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4-(1-Pyrrolidinyl)Benzoic Acid

    • Product Name 4-(1-Pyrrolidinyl)Benzoic Acid
    • Alias 4-Pyrrolidinylbenzoic acid
    • Einecs 239-528-5
    • 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

    216336

    Chemical Name 4-(1-Pyrrolidinyl)benzoic acid
    Molecular Formula C11H13NO2
    Molecular Weight 191.23 g/mol
    Cas Number 4985-47-7
    Appearance White to off-white powder
    Melting Point 178-182°C
    Solubility Soluble in DMSO, slightly soluble in water
    Purity Typically >98%
    Inchi InChI=1S/C11H13NO2/c13-11(14)9-3-5-10(6-4-9)12-7-1-2-8-12/h3-6H,1-2,7-8H2,(H,13,14)
    Smiles C1CCN(C1)C2=CC=C(C=C2)C(=O)O

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

    Packing & Storage
    Packing 100g of 4-(1-Pyrrolidinyl)benzoic acid is supplied in a sealed amber glass bottle with a tamper-evident cap and label.
    Shipping 4-(1-Pyrrolidinyl)benzoic acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. It is handled as a hazardous material, following all relevant transport regulations. The packaging includes clear labeling, safety documentation, and protective padding to ensure safe delivery and compliance during transit.
    Storage 4-(1-Pyrrolidinyl)benzoic acid should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and excessive heat. Store at room temperature (15–25°C). Proper laboratory safety protocols should be followed during storage and handling to minimize exposure and contamination risks.
    Application of 4-(1-Pyrrolidinyl)Benzoic Acid

    Applications of 4-(1-Pyrrolidinyl)Benzoic Acid in Industrial Manufacturing

    Our production-grade 4-(1-Pyrrolidinyl)benzoic acid supports a range of downstream processes in the pharmaceutical, agrochemical, advanced materials, and dye industries. As a direct manufacturer, we deliver consistently high-quality material suitable for integration into specialized formulations requiring precision, compliance, and proven technical performance. The following are verified commercial application scenarios for this raw material based on our extensive supply chain and technical support experience.

    1. Pharmaceutical Intermediate for Local Anesthetic Synthesis

    Many pharmaceutical facilities employ this compound as a key building block during the manufacture of local anesthetics, linking the aromatic acid core with specific alkylamine moieties for tailored pharmacological activity. Stringent industry practices require high chemical purity and precise molar addition to ensure consistent yield and product safety. The compound typically enters the process during amidation or esterification steps to construct the final active ingredient.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) monographs for intermediates and starting materials
    • Directive 2001/83/EC (EU)
    • China Pharmacopoeia (if API export or local supply applies)

    Typical usage ratio

    • 0.2–0.6 molar equivalents per mol of final API, depending on desired ester or amide linkage; chemists adjust the ratio based on synthetic route optimization and impurity profile management.

    Downstream process integration

    • Introduced post-condensation as a coupling partner in the acylation or esterification step, subsequently purified by recrystallization and QC-verified prior to final synthesis or additional modification.

    Final product types

    • Topical anesthetic solutions for medical and dental procedures
    • Injectable anesthetic formulations
    • Finished API powder for further compounding

    2. Intermediate for Systemic Antimicrobial Compounds

    Downstream facilities use this material as an intermediate for constructing benzoic acid-derived antimicrobial agents, leveraging the pyrrolidine functional group to introduce membrane permeability and pharmacokinetic attributes. The compound must meet stringent trace impurity thresholds as defined by human or veterinary drug regulations, and addition levels depend on the overall molecular weight of the final antimicrobial agent.

    Industry compliance standards

    • FDA Guidance for Industry: Q3A Impurities in New Drug Substances
    • Good Manufacturing Practice (GMP) for Intermediates (21 CFR Parts 210 & 211)
    • European Medicines Agency (EMA) guidelines for APIs and intermediates
    • WHO GMP for Pharmaceutical Production

    Typical usage ratio

    • 0.15–0.25 molar equivalents per batch, variable with synthetic target and route efficiency; R&D and pilot-scale data guide any adjustments for commercial scaling.

    Downstream process integration

    • Charged during early-stage heterocycle assembly, facilitating subsequent halogenation or nitration to yield bioactive benzoic acid derivatives; intermediate requires HPLC and NMR confirmation before downstream conversion.

    Final product types

    • Oral and parenteral antimicrobial drugs (finished dosage forms)
    • Bulk API for generic and proprietary drugs
    • Direct supply to veterinary medicine manufacturers

    3. Building Block in Agrochemical Synthesis: Herbicide Formulations

    Leading agrochemical companies integrate this compound when constructing heterocyclic benzoic acid derivatives with targeted phytotoxicity profiles. As regulations for environmental safety and residue enforce tighter controls, the supplied raw material must align with both purity specifications and environmental release limits. Usage levels are dictated by proprietary formulation guidelines and molecular design constraints.

    Industry compliance standards

    • ISO 9001 Quality Management System (for input traceability and QC)
    • Regulation (EC) No 1107/2009 for plant protection product placing on the EU market
    • FAO/WHO Specifications for Pesticides: Raw Materials and Intermediates
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance (for EU supply)

    Typical usage ratio

    • 5–12% by weight in concentrated pre-mix solutions; actual batch usage modifies in accordance with actives loading, target application rate, and regulatory maximum residue allowances.

    Downstream process integration

    • Included during early-stage synthesis to provide aromatic core and secondary amine moiety; followed by chlorination, methylation, or formulation with inert carriers for finished herbicides; subjected to application-specific QC including GC-MS and environmental persistence assays.

    Final product types

    • Pre-emergence and post-emergence herbicide concentrates
    • Soluble granule herbicide formulations
    • Bulk intermediates for further agrochemical synthesis

    4. Precursor for Specialty Dyes and Pigments

    Chemical dye manufacturers employ 4-(1-Pyrrolidinyl)benzoic acid in the customized synthesis of colorants, using its ring structure to introduce electron-donating properties for vivid, high-stability pigment compounds. This application is subject to regulatory purity thresholds specific to textile, food-contact, and industrial-grade dyes. Process optimization focuses on precise input control to maintain batch-to-batch color consistency and performance characteristics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile dye components)
    • EN 71-3 (European standard for migration of certain elements in toys, applicable for some pigment types)
    • ISO 14001 Environmental Management (for waste treatment and emissions)
    • Specific national and international regulations for pigments used in food-contact materials (where relevant)

    Typical usage ratio

    • 1.5–6% by weight in dye synthesis batches, modifiable per chromophore target and required tinctorial strength; formulation laboratories test ratio adjustments during pilot-scale approval.

    Downstream process integration

    • Charged during primary diazotization or aromatic substitution reactions, enabling the creation of pyrrolidine-substituted dye molecules; intermediates then processed by filtration, pH adjustment, and spray drying or microencapsulation for final dispersion forms.

    Final product types

    • Reactive textile dyes
    • Functional pigments for plastics and polymers
    • Food-grade specialty colorants
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-(1-Pyrrolidinyl)Benzoic Acid: A Reliable Building Block from Our Plant

    Bringing Decades of Chemical Manufacturing Experience to Specialty Synthesis

    Our work with fine chemical intermediates spans years spent on reaction scales that range from pilot to full commercial batches. One compound we supply straight from our own factory lines stands out for consistent quality and purity: 4-(1-Pyrrolidinyl)benzoic acid. This compound’s track record with pharmaceutical, agrochemical, and material science companies grows each year. Its affordability, scalable synthesis, and reliability all trace back to our direct oversight of every manufacturing step.

    Model and Consistency: Precision at Scale

    We follow a robust process control approach for this compound, handling raw material sourcing and process monitoring in-house. Our model, known internally as 4PBA-98, reflects the minimum assay by HPLC, with specifications determined by direct customer feedback. The current assay target stands above 98% minimum, most lots ship at over 99%. Key impurities, such as 4-aminobenzoic acid and byproducts from pyrrolidine ring opening, stay below detection thresholds in recent batches. These specification sheets didn’t evolve overnight. They came out of countless in-process checks, calibrating our filtration, solvent recovery, and temperature ramps.

    Unlike trading firms, we develop and refine every protocol to address common bottlenecks from the ground up. This means the product reaches users with no need for repurification or adjustment. We avoid solvent residues, color bodies, or late-eluting peaks that can throw off final application stages.

    Demand Drivers: Why Users Keep Ordering This Molecule

    Chemists reach for 4-(1-Pyrrolidinyl)benzoic acid when they need a well-characterized scaffold for further derivatization. Its main draw comes from the pyrrolidinyl group’s influence on reactivity along the ring system. Downstream, it enters both protected and deprotected syntheses — as a starting material for amide coupling, a handle for N-acylation, or a component in heterocycle diversification. Our customers depend on its uniformity when optimizing reaction conditions: inconsistent batches waste both reagents and troubleshooting time.

    On the pharmaceutical side, researchers value the molecule’s solubility profile. Many closely related para-aminobenzoic acids bring purity challenges or solubility issues that slow down follow-up chemistry. By introducing a pyrrolidine ring in the para position, the compound sidesteps metabolic and solvation drawbacks. This faster dissolution reduces input mass in solvent-intensive extractions or chromatography, saving both time and step costs for any plant already operating at tight margins.

    Agrochemical R&D groups welcome this intermediate because it brings a reliable route to new herbicide and plant protectant scaffolds. Aromatic acids showing tertiary nitrogen function offer routes to stable conjugates and improved soil uptake. Our experience working alongside field chemists means we know how difficult it can be to screen dozens of analogs—so every kilo we ship follows the parameters demanded by high-throughput screening teams.

    Unique Performance Compared to Other Aromatic Benzoic Acids

    We’ve made and tested nearly every variant in the aromatic acid family, so the strengths of 4-(1-Pyrrolidinyl)benzoic acid show up clearly in real-world use. Chemistry built on simple para-amino or para-methyl substitutions delivers only limited differentiation in reactivity and final application profile. By contrast, adding a pyrrolidine group extends reactivity via enhanced basicity and electronic effects, creating new handles for functionalization. Its behavior during amidation and cyclization steps differs predictably from its methyl or ethyl analogs, providing greater selectivity or altered kinetic profiles that can unlock time savings in multi-step syntheses.

    On-process, we’ve seen that its crystalline form grants consistent handling and drying characteristics. There’s less risk of clumping, caking, or batch segregation than seen with some related acids that arrive as sticky, amorphous materials. Our dryer operators minimize loss in tray transfer, and customers rarely face loss during final dispensing, even in humid regions.

    Other suppliers deliver benzoic acid derivatives in grades that meet only a loose technical specification. Drawing directly from our own reactors guarantees customers a single, well-defined source. They don’t have to re-test or requalify each shipment due to supply chain changes. Fewer interruptions keep the discovery pipeline running smoothly.

    Proven Manufacturing Methods and Traceability

    Reliability doesn’t come from paperwork; it comes from controlling every input and outcome. Our process starts with high-purity pyrrolidine, which we source through vetted relationships built over years. Direct addition under controlled exotherm conditions avoids polymerization seen in batch jobs farmed out to unqualified shops. Every tank passes GC analysis both prior to use and after intermediate isolation. This tight loop means that our specification doesn’t depend on luck.

    We record each key control point, including filtration temperatures and drying times. Any deviation triggers real-time review by both operators and in-house QC. These records, along with samples from every batch, enable us to backtrack and resolve any query instantly. As a result, academic and industrial project leaders alike rely on our lot-level documentation for their regulatory or IP filings, knowing that the backstory behind each container stays transparent.

    Over 20% of our shipments directly support European and North American R&D projects. Their regulatory teams regularly require full traceability and impurity data—accuracy only possible with direct in-house manufacturing.

    Safety, Handling, and Practical Experience

    Working at scale introduces practical lessons about stability and safety. 4-(1-Pyrrolidinyl)benzoic acid stores easily in standard containers at ambient temperature, avoiding degradation under routine shipping. Its melting point, consistently confirmed in our lab, avoids trouble during grinding, transfer, and packaging. Handling with standard PPE—gloves, goggles, and dust masks—eliminates exposure risks observed in fussier compounds with higher volatility or allergenic potential.

    We train our staff in cleanroom transfer techniques to avoid contamination and unintentional static buildup, especially during drum filling or large bag packing. We ship every order in fully sealed, lined containers, tested for compatibility with both local and overseas transit times.

    Some clients initially sought alternative derivatives, only to contend with off-spec shipments that introduced unwanted odors or dust. We take these complaints seriously and have tweaked our drying and packaging steps to resolve customer feedback. Our technical support addresses issues that only come from repeated contact with real-world supply scenarios. Anyone facing downstream discoloration or reactivity can speak directly with someone who’s filled, labeled, and tested the batch themselves.

    What Distinguishes In-House Manufacturing from Trading-Route Product

    Open conversations with R&D and manufacturing buyers taught us where trading firms tend to fall short. Intermediary traders often mix product from multiple sub-contractors. Customers wind up with variable form, inconsistent color, and uneven particle size. As original manufacturers, we supply from one facility, using one continuous batch record. Each container matches the last—not just in purity but in density, solubility, and ease of use on the bench.

    We actively share analytical spectra and batch histories, allowing users to compare our material against regulatory requirements or project targets. This transparency reduces onboarding time for new projects, prevents procurement snags, and makes switching from other supply sources pain-free. Some large-scale pharmaceutical partners switched to us after repeated delays and lost batches with multi-vendor trading chains—feedback they gave us directly after site audits.

    Continual Process Refinement: Our Edge

    Our production line reviews each critical stage to refine yields and downtime. Automated temperature, pH, and filtration controls born of operator experience head off problems before they surface in finished product. We adapt tank cleaning procedures in response to customer reports of caking or cross-contamination—these aren’t theoretical tweaks, they come from documented plant floor results.

    Our pilot team investigates route optimization for raw material streams, cutting solvent usage without sacrificing final purity. In recent runs, yield improvements of 3-5% cut overall turnaround and waste, lowering carbon footprint and raw ingredient draw. These tweaks filter down to customers, who notice the difference in pricing and lot reliability.

    What 4-(1-Pyrrolidinyl)Benzoic Acid Means for Our Customers’ Pipelines

    Pharmaceutical R&D teams harness this compound for exploratory candidate synthesis, amorphous solid dispersion studies, and polymorph analysis. Its predictable behavior in coupling, amidation, and cyclization offers stress-free scalability from bench to pilot runs. Regulatory filings gain a head start with our full characterization package—HNMR, FTIR, HPLC, and elemental data supplied with each order.

    Custom chemistry groups draw on its adaptability across protecting group strategies; it tolerates a wide range of deprotection conditions, whether mild basic treatments or strong acid hydrolysis. The pyrrolidine ring resists many undesired side reactions, shrinking the spread of byproducts in purification.

    For those focused on advanced materials, such as dispersants, dyes, or electronic intermediates, this compound’s robust aromatic core stands up to demanding post-functionalization. Chromophore designers in particular find the pyrrolidinyl group boosts conjugation, shifting spectral properties and opening doors for novel light-harvesting or photoactive materials strategies.

    Our Supply Capability: Fast Turnaround, Trusted Scale

    On-demand availability remains at our core. We keep buffer inventories both on-site and at strategic warehouse partners to absorb spikes in demand. For custom projects, we switch between glass-lined and stainless steel reactors to shape volumes with minimal plannable downtime. Rush orders see same-day handling; regular forecasts support multi-ton supply chain planning for longer-term customers.

    Shipping documentation follows every requirement, with harmonized product codes and international transport paperwork attached to each consignment. Customs and client audits confirm our origin and full chain-of-custody—details that prevent costly project interruptions downstream.

    After years serving innovators in new chemical spaces, we’ve built a feedback loop connecting real use cases with hands-on shop floor adjustments. This bond with project chemists, formulation teams, and plant managers makes us more responsive to unplanned challenges and accelerated deadlines.

    Facing Tomorrow: Sustainable Operations and Product Stewardship

    Green chemistry impacts all stages of our production cycle. New solvent recovery systems and inert gas blanketing minimize emissions throughout large-scale reactions. Waste treatment investments reduce both effluent volumes and off-site disposal needs. Recent process intensification on this line dropped average process mass intensity by over 10%, translating to measurable benefit for clients seeking lower environmental impact without built-in cost premiums.

    As regulatory pressures shift, we track global trends in impurity limits, contaminant disclosure, and packaging waste reduction. Whether customers call for REACH registration, ICH Q3D elemental impurity data, or tailored packaging solutions, we address these concerns before they slow down project launches. Environmental responsibility extends to our choice of container liners and outer drums—as standards evolve, so do our solutions.

    4-(1-Pyrrolidinyl)Benzoic Acid: The Manufacturer’s Benchmarks for Success

    Every gram we ship shows what years of hands-on development can achieve. Instead of chasing transient price swings or chasing speculative markets, we prioritize consistency, reliability, and direct support at every stage of the product’s journey from reactor to bench. The relationship we nurture with each buyer—built on practical performance, open dialogue, and responsiveness—lets us improve our product and chip away at the everyday challenges that hold back progress in the chemical and material sciences.

    We bring a manufacturer’s perspective to both small-lot and bulk orders, tailoring batch sizes and shipment logistics to real project needs, not abstract minimums or trading quotas. 4-(1-Pyrrolidinyl)benzoic acid stands out because it works for the people who make new chemistry happen, not just for resellers in the middle. We see its future in every successful experiment, scale-up, and product launch that begins with our materials.