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5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid

    • Product Name 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid
    • Alias 5-[(Piperidin-1-yl)methyl]furan-2-carboxylic acid
    • Einecs 643-631-5
    • 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
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    Specifications

    HS Code

    794961

    Product Name 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid
    Molecular Formula C11H15NO3
    Molecular Weight 209.24 g/mol
    Cas Number 1421373-60-9
    Iupac Name 5-[(Piperidin-1-yl)methyl]furan-2-carboxylic acid
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in DMSO, DMF; slightly soluble in water
    Storage Temperature 2-8°C (refrigerated)
    Smiles C1CCN(CC1)CC2=CC=C(O2)C(=O)O

    As an accredited 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packed in a sealed amber glass bottle labeled "5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid, 25g," featuring hazard and handling instructions.
    Shipping 5-Piperidin-1-ylmethyl-furan-2-carboxylic acid is shipped in tightly sealed containers, protected from moisture and light. It is handled under standard chemical safety protocols and typically transported at ambient temperature. Proper labeling and documentation are included to ensure compliance with regulatory guidelines for safe delivery and handling during transit.
    Storage **5-Piperidin-1-ylmethyl-furan-2-carboxylic acid** should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep at room temperature (15–25°C) in a cool, dry, and well-ventilated area. Ensure the storage area is free from incompatible substances such as strong oxidizing agents. Properly label the container and avoid prolonged exposure to air to prevent degradation.
    Application of 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid

    Applications of 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid in Industrial Manufacturing

    As a specialized chemical raw material, 5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid supports the synthesis of advanced intermediates across several regulated industries. Our direct manufacturing enables strict process control for customers integrating this building block into complex downstream production workflows.

    1. Pharmaceutical API Intermediate Synthesis

    This material serves as a key construct in the development of piperidine- and furan-based pharmaceutical active pharmaceutical ingredient (API) intermediates, especially in small-molecule cardiovascular, anti-infective, and CNS drug pipelines. Its structure enables precise regioselective modifications through N-alkylation and amidation workflows. We supply cGMP-grade batches tailored to support multi-step synthesis with stringent impurity profiles. Typical customers in this segment require transparent traceability records and validated documentation for regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • US FDA 21 CFR Part 210/211
    • EU EMA Guideline on Manufacture of the Finished Dosage Form
    • Chinese Pharmacopoeia (ChP) requirements for chemical drug substances

    Typical usage ratio

    • Batch formulation: 0.5–2.5 molar equivalents relative to the core API structure, depending on the final route and yield optimization studies.

    Downstream process integration

    • Material introduction in protected intermediate stage, often after core piperidine ring formation.
    • Purification and isolation steps performed prior to coupling or further functionalization.
    • Quality control sampling required at each critical stage before release to final API synthesis.

    Final product types

    • Antiviral and antibacterial APIs (e.g., for generic small molecules)
    • CNS disorder drugs in the development pipeline
    • Selected cardiovascular and metabolic disorder candidate drugs

    2. Custom Agrochemical Intermediate Productions

    Major agrochemical formulators utilize this compound for synthesizing high-purity intermediates, often as a core for novel fungicides and insecticides targeting piperidine/furan scaffolds. Production follows ISO-compliant safety documentation, with controlled exposure limits due to sensitivity of environmental release. Our plant supports closed-loop bulk supply for multistep scale-up, emphasizing reproducible purity and compliance with occupational chemical hygiene rules.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for agrochemical raw materials
    • REACH Regulation (EC) No 1907/2006 (Annex II SDS compliance)
    • China Pesticide Registration Guidelines (ICAMA) traceability
    • OHSAS 18001/ISO 45001 occupational health controls

    Typical usage ratio

    • Intermediate formation: 3–10 wt% of total synthetic feedstock, with final ratio tuned according to crop protection target molecule and compliance residue analysis.

    Downstream process integration

    • Reaction input during backbone functionalization step specific to piperidine–furan hybrid pesticides.
    • Used in closed reactor systems to avoid airborne contamination.
    • Final purification prior to coupling with active moieties for target selectivity.

    Final product types

    • Precursor to agricultural fungicides
    • Building blocks for insect growth regulators
    • Platform for new herbicide discovery projects

    3. Advanced Chemical Research & Custom Synthesis

    Specialty chemical research and contract development organizations incorporate this compound into a variety of programs focused on novel heterocyclic molecules. Research-scale and pilot batches support targeted discovery in medicinal and organic chemistry where its furan-carboxylic acid group is critical for fast modification cycles. Our quality system enables flexible lot sizes and multi-parameter batch records for fully traceable R&D support.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • Applicable local occupational exposure limits (OELs)
    • GLP (Good Laboratory Practice, as relevant to contract syntheses)
    • SDS issued according to GHS for laboratory use

    Typical usage ratio

    • Experiment-specific–from 0.1 mmol scale up to 10 g per reaction, subject to project need and synthetic pathway optimization.

    Downstream process integration

    • Custom library synthesis or lead structure functionalization via amide/ester formation.
    • Used at the chemoselective step for preparation of analog libraries in high-throughput screening.
    • Batch splitting for parallel testing of downstream derivatives.

    Final product types

    • Tool compounds for target identification
    • Synthetic reference standards
    • Library elements for high-throughput screening

    4. Fine Chemical Manufacturing for Specialty Polymers

    Industrial fine chemical producers leverage this molecule as a co-monomer or an end-capping agent in specialty polymer synthesis, particularly for adding chemical resistance or targeting modified rheological properties in furan-containing plastics. Manufacturing integrates extensive QC and analytic verification, especially regarding residual monomer content and trace impurities. Regulatory audits examine toxicological and downstream migration data before release for further compounding or consumer applications.

    Industry compliance standards

    • ISO 14001 Environmental Management
    • EU REACH Annex XVII requirements for polymer additives
    • RoHS 2 (Directive 2011/65/EU) for electronic-grade polymers
    • Applicable national chemical registries for end-use polymers

    Typical usage ratio

    • Co-reactant feedstock at 0.5–1.5% by weight of total polymer resin batch; adjusted to tune target chemical or mechanical resistance specifications.

    Downstream process integration

    • Input at pre-polymerization or as a terminator in condensation/polyaddition.
    • Careful control over addition sequence to maximize integration into the backbone structure.
    • Post-reaction purification to minimize leachable residues.

    Final product types

    • Heat-resistant engineering plastics
    • Chemically resistant copolymers for electronics casings
    • Modified furan-acrylic copolymer blends

    5. Precursor for Performance Additives in Rubber Chemicals

    Selected rubber manufacturers employ this intermediate to produce high-performance vulcanization agents and antioxidant functional additives. Its unique ring structure offers benefits in fine-tuning cross-link density and aging characteristics of specialty elastomers. We specialize in impurity-controlled production, supporting downstream integration with full batch-level traceability, safety documentation, and analytical release testing suited for critical material performance in tire compounds and technical rubber goods.

    Industry compliance standards

    • ISO 9001:2015 for rubber compounding chemicals
    • ASTM D3182/ISO 2393 mixing practices
    • Toxicological evaluation according to local environmental regulations
    • REACH registration (as required for downstream additives)

    Typical usage ratio

    • Reactive additive content: 0.2–1.0 phr (parts per hundred rubber), adjusted depending on desired cross-link profile and compound physical specifications.

    Downstream process integration

    • Raw input during banbury mixing or internal mixer stage of compounding.
    • May undergo in-situ reaction with other cross-linking agents.
    • QC approval required for dispersion and compatibility with base elastomer matrix.

    Final product types

    • High-durability tire treads
    • Technical rubber seals
    • Elastomer blends for automotive components
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    Certification & Compliance
    More Introduction

    5-Piperidin-1-Ylmethyl-Furan-2-Carboxylic Acid: Factory Insight and Practical Perspectives

    Introduction and Background

    In the world of fine chemicals, every molecule that comes out of the reactor tells a story about process knowledge, material purity, and production realities. As the team running the core tanks, columns, and controls, we often get asked about products that stand apart for their unique structure and utility. 5-Piperidin-1-ylmethyl-furan-2-carboxylic acid has earned that status in a compact but discerning field of research and applied chemistry. Its backbone features a piperidine ring bridged to a furan, capped by a carboxylic acid group, blending biochemical interest with synthetic opportunity.

    Chemical producers like us recognize straight away when a molecule arrives with more than just theoretical applications. This compound reflects years of incremental process improvements, from initial bench-scale pathways relying on challenging intermediates, to more modern plant-scale operations using robust controls to keep product profiles within specification. The structure alone signals a degree of solubility and reactivity that synthetic chemists know how to appreciate, especially those pushing boundaries in drug development or molecular design.

    Core Manufacturing Process and Standards

    The route to 5-piperidin-1-ylmethyl-furan-2-carboxylic acid demands careful attention. Water and oxygen sensitivity during initial furan handling can easily cause side reactions, generating impurities that plague isolation. Piperidine-based intermediates sometimes emit sharp odors and call for continuous scrubber upkeep, and extracts washed during final purification tend to form stubborn emulsions if not patient with phase separations. Through practice, the plant team has learned which runs react best to gradual base addition, which lots require double recrystallization, and how minor temperature drifts can steer the yield away from the target profile.

    Trace residual solvents remain another constant focus. We run regular gas chromatography checks after vacuum drying, not only to keep solvent residues within the cautious limits expected by biopharma clients, but because in our own lab evaluations, even small amounts can skew results when researchers scale up their next steps. Stability tests in warehouse storage highlight another point: this product keeps best in low-humidity environments with modest temperature handling, and simple attention to airtight packaging pays off. We do the loading ourselves so any off-color, off-odor, or off-grain sample gets rejected before it leaves the plant.

    Molecular Properties and Distinctions

    Researchers looking at this compound’s molecular map spot the logic behind its interest. The piperidine ring adds polar character and, depending on partners, can support secondary reactions that analogs with aliphatic linkages cannot. The furan ring is less common in base-stock chemicals but attracts people developing biaryl scaffolds, since it sometimes survives conditions that destroy benzene-based relatives. The carboxylic acid anchor allows further modification, particularly in peptide coupling or acylation sequences. Comparable molecules can offer one or two of these features, but rarely deliver all three in a single, stable entity.

    Through our in-house NMR and LC-MS screening, we've seen how this combination opens wider process windows than other structurally close building blocks. Less steric hindrance than bulkier bicyclic acids, better solution handling than higher molecular weight piperidines, and distinct from straight-chain acids which often lack the chemical traction for cyclization and bonding work. For custom synthesis clients, this fingerprint of versatility means the same molecule can become a candidate in anti-infective screens, CNS chemistry, or materials design depending only on what gets added next.

    Product Handling and Practical Observations

    In a real manufacturing environment, theory and practice sometimes part ways. Fine chemical plants face not only the challenges of producing the desired structure but of keeping batch-to-batch consistency tight. Over the years, we have gradually pinpointed which shelf-life measures matter for 5-piperidin-1-ylmethyl-furan-2-carboxylic acid: heavy-duty laminated bags, nitrogen flushing for larger quantities, and using small lots for pharmaceutical clients. It is also not a product that favors open containers or slow-moving inventory—our QC team catches degradation faster than it would for more robust acids or amines.

    Most users request the purified form as a white-to-off-white powder, stable if kept dry, susceptible to mild yellowing when left open in high humidity. Slight shifts in powder granularity can show up based on the final crystallization solvent, so we document and share each batch’s grain profile. Every year, at least one customer wants to know if it dissolves better in ethanol or DMSO, and every year, the answer comes out the same: for solubility, both work, but lower water content in the solvent makes for a cleaner reaction.

    User Applications: From Laboratory to Scale-up

    Most requests for this molecule come from pharmaceutical research, especially for early-phase screening and intermediate coupling. Our connections with academic and industrial labs have shown two distinct tracks: One group values the compound for its ability to introduce both the furan and piperidine features into candidate drugs, especially where metabolic stability and receptor selectivity need balancing. A second, equally active segment, pursues materials research, exploiting the heterocyclic pattern for new polymers and specialty coatings.

    During scale-up projects, customer chemists sometimes ask for advice on reaction workups and solvent choices. Based on plant experience, filtration through basic filter aids works reliably, but aggressive acid washes often cause decomposition. From large-scale production runs, we suggest gentle neutralization over direct acidification, which tends to help yield and also reduces off-odors in product isolation. Years of troubleshooting have taught us not to rely on generic workup procedures often found in literature reports, but to adapt, document, and compare at every scale. We also keep a standard library of comparison spectra and chromatograms, so customers working on their own purifications can check progress or resolve problems without guesswork.

    Comparisons to Related Chemicals

    In day-to-day manufacturing conversations, one subject keeps returning: how does this product compare with commonly used alternatives? Even the best catalog descriptions sometimes fail to clarify the practical differences.

    Compared to 2-furoic acid, 5-piperidin-1-ylmethyl-furan-2-carboxylic acid introduces a flexible amine handle, extending its value for bioconjugation and peptide fusion. Unlike N-alkylated pyridine conjugates, this compound preserves more of the native heterocyclic electron pattern without excessive steric drag, making it more reactive in cross-coupling and amidation. For chemists seeking new medicinal scaffolds, these minor adjustments on paper turn into major shifts in real-world reactivity and selectivity.

    From a production standpoint, the biggest contrast comes with purification steps and by-product profiles between similar-looking structures. Some products in this chemical class suffer from persistent colored trace impurities that demand harsh charcoal treatment; our plant team has dialed in the protocol so the final API grades consistently exceed the thresholds big pharma requires, but without over-washing or risking hydrolysis. Time and again, conversations with development scientists confirm they notice product handled by factory-experienced teams performs better, with fewer reruns and less waste in downstream chemistry.

    Quality and Traceability in Real Life

    The chemical industry has always talked about quality, but on the shop floor, words only mean as much as daily process data and robust tracking. 5-Piperidin-1-ylmethyl-furan-2-carboxylic acid is no exception. Each batch comes with its own identity card, tracking every ingredient lot, process change, sampling point, and inspection result. We take stability and impurity tracking seriously because some downstream uses land in clinical settings or as precursor to regulated products. When researchers send back samples for comparison, or ask for impurity profiles not mentioned in the initial spec, the data lives close at hand.

    Having managed product recalls and investigations in the past, we know swift answers matter more to real-world reliability than appending reassurances into marketing brochures. Each load shipped leaves a paper trail that matches sample to drum to palette, with regular stability sampling reported on a rolling schedule for our higher criticality clients. Supporting client audits is much easier with these real production records, not just because it satisfies regulatory asks, but because it roots our reputation in tangible daily discipline.

    User Feedback and Continual Process Upgrades

    Feedback from users forms an ongoing cycle with process improvements in the plant. A recurring theme with 5-piperidin-1-ylmethyl-furan-2-carboxylic acid is feedback on reactivity and side-product formation in larger scale couplings. Early clients flagged modest batch-to-batch color shifts in heated reactions; since then, our team reviewed solvent grade filtering and crystallization rate controls, closing the gap. The handful of customers experimenting with solid-phase synthesis or automated reactors needed a tighter particle size distribution, prompting us to add secondary sieving and inline monitoring ahead of final packaging.

    High-tier researchers prize transparency on what smaller impurities may accompany the main product, especially as their own analytical techniques grow sharper. We regularly supply detailed chromatograms and spectra so methods development teams in pharma and biotech can tailor purification or tolerance limits to their specific programs. Some even report new findings, helping our QC team tweak screening or retention time libraries for the next wave of shipments. For every batch that leaves the factory, learning loops back to everyone on the team—process chemists, operators, and QC analysts—who see how their choices echo in downstream innovation.

    Looking beyond chemistry, we've welcomed plant tours or client visits so researchers can see the real production landscape, from raw material tanks through to isolated product drums. This level of openness fosters mutual respect—and honest insights—for how reactants, water quality, and process timing impact the journey from theory to tangible output.

    Sourcing Confidence and Ethical Practices

    Having worked through supply chain disruptions and global shortages, we recognize the risk buyers face in finding a stable, consistent source of specialty chemicals. Each drum of 5-piperidin-1-ylmethyl-furan-2-carboxylic acid reflects careful sourcing of critical upstream chemicals, direct partnership with trusted supply partners, and proactive inventory buffering during seasonal shortages. Several times over the past few years, weather or logistic events have threatened deliveries, making in-house stock margin and long-term purchasing essential. We communicate early with users about potential delays and keep transparency at the heart of every transaction.

    Beyond logistics, our production staff have a deep commitment to safe and sustainable fabrication. Waste and effluent controls meet or exceed local mandates, with regular third-party checks of our treatment facilities. Hazardous waste gets minimalized through concentrated process design, with full recycling programs for bulk solvents and workup fluids. Everyone in the operation understands that ethical production practices build the foundation of confidence, particularly when working with downstream sectors like pharma and advanced science, where reputation drives purchasing decisions as much as any specification number.

    Guidance for Choosing the Right Product

    Every application cries out for the right fit, so it pays to talk to factory experts before committing to a particular grade or form. For users needing the highest possible purity—often early-stage drug developers—tightest batch specs and fresh manufacture win out over leftovers from bulk runs. For material scientists or intermediates suppliers, cost matters alongside purity, and our team discusses scale-up economics, alternate pack sizes, or custom purity levels case by case.

    As with every specialty molecule, the choice depends not only on application needs but on practicalities in formulation, solvent handling, and downstream chemistry. We have learned from years of phone calls and late-night troubleshooting chats: chemists on the front line do better when they know what’s behind the product—not just in terms of purity and shelf life, but in terms of operator expertise, real-world process choices, and willingness to adapt when surprises arrive in the lab.

    Industry Trends Shaping This Segment’s Future

    Scientists and manufacturers both notice increasing complexity in chemical supply chains and research pipelines. With the rising trend toward more complex, heterocycle-rich APIs and advanced materials, factories that can reliably deliver on molecules like 5-piperidin-1-ylmethyl-furan-2-carboxylic acid are seeing greater demand. Our industry tracked one sharp uptick as biotech firms pivoted to deeper CNS and anti-metabolic research. Each step up in molecular complexity means every intermediate needs tighter consistency, fewer trace metals, and more documentation on origin and handling.

    Meanwhile, regulatory oversight continues to expand, not just for finished drugs but for all input chemicals. Detailed traceability, transparent impurity and residue reporting, and up-to-date compliance filings are no longer just competitive extras—they drive qualification, especially as firms seek to future-proof product registrations in new markets. We field more requests now for reference spectra, route of synthesis breakdowns, and expanded impurity panels from biotech and academic clients.

    Sustainability also shapes purchasing priorities. End users ask not only about green chemistry credentials but practical production choices, such as solvent recovery rates and energy inputs. In the past year, carbon accounting for each batch run has become standard, with teams requesting CO2 footprints or LCA (life cycle analysis) fact sheets alongside the usual certificates of analysis. For those of us in production, this means ongoing investments in solvent recycling, process intensification, and lower-emission transport.

    Frequently Raised Customer Questions and Our Responses

    Customers at all levels—from development chemists to procurement specialists—bring up certain questions nearly every week. Questions arise about storage: airtight packing remains essential, and we advise refrigeration only if stability or humidity becomes a concern for long-term storage. Some ask about particle size and grindability for automated dosing; our production team can screen and check powders by laser or sieve, reporting the distribution by lot before shipment. Solubility comes up as well: water tolerance is limited, but DMSO and ethanol both perform well for most applications, with fine tuning required for more exotic solvent systems.

    Others ask how flexible supply arrangements can be—minimum order size, split shipments, and stock scheduling. As manufacturers, we offer direct one-on-one Q&A for special projects or tight resource timelines, explaining what can change by request and what must remain fixed for consistency. Experienced buyers appreciate up-front discussion of lead times and "make-to-order" cycles, preventing delays on both ends and helping us match plant workload to real demand.

    Ongoing Collaboration and Support

    Every relationship with advanced researchers or process engineers turns into a continuous learning cycle for us as a chemical manufacturer. Your experience in scaling up new reactions or comparing production lots provides direct feedback to our teams on what adjustments drive better consistency or cleaner downstream applications. With every inquiry, from troubleshooting workup tips to new impurity screening requests, we draw on plant-floor reality—not only to pass along what works, but to adapt and refine each batch that leaves our line.

    Having supplied 5-piperidin-1-ylmethyl-furan-2-carboxylic acid to both established and emerging innovators, our goal remains the same: real, ongoing dialogue backed by data and open access to manufacturing expertise. This approach aligns with the current movement toward transparency, robust traceability, and continuous quality improvement, values that customers recognize and value as much as strict technical specification.

    If you have specific requirements, questions about process optimization, or feedback from your laboratory or production line, connect with us to share your perspective. Decades of plant-side experience reinforces our commitment to real-world reliability and collaborative innovation, making even a specialized product like this a catalyst for discovery and progress.