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1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride

    • Product Name 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride
    • Alias DSC
    • Einecs 629-601-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    157122

    Chemical Name 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride
    Molecular Formula C5H7ClN2O2S
    Molecular Weight 210.64 g/mol
    Cas Number 214065-42-2
    Appearance White to off-white solid
    Boiling Point No data available
    Melting Point No data available
    Solubility Soluble in organic solvents such as dichloromethane
    Density No data available
    Purity Typically >97%
    Storage Conditions Store in a cool, dry place and protect from moisture
    Synonyms 1,2-Dimethylimidazole-4-sulfonyl chloride
    Iupac Name 1,2-dimethylimidazole-4-sulfonyl chloride
    Smiles CC1=NC=CN1S(=O)(=O)Cl
    Hazard Statements Irritant; harmful if inhaled or swallowed

    As an accredited 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, sealed with a PTFE-lined cap, labeled with chemical name, hazard warnings, and handling instructions.
    Shipping **Shipping Description for 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride:** Ships in a tightly sealed container under dry, cool conditions. Protect from moisture, heat, and direct sunlight. Classified as a corrosive substance; handle with care. Complies with relevant safety and transport regulations. Ensure compatibility with packaging during shipment. Use appropriate labeling and documentation for chemical transport.
    Storage Store **1,2-Dimethyl-1H-imidazole-4-sulfonyl chloride** in a tightly sealed container under a dry, inert atmosphere (such as nitrogen or argon) at a cool, stable temperature. Protect from moisture and direct sunlight, as the compound is sensitive to hydrolysis and degradation. Store in a well-ventilated area, away from incompatible substances such as strong bases, oxidizers, and water. Use appropriate labeling and safety precautions.
    Application of 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride

    Applications of 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride in Industrial Manufacturing

    As a specialized manufacturer of 1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride, we supply this intermediate to leading manufacturers dedicated to advanced material synthesis and specialty chemical production. Below, we detail relevant, real-world application segments, highlighting essential formulation and regulatory aspects for each scenario.

    1. Pharmaceutical Intermediate Synthesis

    Active pharmaceutical ingredient (API) producers use this compound in the construction of heterocyclic sulfonamide groups, which are integral building blocks for antibacterial and antifungal drugs. Its chlorinated sulfonyl functionality enables efficient coupling reactions with amine-bearing core structures during multi-step organic synthesis, where precise control over purity and yield is critical for successful downstream conversion into APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (GMP) for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) General Chapter <1045>
    • European Pharmacopoeia Monograph 5.08
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Applied at 0.9–1.2 molar equivalents relative to amine substrates; exact ratio depends on target compound and requires adjustment for impurity profile control and conversion efficiency.

    Downstream process integration

    • Charged during the sulfonamidation step following ring closure or core scaffold formation, typically in the presence of mild organic bases and solvents under controlled temperature.

    Final product types

    • Sulfonamide antibiotics
    • Antifungal agents
    • Precursor intermediates for cardiovascular pharmaceuticals

    2. Crop Protection and Agrochemical Formulations

    Agrochemical companies rely on this material as a sulfonylating agent when constructing active sulfonylurea herbicides and related fungicidal compounds. Its reliable reactivity profile ensures it integrates efficiently during key condensation stages, where even minor formulation deviations can impact the selectivity and potency of the resulting agrochemical active.

    Industry compliance standards

    • FAO Specification for Pesticide Ingredients
    • ISO 9001:2015 Quality Management Systems (applied to manufacturing process)
    • REACH Registration (EC No. 1907/2006, for EU-bound exports)
    • US EPA Pesticide Registration Manual, Chemical Standards

    Typical usage ratio

    • Commonly dosed at 0.95–1.1 molar equivalents, based on the target sulfonylurea or sulfonamide crop protection agent; slightly excess dosing may be employed to drive completion at industrial scale.

    Downstream process integration

    • Incorporated after initial core assembly, as part of the sulfonylation step during synthesis of herbicide or fungicide actives, typically followed by ring closure and purification.

    Final product types

    • Sulfonylurea herbicide actives
    • Triazole fungicide bases
    • Select preemergence weed control agents

    3. Specialty Dye and Pigment Manufacture

    Producers of specialty dyes, including those for textiles and electronics, use this molecule to introduce sulfonyl groups onto imidazole-based aromatic rings. This step enhances water solubility and color intensity in high-value pigment and dye formulations, where reproducible reactivity and absence of side reactions govern the performance and batch-to-batch consistency of the end products.

    Industry compliance standards

    • Oeko-Tex® Standard 100 (textile chemicals)
    • EU Regulation (EC) No 1907/2006 (REACH) for industrial dye precursors
    • ZDHC MRSL Level 1–3 (Zero Discharge of Hazardous Chemicals)
    • SATRA TM18: Dye Performance and Quality Control

    Typical usage ratio

    • Blended at 0.7–1.3 molar ratio depending on desired dye solubility and depth; formulation typically optimized for substrate affinity and final product hue.

    Downstream process integration

    • Introduced during the aromatic sulfonylation stage, prior to azo or phthalocyanine core assembly, using solvent-based batch reactors with continuous mixing and real-time QC checks.

    Final product types

    • Reactive textile dyes
    • Electronic ink pigments for display applications
    • Special effect pigments for automotive coatings

    4. Chemical Research and Custom Synthesis Services

    Custom synthesis laboratories, including those engaged in contract research (CRO), select this reagent for the preparation of protected sulfonamide and imidazole derivatives. It serves as a critical intermediate for synthesizing novel bioactive frameworks and analogues under controlled laboratory and pilot-scale conditions, where method development must adhere strictly to safety and documentation requirements.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Accreditation
    • OECD Principles of Good Laboratory Practice (GLP)
    • United States Drug Master File (DMF) requirements for intermediates
    • GMP guidelines for pilot-scale intermediates

    Typical usage ratio

    • Deployed at a 1:1 molar ratio with the reactant of interest; small-scale experimentation may vary by up to 10% depending on reactivity screening results and intended final structure.

    Downstream process integration

    • Employed during functional group installation or protection steps, commonly in combinatorial chemistry libraries or for lead compound generation, under validated batch protocols.

    Final product types

    • Small-molecule research intermediates
    • Protected heterocyclic scaffolds
    • Library compounds for drug discovery screens
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    Certification & Compliance
    More Introduction

    1,2-Dimethyl-1H-Imidazole-4-Sulfonyl Chloride: An Insider's Perspective from the Production Line

    On the Shop Floor: Turning Chemistry into Practical Tools

    The journey from raw starting materials to a ready-to-ship batch of 1,2-dimethyl-1H-imidazole-4-sulfonyl chloride follows more than just a flowchart in a protocol. Each dry kilogram tells the story of intricate handling and close process supervision, where precision controls more than just theoretical yield. Over years spent calibrating our reactors and optimizing work-up procedures, we've learned the subtle quirks that separate this sulfonyl chloride from the crowd.

    Production teams in chemical manufacturing thrive on routine, but few batches pass without something unexpected cropping up. This compound’s sensitivity to moisture demands a particularly attentive workforce and tight plant discipline. Standard moisture control or run-of-the-mill inert gas sweeps rarely suffice. Every person on the line learns that even the tiniest slip in sealing or handling can lead to compromised purity. This is not an academic detail—it shapes the finished product’s performance and reliability, especially in high-stakes synthesis downstream.

    Quality, in our world, stems from diligent upstream selection. We source input chemicals with narrow impurity profiles and ensure careful storage, not because regulations say so, but because we’ve seen what happens when corners get cut. The effect might not always show up in a quick analytical snap, but labs downstream will feel it during scale-up or in side-product formation.

    Product Model and Specifications: Not Just Numbers on a Slip

    Over time, teams on our plant floor and in the lab together have agreed on a distinct baseline. Our process typically yields 1,2-dimethyl-1H-imidazole-4-sulfonyl chloride as a white to pale off-white solid, often presenting as a crystalline powder if handled with care at key points. Chemists will immediately notice differences in appearance that signal a near-ideal synthesis: clean color, proper texture, and no sticky agglomerates.

    Most requests from industrial and R&D clients target material with a minimum assay of 98%, and that is where our QC places the batch release threshold. Many in our field have learned the hard way that chasing every last decimal point beyond this brings sharply rising costs and diminishing returns in actual reactivity on customers’ benches. Low moisture content, consistently below 0.3%, remains essential. Stubbornly high water, even in the low single digits, risks premature hydrolysis; the margins are tight.

    Any experienced chemist knows to scan for hydrochloric acid release and the stability of the sulfonyl chloride in air. That translates into a workable shelf life at room temperature, with simple desiccation rounding out the protection needed for safe transport. The stability windows exceed short-term handling demands, but we steer clear of promising indefinite storage—no process can stop chemistry cold.

    Front-Line Use: Real-World Chemistry in Action

    Fielding questions from users around the globe reveals what buyers value most—not just numbers on a certificate of analysis, but reliable, predictable behavior in real reaction flasks. As a sulfonyl chloride, this chemical draws steady demand in the preparation of specialized sulfonamides, sulfones, and other functionalized heterocycles. Synthetic designers in pharmaceuticals, crop protection, and material science call for this reagent when they need improved selectivity or the chance to install an imidazole motif.

    The pattern stands out in our experience: gram-scale R&D rarely reports trouble, but scale-up into kilo or larger batches quickly tests the consistency of our process. Minor impurities that slip past lesser manufacturers can create batch-to-batch headaches once reactions are run at production scale. Conscientious formulation teams watching for side reactions lean heavily on us to provide reliable, reproducible purity. Nothing sinks a development pipeline faster than a scale-up that fails due to unidentified contaminants.

    For some customers, 1,2-dimethyl-1H-imidazole-4-sulfonyl chloride solves solubility and stability limitations posed by other sulfonylating agents. The presence of electron-withdrawing sulfonyl and two methyl groups improves its volatility profile compared to more hydrophilic analogues. At the same time, its stability in common organic solvents, like dichloromethane and acetonitrile, opens doors to a broader reaction design. Process development teams appreciate that flexibility, especially when handling tight environmental controls or strict residual solvent parameters.

    Real-world use cases often land in tough territory that product brochures skip over. Take, for instance, customers working on API intermediates or fine-tuning bioactive compounds. The selectivity granted by this sulfonyl chloride, thanks to the steric effects of those methyl groups, has allowed multiple drug discovery teams to hit difficult substitution patterns without running into troublesome over-reaction or unwanted side chains.

    The Practical Differences: What Sets This Sulfonyl Chloride Apart

    If every sulfonyl chloride offered identical performance, there’d be little reason for dedicated chemical divisions to obsess over the quirks and value of this specific compound. Our plant’s long engagement with the 1,2-dimethyl-1H-imidazole motif shows its unique pulse. The double methylation strengthens hydrophobic character, mitigating certain unwanted solubilities and boosting shelf stability. Many less-substituted analogues, although familiar, bring a higher risk of hydrolysis and unpredictable decomposition in open-air or hydrated environments.

    Practical differences show up not in spreadsheets but under real reaction conditions. Substitute with imidazole-4-sulfonyl chloride (sans methyls), and experienced process chemists routinely report lower conversion rates or headaches with isolation. The methylated version scopes out a balance: least reactivity sacrificed, greatest process leeway gained. Over the years, client feedback and internal R&D work confirm that this compound’s behavior often helps shave steps from purification or facilitates direct downstream reactions—a distinct advantage when project timetables run short or costs need controlling.

    Heat sensitivity appears somewhat improved, thanks to the stabilizing influence of those methyl groups. There’s more margin to operate at slightly elevated temperatures without sacrificing the reactivity window entirely, a property our technical team first confirmed during comparative stress tests. Handling in modestly equipped labs becomes more straightforward, letting users push conditions with fewer worries about runaway degradation or corrosion.

    Downstream applications in dye chemistry and advanced coatings also favor this variant for its ability to stack up with broad substrate compatibility. For industrial chemists pressed to streamline workflows, the predictability of product formation—minimizing clean-up and avoiding excess reagent waste—makes a daily difference.

    Addressing Real-World Challenges: Moisture, Storage, and Hand-to-Hand Reliability

    Moisture poses an ever-present threat, and nowhere does that lesson come through more sharply than on our plant floor. Staff account for air moisture fluctuations by storing raw reagents and intermediates in dedicated dry rooms. Open transfers or lengthy exposures earn fast correction, as both plant experience and customer returns make clear how quickly tiny water incursions degrade the sulfonyl chloride.

    In logistics, our teams seal batches extra-tight and emphasize layered barriers, not only for transit, but also so end-users open fresh packs that haven’t sweated or absorbed trace humidity. A good desiccant in an inner pouch makes a visible impact. Although these measures add small incremental costs, their payoff comes in customer trust and reduced waste, a balance that only hands-on production crews can rightly appreciate.

    Storage calls for a space away from sources of heat and atmospheric shifts. Plant workers and technical advisers share best practices directly with buyers: keep the drum sealed, ensure access transitions quickly, and rotate stock within a documented time window. Extended shelf-life follows from the sum of minute decisions by every operator on the supply path, not from miraculous packaging.

    Scale-Up: Consistency and the Price of Shortcuts

    Process scale-up exposes quality like few other stress tests. At the pilot stage, smart teams replicate the scale and order of operations from our plant runs as closely as possible. Control in lab glassware rarely signals smooth sailing when the same chemistry gets pushed up to fifty liters or more. Our direct observations match what contract manufacturers report: color, odor, and purity swings can upend the economics of a project quickly if the input sulfonyl chloride isn’t properly managed from the start.

    Shortcuts, whether in drying, purification, or packaging, almost always amplify risk. A few grams of absorbed moisture in a single container may skew results for an entire synthetic campaign—a fact often learned through costly reruns and failed validations. Customers scale up their procurement as confidence in batch homogeneity grows, so our own revenue rests on taking every safeguard rather than promising shortcuts.

    Repeatable success depends on eliminating variables in both the starting material and the work-up: solvents cleaned to tight technical specs, glassware and reactors checked for inertness, and every production log reviewed by hands familiar with every dial and valve on the plant floor.

    Technical Experience: Lessons Learned from Direct Production

    Technical nuance matters at production level. The impact of batch agitation, for example, often appears underappreciated in textbook recipes, yet makes measurable differences in crystallinity and ease of filtration. Through countless production runs, we've learned how agitation profiles, cooling rates, and precise dosing affect more than just visual appearance—they shift impurity uptake and natural filtration times.

    Solvent grade selection rarely stays theoretical. Minor differences in residual ions or trace volatiles influence final assay and shelf stability, prompting our sourcing department to negotiatie robust specs backed by precise COA documentation from our suppliers. This isn't paperwork for the sake of compliance, but a practical shield against reruns and failed lots.

    Plant teams work closely with in-house analytical chemists, spending hours calibrating methods and verifying that production-scale NMR and HPLC still track properly across seasonal swings and equipment upgrades. Small process tweaks can move impurity fingerprints just enough to be flagged during final release testing, a challenge only handled through persistent trial, repeat runs, and real-world feedback loops.

    Supporting Sustainable Practice: Waste Streams and Recovery

    Waste handling forms part of every responsible manufacturer’s landscape. For years, we have organized solvent recovery and acid neutralization programs that feed directly into lower discharge rates and reduced environmental impact. Process teams balance efficiency with long-term responsibility, finding outlets for spent sulfonylating agents or byproducts where feasible rather than defaulting to incineration.

    Plant-side improvements—such as closed-loop capture of evolved HCl and tight distillation of post-reaction solvents—pay back over time by both cutting compliance headaches and keeping waste below regulatory thresholds. This hands-on approach mirrors the expectations of major chemical users who want sustainability without surprise costs buried in fine print.

    Feedback Cycle: Learning from Every Batch

    Manufacturing isn’t static, and neither are the needs of the scientists or engineers who rely on us. Open lines between the technical support desk, R&D labs, and the production line let us fine-tune both real-world specifications and logistic details. Each customer comment, whether an academic group running a unique synthesis or a multinational scaling for industrial output, contributes to adjustments and process innovations.

    Lessons from every return or out-of-spec report become part of our team discussions. Actions follow, as repeat process checks and small plant modifications reduce risk of future hiccups. The cumulative gains might seem invisible batch-to-batch, but regular users notice steadier quality and faster troubleshooting support—features that don’t stem from a template but from decades of accumulated know-how.

    The Way Forward: Integration and Real-World Partnership

    The best results come from open partnership between the production line, technical advisors, and the wide range of end users. Internally, investing in continuous training ensures each operator understands not just the “how” but also the “why” behind every plant guideline and control. Supply partners who uphold strict analytical verification reinforce our own quality system, so trust gets built into every connection along the pipeline.

    With each year, as regulatory demands tighten and application challenges shift, maintaining trust comes down to transparency and willingness to adapt. Our teams don’t view specifications as static barriers, but as dynamic markers based on lab feedback and market realities. Through direct engagement with process chemists, R&D teams, and industrial buyers, we gain a deeper picture of how 1,2-dimethyl-1H-imidazole-4-sulfonyl chloride can enable more efficient chemistry in the field.

    By staying rooted on the production floor, listening as much as directing, we turn every batch into a promise of reliability, not just a number on a spec sheet. The value added by 1,2-dimethyl-1H-imidazole-4-sulfonyl chloride in your synthesis isn’t handed down from distant corporate summaries—it’s shaped by hands-on experience, open feedback, and complete commitment to science-driven progress.