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4-Chloromethyl-2-Methylthiazole Hydrochloride

    • Product Name 4-Chloromethyl-2-Methylthiazole Hydrochloride
    • Alias 4-CMT HCl
    • Einecs EINECS 415-810-4
    • 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

    107033

    Productname 4-Chloromethyl-2-Methylthiazole Hydrochloride
    Casnumber 104532-02-9
    Molecularformula C5H7Cl2NS
    Molecularweight 184.09
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint 180-185°C (decomposes)
    Solubility Soluble in water and DMSO
    Structure Contains a thiazole ring with chloromethyl and methyl substituents, present as a hydrochloride salt
    Storageconditions Store at 2-8°C, protected from light and moisture
    Synonyms 4-(Chloromethyl)-2-methylthiazole hydrochloride
    Smiles CC1=NC=C(S1)CCl.Cl

    As an accredited 4-Chloromethyl-2-Methylthiazole Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 25g amber glass bottle with a screw cap, labeled “4-Chloromethyl-2-Methylthiazole Hydrochloride,” includes hazard warnings.
    Shipping 4-Chloromethyl-2-Methylthiazole Hydrochloride is shipped securely in sealed, labeled containers under dry, cool conditions. Packaging complies with hazardous materials regulations to prevent leaks, degradation, or contamination. The product is typically delivered by certified carriers with proper documentation, ensuring safety and regulatory compliance during transport and storage. Handling instructions are included.
    Storage 4-Chloromethyl-2-Methylthiazole Hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Store away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and secondary containment, and follow all relevant safety protocols for handling hazardous chemicals.
    Application of 4-Chloromethyl-2-Methylthiazole Hydrochloride

    Applications of 4-Chloromethyl-2-Methylthiazole Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Chloromethyl-2-Methylthiazole Hydrochloride for advanced industrial applications across several regulated sectors. Its unique thiazole structure provides a functional building block for specialized downstream synthesis processes.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers rely on this compound as a key intermediate in the synthesis of thiazole-containing drug molecules, especially selective kinase inhibitors and anti-infectives. Production lines incorporate the material during advanced stage coupling reactions to introduce specific halothiazole motifs. End users demand high-purity lots, in line with stringent process validation for regulated end APIs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia 10.0/USP General Notices
    • REACH EC No. 1907/2006 for chemical registration
    • FDA 21 CFR 210/211 for finished pharmaceutical controls

    Typical usage ratio

    • 0.15-0.7 molar equivalents per target API batch, adjusted based on yield and downstream coupling efficiency

    Downstream process integration

    • Introduced after initial scaffold assembly, prior to amide or urea functionalization steps in multi-step synthesis

    Final product types

    • Targeted kinase inhibitor APIs
    • Broad-spectrum antimicrobials bearing thiazole moieties
    • Novel antitumor drug candidates under clinical development
    • Pharmacy compounding intermediates

    2. Agrochemical Intermediate Preparation

    Agrichemical producers utilize this compound during the manufacture of advanced thiazole-based active ingredients, including fungicides and insecticides. Process chemists employ the material to introduce chloromethylated thiazole units during early or mid-stage synthesis, ensuring site-specific reactivity and high conversion rates for crop protection agents.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing quality
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • EPA 40 CFR Part 169 (Pesticide Registration)
    • Globally Harmonized System (GHS) of Classification and Labelling

    Typical usage ratio

    • 15-22% (w/w) as an intermediate reactant in multi-component synthesis, adjusted in context of substrate loading

    Downstream process integration

    • Reacted during intermediate formation, preceding heterocycle ring closure and cross-coupling reactions

    Final product types

    • Thiazole fungicidal actives (e.g., propiconazole derivatives)
    • Insecticides incorporating halothiazole functionalities
    • Seed treatment formulation intermediates
    • Herbicidal precursor substances

    3. High-Performance Dye and Pigment Manufacture

    Specialty dye manufacturers select this intermediate for building complex thiazole-based chromophores in textile, leather, and specialty fiber applications. Its well-defined reactivity enables precise construction of thiazole-linked azo dye scaffolds, leading to products with enhanced color fastness and chemical resistance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in dye production
    • EN 71-3:2019 for colorants used in toys and textiles
    • REACH Annex XVII (restricted dyes)
    • ISO 1833 for fiber identification in dyes

    Typical usage ratio

    • 5-11% (w/w) of total batch weight, adjusted for desired chromophore density and toner blending ratio

    Downstream process integration

    • Incorporated as a nucleophilic component in azo coupling, prior to salt formation and drying steps

    Final product types

    • Textile disperse dyes containing thiazole segments
    • High-performance colorfast pigments for synthetic fibers
    • Leather colorants meeting stringent migration limits
    • Technical inks for industrial applications

    4. Specialty Polymer Additive Production

    Producers of advanced polymeric materials use the compound to functionalize resins for electronics, coatings, and packaging. Its thiazole ring imparts polarity, solvent resistance, and controlled electrical properties, meeting the requirements of custom polymer additive formulations.

    Industry compliance standards

    • ISO 10993-18 for characterization of polymer additives
    • RoHS Directive 2011/65/EU for restricted substances (electronics)
    • UL 94 for flame retardancy of polymerized components
    • Food Contact Regulation (EU) No. 10/2011 as applicable for packaging

    Typical usage ratio

    • 0.5-3% (w/w) as a chain modifier or crosslinkable additive, based on resin backbone and end-use application

    Downstream process integration

    • Added during prepolymer mixing or directly into melt-processable resin blends, often with catalyst or initiator systems

    Final product types

    • Conductive polymer films for flexible electronics
    • High-solvent-resistant engineering plastics
    • Specialty coatings with thiazole-based UV stability
    • Food packaging materials with tailored migration limits

    5. Fine Chemical Intermediate for Flavors and Fragrances

    Manufacturers in the flavors and fine fragrance sector incorporate thiazole intermediates for synthesizing unique aroma chemicals, particularly in sulfur-rich olfactory notes. This compound enables targeted modifications in sulfur heterocycle construction, supporting production of flavor enhancers and aromatic aldehyde derivatives.

    Industry compliance standards

    • FEMA GRAS substances list (Flavor and Extract Manufacturers Association)
    • IFRA Standards (International Fragrance Association)
    • 23 CFR 172.515 – Food additive regulations for flavoring substances
    • ISO 9235 for natural and synthetic fragrance ingredient definition

    Typical usage ratio

    • 0.8-2.2% (w/w) as a precursor reactant, depending on the complexity of target aroma profile

    Downstream process integration

    • Used during the structural elaboration of thiazole-containing side chains, often in early-stage aldehyde synthesis

    Final product types

    • Sulfur note boosters for savory foods
    • Specialty aroma chemicals for premium fragrance accords
    • Flavor compounds for beverage and dairy applications
    • Custom perfume oil intermediates
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-Chloromethyl-2-Methylthiazole Hydrochloride: A Chemist’s Perspective

    Genuine Chemistry from the Source

    4-Chloromethyl-2-methylthiazole hydrochloride stands out in the thiazole family for its role as a versatile intermediate, especially in the synthesis of high-value pharmaceuticals, agrochemicals, and specialty molecules. Speaking directly as a manufacturer, it means rolling up our sleeves and getting hands-on with every step, from raw material selection to final packaging. This kind of dedication pays off in the consistent quality and reliability that downstream processors expect. It’s not theory to us. We monitor every batch, know our process residuals like the back of our hand, and continually update our protocols based on plant-floor feedback and analytical data.

    In our experience, academic descriptions of this molecule often don't capture the practical side of working with it on an industrial scale. Thiazoles can be finicky, particularly once functionalized on the ring. The chloromethyl group adds a layer of reactivity that demands respect when handling, not only during synthesis but during transfer, shipment, and incorporation into the next synthetic stage. Rigorous controls, well-trained operators, and a deep understanding of the process dynamics form the backbone of our daily work.

    Specifications and Quality: Beyond the Lab Bench

    Quality begins with source materials. Common grades available from traders sometimes overlook the impact of even tiny impurities. Years back, working through scale-up issues, we noticed minor contamination—often less than 0.3%—could throw off subsequent reactions, especially in the pharmaceutical sector. We learned the hard way that what goes undetected in bench-scale runs might wreak havoc in a 500-liter reactor.

    Our typical batch of 4-chloromethyl-2-methylthiazole hydrochloride presents as a pale, free-flowing crystalline powder. Analytical chromatograms show a sharp, clean peak with no dragging tail. Water content, checked by Karl Fischer titration, remains far below the threshold where hydrolysis can threaten stability, translating into broader shelf-life and secure storage. Each lot hits a narrow purity window, typically 98.5% or above by HPLC, measured after drying at an industry-standard 105°C. Chloride content is confirmed using established argentometric titration, not just bulk weight calculations, as real-world experience tells us batch yield can sometimes mislead due to residual solvents or lattice water.

    Packing lines move cautiously with this compound. It interacts readily with moisture, so we limit exposure to the ambient air, use strip-sealed Mylar pouches, and back them up in laminated drums. Simple switchovers to less robust methods can let the material cake or lose purity, causing trouble down the line. Over many years and countless batches, we have learned which environmental triggers affect product integrity, and we've designed our logistics chain to minimize those risks.

    Applications: Not Just Another Building Block

    No two customers ask for the same run of 4-chloromethyl-2-methylthiazole hydrochloride. In the real manufacturing world, variability is the norm. Some need the product strictly as a coupling partner for forming thiazole-based active ingredients. In that workflow, a clean, chloride-free batch can mean the difference between a smooth conversion and hours of troubleshooting side-product formation. Others take it further, modifying the methylthiazole ring to produce advanced agrochemicals that meet evolving regulatory and resistance requirements.

    Working at scale also reveals the limits of generic procedures. Automated lines, large vessels, and the movement of hundreds of kilograms at a time expose the material to forces and temperatures rarely seen in a small flask. We’ve witnessed first-hand—during night shifts and long production runs—how batch homogeneity impacts the subsequent yields and purity of end products. Problems such as minor disaggregation or static build-up often show up only above 20-kilogram fills. These real-world lessons have shaped both our process and our recommendations for downstream users.

    Pharmaceutical clients often run multiple synthetic steps in rapid sequence, so consistent input is critical. There’s no room for batch-to-batch drift. Mid-run, deviations in particle size or moisture can jam automated feeders, wasting hours or forcing costly cleanouts. Our team has partnered regularly with process engineers at client sites, troubleshooting remotely or visiting plants to analyze on-the-ground materials—fixing issues that never turn up in specification sheets.

    Fashioning active pharmaceutical ingredients relies heavily on leaving behind no trace of unwanted side products. Unlike some indirectly produced thiazoles, 4-chloromethyl-2-methylthiazole hydrochloride, when executed properly, does not leave behind persistent odor-causing organosulfur fractions. We regularly collaborate with customer labs on studies to map the trace impurity pathways and adapt our cycles to stay ahead of evolving global pharmacopoeia.

    Key Differences from Other Thiazoles

    Within the thiazole arena, differences between substitutions on the heterocycle create a world of distinction in both handling and end-use. Some laboratories and market newcomers expect transposability across the series—swap a methyl for a chloro, or another alkyl, and anticipate similar performance. Experience quickly teaches that a single chloromethyl adds a handling challenge, not to mention downstream synthesis complexity. Handling precautions must address the enhanced electrophilicity and potential methylation of unwanted sites under mild conditions.

    Our operations team often reminds new hires that even thiazole rings with near-identical weights behave radically differently once bordered by reactive halogens. The hydrochloride salt form is selected for a reason: it reduces volatilization and provides a safer pathway for large-scale manipulations. Some open-chain analogs, through their volatility or reactivity, require extensive recovery or abatement systems. The crystalline salt, by contrast, sits comfortably in drum or wide-mouth bottle, reducing occupational hazard and off-gassing concerns—priceless on a busy line with frequent batch turnovers.

    Bulk traders sometimes group thiazole intermediates under a one-size-fits-all approach, overlooking hidden factors such as shelf-stability, temperature excursion tolerance, and reactivity with process solvents. Having watched batches held for extended periods due to customs bottlenecks, we have built protocols around temperature and humidity excursions that are backed by actual stability data, not catalogue assumptions. Cross-contamination worries—sometimes propagated by shared lines in multi-purpose plants—get addressed by routine line flushes and well-documented clean-in-place programs, all built into our in-house traceability system.

    Trace metals, residual solvents, and non-detected organics all show up on our specification sheets, but these are just the tip of the iceberg. For clients making final APIs or high-barrier pesticides, we contribute analytical records derived not just from standard USP/EP or ISO protocols, but from collaborative method development, ongoing stability programs, and decades’ worth of real-world returns and technical queries. Labs using commodity thiazoles from traders may face headaches downstream, spending unexpected time on extra purifications or endpoint tweaking. Our job as the original manufacturer is to take these headaches off the table right from the start.

    Process Learnings and Ongoing Innovation

    Working with thiazole chemistry requires nimble adaptation. As regulatory standards tighten and analytical technology advances, we continually re-examine each process step for efficiency and safety. Standard methods from the old days—batchwise chlorination, open-vessel neutralization, or non-automated washing—no longer meet industry, environmental, or operator safety standards. Our move to closed-transfer reactor systems, in-line pH metering, and automated solvent stripping has shaved hours off cycle times and improved profile consistency.

    We invest in operator education, not just equipment. Morning huddles include process safety reminders, and our shift leaders have authority to halt runs if any condition looks unpredictable. Annual audits from outside regulatory partners, not just internal teams, keep us sharp and meeting evolving client expectations. Our chemists, many of whom started on the plant floor, regularly suggest improvements for higher yield, reduced waste, or shortened campaign times. No flowchart or training video can substitute for practical, lived experience with these materials in large batches.

    Waste handling poses a serious challenge. Even a well-run process creates byproducts that demand responsible disposal or recovery. Over several seasons, we have revamped our side-stream management, integrating solvent distillation, halide recovery, and water recycling circuits. Local environmental partners audit our process waste streams four times a year, and we frequently benchmark our results with industry colleagues to keep tighter control. It’s not just about meeting minimum governmental standards—protecting our workers, neighbors, and the surrounding ecology matter even more when you’re rooted in the community where you operate.

    Supply Security and Customer Support

    Global supply shocks and logistics delays have taught every manufacturer to look well beyond supplier pricing. During periods of solvent shortage or container backlogs, our long-standing vendor relationships and in-house solvent recovery units keep our output stable. We plan raw material inventories with months-long lead time, often holding more stock than is comfortable on the balance sheet, simply because it guarantees our contracts keep running in tight market cycles.

    For critical campaigns, clients often schedule visits or send materials management teams to inspect our warehouses and production lines. We accommodate these requests proactively, involving not just the commercial team but our plant managers, quality assurance leads, and even shop floor operators. Issues and solutions get hashed out face-to-face, over green tea on the packing floor, when necessary, not just by email. Repeat customers often share their production headaches, and our technical support teams work directly with their chemists and engineers, debugging batch records, and conducting root-cause analyses.

    Technical documents and analytical data mean little without the human touch to back them up. Query response times matter. Our technical support team pulls original batch data rapidly, facilitating regulatory filings and troubleshooting issues at the customer site. Long before online portals and self-service dashboards, our business grew through trust, phone calls at odd hours, and a willingness to walk into a problem—not steer away from it. As new uses for this compound arise, we keep our technical teams cross-trained so they understand the context of each new customer inquiry.

    Product Evolution and Commitment to Transparency

    Customer feedback has reshaped our perspective more than any internal brainstorming session. Early on, screening reactivity in actual customer reactions—rather than merely cataloging theoretical conversions—showed us which minor impurities could catalyze unwanted side reactions. These collaborative studies spurred process improvements, helping us reduce non-target halides, clarify recrystallization protocols, and select packaging specifically to minimize shelf-life decay.

    As Asian and European regulations demand ever-stricter data packages, our R&D team now includes process and analytical chemists focused solely on compliance. We submit ongoing stability reports, shelf-life data, and impurity profiles—not just to authorities, but to customers who rely on our documentation to file their own registrations or certifications. We also track environmental and occupational hazards, reporting both aggregate emissions and individual exposure controls, with third-party audits available for customer review.

    Confidentiality remains paramount. Many clients develop proprietary syntheses downstream and expect world-class confidentiality agreements and data security. Our legal and technical teams collaborate to ensure seamless, secure exchanges, from the first quote request through final delivery and ongoing support.

    Conclusion: Why Source Directly from Manufacturers

    Direct sourcing brings tangible benefits. Over time, buyers realize that the value of a high-integrity supplier transcends mere cost per kilogram. Traceable material lot histories, transparent process control, batch-to-batch reproducibility, and hands-on support all add up to real savings in production uptime and end-product yield. Working directly with a manufacturer offers a safety margin against global disruption and ensures technical support no third-party trader can match.

    Real-world manufacturing delivers substance that specs alone can’t promise. With every drum or bag, we stand behind decades of accumulated know-how, human insight, and process rigor. For industries that stake their business on reliable chemistry—medicinal, agricultural, specialty—products like 4-chloromethyl-2-methylthiazole hydrochloride require more than a datasheet; they demand a partner whose experience builds safety, certainty, and success into every shipment.