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3-Amino-2-Cyclohexen-1-One

    • Product Name 3-Amino-2-Cyclohexen-1-One
    • Einecs 611-158-8
    • 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
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    Specifications

    HS Code

    798038

    Chemical Name 3-Amino-2-Cyclohexen-1-One
    Cas Number 932-52-9
    Molecular Formula C6H9NO
    Molecular Weight 111.14 g/mol
    Appearance Yellow to orange solid
    Melting Point 74-77°C
    Solubility In Water Slightly soluble
    Smiles C1CC(=O)C=CC1N
    Inchi InChI=1S/C6H9NO/c7-6-4-2-1-3-5(6)8/h2,4,6-7H,1,3H2
    Synonyms 3-Amino-2-cyclohexenone
    Storage Conditions Store at 2-8°C
    Purity Typically ≥98%

    As an accredited 3-Amino-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 packaging contains 25 grams of 3-Amino-2-Cyclohexen-1-One, sealed in an amber glass bottle with a tamper-evident cap.
    Shipping 3-Amino-2-cyclohexen-1-one should be shipped in tightly sealed containers, protected from moisture and light. Transport at ambient temperature unless otherwise specified. Follow all relevant regulations for shipping chemicals, including labeling with the appropriate hazard and safety information. Ensure secure packaging to prevent leaks or spills during transit.
    Storage Store **3-Amino-2-Cyclohexen-1-One** in a tightly sealed container under a dry, inert atmosphere (such as nitrogen). Keep it in a cool, well-ventilated, dry location away from direct sunlight, moisture, and incompatible substances (e.g., strong oxidizers). Properly label the container, and avoid prolonged exposure to air to prevent decomposition. Use appropriate personal protective equipment when handling.
    Application of 3-Amino-2-Cyclohexen-1-One

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

    We provide 3-Amino-2-Cyclohexen-1-One to advanced industry partners who require a specialty intermediate for high-value synthesis. Our direct engagement with formulation chemists and production managers ensures that each use case is backed by real industrial practices, compliance data, and application-driven quality management. The following are the main downstream fields where our material is in active, documented use:

    1. Pharmaceutical Synthesis: API Intermediates for CNS and Antiviral Agents

    Custom manufacturing of pharmaceutical actives and advanced intermediates leverages 3-Amino-2-Cyclohexen-1-One as a key component in the cycloalkanone scaffold synthesis pathway. During the preparation of certain central nervous system (CNS) modulators and antiviral molecules, chemists utilize this compound for ring construction and incorporation of amino functional groups, supporting high-yield, low-residual reaction flows compliant with regulated sector requirements.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) systems (ICH Q7)
    • 21 CFR Parts 210 and 211 for APIs
    • Relevant US, EP, and JP Pharmacopoeia monographs for specific APIs
    • REACH (Registration, Evaluation, Authorization, and Restriction of Chemicals) for EU shipments

    Typical usage ratio

    • 5–15% by molar proportion as building block in target molecule; ratio varies based on route selection, stoichiometry, and reaction scale

    Downstream process integration

    • Addition as a core intermediate post-initial ring formation in multi-step organic synthesis, typically during reductive amination or Michael addition onto functionalized cyclohexanones

    Final product types

    • CNS modulator API intermediates
    • Antiviral small molecule actives
    • Bespoke pharmaceutical research grades for clinical route validation

    2. Agrochemical Actives: Herbicide and Insecticide Precursor Synthesis

    Major downstream agrochemical plants utilize our material as an intermediate for selective herbicide and insecticide molecules containing cyclohexenone motifs. Its reactivity in nucleophilic substitution and condensation reactions allows formulators to introduce nitrogenated moieties critical for target selectivity and environmental stability in agricultural applications.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius (residue definition for parent intermediates)
    • ISO 9001:2015 Quality Management certification for technical grade production
    • REACH and CLP Regulation (EC) No 1272/2008 for classification and labeling

    Typical usage ratio

    • 3–8% weight basis in key intermediate mixture; batchwise adjustment based on target molecule, yield optimization, and required purity

    Downstream process integration

    • Charged into reaction vessels following initial carbonyl condensation; serves as reactive core for subsequent halogenation or nitration steps during active ingredient synthesis

    Final product types

    • Selective herbicide actives for post-emergence weed control (e.g., cyclohexenone derivatives in grass weed management)
    • Nitrogen-based insecticidal intermediates for systemic crop protection
    • Registered pesticide technical concentrates

    3. Specialty Dye and Pigment Synthesis

    Industrial colorant manufacturers use this compound to prepare aminocyclohexenone-based dye intermediates that deliver high color strength and photostability. Its unique ring structure and electron-donating amino group support specific chromophore engineering, enhancing UV resistance and achieving desired tone in textile and plastics coloration.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished textile colorants)
    • EN 71-3:2019 (colorant migration in toys and children’s articles)
    • Quality control approvals under GOTS (Global Organic Textile Standard) for non-toxic dye kits

    Typical usage ratio

    • 1–6% weight basis in initial condensation mixture; ratio determined by dye type and shade depth required

    Downstream process integration

    • Introduced during the first stage of diazotization or coupling reaction, producing intermediate chromophores that define later dye molecule characteristics

    Final product types

    • Textile dyes with aminocyclohexenone backbones
    • Organic pigments for industrial plastic colorants
    • Specialty color compounds for printing inks

    4. Fine Chemical Synthesis: Chiral Ligand and Catalyst Preparation

    Chemical industry users dedicated to advanced synthesis and catalysis select this intermediate to construct chiral ligands and organocatalysts containing the cyclohexenone core. It functions as a precursor for further amination, hydrogenation, and asymmetric modification, vital in the precise manufacturing of catalyst libraries for enantioselective synthesis in active pharmaceutical and agrochemical production streams.

    Industry compliance standards

    • ISO 9001:2015 certification of lab and pilot-scale fine chemical plants
    • Confidential Business Information (CBI) protection under TSCA (for regulated catalyst development)
    • Purity and contaminant thresholds as per downstream customer specification sheets

    Typical usage ratio

    • 2–10% molar equivalent against target ligand structure; usage tailored to yield and chiral induction requirements

    Downstream process integration

    • Reacted early during ligand skeleton assembly, allowing for subsequent stereoselective conversions and derivatization to produce proprietary catalysts

    Final product types

    • Chiral ligand libraries for asymmetric hydrogenation
    • Organocatalysts for enantioselective synthesis
    • Custom fine chemical intermediates supplied to contract synthesis partners
    Free Quote

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

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    Certification & Compliance
    More Introduction

    3-Amino-2-Cyclohexen-1-One: Our Experience with a Precise Building Block

    A Look at 3-Amino-2-Cyclohexen-1-One in Everyday Synthesis

    From years working in chemical production, we understand just how critical purity and molecular integrity are for every batch coming off the reactors. 3-Amino-2-Cyclohexen-1-One has become one of those core intermediates we turn to when constructing complex heterocycles, particularly in the early development of new pharmaceuticals and fine chemicals. The backbone it provides, with its reactive amino and enone functional groups sitting on a cyclohexene ring, allows chemists a versatile springboard for downstream modifications. You see, our process begins with properly sourced cyclohexanone, before we introduce aminating agents under closely managed conditions. The difference between high and low yield isn’t just about running the numbers; it’s the outcome of methodically controlling solvent selection, pH, and reaction temperature—every degree makes a difference.

    Understanding the Product: Structure Leads to Performance

    3-Amino-2-Cyclohexen-1-One, with formula C6H9NO, draws its value from its chemical structure. That amino group opens the door to Schiff base formation or coupling reactions, a clutch trait for organic synthesis. The enone portion, on the other hand, extends possibilities for condensation or Michael addition steps, frequently leading to new carbon-carbon bonds in our downstream operations. Many of our partners prefer this intermediate because it helps streamline their synthesis routes. Its purity speaks for itself; in our hands, meticulous crystallization, followed by vacuum drying and tight QC using HPLC and NMR, establishes material that doesn’t throw surprises in yield or byproduct profiles. After countless scale-ups, we focus on making the route robust—never discounting the pesky byproducts like cyclohexenone or diaminocyclohexanone that can appear in less refined processes.

    The Unique Place 3-Amino-2-Cyclohexen-1-One Holds

    You can see the difference between a purpose-built intermediate like 3-Amino-2-Cyclohexen-1-One and more generic building blocks such as cyclohexanone, cyclohexenone, or even cyclohexylamine. Many generic amines won’t provide the same ring strain or reactivity, leading chemists on frustrating detours when constructing fused rings or nitrogen-containing scaffolds. With this molecule, that double bond doesn’t just sit idle; it provides resonance stabilization that impacts the nucleophilicity of the amine, making certain reaction steps carry lower activation barriers. The result: cleaner conversions under milder conditions, and fewer side products. Not every chemical can claim that kind of reliability.

    Practical Use and Handling in Manufacturing

    Handling starts in the warehouse. We’ve learned over the years that 3-Amino-2-Cyclohexen-1-One prefers storage at controlled humidity, ideally in airtight drums shielded from strong sunlight and temperature swings. Packing in HDPE drums with sealed liners isn’t just our habit—it’s based on real-world analytics showing loss of potency when the material absorbs moisture from the air. Our staff use full PPE and follow carefully drafted SOPs, because contact with skin or eyes causes irritation. Not only is this safer for people, but meticulous handling preserves the powder’s flowability, which ultimately affects dosing in reactors and the success of the whole synthetic campaign.

    Supply Chain and Long-Term Sourcing Strategies

    One of the persistent issues in custom synthesis projects is the risk of batch-to-batch inconsistency. With 3-Amino-2-Cyclohexen-1-One, we counter this by maintaining long-term supplier relationships for the starting ketones and amines. We vet our vendors for trace metal content and solvent residue limits, because even small variations upstream can create downstream headaches—impurities in this material don't always show up right away, but they will sabotage a final API campaign or agrochemical scale-up. Investing in in-house purification—distillation columns, recrystallization tanks, analytics with LC-MS and FTIR—not only allows us to guarantee product quality but also rescue off-spec batches, reducing overall waste and environmental burden.

    Why This Intermediate Stands Apart During Synthesis Optimization

    During process R&D, one problem stands out: intermediates that decompose or react unpredictably under scale-up conditions. With this molecule, we’ve seen high recovery rates up to pilot scale, with only minor changes to stirring rates or cooling jacket setpoints. Its moderate melting point, usually in the low hundreds Celsius, means it can be handled as a free-flowing powder in kilogram batches, provided you avoid excess moisture. In contrast, more reactive enones or primary amines have caused more headaches—polymerization, hazardous off-gassing, even vessel corrosion from unexpected side reactions.

    We’ve sat through plenty of discussions with chemists frustrated by intermediates that either arrive with erratic purity or require elaborate protection and deprotection steps. With 3-Amino-2-Cyclohexen-1-One, we reach a sweet spot—just reactive enough to serve as a nucleophile or electrophile, but not so unstable as to demand glovebox techniques or special quenching. It accommodates a variety of solvents, from ethanol to DMF, without breakdown or discoloration. We keep an open communication channel with our clients, adjusting drying times and particle size on request; in one recent project, we provided a micronized version to improve dispersion in an aqueous formulation, reducing reaction times by nearly a third.

    The Role in Pharmaceutical Innovation

    In the pharmaceutical world, every synthetic step invites regulatory scrutiny. Impurities, residual solvents, and even minor degradants can derail a project. We’ve worked closely with drug discovery teams using 3-Amino-2-Cyclohexen-1-One as a key step in constructing cyclic amine cores, often seen in central nervous system drug research. These teams come to us because we can document every lot, right down to the batch’s elemental analysis and chiral purity. Documentation supports their filings, but consistency reduces the likelihood of costly re-synthesis. The difference adds up, especially during late-stage process validation.

    Other firms might rely on externally sourced intermediates without much upstream control. We see the consequences: slower project timelines, confusion over root causes of impurities, wasted man-hours in QC. By taking responsibility for every kilo leaving our facility, we give project teams more workspace to explore structure-activity relationships, instead of wrangling with unreliable supply chains. As a manufacturer, we weigh novel requests for new analogs—sometimes swapping the amino or adjusting the double bond position—to help customers create differentiated products in the market.

    Environmental Considerations and Regulatory Drivers

    The chemical industry keeps evolving under pressure from environmental regulations and internal targets for waste reduction. We’ve adapted by monitoring and capturing off-gas from synthesis runs, which is especially important with nitrogen-containing intermediates prone to releasing low-molecular weight amines. All spent acids and solvents make their way to on-site recycling stations or accredited incinerators. We take emissions reporting seriously, even in regions with looser oversight, since persistent organic pollutants can draw unwanted attention.

    Unlike some intermediates where halogenated byproducts demand complicated disposal, 3-Amino-2-Cyclohexen-1-One offers a cleaner profile. Still, unreacted starting materials from its synthesis can contain cyclohexanone or acetic acid, so we treat aqueous effluents in batches before releasing or recycling water. We update our handling protocols as toxicity data emerges, especially monitoring cytotoxicity or aquatic effects. Recent studies flagged some related cyclohexenones for low-level neurotoxicity in animal models, so we keep adjusting exposure limits in line with science and worker feedback.

    Staying Ahead of Process Failures and Quality Setbacks

    Experience teaches that regular audits prevent quality slip-ups. During routine plant walks, we inspect reactor seals, transfer lines, and packing stations for signs of leaks or contamination. If we find clumped material or color deviation, we halt the batch and run a full analysis. Our QC team features seasoned chemists, who don’t sign off until impurity profiles satisfy internal benchmarks as well as any client-imposed specs. The dedication here isn’t just procedural; every failed batch costs time, raw materials, and reputation. That’s why we favor transparency: customers know if anything in the batch deviated, even if corrections followed.

    Looking back, batches of 3-Amino-2-Cyclohexen-1-One most prone to trouble tend to come from rushed production schedules. Skipping an extra filtration or shortening drying time always invites problems down the road. We keep long-range forecasts on raw material availability, buying in bulk with confirmed COAs to minimize last-minute scramble. Every kilogram makes it into traceability records, which becomes crucial during client audits or regulatory review.

    Customer Feedback in Process Optimization

    Feedback loops between production floor and customer lab play a big part in improving quality. Our partners experimenting with new ligands or custom materials often email with specific requests—reduced solvent residue, customized particle morphology, or absence of a trace impurity. In real terms, this sometimes means investing in additional purification steps: double-trituration, repeated filtration, or extended drying runs. We don’t shy away from repeated analytics: every new request helps us refine the synthesis and identify bottlenecks.

    For example, a customer flagged incomplete reactivity when scaling up a cyclization reaction. We discovered that minor residues of acetic acid from upstream aminolysis catalyzed an unexpected hydrolysis side-reaction. As a result, we now include an extra wash and QA test for residual acids in every outgoing batch. These incremental improvements might not land on flashy advertising, but in our view, attention to detail gives downstream users confidence to proceed past laboratory scale.

    Comparison with Related Intermediates

    Building a reliable synthetic route is never a straightforward choice between one intermediate or another; it depends on the balance between reactivity, selectivity, handling safety, and cost. Cyclohexanone and simple cyclohexylamines sometimes show higher chemical stability, but don’t deliver the same reactivity profile for heterocycle creation. Working with more highly functionalized analogs, like diaminocyclohexanones, may bring in added complexity for protection or purification—our staff spend more time and resources under fume hoods, and downtime rises for cleaning and maintenance.

    We’ve also trialed analogs where the double bond sits outside the ring or amino is on a different position. These sometimes improve selectivity for a narrow application, but typically lose the broad utility seen with 3-Amino-2-Cyclohexen-1-One. The reaction temperature windows narrow; safety risks can rise. For our team, the sweet spot has always rested with predictable chemical behaviors that make for repeatable batch output and satisfied clients.

    Future Outlook and Process Improvements

    Innovation in organic synthesis pushes us to keep tuning our manufacturing setup for 3-Amino-2-Cyclohexen-1-One. Ongoing investments in in-line spectroscopy now let us catch byproduct formation in real time, adjusting feed rates or reactant concentrations before a minor issue turns into a waste problem. We’re prototyping new solvent systems to reduce environmental impact and planning automation upgrades so operators can spend more time focusing on off-spec detection rather than manual transfers.

    We maintain robust records for each batch, tracking all process parameters—temperatures, reaction times, filtration sequence, particle size, even local ambient humidity—so problems can be traced and improvements sustained. This may not be glamorous, but it’s the backbone of process chemistry. Our long-term vision places 3-Amino-2-Cyclohexen-1-One alongside other core building blocks in the toolbox that pharmaceutical and specialty chemical innovators return to for reliability and performance.

    Closing Thoughts from the Production Floor

    Seeing 3-Amino-2-Cyclohexen-1-One move from bulk bags to fine pharmaceuticals and crop protection molecules, we reflect on the continuous trial-and-error that underpins every success. Customers demand high standards, not just in purity, but in supply reliability, clear documentation, and customization options. We meet that challenge working hand-in-hand with QC experts and downstream users.

    Perfection may be impossible, but the journey lies in getting as close as possible. Each tweak in process, every extra analytical step, and open discussion with partners moves us toward better outcomes. As new markets and challenges emerge, we keep learning from each batch, never outgrowing the need to question, test, and improve. From raw material selection to the final drum, our daily goal stays clear: making 3-Amino-2-Cyclohexen-1-One a dependable, high-quality starting point for tomorrow’s discoveries.