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3-Ethoxy-2-Cyclohexen-1-One

    • Product Name 3-Ethoxy-2-Cyclohexen-1-One
    • Einecs EINECS 211-366-3
    • 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

    703021

    Iupac Name 3-Ethoxycyclohex-2-en-1-one
    Molecular Formula C8H12O2
    Molecular Weight 140.18 g/mol
    Cas Number 10472-24-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 85-86°C at 2 mmHg
    Density 1.045 g/cm³ at 20°C
    Refractive Index 1.4870-1.4910
    Smiles CCOC1=CC(=O)CCC1
    Melting Point < 25°C
    Solubility In Water Insoluble
    Flash Point 82°C

    As an accredited 3-Ethoxy-2-Cyclohexen-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Ethoxy-2-Cyclohexen-1-One is packaged in a 25g amber glass bottle, tightly sealed with a screw cap for safety.
    Shipping 3-Ethoxy-2-Cyclohexen-1-One should be shipped in tightly sealed, clearly labeled containers, protected from light and moisture. Use compatible, leak-proof packaging materials. Compliance with applicable local and international regulations for chemical transportation is required. Ensure safety data sheets (SDS) accompany the shipment, and handle with care to prevent breakage or spills.
    Storage **3-Ethoxy-2-Cyclohexen-1-One** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep away from incompatible materials such as strong oxidizing agents. Store at room temperature or as recommended by the manufacturer. Ensure proper labeling and avoid moisture contact to maintain chemical stability.
    Application of 3-Ethoxy-2-Cyclohexen-1-One

    Applications of 3-Ethoxy-2-Cyclohexen-1-One in Industrial Manufacturing

    As a direct manufacturing source, we supply 3-Ethoxy-2-Cyclohexen-1-One to downstream industries that demand high-purity intermediates for precise applications. Below, we outline its real-world roles in key industrial sectors, focusing on segment-specific specifications, proven formulation parameters, validated process stages, and representative end product mappings.

    1. Pharmaceutical Intermediate Synthesis

    Our material plays an established role in pharmaceutical API synthesis, notably in the preparation of complex heterocyclic scaffolds found in cardiovascular and central nervous system drug development. Process chemists value its well-defined reactivity during C–C bond formation steps, allowing selective derivatization in tightly controlled environments. Compliance with strict regulatory frameworks underpins this use, and precise metering ensures batch-to-batch consistency for registered intermediates.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Part 210/211 US FDA)
    • EU GMP Directive 2003/94/EC
    • ICH Q7 Guidelines for Active Pharmaceutical Ingredients
    • Applicable monograph requirements from USP, EP, JP (for qualifying intermediates)

    Typical usage ratio

    • 0.5%–5% w/w depending on target molecule’s synthetic route, with higher ratios during early route scouting; optimized to minimize residual levels in API.

    Downstream process integration

    • Charged during stepwise condensation or cyclization reactions following initial functional group activation; typically used in controlled-glass reactors under nitrogen, entering after solvent exchange and preceding downstream work-up or purification columns.

    Final product types

    • Small-molecule API intermediates (cardioprotective, anticonvulsant, and anti-inflammatory candidate structures)
    • Regulated pharmaceutical building blocks supplied to CDMO operations

    2. Agrochemical Active Ingredient Precursor

    In the agrochemical industry, formulators rely on this compound as a reactive enone for constructing key scaffolds in insecticide and herbicide actives. Process development utilizes it during multi-step aromatic modifications, owing to its high selectivity in Michael-type reactions and ability to confer specific activity profiles to pesticide candidates.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH Regulation (EC 1907/2006) for chemical registration
    • Good Laboratory Practice (GLP) for new active substance development

    Typical usage ratio

    • 1%–8% w/w in synthetic feedstock mixtures, with dosage adjusted for desired chain elongation or activity profile of target molecule.

    Downstream process integration

    • Introduced during intermediate-stage coupling reactions, post-initial aromatic halogenation, frequently entering continuous stirred tank reactors equipped for nucleophilic addition and subsequent work-up.

    Final product types

    • Novel insecticide and herbicide active substances
    • Technical-grade crop protection intermediates for downstream formulation

    3. Specialty Fragrance and Flavor Chemical Synthesis

    Specialty fragrance houses use our product as a high-value intermediate in the synthesis of unique keto-ester-based aroma chemicals. Its introduction controls cyclohexenone backbone modifications crucial for fruity, floral, or green-note molecules, allowing predictable performance in fragrance accords and food additive blends.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • FEMA GRAS (Flavor and Extract Manufacturers Association, Generally Recognized as Safe)
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • ISO 9225:2010 for essential oil and aroma chemical production

    Typical usage ratio

    • 0.05%–0.8% w/w, strictly calibrated according to target molecule intensity and volatility profiles in finished fragrances or flavorings.

    Downstream process integration

    • Added after primary cyclization, triggering enol ether formation or selective reduction reactions under controlled vacuum distillation; often processed in jacketed glass-lined reactors with precise temperature gradients.

    Final product types

    • Cyclohexenone-derived aroma chemicals (used in fine fragrance and personal care)
    • Commercial food flavoring compounds/blends

    4. Dye and Pigment Intermediate Manufacturing

    Colorant producers handle this raw material as a masked dicarbonyl unit in the synthesis of specialty dyes, especially in the creation of high-lightfast pigmentary structures for plastics and ink applications. Its well-defined reactivity enables efficient coupling during condensation and subsequent chromophore construction, favoring consistent color quality over large batches.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile colorants)
    • EN 71-3 Safety of Toys (Migration of certain elements in pigments)
    • ISO 9001:2015 and ISO 14001:2015 for dye and pigment manufacturing
    • REACH-compliant registration for colorant chemicals

    Typical usage ratio

    • 2%–12% w/w in chromogenic feed mixtures, set based on color intensity targets and matrix compatibility; higher levels used in masterbatch pigment creation.

    Downstream process integration

    • Dosaged at the condensation stage immediately prior to azo or anthraquinone ring closure, integrated into high-temperature batch reactors with staged solvent removal and pH control, before being isolated and purified via crystallization or extraction.

    Final product types

    • Lightfast plastic colorants for automotive and consumer goods
    • Specialty printing inks and dispersions
    • Textile dyes with enhanced resistance properties

    5. Advanced Polymer Additive and Modifier Synthesis

    Producers of advanced materials implement this compound as a precision functionalizer in the synthesis of specific cyclohexenone-modified polymer additives. Applications involve covalent incorporation into polymer side chains or backbone, improving compatibility and stability in high-performance elastomers, adhesives, and specialty films used in demanding environments.

    Industry compliance standards

    • ISO 10993 (for medical-grade polymers, biocompatibility test guidance)
    • ASTM D256 and D638 (mechanical property standards for plastics)
    • FDA 21 CFR 177.2600 (for indirect food contact elastomeric components)
    • RoHS Directive 2011/65/EU (restricting use of hazardous substances in electronic polymers)

    Typical usage ratio

    • 0.5%–3% w/w relative to total polymer matrix, depending on target functional group density and end-use exposure profile.

    Downstream process integration

    • Employed at pre-polymerization modification stage, added to precursor blends in bulk reactors or solution-polymerization vessels; may also be grafted onto existing chains via post-polymerization functionalization with continuous in-line monitoring for conversion.

    Final product types

    • Functionalized adhesives for electronic assembly
    • Modified elastomers for medical and food-contact use
    • Specialty films with enhanced permeability/UV-resistance
    Free Quote

    Competitive 3-Ethoxy-2-Cyclohexen-1-One prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Tel: +8615371019725

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    Certification & Compliance
    More Introduction

    Introducing 3-Ethoxy-2-Cyclohexen-1-One from the Manufacturer's Workbench

    Our Hands-On Experience Producing 3-Ethoxy-2-Cyclohexen-1-One

    Talk to anyone with decades in fine chemical manufacturing and a few molecules always stand out for their balance of reactivity and reliability in synthesis. 3-Ethoxy-2-cyclohexen-1-one sits firmly in that category. In our daily runs, where product consistency translates directly to downstream results, this compound has built a reputation for clean yields and a straightforward production pathway. The molecule’s structure—an ethoxy group tethered to a cyclohexenone core—offers synthetic flexibility without the volatility found in some similar systems. From the early days, back before analytical controls were fully digital, we discovered a lot about the quirks of this intermediate at bench scale. Moving to production, we learned more from full-batch troubleshooting than any compendium or remote analyst ever could provide.

    Specifications and Batch Consistency: What Really Matters

    Our approach always centers around maintaining high-purity output. With 3-ethoxy-2-cyclohexen-1-one, this usually means controlling the moisture content, strict temperature control during the ethoxylation step, and tight distillation cuts. Minor shifts in these parameters have a clear impact downstream. We keep residual solvents low—not just to hit a number on a report, but because we’ve tracked the effect even small amount of residual alcohol can have later in a client’s synthesis. Over the years, our in-process GC analyses made it clear that subtle adjustments to residence time in the reactor prevent unwanted side-product formation.

    On average, our batches show GC purity upwards of 99%. There are times when an odd impurity pops up—often due to a new operator or a change in raw material supply—but process adjustments iron things out. For those formulating at kilo or ton scale, the reproducibility saves headaches. We store and ship in containers specified by our own trials, noting that inexpensive packaging or a shortcut with liner material creates moisture ingress that rapidly shifts product profile. In short, every drum matters, and our bulk customers see the upside in better process uptime and less scrap.

    Applications That Drive Demand

    Customers come to us for 3-ethoxy-2-cyclohexen-1-one with a range of uses in mind. The most consistent demand has come from organizations making advanced pharmaceutical intermediates. Take a convergent synthesis route: reducing steps, linking critical motifs, and aiming for high throughput. This intermediate brings a valuable functional group and a reactive center that endures tough reaction conditions. It drives down the step count and can keep the route robust even if some conditions flex or drift.

    In agrochemical labs, there’s ongoing interest in cyclic enones for new herbicidal frameworks. Here, ethoxy-modified enones provide key access points for later substitution. With our own R&D time on similar scaffolds, we spotted ring-expansion possibilities and Michael addition routes that wouldn’t work with unsubstituted or methyl-substituted cyclohexenones. This kind of fine-tuned development describes a lot of what’s happening outside the latest trade show headlines. While many look for a silver-bullet intermediate, the priorities at the bench remain cost, availability, and minimal workup.

    Besides pharmaceuticals and crop science, pigment and flavor chemists find value in the unique blend of reactivity and manageable odor profile. Some cyclic enones bring sharp or overpowering notes to the workroom. Ethoxy-functionalization here softens the olfactory footprint, making extended handling in flavor-formulation labs less taxing for both operator and exhaust system.

    Comparing to Other Cyclohexenones: Real-World Differences

    Every year, buyers and formulators ask about the reasons behind picking 3-ethoxy-2-cyclohexen-1-one over a straightforward cyclohexenone or a methyl analog. From the seat of production, distinct advantages show up during scaling and day-to-day handling. For one, incorporating the ethoxy group increases solubility in commonly used organic solvents, especially in formulae needing rapid dissolution. This reduces the bottlenecks we’ve seen with other cyclohexenone derivatives, where non-uniform mixing in process tanks led to downstream fouling.

    Process safety follows closely. Some enone intermediates prone to polymerization or exothermic behavior under moderate heating have caused more than a few nail-biting episodes in chemical plants. The ethoxy group’s electron-donating nature, based on our in-house thermal data, suppresses runaway tendencies and narrows the range of hazardous byproducts. In actual operations, this translates to less need for corrective maintenance and reduced stoppage due to equipment fouling. More stable intermediates always make for better final yields, especially when humidity or ambient temperature fluctuates.

    Another practical point: While methyl- or unsubstituted cyclohexenones bring their own sound reactivity, they often invite side reactions in complex, multi-step syntheses. The ethoxy moiety imparts a balance—enough reactivity for sequential functionalizations, but not so much that every impurity in the starting material comes through in the end product. Downstream, customers report fewer chromatographic purifications and less time running preps, which reflects back on us through repeat orders and less order-to-order troubleshooting.

    Quality at Scale: From Bench to Ton

    It’s one thing to make a few grams for research. It’s another to deliver multiple metric tons of 3-ethoxy-2-cyclohexen-1-one, batch after batch, with purity and reactivity profiles holding steady. Our site has faced reality more than once—a solvent drum out of spec, a reactor jacket failing during winter, unpredictable outages with the filtration system after a string of wet weather days. Each challenge added a note to our process manuals and prompted new controls. Over the years, we brought every learning back to the process floor. Today, our QA team picks up off-spec samples long before they ever hit a finished drum.

    Clients scaling their own syntheses often share war stories about suppliers who can’t transition from kilo lab to plant production. We made it our goal to maintain batch size flexibility within the same process chain—right down to packing, which deals with the reactivity and minor volatility that can cause headaches during shipment. An unlined drum or long ocean-leg shipment spells disaster—and we have the records to prove it. Optimal container materials and multi-layer closures always outperform the bare minimum. We share these findings with clients working in variable storage environments, particularly those who need to split orders across continents.

    Practical Insights on Safety and Storage

    Anyone who spends time managing chemical warehouses quickly learns that cyclohexenone derivatives—while less hazardous than some—require due respect. 3-ethoxy-2-cyclohexen-1-one doesn’t carry the same volatility risk as the lower homologs like cyclohexanone itself, but it can show degradation if exposed to air and light for long stretches. Early on, storage in uncooled environments led to a series of quality complaints. Since then, we specify cool, dark, low-humidity storage. Tracking the impact of even a few weeks at elevated temperature gave plenty of incentive.

    Regular inspection of storage drums reveals patterns, too—many failures come from inadequately sealed bungs or mismatched gasket materials. Our maintenance staff opens finished drums past their nominal shelf life and posts updates for every storage anomaly. Sharing this kind of data with our partners allows them to spot incoming trouble before it requires scrapping a full lot.

    Touching the topic of human safety, contact with exposed arms, even in well-ventilated spaces, causes noticeable skin irritation for some operators. Our production lines adopted improved PPE guidelines based on a handful of minor incidents. Posting these notes in the shipment documents has helped many downstream users avoid similar hiccups.

    Environmental and Regulatory Considerations

    As regulatory frameworks continue to tighten across North America, Europe, and East Asia, authorities expect transparency about intermediate handling and fate. 3-Ethoxy-2-cyclohexen-1-one does not fall in the category of persistent organics or recognized environmental hazards under most regimes. Nevertheless, we treat all emissions with closed-loop collection during distillation and handle aqueous waste with on-site neutralization. We keep batch and emissions data on file for years, reporting as required or in direct response to customer audit requests.

    Every lot manufactured passes through an integrated database for traceability. Our teams conduct annual drills to verify recall readiness—a step that separates robust suppliers from opportunistic traders. In audits, even the questions we can’t answer immediately send us back to the process logs, collecting new data to refine the next round of production instructions. In the long run, these visits drive as much change on the process side as new capital investments do on the equipment side.

    Feedback Loops Drive Improvements

    Sourcing decisions often hinge on trust built through consistent performance. Our regular customers share stories where switching to another supplier’s material disrupted whole synthesis flows—requiring extra purification, longer drying, and sometimes outright rejection of finished product lots. Over time, these shared headaches fueled our own continuous improvement projects. We run scheduled feedback sessions internally, pulling together technical, logistics, and support staff to hash out every minor outage or deviation flagged in customer calls. Each cycle identifies new data points, instrument calibrations, and potential process control tweaks.

    Hardware upgrades remain an ongoing commitment. Years of hands-on maintenance in a live plant—rather than a demo environment—provides real clarity on what fails in practice. For 3-ethoxy-2-cyclohexen-1-one, replacing pump seals with chemically tolerant polymers, lining transfer pipes, and augmenting chilled storage have each produced measurable drops in product return rates. We encourage incoming partners to walk the floor, see the finish of actual goods, and review the logs before entering contracts. Transparency, not fine print, protects both sides.

    The Manufacturer’s Perspective on Innovation

    The feedback loop between our plant and our product development group stays active. Radical advances often happen less by chance than through spots of frustration with conventional methods. A few years back, a client struggled with an uncooperative coupling step where simple cyclohexenone caused unstable adducts and lengthy purification headaches. Collaborative troubleshooting led us to evaluate the ethoxy group’s stabilizing effects, and we ran a suite of controlled trials until results lined up with their targets. That solution now supports a regularly shipped, high-value pharmaceutical route.

    In other instances, batch-to-batch reproducibility took center stage—some customers require multi-ton annual volumes for fragrance synthesis, where minute shifts mean large-scale waste. Extended discussions across engineering, QC, and logistics led us to tighten in-line solvent stripping and adjust the allowable range for raw material composition. This kept lot-to-lot variation below even the strictest customer thresholds. Each iterative change, supported by feedback, keeps pushing performance up and complaint frequency down.

    Lessons Learned and Shared with Clients

    There’s no substitute for time spent on the process floor. Standard operating procedures, no matter how carefully written, only go so far without ongoing practical review. Overhauling pump maintenance following a run of foaming incidents, or training every new operator about subtle color changes during distillation, all form part of the lived experience that shapes our product. For 3-ethoxy-2-cyclohexen-1-one, those details matter as much as molecule counts or certificates of analysis.

    We maintain an open-door policy for customer site visits and technical reviews. Our practical knowledge doesn’t come from perfect textbook conditions—equipment snags, raw material oddities, and day-to-day weather shifts have all left their mark. For clients dealing with sensitive syntheses or scaling up from research, connecting these lessons directly to their needs shortens development cycles and avoids preventable outages. We take pride in helping troubleshoot application specifics—whether that means suggesting alternate solvent use or reviewing flashpoint hazards in a downstream process.

    Looking Ahead: Adapting to Industry Shifts

    We’ve tracked growing interest from researchers looking to build increasingly complex molecules using less conventional intermediates. 3-Ethoxy-2-cyclohexen-1-one offers a blend of stability and synthetic utility that fits these development goals. Investing in better control systems, automated batch monitoring, and in-line analysis methods remains part of our response to these shifts. With every production run, these systems deliver a baseline of quality and traceability that makes it easier to support emerging needs—whether for pharmaceutical, agrochemical, or specialty chemical innovation.

    Across the years, our goal remains steady: manufacture and ship a compound that not only meets the data sheet but performs dependably in every hands-on use. Experiences from daily plant life, long-term customer relationships, and direct troubleshooting remain the backbone of our approach to 3-ethoxy-2-cyclohexen-1-one production. In a market increasingly crowded by third-party re-packagers and synthetic shortcuts, our process knowledge and commitment to real-world solutions set us apart—helping builders, formulating scientists, and production managers alike move projects from bench to bulk without missing a step.