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4-Hydroxypiperidine Hydrochloride

    • Product Name 4-Hydroxypiperidine Hydrochloride
    • Alias 4-Piperidinol hydrochloride
    • Einecs 630-807-7
    • 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

    909140

    Productname 4-Hydroxypiperidine Hydrochloride
    Casnumber 40064-34-4
    Molecularformula C5H11NO · HCl
    Molecularweight 137.61 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 220-225°C (decomposes)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storagetemperature Store at 2-8°C
    Synonyms Piperidin-4-ol hydrochloride

    As an accredited 4-Hydroxypiperidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A tightly sealed, amber glass bottle containing 100g of 4-Hydroxypiperidine Hydrochloride, labeled with hazard information and lot number.
    Shipping 4-Hydroxypiperidine Hydrochloride is shipped in sealed, airtight containers to prevent moisture absorption and contamination. Packaging adheres to standard chemical safety regulations, is clearly labeled, and includes hazard identification. During transit, temperature and handling controls are maintained to ensure chemical stability, with appropriate safety documentation provided as per international shipping requirements.
    Storage 4-Hydroxypiperidine Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Store at room temperature or as indicated on the product label, ensuring proper labeling and restricted access to authorized personnel only.
    Application of 4-Hydroxypiperidine Hydrochloride

    Applications of 4-Hydroxypiperidine Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Hydroxypiperidine Hydrochloride for specialized industrial applications. The downstream sectors outlined below reflect actual, regulated uses where our material provides proven compliance and value in the synthesis of specialty products.

    1. Pharmaceutical Intermediate for Anti-Psychotic Synthesis

    This material plays a critical role as an intermediate in the synthesis of antipsychotic active pharmaceutical ingredients, such as risperidone derivatives. Pharmaceutical processors require a high degree of purity and consistency to meet cGMP standards. The hydrochloride salt ensures solubility and reactivity during condensation stages, which are crucial in preparing piperidine scaffolds. Integration into multi-step synthesis must consider controlled substance filing and strict documentation for traceability.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • USP and EP Monograph requirements for related intermediates
    • FDA Drug Master File (DMF) registration support
    • ICH Q3C for residual solvent control

    Typical usage ratio

    • Typically 1.0–1.5 molar equivalents per target molecule; batch process may adjust for stoichiometric optimization and impurity control.

    Downstream process integration

    • Added during piperidine ring construction in multi-step reactions; usually introduced in protected form and deprotected prior to final coupling with aryl fragments.

    Final product types

    • Atypical antipsychotics (e.g., risperidone analogues)
    • Specialty CNS active intermediates
    • Pharmaceutical reference standards
    • Regulatory registered APIs

    2. Precursor in Crop Protection Active Ingredient Manufacture

    Chemical crop protection manufacturers employ this hydrochloride for synthesis of select piperidine-based insecticides and fungicides. The chemical’s reactivity enables conversion into key nitroxyl and heterocyclic structures under precisely monitored conditions. Batch scale-up requires validated cleaning, according to agricultural grade and residue management guidelines, to prevent cross-contamination across actives. Final pesticides undergo extensive field testing before sale.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Agricultural Pesticides
    • ISO 9001:2015 for manufacturing traceability
    • REACH registration (EC 1907/2006) for Europe
    • US EPA active ingredient listing (as applicable to downstream product)

    Typical usage ratio

    • Ranged from 10–35% of total reactant mass in heterocycle formation, adjusted depending on the required transformation and scale.

    Downstream process integration

    • Added to closed reactors during initial nitrogen-heterocycle assembly; monitored to prevent oxidative degradation before downstream halogenation or esterification steps.

    Final product types

    • Piperidine-substituted insecticides (e.g., pyridinecarboxamide derivatives)
    • Systemic fungicides
    • Intermediate actives for plant protection blends
    • Stabilized pesticide technical concentrates

    3. Building Block in Specialty Polymer Synthesis

    The raw material serves as a monomeric precursor in the synthesis of selected polyamide and polyimide engineering plastics. Its defined functionality enables the creation of macromolecules with tailored flexibility and solvent resistance. Reaction planning must address batch purity, moisture content, and acid-base neutralization to optimize polymer chain uniformity. Attentive quality control is maintained throughout polymerization, extrusion, and pelletization.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems
    • ASTM D638 for tensile properties of plastics
    • RoHS Directive 2011/65/EU for hazardous substances
    • REACH Article 33 for downstream notification

    Typical usage ratio

    • 5-20% by weight of total monomer input, based on desired thermoplastic or thermosetting properties; precision metering required for molecular weight consistency.

    Downstream process integration

    • Fed into continuous or batch polymerization vessels; reacts via condensation or addition mechanisms to yield polymer backbones with functionalized side groups.

    Final product types

    • Thermoplastic polyamides for automotive assemblies
    • Polyimide films for electronic insulation
    • Custom-engineered plastics with enhanced solvent resistance
    • Compounds for specialty coatings and adhesives

    4. Intermediate for Active Pharmaceutical Ingredient (API) Synthesis in Antiviral Drugs

    Leading antiviral API manufacturers utilize 4-Hydroxypiperidine Hydrochloride as a precursor in the preparation of neurotropic antiviral agents. Its role includes selective ring substitution and protection, enabling further N-alkylation or acylation. Operations maintain strict supply chain transparency and impurity profiling, in accordance with pharmacopoeial and import/export regulations. Control labs monitor reaction endpoints for batch release.

    Industry compliance standards

    • ICH Q7 active pharmaceutical ingredient controls
    • Ph.Eur. and USP for related substances
    • FDA API importation requirements (21 CFR Part 314)
    • Chinese Pharmacopeia standards for raw material sourcing

    Typical usage ratio

    • Between 1.1–1.3 molar equivalents per active molecule; frequent adjustments made for scalability based on impurity clearance data.

    Downstream process integration

    • Engaged in N-substitution reactions and subsequent cyclization stages before ultimate deprotection leading to final API assembly.

    Final product types

    • Piperidine-derived antiviral APIs
    • Advanced pharmaceutical building blocks
    • Vial/bulk tablet formulations (downstream from API)
    • Licensed intermediates for global pharma supply

    5. Fine Chemical Intermediate for Photoinitiator Synthesis

    This chemical acts as a structural unit for the synthesis of specialty photoinitiators used in UV-cured inks and coatings. It enables the preparation of stable oxime-ether structures through nucleophilic substitution and hydrochloride salt-handling techniques. Manufacturers design reaction protocols to prevent moisture uptake and achieve target molecular weight distributions. Scale-up requires recyclable solvent systems to meet regulatory requirements for volatile organic compound (VOC) emissions.

    Industry compliance standards

    • ISO 14001:2015 for environmental management systems
    • EN 71-3 limits for heavy metals in coatings (relevant for food packaging/children’s products)
    • REACH SVHC listing control
    • EPA TSCA Listing for US commerce

    Typical usage ratio

    • Usually 7–15% by total mass of photoinitiator batch, recalibrated for molecular structure or UV-responsiveness of finished product.

    Downstream process integration

    • Dosed at the nucleophilic addition stage, then purified by fractional crystallization before final coupling or polymer attachment in photoinitiator lines.

    Final product types

    • UV-curable photoinitiators for digital printing
    • Chemical precursors for 3D printing resins
    • High-performance coatings for electronics and packaging
    • Photo-reactive intermediates exported globally

    6. Precursor for Synthesis of Fine Fragrance Intermediates

    Manufacturers of fine fragrance chemicals select this material for producing select piperidine-based aroma and flavor intermediates. The hydrochloride salt ensures reactivity and stability during condensation and reductive amination, essential in generating target odorant molecules with defined aromatic profiles. Careful batch record-keeping matches IFRA recommendations for safe downstream use and enables full transparency for end-user documentation.

    Industry compliance standards

    • IFRA Code of Practice for fragrances
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9001:2015 for batch traceability
    • REACH Annex XVII (cosmetic restrictions where applicable)

    Typical usage ratio

    • Ranging from 4–12% of formulation mass in fine fragrance intermediates, adjusted for target volatility and olfactory threshold of the final blend.

    Downstream process integration

    • Introduced at the selective amination or cyclization step; usually neutralized and extracted to achieve high purity for downstream compounding with aldehyde or ester groups.

    Final product types

    • Piperidine-based fragrance intermediates
    • High-impact aroma chemicals for perfumes
    • Flavor ingredients for food and beverage applications
    • Specialty bases for luxury personal care lines
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    Certification & Compliance
    More Introduction

    4-Hydroxypiperidine Hydrochloride: A Key Intermediate Driving Complex Synthesis

    The Chemistry Behind 4-Hydroxypiperidine Hydrochloride

    In our work, producing 4-Hydroxypiperidine Hydrochloride is less about sheer output and more about fine-tuning at every stage. This compound reveals its value in the hands of process chemists who face regular challenges in developing pharmaceutical candidates or manufacturing specialty products. Our approach centers around stable hydrochloride form, offering reliable solubility and handling characteristics crucial for repeatable downstream chemistry. The backbone structure—the piperidine ring—remains highly sought after, but the introduction of a hydroxy group at the 4-position adds flexibility that chemists appreciate when looking to expand reaction possibilities.

    Bringing together precise raw materials under tight temperature and pH control, we ensure a consistent crystalline product, free of unwanted residuals or side products. Experienced chemists often notice significant differences between grades of this intermediate. Technical know-how at our manufacturing floor allows us to push purity levels, reduce moisture, and minimize color, satisfying even the most demanding API projects.

    What Sets Our 4-Hydroxypiperidine Hydrochloride Apart

    Similar-looking products can drift in quality or reactivity due to subtle differences in process or feedstock. Over years, our process development team has eliminated variable crystal habits, monitored particle size ranges, and established strict limits on chloride and residual solvent contents. These material attributes aren't just academic; they matter to anyone hoping to scale-up a synthesis without mid-batch hiccups or costly purification headaches.

    Not every version of 4-Hydroxypiperidine Hydrochloride will behave the same in coupling or alkylation steps. Stability in long-term storage has seen significant improvement. Physical form—bead, flake, powder—can affect solvent wetting and subsequent reactivity. Chemical engineers working at lab scale sometimes overlook powder flow or dissolution rates. At the plant level, we engineer our product for maximum compatibility with automated dosing, pneumatic transfer systems, or direct feed to reactors. Reduced dusting, lower caking tendencies, and optimized bulk density come as a result of targeted process changes and continuous feedback from long-term customers.

    Experience with Challenging Reactions

    Synthetic chemists commonly turn to 4-Hydroxypiperidine Hydrochloride as a robust nucleophile or building block for nitrogen-containing scaffolds, especially in drug development. Our team’s first-hand experience supporting custom synthesis projects highlights the importance of contaminant control—trace byproducts from over-reaction or incomplete quenching can poison downstream catalysts, leading to poor yields further along the route.

    Seeing how different customers use this intermediate informs our manufacturing strategy. Some require strict moisture limits to prevent hydrolysis of sensitive acylating agents, while others focus on minimizing batch-to-batch color variation to avoid unpredictable product isolations. Years of technical service stories underline that consistent reactivity and reliable documentation save resources on the customer end. This reduces failed batches and last-minute troubleshooting, giving process chemists and QC analysts greater confidence.

    Harnessing Versatility in Synthesis

    A core strength of 4-Hydroxypiperidine Hydrochloride stems from how it bridges functional group chemistry. The piperidine ring positions nitrogen in the right orientation for nucleophilic substitution, while the hydroxy group brings a handle for O-alkylation, esterification, or carbamate formation. Working directly with pharmaceutical innovators, our technical advisors guide customers on which solvent systems extract the best yield, how different acid scavengers influence conversion, and what purification techniques most effectively clear minor impurities.

    Because salt forms change solubility and handling parameters, the hydrochloride salt stands out for those working in aqueous or polar organic environments. It resists degradation compared to the free base, retaining integrity during long shipping or storage. In contrast, free base forms might suit nonpolar environments but lose out on processability in larger reactors. Early pilot-scale customers have noted reduced static buildup and easier weighing with our hydrochloride product, removing friction from material moving and blending steps.

    Pharmaceutical Pathways: From Intermediate to Active Ingredient

    A clear application for 4-Hydroxypiperidine Hydrochloride appears in the construction of heterocyclic active pharmaceutical ingredients. Antipsychotics, analgesics, and several central nervous system agents build out their core ring systems using our crystalline intermediate. Many research teams have used this compound to link aromatic systems or introduce additional heteroatoms, leading to faster SAR cycles and direct access to proprietary compounds. One global innovator scaled-up a new CNS candidate in record time after switching to our low-residual product. They credited reduced impurity load and faster filtration times for keeping the project on schedule.

    Our in-house process chemistry service often gets called in to consult on late-stage route modifications. People developing active ingredients need intermediates guaranteed to comply with ICH residual solvent and heavy metal guidelines. We support these efforts through validated cleaning protocols, carefully controlled utility streams, and documentation ready for regulatory filings. Chemists studying new salt forms or prodrugs based on piperidine often share positive results after transitioning from generic material to our meticulously controlled lots.

    Technical Insights: Quality, Impurities, and Process Sustainability

    Unlike resellers, we control every input—water, acid, solvent—and measure each critical parameter at every scale. Instrumentation on the production line spots out-of-spec material, not just at the final QC step, but right as it emerges from reaction and isolation. Our experts understand how impurities develop and track every batch. Optimized batch washing protocols and multiple filtration steps result in levels of color and residual solvent suitable for even injectable-grade development.

    Process optimization doesn’t stop at the lab. We invest in solvent recovery, closed-system transfers, and energy-reducing crystallization. Materials scientists at our facility work on granular flow, tweak drying schedules, and run simulated transport studies, delivering a solid form ready for harsh supply chain conditions. Sustainability concerns matter—solvent recycling and careful pH neutralization not only minimize environmental impact but also produce a cleaner final product.

    Application Diversity Beyond Pharmaceuticals

    Applications of 4-Hydroxypiperidine Hydrochloride reach beyond drug synthesis. Polymer designers searching for nitrogen-functionalized building blocks now include this product in their toolkit, modifying macromolecular chains and tuning mechanical properties. Team members support agricultural chemistry firms working on new active ingredients, where the compound’s dual reactivity helps develop water-dispersible formulations. During project feedback sessions, researchers cited higher reaction conversion and easier scale-up with high-purity materials.

    Advanced electronics manufacturers experimenting with new functional resins have called for intermediates with low ionic contamination. Batch certificates with full impurity profiling, retained samples for years, and rapid technical support help these partners maintain stringent standards. Research customers often revisit our material during multi-stage syntheses because variability in handling or shelf life directly impacts performance of their finished projects.

    Comparison with Other Piperidine Intermediates

    Someone choosing between 4-Hydroxypiperidine Hydrochloride and related compounds such as 4-Piperidone or 4-Aminopiperidine Hydrochloride needs to weigh reactivity and synthetic tractability. The hydroxy group at the 4-position provides a unique point for further transformation, suited for selective O-derivatization, whereas the ketone or amine functionalities demand different protecting group strategies. Over-reliance on generic analogues often leads to longer process cycles and more wasted starting material.

    Process chemists running pilot plants often report dosage and mixing issues with hygroscopic amines or volatile ketones compared to the stable hydrochloride salt of 4-Hydroxypiperidine. In one example, a customer noted that troublesome filtration steps during workup disappeared by switching over. Solubility in polar media and resistance to hydrolysis under moderate conditions give this product an edge in multi-step reactions where other forms require additional stabilization.

    Challenges and Solutions through Real-World Manufacturing

    Every project brings new requirements—higher throughput, cleaner impurity profiles, less environmental footprint. As product demand grew over the years, scaling up from kilo-lab to multi-ton runs required tighter process controls. Equipment was retrofitted to maintain strict acid/base ratios, and real-time analytical methods flagged deviation from set moisture and pH thresholds. Collaboration between lab, production, and warehouse staff closed the gap between analytical standards and on-the-ground logistics. Material shipped on time, clean and ready, no surprises at the point of use.

    There have been instances where end-users received materials with excessive caking, inconsistent flow, or unexplained byproducts from less-experienced vendors. Our traceable raw material sourcing and in-house testing facilities made it possible to investigate issues jointly with customers. Through technical troubleshooting, root-cause analysis, and, when necessary, tailored post-synthesis purification, we helped salvaged valuable batches and trained downstream partners to adjust process parameters based on real data.

    Benefits to Research Teams and Process Development Scientists

    Our ongoing relationship with research and scale-up chemists means every lot comes with technical insight, not just a product specification sheet. Fermentation labs and CROs working with small amounts benefit from custom packaging options and a staff on call for technical queries. Large-scale manufacturers gain from proven logistics, robust supply chains, and flexibility in accommodating special delivery needs or documentation requests.

    Feedback loops with academic groups, industrial teams, and external consultants feed directly into process improvements. Knowing exactly what an R&D scientist expects for a new route or patented intermediate helps us maintain high quality material. Years of close collaboration with downstream users weighs more than a generic compliance claim could ever do.

    Keeping Pace with Industry Demands

    As markets expand into more complex, highly regulated molecules, demand for reproducible intermediates like 4-Hydroxypiperidine Hydrochloride continues to rise. Navigating evolving requirements from global regulators, advanced QA systems assure traceability and transparent documentation. Independent audits, data integrity protocols, and real-time cycle analysis safeguard every lot delivered. Sustainable production aligns with environmental and safety expectations.

    Continuous investment allows us to upgrade detection limits for heavy metals and volatile organic residues, respond quickly to customer requests, and maintain flexible plant scheduling for urgent projects. Our roots in the chemical industry teach us to match practical know-how with technological advances, ensuring each kilogram meets or exceeds the performance standards that global pharmaceutical and fine chemical firms rely on.

    Conclusion: Bringing Chemistry and Experience Together

    Reliable supply of 4-Hydroxypiperidine Hydrochloride hinges on science, process, and trusted partnerships. Real-world expertise—developed through hands-on process, daily challenges, and customer-driven improvement—cements our role as more than just a supplier. Those who use our intermediate, whether running a single synthesis in a startup lab or advancing major pharmaceutical development, find value in proven material, straightforward support, and solutions to every stage of scale-up.

    From custom synthesis consultation to logistics solutions, detailed impurity tracking, and diverse packing formats, our approach keeps chemistry practical and production predictable. We invite collaborators focused on results—process efficiency, compliance, safety, and innovation—to discover new potential unlocked by a thoughtfully manufactured 4-Hydroxypiperidine Hydrochloride.