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2,5-Dichloro-3-Methylthiophene

    • Product Name 2,5-Dichloro-3-Methylthiophene
    • Alias 2,5-Dichloro-3-methylthiophen
    • Einecs 'EINECS 242-098-9'
    • 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

    357595

    Cas Number 16619-57-1
    Molecular Formula C5H4Cl2S
    Molecular Weight 167.06 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 210-212°C
    Density 1.398 g/cm3
    Refractive Index 1.568
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Flash Point 93°C
    Synonyms 2,5-Dichloro-3-methylthiophene

    As an accredited 2,5-Dichloro-3-Methylthiophene 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 100 grams of 2,5-Dichloro-3-Methylthiophene, sealed with a screw cap, labeled with hazard warnings.
    Shipping 2,5-Dichloro-3-Methylthiophene is shipped in tightly sealed containers made of compatible materials, protected from light and moisture. It should be handled as a hazardous chemical, transported according to relevant regulations (such as DOT or IATA), and accompanied by proper documentation and hazard labeling to ensure safe and compliant delivery.
    Storage 2,5-Dichloro-3-methylthiophene should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Store in a cool, dry, and well-ventilated area. Ensure the storage area is equipped to contain spills. Proper chemical labeling and access for authorized personnel only are essential for safety. Avoid extreme temperatures during storage.
    Application of 2,5-Dichloro-3-Methylthiophene

    Applications of 2,5-Dichloro-3-Methylthiophene in Industrial Manufacturing

    We manufacture 2,5-Dichloro-3-Methylthiophene to exacting standards for demanding industrial use. Below are key application sectors and integration pathways for this intermediate chemical in actual downstream production environments.

    1. Pharmaceutical Intermediates for Thienopyridine Synthesis

    Within the active pharmaceutical ingredient (API) supply chain, 2,5-Dichloro-3-Methylthiophene functions as a critical intermediate during the synthesis of thienopyridine core structures, such as clopidogrel and related antiplatelet compounds. The compound’s dual chlorine substituents enable site-selective nucleophilic aromatic substitution and further cyclization steps, supporting precise structure-activity relationships in target molecules. Purity and trace impurity control remain essential for release into regulated API plants.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4, Part II
    • 21 CFR Part 211 (United States cGMP for finished pharmaceuticals)
    • USP General Chapters — Residual Solvents, Elemental Impurities (as applicable to intermediates)

    Typical usage ratio

    • Reactant mesh: typically 1.0–1.1 molar equivalents per molecular unit of target thienopyridine core
    • Adjustment based on desired yield and downstream impurity profile

    Downstream process integration

    • Charged in initial heterocyclic scaffold condensation with nitrogen donors
    • Feeds into halogen-exchange transformations and metal-catalyzed coupling steps
    • Processed via well-controlled solvent systems, usually under inert atmosphere

    Final product types

    • Clopidogrel bisulfate active pharmaceutical ingredient
    • Ticlopidine hydrochloride API
    • Pharmaceutical solid dosage forms containing thienopyridine cores

    2. Advanced Agrochemical Building Blocks

    Agrochemical manufacturers deploy this methylthiophene derivative as a building block to generate sulfur- and chlorine-bearing heterocyclic pesticides and fungicides. The material offers a reactive handle for cross-coupling and substitution steps in the protected assembly of bioactive agents. Its selectivity in substitution reactions limits side-product generation, supporting high process yields and precise regulatory documentation of starting materials.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticide Intermediates
    • ISO 9001:2015 Quality Management for Chemicals
    • EU REACH Registration (EC No. 1907/2006) — Safety Data and Toxicology
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticide Registration)

    Typical usage ratio

    • 0.7–1.2 equivalents per crop-protection active unit, depending on targeted bioactive structure
    • Basis: varies by fungicide or insecticide synthetic route

    Downstream process integration

    • Introduced in early-stage sulfonation or chlorination steps
    • Actively converted via Suzuki or Stille coupling onto aromatic systems
    • Processed in batch or continuous reactors depending on crop-protection compound

    Final product types

    • Thienopyridine-based fungicides
    • Novel thiophene-chlorinated herbicides
    • Specialty insecticidal active compounds

    3. Electronic Materials and Conductive Polymers

    Producers of electronic components and polymeric conductors use 2,5-Dichloro-3-Methylthiophene as a functional monomer in the synthesis of thiophene-based conductive polymers. The electron-rich thiophene ring, in combination with strategic halogenation, facilitates oxidative polymerization and targeted doping with molecular dopants. Careful specification of impurities and side-chain composition impacts polymerization kinetics and performance in device integration.

    Industry compliance standards

    • IEC 62321 – Determination of certain substances in electrotechnical products
    • RoHS Directive 2011/65/EU – Restriction of Hazardous Substances
    • ISO 9001 for Electronic Chemicals
    • Customer-specific electronic materials specifications

    Typical usage ratio

    • 10–50 wt% as co-monomer in batch oxidative or electrochemical copolymerization
    • Adjusted for polymer backbone regularity and conductivity targets

    Downstream process integration

    • Injected into controlled monomer feed in oxidative polymerization reactors
    • Processed in inert, low-moisture environments to avoid halogen elimination
    • Blended and doped prior to device casting or coating

    Final product types

    • Poly(3-methylthiophene) derivatives
    • Conductive polymer films for printed electronics
    • Sensors and flexible circuits incorporating functionalized thiophenes

    4. Fine Chemicals and Specialty Dye Production

    Producers of high-value specialty dyes and pigments utilize this dichloro-methylthiophene as a key intermediate for constructing complex aromatic and heterocyclic colorant backbones. The electron-donating methyl and electron-withdrawing chloro groups enable selective functionalization and extended conjugation, essential for tailoring light absorption and fastness properties in advanced dyes. Stringent control over lot-to-lot consistency ensures predictable color yield in batch and continuous colorant manufacture.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (relevant for input chemicals in dye manufacture)
    • REACH SVHC documentation for colorant intermediates
    • GHS/CLP Regulation (EC) No 1272/2008 for chemical labelling
    • ISO 9001 for colorant and dye intermediate manufacturing

    Typical usage ratio

    • 5–20 mol% relative to total heterocycle-forming reactants in the stepwise synthesis of chromophores
    • Adjusted to manage color shade, intensity, and solubility

    Downstream process integration

    • Feeds into Friedel–Crafts acylation or substituted amidation for dye scaffold formation
    • Integrated in multistep synthesis with targeted halogenation and alkylation
    • Undergoes purification for low impurity dye intermediates

    Final product types

    • Organic pigments for inks and plastics
    • Specialty dyes for textiles and coatings
    • High-performance colorants for automotive and electronics

    5. API Impurity Reference Standards Manufacturing

    Specialty reference laboratory manufacturers isolate and purify 2,5-Dichloro-3-Methylthiophene to use as a certified reference standard for impurity profiling in pharmaceutical quality control. Its known profile supports the quantitation of trace levels in related API batches, especially for structurally close thienopyridine or thiophene APIs. Rigorous certification, documentation, and trace-level purity analysis underpin this application for leading pharmaceutical QC labs worldwide.

    Industry compliance standards

    • Ph. Eur. and USP Reference Standard Monographs
    • ISO/IEC 17025 — Testing and Calibration Laboratories
    • ICH Q3A/B Impurity Guidelines (Identification and Qualification)
    • FDA 21 CFR Part 11 (Electronic Records Requirements for Data Integrity)

    Typical usage ratio

    • Ultra-trace, sub-ppm levels in spike-recovery testing and calibration lines for HPLC, GC-MS, or LC-MS systems
    • Prepared as standardized solutions for repeatable calibration work

    Downstream process integration

    • Purified to >99.9% by preparative chromatography
    • Certified with full spectral characterization and exact assay testing
    • Packaged in hermetically sealed ampoules for distribution

    Final product types

    • Certified impurity reference standards
    • Pharmacopeial calibration kits
    • Traceability solutions for routine pharmaceutical QC
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    Certification & Compliance
    More Introduction

    2,5-Dichloro-3-Methylthiophene: Crafting Quality in Chemical Synthesis

    Our Experience as Manufacturers

    Years spent in the chemical manufacturing world have taught us that every intermediate brings its own strengths and challenges to the bench. 2,5-Dichloro-3-methylthiophene is one of those critical building blocks that keeps showing its value in specialties and advanced applications. Chemical plants, especially those focused on pharmaceutical actives and agrochemicals, look for starting materials with tight specifications, predictable reactivity, and reproducibility. This molecule promises just that, and as a team that synthesizes it from the ground up, we see firsthand how carefully controlled processes make all the difference for downstream users.

    Our product delivers the high purity (usually above 98% by GC) chemists count on to keep side reactions at bay. The compound appears as a light-yellow liquid, a form that's easily measured, transferred, and stored in labs and manufacturing environments. The molecular structure, featuring two chlorine atoms at the 2 and 5 positions along with a methyl group at the 3 position on the thiophene ring, provides both steric and electronic characteristics sought after in synthetic chemistry. Unlike less substituted thiophenes, it offers selective sites for further functionalization — a reason it attracts interest among R&D teams developing new molecular entities.

    Specification Details and Consistency

    Consistency forms the backbone of our reputation as direct manufacturers. We use carefully sourced raw materials, under tightly monitored temperature and pressure controls, to maintain batch-to-batch uniformity. The synthetic protocol, including chlorination and methylation, follows a closed-loop monitoring system to catch impurities below the threshold levels (typically less than 1% for any single impurity, by our analysis). Our finished 2,5-dichloro-3-methylthiophene meets a water content specification below 0.5%, so users avoid hydrolytic degradation in moisture-sensitive syntheses.

    Each batch passes through a dedicated distillation train, separating the desired product from close-boiling byproducts. Sampling crews take vials from each drum and run GC-MS and NMR validation, cross-checking against previous lots as well as published literature. We never skip these steps, as downstream complaints about reactivity or solubility almost always tie back to lapses in the early stages of production. Decades of feedback — both positive and corrective — from long-term clients have shaped our inspection routines.

    Working with 2,5-Dichloro-3-Methylthiophene

    Research routes for new pharmaceuticals and agrochemicals keep returning to substituted thiophenes as privileged scaffolds. Our experience with regulatory filings exposed us to the recurring need for this compound in advanced intermediates and fine chemical libraries. Chemists gravitate to it for its clean reactivity, especially on the unsubstituted positions of the ring. The presence of two chlorine atoms offers anchor points for various cross-coupling and substitution reactions, expanding the playbook for medicinal chemistry and development teams.

    Formulations involving 2,5-dichloro-3-methylthiophene often depend on its unique balance of electron withdrawal and ring activation. The methyl group at the 3 position blocks regioselectivity, steering further functionalization toward the open 4-position or facilitating reductive coupling. This makes our product a reliable starting point for new library members or patentable active molecules. Some of our customers design thiophene-based ligands from scratch, while others focus on scale-up and pilot production tied to this versatile intermediate.

    We see a steady pipeline of requests from innovators working in performance materials as well, where designing structure-property relationships needs precision at the atomic level. Our formulation team keeps track of customer feedback to refine downstream compatibility, especially for those running automated synthesis or parallel chemistry protocols. The product’s physical properties — manageable viscosity, moderate polarity, and reasonable volatility — blend well into existing workflows, limiting downtime or equipment recalibration.

    How It Differs from Other Thiophenes and Chlorinated Intermediates

    Over the years, we’ve handled a wide range of chlorinated thiophenes, each with its own challenge. Simple thiophene offers little selectivity, often demanding lengthy protection-deprotection sequences. Mono-chlorinated thiophenes suit some applications but lack the tunable reactivity that the 2,5-dichloro motif brings. Introducing a methyl group at the 3 position as we do in our product changes the chemistry, making it possible to access chemical space otherwise blocked with unsubstituted rings.

    Customers sometimes ask whether it’s worth choosing this compound over related analogs. In our view, 2,5-dichloro-3-methylthiophene’s pattern of substitution prevents unwanted side reactions and leads to higher yields for targeted couplings, especially in Suzuki or Buchwald-Hartwig cross-coupling chemistry. We’ve tracked scale-up data and batch records from partner pilot plants; these show better yields and purer end-products when starting from this specific compound, compared to congeners like 2,3-dichloro- or 2,5-dibromothiophenes.

    The Role of Quality and Traceability

    In practice, what keeps clients confident returning to us isn’t just the technical properties of the molecule; it’s the traceable path from raw material to finished drum. We design control points throughout synthesis to record time, temperature, pressure, and addition rates along the way. These records stay archived for every batch, accessible at audit and on demand by clients with documentation requirements. We support filings for regulatory bodies and quality management systems along the supply chain, so every kilogram delivered tallies with a clear data trail.

    We also keep direct feedback channels open for upgrading or troubleshooting customer experience. If a batch shows performance anomalies in a reaction, our technical support team engages immediately, running side-by-side comparatives with retained samples and adjusting future runs if needed. This dynamic response wasn’t possible back in the early days of manual batch records and paper logs; today’s digital tracking gives us a flexible edge and a culture of constant learning.

    Process Optimization — Lessons from the Plant Floor

    From a manufacturer’s perspective, maximizing both yield and worker safety sets the agenda. Our production teams work in training cycles to identify bottlenecks in purification or reaction setup. Reactor cleaning protocols, drum labeling, and in-process controls all come out of lessons learned from actual downtime and operational interruptions. By reducing off-specification runs, we keep unnecessary rework and waste to a minimum. Losses from side reactions can be costly both in raw material use and in hours lost for reprocessing, so process improvement meetings focus on efficient transfer and accurate distillation cuts.

    In earlier years, occasional troubleshooting pinpointed corrosion issues in process lines carrying chlorinated organics. Shifting to corrosion-resistant alloys for key transfer lines and seals reduced downtime and contamination risk. Similarly, we responded to feedback about odor management and safe handling, investing in vapor containment hoods and sealed pump systems for transfer. These steps were driven not by regulatory pressure but by on-the-ground feedback and an understanding of the hazards specific to chlorinated thiophenes.

    Supporting the Pharmaceutical and Agrochemical Sectors

    Demand for 2,5-dichloro-3-methylthiophene closely follows the cycles of innovation in pharmaceuticals and crop protection. As drug molecule complexity climbs, reliance on tailored building blocks like chlorinated thiophenes grows. Our main clients share the need for kilogram-to-multiton supply, each with specific requirements for documentation, purity, and on-time delivery. We’ve learned that early-stage projects often start with gram-scale orders, scaling up quickly as projects move to phase II trials or field studies for agrochemicals.

    Our production planning team watches market signals to align capacity expansions with customer trial phases and commercial launches. In years marked by regulatory changes or sudden shifts in compound portfolios, we adapt supply schedules to avoid bottlenecks. Recently, increased scrutiny on impurity profiles and trace contaminants means that we run extended chromatography and advanced analytics to ensure compatibility with pharmaceutical-grade applications. For some end uses, we provide further cleaning steps, giving chemists a head start on downstream purification.

    Insights from End-User Experiences

    Not every batch walks the same path — we’ve seen 2,5-dichloro-3-methylthiophene used in work targeting cancer therapies, as well as crop science breakthroughs. Relationships with customer teams let us track success stories and gather detailed performance data, especially in multi-step syntheses. Chemical engineers appreciate the predictable boiling point and defined reactivity; analytical chemists turn to our batch data during impurity investigations.

    Learning from each application, we’ve improved not only the chemical itself, but also the container materials and label durability for extended storage. There’s no substitute for field data, particularly when intermediates travel long distances in varied conditions. Issues with temperature swings, moisture ingress, or labeling confusion are all brought back to our operations team for fast resolution and continuous improvement in packing and logistics.

    The Sustainability Angle

    As direct manufacturers, we feel a responsibility to environmental performance, not just for compliance but as a matter of principle. Chlorinated organics require robust emissions controls, and decades of investment in scrubber systems and closed vapor loops cut emissions to well below regulatory limits. We recover heat from exothermic reactions, channeling it to pre-warm raw material feeds, which cuts energy waste plant-wide. For waste product streams, we operate neutralization and incineration systems before safe disposal, audited regularly by independent agencies.

    Input materials sourcing has shifted toward partners with transparent supply chains and certified practices. We scrutinize every link — from mine to feedstock processor — for environmental and labor credentials. This approach reduces risks in our supply chain and aligns us with partners who share long-term goals for responsible chemistry. Responding to increasing requests for “green” process documentation, we continue gathering and sharing data on solvent recovery, closed-loop operations, and process intensification.

    Scaling, Custom Solutions, and Flexibility

    No two customers request exactly the same thing, and that’s where our cumulative on-floor expertise sets us apart. Projects seeking custom specifications on assay or packaging bring out the best in our team, who handle fine-tuning every order in line with customer feedback. Modifications to the distillation route, solvent choices, or drying cycles for specific project needs receive detailed attention in plant meetings. As manufacturers, we actively invite this level of collaboration, knowing it leads to better-designed products and solutions.

    On request, we can trace specific synthesis variables and offer extra product analyses — such as residual solvent reports or impurity fingerprints — supporting client filings or special formulation needs. For multinational programs needing locked process parameters, we document every change and run periodic full validations to support reproducibility. The open-door policy between our lab, production, and quality assurance teams means every special order, whether for a few kilograms or larger scale, gets treated with the rigor and respect it deserves.

    Looking Ahead: Innovation Roots in Manufacturing Practice

    Our own R&D team keeps a steady eye on new catalytic methods or alternative feedstocks that could improve future batches. Current test runs focus on lowering solvent use and expediting cleaning cycles, further reducing emissions and downtime. Materials science collaborations aim to reduce odor and vapor risks during shipping. Practical lessons from warehouse to reactor continue to inform both incremental and step-change improvements in our plant.

    We draw innovation from real-world operator feedback, supplier partner updates, and — ultimately — the inventive ways our clients deploy 2,5-dichloro-3-methylthiophene. No two projects mirror one another, so ongoing dialogue remains the backbone of our ongoing improvement. As regulations change and the demand for specialty building blocks grows, we rely on accumulated manufacturing practice and a commitment to transparent communication across all stakeholders.

    Direct Experience: The Real Value Add

    After years on the shop floor and in client meetings, it’s clear that quality, operational transparency, and flexible support secure more loyalty than buzzwords or claims. Our responsibility, as manufacturers of 2,5-dichloro-3-methylthiophene, is to deliver consistency — not just in chemical purity, but in every aspect of the customer experience. Whether developing a new therapy or advancing specialty materials, teams count on reliable partners who fundamentally understand the chemistry and the demands of production, shipping, and long-term storage.

    Being present through each stage of synthesis, quality assurance, and customer support allows us to continually refine the product. Our best ideas don’t come from marketing; they come from seeing what works in practice, listening to customer pain points, and solving the unique puzzles that every batch presents. In every ton produced or test vial shipped, our knowledge and investments reflect not only today’s needs, but also a vision for the future of responsible chemical manufacturing.