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3-Hydroxypiperidine Hydrochloride

    • Product Name 3-Hydroxypiperidine Hydrochloride
    • Alias 3-Piperidinol Hydrochloride
    • Einecs 239-210-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    610438

    Product Name 3-Hydroxypiperidine Hydrochloride
    Cas Number 1136-18-7
    Molecular Formula C5H11NO · HCl
    Molecular Weight 137.61 g/mol
    Appearance White to off-white crystalline powder
    Purity Typically ≥98%
    Melting Point 230-234°C (decomposes)
    Solubility Soluble in water
    Storage Temperature 2-8°C
    Synonyms 3-Piperidinol hydrochloride
    Ph 1 Solution 4.0-6.0
    Iupac Name Piperidin-3-ol hydrochloride

    As an accredited 3-Hydroxypiperidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed 100g amber glass bottle, labeled with chemical name, concentration, safety symbols, and batch information; tamper-proof cap included.
    Shipping 3-Hydroxypiperidine Hydrochloride is shipped in secure, sealed containers, protected from moisture and light. The packaging complies with chemical safety regulations, often utilizing UN-approved bottles or jars with proper labeling. It is handled and transported as a non-hazardous material, following standard chemical shipping procedures to ensure safe delivery.
    Storage 3-Hydroxypiperidine Hydrochloride should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Ensure the storage location is free from incompatible substances such as strong oxidizing agents. Always follow proper chemical storage regulations and safety guidelines.
    Application of 3-Hydroxypiperidine Hydrochloride

    Applications of 3-Hydroxypiperidine Hydrochloride in Industrial Manufacturing

    3-Hydroxypiperidine Hydrochloride serves as a key intermediate for multiple high-value segments within pharmaceutical, agrochemical, and advanced material synthesis. Our expertise as a direct manufacturer supports volume customization and strict quality adherence in these critical sectors.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers use 3-Hydroxypiperidine Hydrochloride to build select piperidine-based skeletons, especially for CNS-active agents and antihistamines. It introduces a hydroxylated ring structure vital for molecular modification. Our customers apply the material in N-alkylation and reductive amination sequences, predominantly within multi-step API synthesis. This intermediate supports controlled batch and continuous production, under strict validation, to ensure regulatory submission readiness and batch consistency demanded by finished dosage manufacturers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) monograph requirements
    • USP General Chapter standards

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents per target molecule, depending on API scaffold complexity
    • Adjustments according to impurity control and yield optimization during scale-up

    Downstream process integration

    • Introduced during early-to-intermediate synthesis stage
    • Participates in alkylation or hydroxylation reactions, based on API pathway
    • Feeds directly into subsequent protection or deprotection cycles
    • Supports closed-system liquid phase or solid-phase batch synthesis

    Final product types

    • Active pharmaceutical ingredients (e.g., certain antihistamines, antiemetics)
    • Generic CNS drugs
    • Custom high-value specialty APIs
    • Intermediates for patented small molecule development

    2. Agrochemical Intermediate Synthesis

    Leading agrochemical formulators utilize 3-Hydroxypiperidine Hydrochloride for ring-closed intermediates, critical in next-generation insecticides and herbicide actives. The material enters manufacturing protocols requiring high selectivity in ring modification, supporting downstream chlorination, amination, or coupling reactions. Producers benefit from its high purity profile, reducing side-product formation and facilitating downstream product registration.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH registration, evaluation, and authorization regulations (EU)
    • US EPA 40 CFR part 174/180 chemical requirements
    • ISO 9001:2015 quality management for fine chemicals

    Typical usage ratio

    • Typically between 0.9 and 1.3 equivalents per mole of target compound
    • Variation according to target molecule and waste minimization targets

    Downstream process integration

    • Feeds into initial heterocycle assembly or late-stage active functionalization
    • Applied in both batch and continuous stirred-tank reactor setups
    • Subjected to acid/base workup and solvent partition to maximize conversion
    • Utilized prior to halogenation or sulfonation, as dictated by the synthesis scheme

    Final product types

    • Insecticide intermediates (e.g., neonicotinoid skeletons)
    • Precursor for novel herbicidal scaffolds
    • Building block for fungicidal molecules
    • Intermediate for plant growth regulators

    3. Advanced Material Synthesis for Polymer Modifiers

    Manufacturers of specialized polymers and copolymers incorporate 3-Hydroxypiperidine Hydrochloride to introduce controlled secondary amines and hydroxyl groups into backbone structures. This compound enhances hydrophilicity and improves cross-linking efficiency, especially in polyurethane and epoxy resin systems. Reliable lot-to-lot consistency is essential for meeting demanding mechanical property and curing performance criteria in finished advanced materials.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing quality assurance
    • REACH Compliance (Europe) for polymer additives
    • ASTM D256/D638 for mechanical testing in composites
    • RoHS Directive (if used in E&E polymers)

    Typical usage ratio

    • Normally 2-6 wt% within polymerization mixtures
    • Optimized based on cross-link density and matrix flexibility requirements

    Downstream process integration

    • Introduced at liquid blending or pre-polymer formation stage
    • Can serve as a chain extender or functional group donor during curing
    • Processed under inert atmosphere to prevent hydroxyl loss
    • Temperature-controlled addition to manage reactivity during scale-up

    Final product types

    • Hydroxyl-functionalized polyurethane foams
    • Specialty coating additives
    • Amphiphilic block copolymers for advanced membranes
    • Cross-linked epoxy engineering components

    4. Fine Chemical Production for Chiral Ligand Precursors

    Producers of chiral ligands and catalyst supports employ 3-Hydroxypiperidine Hydrochloride as an essential mono-hydroxylated piperidine. Its high purity and amine reactivity help develop enantioselective ligands and auxiliaries through functional group transformation and asymmetric modification. The material’s defined chemical structure supports rigorous analytical traceability, supporting manufacturers focused on specialty organometallic and catalytic chemistry.

    Industry compliance standards

    • ISO 17025 laboratory quality management
    • REACH substance registration for specialty chemicals
    • Chemical Hazard Communication (OSHA GHS criteria)
    • Responsible Care® program for EHS management

    Typical usage ratio

    • Utilized at 1.0–1.5 equivalents per chiral ligand moiety
    • Changes based on required stereoselectivity and final product complexity

    Downstream process integration

    • Incorporated during ligand scaffold assembly
    • Participates in site-selective substitution and cyclization reactions
    • Refined under inert conditions for maximum chiral retention
    • Feeds into downstream transition metal complex synthesis

    Final product types

    • Chiral ligands for enantioselective catalysis
    • Organometallic catalyst supports
    • Complex asymmetric synthesis auxiliaries
    • Fine chemical intermediates for R&D and pilot plants

    5. Chemical Research and Custom Synthesis Services

    Contract manufacturing organizations (CMOs) and custom synthesis laboratories depend on the consistent quality of 3-Hydroxypiperidine Hydrochloride for exploratory raw material provisioning, pilot runs, and customer R&D requests. Its defined salt form ensures precise molarity control, enabling kinetic studies, analytical method development, and structure-activity relationship work in both academic and commercial research settings.

    Industry compliance standards

    • GLP (Good Laboratory Practice) guidelines
    • ISO 9001:2015 certification for laboratory supply
    • REACH registration under “research and development” exemptions
    • National Chemical Inventory Reporting (TSCA, EU, China IECSC)

    Typical usage ratio

    • Usually 0.95–1.0 molar equivalents for reference synthesis and analytical controls
    • Range adapted to experimental method or library construction target

    Downstream process integration

    • Dosed directly into small-scale reaction vessels or automated synthesizers
    • Used for nucleophilic functionalization and amide bond construction
    • Supports parallel synthesis, high-throughput screening, and method validation
    • Routinely analyzed via HPLC, NMR, and LC-MS for QA/QC documentation

    Final product types

    • Analytical reference standards
    • Research intermediates for structure elucidation
    • Compound libraries for drug discovery
    • Specialty project pilot samples
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    Certification & Compliance
    More Introduction

    Introducing 3-Hydroxypiperidine Hydrochloride: Meeting Modern Chemical Requirements

    Industry Insight from a Chemical Manufacturer

    Over decades of hands-on work in fine chemical synthesis, I’ve witnessed countless molecules come and go through production lines. Each compound speaks to a certain market demand, but a few endure and carve out an essential space in both research and commercial applications. 3-Hydroxypiperidine Hydrochloride is one such product that has gained the respect of synthetic chemists and formulation teams alike. This isn’t a compound cobbled together as an afterthought; it’s born from both experience and a tight focus on the stringency demanded by modern chemical and pharmaceutical workflows.

    Core Properties That Matter

    Our 3-Hydroxypiperidine Hydrochloride, typically offered under CAS number 695-87-4, brings together a clean, well-characterized heterocyclic structure with a stable hydrochloride form that eases handling and measurement. Most of our batches reach a purity level above 99%, analyzed by both HPLC and GC for organic trace impurities—critical for anyone targeting reproducible, reliable synthetic results. Unlike generic samples you may encounter, we do not cut corners. Our team leverages in-house recrystallization and drying protocols that slash the possibility of moisture or volatile contamination.

    Instead of accepting minimal control, we verify every lot’s melting point and confirm stability during storage. The white crystalline powder maintains notable solubility in polar solvents, especially water and methanol, which speeds up formulation tasks. This brings down barriers for researchers who don’t want to waste time troubleshooting solubility or batch-to-batch inconsistencies. Ease of weighing and solubilizing streamlines workflows and keeps projects on track.

    Applications That Demand Reliability

    Over the years, the most consistent feedback I receive from clients has come from those working in either early-phase drug development or materials science. 3-Hydroxypiperidine Hydrochloride stands out as a preferred building block in the synthesis of piperidine-based drugs and specialty organics, especially those requiring precise positional selectivity. I’ve seen it used for introducing hydroxylated piperidine fragments into CNS-active pharmaceutical candidates and optical brighteners. Because of its structure, it behaves predictably during reductive amination and ring closure steps—two reaction classes notorious for making or breaking process reliability.

    A major advantage: its hydrochloride salt form keeps the molecule stable throughout intricate, multistep syntheses. Whether in classic batch reactors or automated flow setups, this compound resists degradation better than the free base in humid or warm environments. Quite a few contract manufacturers have told us that the move to the hydrochloride form drastically reduced their material losses and time spent monitoring for decomposition.

    An Edge Over Comparable Intermediates

    It’s not rare for procurement teams to lump 3-Hydroxypiperidine Hydrochloride with other piperidine derivatives or related amines. This misses some big differences in reactivity and downstream processing predictability. For example, 3-hydroxy substitutions change the electron density around the ring, which alters its reactivity compared to 2-hydroxy or N-substituted alternatives. Some of our long-time partners point out that, in their hands, the regioisomeric form can lead to unwanted byproducts and problematic side reactions if chosen without caution.

    The hydrochloride salt brings several handling benefits. Many researchers have vented to us about how the free base version absorbs water from the air within hours, especially if exposed during weighing. Hygroscopic behavior may seem minor until you’re halfway through a scale-up, and your yield calculations start drifting from their predicted values. By supplying the hydrochloride, we’ve given development teams more freedom to plan larger-scale syntheses with confidence, reducing downtime for troubleshooting moisture ingress.

    Meeting the Needs of Medicinal and Process Chemists

    Success in pharmaceutical chemistry doesn’t just stem from chasing novelty but by controlling each transformation. More than once, clients have confided that mediocre intermediates led to weeks’ worth of delays due to unpredictable reactivity. With 3-Hydroxypiperidine Hydrochloride, the tight lot-to-lot consistency has proved more valuable than any claim of high purity listed on paper.

    Formulators who rely on scale-appropriate documentation appreciate our transparency regarding analytical characterization and impurity profiling. We’re proactive: we release spectral data and chromatographic traces for every batch, not only for regulatory compliance but to reinforce trust—especially as teams transition from milligram discovery work to kilogram process chemistry.

    Supporting Synthesis Beyond the Lab Bench

    Beyond drug development, agrochemical researchers and materials scientists are putting 3-Hydroxypiperidine Hydrochloride to work in next-generation synthesis. We’ve supplied kilo-scale material for multi-step preparations of specialty monomers and advanced dye intermediates. The clean reaction profile in amide coupling and Michael addition steps often decides whether the finished product meets final spec. Raw material purity and salt selection have a real effect on finished goods—not just analytical benchmarks.

    Years of batch production have shown how small process improvements make a difference. A focus on achieving consistent particle size distribution helps downstream filtration and washing, particularly for teams with stringent purification needs. Where some suppliers overlook grinding and sieving steps, demanding users see the difference during bulk handling. Our experience has taught us that manageable powder flow and low dusting do more than protect worker safety; they reduce the risk of accidental loss or cross-contamination.

    Reliable Supply Chains Matter

    Markets shift unpredictably. Tight timelines and ambitious R&D milestones force sourcing managers to demand more than just a list of generic specifications. As a direct manufacturer, we commit to holding buffer inventory in climate-controlled conditions. Open communication lines with clients catch potential supply gaps before they turn into emergencies. A few years back, a supply chain disruption of another key heterocycle left several clients in a bind. We responded within days by prioritizing extra runs of 3-Hydroxypiperidine Hydrochloride, demonstrating the value of direct, transparent relationships between end users and manufacturers.

    We don’t view logistics as an afterthought. Our team regularly reviews packaging integrity, shipment tracking, and customs compliance. Strong packaging keeps material fresh until the minute it is weighed into a jacketed vessel, not just the day it ships from our loading bay. If issues arise during customs clearance or on-site receipt, dedicated support from chemists—rather than third-party reps—makes troubleshooting immediate, not bureaucratic.

    Regulatory Readiness and Safety Considerations

    Safety is built into the process, not bolted on. In our experience, working directly with regulatory teams from finished product companies helps us anticipate the required documentation. Whether it’s for GHS labeling, COA transparency, or preclinical submission, we include thorough substance reports and up-to-date safety information. Any unusual impurity or batch trend triggers a review, not a hope that it will slip through the cracks.

    We invest in up-to-date environmental and health training, ensuring that the same hands responsible for synthesis understand the practical implications of GHS and REACH compliance. This extends beyond paperwork—our own floor-level procedures exceed warehouse-grade air and particulate controls so the delivered product consistently reflects the safety profile users expect.

    Practical Guidance for End Users

    Progress in chemical manufacturing comes from listening. Over the years, we’ve tailored our approach according to feedback on what labs and plants truly need. Some researchers requested smaller pack sizes to reduce the risk of exposure or spoilage for low-throughput projects, so we adjusted. Others pushed for specific solubility profiles to ease integration into automated synthesis platforms, prompting investments in further analytical testing. Flexibility and a willingness to listen allow us to help clients sidestep common bottlenecks.

    Maintaining an open line to users—from bench chemists to plant managers—lets us catch emerging problems before they balloon. Not long ago, a customer flagged an inconsistency in water content after switching storage sites. Our technical team jumped in to cross-reference production logs and expedited stability tests. Fast response kept the end user’s timeline intact and ensured the product met the revised specification.

    Comparing to Other Suppliers and Molecules

    Markets feature plenty of piperidine derivatives and third-party brands. Still, not every option stands up during real-world stress. Some buyers will gamble with low-priced, unverified batches or settle for unqualified intermediates. Several project teams have shared stories where these decisions cost them weeks due to failed reactions or frustrating purification steps. 3-Hydroxypiperidine Hydrochloride from our plant performs the way it should—batch after batch.

    Differences stand out in packed-bed reactors and scale-up environments. A salt with variable moisture or inconsistent particle size can clog lines or alter reaction rates. The consistency from our plant, proven by dozens of kilo-lot audits, removes this uncertainty. Repeat business from sophisticated labs validates the long-term approach over transactional convenience.

    Continuous Improvement and Customer Partnerships

    Partnerships with downstream clients have shaped every step of our process. Experienced buyers know quality doesn’t just come from a certificate but from honest dialogue. We host regular audits and invite partners to inspect facilities, track raw material sources, and follow process change logs. Questions about production routes, impurity controls, or logistical support are answered from direct experience—not by reading off spec sheets.

    Continuous training and technology upgrades, informed by both customer feedback and regulatory trends, strengthen our product line every year. Rather than chasing every new synthetic fad, our aim focuses on eliminating pain points—whether they’re related to reactivity quirks, regulatory hurdles, or physical handling. This approach has helped us cement trust across long-standing client relationships and supported the emergence of new innovations.

    Looking Ahead: The Role of 3-Hydroxypiperidine Hydrochloride

    The demand for reliable building blocks will only grow as more research teams work on challenging targets. Automated platforms, more advanced analytical techniques, and increasingly complex regulatory scrutiny mean no one can afford unreliable intermediates. Our plant operates with these realities in mind; processes are tuned to meet not only today’s requirements but also anticipated shifts in market demands and compliance oversight.

    We see 3-Hydroxypiperidine Hydrochloride as more than just a chemical input. It enables innovation across pharmaceutical, agrochemical, and materials applications. Every batch that leaves our facility is a direct result of decades of accumulated experience, ongoing collaboration with the end user, and a relentless commitment to adapting alongside client needs. This commitment upholds the reliability behind every kilo and ensures that those who depend on this compound can focus on their groundbreaking science, not second-guess the quality of their raw materials.

    Conclusion

    Manufacturing is more than production. It’s stewardship—of quality, of client trust, and of the continuous drive to get things right. 3-Hydroxypiperidine Hydrochloride stands as a testament to what’s possible when rigorous science, direct accountability, and attentive service converge. We earn our place in the supply chain every day by proving, in deed rather than word, that quality and partnership deliver measurable progress in every reaction our materials support.