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HS Code |
382027 |
| Product Name | 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal |
| Molecular Formula | C10H17NO4 |
| Molecular Weight | 215.25 g/mol |
| Appearance | White to off-white solid |
| Cas Number | 180548-29-0 |
| Solubility | Soluble in water and most organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C (Refrigerated) |
| Chemical Class | Protected amino acid derivative |
| Smiles | NC1CCC(C(=O)O)C(C1)=O.OCC(OCC)O |
| Synonyms | Ethylene ketal of 1-amino-4-oxocyclohexanecarboxylic acid |
As an accredited 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is securely sealed in a 25g amber glass bottle with tamper-evident cap, labeled with chemical name, batch number, and hazard symbols. |
| Shipping | 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal is shipped in tightly sealed containers to prevent moisture and air exposure. Transport is typically conducted under ambient conditions unless otherwise specified. All shipments adhere to relevant chemical transportation regulations, including labeling and documentation for safe handling and compliance with local and international shipping standards. |
| Storage | Store **1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal** in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from strong oxidizing agents and acids. Recommended storage temperature is 2–8°C (refrigerator). Always follow appropriate safety procedures, including the use of gloves and protective eyewear, when handling this compound. |
Applications of 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal in Industrial ManufacturingAs a specialized manufacturer, we supply 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal for targeted use in chemical synthesis, active ingredient production, and advanced polymer systems. Below is a detailed overview of several direct downstream application sectors, including industry-specific requirements on regulatory compliance, formulation ratios, line-integration stages, and the typical end products manufactured using this material. 1. Pharmaceutical Intermediate for Peptide SynthesisPharmaceutical manufacturers incorporate this material as a key intermediate in complex peptide synthesis—especially for novel cyclic peptide analogues and APIs. Its unique protected amine and carboxylic acid functionalities help streamline multi-step reactions, promoting efficient building block assembly and minimizing by-product formation. Facilities integrate it primarily at initial condensation steps, leveraging its selective reactivity under controlled solution-phase or solid-phase methods. Industry compliance standards
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2. Building Block in Fine Chemical SynthesisChemical manufacturers utilize this specialty acid as a precise intermediate when engineering small-molecule fine chemicals, including chiral auxiliaries and cyclohexanone derivatives. Its ethylene ketal protection allows easy handling and selective deprotection, vital for multi-step syntheses that demand exact stereocontrol and functional group compatibility. This material supports high-purity product isolation at desired steps, reducing downstream purification requirements and overall cycle time. Industry compliance standards
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3. Monomer for Specialty Polyamide ProductionPolymer chemists employ this protected amino acid derivative as a niche monomer for engineering polyamides with defined ring-structured motifs. Its protected form prevents premature cross-linking and supports step-growth polymerization in melt or solution processes, prior to controlled deprotection and imidization. This approach ensures high molecular weight development, reproducible polymer architecture, and facilitates further functionalization downstream. Industry compliance standards
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4. Advanced Intermediate for Agrochemical SynthesisAgrochemical companies incorporate this cyclohexane-based intermediate into synthesis routes for new-generation pesticides and plant growth regulators. The ethylene ketal-protected form confers chemical stability during the stepwise introduction of functional groups, especially for developing active ingredients requiring ring rigidity and differentiated side chains. It performs as a controlled-release core substrate or as part of multi-functional active ingredient synthesis in strictly regulated batch processes. Industry compliance standards
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5. Intermediate for Fragrance and Flavor Compound SynthesisFine fragrance producers and flavor compound manufacturers utilize this ketal-protected cyclohexanecarboxylic acid as a masked intermediate for developing saturated cyclic ring compounds that serve as aroma impact molecules. The stable ethylene ketal enables selective transformations—like alkylation, reduction, or esterification—without premature ring opening, offering precise control over isomer formation and supporting purity requirements for both cosmetic and food-grade markets. Industry compliance standards
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Long experience has taught our team that every step in the manufacturing of specialty amino acids requires close attention to consistency, reliability, and quality. For chemists seeking to add complexity to molecular scaffolds or introduce protecting groups efficiently, a reagent with the right balance of stability and reactivity stands out. 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal belongs in this category, opening new doors for design in research labs as well as production processes.
With the systematic name corresponding to its core cyclohexanecarboxylic acid structure, this compound introduces both amino and ketal functionalities. The ethylene ketal group, anchored to the cyclohexanone moiety, protects the underlying carbonyl group during synthetic work. By including an amine and a carboxylic acid in the same molecule, the material brings a range of options for downstream chemistry: peptide coupling, amide formation, reductive chemistry, and further modifications.
As a manufacturer who controls every stage of synthesis, we focus on delivering batches with narrow purity windows, using only verified raw materials and thorough analytical follow-through. The typical assay for 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal measures above 98% by HPLC, while moisture and residue-on-ignition benchmarks fall within tight parameters. The technical team carefully verifies the intermediate and final product at multiple points using HNMR, IR, and mass spectrometry, which lets us catch any byproducts before they reach customers.
We ship the product as a white to off-white crystalline solid. Standard packaging minimizes exposure to air and moisture, since the integrity of the ethylene ketal group relies on dry storage conditions. For packaging, we work with solid HDPE or amber glass, tailored to safeguard the ketal protecting group while keeping transport easy from lab to lab. Batch-to-batch variations remain minimal due to our production controls, and all lots come with full analytical documentation on request.
Researchers and process chemists who handle sensitive carbonyl compounds often need to mask certain groups in early synthetic stages, then reveal them again under specific deprotection conditions. In practice, the ethylene ketal on this molecule performs effectively as a protecting group for the cyclohexanone core. Many of our partners in pharmaceutical R&D select this derivative to prevent undesired side-reactions that would otherwise affect the parent ketone or carboxylic acid functions.
One clear advantage arises during multi-step synthesis: without a protecting group, cyclohexanone rings face nucleophilic attacks or enolization, especially under harsh conditions needed for coupling the amino moiety to other fragments. The ethylene ketal group improves resistance to those conditions—holding the structure intact until selective cleavage is required. Customers in the peptide and advanced intermediate sectors often remark that this feature lets them avoid yield loss and multiple purification cycles.
Deprotection is easily handled with mild acid, which saves both process time and the need for exotic reagents. Lab-scale and pilot manufacturing reports confirm fewer impurities after ketal removal, since the group comes off cleanly and leaves a standard cyclohexanone for further extension or ring contraction reactions.
Commercial cyclohexanecarboxylic acid derivatives differ in several ways that matter to practicing chemists. When comparing this ethylene ketal-protected form to plain cyclohexanone or -carboxylic acid derivatives, the protected group presents a tangible benefit. The compound we produce handles exposure to basic and nucleophilic reagents that would otherwise damage a free ketone, enabling more robust synthetic routes.
Other protecting groups, such as diethyl ketals or acetal variants, often break under conditions where the ethylene ketal endures. Based on hands-on feedback from process chemists, our ketal derivative offers greater selectivity in sequential reactions. Some alternative amino-cyclohexanecarboxylic acid compounds lose the delicate balance between stability and accessibility, but the ethylene ketal allows selective unmasking, extending the usability for both protection and deprotection strategies.
Unlike many bulk chemicals or inexpensive building blocks, our product arrives with full traceability and batch documentation—an essential requirement in regulated or high-specification sectors. In-house retention samples and analytical archives ensure that queries concerning batch consistency or product drift can be resolved rapidly without guesswork. This approach distinguishes materials built for rigorous synthetic work from general-purpose reagents.
Much of the engagement around 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal happens at the intersection of medicinal chemistry, process development, and pilot plant operations. For scientists working in drug discovery, the molecule gives a reliable scaffold for amide bond formation, cyclization, and heterocycle construction. The protected ketone enables flexible synthetic planning, whether the route aims for linear peptides, macrocycles, or other advanced targets.
Custom synthesis teams frequently use this building block for constructing analogs of lead compounds. Each batch runs through our pilot reactors and purification columns, mimicking the exact conditions faced in scale-up. This practice leads to less troubleshooting and fewer delays as chemistry moves from milligram to kilogram lots.
Scale-up work requires predictable reaction profiles and low byproduct formation. Over several years, our technical team has dealt directly with project chemists to fine-tune the physical characteristics of this product—making sure it dissolves quickly in typical organic solvents and handles smoothly, even at higher concentrations. Routine pilot plant trials confirm batch reproducibility, an asset that lowers total cost for downstream users.
Our team maintains a feedback loop between laboratory, pilot, and quality control groups. This structure ensures that our analytical process not only meets regulatory standards but also continuously adapts to the requirements of evolving chemistries in the field. Customer-driven assays, including impurity profiling and chiral analysis, guide incremental product improvements and help maintain leading-edge relevance in the sector.
Degradation studies run regularly on retained lots, confirming that the ethylene ketal resists most hydrolysis and byproduct formation, so shelf-life remains predictable. Routine side-by-side trials with earlier-generation materials show fewer hydrolytic side products, particularly in humid climates or during repeated handling. These checks tie production directly to chemical realities in end-user labs—not abstract benchmarks.
Chemical supply can hinge on everything from global logistics to the reliability of source materials. To secure continuity, each batch of 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal comes from documented synthetic lots, always managed in-house from initial charge to final packaging. We never rely on toll manufacturing or external purification for critical intermediates, sidestepping the compliance and traceability gaps that can emerge elsewhere.
The purity of raw inputs directly affects the final product. Raw material sources pass strict audits; our documentation logs each transfer and process modification. This transparency guards against drift in quality and ensures all feedback—positive or negative—feeds back into manufacturing protocols.
Our manufacturing process emphasizes recovery of solvents, reduction of waste streams, and containment of process emissions. Newer iterations of our synthetic route recover and recycle both organic solvents and water washes, lowering overall environmental footprint. Lesser reliance on one-time-use reagents and greater focus on filterable catalysts have both improved waste handling and operator safety.
We continually audit both upstream and downstream stages of production for environmental impact, working towards improved atom economy and fewer process steps. Trials with greener solvents and alternative energy sources—confirmed by pilot runs—feed directly into scheduled upgrades at the main plant. Some downstream partners have integrated our findings as part of their own sustainability reporting.
Every manufactured lot reflects years of practical experience in fine chemical synthesis and bulk handling. While the structure and utility of 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal depend on robust scientific principles, its usefulness finds real-world support from direct application data, customer research, and the lessons learned from troubleshooting. Beyond analytic control or process optimization, confidence in this product stems from dozens of collaborative projects and tangible advances in yield and selectivity across several fields.
As a supplier who operates synthesis, purification, and audit functions under one roof, we take a long view—investing in both the people and the technology that deliver specialty reagents with evolving needs in mind. Our material has supported both short tactical campaigns in medicinal chemistry and planned multiton campaigns for advanced chemical manufacturing. Without continual two-way communication with field chemists and production engineers, none of this progress would have been possible.
We encourage chemists—whether in academic settings or industrial labs—to reach out with new ideas, process feedback, or special project needs. Insightful feedback from customers over years of partnership has pointed the way to higher-purity batches, more consistent particle properties, and packaging protocols that withstand even the most demanding transport routes. Adjustments to drying, screening, and final quality verification all trace back to real-world uses, not hypothetical guidelines.
Some customers rely on us for rapid turnaround on kilogram lots; others seek small batches for intensive method development. Our experience in balancing these needs has taught us that responsiveness trumps automation, and that every modification has to stand on a foundation of proven chemistry as well as practicality.
The goal is not simply to deliver a compound, but to cultivate reliability. Through continuous dialogue with process engineers and R&D scientists, improvements move quickly from pilot trials to standard production. Our plant maintains detailed records to track new synthetic routes, process bottlenecks, and user feedback. This culture of candor has led to both technical refinements and improved scheduling accuracy.
For example, solvent handling has evolved over years of batch and continuous production runs. Switching to more efficient washes, updating filtration steps, and using real-time moisture monitoring all came from review meetings with end users seeking better product throughput and less waste. These changes did not come from an abstract directive, but from laboratory and production teams sharing one domain: practical chemistry.
Consistent safe practice forms the basis of all production activities. Our team receives regular hands-on training in specialized handling of ethylene ketal-protected intermediates, updating protocols whenever staff or regulatory feedback points to improvement. Precise calibration of safety infrastructure, from local exhaust down to specialized PPE, ensures both material integrity and operator well-being.
We require team members to validate not just the identity of each batch but its suitability for intended applications under real use cases. This vigilance extends through storage, packaging, and shipment, logging possible deviations quickly and rectifying them before materials reach customer benches.
Continuous analysis of customer needs steers both ongoing development and new product design. Recent upgrades in instrumentation for purity verification and moisture content allow ever-tighter specification limits, reducing the need for sample re-analysis downstream. These technical improvements align with our steady commitment to open, fact-driven dialogue with application chemists—allowing us to point to validation results, not aspirational claims.
Trust builds batch by batch, feedback by feedback, improvement by improvement. Our long-standing relationships with customers offer clear evidence that materials such as 1-Amino-4-Oxocyclohexanecarboxylic Acid Ethylene Ketal serve not as interchangeable commodities, but as essential, tailored intermediates for solving specific synthetic challenges. This outlook inspires us to maintain and raise standards in purity, documentation, and customer support—so end-users can focus on chemistry that matters.