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4-(Chloromethyl)-2-Methyl-1,3-Thiazole

    • Product Name 4-(Chloromethyl)-2-Methyl-1,3-Thiazole
    • Alias 4-(Chloromethyl)-2-methylthiazole
    • Einecs 410-420-7
    • 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

    986185

    Chemicalname 4-(Chloromethyl)-2-Methyl-1,3-Thiazole
    Casnumber 147040-02-8
    Molecularformula C5H6ClNS
    Molecularweight 147.63
    Appearance Colorless to pale yellow liquid
    Boilingpoint 80-82°C at 10 mmHg
    Density 1.24 g/cm³
    Solubility Slightly soluble in water
    Refractiveindex 1.587 (approximate)
    Flashpoint 86°C
    Synonyms 2-Methyl-4-(chloromethyl)thiazole
    Pubchemid 11617653
    Smiles CC1=NC=C(S1)CCl
    Inchikey LKUXVMZQBWQOJY-UHFFFAOYSA-N

    As an accredited 4-(Chloromethyl)-2-Methyl-1,3-Thiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of 4-(Chloromethyl)-2-Methyl-1,3-Thiazole, sealed with a screw cap and labeled for laboratory use.
    Shipping 4-(Chloromethyl)-2-Methyl-1,3-Thiazole is shipped as a hazardous material, typically packed in sealed, chemical-resistant containers. It must be transported in accordance with local and international regulations (such as DOT, IATA, or IMDG), ensuring protection from moisture, heat, and incompatible substances. Proper labeling and documentation are mandatory for safe handling.
    Storage Store 4-(Chloromethyl)-2-methyl-1,3-thiazole in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from incompatible materials such as strong oxidizers, strong acids, and bases. Ensure the storage area is free from sources of ignition and follow appropriate chemical safety protocols. Proper labeling and secondary containment are recommended.
    Application of 4-(Chloromethyl)-2-Methyl-1,3-Thiazole

    Applications of 4-(Chloromethyl)-2-Methyl-1,3-Thiazole in Industrial Manufacturing

    As the original manufacturer of 4-(Chloromethyl)-2-methyl-1,3-thiazole, we supply this intermediate for tightly controlled and traceable use across several specialized chemical sectors. Below, we outline key downstream application segments, with process-focused details supporting our industrial clients’ formulation and regulatory demands.

    1. Pharmaceutical Intermediate Synthesis (Thiazole-containing APIs)

    Our material plays a crucial role as a building block in the synthesis of select active pharmaceutical ingredients, such as thiazole-based antimicrobials and neuroprotective agents. Pharmaceutical processors utilize it primarily in N-alkylation and thiazole ring functionalization during multi-step syntheses, under cGMP-compliant conditions where control of impurities and precise stoichiometry directly influences yield and product purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP regulations)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements
    • US Pharmacopeia (USP) monograph requirements

    Typical usage ratio

    • 0.15–0.7 molar equivalent, adjusted per target molecule synthesis pathway and impurity profile restrictions

    Downstream process integration

    • Employed during the alkylation step of thiazole pharmaceutical intermediate assembly
    • Handled inside validated reactor trains and protected environments to prevent side reaction and cross-contamination
    • Integrates with in-process quality testing for residual solvents and thiazole-related substances

    Final product types

    • Thiazole-based antibiotics (e.g., sulfathiazole derivatives)
    • Neuroprotective drug intermediates
    • Chemically defined raw materials for research-grade APIs

    2. Agrochemical Actives Manufacturing

    The thiazole-based structure incorporates efficiently into agrochemical molecule synthesis, including certain fungicide and insecticide active ingredients. Agrochemical formulators use this compound for constructing bioactive moieties, requiring stringent adherence to international residue and environmental standards due to its chemical reactivity and the ecological impact of the final crop protection products.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EU REACH Regulation (EC) No 1907/2006 for ingredient assessment
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • China GB 2763: National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.1–0.4 molar equivalent per final agrochemical molecule, ratio refined according to target yield and process selectivity

    Downstream process integration

    • Introduced in controlled reaction steps for C–N bond formation or thiazole functionalization
    • Processed within closed systems to prevent operator exposure and environmental emission
    • Downstream purification includes chromatographic or crystallization steps to achieve regulatory purity limits

    Final product types

    • Thiazole-based broad-spectrum fungicides
    • Insect growth regulators with substituted thiazole cores
    • Precursor intermediates for crop-protection formulations

    3. Flavors and Fragrances Intermediate

    The thiazole ring imparts characteristic toasted and nutty notes, making this material a valued precursor in creating food-grade thiazole compounds for the flavors sector. Only facilities with certified food contact compliance employ this intermediate, and dosage must stay within specific limits to meet regulatory approvals, residue controls, and consumer safety standards.

    Industry compliance standards

    • US FDA 21 CFR 172.515 – Synthetic flavoring substances and adjuvants
    • European Regulation (EC) No 1334/2008 on flavorings and food ingredients
    • IFRA Code of Practice (for fragrance applications)
    • ISO 22000 Food Safety Management Systems

    Typical usage ratio

    • Max 10 ppm in food flavor compositions; typically introduced at 1–5 ppm, final usage strictly depends on end-product application and regional regulatory threshold

    Downstream process integration

    • Reacted at controlled temperatures for high-purity thiazole flavor generation
    • Blended into concentrated aroma bases used in the final food or beverage matrix
    • Incorporated in closed-batch reactors with full traceability for batch verification and contamination control

    Final product types

    • Roasted meat, savory and bread flavorings for food processing
    • Nutty and toasted notes for snack and bakery products
    • Fine fragrance intermediates for perfumery

    4. Specialty Dye and Pigment Precursors

    Chemical sectors producing advanced dyes and pigments utilize thiazole derivatives for constructing colorfast, light-stable molecule frameworks, especially for textile and plastic applications. Control of material addition, purity, and end-use compliance with colorant safety standards is essential, with processing steps optimized for maximum chromophore yield and minimal residual solvent.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile and leather safety requirements)
    • EN 71-3: Safety of toys – Migration of certain elements (for pigments in toys)
    • ISO 9001:2015 Quality Management Systems
    • GHS (Globally Harmonized System) labeling and handling requirements

    Typical usage ratio

    • 0.05–0.3 mol per mole of final dye molecule; process technicians adjust according to desired color depth and product application segment (fiber, polymer, ink)

    Downstream process integration

    • Added during the thiazole ring-coupling reaction in preregistered pigment synthesis steps
    • Mixed in high-shear reactors prior to diazotization or condensation
    • Involves subsequent washing and filtration to remove free thiazole and minimize contamination

    Final product types

    • Yellow and orange azo dyes for textiles
    • Light-stable pigments for plastics and coatings
    • Color additive intermediates for inks and printing

    5. Specialty Polymer and Resin Modification

    Advanced polymer manufacturers employ this compound to introduce heterocyclic features, providing enhanced UV resistance and chemical durability in engineering resins and functional coatings. Process engineers determine the precise point of addition to maximize integration into the polymer backbone and achieve properties critical for automotive, electronics, and industrial equipment components.

    Industry compliance standards

    • UL 94 Flammability Standard (for polymer components)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics)
    • ISO 14001 Environmental Management Systems
    • REACH Annex XVII (restrictions on use of certain hazardous substances in polymers)

    Typical usage ratio

    • 0.2–1.0 wt% by resin mass, adjusted for compatibility with polymer structure and target end-product mechanical properties

    Downstream process integration

    • Introduced in the initial polymerization stage or as part of specialty resin compounding
    • Processed at controlled temperatures to ensure homogenous integration into the polymer matrix
    • Accompanied by QC for residual monomer and mechanical performance analysis

    Final product types

    • High-durability automotive trim and under-hood components
    • Corrosion-resistant coatings for industrial machinery
    • UV-resistant electronic enclosures
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    Certification & Compliance
    More Introduction

    Introducing 4-(Chloromethyl)-2-Methyl-1,3-Thiazole

    What Sets This Molecule Apart

    Our daily work in chemical manufacturing revolves around precision, predictability, and reliability. Among the portfolio of heterocyclic building blocks, 4-(Chloromethyl)-2-Methyl-1,3-Thiazole plays a crucial role where high reactivity and selectivity are essential. After years of direct experience on the production line and in synthesis labs, it's clear this compound stands out, not just for its structure, but for the capabilities it opens up to downstream users in fine chemicals, agrochemical, and pharmaceutical development.

    Our chemists work with this molecule due to its unique balance of reactivity and stability. The chloromethyl group at the 4-position translates into a versatile functional handle, allowing nucleophilic substitution reactions to take place cleanly. The methyl substitution at the 2-position of the thiazole ring offers extra lipophilicity that suits medicinal chemistry programs looking to tweak metabolic and physicochemical properties. Unlike simple thiazoles, where selective functionalization calls for labor-intensive, multi-step methods, this compound lets synthetic chemists streamline their routes.

    Customers often ask what sets 4-(Chloromethyl)-2-Methyl-1,3-Thiazole apart from its analogs such as 4-(bromomethyl)-thiazoles or unsubstituted thiazole cores. Experience shows the fine control over halogen reactivity here. The chloromethyl group reacts less violently compared to its bromo analog, affording smoother handling during large-scale alkylation reactions. This reduces side-products, saves time on purification, and cuts waste. For facilities pushing for greener practices or those that face blending logistics with sensitive intermediates, this attribute decreases batch-to-batch unpredictability. The methyl group distinguishes it from simple 4-(chloromethyl)thiazole as well. By modifying the electron density of the ring system, it influences regioselectivity when the molecule gets involved in further transformations.

    Specifications: Going Beyond the Commodity Approach

    We manufacture 4-(Chloromethyl)-2-Methyl-1,3-Thiazole to a purity exceeding 98%, using a controlled distillation process honed from years of in-house process optimization. Moisture and residual solvent analyses run on every lot, aligning with the QC practices that have driven most of our relationships with R&D labs and scale-up partners. What matters here is not just analytical data, but the assurance that the batch you receive today will mirror the batch next month—without unexpected changes in color, odor, or impurity profile.

    Our model for this product reflects the particular needs of synthetic chemists. Packaging avoids interaction between the chloromethyl functionality and container material. We deliver in glass, because years of observing trace metal leaching in other packaging reinforced the learning that small details ripple out into the quality of the subsequent synthesis. We listen to customers who push these molecules into gram-to-multikilogram quantities. For one international partner, customizing fill sizes reduced their open-handling steps, which led to sharp decreases in both operator irritation and process downtime.

    Understanding Customer Challenges

    Working as a manufacturer rather than a middleman gives a close look at the bottlenecks and opportunities in thiazole chemistry. Chemical intermediates linger in facilities for weeks at a time. Stability and shelf life matter more than a datasheet can convey. If a product breaks down under ambient warehouse conditions or starts to polymerize, the lost time and extra cost can cascade through projects. Our team saw how one batch handled poorly by a third-party led users downstream to troubleshoot mystery impurities that faded only when trace moisture levels were dropped below 0.1%. These lessons led us to humidity-controlled storage and a more robust internal release protocol.

    Global suppliers may talk a good game about flexibility, but from the perspective on the production floor, changing parameters mid-campaign rarely ends well. Instead of chasing last-minute fixes, we focus on reproducibility—tweaking conditions such as crystallization temperature or distillation pressure only after confirming improvements with rigorous pilot runs. Customers send us feedback about actual in-lab experience, not marketing claims, and those stories refine our methods more than any third-party literature survey. It's common for a chemist procuring intermediates for a multi-step synthesis to worry about variability. Contracts won and lost can pivot on some minor impurity or a stuck solvent band, and only manufacturers who stick by their product through these challenges win repeat partners.

    Why 4-(Chloromethyl)-2-Methyl-1,3-Thiazole Matters

    This molecule matters because it bridges gaps in modern synthetic routes. Pharmaceutical companies value it as a scaffold for bioactive targets. Agrochemical developers deploy it in the creation of advanced fungicides or herbicide candidates, where the thiazole ring system imparts selectivity while the chloromethyl group enables clean, adjustable coupling to varied moieties. Specialty chemicals teams use it for material science innovations, from UV stabilizers to polymer cross-linkers. During the past decade, demand has trended in step with needs for smaller, more flexible synthetic handles on complex molecules. This compound’s blend of nucleophilic substitution availability and fine-tuned electronic properties gives researchers a foundation for creative problem-solving.

    Relying on a tested, high-quality version of 4-(Chloromethyl)-2-Methyl-1,3-Thiazole lets chemists focus on making discoveries—not on double-checking incoming intermediate quality. The stories we hear most involve shortened synthesis timelines, fewer side-reactions, and less time battling batch inconsistency. While distributors may shift risk upstream, a producer answers for every lot. It's our name and our site’s record on the line if an intermediate behaves unpredictably during scale-up. Direct engagement with chemists—on the phone, through shared data, or onsite—brings feedback that closes the loop between bench-top chemistry and large-scale manufacturing.

    Experience-Driven Continuous Improvement

    Getting a molecule to market quickly may seem attractive, but in chemical manufacturing, patience in process development pays off in reliability. Our scale-up journey with 4-(Chloromethyl)-2-Methyl-1,3-Thiazole taught that subtle shifts, like stirring rate or fraction-cut points in vacuum distillation, dramatically impact purity and color. Early batches yielded variable results, so we mapped impurity sources from raw material suppliers to filtration media. Where other factories tolerated minor byproducts, our team drilled down until every material input met tight specifications.

    It’s one thing to achieve high nominal yield; it’s another to replicate that output day after day with documented purity and minimal environmental footprint. We learned the hard way that a shortcut taken to reduce energy during chloromethylation invariably caused color body formation, requiring rework and extra solvent. Learning from setbacks distinguished our operation, because we didn’t just adjust on paper. Standing by each batch and adjusting hands-on in real time cemented our process resilience.

    On the supply side, market volatility in thiazole feedstocks remains a challenge. Raw material pricing can swing on short notice, but our long-term partnerships with base chemical producers allow us to blunt these impacts. During the last spike, we leveraged group purchasing to buffer extreme fluctuations, sparing our customers from price whiplash and keeping lead times short. The depth of a producer’s supply network doesn’t show up in a spec sheet, but it saves project managers from lost weeks during crunch periods.

    Practical Differences From Other Intermediates

    From a technical standpoint, the presence of both the methyl and the chloromethyl substituents defines this product’s sweet spot. Chemists seeking simple thiazole options often hit a wall due to the lack of functional differentiation. The 2-methyl group, missing in unsubstituted 1,3-thiazoles, influences hydrophobicity and metabolic stability, which is a subtle but important detail for drug discovery and materials work alike. For nucleophilic substitution reactions or cross-coupling, the chloromethyl position at C-4 delivers faster, more predictable outcomes than opening a ring or starting from less functionalized precursors.

    Those who have worked with 4-(Bromomethyl)-2-Methyl-1,3-Thiazole or 4-(Iodomethyl) analogs recognize the practical hazards—volatility, aggressive byproduct formation, and storage decay. Chlorine substitution hits a middle ground: active enough to ensure robust coupling, yet not so reactive that minor handling variances ruin a batch. In reaction development, this difference means real time and material savings. One customer shifted from using a bromo variant and cut waste solvent volume by a third, thanks to cleaner workups and steadier side-reaction profiles.

    The choice of substituents also affects environmental management. Our experience has shown that even modest improvements in overall yield or decrease in hazardous byproducts translate directly into lower regulatory burdens and easier waste treatment. The compound's chemical properties mean waste streams contain less organohalide load—something that matters for industrial partners watching their compliance metrics.

    Meeting Application Demands Through Manufacturing Experience

    Whereas some suppliers pitch a wide net, focusing on broad utility, our approach leans into conversation with chemists at the application level. For agrochemical groups, many actives depend on advanced thiazole intermediates. Years of supporting process chemists during pilot plant-to-commercial transition gave us first-hand insight into the knock-on effects that upstream intermediate quality inflicts on scale-up trouble. By working directly with those users, we’ve fine-tuned our thiazole’s profile. The resulting chromatic clarity and low salt content reduce concerns about spot formation in herbicide blends or unpredictability in formulation shelf life.

    Drug discovery and medicinal chemistry teams have their own requirements for documentation, traceability, and rapid batch release. We engage in proactive sharing of impurity profiles and stress-test data tailored to support regulatory submission. In one collaborative project, access to batch-specific stability data allowed a customer to skip a lengthy requalification step, accelerating their path to IND submission. These steps, from GMP-aligned protocols to on-demand supply chain reporting, evolved not out of abstract frameworks, but from countless conference-room postmortems where ideas from the bench forever shaped how we operate.

    Handling feedback and recalibrating protocols, batch after batch, is what distinguishes the manufacturer’s perspective. Rather than spinning generic talking points about “cutting edge productivity” or “universal compatibility,” our interest falls on avoiding the errors we once made. Each adjustment—from nitrogen-blanketed packaging to just-in-time delivery windows—stems from actual incidents, such as loss of reactivity traceable to subtle oxidation in half-filled containers or delays during customs clearance exacerbated by ambiguous labeling.

    Pragmatic Discussion on Safety, Compliance, and Handling

    Manufacturing and shipping reactive intermediates such as 4-(Chloromethyl)-2-Methyl-1,3-Thiazole brings responsibility. Real-world plant environments reward those who take diligence as seriously on the warehouse floor as they do in executive suites. We invest in comprehensive training and process audits—from basic PPE reminders to regular plant walkthroughs. An operator error or a labeling oversight can catapult a small issue into project chaos. Years prior, a mislabeled container set back a partner’s full batch by days, prompting an overhaul not only in our own packaging SOPs but in our upstream audit schedule.

    Compliance goes beyond ticking boxes. Batch records and traceability protocols live up to higher scrutiny than those from transient traders. Our production site opens its records for periodic review, not out of obligation, but because real transparency earns long-term trust. Customers exploring new synthesis routes often need access to risk profiles and impurity trend charts before integration into their proprietary steps. Our willingness to hand over everything—right down to detailed cleaning logs—comes from a belief that short-term obfuscation never pays.

    We also support partners by sharing lessons learned. Safe handling of labile thiazoles means maintaining anhydrous conditions and appropriate cold storage—knowledge earned from batches lost before these practices became embedded. In particular, the risk of slow decomposition from atmospheric moisture, especially in high humidity regions, amplified the importance of not just documenting each lesson, but passing it along to customers at order placement. Technical support rarely appears atop a distributor’s feature list, yet, at a manufacturer, we learn that a short conversation often heads off costly trial and error.

    Solutions Rooted in Practice

    Enhanced intermediate reliability stems from four pillars: robust raw materials, precise in-process controls, operator training, and user-oriented support. The industry often rewards shortcuts and narrow margins in the short term, but our history with this compound exposed the eventual costs of this approach. By focusing on chemical reality over marketing spin, we deliver a product that stands up to scrutiny and a team that’s ready to troubleshoot in real time.

    Repeat customers, especially in pharmaceutical and agroscience development, know us for rolling up sleeves during pilot run hiccups or regulatory documentation crunches. Our best ideas for improving 4-(Chloromethyl)-2-Methyl-1,3-Thiazole synthesis came from honest post-mortem sessions rather than top-down executive edicts. Suggestions from plant-floor chemists, often overlooked in process design meetings, led to double-sealed containers that stopped cross-contamination issues dead in their tracks.

    Problems do arise—whether raw material purity dips, shipping delays intervene, or regulatory hurdles demand revalidation of an entire sub-lot. In each case, the solution emerges from direct engagement. One partner, faced with an unexpected shift in impurity profile during a crucial campaign, worked with our technical team to adjust downstream process parameters. The solution required joint root-cause analysis, not just a shipment of free material. Outcomes like these, repeated project after project, affirm the lasting value of a manufacturer willing to stand up and be counted when it matters.

    Looking Forward, Sticking to Experience

    Fashions in chemistry shift every few years. Heterocycle emphasis cycles between project needs and fresh regulatory scrutiny. The core lessons learned from manufacturing 4-(Chloromethyl)-2-Methyl-1,3-Thiazole stay relevant regardless of these swings. Staying close to raw material sources, investing in pilot data before plant trials, bringing frontline technical staff to customer meetings—all these practices outlast the market’s latest buzzwords. The molecule’s value endures as long as its quality matches the stakes in application.

    We meet with global partners who often ask how to hedge against disruptions, what next steps to take as new regulations hit, how to extend shelf life, or whether recycled solvent streams could fit particular grades. These questions get honest answers only from people who make and live with the consequences of each step in the process. Our commentary comes not from recycled marketing, but from cumulative trial, honest error, and continuous improvement.

    In all, 4-(Chloromethyl)-2-Methyl-1,3-Thiazole stands out because it’s produced for the realities chemists actually face, not for abstract catalog needs. Its distinctiveness flows from direct feedback loops, harsh scrutiny of every failure, and a commitment to act on lessons learned. Our hope is that, as you plan your next synthesis, you benefit from the same blend of reliability, insight, and adaptability that informs all we do as manufacturers.