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2-Chloro-5-Methylthiazole

    • Product Name 2-Chloro-5-Methylthiazole
    • Alias 2-Chloro-5-methyl-1,3-thiazole
    • Einecs 629-172-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    247237

    Chemical Name 2-Chloro-5-Methylthiazole
    Molecular Formula C4H4ClNS
    Molecular Weight 133.60 g/mol
    Cas Number 35144-22-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 164-166°C
    Density 1.28 g/cm³
    Synonyms 2-Chloro-5-methyl-1,3-thiazole
    Purity Typically ≥98%
    Refractive Index 1.570 (at 20°C)
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Conditions Store in a cool, dry place, tightly closed
    Smiles CC1=CN=C(S1)Cl
    Ec Number 252-385-1

    As an accredited 2-Chloro-5-Methylthiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 g of 2-Chloro-5-Methylthiazole is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2-Chloro-5-Methylthiazole is shipped as a chemical reagent, typically in tightly sealed containers to prevent leaks and contamination. It is transported according to applicable regulations for hazardous materials, with proper labeling and documentation. Ensure storage in a cool, dry, well-ventilated area, away from incompatible substances, and handle with appropriate safety precautions.
    Storage 2-Chloro-5-methylthiazole should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and keep away from heat. Ensure appropriate chemical labeling and secondary containment to prevent spills or leaks. Store in accordance with all local and national regulations.
    Application of 2-Chloro-5-Methylthiazole

    Applications of 2-Chloro-5-Methylthiazole in Industrial Manufacturing

    2-Chloro-5-Methylthiazole serves as a high-purity intermediate chemical in the synthesis of various specialty chemicals. Our direct manufacturing ensures consistent quality and reliable supply for downstream partners operating in regulated, process-intensive sectors.

    1. Agrochemical Synthesis — Production of Crop Protection Actives

    Leading agrochemical formulators use this compound as a critical building block for thiazole-derived active ingredients. The chlorine and methyl substituents offer distinctive reactivity in thiazole ring construction, supporting the synthesis of herbicides, fungicides, and insecticides. During the multi-step production process, this intermediate couples through specific nucleophilic substitution and cyclization reactions, ensuring precise molecular targeting attributes. Our clients require traceability and batch-to-batch reproducibility for all incoming materials.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (EC 1907/2006) registration and compliance
    • OECD Good Laboratory Practice (GLP) Guidelines
    • China National Standard GB 2763 (Maximum Residue Limits for Pesticides)

    Typical usage ratio

    • 5%–15% by weight in stepwise synthesis of target thiazole actives; final ratio adjusted based on target molecule and stoichiometry

    Downstream process integration

    • Used during early-stage thiazole core assembly before downstream heteroaryl modifications
    • Frequently incorporated via nucleophilic aromatic substitution or via thioamide intermediates
    • Batch-wise addition to maintain control over exothermicity and purity

    Final product types

    • Triazole-based fungicidal actives
    • Selective post-emergent herbicides
    • Systemic seed treatment insecticides

    2. Pharmaceutical Intermediates — Synthesis of APIs

    API manufacturers select this raw material for constructing specific thiazole pharmacophores found in several anti-infective, anti-tubercular, and CNS drug molecules. Its role includes serving as a functionalized halogen donor in hybrid molecules and as an electrophilic partner in cross-coupling reactions. Consistency in purity, residual solvent control, and trace metal levels critically influence downstream API yield and compliance. Our manufacturing covers full documentation for audit readiness in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF monographs for relevant intermediates
    • EDQM CEP certification process
    • 21 CFR Part 211 (US FDA cGMP Regulations)

    Typical usage ratio

    • 3%–10% by molar input relative to total intermediate weight, staggered over multiple reaction steps depending on the API route

    Downstream process integration

    • Introduced during core thiazole ring formation or late-stage halogenation
    • Applied in both batch and continuous flow systems per process scale
    • QC sampling at input and post-reaction isolation stages to confirm identity and limit impurities

    Final product types

    • Anti-tuberculosis agents featuring thiazole moieties (e.g., thioamides)
    • Newer CNS drugs — thiazole-substituted heterocycles
    • Broad-spectrum antibacterial agents

    3. Flavor and Fragrance Ingredient Manufacturing

    Major fragrance and flavor compound producers utilize this material for constructing sulfur-containing aromatics, providing a roasted, nutty, or meaty note in food mimetics and fine fragrances. The regulated use of thiazole derivatives requires stringent dosing and residual solvent monitoring. It enters the production process via controlled synthesis and subsequent purification steps for compliance with food and fragrance safety requirements.

    Industry compliance standards

    • US FDA 21 CFR 172 (Food Additives Permitted for Direct Addition to Food)
    • IFRA Standards for Aromatic Ingredients
    • EU Regulation (EC) No 1334/2008 on Flavorings and Food Ingredients
    • FEMA GRAS List (Flavor and Extract Manufacturers Association)

    Typical usage ratio

    • 0.01%–0.5% in finished fragrances or flavor formulations; adjusted per final profile and end-use requirements

    Downstream process integration

    • Acts as a precursor and key reactant in assembling sulfur-containing aroma chemicals via condensation reactions
    • Processed under vacuum and controlled temperature to minimize off-notes
    • Purification via distillation or preparative chromatography before blending

    Final product types

    • Roasted coffee and nut flavorings for food applications
    • Top note enhancers in fine perfume bases
    • Savory flavor blocks for processed foods and instant seasonings

    4. Specialty Chemical Synthesis — Advanced Material Coatings

    Developers in high-performance coatings and electronics chemicals incorporate this intermediate to introduce thiazole-derived units into polymers and specialty resins. The unique reactivity profile enables the creation of corrosion-inhibiting agents, adhesion promotors, and functional coating monomers. The production sequence requires accurate metering, and the presence of specific chemical handles supports downstream post-polymerization modification.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • RoHS Directive (EC) 2011/65/EU for electronics-related chemicals
    • UL Environmental Claim Validations for surface coatings
    • GHS/CLP Regulation (EC) No 1272/2008 for hazard labeling

    Typical usage ratio

    • 2%–8% of total monomer or additive batch, adapted for desired functional group density and performance

    Downstream process integration

    • Fed into resin manufacturing prior to chain extension or cross-linking
    • Serves as a functional monomer or end-capping agent
    • Monitored by stoichiometry and reacted under inert atmosphere to preserve integrity

    Final product types

    • Corrosion-resistant metal primers
    • Adhesion enhancers for electronic device coatings
    • Specialty finished polymers with thiazole pendants
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    Certification & Compliance
    More Introduction

    2-Chloro-5-Methylthiazole: A Backbone for Fine Chemical Synthesis

    Understanding 2-Chloro-5-Methylthiazole from a Manufacturer’s Bench

    Every batch of 2-Chloro-5-Methylthiazole we produce carries more than just a chemical structure—it reflects diligent process management, years of experience scaling up thiazole derivatives, and ongoing commitment to customer-oriented manufacturing. Over the years, this compound has found its way onto the order sheets of agricultural labs, pharmaceutical synthesis teams, and fragrance developers. Whether we see the demand spike due to a new pesticide discovery, or a custom reagent for a medicinal chemistry lab, the chemical’s value keeps growing in downstream applications.

    We don’t simply list 2-Chloro-5-Methylthiazole as one item among many. Its chemistry belongs in the thiazole family, marked by the five-membered ring with sulfur and nitrogen atoms that brings unique properties. The chloro-substitution at the 2-position gives it a reactive handle for many coupling or substitution reactions, while the methyl group at the 5-position alters its reactivity and makes it stand apart from similar analogues in this class. Our recurring collaborations with contracted R&D groups have shown the difference this single methyl group can make—for instance, it can influence regioselectivity in heterocycle-building routes, or tweak physicochemical behavior in intermediates for pharmaceuticals or agrochemicals.

    For project teams on the chemistry side, process purity and the quality of the raw material mean yield, project timelines, and reliable structure-activity relationships. Our technical team set up robust quality protocols during every batch cycle. Over the years, some colleagues have asked for specifications that balance purity, moisture content, melting point, and isomer ratio. With each discussion, we’ve had to weigh risers in yield against achievable purity thresholds. Our typical manufacturing process delivers 2-Chloro-5-Methylthiazole in liquid form, with purity routinely exceeding 98.5% by GC—though on occasion, customers developing highly sensitive pharmaceutical actives require material up to 99.5% or tighter specification. For highly regulated industries, we retain critical traceability documentation on every batch release.

    Routines and Realities—From Reactors to Finished Product

    This product is manufactured using controlled chlorination over a methylthiazole substrate. Time, temperature, and feed rates of the chlorinating agent all vary according to the volume of production and client-specific requirements. As reaction scale increases, managing byproduct removal and heat control becomes a challenge we’ve learned to anticipate. With each incremental upgrade in our reactor capacity, our technical staff has implemented new in-line monitoring equipment—every change shaped by what previous batches taught us.

    Working with thiazoles means taking care with storage and personal handling. Many thiazole derivatives emit a characteristic odor and 2-Chloro-5-Methylthiazole is no different. Our plant team maintains strict air handling, and we recommend customers utilize well-ventilated transfer systems. Clients who formulate at pilot or commercial scale also value advice on compatibility with sealants and process equipment, since thiazoles can be aggressive to some polymers and certain elastomers. It isn’t just about “product in a drum”—it’s about how product moves through mixers, hoppers, and agitation systems on the floor.

    Most distributors only echo technical data sheets, but needs on the production floor go deeper than numbers. Seasonal humidity trends, variations in bulk packaging, and even regional shipment routes all play a part in how the material arrives and blends at the customer’s site. By sharing these hands-on discoveries, we’ve helped clients avoid stops in production and reduce the risk of slowdowns during scale-up batches. The more transparent everyone can be about downstream requirements, the smoother the process.

    Differentiating 2-Chloro-5-Methylthiazole from Other Thiazoles and Halothiazoles

    At first glance, 2-Chloro-5-Methylthiazole shares a structural motif with many other thiazole derivatives. In practice, no two thiazoles behave quite the same when subjected to coupling, alkylation, or nucleophilic substitution. Substitution patterns, particularly the presence of a methyl group at position 5 along with chlorine at position 2, reroute electron density and shift solubility or boiling point. Technicians observing a “simple swap” with a 2-chlorothiazole instead of the methylated version often see unexpected drawbacks: altered reactivity with key nucleophiles, reduced selectivity in step growth reactions, or lower yield when scaling up to multi-kilogram.

    We see chemists in agricultural R&D prefer 2-Chloro-5-Methylthiazole when seeking to build pre-emergent herbicides targeting enzymes sensitive to both the hydrophobicity and the electron-donating effects of the methyl group. This seemingly minor shift can push the molecule’s profile closer to target binding, or reduce its off-site environmental drift. On the pharmaceutical stage, medicinal chemists often request multiple halothiazoles for structure-activity exploration, but find the methylthiazole version demonstrates improved metabolic stability or synthetic accessibility for later building blocks. Even in perfumery, certain top-note or “spicy” base profiles benefit from the additional character imparted by this specific structure.

    When customers ask us to compare 2-Chloro-5-Methylthiazole to 2-Chlorothiazole, we reference not only boiling points or reactivity but also performance in downstream synthesis. The methylated version tends to have a higher boiling point, offers different partition coefficients in solvent extraction, and may impart more process losses or residues if not handled with precision during distillation. Our plant operators keep these factors in mind when tailoring order size and packaging to reduce waste, and our technical teams document environmental emission data for responsible disposal. This hands-on insight only comes from years of monitoring, troubleshooting, and supporting client troubleshooting during tech transfer.

    From Lab Bench to Commercial Rollout: Practical Uses and Challenges

    In the agricultural sector, 2-Chloro-5-Methylthiazole finds ready utility in constructing advanced intermediates for herbicides and fungicides. Chemists who specialize in thiazole ring construction gravitate toward this molecule, leveraging its unique substitution pattern to design new actives that evade resistance in weed populations or fungal blights. The reactivity of the chloro group at position two makes it suitable for nucleophilic substitution, permitting diverse derivatization. Since the methyl group can attenuate the electron-withdrawing effect of the chlorine, it also influences how the molecule participates in palladium-catalyzed coupling reactions. These fine-tuned differences allow R&D teams to position novel actives with very distinct biological profiles, without requiring massive overhauls of existing manufacturing assets.

    In the pharmaceutical landscape, 2-Chloro-5-Methylthiazole serves as both a core building block and a trusted intermediate. We’ve seen project chemists select this molecule to enable sulfur or nitrogen substitutions, or as a starting point to create libraries for anti-infective or anti-inflammatory indications. Its robust ring system stands up to long synthetic sequences, even when subjected to high-temperature transformations or metal-catalyzed couplings. We continually engage with clients who count on reliable, reproducible batches—because any deviation in impurity profiles can ripple through to the final active ingredient.

    Even beyond these core markets, teams in the flavors and fragrances sector pursue the slightly smoky, peppery, and savory notes that come along with methylthiazole units, adjusting concentration and blending for rich “gourmand” profiles. Not all thiazole analogues lend this nuance; we’ve found customers frequently select this specific methylated variant when they require a warm top note or earthy backbone. By keeping open lines with fragrance houses on the best application approaches, we’ve tracked formulation trends and shared best practices for both solubility and controlled release.

    The Manufacturer’s Lens: Quality, Traceability, and Regulatory Watchpoints

    Maintaining consistent quality is harder than most outsiders realize. Lab-scale synthesis gives way to much more challenging dynamics in plant operations—where batch reactors, feedstock controls, temperature gradients, and sampling procedures determine what leaves the line. Frequent sampling, instrument calibration, and multi-point in-process controls help to catch outliers before they make it to packaging. In our facility, we draw on cross-disciplinary input, including QC chemists, maintenance techs, and logistics managers, to ensure every kilogram matches tight client requirements.

    Strict traceability features in every shipment of 2-Chloro-5-Methylthiazole we send. Our clients in pharmaceutical and crop-protection industries require it. Each produced batch is coded and documented, with access to Certificates of Analysis and detailed impurity profiles. In areas requiring control for regulated chemical precursors, we advise project leaders on regulatory watchpoints—whether they stem from local, regional, or international oversight. Years spent following regulatory regimes in Europe, North America, and Asia taught us: requirements can change and do so unexpectedly. Keeping raw material, synthetic intermediates, and finished product documentation up to date speeds client audit approvals and smooths new route evaluations.

    Working at plant scale also brought us face to face with the realities of safe handling and responsible waste management. Fumes produced by 2-Chloro-5-Methylthiazole or its analogues can carry both strong odors and environmental impacts. Our facility uses closed transfer and filtration steps, air scrubbing, and proper PPE at every handling station. Once downstream users at customer sites shared concerns about residual odors in end formulations, our technical support teams collaborated to develop better storage, ventilation, and even on-site neutralization options. Our safety and compliance staff constantly reassess these protocols to align with health, safety, and environmental guidelines.

    Packaging, Lead Times, and Battlefield Lessons from Bulk Shipments

    Packaging options set the stage for every logistics plan. We offer 2-Chloro-5-Methylthiazole in carbon steel drums, polyethylene-lined containers, and specialty jerricans. Certain clients running continuous reactors or pilot campaigns benefit from flexi-bags or larger bulk tanks, designed for efficient direct feed into process streams. Storage stability stays critical—thiazoles can degrade in the presence of strong acids, bases, or sustained UV light exposure. Customers periodically seek advice on optimizing warehouse conditions to extend shelf life, and our plant engineers draw on years of data tracking temperature fluctuations and degradation curves for best recommendations.

    Lead times fluctuate, especially when major agricultural product launches or pharmaceutical approval cycles take off. Raw material inefficiencies can throw off production forecasts. Over the years, through trial and misstep, we’ve adopted more flexible procurement strategies—holding strategic inventory, building multi-step contingency capacity, and maintaining lines to diversified raw suppliers. Strong forecasting relationships with steady clients allow us to align production runs, minimize stoppage, and schedule planned maintenance without disrupting supply. For projects with extremely sensitive timelines—such as clinical-stage pharmaceuticals—we coordinate advance batches, staggered testing, and just-in-time shipments to ensure uninterrupted R&D or pilot production.

    Experience has taught us the importance of planning for customs, shipping lane disruptions, and seasonal weather patterns. In the past, cargo stuck in heatwaves or monsoon transit periods risked reduced product quality or outright loss. We support customers by proactively tracking cross-border documentation and by alerting them to local conditions that may threaten shipment reliability. Consistent communication, both internally and externally, keeps missteps at bay and builds lasting, productive business relationships.

    Facing Forward: Innovation, Sustainability, and Remaining Responsive

    Sustainable production of thiazole derivatives presents ongoing challenges. The feedstocks, chlorinating reagents, and solvents involved come with environmental footprints and safety considerations. Our lab teams keep pressure on themselves to fine-tune reaction parameters, minimize byproducts, and seek greener input streams. Solvent and wash recovery systems reclaim value and reduce overall emissions. Waste management ranks high on our operations agenda; we invest in neutralization and on-site water treatment to ensure responsible discharge. Staying alert to future legislation and evolving best practices shields customers from regulatory risk and affirms our commitment to manufacturing as a responsible partner.

    We maintain open channels with clients and supply chain partners, sharing ongoing findings about process optimization and identifying pain points that could impact end-use performance. By keeping quality, safety, and responsiveness central, we demonstrate the value that only a manufacturer with years of hands-on experience can offer. Over the lifecycle of this product—whether it moves from R&D bench to ton-scale reactor, or stays in the small-batch specialty sector—the practical lessons of the manufacturing floor make the largest impact on customer outcome.

    2-Chloro-5-Methylthiazole: Beyond Commodity Status

    Producing 2-Chloro-5-Methylthiazole at scale draws on both chemical knowledge and operational experience. Every technical challenge in production, every feedback loop from clients navigating new formulations, and every step in compliance preparation combines to shape a product line that’s known for reliability and practical support. Years spent on the production side show how small structural differences—like the methyl group at position five—can completely redirect a project’s pathway or define the edge between success and a bottleneck in process.

    Fine chemicals, especially pivotal building blocks like 2-Chloro-5-Methylthiazole, ask for more than a transactional approach. Staying responsive, curious, and thorough in both manufacturing and client support continues to set us apart. For any team searching for a thiazole reagent that balances reactivity, predictability, and application flexibility, this molecule stands out—not on paper, but in the real-world lab work where process integrity and project momentum matter most.