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HS Code |
250974 |
| Chemical Name | Ethyl 4-Piperidinecarboxylate |
| Molecular Formula | C8H15NO2 |
| Molar Mass | 157.21 g/mol |
| Cas Number | 4543-09-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 239-241°C |
| Density | 1.025 g/mL at 25°C |
| Smiles | CCOC(=O)C1CCNCC1 |
| Inchi | InChI=1S/C8H15NO2/c1-2-11-8(10)7-3-5-9-6-4-7/h7,9H,2-6H2,1H3 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as ethanol, DMSO, chloroform |
As an accredited Ethyl 4-Piperidinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of Ethyl 4-Piperidinecarboxylate is supplied in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | Ethyl 4-Piperidinecarboxylate is typically shipped in tightly sealed containers to prevent leakage and contamination. It should be stored and transported at room temperature, away from heat sources and incompatible substances. Proper labeling and adherence to local and international chemical transport regulations are required to ensure safety during shipping and handling. |
| Storage | Ethyl 4-piperidinecarboxylate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from moisture, heat, and direct sunlight. Ensure proper labeling and restrict access to trained personnel. Follow all applicable safety guidelines to prevent spills or accidental exposure. |
Applications of Ethyl 4-Piperidinecarboxylate in Industrial ManufacturingEthyl 4-Piperidinecarboxylate is an advanced heterocyclic intermediate supporting multiple sectors within the chemical industry. Our manufacturing process assures pharmaceutical-grade and industrial-grade quality consistency, facilitating integration across specialized production chains. Below are key downstream applications, with specific compliance, formulation, process, and end-product considerations for each. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies incorporate this material as a core intermediate when producing select APIs, especially within CNS agents and antipsychotic drug classes. Within GMP-compliant synthesis, the compound serves as a building block in multistep reactions, contributing to the formation of piperidine pharmacophores after amidation or further ester transformations. Integration into synthesis routes involves targeted feed ratios tailored to the specific molecular pathway, with extensive in-process purity controls throughout. This approach supports downstream formulation of prescription-grade APIs for neurological and psychiatric therapies. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingProducers of crop protection agents use this compound as a piperidine moiety source in the preparation of selective herbicide and insecticide actives. Its role is primarily in the formation of tertiary amines through nucleophilic substitutions or ester hydrolysis, typically under regulated environmental conditions. Processing often demands adherence to global pesticide safety and purity benchmarks, with full traceability and documentation at each blending or reaction stage. Handling precise dose levels is necessary for both efficacy and avoidance of residual impurities in final agrochemicals. Industry compliance standards
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3. Fine Chemical Synthesis for Specialty CoatingsIn advanced materials manufacturing, the ester compound functions as a key intermediate in the customization of specialty resins and polymerizable precursors. Epoxy and polyurethane coating producers utilize it to introduce heterocyclic functionalities, improving film flexibility, adhesion, or chemical resistance. Batch process control and solvent purity requirements are critical during polymer precursor modification stages. Formulators must adjust the input ratio to balance film property targets with downstream compatibility for blending and curing operations. Industry compliance standards
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4. Fragrance and Flavor SynthesisProducers in the aroma chemicals sector use the compound as an intermediate in synthesizing key piperidinyl derivatives found in select fragrances and flavor modifiers. The compound’s structure assists with building nitrogen-containing ring systems during multi-step synthesis, enabling the production of aroma ingredients used in food, beverages, and perfumes. Processes require food or fragrance-specific controls, often referencing IFRA or FCC standards, with tight management over impurity profiles. Small-scale syntheses often optimize the ratio for both yield and organoleptic profile development, minimizing side products detrimental to sensory characteristics or downstream compliance. Industry compliance standards
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5. Research and Development Chemical SynthesisSpecialty chemical R&D laboratories and pilot-scale manufacturers apply the compound when developing novel molecules, including pharmaceutical candidates, enzyme inhibitors, or advanced material monomers. Syntheses require analytic-grade purity and full batch traceability, with process design often tailored for structure-activity exploration. R&D workflows may leverage variable loading ratios to optimize reaction outcomes and evaluate molecular frameworks for activity, solubility, or reactivity in new compound libraries. Documentation aligns with general research safety guidance and chemical handling protocols, adapting to specific project requirements. Industry compliance standards
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