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HS Code |
625006 |
| Product Name | 1-Boc-2-Methyl-Piperidin-4-One |
| Cas Number | 144282-99-1 |
| Molecular Formula | C11H19NO3 |
| Molecular Weight | 213.27 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 98% |
| Melting Point | 68-72°C |
| Solubility | Soluble in organic solvents (e.g., DCM, EtOAc) |
| Smiles | CC1CC(=O)CCN1C(=O)OC(C)(C)C |
| Inchi | InChI=1S/C11H19NO3/c1-8-6-9(13)7-12(8)10(14)15-11(2,3)4-5/h8H,6-7H2,1-5H3 |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 1-Boc-2-Methyl-Piperidin-4-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle, sealed with a screw cap, and labeled with “1-Boc-2-Methyl-Piperidin-4-One.” |
| Shipping | **Shipping Description:** 1-Boc-2-Methyl-Piperidin-4-One ships in tightly sealed, chemical-resistant containers, protected from moisture and light. The package is clearly labeled according to regulatory standards (GHS/CLP) for non-hazardous chemicals, and shipped via ground or air, prioritizing safe, compliant transit at ambient temperature. Shipping documentation and safety data are included with every order. |
| Storage | 1-Boc-2-Methyl-Piperidin-4-One should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a dry, well-ventilated area, away from incompatible substances such as strong acids or bases. Avoid excessive heat and ignition sources. Proper labeling and adherence to general laboratory chemical storage guidelines are recommended for safety. |
Applications of 1-Boc-2-Methyl-Piperidin-4-One in Industrial ManufacturingAs the original manufacturer of 1-Boc-2-Methyl-Piperidin-4-One, we supply this protected heterocycle to leading chemical producers. This intermediate enables precise functionalization in several high-value synthesis routes. Below are the principal industrial application scenarios with processing and compliance details tailored for formulation chemists and technical buyers. 1. Pharmaceutical Active Ingredient SynthesisOur product holds consistent demand from API manufacturers who use it in multi-step routes to develop piperidine-based drug molecules. Production teams rely on the Boc-protection to manage regioselectivity during N-alkylation and C-functionalization. Following proprietary deprotection, the intermediate advances to the next synthetic stage. Documentation and batch-level traceability support regulatory submissions for finished dosage forms. Industry compliance standards
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2. Advanced Agrochemical SynthesisAgrochemical formulators employ this intermediate in the construction of specialty active molecules with controlled-release profiles. The Boc-protected structure enables site-specific reactions before nitrogen deprotection, minimizing undesired side-products in the synthesis of commercial pesticides and fungicides. Quality teams require analytical documentation for regulatory clearances in major agricultural markets. Industry compliance standards
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3. Fine Chemical Intermediates for Specialty SynthesisCustom synthesis contractors utilize 1-Boc-2-Methyl-Piperidin-4-One as a modular building block in the development of tailored fine chemicals, including chiral auxiliaries and research intermediates. It supports route scouting and scale-up for complex heterocyclic scaffolds where high purity and selectivity are prioritized. Detailed batch records and spectral documentation enable end-users to validate input material quality for subsequent transformations. Industry compliance standards
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4. Custom Synthesis for CRO/CDMO ProjectsContract research and manufacturing organizations (CRO/CDMO) integrate our intermediate in their client-driven route development and scale-up programs. The compound allows for secure introduction of the piperidine core with optional deprotection based on multi-stage synthesis timelines. Documentation of lot-to-lot consistency, impurity profiling, and regulatory declarations are critical to fulfill customer project and audit requirements. Industry compliance standards
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In laboratory and industrial settings, the quest for reliable and versatile intermediates leads time and again to compounds like 1-Boc-2-Methyl-Piperidin-4-One. Produced at scale through careful synthesis, this compound opens new avenues in pharmaceutical development and specialty chemical manufacture. Having spent years refining our process, we see, every day, how its structure and reactivity shape research pipelines and manufacturing routes. Our experience with 1-Boc-2-Methyl-Piperidin-4-One, with its N-Boc protection and methyl group at the second position, has equipped us to address the complexities chemists face.
Sourcing this compound directly from the manufacturing floor avoids issues commonly found with third-party intermediaries. Facilities designed around ISO standards, tight control on temperature, and pure feedstocks ensure consistent appearance and reliability. Over the years, we’ve scaled up from pilot batches to commercial lots, delivering a product that chemists trust to perform as expected across projects large and small. This reliability matters most when new drug candidates depend on the unique characteristics of the piperidinone core.
Every substituent on a piperidinone framework influences reactivity and selectivity. Shifts in electron density, changes to steric bulk, all affect subsequent transformations. The 2-methyl modification on the ring changes behavior in coupling reactions and controls outcomes in asymmetric synthesis. Our team has studied how this subtle alteration, combined with Boc protection, guides the reaction profile toward desired products. This informs choice of solvents, reaction conditions, and downstream purification, benefiting chemists every time they reach for our material.
N-Boc protection provides a stable, removable group that stands up to basic and neutral conditions, yet cleaves under mild acid. Chemists can process 1-Boc-2-Methyl-Piperidin-4-One through multiple steps with confidence the nitrogen will not react prematurely. The result is a practical intermediate, well-suited for stepwise construction of more complex molecules, particularly in drug discovery where protecting groups often make or break a synthetic sequence. We see this in requests for kilo quantities to build combinatorial libraries, as well as gram-scale custom lots for specialty studies.
The process to prepare 1-Boc-2-Methyl-Piperidin-4-One demands more than just following a published route. It draws on years of process optimization: tracking side-products, anticipating variability in raw materials, and devising work-up steps that minimize loss while maximizing purity. In our early days, scale-up revealed bottlenecks that academic write-ups never mention. For instance, controlling moisture during Boc protection minimized hydrolysis, while precise temperature ramps in the ring-forming step limited unwanted dimerization or oligomer formation.
Technicians monitor each phase of synthesis, testing for byproducts and confirming Boc incorporation by NMR and HPLC. We invest in in-house analytics to catch deviations before the final packaging, offering our partners data-backed assurance. Each new batch builds on the lessons of the last. Feedback from medicinal chemists has prompted tweaks to particle size, color, and even packaging options. Supplying 1-Boc-2-Methyl-Piperidin-4-One is a partnership, each batch a collaboration born from two-way communication between bench chemist and manufacturer.
Demand for 1-Boc-2-Methyl-Piperidin-4-One traces to real challenges in modern chemistry, not theoretical speculation. Projects as varied as opioid antagonists, CNS modulators, and antibacterial candidates all depend on building blocks that offer selectivity and flexibility. The 4-ketone moiety invites reductive amination, alkylation, or further elaboration into complex polycyclic scaffolds. Protecting group strategies gain new options with N-Boc, given the ease of deprotection and compatibility with a wide solvent spectrum.
Research chemists favor our material for its reproducible reactivity. The N-Boc group resists side reactions that unprotected piperidinones can succumb to, while the 2-methyl provides a handle for tailored diversification. Some teams build on this compound to access selective dopamine receptor ligands, others use it as a key fragment to introduce chiral centers downstream. In each setting, success depends on starting with a consistent intermediate; surprises in melting point, residual solvents, or color waste weeks of work. We’ve focused our process on minimizing those risks so chemists can focus on innovation.
Several factors distinguish the N-Boc-2-methyl derivative from other piperidinones and similar cyclic ketones. Traditional 4-piperidinones, lacking N-protection, often show instability or unwanted side-reactions early in a synthetic scheme. The 2-methyl variant further resists oxidation and makes the product less hygroscopic, reducing caking in ambient air. Over time, we've documented longer shelf-life in properly sealed containers, a direct benefit for research programs with unpredictable timelines.
Compared to smaller production houses, larger scale enables us to control impurity profiles and particle size distribution. These factors control filtration rates and allow smoother integration into automated systems. Some chemists attempt in-house synthesis, but by the time chromatography, failed workups, and waste management are considered, the value of dedicated production becomes clear. We’ve documented cost savings by supplying ready-to-use batches, freeing up skilled staff to focus on value-added research instead of troubleshooting starting material prep.
Ingredients like 1-Boc-2-Methyl-Piperidin-4-One challenge manufacturers to stay ahead of evolving research needs. New reaction methodologies and regulatory shifts around residual solvents mean yesterday’s standards won’t always satisfy tomorrow’s requirements. Feedback loops drive improvement: our early partners flagged traces of starting amines as problematic in highly sensitive reactions. Working with procurement and QA led to tweaks in our purification, reducing those residuals below the most demanding specifications. Today, each batch is profiled for trace organics and moisture, realigning processes as regulators adjust allowable thresholds.
The technical team remains on call to answer how our process integrates with downstream chemistry. Early concerns about shelf-life in glass versus plastic prompted a switch to higher barrier containers, especially for research sites operating in variable humidity. As part of our commitment to clear technical data, lot-specific documentation covers not just assay and appearance but also nuanced attributes like polymorphism and micro-contaminants. We see this as fundamental, not a favor to our customers, but as the baseline for responsible chemical manufacturing.
Over the years, manufacture of heterocyclic intermediates shifted toward greener methods. Early syntheses for 1-Boc-2-Methyl-Piperidin-4-One involved solvents like dichloromethane and stoichiometric reagents, which presented safety and disposal headaches. Responding to these challenges, process engineers shifted to more benign solvent systems and implemented solvent recovery protocols. Each modification not only improves our own environmental scorecard; it ripples downstream to end users tasked with managing chemical waste.
On the safety side, even seasoned chemists deserve accurate technical detail before using complex compounds. Each drum shipping from our warehouse carries batch-specific safety information and guidance. With close ties to industrial hygiene specialists, we’ve refined handling guidance to minimize exposure risks during weighing and transfer. Past incidents elsewhere highlighted how minor oversights in handling derivatives like ours can delay whole campaigns or trigger expensive clean-ups. Our approach is straightforward: where potential hazards exist, clear data and practical measures reduce them early, saving effort for all parties.
Innovative medicinal chemistry leans on modular building blocks that let chemists assemble and modify molecular scaffolds efficiently. 1-Boc-2-Methyl-Piperidin-4-One stands out as a prime example—a compact, functionally-rich unit incorporated in both early-stage hits and late-stage lead optimization. Sometimes a structure–activity relationship hinges on subtle changes to a ring size or an N-protecting group; our compound enables those decisions without delays. Over several project lifecycles, we’ve seen it move from a narrow research niche into a staple across drug discovery firms and biotech startups alike.
We regularly collaborate with research teams on customized lots, adjusting impurity profiles, and developing formats that streamline integration into automation. Our team maintains a living archive of prior projects, documenting scale-up milestones, pitfalls avoided, and emerging analytical needs. This ongoing dialogue means shipments arrive not just on time, but truly ready for use. In a business where competitive timelines drive success, this responsiveness means as much as any line on a technical data sheet.
For both contract manufacturers and in-house R&D labs, downtime tied to intermediate shortages can stall entire programs. Gaps as short as a few days complicate project planning, strain budgets, and can even impact regulatory timelines. Recognizing this, we built our production cycles to anticipate peaks in demand. Resilient supply chains, buffer stocks, and transparent lead time communication keep projects on track. Our experience shows that, far beyond the purchase price, the true value of a specialty intermediate lies in its guarantee of availability and predictable performance.
In regulated environments, compound traceability and batch-to-batch uniformity support both quality audits and product registrations. We invest in record-keeping that stays with every drum and bottle, so partners meet documentation standards set by regulators worldwide. At multiple steps in the process, automated checks flag variances, prompting real-time interventions, not after-the-fact corrections. This persistence, learned through both routine campaigns and high-stakes custom syntheses, lets our partners forecast with confidence.
No chemical manufacturing project escapes setbacks. Early syntheses of 1-Boc-2-Methyl-Piperidin-4-One taught our staff plenty about process limits. Batch reactions sometimes stalled; subtle shifts in raw material source forced last-minute recalibration. Initially, purification after Boc protection created recovery losses or color impurities that complicated downstream product analysis. Facing these, our technical team worked with reactor operators and bench chemists to map failure points, build corrective protocols, and share lessons across shifts.
Today’s success rides on those lessons. Increasing yields by even a modest percent translates directly to greater security of supply for every partner. Our plant layout, originally suited for a different portfolio, now adapts reactor space and filtration equipment to meet changing project priorities. QC analytics, once performed only at release, now sample intermediate steps as well, flagging risks earlier. The net result: an improved, smarter workflow refining material run after run.
The role of 1-Boc-2-Methyl-Piperidin-4-One will only grow as synthetic routes demand new levels of flexibility and reliability. Platform chemistries tapping into this intermediate expand not only by classical organic means, but via biocatalysis and continuous flow. We’ve invested in parallel route development, simulating different conditions on the same starting lot to supply a broader customer base. Partners exploring new reactivity patterns or alternative protecting groups bring fresh ideas; their curiosity shapes our ongoing process evolution.
Documentation practices now anticipate feedback not just from commercial partners, but from regulatory submissions and environmental reporting. Global changes in supply chain expectations, particularly as regions adopt stricter import controls, place a premium on clear provenance, trace impurity levels, and sustainable production. The flexibility built into our plant from lessons with this intermediate arms us to respond quickly as external requirements shift. We see this as an essential part of manufacturing, not an add-on to our core competency.
Reflecting back on a decade with 1-Boc-2-Methyl-Piperidin-4-One, the advance of synthetic methodology and analytical rigor has turned this molecule into a benchmark for reliability. Our close collaboration with chemists worldwide, direct investment in plant improvement, and strict adherence to evidence-backed process control define what we deliver with each shipment. Every bottle that leaves our facility carries the weight of accumulated experience—decisions made, problems solved, partnerships forged on the solid ground of mutual trust and technical respect.
This journey is far from finished. Chemical manufacturing requires vigilance, adaptability, and an honest reckoning with both strengths and stumbles. For every new project built on the scaffold of 1-Boc-2-Methyl-Piperidin-4-One, we push for higher standards, quicker iterations, and deeper support. Chemistry’s future will demand no less, and we remain committed to rising up alongside our partners in every endeavor.