Products

N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride

    • Product Name: N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride
    • Alias: Chlorimuron-ethyl
    • Einecs: 259-559-4
    • 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

    633622

    Product Name N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride
    Cas Number 4318-56-3
    Molecular Formula C10H14Cl2N2
    Molecular Weight 233.14 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 163-166°C
    Solubility Soluble in water and methanol
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, tightly sealed
    Synonyms 4-Chloro-2-methyl-N,N-dimethylformanilide hydrochloride
    Application Pharmaceutical intermediate

    As an accredited N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g supplied in a sealed, amber glass bottle with a tamper-evident cap, labeled with product name, formula, and hazard warnings.
    Shipping **Shipping Description:** N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride is shipped in sealed, moisture-resistant containers under ambient conditions. The package is clearly labeled with appropriate hazard and safety information. Standard chemical shipping regulations are observed to ensure substance integrity and personnel safety during transit. Handle with care and avoid direct contact or inhalation.
    Storage N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area at room temperature, away from incompatible substances such as strong oxidizing agents. Ensure the container is clearly labeled, and access is restricted to trained personnel. Follow all relevant safety regulations and handling guidelines.
    Application of N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride

    Applications of N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride in Industrial Manufacturing

    As a specialized producer, we serve chemical sectors with N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride, ensuring precise material quality for downstream manufacturers. This intermediate plays a critical role in multiple industries where process integrity, compliance, and performance rely heavily on component selection and use.

    1. Agrochemical Synthesis: Herbicide Intermediate Manufacturing

    Large-scale agrochemical operations rely on this compound as a core intermediate for modern post-emergent herbicides. Direct incorporation into the active synthesis phase enables tightly controlled reactions, supporting yield, by-product minimization, and consistent active content in final herbicide formulations. Downstream production plants integrate precise feedstock dosing, monitored through in-line analytics, meeting market demand for reliable crop protection solutions.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)
    • U.S. EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) standards
    • China National Standard GB 2763 for pesticide residue control

    Typical usage ratio

    • 5-30% by mass in the total intermediate feed for triazine and related herbicide APIs; exact ratio varies by specific formulation and reaction pathway

    Downstream process integration

    • Metered addition after base reaction stage, followed by high-temperature condensation under inert atmosphere
    • Enters amidine functionalization step for subsequent coupling reactions

    Final product types

    • Selective cereal crop herbicides
    • Broadleaf weed control actives
    • Premix herbicide concentrates
    • Herbicidal ingredient technical powders

    2. Pharmaceutical Intermediate Manufacturing (Active Ingredient Synthesis)

    Advanced pharmaceutical plants use this material as a pivotal intermediate in active pharmaceutical ingredient (API) routes, particularly for select antihypertensive and anti-infective drug substances. Chemists adjust molar equivalents for target conversion, implementing rigorous in-process controls to ensure batch traceability. Its structural features facilitate downstream heterocyclic formation or as a protecting group in multi-stage synthesis schemes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopeia (Ph. Eur.) monographs for intermediates
    • China Pharmacopoeia (CP) for API manufacturing standards

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to primary amine or carboxyl precursor, determined by process optimization and regulatory requirements

    Downstream process integration

    • Dosed in pre-final condensation or cyclization step, under controlled temperature and solvent regime
    • Integration with automated synthesis reactors for batch or continuous operation

    Final product types

    • Pharmaceutical APIs (antihypertensives, anti-infectives)
    • API intermediate bulk compounds
    • Key intermediates for cardiovascular drug manufacturing
    • Contract-manufactured advanced intermediates

    3. Veterinary Drug Intermediate Production

    Many veterinary medicine producers deploy this substance during the core intermediate stage for synthesis of licensed animal health products and actives. Quality control personnel conduct extensive analytical verification on incoming batches for use in regulated environments. Technicians monitor reaction conversion to minimize impurity formation, directly linking to later process steps including salt formation and crystallization for lower-dose veterinary actives.

    Industry compliance standards

    • VICH GL 35 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 500–599 Veterinary Drugs
    • EU Regulation (EC) No 726/2004 for veterinary medicinal products
    • China Veterinary Pharmacopeia

    Typical usage ratio

    • 3-20% by weight in multi-step synthesis routes, depending on reaction scale and yield requirements

    Downstream process integration

    • Charged during nucleophilic substitution or amidine introduction step
    • Feed control integrated with online purity monitoring and process automation

    Final product types

    • Livestock and companion animal drug APIs
    • Veterinary premix actives
    • Final injectable and oral veterinary formulations
    • Animal nutritional supplement intermediates

    4. Fine Chemicals and Dye Intermediate Synthesis

    Specialty dye and pigment producers select this material for functionalization and selective substitution in downstream coupling reactions. Plants often adjust the input rate according to desired chromophore structure and end-use requirements, ensuring precise color hue and stability. Teams monitor reaction endpoints through high-precision analytical tools, maintaining consistent product character and meeting colorant performance specifications for industrial and consumer uses.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems (chemical, dye & pigment industry)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • Oeko-Tex Standard 100 (for textile dye stuff safety)
    • China Industrial Standard HG/T 3706 for dye intermediates

    Typical usage ratio

    • 2–10% of total reactant mass in dye intermediate production; adjusted by desired functional group density

    Downstream process integration

    • Added at diazotization or coupling stage following initial aromatic amination
    • Blending with secondary amines and functional group donors in closed system reactor trains

    Final product types

    • Monoazo and disazo dye intermediates
    • High-performance industrial pigments
    • Textile, inkjet, and plastic colorants
    • Specialty chemical intermediates for further processing

    Free Quote

    Competitive N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride: Practical Insights From the Manufacturer’s Bench

    Bringing Reliable Chemistry to Modern Labs

    Working right at the intersection of raw material sourcing, scale-up synthesis, and daily production, our team has gained a close-up view of the real-world impact of N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride. This particular molecule, often referred to within the industry by its short name or as part of custom formulations, forms an important node in fine chemical manufacture. Factories, research units, and pilot plants all find use for this compound in various forms, but the demands of each operation differ widely. We create our batches with direct feedback from process chemists and engineers, responding to the challenges they face, whether related to yield optimization, purity adjustments, or downstream compatibility.

    On our floor, chemistry never stays on paper. It converts into reactors churning at different throughputs, vacuum pumps humming day and night, constant attention to each crystallization endpoint. Our staff monitors appearance, odor, solubility, and checks for contamination before anything leaves the plant. Because of its hydrochloride form, this compound offers good handling properties, storing well under typical lab and warehouse conditions. Our process eliminates lot-to-lot variability by controlling each reagent ratio and adjusting the reflux parameters, informed by years spent understanding how side products can form under different temperatures or hold times. These continuous tweaks now allow us to produce each lot with both high assay and a clean impurity profile.

    A Closer Look at Our Synthesis and Purification Steps

    Scaling up from lab beakers to industrial reactors brings plenty of surprises. Our teams discovered early that slight tuning of methylation conditions and acidification influences not just purity, but how quickly filtration and drying can wrap up the batch. We employ standardized glass-lined reactors, keeping both the amine source and chloro-tolyl components at controlled feed rates. Sampling is not a box-ticking exercise on our line—it’s a way to solve problems before they grow. Problems like unreacted starting material, color bodies, or troublesome moisture traces do not go unnoticed. Our batch tracking system keeps records of adjustments, so every deviation becomes a learning point for future runs.

    Adding hydrochloride at the right time matters especially for downstream users who require stable, easy-to-dose powders free of clumping or bridging. The result is a form that weighs out with precision, stays free-flowing on the shelf, and responds predictably in both bench chemistry and automated lines. Years of hands-on synthesis have taught us to take nothing for granted—from agitator speeds affecting slurry formation, to how room temperature or humidity drift affects final packing. We control these variables so our customers get a batch that matches their expectations for performance, not just a compliance checkbox.

    Understanding the Role in Synthesis Pathways

    N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride often appears deep within multi-step synthetic routes—not as a showpiece molecule but as a versatile intermediate supporting a vast number of transformations. This product shows its value in medicinal chemistry and agrochemical precursor work, helping build heterocyclic frameworks or serving as a tailored reactant in substitution, cross-coupling, or reductive amination. From first contact with our customers in process development, the feedback is clear: predictable reactivity now means fewer headaches down the line, especially during scale-up or regulatory submission.

    The QC and development staff at our facility engage directly with scientists who run test reactions or validate impurity profiles. In our own pilot labs, we’ve run mock reactions requested by clients building API libraries or agrochemical scaffolds. Each time, we gain a clear sense of how subtle impurities or changes in crystalline form influence downstream splitting or purification. As manufacturers, we do much more than fill drums – our support covers custom particle size fractions, help with regulatory submissions, and troubleshooting of scale-dependent solubility. Our expertise comes from solving real failures, like resin fouling during purification or waste stream issues during hydrolysis, not just relying on published procedures.

    Specifications Shaped by Practical Production

    Chemistry textbooks will list plenty of data: molecular weight, melting point, or solubilities. These facts matter, but on our scale, numbers only go so far. We adjust our product specifications based on what hundreds of downstream reactions and production hiccups have shown us. Most buyers want a white to off-white crystalline powder, but we go further—checking bulk density for automated feeders, making sure moisture content stays within a band suitable for powder handling equipment, and checking for stability under normal warehouse lighting.

    Tech staff at our plant regularly cross-check new methods, because suppliers advertising generic “high purity” often ignore trace side products that can cause headaches in later synthetic steps. Our typical lots exceed 98% assay, with tight limits set for residual solvents and known structural isomers. Each parameter responds to a specific real-world demand, whether it’s reactivity in a Suzuki coupling or azole ring closure. Rather than just ticking off generic international standards, our approach hones in on the requirements that matter for industrial, pilot, and R&D users alike.

    What Sets This Product Apart

    Quality and safety are not up for debate. Our N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride takes center stage because it builds on practical experience, not just a checklist. From the start, we sourced clean amine precursors and process acids, upgrading our distillation units to avoid reaction byproducts known to plague other supply chains. Over time, we’ve benchmarked our compound against market samples, finding that uncontrolled feedstock quality or skipping proper drying steps leaves competitors with higher color bodies and unpredictable solubilities.

    Our focus extends to the details that matter for day-to-day users. For example, particle size distribution does more than look nice on paper. We’ve found that consistent micronization cuts down on static buildup in automated hoppers and enables reliable weighing even in high-throughput plants. Our technical staff run actual dosing simulations, using the same feeders and balances our customers rely on. Overdried product might dust too much; high moisture causes clumping under warm conditions. Experience has taught us the sweet spot, and we tune each batch accordingly.

    Practical Uses and End Applications

    Year after year, process chemists and development scientists return for this compound because it enables workflows that demand more than theoretical performance. As an intermediate for building key aromatic or heterocyclic fragments, this material finds its way into pharmaceutical research, specialty agrochemicals, and advanced polymers. Only consistent reactivity and a well-controlled impurity profile can support the preparation of active ingredients or specialty ligands where yield and selectivity matter more than just raw output.

    Researchers in our client labs talk about cutting days off project timelines because our product dissolves predictably and doesn’t throw up new TLC spots or unaccounted-for masses in qNMR analysis. For process scale plants prepping batches of a few kilograms to a few tons, the need for a reliable input chemical translates to higher confidence through pilot and into final campaigns. We understand that one rogue impurity can derail an entire batch, so our upstream controls and in-process analytics serve as the front line of defense for anyone betting on downstream process reproducibility.

    Field Learnings: Avoiding Pitfalls and Surprises

    Direct conversations with our partners exposed common issues around variability found from off-the-shelf or poorly documented sources. Examples include sticky residues on dryer trays, batch yellowing from uncontrolled acid addition, and slow filtration times triggered by undetected particle agglomeration. Through collaboration with synthetic organic chemists and process engineers, we targeted these pressure points by tuning every step from acidic workup pH adjustment, to antisolvent selection, to final vacuum drying cycles.

    Every batch teaches us something new. We pushed filtration rates up and dust generation down, guided by user-reported headaches in automation or sampling. Protection from atmospheric moisture during late-stage packaging cut down on field complaints of flow or fill issues. We view these incremental improvements as the result of years on the floor, not just standardized specs. This way, chemists in our customer labs spend less time problem-solving unexpected side effects and more time pushing science forward.

    Differences From Other Similar Materials

    In today’s market, many claim parity with the benchmark. Our approach sets us apart on two major fronts: hands-on process control and total transparency. Instead of only advertising minimum purity, we provide full impurity profiling and batch-specific analysis, offering a view of what microcomponents exist and how they affect the intended syntheses. Competitor samples sometimes skip important purity markers. Direct comparisons on test benches showed tighter melting profiles, cleaner solution color, and less tendency to cake following extended storage—all results of methodical process improvements made over years.

    Our compound’s hydrochloride form brings added benefits for those working with water-sensitive substrates. Handling ease, consistent bulk density, and absence of fine particulate clumping gives formulators and process operators more control during metering and blending. We have fielded multiple technical inquiries and conducted side-by-side application studies, demonstrating higher reproducibility and faster throughput where our material replaced less-controlled alternatives.

    Supporting Safe Handling and Sustainable Practice

    Decades spent scaling and managing fine chemical manufacture have reinforced the importance of both human and environmental safety. From the earliest R&D discussions to current plant operations, our team keeps environmental impact top of mind. Waste minimization, solvent recovery, and responsible effluent treatment do not just serve compliance—they help maintain reliable supply lines and reduce risks to both users and neighbors alike.

    We actively share safe handling guides, layouts for effective powder control, and relate experienced-based solutions for common challenges such as dust containment or worker exposure minimization. These insights are born out of trial, improvement, and a culture that puts employee health on par with batch yield. By making sure all personnel—ours and our clients’—are equipped with up-to-date chemical information, we support broader industry efforts to create cleaner and safer workspaces, while consistently meeting the production targets expected in pharmaceutical and specialty chemical supply chains.

    Constant Feedback Loops: Listening, Learning, Adapting

    In the world of chemicals, every loss of reactivity, every batch that won’t filter quickly, or every off-color sample has a root cause. Feedback loops drive us to adapt—data comes back from the loading dock, the lab bench, and on down the chain of custody. Updates to drying techniques, in-process analytics, or site workflows feed directly into how we tune future lots. Conversations with users have sparked everything from custom drum linings to anti-static packaging, each addressing a detail that impacts the real user experience.

    Our commitment is not only to robust quality but to project-specific partnerships. New reaction classes and expanded demand in high-throughput screening constantly push us to ask what we can improve next. By anchoring synthesis and purification protocols in these direct experiences, we ensure every batch becomes stronger than the last. Our technical desk remains open to all client feedback because in our view, incremental advances across safety, reproducibility, and application support drive not just market success, but the progress of chemistry as a whole.

    Final Thoughts from the Factory Floor

    Supplying N-(4-Chloro-O-Tolyl)-N,N-Dimethylformamidine Hydrochloride means taking direct responsibility for every step—from the state of the starting materials to the reliability of each packed drum going out the gate. The process is anything but routine. Staff confront surprises, chase down odd color shifts, troubleshoot clumping, and work long nights to meet timelines. These experiences shape the confidence we offer to every customer, whether their destination is a kilo scale organic research lab or a large-volume specialty plant. By acting on years of cumulative hands-on learning, our teams produce more than just a catalog entry—they deliver a product that makes downstream chemistry safer, simpler, and for many, a little more predictable in an unpredictable world.

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