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1-Isopropyl-4-Piperidone

    • Product Name 1-Isopropyl-4-Piperidone
    • Alias 4-Piperidone, 1-isopropyl-
    • Einecs 613-116-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    123764

    Cas Number 35047-07-3
    Iupac Name 1-Isopropylpiperidin-4-one
    Molecular Formula C8H15NO
    Molecular Weight 141.21
    Appearance Colorless to pale yellow liquid
    Boiling Point 250-252 °C
    Density 0.96 g/cm3
    Solubility Soluble in organic solvents
    Smiles CC(C)N1CCC(=O)CC1
    Inchi InChI=1S/C8H15NO/c1-7(2)9-5-3-8(10)4-6-9/h7H,3-6H2,1-2H3
    Storage Temperature Store at room temperature
    Refractive Index 1.471

    As an accredited 1-Isopropyl-4-Piperidone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 500 grams, tightly sealed with a tamper-evident cap, labeled with chemical name, purity, hazard warnings, and batch number.
    Shipping **1-Isopropyl-4-Piperidone** is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. It is transported as a hazardous chemical, compliant with international regulations. Adequate labeling, documentation, and safety precautions are followed to ensure secure delivery. Store and handle away from heat, moisture, and incompatible materials during shipping.
    Storage **1-Isopropyl-4-Piperidone** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep it protected from moisture and direct sunlight. Use in a chemical fume hood, and always label the container clearly for safety and compliance purposes.
    Application of 1-Isopropyl-4-Piperidone

    Applications of 1-Isopropyl-4-Piperidone in Industrial Manufacturing

    As an original manufacturer, we supply 1-Isopropyl-4-Piperidone to key industrial sectors. This material demonstrates consistent performance in demanding chemical syntheses for downstream manufacturing. Its specific functional group enables advanced chemical transformation across regulated industries.

    1. Pharmaceutical Intermediates for CNS-Active Compounds

    Pharmaceutical companies use 1-Isopropyl-4-Piperidone as a defined intermediate in multi-step synthesis routes for central nervous system (CNS) drug development. Medicinal chemists apply its piperidone moiety for the introduction of isopropyl substitution, enabling unique pharmacological profiles in target molecules. This compound typically enters API manufacturing by acylation or alkylation methods, ensuring precise control over intermediate purity required for further conversion. The process demands robust analytical verification to comply with regulatory pathways for clinical candidates and commercialized drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) general chapters applicable to intermediates
    • EDQM and EudraLex Volume 4 regulations for intermediates used in EU APIs
    • FDA 21 CFR Part 211 and 210 requirements governing drug substance synthesis

    Typical usage ratio

    • Used at 0.6–1.2 molar equivalents relative to core scaffold, based on structure-activity targets and yield optimization
    • Final charge adjusted in response to reactivity of subsequent synthetic step

    Downstream process integration

    • Added after initial condensation or reduction stage during multi-step synthesis
    • Reacted in controlled reactor vessels under nitrogen to limit oxidation
    • Purified by fractional distillation or crystallization before transfer to the following coupling step

    Final product types

    • CNS-related small molecule APIs (active pharmaceutical ingredients)
    • Experimental medicinal chemistry scaffolds
    • Reference standards for analytical testing
    • Commercial CNS drug intermediates

    2. Agrochemical Synthesis for Heterocyclic Pesticides

    Agrochemical producers incorporate 1-Isopropyl-4-Piperidone as a key building block for novel heterocyclic pesticide synthesis. Its chemical configuration supports selective N-functionalization, providing a basis for active ingredients with improved environmental fate. Utilization starts from the mid-stage route, allowing for targeted construction of piperidinyl-based herbicides and insecticidal compounds. Rigorous traceability, in-process controls, and batch documentation underpin the compliance expectations of this sector.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for regulated agrochemical intermediate manufacturing
    • ISO 9001 quality management systems
    • CropLife International product stewardship code
    • REACH Annex VII-XI as applicable for notified agricultural substances

    Typical usage ratio

    • Dosage ranges from 0.7–1.5 molar equivalents, depending on the desired active structure and conversion rate
    • Adjusted for reaction scale and downstream compatibility

    Downstream process integration

    • Introduced in a cyclization or amination stage after primary skeleton formation
    • Processed in closed reactors equipped with solvent recovery for environmental protection
    • Undergoes in-line purity analysis and stability checks before further chemical modification

    Final product types

    • Heterocyclic herbicidal intermediates
    • Insecticide precursors with piperidine core structures
    • Development substances for regulatory submission dossiers
    • Bulk intermediates for custom synthesis contracts

    3. Fine Chemical Manufacture for Specialty Catalysts

    Chemical processing facilities utilize 1-Isopropyl-4-Piperidone as a structural component in crafting nitrogen-based ligands for manufacturing specialty catalysts. Its unique substitution is essential in forming piperidine-derived chelating agents that support transition metal catalysis in polymerization and hydrogenation reactions. Process engineers incorporate this raw material during tailored ligand synthesis under inert conditions to maintain integrity and functional performance in the final catalyst product.

    Industry compliance standards

    • ISO 9001 and ISO 14001 integrated management systems
    • Responsible Care chemical product stewardship guidelines
    • Customer-approved technical and quality agreements
    • GHS-compliant hazard labeling and documentation

    Typical usage ratio

    • Employed at 1.0–1.4 equivalents relative to metal precursor feed, metered to optimize chelation and catalyst performance
    • Ratio adjusted according to ligand to metal stoichiometry in coordination complexes

    Downstream process integration

    • Charged during controlled ligand formation under nitrogen atmosphere
    • Blended with metal salts or organometallics for direct complexation
    • Quality checks for ligand structure and activity precede batch approval

    Final product types

    • Nitrogen-based ligand intermediates
    • Transition metal catalyst systems for industrial polymer synthesis
    • Specialty reduction and hydrogenation catalysts
    • Catalyst-ligand blends for process development

    4. Custom Synthesis in Flavors and Fragrance Intermediates

    Flavors and fragrance houses contract the custom synthesis of select precursors using 1-Isopropyl-4-Piperidone. Its amine-reactive carbonyl assists in building complex heterocyclic molecules with aromatic profiles for specialty scent compounds. Production chemists feed this raw material after initial aromatic core construction, applying mild hydrogenation and condensation steps for high-purity conversion. Strict limits on trace contaminants and product batch reproducibility remain central to business-to-business supply.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 22716 Good Manufacturing Practices for cosmetic ingredients
    • EU Regulation (EC) No 1223/2009 for cosmetic products
    • REACH protocols for intermediates (when applicable)

    Typical usage ratio

    • Processed at 0.5–1.0 equivalents relative to aldehyde or aromatic core to achieve selectivity in end structure
    • Ratio set based on molecule complexity and required odor threshold

    Downstream process integration

    • Charged during intermediate coupling steps post-aromatic formation
    • Hydrogenated in temperature-controlled vessels to avoid byproduct formation
    • Purity checked by GC-MS and HPLC before customer release

    Final product types

    • Fragrance heterocycle intermediates
    • Odorant precursors for custom blends
    • Aroma compound reference materials
    • Flavors industry restricted-use intermediates

    5. Research Chemicals for Analytical Reference Standards

    Analytical laboratories and research reagent suppliers use 1-Isopropyl-4-Piperidone to produce calibrants and method development reference standards for small molecule analysis. It permits the construction of N-substituted standards for chromatographic calibration and stability studies. Labs rely on the well-defined structure to trace impurity profiles and support mass spectrometric method qualification. All synthesis occurs in line with traceability and analytical validation requirements for regulated environments.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory competence
    • USP General Chapter <11> for reference standards
    • GLP for laboratory synthesis of analytical intermediates
    • Documentation in accordance with NIST traceability policy

    Typical usage ratio

    • Used at 0.95–1.10 equivalents depending on analytical derivative formation
    • Adjusted according to calibration curve and intended analytical response

    Downstream process integration

    • Added at the derivatization step following core structure synthesis
    • Controlled by weighing protocols for traceable batch records
    • Purity characterized by NMR and LC-MS before vialing for sale

    Final product types

    • Certified analytical reference standards
    • Chromatography calibrant sets
    • Mass spectrometry validation kits
    • Research-grade piperidone derivatives
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    Certification & Compliance
    More Introduction

    Introducing 1-Isopropyl-4-Piperidone: A Practical Perspective from the Manufacturer

    Understanding 1-Isopropyl-4-Piperidone in the Context of Fine Chemical Manufacturing

    Navigating the chemical landscape, we see many compounds come and go, but some carve out a spot in synthetic chemistry that few others rival. 1-Isopropyl-4-Piperidone is one of those steadily reliable intermediates, valuable in both scale-up environments and fine-tuned lab synthesis. Years spent in the reactor halls and on the QC bench have taught us to appreciate the straightforward behavior and robust demand for this molecule, especially among developers hunting for efficiency and selectivity in their pathways.

    Our facility maintains consistent output of this piperidone variant, owing both to established downstream customers in pharmaceutical synthesis and the energetic needs from certain specialty chemical segments. 1-Isopropyl-4-Piperidone makes its mark in places that depend on reproducibility — laboratories that can't tolerate questionable purity or unpredictable side-products simply don't entertain risky suppliers. Our process engineers pushed for strict reaction controls, and we built our purification routes to minimize residual contaminants, particularly ones that would cause headaches downstream such as overalkylated piperidine byproducts. In practice, requests for supporting analytical packages increased as regulatory and compliance standards climbed, so we kept pace by standardizing batch-to-batch HPLC, NMR, and GC-MS profiles.

    Key Features and Specifications of 1-Isopropyl-4-Piperidone

    Batch reviews regularly show a colorless to pale yellow liquid, with an odor profile that experienced chemists recognize from nitrogen-containing heterocycles. Our standard offering usually hits a purity level above 98%, confirmed through high-resolution techniques — a necessity for customers planning to push piperidone chemistry toward active pharmaceutical ingredients. Moisture control matters; we intentionally lower water content before packaging, as elevated levels can impact selectivity in reductive amination and hinder downstream yields. After encountering some inconsistent results in early years, we now employ a vacuum drying sequence and nitrogen-blanketed packaging, which proved their worth when certain clients tested our materials' stability after prolonged storage.

    The chemical holds a molecular weight suitable for practical handling, with a boiling range that keeps it well below exothermic risk but high enough to prevent unintentional evaporation during open bench manipulations. Each outgoing lot receives a certificate with the full slate of physical constants, including melting and boiling points, refractive index, and elemental analysis, so users spend less time running their own confirmations and more time progressing their synthesis.

    Distinct Advantages Compared to Other Piperidones and Nitrogen Heterocycles

    Those who have spent time scaling up piperidine chemistry know not all piperidones behave the same way. As manufacturers, we see frequent requests for various N-substituted and 4-substituted piperidones. Comparing 1-Isopropyl-4-Piperidone with more common analogues like N-methyl or 4-phenyl options, we notice immediate differences in reactivity, especially in nucleophilic acyl substitution and at the enamine stage. The isopropyl group alters both steric and electronic characteristics, often reducing overreactions during further functionalization and helping route selectivity when targeting specific side chains.

    We learned early not to lump all piperidones together, especially after some partners found lower regioselectivity and tougher purification challenges with N-ethyl or other bulkier alkyl variants. Through our own side-by-side test reactions, 1-Isopropyl-4-Piperidone delivered a consistently cleaner profile in reductive cyclization and alkylation steps, with less competing amination. This proves especially useful for project leaders facing tight impurity thresholds and significant downstream analytics. It helps that, compared to ketonic piperidones with more activated alpha positions, this compound shows improved shelf life and fewer polymerization issues when stored under inert conditions.

    Applications in Pharmaceutical and Specialty Chemical Synthesis

    Every time our team interacts with advanced pharmaceutical synthesis groups, the use cases for 1-Isopropyl-4-Piperidone underline its flexibility. Many researchers lean on it as a precursor for building block scaffolds where specific N-substitutions lead to the right pharmacophores or therapeutic profiles. We've followed several published synthetic pathways closely, including those for pain management and central nervous system therapeutics, watching chemists favor isopropyl substitution for improved solubility and metabolic resistance.

    The specialty chemical space draws on its structural stability for advanced resin precursors and even in certain agricultural chemistry applications. A recent collaboration with a polymer research group led to experimentation around how this piperidone’s steric bulk influences copolymer backbones. The trial batches prompted a series of debates about ring-opening kinetics and end-group compatibility, but they kept ordering for further pilot-scale evaluation, suggesting the material’s performance impressed them enough to justify follow-up studies.

    As a manufacturer, we focus on offering predictable supply — both in terms of volume and quality. Users developing novel therapeutics or specialty functional materials need more than an off-the-shelf compound; they want batch reliability, immediate technical support, and a supplier who can adapt specifications as discovery work progresses. Over the years, we’ve adapted several formulations in response to sometimes obscure requests, such as extra-tight residual solvent levels or certificate-backed microbiological controls for bioprocess integrations.

    Safety and Handling: What Decades in Manufacturing Have Taught Us

    Factories learn through experiences — often through minor mishaps brought on by hasty handling or overlooked incompatibilities. 1-Isopropyl-4-Piperidone, like most nitrogen heterocycles, rewards careful storage and conservative handling practices. We keep ambient storage temperatures in check, relying on sealed vessels with well-maintained gaskets to prevent moisture or oxygen intrusion. Starting batch production always involves a briefing on its volatility and reactivity with strong acids or oxidizers, based on some cautionary tales from early scale-ups.

    Transportation history shaped improvements in our own logistics. Early shipments in generic drums sometimes led to slight off-spec profiles at receipt, rarely due to manufacturing error, but instead linked to temperature excursions or delays. Now, we contract temperature-controlled logistics partners for longer hauls and only release stocks after double-verifying both packaging and the tight seal integrity. For clients running solvent-based preps, we frequently share tips from our own solvent compatibility trials — DMF and DMSO excel, while moisture-rich media add unnecessary headaches.

    Safety protocols in our chemical park mandate closed-system loading and dedicated PPE for all handlers. The irritating nature of vapor concentrations seems obvious, yet even experienced operators new to this compound sometimes underestimate the sensitivity of exposed skin or mucous membranes. Documentation and ongoing training prevent repeat mistakes, and teams tasked with large batch transfers always double-check emergency shower and eyewash stations before beginning.

    Managing Supply Chain Pressures and Quality Consistency

    Anyone committed to genuine manufacturing knows markets shift, and raw material shortages or regulatory changes can hit without warning. Our production planning team tracks isopropylamine and piperidone precursors as closely as sales forecasts. This attention kept us operational through several spikes in global solvent prices, and we continue to maintain buffer inventories to avoid passing abrupt market volatility onto our customers. Years spent building relationships with reliable feedstock partners paid off, no small feat considering the commoditization pressures in some corners of the piperidine supply chain.

    Developers require more than basic technical answers; they want solution-oriented partners ready to solve unpredictable issues. We once encountered a sudden uptick in orders from a sector that previously stayed quiet, putting pressure on both reactor availability and downstream purification. Prioritizing long-term relationships over short-term profits, we extended shifts and onboarded additional QC techs to maintain batch quality under the heavier load. No shortcuts went into production, and the batch-to-batch consistency — validated via side-by-side chromatograms and impurity profile overlays — confirmed we made the right call. 

    Batch variation remains one of the most common technical complaints in the global fine chemicals market. Thanks to automated monitoring and strict in-process controls, our team catches deviations before release, and years of investing in modern analytics enables direct dialogue with clients when questions arise. Feedback loops drive improvement, and process tweaks come from both customer needs and our own drive to outpace tolerances set by regulatory authorities.

    Continuous Improvement and Technical Support

    Not all syntheses scale neatly from beaker to plant. Troubleshooting unexpected stalling in a reductive amination route or a cross-coupling reaction often leads chemists back to the drawing board, where the purity and reactivity of their piperidone intermediate makes all the difference. Our technical staff field dozens of questions each month about compatibility, reaction optimization, and even alternative formulation options. Several times, a rapid phone consultation uncovered either off-beat solvent effects or simple procedural oversights, saving our partners hours or days of fruitless troubleshooting.

    As synthesis techniques evolve, so do demands for greater transparency and documentation. Customers, especially those working under GMP or in pilot programs, expect not just purity specs, but robust traceability records and vendor audit-readiness. Our team invested early in electronic record-keeping and shipment tracking, so technical support never waits on paperwork. From manufacturing deviations logs to revalidation protocols, we stay prepared for deep-dive regulatory reviews. 

    Some areas of specialty chemistry turned to custom-tailored grades (for example, extra-dry or ultra-pure batches) and our production responded. Engineers flex equipment setups to meet new demands, and direct communication means chemists speak to other chemists, not intermediaries. We often remind new customers that fine chemical manufacturing rewards agility just as much as consistency.

    Environmental and Regulatory Considerations

    Manufacturing any piperidone compound at scale involves a steady focus on compliance and environmental impact. Authorities tightened effluent discharge limits over the years, driving us to overhaul legacy solvent recovery units and update wastewater pretreatment protocols. Modernized scrubbers and containment tanks reduced emissions, and extensive waste tracking helps address both regulatory reviews and sustainability expectations.

    Our experience highlights that regulatory compliance isn’t just a box to check; it forms the backbone of a responsible manufacturing operation. Each year brings another audit round, and both ISO certifications and local environmental reporting push us to document every process change and equipment upgrade. These steps build trust with long-term customers, who need the assurance of both product safety and sustainable practices further down their own supply chains.

    Lessons learned from earlier supplier audits taught us how quickly an overlooked residue or late paperwork can unravel project timelines. At every new process launch, our regulatory team updates safety data sheets, tracks new classification changes, and maintains open communication lines with government agencies. The end goal has always been straightforward: keep product flowing without regulatory hang-ups or unnecessary paperwork delays.

    Looking Toward New Applications and Collaboration

    From the production floor to the customer’s bench, we value open dialogue and thoughtful technical exchange. Early conversations with researchers often prompt us to challenge our own manufacturing boundaries. Several recent collaborations sought structural modifications, including tailored salt forms, alternate isopropyl substitutions, or coupled piperidone scaffolds. Some of these partnerships ran through multiple trial phases, with incremental tweaks and process validations at each stage, before finding commercial viability.

    Growing interest in sustainable chemistry caused us to seek lower-solvent, reduced-waste synthesis routes, both for in-house production and for knowledge transfer to development partners. These changes yielded measurable improvements both in process yield and environmental footprint, two metrics demanded by procurement and R&D teams alike. Ideas for further adaptations continue to roll in from customers who use our piperidone in ways we haven’t yet explored — something that energizes both our R&D chemists and reactor operators.

    Participating in the evolution of 1-Isopropyl-4-Piperidone applications, we act as both supplier and collaborator. Our experience affirms that even well-established intermediates like this one gain new relevance as technologies advance, new therapies progress, and specialty applications move to pilot and commercial scale. The direct line of communication between synthesizing chemist and manufacturing engineer translates to steady improvement, higher yields, and solutions to technical snags that can be solved only by those with deep experience in both theory and practice.

    Conclusion: Commitment to Quality and Partnership

    Our journey with 1-Isopropyl-4-Piperidone runs deep — from process development in our own labs to technical support across a wide spread of innovative applications. We built quality, safety, and reliability into every shipment, learning from each production campaign and every customer demand. We meet market needs by adjusting batch specifications, improving analytics, and providing real-world advice. The collective effort from production, safety, logistics, and technical support turns out a material trusted by leading synthetic chemists and process engineers worldwide. Our commitment is to maintain this standard, listening closely to partner feedback and responding with action, not promises. 1-Isopropyl-4-Piperidone stands as proof that dependable manufacturing opens new doors for invention and discovery, now and for the road ahead.