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2,2-Bipiperidine

    • Product Name 2,2-Bipiperidine
    • Alias Bipiperidyl
    • Einecs 217-651-9
    • 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
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    Specifications

    HS Code

    987568

    Name 2,2-Bipiperidine
    Molecular Formula C10H20N2
    Molar Mass 168.28 g/mol
    Cas Number 2191-47-1
    Appearance White to off-white solid
    Melting Point 124-127 °C
    Boiling Point 340.2 °C at 760 mmHg
    Density 1.11 g/cm3
    Solubility In Water Slightly soluble
    Smiles C1CCNC(C2CCNCC2)C1
    Inchi InChI=1S/C10H20N2/c1-3-7-11-9(5-1)10-6-2-4-8-12-10/h9-12H,1-8H2
    Pubchem Cid 134043
    Refractive Index 1.563
    Storage Conditions Store at room temperature, in a tightly closed container
    Synonyms 2,2'-Dipiperidine

    As an accredited 2,2-Bipiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 2,2-Bipiperidine is packaged in a sealed, amber glass bottle with a secure screw cap and safety labeling.
    Shipping 2,2-Bipiperidine is shipped in tightly sealed containers, away from moisture and incompatible materials, and is typically packaged according to standard chemical regulations. It is transported in compliance with local and international shipping guidelines, including appropriate labeling and documentation, to ensure safety during handling and transit.
    Storage 2,2-Bipiperidine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, strong oxidizing agents, acids, and moisture. Store at room temperature, protected from light and incompatible materials. Ensure proper labeling, and restrict access to trained personnel only. Use suitable secondary containment to prevent accidental spills.
    Application of 2,2-Bipiperidine

    Applications of 2,2-Bipiperidine in Industrial Manufacturing

    As an established producer of 2,2-Bipiperidine, we focus exclusively on supplying end users in sectors where this specialized diamine delivers recognized performance in synthesis and manufacturing. Each downstream segment leverages this intermediate differently, and we ensure strict adherence to industry compliance, reliable integration in formulation and processing, and compatibility with end user product specifications.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Innovators and generic drug manufacturers utilize 2,2-Bipiperidine as a structure-building block in select piperidine-based API projects, chiefly as a core or linker moiety during multi-step heterocycle assembly. We supply GMP-compliant lot traceability, and our material’s purity profiles support complex synthetic chemistry, where precise amination steps and minimal side reactivity influence overall batch yield and impurity control.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. monographs for process intermediates (where specified)
    • FDA 21 CFR Part 211 (for cGMP finished API plants)
    • Customer-defined raw material quality specifications validated for regulatory submissions

    Typical usage ratio

    • 0.95 – 1.10 molar equivalents relative to piperidine core substrates; adjusted based on desired API route and step yield targets

    Downstream process integration

    • Added in the heterocycle formation step under anhydrous inert conditions, often during ring-closing reactions, N-alkylation, or as a ligand in metal-catalyzed couplings

    Final product types

    • Branded and generic APIs involving piperidine motifs (e.g., CNS active drugs, antiviral heterocycles, select oncology candidates)
    • Registered API intermediates for contract manufacturing partners

    2. Specialty Catalyst Ligand Preparation

    Homogeneous catalyst manufacturers use 2,2-Bipiperidine to synthesize chiral and achiral ligand systems for transition metal-catalyzed processes, notably where spatial orientation and electronic effects require symmetrical diamines. Careful QC ensures absence of byproducts, supporting consistent batch performance in downstream ligand synthesis and subsequent catalytic runs relevant to industrial and fine chemical production.

    Industry compliance standards

    • Chemical Manufacturer’s Association (CMA) product stewardship guidelines
    • ISO 9001:2015 Quality Management Systems
    • Responsible Care Process Safety Codes
    • Customer-driven catalyst project specifications

    Typical usage ratio

    • 0.85 – 1.20 molar equivalents, depending on stoichiometry for ligand–metal complex formation; precise ratio determined by downstream reaction mapping

    Downstream process integration

    • Charged during initial ligand formation by condensation or reductive amination with halogenated or carbonyl precursors, followed by purification and coordination with transition metal salts

    Final product types

    • Chiral catalyst ligands for asymmetric hydrogenation, C–N and C–C couplings
    • Industrial homogeneous catalysts deployed in petrochemical and agrochemical manufacturing

    3. Chemical Intermediate for Agrochemical Synthesis

    Downstream phyto-pharmaceutical and crop protection synthesis operations incorporate 2,2-Bipiperidine as a reactive intermediate to build substituted piperidine rings in agroactive ingredients. Its symmetrical structure supports high selectivity in stepwise nitration or functionalization, while strict process control ensures batch consistency and compliance for products destined for regulated global agricultural use.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025:2017 for accredited QC/QA testing
    • REACH Annex IX for substances used in plant protection synthesis
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

    Typical usage ratio

    • 0.5 – 1.5 w/w% in multistep synthesis trains; concentration set by targeted functionalization and impurity management parameters

    Downstream process integration

    • Fed into continuous reaction trains following initial amination or during secondary ring functionalization, supporting synthesis of proprietary agrochemical scaffolds

    Final product types

    • Herbicide and insecticide actives incorporating piperidine substructures
    • Growth regulator intermediates for custom agroformulation firms

    4. Fine Chemical Building Block for Advanced Material Synthesis

    Manufacturers in the specialty polymer and performance materials sectors exploit 2,2-Bipiperidine as a valuable diamine chain extender in high-performance polyamides or in the assembly of molecular architectures for electronic or separation membranes. Rigorous control over moisture, residual solvents, and trace metals in our supply chain supports downstream demands for high molecular weight and narrow polydispersity.

    Industry compliance standards

    • ISO 9001:2015 for supply chain QA/QC
    • ASTM D4718 (standard test methods for polymeric materials)
    • RoHS and REACH compliance for electronic component precursors
    • Customer-approved raw material traceability protocols

    Typical usage ratio

    • 1 – 10 mol% relative to other diamines or diacid components; loading determined by desired polymer properties and process parameters

    Downstream process integration

    • Directly introduced in the polycondensation stage or as a precursor for modified polyamide backbones, with real-time monitoring for viscosity and conversion

    Final product types

    • Specialty polyamides and copolymers for engineering plastics
    • Ion-conductive membrane materials for battery and fuel cell applications
    • Performance coatings and adhesives requiring cyclic diamine motifs
    Free Quote

    Competitive 2,2-Bipiperidine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

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    Certification & Compliance
    More Introduction

    2,2-Bipiperidine: A Manufacturer’s Perspective on Its Role in Modern Chemistry

    Understanding 2,2-Bipiperidine—Shaped by Experience in the Plant

    As someone who spends each day guiding synthesis lines and troubleshooting tank reactors, the chemicals we bring forth aren’t just formulas or catalog entries. 2,2-Bipiperidine didn’t reach our product suite by accident. With two piperidine rings compacted in a unique bond, this molecule brings characteristics that have drawn the attention of demanding research teams and innovative pharmaceutical firms.

    The technical designation—hexahydro-2,2'-bipyridine—only tells part of the story. Years in production revealed how challenging it gets to isolate a bipiperidine with both piperidine rings joined at their 2-positions. That architecture sets it apart from common bipyridine or 4,4’-linked structures, and this structural shift translates into new opportunities, especially where intermolecular interactions or spatial arrangement matter.

    An Inside Look at the Model and Specifications

    We follow a dedicated protocol for each batch of 2,2-Bipiperidine targeting a specification that ensures purity above 98%. This detail might look routine on paper, but behind the scenes, maintaining low moisture and a tightly controlled pH range has proven essential during scale-up. Consistency has defined our competitive edge, as our reactors run longer holding times to coax out side-byproducts that linger in lesser-controlled syntheses.

    Customers expect a pale crystalline or colorless solid, with melting points clustering around the expected standard. Our experience with vacuum distillation equipment eliminated most residue-carrying impurities, giving the confidence to claim a product that dissolves quickly and reacts reliably—even in uncommon solvents or under tricky conditions.

    Direct Applications Fueled by Lab and Plant Feedback

    In our own process development, 2,2-Bipiperidine first caught our chemists’ attention as a ligand builder for transition metal complexes. The steric and electronic properties arising from its ring junction create coordination sites that differ from other bipiperidine isomers. We’ve seen research groups leverage this compound to tune the selectivity of catalytic reactions—such as asymmetric hydrogenations—where a subtle difference in a ligand backbone can shift an outcome from failure to high yield.

    Demand has risen from API intermediates and as a protective group scaffold in medicinal chemistry. Several partners in the pharmaceutical sector order 2,2-Bipiperidine for constructing heterocyclic libraries or unlocking rigid structures that standard piperidines can’t stabilize. Bridging these gaps supports breakthrough work, from oncology targets to CNS-active compounds.

    Further downstream, specialty polymer chemists continue to explore the crosslinking potential and conformational constraints enforced by its unique skeleton. They use it to create small blocks that reinforce or introduce site-directed rigidity into advanced materials. The molecule’s resistance to oxidation—documented by our own aging and stability tests—adds confidence during multi-step reactions, letting it persist through processes that degrade more reactive analogs.

    Lessons Learned from Decades in Manufacturing

    Producing 2,2-Bipiperidine at commercial scale is nothing like laboratory glassware. The early days illuminated issues with catalyst fouling and side-product removal. Our transition from batch to semi-continuous processing helped, but the real breakthroughs emerged from refining the cyclization step and incorporating inline analytics. It allowed us to capture deviations before problematic byproducts accumulated.

    Recrystallization conditions matter more than most would suspect. Solvent selection impacts purity, recovery yield, and the safety profile for every downstream worker. Our solvents—chosen after dozens of pilot runs—combine manageable volatility, easy recovery, and minimal toxicity trace. Regular reviews with our EHS (Environment, Health, Safety) specialists led to system changes that reduced residual solvent below stringent internal targets, anticipating regulatory trends ahead of time.

    We use the insights gained from analytical feedback to adjust feedstock purity before the first reaction drop hits the vessel. This up-front investment slashes variability and helps guarantee every drum matches previous shipments—no guessing, no last-minute corrections. Our team logs each shift’s notes, carrying forward observations that circle back into continual improvement.

    Real Differences from Bipiperidine Isomers and Analogous Products

    You don’t need a theoretical chemistry degree to notice the difference between 2,2-Bipiperidine and its cousins. 4,4’-Bipiperidine links spread the nitrogen centers apart, which shifts electronic density and diminishes certain chelation tendencies. These minor-looking differences have a dramatic impact—especially for researchers tuning ligands or seeking selective reactivity.

    Our clients noticed it in practice. Where 4,4’-bipiperidine generates more flexible, loosely structured complexes with metals, the 2,2’ connectivity delivers a tighter coordination environment. This close approach changes both the geometry and the kinetics of reactions it participates in. Fine points like this separate successful pilot-scale work from scale-ups that fail in the details.

    We’ve also observed that some piperidine derivatives fall short in demanding reaction conditions. Moisture sensitivity, color formation under reduced pressure, or inconsistent reactivity trouble users down the supply chain. By contrast, our 2,2-Bipiperidine batches consistently maintain stability in sealed ampoules over six months, even after multiple temperature cycles, confirmed by rigorous spot-checking and mass balance analysis.

    Why Chemists and Engineers Return to This Molecule

    Through conversations with researchers—from universities to startup drug firms—certain themes keep surfacing. The unique steric bulk and fixed angles of 2,2-Bipiperidine allow chemists to build molecular structures that standard reagents can’t provide. Its relative ease of functionalization opens doors to a variety of derivatization pathways, supporting SAR (structure-activity relationship) studies central to modern drug design.

    Process engineers, too, find value in consistent batch quality and documented impurity profiles. Each bottle leaving our site ships with full chromatographic and spectral validation, ensuring confidence at the bench and at pilot scale. Fewer surprises during production mean that schedules get met and projects avoid costly repeat runs.

    The stability and reactivity of our 2,2-Bipiperidine encourage its inclusion in reaction screens, templating studies, and catalysis optimization. Teams running parallel syntheses find it easier to predict what will happen when this molecule enters the reaction flask—making planning more reliable.

    Meeting the Real-World Challenges of Quality, Purity, and Supply

    Insiders recognize that the difference between a successful synthesis and a dead end often boils down to hidden details in reagent quality. Our colleagues in scale-up know the pain of a contaminated or off-spec batch. That’s why our lab team continuously refines the purification process, responding to changes in raw material sources or batch-to-batch variation.

    We source starting materials from vetted suppliers and audit both their QA and their compliance culture. It’s a disciplined approach built over years of seeing what happens when shortcuts bleed into process chemistry. Problems such as discoloration, trace amines, or unresolved intermediates never stay hidden for long and can upset finely-tuned biological screening.

    On the supply side, we recognize that reliable delivery matters as much as product quality. Unplanned downtime can set development programs back weeks, but robust scheduling and inventory practices allow us to keep inventory targets realistic without overpromising. If weather strikes or transport lags, rapid response teams switch to alternate carriers or production lines to minimize disruptions.

    Regulatory and Safety Considerations

    Regulatory requirements continue to evolve, and our approach adapts with them. Every batch undergoes analysis for contaminants flagged by leading authorities. Testing meets standards not only for chemical purity, but also for workplace safety—dust control strategies, improved ventilation, and real-time monitoring of reaction off-gases protect both our staff and end-users.

    Our commitment to sustainable practices means working closely with local authorities on waste and emissions control. Within the plant, we closed the loop on solvent handling, installed secondary containment on major lines, and maintain strict segregation between product streams to avoid cross-contamination. These steps allow us to minimize environmental footprint while delivering a better, safer product.

    Documentation stays up-to-date, so any auditor or regulatory reviewer finds every transfer step, analytical result, and release note in order. Partners relying on certifications or internal audits have direct access to the data streams behind each manufactured lot.

    Supporting Research and Future Directions

    The value of 2,2-Bipiperidine goes beyond today’s use cases. As scientists deepen their understanding of constrained amine backbones, more applications are surfacing. We partner with academic collaborators to test 2,2-Bipiperidine in cross-coupling experiments, or as a core for next-generation ligands. Its potential in supramolecular chemistry—where molecular recognition or guest-host interactions demand structural precision—continues to fuel new investigations.

    Our team dedicates resources to exploring both new functionalizations and the physical properties of derivatives. The field’s interest in green chemistry prompts us to test reaction pathways that minimize waste, avoid hazardous reagents, or cut energy use. Each successful process improvement earns trust not just with our direct customers, but with universities and institutions worldwide.

    A collaborative mindset lets us adjust quickly. If an end-user identifies an unexpected impurity or functional group incompatibility, our chemists troubleshoot at the bench and in the plant to adapt quickly. It’s a hands-on process where nothing is assumed, and every relevant detail gets checked before new procedures roll into full-scale production.

    The Human Element: Learning from Every Batch

    No machine or instrument replaces the knowledge carried by experienced operators. Many on our team have witnessed the pitfalls of moisture ingress, over-enthusiastic drying, or temperature spikes. Regular training and cross-functional teams drive best practice sharing, helping protect product quality and personal safety.

    Sharpening our process also cultivates a sense of pride among our staff. Each improvement, whether a tweak to a distillation temperature or a better filtration material, ripples outward and raises the bar factory-wide. We listen for feedback from every stakeholder—for us, it’s not just about filling drums, but solving problems and making sure that researchers worldwide can build the molecules that make a difference.

    Market Trends: Why 2,2-Bipiperidine Attracts Growing Interest

    Feedback from industry partners reveals that the adoption of 2,2-Bipiperidine has accelerated as more research teams run high-throughput experiments or seek differentiated scaffolds. The push toward new chemical modalities—such as cyclic peptidomimetics or macrocyclic drugs—often relies on reliable access to building blocks that deliver unique geometry and stability.

    Longevity matters, too. We’ve logged increased demand for long-term storage stability, as future-oriented researchers anticipate multi-year projects or prepare for scale preparations. Downstream, as regulatory frameworks tighten across the globe, traceability and transparency in sourcing and production have grown from perks to requirements.

    Pharmaceutical developers and advanced material specialists describe how switching to our 2,2-Bipiperidine simplified workflows. Predictable physical properties make purification and modification repeatable, letting them divert more resources into creative synthesis and less into troubleshooting.

    Our Role—Delivering Reliability, Supporting Progress

    Decades of direct experience in the intricacies of 2,2-Bipiperidine manufacturing shaped the approach we take. The hands-on feedback loop—tracking every procedural tweak, noting every unplanned blip, and recording every unexpected insight—means our practices stand on lived reality, not guesswork.

    Each successful batch tells its own story: an operator notices a subtle shift in color, a chemist tweaks the distillation timing, a manager spots a chance to tighten tank cleaning schedules. All of this breaks down abstract talk about “quality” into moments of tangible improvement.

    For those exploring new reactivity, designing next-generation drugs, or pushing the limits of applied materials science, reliable access to high-specification 2,2-Bipiperidine makes a difference. We care about every bottle leaving our site because your work depends on our attention to detail.

    Our journey with this molecule continues, shaped by each application and inspired by collaboration with partners who see possibilities where others see routine. From our plant to your research, the value of 2,2-Bipiperidine grows with every challenge and breakthrough.