ensure safe and legal delivery to laboratories or licensed recipients.
    Storage **2-(4-Chlorophenyl)pyrrolidine** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Avoid exposure to direct sunlight and moisture. The storage area should be clearly labeled, and access restricted to qualified personnel. Ensure appropriate safety measures and protective equipment are available nearby.
    Application of 2-(4-Chlorophenyl)Pyrrolidine

    Applications of 2-(4-Chlorophenyl)Pyrrolidine in Industrial Manufacturing

    2-(4-Chlorophenyl)Pyrrolidine serves as a crucial intermediate and building block across select chemical industrial sectors, contributing technical value in pharmaceutical active ingredient synthesis, fine chemical manufacturing, research-grade reference standards, and crop protection compound development. All applications described below represent established, regulatory-compliant downstream uses where our product meets recognizable industry requirements for purity, supply consistency, and integration into finished goods manufacturing.

    1. Pharmaceutical API Intermediate Synthesis

    This compound plays a key role as a structural intermediate in the synthesis of certain pharmaceuticals, especially within CNS-acting agent pathways. Downstream formulators use this raw material to construct targeted heterocyclic scaffolds, optimizing yield and selectivity in the multi-step API production process. Typical use requires stringent documentation, audited batch traceability, and attention to impurity profiles to align with regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 (GMP for drugs)
    • EU EudraLex Volume 4 GMP
    • USP/EP monographs for specified APIs (where applicable)

    Typical usage ratio

    • Used in stoichiometric ratios as per target compound’s synthetic step, often ranging 0.8–1.2 molar equivalents relative to the immediate precursor. Ratio may be refined based on yield optimization trials and impurity control requirements demanded by the final API specifications.

    Downstream process integration

    • Introduced during one of the core or late-stage synthetic transformations (e.g., reductive amination or cyclization steps) in multi-step batch reactors, after primary ring construction but before final deprotection or crystallization. Common in cGMP kilo-lab or pilot-scale reactors as well as validated full-scale production lines.

    Final product types

    • Central nervous system (CNS) agent APIs
    • Intermediates for analgesics or anti-psychotic commercial drugs
    • Chirally pure pharmaceutical substances for human or veterinary use (subject to regulatory approval)

    2. Fine Chemical Synthesis (Custom Organic Building Block)

    In the fine chemical sector, this pyrrolidine derivative functions as a tailored starting material in the assembly of complex heterocycles and specialty organic compounds, supporting the synthesis of advanced research molecules and catalog compounds. Fine chemical manufacturers choose this material when precise substitution patterns and high purity are required for downstream transformations and SAR studies.

    Industry compliance standards

    • ISO 9001 certified quality management systems
    • Chemical safety and environmental handling per local regulations (e.g., REACH registration, TSCA for US-based production)
    • Specialty fine chemical supplier qualification audits

    Typical usage ratio

    • Integration at 0.5–1.5 molar equivalents in custom synthesis. Final proportion determined by the complexity of target molecule, desired substitution, and minimization of downstream purification steps.

    Downstream process integration

    • Added in the sequence during catalytic substitution, alkylation, or cross-coupling reactions, often as the nucleophilic partner forming new linkage points in bench-scale or automated microreactor systems.

    Final product types

    • Reference standards for pharmaceutical R&D
    • Intermediates for agrochemical R&D
    • Custom-built scaffolds for lead compound discovery
    • Small-batch specialty organics for chemical libraries

    3. Agrochemical Active Ingredient Manufacturing

    Leading agrochemical producers utilize this raw material within controlled synthesis routes to produce certain pyrrolidine-based crop protection actives. The compound offers selective reactivity ideal for producing new-generation herbicide and insecticide intermediates. Downstream processes emphasize reaction efficiency, batch reproducibility, and compliance with environmental safety assessments central to pesticide registration dossiers.

    Industry compliance standards

    • FAO & WHO pesticide specification standards
    • OECD GLP (Good Laboratory Practice) for active ingredient synthesis
    • ISO 14001 environmental management (in production site)
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market

    Typical usage ratio

    • Structured batchwise at 1.0 molar equivalent against the acylating or coupling partners. Actual use level depends on required selectivity and target impurity profile set by downstream regulatory requirements.

    Downstream process integration

    • Incorporated during the intermediate formation stage in closed batch reactors or continuous stirred-tank reactors (CSTR), preceding final formulation into technical-grade actives for product registration and pilot-plant scale-up.

    Final product types

    • Pyrrolidine-based fungicide or insecticide active substances
    • Herbicidal intermediate compounds supplied for further etherification/functionalization
    • Analytical standards for pesticide residue testing

    4. Analytical Reference Standards for Forensic and Academic Research

    Certified reference material producers incorporate 2-(4-Chlorophenyl)Pyrrolidine as a structural template for forensic, pharmaceutical, and toxicological reference standards supplied to accredited laboratories. Proper documentation of batch origin, purity validation, and traceability ensures these materials meet national and international standards essential for regulated analytical use.

    Industry compliance standards

    • ISO 17034 (General requirements for the competence of reference material producers)
    • Relevant pharmacopeia reference standard protocols (USP, EP, JP)
    • Accreditation requirements under ISO/IEC 17025 for using certified reference materials
    • National forensic laboratory procurement standards

    Typical usage ratio

    • Prepared as a pure standard or calibrated mixture, with concentration adjusted to calibration range relevant for HPLC, GC-MS, or LC-MS applications (normally 1–100 μg/mL in solution, with solid reference purity exceeding 98%).

    Downstream process integration

    • Processed through high-purity crystallization or preparative chromatography, aliquoted into certified vials, and distributed with batch-specific certificates of analysis (COA) and stability data for direct use in instrument calibration or method validation.

    Final product types

    • Certified forensic reference standards for law enforcement or toxicology labs
    • Analytical standards for method validation in pharma QC
    • Custom reference compounds for university and private research institutions
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    Certification & Compliance
    More Introduction

    2-(4-Chlorophenyl)Pyrrolidine: A Closer Look From a Manufacturer's Perspective

    The Story Begins in the Lab

    Every so often, a compound finds its place in our production schedules not because it's the easiest to make, but because the research community keeps asking for it. 2-(4-Chlorophenyl)Pyrrolidine fits that mold. As a manufacturer pouring years into chemical synthesis, we see trends come and go, but requests for this particular structure keep steady for good reasons.

    The skeleton of 2-(4-Chlorophenyl)Pyrrolidine stands out. Chemists don’t just chase after anything with a pyrrolidine ring. When the 4-chlorophenyl group attaches at the second position on the ring, the molecule’s personality changes, offering reactivity that suits a whole line of downstream applications.

    Model and Process Details From the Production Floor

    There’s a simple truth in manufacturing: what you synthesize matters just as much as how you synthesize it. For this compound, we’ve stuck with a route that minimizes both the water footprint and cumbersome byproducts. We control the batch size, monitor impurity profiles, and lean on robust phase separation to clean up each lot before it moves to final purification.

    Those months spent calibrating the process left a mark—impurity levels typically stay several times lower than the thresholds set by most labs. Hydrogenation remains the trickiest step, especially avoiding over-reduction or unwanted side reactions at the aromatic ring. By dialing in temperature and pressure throughout, our technicians eliminate repeat runs and wasted solvents.

    Synthesis involves more than perfecting a recipe. It’s the hands in the glovebox, the eyes on the color changes, and the quick judgment on an NMR reading. This blend of skill and persistence shows in the clean, pale solid that comes off our line. Each batch is tracked by its lot number, but the uniform appearance and lack of smoky undertones always signal when the synthesis hits the mark.

    Physical Characteristics and Testing Rigor

    A chemical’s reputation rides on consistency as much as its intended function. 2-(4-Chlorophenyl)Pyrrolidine displays as a fine to crystalline powder, off-white with a faint tint depending on minor batch variances, thanks to residual moisture exposure. The melting point stays tight within a two-degree window, a direct result of slow crystallization at the end of the process—moving too fast at this stage means more labor later filtering out mother liquor.

    Gas chromatography and NMR confirm the main isomer and rule out contamination from aromatic chlorination byproducts. We find that some users prefer additional HPLC runs, though our typical end-user base accepts the standard GC-NMR combo for proof of purity. In the rare event that a batch doesn’t meet this mark, quarantine and reprocessing follow stringent internal procedures. Our plant’s quality control team walks the labs with a simple mantra—if you wouldn’t use the sample in your own experiment, don’t release it.

    Recognizing Real-World Uses

    Everyone who works in chemical production knows that most building blocks have at least a half-dozen possible lives ahead of them. For 2-(4-Chlorophenyl)Pyrrolidine, its main value comes as a synthetic intermediate. Many customers use it to lay the foundation for chiral drugs and develop structure-activity relationship libraries. It slots neatly into routes where functional group tolerance matters.

    Biosciences teams look for stability under mild conditions, and this compound stays intact during key transformations like reductive aminations or Suzuki couplings. In agricultural research, teams want new scaffolds for lead optimization without dramatically increasing regulatory review workload—the compound’s consistent behavior and clear analytical profile help keep studies on schedule.

    Through random bumps and operator error, this compound rarely throws surprises. It stores well with basic precautions: dryness, a sealed vessel, and reasonable temperatures. On startup orders, we walked a few clients through dissolving issues—solubilizing in polar aprotic solvents solves most handling concerns.

    Fresh Experience, Not Hype

    A manufacturer’s relationship with a molecule isn't about reading off a spec sheet. Over the years, you learn quirks: 2-(4-Chlorophenyl)Pyrrolidine crystallizes beautifully from ethanol, but half a percentage point too much water introduces cloudiness. Trying to force down the price by using a cheaper base during ring closure almost always increases downstream clean-up costs. Each time cost accountants push for raw material changes, the lab reminds them that purity lost early is almost impossible to regain later.

    Clients sometimes ask if this compound works as a substitute for close analogs. Our answer is always anchored in practical runs. Compared to the parent pyrrolidine, the 4-chlorophenyl group brings greater rigidity and hydrophobic character. This difference shows up clearly during chromatography and in solvent selection for chemical transformations. 2-(4-Chlorophenyl)Pyrrolidine’s electronics and steric profile lead to different regio- and chemoselectivity during subsequent synthesis steps.

    Choosing this compound means buyers gain more control during functionalization—either protecting the amine or attacking the ring. Some research groups try to swap in cheaper phenylpyrrolidine analogs, only to learn after weeks of screening that the substitution pattern matters more than most budget predictions.

    What Sets It Apart in Our Eyes

    There’s a steady market of phenyl-substituted heterocycles, and manufacturers like us see sales peaks driven by new research publications. Most companies keep inventories of 2-phenylpyrrolidine or its methylated siblings, but direct analogs like 3-(4-chlorophenyl)pyrrolidine end up with very different chemical personalities. Some lack thermal stability; others decompose slowly during purification.

    We stick with this exact substitution because requests always gravitate towards it. The 4-position chlorine is not only a synthetic handle (for later cross-coupling), but it adds electron-withdrawing effect that tightens the amine’s behavior during functionalization. Comparing with the meta- or ortho-chlorophenyl variants, this compound handles tougher redox manipulations—customers report higher yields in downstream amide formation and reduced over-alkylation rates.

    Running head-to-head tests with other suppliers, differences emerge in shelf life, product clarity, and impurity profiles. Heat cycling samples tells the inside story, revealing which batches carry over latent moisture or traces of catalyst. Years of troubleshooting and learning from returned goods gave us an edge in refining wash steps and optimizing vacuum drying routines. These may sound like minor tweaks, but they add up to notable differences in repeatability and overall project costs for buyers.

    Impact on Downstream Research

    Our end users include university labs pushing new molecular probes, pharma companies conducting SAR campaigns, and industrial R&D groups building libraries for screening. Feedback comes straight from people running reactions, not just ordering from catalogs. They notice when a batch provides reproducible NMR signals, no stubborn losses during transfer, and no ghost peaks showing up under routine analysis.

    This compound’s handling properties—low tendency to absorb atmospheric moisture and minimal static clumping—mean fewer headaches during formulation. For a few, this makes the difference in project timelines. Complaints about sticky powders or batches that won’t dissolve cleanly have led us more than once to start fresh with raw material screening.

    Those details make it clear why quality matters. Medicinal chemistry teams expect tighter turnaround, higher demand for purity, and a need for unambiguous characterization. We built our process to keep up with this pace—not just increasing reactor throughput, but building in decision points where real chemists review and intervene long before final approval.

    Troubleshooting and Continuous Improvement

    Every production year brings new surprises. We’ve seen raw material volatility upset timelines, reactor equipment failures, or the need to revalidate cleaning protocols between lots. Knowing these risks means building slack into schedules, appointing backup technicians, and maintaining a full set of reference standards for analytical comparison.

    Sometimes a synthetic step presents an unexpected impurity or, worse, an off-color batch. For 2-(4-Chlorophenyl)Pyrrolidine, early identification of air-sensitive byproducts led to major headway. One season, a new MCQ (moisture content quantification) method reduced quarantine time on questionable batches by half, letting customers receive material without needless delay or risk.

    Technical solutions only go so far without open feedback. We encourage direct dialogue with researchers and production chemists, often sending samples alongside lots in order to collect performance reports. More than once, we’ve adjusted filtration schedules or adopted new drying regimes purely on user feedback—sometimes a slight improvement quickly becomes a standard step in our workflow.

    Global Reach: Regulation, Safety, and Logistics

    Living with export controls and evolving regulatory frameworks comes with the territory. Pyrrolidine derivatives, especially those with aryl substituents, attract scrutiny from regional authorities. To keep logistics smooth, we keep all compliance documentation ready and keep channels of communication open with customs officers. Delays rarely surprise us because we watch global regulatory updates, and our teams fill out the necessary paperwork before shipping.

    In a reality where chemical sourcing keeps getting more complex, shipment remains a sticking point for some buyers. We package the finished compound in containers certified against static build-up and moisture ingress. These aren’t afterthoughts; ruined batches matter to customers’ budgets and to our relationship with clients. Working closely with carriers, we've selected routes that reduce exposure to drastic temperature changes, ensuring no impact to batch integrity.

    Safety checks cover more than environmental guidelines. Before shipping, each package gets a double inspection. Our internal training doesn’t just cover documentation—it includes regular review with freight handlers and hands-on sessions for responding to breakage in transit. Over the years, this has cut the occurrence of shipping mishaps and given us a base of logistics partners who respect the care necessary for specialty chemicals.

    Future Outlook and Trends

    Market analysts try to predict whether demand will shift, but on the shop floor, we base forecasts on practical conversations. Recent years brought interest from newly funded biotech startups and agricultural research initiatives. These newcomers push for smaller batch sizes, faster lead times, and more documentation, especially analytical support. The requests align with a shift toward personalized research—rapid iterations, high-throughput screening, and exploratory synthesis.

    We use this feedback not to chase every fleeting trend but to drive continuous process improvement. Batch scaling protocols are a current focus, optimizing both for hundred-gram lots and multi-kilogram campaigns. Our staff remains cross-trained, able to adapt to fluctuating workload between research and industrial-scale projects, making sure no production slot stays idle.

    In the near future, advances in flow chemistry and new catalytic methods may open up more sustainable or selective routes for 2-(4-Chlorophenyl)Pyrrolidine. We closely watch publications and vendor pitches, surveying for new partners whose platforms offer reductions in waste or better recovery rates for costly reagents. This isn’t just a pitch to green credentials—we track solvent recovery down to small percentages, seeing real payoff in cost and environmental reporting.

    Increased scrutiny from regulatory bodies means more paperwork, more batch traceability, and higher documentation standards. We accept this as the price of doing business in a sector under the microscope, and we have adjusted our SOPs to match. Research and compliance walk hand-in-hand—getting both right earns trust and builds the long-term relationships we value.

    Final Thoughts From the Production Line

    Making 2-(4-Chlorophenyl)Pyrrolidine teaches lessons that go beyond chemical recipes. Each order reflects the sum of learned hard truths, small process improvements, and honest conversations with end users across the world. Consistency matters most: not just in analytical printouts, but in customer experience from sampling to final application.

    We treat this compound not as just another entry on a product list, but as a reflection of the craft, attention to detail, and practical ownership that separates seasoned manufacturers from a field of remote suppliers. These habits draw clients back, building trust batch after batch—whether for discovery chemistry or scaled pilot plant needs.

    By keeping each step under the eyes of people who care about the outcome, from raw material to final drum in the warehouse, we believe that real quality can be recognized, not just claimed. For us, that belief isn’t abstract. It’s what lets our partners move forward, confident they’re building science on a strong foundation.