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2-Thiopheneacetyl Chloride

    • Product Name 2-Thiopheneacetyl Chloride
    • Alias Thiophene-2-acetyl chloride
    • Einecs 240-111-3
    • 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

    708683

    Cas Number 39098-97-0
    Molecular Formula C6H5ClOS
    Molecular Weight 176.62 g/mol
    Appearance Clear colorless to pale yellow liquid
    Boiling Point 117-119°C at 15 mmHg
    Density 1.291 g/mL at 25°C
    Flash Point 97°C
    Purity Typically ≥98%
    Refractive Index n20/D 1.604
    Solubility Reacts with water; soluble in common organic solvents
    Chemical Structure CC(=O)Cl attached to 2-position of thiophene ring
    Storage Temperature Store at 2-8°C

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

    Packing & Storage
    Packing 2-Thiopheneacetyl Chloride, 100g, is packaged in a sealed amber glass bottle with a tamper-evident cap, labeled with hazard symbols.
    Shipping 2-Thiopheneacetyl chloride is shipped in tightly sealed, corrosion-resistant containers, protected from moisture and incompatible substances. It is transported as a hazardous material under appropriate regulations, including labeling for corrosive and flammable substances. The shipment must be accompanied by a safety data sheet and handled by trained personnel using suitable protective equipment.
    Storage 2-Thiopheneacetyl chloride should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen, to prevent moisture ingress. Keep it in a cool, dry, and well-ventilated area, away from heat, direct sunlight, and incompatible materials such as water, alcohols, amines, and strong bases. Store in a chemical fume hood or designated corrosives cabinet if possible.
    Application of 2-Thiopheneacetyl Chloride

    Applications of 2-Thiopheneacetyl Chloride in Industrial Manufacturing

    As the direct manufacturer of 2-Thiopheneacetyl Chloride, we support key chemical sectors with consistent quality and compliance to demanding downstream specifications. Our experience spans multiple specialized applications, with precise formulation and integration guidance across advanced organic synthesis, pharmaceutical intermediates, and specialty material industries. Below, we detail distinct industrial use cases with concrete compliance and processing information tailored to each downstream scenario.

    1. Synthesis of Thienopyridine Pharmaceutical Intermediates

    Our material finds extensive application in the production of thienopyridine-class drug intermediates, notably for active ingredients including anti-platelet agents. Process chemists rely on its acylation reactivity to introduce the thiopheneacetyl moiety at critical heterocyclic sites, influencing bioactivity and downstream molecule assembly. The raw material enters the synthetic route during secondary amine acylation, shaping the core scaffold of several branded therapeutics.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – FDA 21 CFR Part 210/211
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for APIs
    • USP General Chapter <467> Residual Solvents

    Typical usage ratio

    • Usage from 0.8 to 1.2 molar equivalents relative to amine substrate; chemists adjust within this range based on purity and step yield targets

    Downstream process integration

    • Introduced in the acylation step of multistep API intermediate synthesis (typically after initial thiophene ring derivatization and prior to cyclization)

    Final product types

    • Thienopyridine API intermediates
    • Branded and generic anti-thrombotic drug substances (after further synthesis)
    • Research compounds for cardiovascular indications

    2. Agrochemical Ingredient Manufacturing: Herbicide & Fungicide Synthesis

    Both leading and contract agrochemical manufacturers use this specialty acyl chloride to produce key intermediates for heterocyclic-based crop protection agents. It enables selective thiophene group functionalization within pyrazole, pyrimidine, and related structures, supporting the synthesis of new-generation fungicide and pre/emergent herbicide actives. Process control during acylation determines impurity profile and biological selectivity of the end product.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical raw material quality management
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • GB 2763 China's Maximum Residue Limits (MRLs) for Pesticides

    Typical usage ratio

    • Employed at 0.95 to 1.1 molar equivalents relative to nucleophilic counterparts; operators may further adapt according to impurity thresholds and cost optimization directives

    Downstream process integration

    • Fed into batch or continuous acylation reactors as the acyl donor during the early step of active ingredient backbone assembly, often under strictly anhydrous conditions to ensure cleaner conversion

    Final product types

    • Thienyl-containing fungicide intermediates
    • Heterocyclic herbicide intermediates
    • Biologically active agrochemical products following further downstream transformation

    3. Electronic Materials: Organic Semiconductor Synthesis

    Specialty materials manufacturers utilize this raw material for crafting building blocks in organic semiconductors, particularly in the preparation of oligothiophene-acyl derivatives designed for field-effect transistors and solar cell applications. Its integration supports high-purity, low-defect aromatics crucial for electronic device reliability, with batch traceability needed to fulfill advanced industry protocols.

    Industry compliance standards

    • IEC 62899-202: Standards for Printed Electronics
    • ISO 14001: Environmental Management for electronics manufacturing
    • RoHS Directive 2011/65/EU (for materials and process chemicals)
    • JIS C0907: Japanese standards for organic electronic materials

    Typical usage ratio

    • Used between 0.9 – 1.15 equivalents per condensation partner; formulation fine-tuned to maximize conjugation length, minimize residual acyl chloride below 50 ppm in purified material

    Downstream process integration

    • Participates in initial monomer acetylation during the synthesis of oligothiophene or donor-acceptor copolymers; subsequent purification steps remove secondary by-products for material device casting

    Final product types

    • Oligothiophene monomers for OFET production
    • Solution-processable semiconducting polymers
    • Organic photovoltaic active layers

    4. Synthesis of Specialty Fragrance and Flavors for Fine Chemicals

    Flavor and fragrance manufacturers use this ingredient to introduce sulfur-containing heterocycles to aroma compound structures via Friedel–Crafts or Schotten–Baumann reactions. The thiopheneacetyl motif imparts signature earthy, roasted, or sweet notes valued in high-concentration perfumery bases and select food flavorings. Operators pay special attention to downstream hydrolysis and purification, given regulatory purity targets for final use.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association, Amendment 51)
    • FEMA GRAS (Flavor and Extract Manufacturers Association Generally Recognized as Safe List)
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • Kosher and Halal production guidelines when applicable

    Typical usage ratio

    • Dosed at 1.0 to 1.3 equivalents in key acylation steps, with minor ratio adjustments guided by sensory panel feedback and downstream distillation efficiency

    Downstream process integration

    • Applied in aroma chemical synthesis as an acyl donor to aromatic alcohols and amines, with particular control over reaction temperature and catalyst concentration to limit formation of non-volatile residues

    Final product types

    • Sulfur-heterocyclic aroma compounds for fine fragrance bases
    • Specialty food grade flavorings (within strict concentration limits)
    • Complex aromatic blends for high-value perfumery and essences

    5. Advanced Dye and Pigment Intermediate Manufacturing

    Producers of specialty dyes employ this raw material for introducing thiopheneacetyl groups into extended conjugated systems, supporting enhanced chromatic stability and brightness for technical textiles and polymer films. This step remains sensitive to moisture, demanding rigorous solvent drying protocols, with colorfastness and migration testing scheduled according to anticipated end uses.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textiles)
    • REACH Regulation (EC) No 1907/2006 for pigment registration
    • ISO 105-C10:2014 for color fastness to washing
    • ASTM D4828: Standard Test Method for Practical Washability of Organic Dye Compounds

    Typical usage ratio

    • Loaded at 0.85 to 1.2 equivalents depending on the reactivity of other chromophore precursors and targeted color intensity

    Downstream process integration

    • Incorporated during acylation and condensation reactions for forming dye intermediate scaffolds prior to final coupling or sulfonation; process engineers maintain batch traceability to confirm pigment batch reproducibility

    Final product types

    • Color-stable organic dyes for technical and automotive textiles
    • Polymer-soluble pigment dispersions
    • Photostable specialty inks for advanced printing applications
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    Certification & Compliance
    More Introduction

    Introducing 2-Thiopheneacetyl Chloride – From Our Production Floor to Your Innovation

    A Synthesis Cornerstone in Heterocyclic Chemistry

    Many of our long-standing customers know the importance of fine-tuned building blocks in advancing both research and bulk chemical synthesis. Over the years, the requests for targeted halogenated acyl intermediates kept growing, especially from partners working in pharmaceutical and advanced materials fields. In direct response, our facility expanded to produce 2-Thiopheneacetyl Chloride, a compound now critical for synthesis routines involving thiophene frameworks. This product, bearing CAS number 39098-97-0 and molecular formula C6H5ClOS, isn’t just an incremental offer—it reflects decades of hands-on experience in thienyl chemistry and chlorination expertise.

    Any chemist who’s run electrophilic acylation or managed sensitive nucleophilic additions with thienyl residues understands why this chloride stands out. Simple structural analogs, such as acetyl chloride or benzoyl chloride, lack the electron-rich and conjugatively active thiophene ring. That tiny advance—a sulfur atom in place of a benzene carbon—translates to major divergences in reactivity, solubility, and synthetic application. Our QC team tests every batch on parameters we know matter: chlorine content, purity by HPLC and NMR, and stability under ambient warehouse conditions.

    Why Tiered Quality Control Matters

    Unlike distributors who source from multiple small producers or blend for price-point advantage, our goal centers on batch consistency from raw input to final packing. The thiophene starting material undergoes rigorous purification to remove isomeric and non-aromatic sulfides, ensuring clarity of the acyl chloride stage downstream. Purity doesn’t just serve documentation—it addresses the life span and behavior of the intermediate in the customer’s own synthesis. When major R&D groups tested cross-coupling and Friedel-Crafts applications with our 2-Thiopheneacetyl Chloride, they saw a repeatability in reaction profiles they couldn’t secure with lower-quality imports.

    We constantly compare our material against imported and domestic alternatives using blind spectral analysis, yields in pilot reactions, and sealed-tube longevity assessments. Signal-to-noise ratio in 1H NMR, for example, directly correlates to smoothness in downstream scaleup, minimizing hazardous byproduct formation. Product from our reactors displays a sharp, clean acyl chloride peak without tailing or baseline drift, which can be a headache in work-up if the material is handled roughly or carries residual solvents.

    Applications – Beyond Simple Derivatization

    Colleagues in pharmaceutical and crop-protection industries report that 2-Thiopheneacetyl Chloride is often the lynchpin for assembling new heterocyclic scaffolds. Whether you’re forming amide bonds with nucleophilic amines, running carbon-carbon couplings, or designing ligands for metal-catalyzed transformations, the unique electron-rich nature of the thiophene ring often enables routes that a phenyl equivalent simply blocks. Our own R&D staff has leveraged this intermediate to build libraries of bioactives—testing not just the core structure but functionalization along different ring positions.

    Several specialty materials suppliers turn to thiophene derivatives as precursors for organic semiconductors and photovoltaic research. The enthusiasm for thiophenes—owing to their pi-electron mobility—means acyl chlorides in this family often see use much earlier in protected, modular syntheses. Comparing with classic acetyl chloride, which quickly hydrolyzes and offers far less scope for backbone design, our product delivers reactive selectivity that’s tough to replace.

    What Makes Manufacturing Challenging (and How We Respond): A Producer’s Perspective

    Handling acyl chlorides, let alone those based on electron-rich heterocycles, presents a pronounced challenge during scale-up. The volatility and reactivity make containment and operator safety non-negotiable priorities. Our reactors use temperature- and pressure-controlled feed systems, combined with in-line HCl neutralization and vapor management. It isn’t unusual to hear about off-spec batches from smaller outfits due to inadequate moisture exclusion; even modest contact with air can destroy the product’s integrity.

    Every year, we analyze loss points at different production stages and invest in improved materials of construction—insisting on lined vessels and automated controls. From shipment to customer, packaging in amber glass ampules or fluoropolymer-lined drums maintains acyl purity, avoiding both UV-induced decomposition and hydrochloric acid corrosion. We never use repurposed containers or inadequate liners, which sometimes show up in reseller-sourced stock and betray their origin through yellowing or stench upon opening.

    Regulatory and Handling Experience

    While our product ships under standard DOT and IMDG codes, team members receive regular hazmat recertification and practical training on both transport and emergency protocols. We maintain clear documentation for all export and domestic shipments, reflecting direct manufacturer-to-customer traceability rather than murky third-party reporting.

    Onsite monitoring detects early warning signs for HCl evolution—fluoropolymer seals, active vapor scrubbing, and storage at low temperatures remain proof against unwelcome surprises. Our decades dealing with sensitive chlorides and homologues means customer queries land with field chemists, not call center scripts.

    Continuous Improvement: Batch Reproducibility and Process Safety

    We never treat our synthetic method as “finished.” Each quarter, our technical team revisits feedstock sourcing, plant hygiene SOPs, and performance benchmarks in both small and tonne-scale runs. Early years in chlorinated handling showed us even minor tweaks to feed ratio, light exposure, or agitation speed influenced downstream utility. At this point, collaborating directly with polymer chemists and medicinal R&D teams has convinced us to lock in tighter controls on isomeric purity and moisture boundaries.

    Instead of trading on batch-to-batch variability—an all-too-common practice among intermediaries—we require alignment with primary spectra and proof-of-function across customer test protocols. If a customer’s amide bond formation, for instance, produces lower yield or unexpected byproduct, we repeat the same reaction in our labs using retained samples. More often than not, reproducibility shows its worth by nailing down process bottlenecks that have nothing to do with the acyl chloride itself, but occasionally, it flags a subtle drift in pH or color that deserves a corrective in the next production cycle.

    Comparing to Other Chlorinated Acyl Intermediates

    Studied side-by-side, 2-Thiopheneacetyl Chloride features a smarter blend of reactivity and ring-system bias compared to benzoyl or pivaloyl chloride. The heterocyclic sulfur offers electron-donating properties, supporting unusual electrophilic substitutions or metal-catalyzed processes, which experienced synthetic chemists demand. Customers chasing advanced conjugation or tailored pharmaceuticals stick with thiophene chemistry, unable to achieve the same pharmacophore or material effect with straightforward aromatic or saturated acyls.

    Several universities partner with us—or benchmark our material against competitor samples—precisely because a poor-quality batch undermines months of downstream kinetic analysis. Impurities from uncontrolled chlorination often poison catalytic systems or introduce colored side-products, so tracking and verifying each batch all the way back to its starting thiophene is integral to our operational playbook.

    Solving Real-World Industry Challenges

    Requests sometimes arrive for reliability across multi-tonne annual volumes, other times from low-volume, just-in-time pilot runs. We treat each order with acute awareness of shelf-life or reactivity risks under field conditions. If a medicinal chemist wants insight on handling traces of acid or gets frustrated with hydrolysis even at low humidity, we share our own protocols—based on years of accidental exposures and stored-sample decomposition. From there, our technical bulletins offer not just storage advice but follow through with cleaning and deactivation methods for vessels or residues, using only field-validated techniques.

    Batch recalls or quality misses from competitors end up circulating through industrial grapevines. We’ve responded more than once to emergency queries from labs running clinical candidate syntheses on tight timelines, where a contaminated acyl chloride batch could cost weeks of lost productivity or a failed patent claim. Our team’s focus falls on supporting the customer’s actual workflow, not just ticking a spec sheet box and shipping a drum.

    Industry Collaboration—Why Direct Manufacturing Pushes Progress

    We’ve observed how collaboration between original manufacturers and end-users can fast-track new reaction designs and analytical techniques. Because the product enters customer workflows at delicate or novel stages, it often reveals pain points no spec sheet covers—from unexpected hydrolytic drag at the solid-liquid interface to compatibility with freshly designed ligands.

    We maintain open channels for joint troubleshooting and pre-shipment batch testing, with select accounts running parallel reactions and sharing results in real time. By keeping manufacturing, analytics, and user feedback under one roof, small but vital improvements—shifts in batch filtration, tweaks in sulfur content, improved cold storage routines—translate into incremental successes for both parties.

    Handling, Storage, and Risk Minimization—Practical Lessons Earned

    A core lesson across our product lines concerns the truth that stability starts at the production floor and traces all the way to the end user's flask. We favor smaller batch sizes, just-in-time shipping, and allocation of surplus only to short-turnover storage. Too much time in ambient conditions, or shipment in poorly sealed packaging, undercuts acyl stability and puts both workflows and budgets at risk.

    Staff in our warehouses handle only one major chloride intermediate at a time, to prevent cross-contamination or mislabeling. Regular, documented lot rotation, along with double-barrier packaging, keeps risks of hydrolysis and adulteration exceptionally low. This discipline matters especially for 2-Thiopheneacetyl Chloride, where the product’s scent and appearance rapidly betray water uptake or sunlight exposure.

    Looking Forward—New Opportunities in Thiophene Chemistry

    Every year, customer applications expand. Specialty pigment projects use our acyl derivative as a springboard for novel dye synthesis. Peptide chemists push it into new N-terminal modifications, while polymer labs probe its suitability for fresh donor-acceptor materials. Each of these projects leans not just on raw supply but on the expertise in navigating reactivity, handling risks, and iterative quality control that years in the field have taught us.

    Our commitment to supporting these communities leads us to reinvest in pilot plant upgrades, better environmental management for chloride effluents, and more granular traceability from precursor to packaged lot. We share case studies, collaborate on custom specs, and maintain a technical helpdesk fully staffed by practicing chemists.

    Why Our Direct Manufacturing Story Matters—A Final Word from the Floor

    These aren’t just talking points but statements from years spent troubleshooting, optimizing, and watching our material shape customer research outcomes. Direct manufacturing links us to end users in a feedback loop of proof, challenge, and improvement. No speculator, broker, or uninvolved distributor can fill that gap. Each kilogram that leaves our warehouse reflects not only process control and careful handling but an ongoing pledge to those who depend on reliability for their next synthesis step.

    For any partner needing consistent, verified, and transparent supply of 2-Thiopheneacetyl Chloride, we bring that perspective—a blend of experience, accountability, and willingness to adapt. It's a promise forged through time, trials, and real-world chemistry: your success depends on what happens before a drum ever reaches your dock, and we treat that responsibility with the seriousness the industry—and your research—demands.