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1-Acetylpiperidine

    • Product Name 1-Acetylpiperidine
    • Alias N-Acetylpiperidine
    • Einecs 205-803-0
    • 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

    459074

    Chemical Name 1-Acetylpiperidine
    Molecular Formula C7H13NO
    Molar Mass 127.18 g/mol
    Cas Number 4655-34-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 220-222 °C
    Melting Point -7 °C
    Density 0.982 g/cm3 at 20 °C
    Refractive Index 1.4840 - 1.4860
    Solubility In Water Slightly soluble
    Flash Point 90 °C
    Purity Typically ≥98%
    Storage Temperature Below 30 °C
    Smiles CC(=O)N1CCCCC1
    Synonyms N-Acetylpiperidine

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

    Packing & Storage
    Packing 1-Acetylpiperidine is packaged in a 100 mL amber glass bottle, sealed with a leak-proof cap, and labeled with hazard warnings.
    Shipping **Shipping Description for 1-Acetylpiperidine:** 1-Acetylpiperidine should be shipped in tightly sealed containers, protected from moisture and incompatible substances. The package must comply with local hazardous material regulations, be clearly labeled, and include safety documentation. Transport under ambient temperature is generally suitable. Ensure handlers are trained in proper chemical safety procedures and emergency response actions.
    Storage 1-Acetylpiperidine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. The storage area should be clearly labeled, with proper chemical safety measures in place to prevent leaks or spills. Always follow local regulations and safety guidelines for storage and handling.
    Application of 1-Acetylpiperidine

    Applications of 1-Acetylpiperidine in Industrial Manufacturing

    1-Acetylpiperidine serves as a specialized intermediate in multiple controlled and quality-centric industrial supply chains. Its role extends across a spectrum of downstream sectors, each characterized by stringent regulations and formulation precision. Below, we detail the principal fields where our direct manufacturing customers incorporate this material for value-added production, with clear distinctions for compliance, formulation, process position, and final product categories.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    1-Acetylpiperidine is primarily sourced by API plants to synthesize piperidine-containing drug molecules including anesthetics, antipsychotics, and antihypertensive agents. The raw material enters amidation, alkylation, and deprotection steps as a masked amine, providing controlled release of the piperidine ring during multi-step synthesis. This route supports high assay and purity control, meeting drug-grade obligations throughout scale-up and process validation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph references
    • U.S. FDA cGMP Parts 210/211
    • China Pharmacopoeia (ChP) quality requirements

    Typical usage ratio

    • 0.8–1.3 molar equivalents relative to core API precursor; optimized according to targeted conversion, with ratio adjustments based on impurity profiles and scale-up yield data.

    Downstream process integration

    • Introduced during the protected amination or ring construction stage of multi-step batch synthesis; reacted under controlled temperature and nitrogen atmosphere; follows solvent extraction and purification prior to downstream condensation or hydrolysis.

    Final product types

    • Pharmaceutical actives such as perazine, risperidone, and lacosamide
    • Finished dosage forms: tablets, injectables containing synthesized APIs

    2. Agrochemical Synthesis for Herbicide and Pesticide Formulations

    Downstream agrochemical manufacturers employ 1-acetylpiperidine as a building block for the synthesis of heterocyclic pesticide active substances, including selective herbicides and insecticides. The molecule contributes nitrogen-bearing intermediate structures, supporting carbon–nitrogen bond formation in key ring-closing and chain-extension sequences, critical for yield consistency across large batch productions.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • EU REACH registration and authorization
    • China National Pesticide Standards (GB/T 1604)
    • ISO 9001:2015 for chemical processing

    Typical usage ratio

    • 5–12% weight/weight as precursor constituent in active ingredient synthesis. Target loading depends on stoichiometry and required conversion efficiency for specific herbicide or insecticide products.

    Downstream process integration

    • Dosed into condensation or cyclization process vessels; added to batch or semi-continuous manufacturing lines for compound assembly; undergoes distillation and in-process impurity removal before downstream formulation and blending with adjuvants or carriers.

    Final product types

    • Active pesticide ingredients such as piperidine-substituted phenylureas
    • Commercial herbicide or insecticide formulations for crop protection

    3. Chemical Synthesis of Specialty Flavors and Fragrances

    Flavors and fragrance compounders incorporate 1-acetylpiperidine as a precursor for nitrogen-containing aroma chemicals, including select musks and heterocyclic flavor modifiers. Its defined reaction profile enables construction of stable intermediates with tailored volatiles, supporting regulatory-compliant, batch-to-batch consistency for both fine fragrance and food-use approvals.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • U.S. FEMA GRAS status for specific derivatives
    • EU Food Additive Legislation (EC 1334/2008)
    • ISO 22716: Cosmetic GMP Guidelines (for fragrance manufacturing)

    Typical usage ratio

    • 0.3–2.0% of total synthetic batch, determined by the specific aroma molecule being targeted and restricted within industry-specified limits to avoid over-concentration.

    Downstream process integration

    • Fed into cyclization, reductive amination, or acylation reaction steps; processed using food- or perfume-grade solvents; followed by fractional distillation, vacuum stripping, and purity adjustment to meet fine chemical benchmarks.

    Final product types

    • Heterocyclic aroma chemicals (e.g., piperidyne musks, tobacco notes)
    • Finished fragrance oils
    • Complex compound flavors for confectionery or beverages

    4. Intermediate for Polymer Modifier Synthesis

    1-Acetylpiperidine functions as a functionalized intermediate in the modification of polymer chains, especially where controlled amine functionality is required to adjust polymer flexibility, adhesion, or crosslinking density. Manufacturers rely on its reproducible purity profile to build specialty polyamides and coatings with predictable thermal and mechanical properties for demanding downstream industrial applications.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • ISO 9001 for chemical quality management
    • ASTM D256 for polymer impact resistance (as applied to finished materials)

    Typical usage ratio

    • 0.5–5% by polymer weight, modulated based on required chemical modification degree, in correlation with targeted mechanical and thermal property enhancements.

    Downstream process integration

    • Pre-blended into monomer feed streams or added at the in situ modification stage during polycondensation; participates in chain extension, end capping, or side-group insertion; followed by extrusion, granulation, and post-synthetic finish treatments.

    Final product types

    • Specialty polyamide resins with improved flexibility
    • Modified polyurethanes for sealant and coating formulations
    • Engineering plastics and adhesive systems
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    Certification & Compliance
    More Introduction

    1-Acetylpiperidine: Manufacturing Perspective and Industry Value

    Grounded Quality Rooted in Chemistry

    We have spent years refining the production of 1-Acetylpiperidine from fundamental raw materials. This compound brings something quite specific to the chemical industry. At our facility, we watch it take shape batch after batch, always aiming for pure, off-white crystalline powder with distinct acetyl and piperidine notes easily detected by anyone accustomed to the smell of such chemicals. The end product usually ranges from 98% to over 99% purity, measured by GC and confirmed with NMR, and we routinely see sharp melting points and clear solubility characteristics indicative of tight process controls.

    Our operators regularly check every step of our acetylation process—the way temperature, agitation, and pH interact—since slight variations show up downstream. Even with technology, nothing beats the trained eye of technicians who can read the results outside the lab sheet. A well-formed batch doesn’t clump, doesn’t yellow, and dissolves rapidly in organic solvents—an assurance to anyone intending to take it to the next synthetic stage.

    What 1-Acetylpiperidine Actually Does

    By itself, 1-Acetylpiperidine rarely becomes a final consumer product. We understand its main attraction rests in its ability to function as a robust intermediate. It finds frequent use across pharmaceutical synthesis, especially in the creation of certain APIs and active metabolites. Medicinal chemists count on it for targeted derivatizations—the acetyl group acts both as a protecting agent and a potential handle for further modification.

    Industrial labs often reach for this molecule during scale-ups. It suits research and pilot development, since its reliable reactivity and manageable toxicity profile fit the routine protocols—unlike more volatile or unpredictable cyclic amines which need extra containment.

    We supply both standard and custom batch sizes. Most requests stay within the kilogram to multi-metric-ton range, reflecting its application in batch synthesis over continuous flow, since the utility comes down to producing specific analogs or fragments rather than baseline commodities.

    Our conversations with formulators and project managers often revolve around yield, work-up efficiency, and downstream isolation. This compound stands out because it can cleanly introduce the acetyl group without encouraging polycondensation or requiring elaborate purification every time—which reduces waste and saves hours across a campaign.

    Specifications Shaped by Application

    A typical specification sheet for our production includes a defined melting point—usually between 36°C and 39°C—a GC area percentage above 98%, a drying loss below 0.5%, and controlled heavy metal content. We routinely screen each lot for residual solvents, following ICH Q3C thresholds, even though the acetylation route doesn’t leave behind common toxins when well-controlled.

    Particle size is another consideration. Some customers working with automated feeders or precise weighing request a coarser cut to prevent static and dusting, while others favor fine powder for quick dissolving. Rather than rely on one default setting, we adjust sieving to reflect this direct feedback. Over time, we’ve witnessed how a misjudged particle cut can slow a batch or force laborious reprocessing.

    Color, too, matters—impurities tend to discolor a product, showing brown or yellow hues if acetyl donors degrade or if basification happens too late. Clean, off-white product signals both correct process timing and adequate storage. These subtle details don’t always get attention in a spec sheet but tell a story to any experienced formulator working at the bench.

    Comparing to Close Relatives and Substitutes

    Within our catalog, a handful of related compounds often come under comparison: piperidine itself, N-alkylpiperidines, unacetylated amines, and other nitrogen heterocycles. Piperidine remains widely used, but if you need better selectivity in acylation or want to avoid reactive amine side chains, our acetylated version becomes the logical step.

    Chemists sometimes consider direct acylation on unprotected piperidine rings. From experience, this raises issues—side reactions, tar formation, and poor yields when working with elaborate substrates. 1-Acetylpiperidine simplifies the task, offering a blocked nitrogen that reacts in a more controlled, efficient manner.

    Compared to other N-acylated piperidine derivatives, the acetyl group also offers a cleaner cleavage path in deprotection, minimizing complexity in scaling up. Some experimenters try cheaper mono-alkyl substitutes, but these often come with off-odors and unstable byproducts that complicate already tight timelines. Once a team faces a batch failure or an unexpected impurity peak, they tend not to risk it again—they look for a stable, tried-and-tested intermediate. This is where 1-Acetylpiperidine earns its keep.

    Troubles and Solutions in Manufacturing

    Any manufacturer worth their salt knows unexpected results sometimes turn up, even with familiar processes. The acetylation step depends on the quality of both piperidine and acetyl sources—clogged lines, temperature spikes, or delays in quenching can shift the impurity profile over several batches. Through repeated runs and scale increases, we learned that running too hot shortens reaction cycles but feeds formation of diacetylated impurities—trace, yet stubborn during crystallization.

    Our in-house troubleshooting strategies avoid last-minute “fixes” because they often create downstream issues. Instead, we prioritize sourcing from validated suppliers, keeping raw materials within narrow acceptance ranges. Maintenance on reactors and attention to cleaning schedules remains essential. It’s easy to overlook a fraction of residue left in lines, but over months this accumulates, leading to contamination events that can threaten dozens of kilograms in a run.

    On the environmental side, the acetylation process can generate acetic acid as a byproduct. We built reclaim and scrubbing systems to capture and neutralize this, turning waste back into a useful feedstock in other syntheses. One repeated request from customers is proof that we manage volatile organic release responsibly; laboratory data and emissions logs—open to scrutiny—go a long way toward building trust over one-off claims.

    Usage—Perspective After Years in Production

    Talking with development chemists day in, day out, it’s clear that the value of 1-Acetylpiperidine is practical. The molecule grants a measured level of reactivity, neither so dormant as to require forcing conditions nor so reactive that it triggers side reactions. It serves as a backbone for making intermediates used in antihistamines, nervous system agents, or agrochemicals. Many generic programs hinge on access to a predictable, high-quality acetylated piperidine for pilot work before any scale-up is possible.

    In a pilot plant, the small details stack up—a batch won’t move if the intermediate refuses to dissolve or if downstream crystallization forms persistent oils. Production managers have shared how a switch to a poorly made lot, out of fear of cost, damaged timelines for months. Many now opt for reliability; better to pay an experienced acetylpiperidine manufacturer than handle the mess of failed purifications or rework. Experience shows that reusing trusted intermediates builds speed and confidence in multi-step synthesis pipelines, and nothing slows a team like unexpected lot-to-lot variance.

    The way a manufacturer approaches drying, even packing, becomes important. Without adequate vacuum drying at the final stage, residual moisture can reduce crystallinity and encourage slow decomposition—something noticed by sharp analysts who test each delivery. We check not only primary chemical purity but also microtraces of water, as moisture can seed unexpected byproduct formation in later reactions.

    Quality packing makes shipment easier. Our shipments use lined, sealed drums—once we permitted cheaper alternatives and lost credibility after a few moisture-affected lots. Now, quality assurance reviews each drum before it leaves our loading bay.

    Safety, Handling, and Transparency

    Some compounds demand extra vigilance, and 1-Acetylpiperidine deserves respect without being particularly hazardous compared to many solvents or amines. Gloves, goggles, and well-ventilated workspaces make for a solid baseline. Over many years, we received only a handful of concerns from handlers, mainly linked to skin or respiratory irritation—the kind easily remedied with training and proper PPE.

    We remain transparent about assessed risks. Our documentation provides clear guidance without overstating or understating hazards. Genuine safety means sharing observed effects and listening to users. Should new data come to light about degradation, toxicity, or environmental persistence, we update our protocols without delay. Compliance with REACH and other chemical codes matters—but nothing matters as much as the real well-being of teams handling each batch, whether in our plant or a customer’s facility.

    Supply Reliability Through Process Know-How

    A big part of manufacturing value is reliability. It takes years to build enough stock and redundancy in supply chains. We hold safety stock based on market trends—avoiding both overproduction and sudden shortages. Unexpected surges from generic pharma launches or changes in regulatory approvals can drive up spot market pricing, but we have built options into our sourcing and stock holding to buffer regular clients.

    Defaulting to consistent scheduling grants project leaders peace of mind, knowing a planned campaign won’t stall due to unavailable intermediates. Our customers often operate tight development windows and cannot risk supply chain unreliability.

    Our philosophy pivots on bridging the gap between bulk chemical production and fine chemical precision. Flexibility only means something when backed by solid on-site analytical methods—GC, HPLC, Karl Fischer for water, in-process NMR for trace checks. We calibrate and validate daily, so any deviation is caught before shipments head out. Both the chemical yield and the measured purity tell the real story, and we’ve learned not to trust paperwork alone.

    1-Acetylpiperidine In the Broader Market

    The demand for this molecule rises and falls based on trends upstream—new pharmaceutical compounds using piperidine scaffolds, new agrochemical candidates, even developments in specialty polymers. Our perspective, shaped over decades, is that investment in consistent core intermediates pays off for everyone in the supply chain.

    Price fluctuations occur, particularly during regional shortages or supply interruptions from global events. Our approach blends long-term contracts with spot sales—bulk buyers get priority, but we reserve capacity for emerging smaller users in academic or pilot settings. New methods or routes using this intermediate arise regularly. We are open to joint development and scale-up partnerships, understanding that a single molecule can anchor dozens of modern chemical advances.

    While generic distribution models focus on margins, a manufacturer’s concern runs deeper: product performance, customer support, and integrity. Whether supplying a kilogram or a metric ton, we stand behind both the product and our track record. Feedback—whether praise or a complaint—feeds directly into our improvement cycles.

    Conclusion: Value Through Expertise

    Years of running acetylation reactions, troubleshooting crystallizations, and shipping product worldwide shapes our view of 1-Acetylpiperidine: it’s more than just an ingredient or catalog number. The difference comes not just from purity or numbers on a certificate but from decades of collaborative work with chemists, process engineers, and project managers across industries. When you work with a manufacturer committed to continuous learning and open dialogue, you get the reliability that underlies lasting progress in chemical innovation—centering the product and the people using it at the core of each development.