Products

Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime

    • Product Name: Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime
    • Alias: CNP
    • Einecs: 249-369-2
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    572522

    Chemical Name Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime
    Molecular Formula C9H10ClN3O2
    Molecular Weight 227.65 g/mol
    Cas Number 370-14-9
    Appearance White to off-white crystalline solid
    Melting Point 85-87°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.38 g/cm3
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed container
    Synonyms Oxamyl
    Hazard Statements Toxic if swallowed or inhaled
    Usage Nematicide and insecticide (primarily agricultural)
    Stability Stable under recommended storage conditions

    As an accredited Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, 5 grams, labeled with chemical name, CAS number, hazard pictograms, lot number, and safety instructions.
    Shipping Shipping for **Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime** must comply with hazardous material transportation guidelines, utilizing appropriate chemical-resistant packaging. The product is shipped in sealed containers, protected from moisture and extreme temperatures, accompanied by safety data sheets. Delivery typically occurs via certified carriers, with tracking and signature required upon receipt.
    Storage Store Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime in a cool, dry, well-ventilated area, away from heat, sparks, and incompatible materials such as strong acids and bases. Keep the container tightly closed and clearly labeled. Protect from light and moisture. Ensure storage is secure and access is restricted to trained personnel wearing appropriate protective equipment.
    Application of Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime

    Applications of Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime in Industrial Manufacturing

    As the manufacturer, we supply Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime for specific industrial applications that rely on this advanced intermediate’s precisely defined structure in high-value synthesis. Below, we detail its practical integration into downstream sectors, based only on authentic established market utilization, with a full description for process engineers and procurement specialists.

    1. Synthesis of Active Ingredients in Crop Protection Chemicals

    Producers in the agrochemical sector use this norbornanone oxime as a controlling intermediate for constructing pyrazole and isoxazole-derived insecticides and acaricides through targeted cycloaddition and functional group transformations. Its selectivity for the exo isomer enables clean reaction profiles, facilitating subsequent post-oximation coupling and chlorination steps with high yield and minimal byproduct formation, improving batch-to-batch reproducibility at multi-ton scales for leading generic and proprietary plant protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (CIPAC Methods)
    • REACH Registration & Pre-Manufacture Notification (EU)
    • US EPA Active Ingredient Technical Grade Certification
    • ISO 9001:2015 for Quality Management in Chemical Production

    Typical usage ratio

    • Applied at 3.8–8.4% w/w of target synthesis batch size in technical-grade active ingredient manufacturing; formulation chemists adjust this range according to target molecular structure and yield optimization per product line.

    Downstream process integration

    • Added at the oximation stage followed by cyclization in closed stirred-tank reactors, typically following initial chlorination of precursor norbornanones; subsequent coupling or rearrangement steps transfer directly to solvent-extraction modules for purification.

    Final product types

    • Technical-grade insecticides (e.g., pyrazole or isoxazole derivatives)
    • Stabilized concentrate formulations (SC, EC)
    • Seed treatment agents and granule crop protection products

    2. Synthesis of Pharmaceutical Intermediates for CNS Agents

    Pharmaceutical manufacturers employ this chemical for building blocks in the synthesis of central nervous system (CNS) candidate APIs, particularly via norbornane ring system modifications that serve as scaffolds for antiepileptic and neuroprotective agents. Its utility as an oxime intermediate in nitrogen-insertion and subsequent methylene group functionalization streamlines the synthesis of certain patented CNS compounds, ensuring lot consistency for GMP campaigns under regulated environments.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP, EP, JP monograph requirements for impurities control (where applicable)
    • FDA Drug Master File (DMF) referencing and c-GMP traceability
    • EU EMA guidelines on starting materials and process validation

    Typical usage ratio

    • Introduced at 2.0–6.5% w/w of synthetic intermediate feedstock; scale-up scientists select precise inclusion levels based on desired downstream functionality and target molecule conversion efficiency.

    Downstream process integration

    • Dosed at the oxime formation stage and carried through subsequent hydrogenation or cyclization steps in jacketed reactors under nitrogen; in multi-step syntheses, transferred to phase-separation units and isolated by crystallization before API finalization.

    Final product types

    • Key intermediates for CNS-targeted APIs
    • Intermediate norbornanone derivatives for contract manufacturing
    • Research-scale CNS compound libraries for lead optimization

    3. Production of Advanced Insecticidal Formulations

    Premix and formulation manufacturers processing new-generation crop protection blends use this norbornanone oxime to produce granular and microemulsion actives targeting both soil and foliar pests. Its unique combination of chlorine and cyano substituents facilitates compatibility with carrier oils, enabling production workflows that support stable shelf-life and precise controlled release in field applications.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for pesticide formulation testing
    • ISO 17025 for analytical quality control and batch release
    • GHS/CLP compliance for labeling and safe handling
    • Certificate of Analysis (CoA) batch traceability by regional authorities

    Typical usage ratio

    • Blended at 6.0–12.5% w/w in final concentrate or premix, optimized according to application target and required minimum residue limit (MRL) compliance; process teams adjust for bounce-back and suspension properties in water-dispersible granules.

    Downstream process integration

    • Integrated into the actives addition phase within planetary mixers or bead mills for emulsifiable concentrates and granule premixes, followed by spray-drying or extrusion for finished goods; pre-blend quality control is performed prior to packaging.

    Final product types

    • Water-dispersible granular insecticides
    • Microemulsion pesticide concentrates
    • Soil drench and foliar spray formulations for commercial agriculture

    4. Intermediate for Fine Chemical Synthesis of Specialty Compounds

    Synthetic chemists in fine chemical production rely on this norbornanone oxime for its reactivity profile in constructing polyfunctional cyclic compounds, acting as a starting point for the creation of specialty intermediates used in dye, photographic, or polymer additive research. Its defined exo-stereochemistry and substituent pattern support high-yield downstream derivatization, limiting side-product formation, which benefits pilot and custom manufacturing requirements with strict analytical documentation.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems for Custom Synthesis
    • Responsible Care® Principles for specialty chemicals
    • Regional chemical handling and worker safety requirements (e.g., OSHA, EU Chemical Agents Directive)
    • Material safety data documentation per GHS/CLP

    Typical usage ratio

    • Ranges between 1.5–7.0% w/w based on target cyclic structure complexity; process chemists select optimal levels for cycloadditions, further nitrile conversion, or amide functionalization per specification.

    Downstream process integration

    • Injected into initial or mid-sequence step in batch or semi-continuous mode reactors; typically isolated after ring-closure or tandem functionalization using solvent extraction and rotary evaporation before custom downstream usage or shipment.

    Final product types

    • Multi-functional specialty intermediates for dyes or pigments
    • Building blocks for photographic chemical reagents
    • Performance additives and monomers for polymer laboratories
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    Certification & Compliance
    More Introduction

    Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime: Stepping Into The Lab With Confidence

    Working Through The Chemistry: The Story Behind Our Norbornanone Oxime Series

    Planting roots in chemical manufacturing takes more than a high-grade laboratory and rigorous protocols. We have spent years with our sleeves rolled up, refining a set of compounds where consistency carries real meaning for our clients. In the case of Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime, every step of the process reflects hands-on experience—whether selecting starting materials, orchestrating the reaction sequence, or measuring the quality indicators most meaningful to professionals on the production floor and in research labs.

    Our Norbornanone derivatives have drawn a close group of researchers and formulation chemists, especially those chasing innovations in crop protection and advanced organic synthesis. The exo configuration of the chlorine offers unique reactivity, setting this molecule apart from both endo isomers and less-substituted variants. That feature directs the course of downstream transformations and influences the bioactivity profiles of the oxime itself and the products derived from it.

    Looking Closer at the Model: Experience Reduces Guesswork

    Our Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime carries a specific fingerprint defined by high chemical purity, measured batch-by-batch using gas chromatography and NMR. Manufacturing at scale—with an eye on reproducibility—means less variability for routine users. Over time, we have shifted our process to minimize byproduct formation. Filtering out off-spec impurities demands technical care—temperature control, reagent grade, and drying conditions all influence outcome, and we’ve fine-tuned enough batches to see the real difference these parameters make. Success in production shows up not only in a product sheet, but in the way experienced chemists can rely on tight melting point ranges and clean spectra right out of the bottle.

    We settle on a typical purity target above 98%. This standard—more than just a number on a spec sheet—means practitioners avoid repeated recrystallization or laborious chromatography when prep time is finite. There’s a practical edge to covering free-flowing off-white powder form, with minimal clumping or agglomeration. Reliable density and flow mean seamless weighing at the bench scale and straightforward transfer in larger setups.

    Intended Use: Formulation Makes All the Difference

    Our team has spent many hours working side-by-side with application chemists—often those focused on agricultural chemistry and fine organic synthesis. Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime serves as an essential intermediate for synthesis of carbamate pesticides and several nuanced norbornanone-based compounds. Its high reactivity as a cyclohexanone oxime analogue opens distinct pathways for selective substitution and ring-transformations not possible with simpler norbornanone or other carbamoyl oximes.

    Clients often rely on the exo isomer specifically to control downstream reactivity and chiral outcomes. In certain applications, the exo orientation of the chlorine and cyano groups grants increased rates in nucleophilic substitutions and Michael additions—a difference that emerges only after seeing side reactions in the presence of trace impurities or alternative stereochemistry. Speaking with several synthetic chemists in the agrochemical research sector, we repeatedly hear the same: predictability of the active’s behavior from batch to batch matters more than almost any single chemical property.

    Specifications: More Than Just A List

    Publishing a spec line is easy, but real-world manufacturing shows there’s more to quality than ticking off numbers. The melting point, for example, carries a direct link to purity and correct exo-isomer content. Consistent melting points between 114–116°C reveal a careful balance of recrystallization, drying, and storage protocols—not just a checkbox. We have experimented with humidity ranges and container linings, observing firsthand the influence on the stability of O-(Methylcarbamoyl)Oxime functionality over time.

    Handling characteristics, such as hygroscopicity and static charging, strongly affect both weighing by hand and dosing by automation. Early batches tended to cling to scoops or stick to polypropylene, so our technicians optimized particle size to reduce fine dust and improve pourability. These small process improvements yield practical gains: less waste, safer handling, fewer product losses during transfer. Moisture content, typically measured below 0.5%, correlates directly with shelf life and reproducibility in preparation of derivatives.

    Applications: Purpose-Driven Chemistry

    Customers use the compound chiefly as a synthetic intermediate. Its O-(Methylcarbamoyl)Oxime group stands out as a carbamoyl source for coupling and cyclization reactions not easily tackled with simpler oximes. For pesticide research, the norbornanone backbone brings rigidity, aiding the introduction of chirality and controlling the three-dimensional layout in active molecules.

    Our supply chain colleagues highlight a point that often gets overlooked: the end-to-end traceability of each batch provides customers with an audit trail for regulatory registration and patent validation. In fields governed by regulatory scrutiny, uncertainty in raw material origins leads to headaches downstream—litigation, recalls, and patent disputes. Fully documented synthetic history becomes an insurance policy for clients charting a new active ingredient or process chemistry with the potent norbornanone core.

    Research teams favor the compound when performance must be replicated across locations—whether for multi-site residue analysis or multilab screening projects. Having managed direct technical service with several large field trial platforms, we’ve seen firsthand how a poor batch can stall entire projects, wasting personnel time and trial acreage. Robust internal standards, short lead times, and harmonized output across facilities aren’t optional extras; they are hard-won features arising out of years of feedback and investment.

    Comparing Norbornanone Oxime Variants In The Real World

    Chemists face abundant options—endo versus exo, simple cyano versus multi-substituted derivatives. What sets our Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime apart is the combined orientation of both chloro and cyano at the specified positions, joined to an O-(methylcarbamoyl) oxime group. In bench tests, endo isomers demonstrate sluggish reaction rates in standard nucleophilic and acylation conditions compared to our exo product. Moreover, the dual substitution pattern introduces electronic effects into the norbornanone ring system, shifting selectivity in late-stage derivatization. This structural feature can make or break a project, so manufacturers who know the ring system at an atomic level have an edge in troubleshooting and method development.

    We routinely receive samples from laboratories struggling with cross-contamination in building-block stocks supplied by traders with unclear chain of custody. By focusing on a closed-loop, direct-from-process model, our oxime delivers both purity and batch-stability needed for critical scale-ups. Each time a lab avoids a failed scale reaction or surprises during a registration submission, that reflects the silent work done by controlling stereochemistry, reactant stoichiometry, and storage conditions back at the source.

    In the early days, some users would substitute more basic norbornanone oximes in preliminary applications, thinking they could later “upgrade” to the chloro-cyano exo version for optimization. In practice, this approach wastes time. Slight molecular differences lead to major shifts in reaction rates and product profile, so starting with the right isomer avoids endless rework and surprises. Our specialized oxime brings reproducibility for method development, and the well-characterized batch histories mean customers hold confidence for their analytical records and patent files.

    Supporting Responsible Chemistry: Batch Control and Transparency

    Care in the lab flows out of more than process diagrams and theoretical yields. Traceability and environmental responsibility both start on the shop floor. We use only locally sourced raw materials whenever possible, reducing long-distance transport risks and volatility that plague global chemical logistics. By keeping all processing under one roof, our chain of responsibility isn’t clouded by third-party brokers, licensing agents, or untraced byproducts.

    Every drum of Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime exits the facility with a complete batch history. This means solvent batches, operator logs, environmental controls, and deviation reports tie each gram to a story—sometimes a challenge with a crystallizer, sometimes a mid-stream tweak in catalyst recipe, sometimes a process control innovation borrowed from another product line. Failures, adjustments, and improvements all get absorbed into the collective experience of the shop. Years of delivering this compound have shown that the discipline of documenting each detail does more than establish trust for audits—it strengthens internal knowhow, preventing repeat errors and keeping the knowledge pool robust for future hires.

    On Safety, Handling, and User Experience

    Hands-on work with oximes and carbamoyl derivatives never turns mundane. For operators and bench chemists alike, familiarity with handling pays dividends in minimizing waste and mishaps. We ship the product in tightly sealed, HDPE-lined drums or tamper-evident polyethylene containers, with an inner foil barrier to protect against incremental hydrolysis or solvent absorption. Controlled humidity and out-of-light procedures anchor the long-term storage stability you’d expect for fine chemicals that end up in regulated industries.

    A chemical manufacturer's job doesn’t end at the factory door. Years fielding user calls about stability, clumping, and safety make that clear. We address FAQs on solubility, off-odors, bridging, and cross-reactivity weekly, and we keep iterating our process based on what customers face on the ground. Direct communication means a technical specialist—not a generic sales rep—answers when a user reports a crystallization issue or incompatibility in synthesis. This feedback culture pushes real improvements, grounding us in the actual workflows of formulation teams and scaling chemists.

    For newer users, a few precautions pay. Wearing gloves, keeping the material capped, and storing in a cool, stable location go a long way. Our team has learned from every mislabeled container and accidental spill; little lessons make for less downtime and safer benches.

    Sustainability and Change: Meeting New Standards

    Responsible chemistry means conscious choices at every stage. We have worked to optimize solvent recovery in our norbornanone process line. Every kilogram of recycled acetonitrile, every controlled release of mother liquor, reduces environmental footprint and tightens our cost structure. Regulatory regimes in Europe and Asia keep moving the bar higher—a reality most in chemical manufacturing see as an ongoing push, not a one-shot compliance hurdle.

    By removing chlorinated solvents from our process, we eliminated one major source of hazardous waste—and found that attention to sustainable alternatives improved batch reproducibility. Feedback from customers in green-chemistry research circles spurred us to review catalyst use and drying agent selection; now, each new pilot run incorporates a sit-down with environmental compliance and process development. Success here boils down to the team’s willingness to wrestle with difficult optimizations until a cleaner, financially viable solution emerges.

    Our local regulators audit air and water emissions regularly, sparking continuous improvement. Documentation of reuse streams, waste tracking, and staff training anchor a process that matches technical ambition with stewardship. Bridging chemical performance to a transparent, sustainable production model remains a daily challenge, but the benefit shows up in supply security, cost competitiveness, and, frankly, pride of craft.

    The Human Factor: What Decades in Manufacturing Reveal

    Molecules only tell half the story. The chain includes operators who know the quirks of stuck filters, maintenance mechanics patching up a seized reactor, and QC technicians spotting a faint impurity band Tuesday at midnight. These people catch variations before they become customer problems. By investing in continuing technical education and process cross-training, we foster a crew who can adapt—whether a supply crunch hits or a customer needs a rush batch with a new testing protocol. More than any isolated process tweak, this focus on human capital keeps the plant nimble.

    Cultural lessons matter, too. Missteps—like launching a shipment before double-checking the exo-to-endo ratio, or shortchanging drying time in a rush—buffed our humility and made us double down on audits and checklists. Supplier relationships became a technical partnership, not just a transaction, after living through a recall triggered by an unnoticed raw material change a decade ago. Everyone on the team knows reputation builds one delivery at a time, tested by how we manage complaints as much as by celebrating smooth campaigns.

    Solutions For Tomorrow: Customer Collaboration

    We keep in close conversation with engineers, formulation chemists, and IP professionals who depend on our Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime. Some look for custom lot sizing or unique pack formats. Others ask for a rush method validation or documentation tailored to jurisdictional requirements. Our technical development group can adapt batch scale, impurity profiling, and shipment timelines to fit project needs, often drawing on experiences from other product lines or failed pilot campaigns. This real-time adaptation transcends the generic “customization” catchphrase so common in commodity markets.

    The shared goal among users and producers lies in consistency, transparency, and fit-for-purpose chemistry. We have seen time and again that up-front investment in validation and user testing saves everyone time, money, and aggravation over the long run. Efforts spent clarifying requirements and sharing process details do much to forestall myths, cross-lab inconsistencies, and late-stage fire drills. A deeper partnership between manufacturer and user means fewer surprises and better science—critical in regulated markets and cutting-edge research alike.

    Looking Forward: Setting the Standard in Norbornanone Oximes

    Possessing in-house control over every aspect of production—from raw input vetting to final batch QC—moves Exo-3-Chloro-6-Cyano-2-Norbornanone O-(Methylcarbamoyl)Oxime out of the “commodity” camp. Our experience demonstrates that each detail—from isomer control to user feedback cycles—gives researchers and formulators a head start in both technical success and regulatory clarity. The combination of robust documentation, direct technical support, consistent product performance, and a genuine focus on environmental stewardship let us serve both the needs of the present and the expectations of the future.

    Across hundreds of batches and thousands of user inquiries, we have seen this oxime deliver value best in the hands of those who demand more than a chemical name and a purity number. Our commitment to hands-on involvement, transparent reporting, and tight process control means our customers and partners step into their next experiment or synthetic campaign with tangible confidence. The next wave of advances in carbamate chemistry and norbornanone derivatives will be built on a foundation formed as much on trusted relationships and purposeful process improvement as on the underlying molecular architecture.

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