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HS Code |
181876 |
| Chemical Name | 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester |
| Molecular Formula | C8H13NO3 |
| Molecular Weight | 171.19 g/mol |
| Cas Number | 105-53-3 |
| Appearance | White to off-white solid |
| Melting Point | 58-62°C |
| Solubility | Soluble in organic solvents like methanol and ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Shipping | Shipping of **4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester** is conducted in compliance with chemical safety regulations. The compound is securely packaged in airtight containers to prevent moisture and contamination, and shipped at room temperature. Appropriate labeling and documentation are provided to ensure safe handling, transport, and customs clearance for laboratory and industrial use. |
| Storage | 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Avoid exposure to moisture and incompatible materials such as strong oxidizers. Store at room temperature unless specified otherwise on the manufacturer's label. Always keep out of reach of unauthorized personnel. |
Applications of 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester in Industrial Manufacturing4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester serves as a critical intermediate in advanced synthesis routes across several downstream sectors. As the primary manufacturer, we have observed its broad adoption in regulated and specification-driven production lines that require consistent performance and compliance. Below, we present actual industrial applications, covering key compliance, formulation ranges, process stages, and end products for each field. 1. Pharmaceutical Intermediates for CNS Drug SynthesisDownstream pharmaceutical manufacturers use this material to build complex heterocyclic scaffolds essential to central nervous system (CNS) drug candidates. Its structure enables site-selective alkylation and amide formation for active pharmaceutical ingredient (API) synthesis. Our customers integrate this raw material in the multistep route leading to advanced intermediates for anti-psychotic and anti-epileptic medications, respecting stringent process controls throughout each stage. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisThe ester compound forms a crucial skeleton in the assembly of substituted piperidine rings found in modern agrochemical actives. Agrochemical processors incorporate it in controlled-scale synthesis lines, targeting insecticides and plant growth regulators. The raw material supports high-purity technical grade outputs by delivering reliable conversion yields under well-defined reaction conditions. Industry compliance standards
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3. Specialty Polymer Modifier ManufacturingIn specialty polymer processing, downstream producers employ this chemical as a niche modifier for engineering thermoplastics and coatings. Its molecular structure imparts controlled polarity and enables further functionalization for improved surface adhesion, flexibility, and chemical resistance in polyamide and polyurethane systems. Use of the ester is closely monitored to maintain reproducibility and conformity with end-use certifications. Industry compliance standards
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4. Building Block for High-Performance Organic SynthesisThe compound operates as a foundation in the synthesis of advanced organic molecules for fine chemicals and performance additives. Custom synthesis houses and research-driven manufacturers utilize this ester to construct piperidine-based frameworks for catalysts, colorants, or specialty reaction intermediates, achieving high selectivity and targeted reactivity. Industry compliance standards
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5. Intermediate for Peptidomimetic Compound SynthesisPeptide pharmaceutical developers and contract research organizations leverage this material in the construction of peptidomimetic structures, substituting for standard amino acids to enhance compound stability and target receptor interaction. Controlled input and process analytics define its role, ensuring quality at every transformation from oligomer formation to final coupling. Industry compliance standards
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6. Intermediate for Functional Dyes and Pigment SynthesisProducers of high-grade specialty dyes draw on this compound for the formation of modified piperidine rings that enhance color stability and fastness in textile and ink formulations. The ester enables tailored nucleophilic substitution and condensation reactions essential for manufacturing heat- and light-stable dye molecules under tightly controlled plant conditions. Industry compliance standards
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In the fine chemicals industry, we often focus on reliability, purity, and process readiness. 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester, also recognized by its model code OPC-3-CAEE, stands out as a key intermediate. Years of manufacturing this compound have shown that it consistently delivers more than just high-grade material to our partners; it drives progress for chemists looking to build advanced molecules with fewer headaches.
Producing OPC-3-CAEE is not about churning out large volumes—it’s about securing tight specifications batch after batch. This ester, with a molecular formula C8H13NO3, offers both the flexibility needed for diverse reaction planning and a dependable foundation for pharmaceutical and research applications. The ethyl ester group confers increased solubility in organic solvents, allowing more straightforward handling during multi-step synthesis. Our teams track every critical variable on the production line, from the temperature intervals during cyclization to the purity achieved after final distillation. We’ve found that yields only matter when the product performance matches or exceeds expectations in downstream use.
A bench chemist might look at OPC-3-CAEE as just one more intermediate. Walk into a kilo lab or a pilot reactor suite, and you realize it’s a pivot point in many synthetic routes. Structure-wise, that oxo-piperidine ring anchors stability and reactivity in a way that other cyclic compounds often can’t. It takes stress out of subsequent coupling reactions, giving chemists a break from re-doing purification or troubleshooting inconsistent performance.
Through years on the plant floor, we’ve noticed that shifting from piperidine carboxylic acids in their free form to the ethyl ester derivative cuts unnecessary bottlenecks. Free acids sometimes trap unwanted water and pull in impurities at unexpected stages. OPC-3-CAEE addresses this; the esterification provides better shelf life and less tendency to hydrolyze when stored in correctly sealed containers. Our direct customers in API and agrochemical development point to this property as a deciding factor between meeting delivery deadlines and missing them.
As someone who has supervised many production batches, I can tell you that quality does not come from paperwork but from repeated, real-time observation and process refinement. We’ve set our purity benchmarks for 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester at 98% or higher (by HPLC). Prioritizing dryness and minimal residual solvents, we move quickly from final distillation to hermetic packaging. Each lot moves directly to a monitored storage environment because small lapses—humidity spikes, temperature drops—can impact both crystallinity and downstream usability.
This compound generally appears as a pale white to off-white crystalline solid, and we found over time that maintaining consistent morphology simplifies subsequent weighing, dissolving, and filtration on your end. During packaging, our technicians inspect for caking or discoloration, recognizing that even subtle appearance changes can signal unwanted side reactions or by-products from the final step.
The synthesis of OPC-3-CAEE traces back to foundational work in piperidine derivatives chemistry. In our facilities, the biggest hurdles rarely come from exotic chemistry—they come from reproducibility at scale. We’ve adjusted batch reactor agitation rates, optimized esterification agent addition profiles, and developed in-house GC-MS methods to track minor impurity profiles that standard catalogs rarely report. These tweaks come from the troubleshooting mindset you earn through years of hands-on work, not from documentation alone.
One of our key observations lies in the exit purity after work-up. Earlier in our production history, small temperature surges during final evaporation caused side-product accumulation that only appeared months later in customer feedback. Installing improved thermal sensors and adjusting ramp rates brought those under control. Now, each lot’s impurity pattern stays within tight windows, reducing the risk of headaches both for us and for synthetic chemists downstream. We have also learned to be cautious about the raw material provenance. Even the best esterification catalysts can be hampered by low-grade piperidine sources, so each lot undergoes screening before synthesis.
Not all cyclic carbons offer the same reliability in reaction development. OPC-3-CAEE distinguishes itself from other piperidine-based esters and acids by offering unique stability in the face of harsh conditions. Compared to methyl or tert-butyl esters, the ethyl ester brings a balance between rate of hydrolysis and workable shelf life. While tert-butyl esters might prolong storage, their de-protection often demands more aggressive conditions, introducing risk of damaging fragile substituents elsewhere in your target molecule.
The 4-oxo function at the ring creates a specifically reactive site for condensation, alkylation, or amide formation. Not every piperidine carboxylic acid, even as an ester, matches this pattern. Many product developers initially try standard carboxylic acids and pivot back to the ethyl ester after struggling with solubility issues or sluggish kinetics. Our regular research collaborators tell us OPC-3-CAEE shortens their overall synthesis by one or two steps compared to the direct use of free acids or piperidine-3-carboxylic acid methyl ester.
Companies looking for kilo-scale orders ask us about consistency between batches. For OPC-3-CAEE, this extends to exact melting point windows, moisture content, and residual solvent levels. We run each batch under the same reaction parameters logged during scale-up validation. This kind of repeatability reassures process engineers aiming for regulatory approval on their own end products.
One example stands out: a pharmaceutical startup aimed to integrate OPC-3-CAEE as a building block for a new CNS-active compound. Early attempts with off-the-shelf material from general resellers stalled at yield variability and inconsistent by-product profiles. We offered material with certified impurity maps and tailored particle size. They reported conversion rates rose by almost 20% and purification times dropped sharply, getting their process development timeline back on track. This may sound straightforward, but it represents years of commitment at the manufacturing level to detail, troubleshooting, and supply chain vigilance.
Many requests come in from partners who want subtle changes—sometimes a tweak in particle size, sometimes a tighter limit on by-products after esterification. Manufacturing directly means we can redesign part of the protocol for targeted requirements. We know that even small traces of unreacted acid or starting amine lead to unexpected chromatographic tailing or loss in yield; the solution is to build process windows with actual downstream chemistry in mind, not just box-checking a generic spec list.
Another industry demand focuses on handling and packaging for air- and moisture-sensitive operations. Large volumes sit in climate-controlled drums with nitrogen blanketing, while smaller research packs use vacuum-sealed, double-lined bags. These decisions evolved over time with direct input from users who saw real-world impacts—clumping, minor hydrolysis, or inconsistent dosing in automated equipment.
Producing 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester at industrial scale means paying special attention to cleanroom protocols and chemical containment. The raw materials, boron-based catalysts, and piperidine derivatives all demand careful handling. We maintain sealed lines and closed containment vessels during reaction and workup, minimizing exposure to operators. Feedback cycles emphasize cross-checking batch numbers with production records and the latest lab data before any product exits our gates.
Years spent in manufacturing have taught us to adapt quickly to new analytical techniques developed at the customer level. New mass spectrometry methods or impurity quantification routines, once shared back to us, feed into our next round of quality and process controls. It’s a two-way street: we learn from every round of customer validation, and operational procedures continue to evolve. The resulting improvements often benefit all customers, not just those who flag a challenge for one project.
As the landscape shifts toward green chemistry and higher throughput drug discovery, the bar rises for every intermediate we produce. For 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester, new chemistries put greater strain on purity, traceability, and waste minimization. We installed solvent recovery units over the past two years—cutting down emissions and yielding a more sustainable process cycle. In the lab, new detection hardware picks up minor off-color impurities that went unnoticed before. Every major upgrade followed either an operator’s suggestion or a key customer’s input after extended trial batches.
Our responsibility as a manufacturer means regular investment in batch records, training, and process documentation. The days of loose records and “good enough” approaches are fading. Our technicians and engineers now cross-verify each analysis and double-check each loading. Buying our materials lets customers build greater confidence into their own process validations and risk assessments.
Building reliable pipelines for chemical innovation starts with dependable, transparent manufacturing. 4-Oxo-Piperidine-3-Carboxylic Acid Ethyl Ester draws its value not just from a chemical blueprint but from the teams and systems that shape each batch. Every decision along the production line—refining purification steps, monitoring impurity maps, integrating smarter detection tools—is rooted in lived experience and direct feedback from the laboratories our products support.
For synthetic researchers, process engineers, and pilot plant operators, OPC-3-CAEE offers more than a reagent; it’s a platform for building increasingly complex chemical architectures. Consistency, clarity in specification, and ongoing supply chain management define its true impact. Our drive to refine every step of production turns a single piperidine derivative into a dependable cornerpiece for modern synthesis. In a world pushing the edge of chemical invention, details like these mark the difference between forecasted timelines and actual results.