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4-(1-Pyrrolidino)Benzaldehyde

    • Product Name 4-(1-Pyrrolidino)Benzaldehyde
    • Alias PBAL
    • Einecs 207-114-3
    • 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

    436474

    Chemicalname 4-(1-Pyrrolidino)Benzaldehyde
    Casnumber 59774-94-8
    Molecularformula C11H13NO
    Molecularweight 175.23 g/mol
    Appearance White to off-white solid
    Meltingpoint 83-86°C
    Solubility Soluble in organic solvents such as ethanol and chloroform
    Purity Typically >98% (varies by supplier)
    Smiles C1CCN(C1)C2=CC=C(C=C2)C=O
    Inchi InChI=1S/C11H13NO/c13-9-10-3-5-11(6-4-10)12-7-1-2-8-12/h3-6,9H,1-2,7-8H2

    As an accredited 4-(1-Pyrrolidino)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-(1-Pyrrolidino)Benzaldehyde, 10g, is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping **Shipping Description:** 4-(1-Pyrrolidino)Benzaldehyde is shipped in tightly sealed containers, protected from light and moisture, and compliant with local regulations. It is packaged according to chemical safety standards, typically as a solid in glass or plastic bottles, labeled with hazard identification. Transport may require temperature control and documentation for regulated substances.
    Storage 4-(1-Pyrrolidino)benzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep it separate from strong oxidizing agents and acids. Store at room temperature and ensure all labeling and safety data are clearly accessible. Use appropriate precautions to prevent inhalation, ingestion, and skin contact.
    Application of 4-(1-Pyrrolidino)Benzaldehyde

    Applications of 4-(1-Pyrrolidino)Benzaldehyde in Industrial Manufacturing

    4-(1-Pyrrolidino)Benzaldehyde plays a critical role across several chemical manufacturing sectors due to its specific reactivity and unique structure, supporting the synthesis of downstream specialty compounds with tightly controlled purity and consistency. Our focus as an established manufacturer is on supplying consistent quality to customers operating in regulated, high-integrity process environments.

    1. Key Intermediate in Pharmaceutical Active Ingredient Synthesis

    This compound serves as a core building block in the multi-step synthesis of select pharmaceutical actives, particularly within the research and production of central nervous system stimulants and certain psychoactive therapeutics. Its specific aromatic-aldehyde structure enables targeted condensation reactions, which are fundamental for downstream manufacturers seeking precise control over molecular architecture and stereochemistry within regulated drug production pipelines.

    Industry compliance standards

    • ICH Q7 GMP for API Manufacturing
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia Monograph 2.2
    • Good Laboratory Practice (GLP), OECD Guidelines

    Typical usage ratio

    • Employed at 0.12–0.35 molar equivalents relative to primary amine reactants; adjusted according to specific molecular target and yield optimization requirements in the active ingredient route.

    Downstream process integration

    • Introduced during the initial condensation or reductive amination stage of production, often followed by chromatographic purification or crystallization of intermediate compounds in a dedicated synthesis suite.

    Final product types

    • Pharmaceutical intermediates for CNS active APIs
    • Bulk APIs in generic and branded psychoactive drug portfolios
    • Custom research chemicals for medicinal chemistry development

    2. Essential Reagent for Specialty Dye Synthesis

    In the fine chemical sector, especially for specialty colorants and fluorescent markers, this benzaldehyde derivative provides a defined aromatic substrate for condensation with heterocyclic compounds. Manufacturing partners select this compound for controlled formation of imine or Schiff base structures incorporated in synthetic dyes that require high purity profiles and consistency for downstream application in textile, imaging, or diagnostic solutions manufacturing.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems
    • Oeko-Tex Standard 100 for textile-related chemicals
    • TSCA Inventory (USA) for chemical inputs

    Typical usage ratio

    • Integrated at 0.18–0.52 weight percent in dye formulation batches depending on target chromophore yield and batch size requirements.

    Downstream process integration

    • Participates in the initial dye core-building reactions, typically under controlled temperature and pH; downstream processing includes solvent extraction and vacuum drying to achieve pigment stability suitable for end-use applications.

    Final product types

    • High-performance synthetic and fluorescent dyes
    • Colorants for industrial textile printing
    • Dye markers in chemical traceability solutions

    3. Building Block for Organic Electronic Material Precursors

    Manufacturers in the organic electronics sector utilize this benzaldehyde as a precursor for synthesizing intermediate molecules used in the production of organic semiconductors, OLEDs, and conductive polymers. Its structural compatibility with conjugated backbone extension allows integration into electronic-grade monomers, ensuring the electrical characteristics essential to next-generation display and sensor devices.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Lead-Free Manufacturing)
    • IEC 62474 Declarable Substance List (Materials for Electronics)
    • ISO 14001:2015 Environmental Management Systems
    • IPC-4101B for base materials in electronics

    Typical usage ratio

    • Used at 0.06–0.22 mol fraction relative to the total organo-reactive species, adjusted for desired conjugation length and device performance requirements in final organic layers.

    Downstream process integration

    • Activated during early-stage synthesis of monomer or oligomer segments destined for spin-coating, vapor deposition, or inkjet processing in semiconductor wafer or film lines.

    Final product types

    • OLED display organic emitter layers
    • Organic field-effect transistor (OFET) active materials
    • Low-voltage conductive polymer films

    4. Intermediate in Industrial Fragrance and Aroma Compound Synthesis

    This raw material supports fragrance compound manufacturers by acting as a structural intermediate in the multi-step construction of cyclic aroma chemicals, especially those with pyrrolidine or substituted aromatic backbones. Specialists in fine fragrance, flavor, and sensory additive production value its consistency for batch processes focusing on both bulk and high-purity niche aroma molecules meeting international flavor and fragrance protocols.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • ISO 9235:2013 Natural Aroma Chemicals definition (for synthetic/natural distinction)
    • US FDA 21 CFR 172.515 (Food Additive Regulations for Flavors)
    • GMP for Food and Cosmetic Ingredients (FSSC 22000 when applicable)

    Typical usage ratio

    • Added at 0.07–0.21 molar equivalents in complex aroma compound synthesis; specific dosage determined by target aldehyde content and downstream olfactory profile calibration.

    Downstream process integration

    • Initiates chain-building reactions in flavor/aroma molecule production, preceding successive alkylation, acylation, or reduction in specialty organic synthesis reactors, followed by phase separation and purification to meet IFRA and food-grade purity targets.

    Final product types

    • Pyrrole-substituted aroma compounds
    • Special fragrance intermediates for perfumery
    • Flavoring agents in processed foods and beverages
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    More Introduction

    4-(1-Pyrrolidino)Benzaldehyde: A Closer Look From a Manufacturer’s Perspective

    Introduction to 4-(1-Pyrrolidino)Benzaldehyde

    Any expert involved in organic synthesis understands how essential intermediate compounds shape both the process and the final result downstream. 4-(1-Pyrrolidino)Benzaldehyde, with its direct connection between a pyrrolidine ring and benzaldehyde structure, has gathered attention in the fine chemicals sector due to its versatility. Our facility focuses on high purity 4-(1-Pyrrolidino)Benzaldehyde for specialized research and industrial usage.

    Molecular Structure and Purity Standards

    This compound, sometimes referenced in shorthand as 4-PBAl, stands out for its clean linkage between the benzene and pyrrolidine rings, which significantly impacts reactivity during further synthesis. We consistently see demand for this structure in routes involving substituted phenyl derivatives—particularly as a precursor for condensation reactions where steric control is critical.

    Our in-house analytical package guarantees purity levels above 98% for 4-(1-Pyrrolidino)Benzaldehyde. Rigorous GC and HPLC checks occur before any material leaves production. Most requests focus on quantities in the 100-gram to multi-kilogram range, and our bulk process ensures tight consistency from batch to batch. Lower impurities translate into cleaner downstream chemistry for our customers, which remains non-negotiable in research and pilot plant settings. Every lot enables traceability to help clients meet regulatory or internal quality requests without hesitation.

    Physical and Handling Properties

    As a crystalline powder, 4-(1-Pyrrolidino)Benzaldehyde resists caking during reasonable humidity fluctuations, as confirmed during our routine stability runs. The melting point falls well above ambient, so users see limited volatility or loss during standard handling. Our packaging team uses sealed containers designed to prevent photodegradation, preserving both shelf life and activity. Over the last decade, we’ve invested in controlled environments for weighing and dispatching sensitive intermediates like this one, ensuring workers’ safety and uncompromised material quality.

    Real-World Usage and User Groups

    We manufacture 4-(1-Pyrrolidino)Benzaldehyde directly with the practical needs of synthetic chemists and R&D groups in mind. Most applications trace back to two themes: advanced pharmaceutical intermediate synthesis and exploratory work in organic electronic materials. The aldehyde group’s reactivity gives our clients plenty of options, from reductive amination—where nitrogen-based functionality matters—to multistep synthetic pathways for heterocyclic compounds. Multiple academic groups have published work with this intermediate as a starting aldehyde, often aiming for innovative ligands, chiral catalysts, and model drug candidates.

    Development chemists frequently ask for insights about modification steps possible using 4-(1-Pyrrolidino)Benzaldehyde. One observed trend: The electron-rich pyrrolidine ring not only boosts nucleophilicity but also directs selectivity during enamine formation. Our technical team assists customers who explore analog synthesis or require help scaling the compound from milligram to production levels.

    Addressing Production Consistency and Safety

    Reproducibility forms the backbone of our production philosophy. Small changes in temperature, solvents, or catalyst selection alter crystallization and final compound appearance, sometimes undetectable without close analysis. Our operators run each batch under close monitoring, adjusting conditions in real time if deviations appear. Since trace contamination in aldehyde intermediates can derail entire synthetic campaigns, we stress attention to glassware cleanliness and solvent drying.

    Worker safety stays front-and-center. Our SOPs require handling in ventilated enclosures, and our experienced team assesses both inhalation risk and potential exposure at every production stage. These safety checks draw from both published literature and firsthand operational data, rather than generic recommendations. Packaging features clear hazard markers, and our logistics process guarantees that each order arrives in uncompromised condition directly from our facility.

    Comparing 4-(1-Pyrrolidino)Benzaldehyde to Similar Compounds

    It’s common for some clients to weigh the pros and cons between 4-(1-Pyrrolidino)Benzaldehyde and related aldehydes—such as plain benzaldehyde, 4-dimethylaminobenzaldehyde, or 4-piperidino benzaldehyde. Based on decades of lab trial feedback, direct substitution with more basic amines typically changes product yields and selectivity. The pyrrolidine moiety combines moderate ring strain and strong electron-donating effects, balancing reactivity and stability. Its slightly higher lipophilicity, compared to the piperidine variant, changes solubility in specific solvents and can affect downstream crystallization.

    Replacement with smaller amines like dimethylamino groups frequently leads to shifts in boiling point and odor profile, but the key difference comes through in the electronic environment. For multi-step syntheses aiming at nitrogen-heterocycle scaffolds, the unique characteristics of the pyrrolidino ring lead to more predictable reactivity and fewer byproducts. Data from our process labs shows less batch-to-batch variation when the 4-pyrrolidino group is employed, partly because the ring is more conformationally locked than open-chain analogs.

    We often field questions about alternatives for scale-up, particularly in cost-driven projects. Our advice usually centers on the downstream impact of the substituent: if selectivity and reproducibility matter more than cost per kilo, 4-(1-Pyrrolidino)Benzaldehyde justifies itself even at higher price points. Chemists working on patent-sensitive formulations have noted its lower impurity profile in repeated runs, leading to fewer purification cycles later on.

    Challenges in Sourcing and Scale-Up

    As a manufacturer, we’ve watched demand for 4-(1-Pyrrolidino)Benzaldehyde increase as synthetic methodologies evolve. Twenty years ago, this was seen as a niche intermediate—ordered in grams or tens of grams, mainly by academic groups. Recent upticks in demand reflect a broader willingness among commercial players to explore more complex starting materials for green synthesis and innovative molecules. Every step up in scale uncovers subtle new challenges, from raw material procurement to solvent recycling.

    The biggest headaches often come from precursor availability or changes in regulatory frameworks that affect precursor chemicals. Our procurement team keeps close tabs on supply chains for the chemicals feeding into this synthesis route, since any disruption raises both direct costs and lead times. We network with primary suppliers to ensure that all materials carry necessary documentation and that every input has a transparent production lineage. This diligence helps both our clients and our own QA group when it comes to regulatory reviews by health or environmental bodies.

    Another persistent challenge is batch consistency during scale-up. Some reactions that behave perfectly in the flask show quirks in 10-kg reactors, often requiring adjustment in stirring speed or cooling rates. Since aldehyde products are prone to oxidation, we use real-time monitoring and rapid isolation to cut side-product risks. Detailed feedback from our on-site technical team enables quick troubleshooting, reducing off-spec production to less than one percent of annual throughput. As a result, clients running pilot batches or first time-ups have reliable backing for every scale transition.

    Environmental Considerations

    Chemists today face ever-tighter controls on waste streams, so we designed our process to minimize loss and maximize solvent reclaiming. By using a closed-system approach with multi-stage solvent recovery, we cut down on both emissions and operational costs. Every solvent used in the 4-(1-Pyrrolidino)Benzaldehyde synthesis cycle enters our on-site recycling program, keeping hazardous waste handling to a minimum. We run annual reviews to identify improvement areas, using both in-house and third-party audits. This level of scrutiny not only helps with environmental reporting but also reassures customers under increasing sustainability pressure from their own stakeholders.

    We also maintain a focus on worker and community safety. Every stage of storage, transport, and production undergoes risk analysis. Detailed tracking of inventory and usage, combined with short lead times, keeps on-site volumes low and manageable. Through this approach, we remain responsive to changing regulations on hazardous materials and can adjust internal processes to stay ahead of the curve.

    Quality Control and Analytical Backing

    Rigorous quality control underpins every shipment from our facility. Each lot undergoes identity confirmation by NMR and FTIR, with regular mass spectrometry spot checks based on project needs. Our team also checks for measurable impurities—often specific aldehyde analogues or residual solvents—so users can rely on predictable reactivity during downstream chemistry. These protocols reflect our experience both with this compound and with related nitrogen-bearing benzaldehydes, where cross-contamination sometimes creeps in during rapid-fire campaign synthesis.

    Some clients need custom analytical documentation: enantiomeric excess for chiral syntheses or extended impurity profiles for regulatory submissions. In those cases, we set up collaborative testing protocols and cross-check methods between our QC lab and the customer’s team, catching small inconsistencies before they cause issues down the line. This kind of partnership ensures that the data supporting every shipment matches demanding research and manufacturing needs worldwide.

    Insights From Field Experience

    We don’t just ship 4-(1-Pyrrolidino)Benzaldehyde; we follow how our material performs in real applications. Multiple customers share performance feedback on specific synthetic routes, crystal growth processes, and bulk conversion steps. These conversations have pointed out several concrete observations. For instance, in reductive amination chemistry, the compound can require slight solvent tweaks to minimize byproduct formation. In larger Grignard-type reactions, scale-up labs often prefer our higher-purity grade, as trace impurities in other grades prompted reaction sluggishness.

    We also see that in multistep organic synthesis, repeated purification often becomes a bottleneck, slowing progress and bleeding yield. With high-quality 4-(1-Pyrrolidino)Benzaldehyde, researchers consistently report increased batch yields and streamlined purification protocols. This isn’t just anecdotal: On average, users report a drop in column chromatography cycles when starting with high-purity lots. That translates into sizable time and cost savings over longer campaigns.

    Practical details always matter to frequent users: storage temperature, packaging design, and shelf life impact workflow efficiency. Our containers feature moisture barrier technology and tamper-evident seals. Based on in-house monitoring, material stored in these conditions remains stable for at least a year without significant color or purity drift—a notable improvement over generic-packaged alternatives.

    Supporting the Path to New Discoveries

    Our commitment to 4-(1-Pyrrolidino)Benzaldehyde goes beyond bulk manufacturing. We support customers who push into new territory—whether that’s using the compound for medicinal chemistry discovery, photonic material research, or entirely new fields. By collaborating directly with end-users, we share troubleshooting tips and best practices that bypass trial and error. Providing insight into reaction setups, solvent choices, and alternative purification paths motivates our laboratory team as much as the final product quality itself.

    Feedback loops between our manufacturing and R&D branches accelerate improvements both in production yield and in material performance. This approach means we don’t simply respond to new trends; we help drive technical progress in sectors that count on reliable chemical intermediates. Through this ongoing knowledge exchange, we’ve played a small part in helping academic and corporate innovators unlock new synthetic methods and refine their own discovery pipelines.

    Why 4-(1-Pyrrolidino)Benzaldehyde Holds a Place in Advanced Synthesis

    The consistent uptake of 4-(1-Pyrrolidino)Benzaldehyde reflects its reliability as a building block for emerging technologies. Chemists aiming for next-generation pharmaceuticals, catalysts, or specialty polymers look to it for the selectivity and reproducibility it brings to key synthetic steps. Its distinctive substitution pattern changes molecule orientation, influencing both kinetics and outcome purity. Each user group—from university research teams to commercial pharmaceutical developers—values confidence in the material that connects ideas to tangible results.

    Over years of batch runs, troubleshooting, and field feedback, we’ve come to trust that reliable intermediates make all the difference when deadlines are tight and product lifecycles shrink. Providing a high-standard 4-(1-Pyrrolidino)Benzaldehyde isn’t only about supplying a reagent; it means supporting safe, efficient, and effective chemical innovation at multiple scales. We remain committed to delivering quality, safety, and experienced guidance for this crucial intermediate—helping each customer advance toward their next breakthrough.