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HS Code |
721723 |
| Product Name | Benzyl 4-Hydroxy-1-Piperidinecarboxylate |
| Molecular Formula | C13H17NO3 |
| Molecular Weight | 235.28 g/mol |
| Cas Number | 57716-12-6 |
| Appearance | White to off-white solid |
| Melting Point | 77-79°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Storage Conditions | Store at 2-8°C, dry and away from light |
| Chemical Structure | Benzyl carbamate ester of 4-hydroxy piperidine |
| Smiles | O=C(OCc1ccccc1)N2CCC(CC2)O |
| Inchi | InChI=1S/C13H17NO3/c15-11-7-10-14(8-9-11)13(16)17-12-5-3-2-4-6-12/h2-6,11,15H,7-10H2,1H3 |
As an accredited Benzyl 4-Hydroxy-1-Piperidinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of Benzyl 4-Hydroxy-1-Piperidinecarboxylate, labeled with hazard information and batch details. |
| Shipping | Benzyl 4-Hydroxy-1-Piperidinecarboxylate should be shipped in tightly sealed containers, protected from light and moisture. It must be packaged according to relevant safety regulations, with appropriate labeling and documentation. During transit, keep it at room temperature, away from incompatible substances. Ensure compliance with local and international hazardous materials shipping guidelines. |
| Storage | Store Benzyl 4-Hydroxy-1-piperidinecarboxylate in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from light and moisture. Use in a chemical fume hood, and ensure all safety procedures are followed during storage and handling. |
Applications of Benzyl 4-Hydroxy-1-Piperidinecarboxylate in Industrial ManufacturingAs a dedicated chemical raw material manufacturer, we supply Benzyl 4-Hydroxy-1-Piperidinecarboxylate to advanced industrial sectors with trackable application value. Our technical support and process knowledge enable downstream partners to maximize performance, regulatory compliance, and production efficiency in key areas. Below is an overview of the compound’s validated roles across specific industries. 1. Pharmaceutical Intermediate for Piperidine-based APIsPharmaceutical syntheses frequently adopt Benzyl 4-Hydroxy-1-Piperidinecarboxylate as a critical intermediate in manufacturing antihistamines and CNS agent APIs, such as piperidine-based antipsychotics. This compound’s functional group profile supports targeted transformations in key step reactions regulated under stringent cGMP and ICH Q7 guidelines. End uses focus primarily on prescription medications with established active molecular scaffolds. Industry compliance standards
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2. Chemical Building Block for Custom Fine ChemicalsContract development and manufacturing organizations (CDMOs) and specialty chemical producers utilize this piperidinecarboxylate derivative as a functionalized scaffolding unit in assembling fine chemicals, including halogenated intermediates and custom ligands for agrochemical discovery. In these applications, rigorous adherence to ISO-certified QA systems underpins batch consistency and audit traceability. Industry compliance standards
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3. Functional Component in Agrochemical SynthesisProducers of crop protection active ingredients integrate Benzyl 4-Hydroxy-1-Piperidinecarboxylate as a functional amine source during the development of specialty herbicides and insecticides. Emerging regulatory frameworks, especially Europe’s PPP (Plant Protection Products) standards and China’s ICAMA protocols, require close attention to batch traceability and impurity profiling for all intermediates. Industry compliance standards
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4. Precursor for Specialty Polymer and Resin ModifiersHigh-performance polymer blends and thermosetting resins sometimes employ this compound as a reactive modifier, especially in developing piperidine-based hardeners and chain extenders for specialty polyurethanes or epoxy systems. Polymer formulators select this intermediate for its defined piperidine functionality, supporting targeted property enhancements per UL or EN polymer industry testing regimes. Industry compliance standards
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5. Key Intermediate in Custom Fragrance and Aroma ChemistryIndustrial fragrance houses employ Benzyl 4-Hydroxy-1-Piperidinecarboxylate as a backbone intermediate in synthesizing aroma chemicals and fixatives with piperidine features. This step ensures compliance with international fragrance association purity and safety requirements, alongside strict limits on trace impurities designated by IFRA standards. Industry compliance standards
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Benzyl 4-Hydroxy-1-Piperidinecarboxylate has seen a quiet but steady rise in the portfolio of intermediates used for pharmaceutical research and fine chemical synthesis. As the manufacturer who actually carries out the reactions, runs the purification, and bottles the final compound, our insights into this material go far beyond what a catalogue or distributor’s page might say. There’s plenty of background behind each batch, each improvement, and each observation made during daily production. In this commentary, I’ll spell out what sets this compound apart, how our team approaches quality, and what it means for real-world labs that use or compare Benzyl 4-Hydroxy-1-Piperidinecarboxylate with similar molecules.
Working directly with Benzyl 4-Hydroxy-1-Piperidinecarboxylate, we have come to respect its unique niche. The compound’s structure—a benzyl ester linked to a 4-hydroxypiperidinecarboxylate backbone—offers a distinct profile of reactivity, solubility, and downstream value in synthetic routes. It has become a staple for those pursuing the development of central nervous system drugs or advanced intermediates in heterocyclic chemistry. That’s not an accident. The benzyl protection confers useful properties during multi-step synthesis, especially for researchers aiming for selectivity when modifying the piperidine ring.
We see scientists choosing this intermediate over other piperidine esters precisely for its stability under certain reaction conditions. The benzyl group can be gently removed by catalytic hydrogenation, a mild and highly predictable transformation. A few years ago, one of our regular customers shared their work optimizing the synthesis of a proprietary API, and Benzyl 4-Hydroxy-1-Piperidinecarboxylate solved their challenge where methyl or ethyl esters fell short—the selectivity during deprotection and the cleaner removal of the benzyl group paid dividends that a less-experienced supplier wouldn’t notice.
Every stage—starting material assays, reaction monitoring, purification choices—shapes the final product’s utility and consistency. Out of the various lot numbers we've produced, the ones that win customer praise usually trace back to raw materials we triple-check. There isn’t just a checklist; it’s hands-on. I’ve spent time on the prep bench scrubbing glassware or logging HPLC runs late into the evening, chasing a stubborn side product, because I know the headaches those residuals cause during scale-up at the customer’s plant.
Our reactors have seen hundreds of batches. That means we catch subtle shifts: a new supplier on benzyl alcohol, a change in the catalyst source, or just humidity creeping in at the drying step. More than once, tiny tweaks delivered noticeably purer lots, easily passing the NMR and GC-MS specs research chemists depend on. I recall one run where trace acid from the initial condensation threatened to depress yield at scale, so we implemented a non-trivial modification—switching the order of quenching steps and extending filtration time. That difference didn’t show up on the spec sheet, but it meant researchers downstream avoided headaches.
Comparing Benzyl 4-Hydroxy-1-Piperidinecarboxylate to its cousin compounds, we notice several practical differences. The benzyl ester variant delivers slower hydrolysis kinetics in aqueous buffers, giving chemists a useful lever for temporary protection schemes. You don’t get as much leeway when using methyl or ethyl esters, which tend to succumb to base or acid much more quickly. This property shapes how scientists design their steps—especially in projects dealing with fragile or highly functionalized intermediates.
Over years of production, we’ve learned to appreciate nuances in each lot—variations in appearance, flow properties, and even odor signals hidden impurities or slight changes in reaction efficiency. The off-white to pale yellow crystalline look marks a quality batch, and any stickiness or discoloration means going back to examine solvent grades and temperatures for the re-crystallization. We track our own statistics: pourability, filterability, and solvent retention, because no matter what the certificate says, laboratory staff have to physically use the material. Every technician has had the experience of battling a clumpy, hard-to-weigh solid, so we pursue physical consistency as much as purity.
Every shipment leaves with a specification sheet, but the real work lies in living up to more than just the stated purity. Our GC and HPLC records regularly exceed 98% area purity, but we don’t rest at that number. Each customer and every application puts its own emphasis: some want the lowest possible water content for sensitive coupling reactions, others want smooth filtration to avoid losses after saponification. We keep a long-form history on solvent residues, knowing that a little leftover toluene or methanol, even within limits, may affect chromatographic separations or later hydrogenations.
True performance emerges during real-life application. A kilo-scale end-user once called with a complaint about unexpected foam in their dissolution step—the culprit was a barely perceptible trace amine impurity, amplified at scale. That day reminded us to push the limits on side-chain neutrality during the last workup, even if most small-scale researchers would never see the problem. Repeated analysis and minor changes in aqueous extractions led us to improve downstream yields and save colleagues hundreds of hours. Crystalline grade, sub-1% moisture, negligible color—as a producer, those are points of pride, and our notes always include direct staff observations, not just automated printouts.
In real-world organic synthesis, the utility of Benzyl 4-Hydroxy-1-Piperidinecarboxylate isn’t measured by generic textbook metrics. It’s the in-lab feedback that guides us. The bulk of our customers use this material in intermediate steps toward piperidine-based APIs or research ligands. We’ve helped scale this product from 100 g trial batches in a university fume hood to industrial campaigns of several hundred kilograms. Certain projects focused on total synthesis routes where regioselective protection of the 4-hydroxypiperidine ring paved the way for multiple further elaborations, particularly in chiral drug targets. Every scale brings new hurdles—vacuum filtration goes from hand-poured Buchner funnels to automated Nutsche filters, and every adjustment downstream affects how researchers can work.
Many experienced researchers comment on the reliability in catalytic debenzylation—benzyl removal under hydrogen at low pressure with standard palladium catalysts avoids over-reduction of sensitive adjacent groups. Comparatively, methyl or ethyl groups need harsher conditions for cleavage, risking broader side reactions. Several partners relayed stories where switching to our Benzyl 4-Hydroxy-1-Piperidinecarboxylate unlocked a previously intractable synthetic sequence, simply because the final step became gentler, higher yielding, and easier to purify.
We deal with questions about differences between this material and other 4-hydroxypiperidine esters almost daily. Most stem from practical constraints in the lab. Benzyl esters give a stability edge for complex multi-step syntheses, lining up neatly with protecting-group strategies across heterocycle chemistry and advanced medicinal chemistry projects. On the other hand, simple alkyl esters offer faster cleavage times but trade away stability during storage and prolong purification steps.
Every batch that leaves our hands contains years of cumulative knowledge. We’ve hammered down sources of batch-to-batch color variation and tracked them back to fractional milliliter shifts in solvent swap-outs. While some may consider appearance a minor concern, the reality is that visible differences signal deeper issues that often only come out at scale. When a batch suddenly becomes more hygroscopic, customers pick up the phone—they rely on our insights to troubleshoot whether drying temperature, crystallization rates, or atmospheric exposure explain the change. Our records, including dozens of production logbooks and years of retained samples, let us trace trends and answer these questions with evidence.
Recent trends in the pharmaceutical industry push for higher transparency and traceability. Our in-house analytical lab has grown to handle new demands: full trace metal analyses, expanded impurities testing, and more robust stability studies. Now, projects receiving Benzyl 4-Hydroxy-1-Piperidinecarboxylate increasingly cite ICH guidelines in their documentation, and we field requests for reactivity profiles under specific forced-degradation conditions. Instead of considering this a burden, we see a chance to show what direct experience in synthesis and handling brings. We don’t outsource development or quality control—our hands-on approach means that we adapt methods and run custom verifications as requests evolve.
There is no shortcut for long-term customer trust. We've seen customers return year after year because they know the team, recognize actual faces, and receive support far beyond what an anonymous order desk provides. That rheological problem with viscous filtrate last autumn? Our QA supervisor remembers the issue and can recount not only the lab fix but also the day it happened, who noticed, and how it was blocked in subsequent campaigns.
Many outside the synthetic chemistry field underestimate the cumulative impact of small process changes on Benzyl 4-Hydroxy-1-Piperidinecarboxylate. Over time, we have shifted from batch distillation under nitrogen to continuous solvent recovery, reducing thermal stress on intermediates and lowering unwanted discoloration. These changes came directly out of observations made by seasoned plant operators—not from consulting firms or generic best-practices documents.
As an organization relying on legacy and modern equipment, we routinely balance reactor throughput and safety. Each time we observe a rare impurity that only shows in long-hold reactions or seeers during transfer, it gets analyzed, catalogued, and factored into subsequent procedures. This internal database becomes invaluable for troubleshooting not just our process, but those of every customer who needs to use Benzyl 4-Hydroxy-1-Piperidinecarboxylate for their own route development or kilo-scale manufacture. Over decades, our focus has shifted—early years emphasized yield, but now customer feedback has made us raise the bar for consistency, ease of handling, and in-process predictability.
Solving issues stemming from Benzyl 4-Hydroxy-1-Piperidinecarboxylate use means listening to researchers and process chemists every day. Some challenges arise in coupling reactions where trace acid or water throws off sensitive downstream steps. We offer not just quality documents but also recovery suggestions, alternate drying conditions, and, for advanced users, nonstandard analytical data. Some clients want to trap every last fraction post-filtration or request process audits; we work with them at the bench or on the phone, using our own archived samples to support troubleshooting.
As the direct producer, we rarely face insurmountable issues. Scaling up makes every minor variability more obvious, so we advise rigorously documenting all procedures—recording every deviation, change in supplier, lot number, or environmental factor. Over the years, these notes have paid enormous dividends—reducing scrap, improving downstream product quality, and cutting time to market for our partners. One longtime collaborator credits process transparency with improving their FDA filing, since comprehensive documentation now starts at the raw material, not the API stage. That’s only possible through continuous communication with the manufacturing team.
Selecting Benzyl 4-Hydroxy-1-Piperidinecarboxylate over structurally similar compounds involves more than reading off the chemical name or the analytical data. Customers with experience in synthetic scale-up ask the hard questions up front: what are the by-products, is there a trend in residual benzyl alcohol content after storage, how does the crystalline form perform in real filtration? We’ve fielded questions about polymorph stability, photodegradation under ambient light, and the best solvent for dissolution before incorporation in a stepwise route.
Each answer traces back to hundreds of batches, customer trials, and in-house experiments. We have learned what small imperfections lead to headaches, so we report honestly whether a given lot leans towards fine or coarse particle size, and which handling quirks arise. Several clients discovered, mid-project, that switching from methyl to benzyl esters in their scheme reduced decomposition during late-stage steps, increased overall yield, and reduced column purifications needed. Experiences like these help other researchers avoid costly dead-ends and highlight where Benzyl 4-Hydroxy-1-Piperidinecarboxylate’s specific profile excels.
We’ve seen the market—and regulations—evolve. Sustainability pressures prompt more careful solvent recovery and greener chemistry choices, where possible. Our own protocols now emphasize reduced waste, safer handling of residual solvents, and minimized process emissions. This translates into fewer complaints, improved environmental profiles, and, over time, more affordable products for researchers and manufacturers alike. As suppliers of Benzyl 4-Hydroxy-1-Piperidinecarboxylate, these patterns push us to re-examine not just cost or specification sheets, but every step along the production cycle.
We share our findings with other chemists—whether it’s a warning on temperature sensitivity during storage, notes on safe handling of fine dusts, or suggestions on minimizing unwanted hydrolysis during sample preparation. Discussions with other manufacturers, regulatory bodies, and universities have improved both our in-house methods and the outcomes for our users. These conversations don’t come from marketing—they follow after solving real issues, testing new routes, and repeatedly validating improvements.
Years on the floor, in the lab, or working with partnering organizations have taught us that chemicals such as Benzyl 4-Hydroxy-1-Piperidinecarboxylate aren’t just items on an inventory. For us, they serve as ongoing listening posts to industry trends, vehicles for collaboration, and challenges that test both technical skill and communication. Every day brings questions from real labs about improved isolation, alternative solvents, or side reactions. Our answers are grounded in what has worked—and what still needs work—based on both success and hard-learned mistakes.
By producing Benzyl 4-Hydroxy-1-Piperidinecarboxylate ourselves, and supporting it from materials sourcing to shipment, we engage with the researchers actually using it. We believe this hands-on approach sets real manufacturers apart from resellers who may never set foot in a synthesis suite. Our perspective doesn’t just shape products; it shapes future ideas, methods, and the success of everyone working to advance innovative chemistry.