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2-Acetyl-5-Bromothiophene

    • Product Name 2-Acetyl-5-Bromothiophene
    • Alias 2-Acetyl-5-bromothiophene
    • Einecs 253-698-9
    • 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

    529306

    Chemical Name 2-Acetyl-5-Bromothiophene
    Cas Number 13684-57-6
    Molecular Formula C6H5BrOS
    Molecular Weight 205.07
    Appearance Yellow to light brown solid
    Melting Point 43-45°C
    Boiling Point 152-154°C at 14 mmHg
    Density 1.675 g/cm3
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Smiles CC(=O)c1ccc(Br)s1
    Inchi InChI=1S/C6H5BrOS/c1-4(8)5-2-3-6(7)9-5/h2-3H,1H3
    Storage Conditions Store at room temperature, away from light and moisture

    As an accredited 2-Acetyl-5-Bromothiophene 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 25g of 2-Acetyl-5-Bromothiophene, tightly sealed with a screw cap, labeled with hazard precautions.
    Shipping 2-Acetyl-5-Bromothiophene is typically shipped in sealed, chemical-resistant containers to prevent leakage and contamination. Transport complies with international regulations for hazardous materials, including appropriate labeling and documentation. Packages should be protected from physical damage, moisture, and extreme temperatures. Handling and shipping are performed by authorized personnel, using recommended safety precautions.
    Storage 2-Acetyl-5-Bromothiophene should be stored in a tightly sealed container, away from heat, moisture, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separate from incompatible materials such as strong oxidizing agents. Ensure labeling is clear and compliant with safety guidelines. Use secondary containment to prevent leaks or spills, and access should be restricted to trained personnel.
    Application of 2-Acetyl-5-Bromothiophene

    Applications of 2-Acetyl-5-Bromothiophene in Industrial Manufacturing

    2-Acetyl-5-Bromothiophene plays a critical role as an advanced intermediate in the synthesis of complex molecules within several highly regulated manufacturing sectors. By providing targeted reactivity and unique substitution patterns, this compound enables controlled downstream transformations with strict process and compliance requirements. Below we present the principal downstream industries, integration details, and final product pathways supported by industrial-grade 2-Acetyl-5-Bromothiophene.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers regularly incorporate this advanced thiophene in the multi-step synthesis of targeted small-molecule APIs, exploiting the brominated ring for selective cross-coupling reactions such as Suzuki, Stille, or Buchwald–Hartwig, and the acetyl group for subsequent functionalization. Its high chemical purity ensures reliable integration into GMP-compliant API routes for syntheses, including thiophene-containing drug scaffolds. Formulation chemists carefully monitor impurity profiles to comply with stringent pharmacopoeial specifications, optimizing reaction ratios for scalable commercial processes. Downstream process engineers ensure that the intermediate is introduced at the correct process stage for controlled halide/acetyl substitution and subsequent cyclization, amidation, or other API-building reactions. Final APIs containing thiophene substructures address therapeutic indications across oncology, anti-inflammatories, antivirals, and CNS applications.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • European Pharmacopoeia (Ph. Eur.) standards for impurities
    • US FDA 21 CFR Part 211 cGMP for finished pharmaceuticals
    • Japanese Pharmacopoeia (JP) API impurity guidelines

    Typical usage ratio

    • 10–40% molar equivalent in API synthetic route, fine-tuned based on targeted halogen or acetyl incorporation, stoichiometry set by batch synthesis scale

    Downstream process integration

    • Enters mid-stage of small-molecule API synthesis
    • Used in heterocyclic coupling steps where thiophene is required
    • Subject to controlled precipitation, filtration, and purification
    • Final API isolated after further transformation of intermediate

    Final product types

    • Anti-inflammatory APIs (e.g., thiophene-based NSAIDs)
    • Antitumor active ingredients using bromothiophene cores
    • Specialty antivirals with heteroaromatic frameworks
    • CNS modulating drugs with thiophene moieties

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical companies employ 2-Acetyl-5-Bromothiophene as a raw material for the creation of selective herbicide and fungicide actives, where the electron-rich thiophene ring provides desirable biological interactions. The compound facilitates the development of new crop protection products via palladium-catalyzed coupling, electrochemical bromine displacement, or ketone modification. Technical-grade batches require compliance with global agrochemical registration standards and environmental safety data, supporting downstream process reproducibility. Formulators carefully adjust the intermediate’s dosage depending on the mode of substitution and the required crop selectivity. In technical production, the intermediate is usually introduced post-nitration or ring-closing and enables the construction of diversified agrochemical scaffolds prior to formulation, stabilizing agents, or emulsification. Downstream companies supply a broad range of registered crop protection products optimized for geographical regulatory acceptance.

    Industry compliance standards

    • OECD Test Guidelines for chemical safety (including 5 Batch analysis)
    • EU Regulation (EC) 1107/2009 for Plant Protection Products
    • US EPA 40 CFR Part 158 for pesticide registration
    • GLP (Good Laboratory Practice, OECD/EPA) for technical-grade intermediates

    Typical usage ratio

    • 20–35% by mol in synthetic multistep pathways, adjusted on the basis of agrochemical actives' required loading and environmental fate studies

    Downstream process integration

    • Inserted after preliminary aromatization or functionalization
    • Key substrate for bromine coupling, exchange, or ring expansion steps
    • Purified immediately before final bioactive assembly
    • Downstream handling includes solvent exchange, extraction, and crystallization

    Final product types

    • Post-patent herbicides with thiophene-based binding domains
    • Systemic fungicides with aromatic sulfur heterocycles
    • Pre-emergent weed killer actives containing bromothiophene
    • New mode-of-action insecticides in regulatory trials

    3. Organic Electronic Materials Synthesis

    Manufacturers operating in the organic electronics industry utilize 2-Acetyl-5-Bromothiophene as a monomer precursor in the production of functionalized thiophene polymers, especially for organic semiconductors and photovoltaic materials. The brominated acetylthiophene unit supports controlled polymerization steps—a key factor for optimizing electrical mobility and optoelectronic efficiency. Electronic material formulators must comply with RoHS hazardous substance limitations, cleanroom protocols, and analytical quality controls. Usage ratios vary according to the targeted molecular weight and degree of polymer chain extension. Integration occurs during the Suzuki or Stille coupling polymerizations, where the intermediate reacts with co-monomers under catalysis, followed by controlled precipitation and molecular weight determination. The resulting conductive polymers enable development of next-generation flexible displays, organic solar cells, and thin-film transistors.

    Industry compliance standards

    • IEC 62321 (RoHS screening for hazardous substances)
    • REACH Regulation (EC) No 1907/2006 for SVHC assessment
    • ISO 9001:2015 QMS for electronic material manufacturing
    • ISO 14644 cleanroom standards (fabrication environments)

    Typical usage ratio

    • 0.1–10% by weight in monomer feeds, dependent on target polymer chain and electronic performance, with lower end use for dopant/functionalization and higher for main-chain inclusion

    Downstream process integration

    • Added to monomer blend before polymerization
    • Undergoes controlled coupling with other aromatic units
    • Process includes precipitation, drying, and molecular weight adjustment
    • End product cast into electronic layers, films, or inks

    Final product types

    • Organic photovoltaic (OPV) absorber materials
    • OLED conductive polymer films
    • Flexible printed circuit substrates
    • Thin-film transistor semiconductor layers

    4. Fragrance and Flavor Intermediate Manufacturing

    Specialty aroma compound producers employ 2-Acetyl-5-Bromothiophene as a heterocycle intermediate in the design and synthesis of sulfur-containing notes for fine fragrance and flavor formulations. Its unique backbone imparts rich, earthy, and spicy nuances after downstream manipulation of the acetyl or bromine group. All stages adhere to food and fragrance chemical purity standards as defined by global and regional agencies. Chemists tailor the usage rate strictly based on olfactory intensity and regulatory residue limits. The intermediate enters the process after initial feedstock blending and pre-functionalization, often participating in selective reduction, acylation, or substitution reactions before distillation and fraction collection. Downstream use focuses on delivering high-impact aroma chemicals and flavoring agents for integration in specialty consumer products.

    Industry compliance standards

    • IFRA Standards for fragrance material safety
    • FEMA GRAS (Flavor and Extract Manufacturers Association Generally Recognized As Safe)
    • EU Regulation (EC) No 1334/2008 for flavoring substances
    • US FDA 21 CFR 172 (food additives, flavoring agents)

    Typical usage ratio

    • 0.01–0.1% by weight in formulation intermediates, optimized for specific flavor threshold or fragrance profile, with maximum levels defined by toxicological and GRAS recommendations

    Downstream process integration

    • Integrated post-feedstock pre-treatment
    • Reaction with reducing agents or acyl donors
    • Fractionated after main chemical transformation
    • Quality controlled for average purity, absence of halogen residue, and aroma profile

    Final product types

    • Flavor bases for savory or meaty profiles in processed foods
    • Fine fragrance aroma molecules for high-end perfumery
    • Spicy and earthy note ingredients for beverage and tobacco flavors
    • Specialty olfactory markers for aroma encapsulation technologies
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    Certification & Compliance
    More Introduction

    2-Acetyl-5-Bromothiophene – Our Perspective as the Producer

    Everyday Work with 2-Acetyl-5-Bromothiophene

    At our facility, 2-Acetyl-5-Bromothiophene shows up almost daily in conversations among our chemists. Our team has worked side by side with this compound for over a decade, so there’s nothing unfamiliar or distant about it. Many clients wonder about the uses and differences compared to other thiophene derivatives. Our viewpoint comes from a long track record in organosulfur chemistry, hands-on production experience, and direct interactions with research teams that depend on quality and reliability.

    In the lab, 2-Acetyl-5-Bromothiophene is not an ornament or shelf-warmer. The white to pale-yellow crystalline powder with a distinct, sharp odor demands thorough attention at every step. Technicians rely on its defined melting point and consistent TLC performance. Our samples regularly show purity above 98% by GC, which saves time for formulation partners and limits surprises in downstream syntheses.

    Thiophene chemistry often enters unpredictable territory, especially with halogenated and alkylated rings. Yet, this compound's bromine group opens countless possibilities in cross-coupling reactions, from Suzuki-Miyaura to Stille protocols. Its acetyl functional handle brings more flexibility for nucleophilic additions and further functionalizations. We’ve learned direct from feedback that research chemists, material science innovators, and pharmaceutical teams all return to this compound because alternatives rarely match its versatility.

    Why 2-Acetyl-5-Bromothiophene Holds Value

    Behind the dry technical descriptions lives a set of real-world problems 2-Acetyl-5-Bromothiophene helps address. In API research, medicinal chemists knew for years they could build out heterocyclic frameworks with this intermediate. Process teams trust that its reactivity profile brings fewer side reactions during scale-up; we’ve heard first-hand from several pilot plant managers that their transition from gram to kilogram scale needs high-purity, low-particulate material to prevent equipment fouling. Our QC team checks batches for residual solvents and trace metals, since these contaminants often frustrate researchers looking for cleaner downstream reactions.

    Industrial customers running OLED material screening programs voiced to us that they prize steadiness in supply; no one wants a halted program due to erratic impurity levels or delays in customs. Experience taught our team to prioritize regularity in composition and packaging, because syntheses that employ this compound to construct extended π-conjugated systems, like polythiophenes or arylthiophenes, do not forgive off-odors or batch-to-batch variation.

    Comparing to Other Thiophenes

    Many new clients ask, “Why not use simpler acetylthiophenes, or skip to a dibromo derivative?” From the years we’ve run both large and specialty campaigns, we see that 2-acetyl-5-bromothiophene strikes a practical balance. For researchers requiring selectivity in controlled halogenations, this mono-brominated version stands apart from both the unsubstituted and di-substituted analogs. Pure acetylthiophenes often lack the orthogonal reactivity necessary for late-stage diversification. On the other hand, heavily brominated thiophenes present solubility headaches or environmental burdens during handling.

    Products such as thiophene-2-carboxaldehyde, 2-acetylthiophene, and 2-bromothiophene turn up in our reactors too, but each one carries distinct quirks. 2-Acetylthiophene, for example, misses out on the potential for rapid cross-coupling at the 5-position; likewise, bromothiophenes without the acetyl group rarely headline as intermediates in complex molecule assembly.

    Some think more bromine or larger acetyl groups might mean greater flexibility, but reality looks different in process control and yield. Several large-scale clients who experimented with 2,5-dibromothiophene found increased waste streams, complicated post-reaction workups, and unnecessarily high purification costs. Semi-conductor industry chemists ring us regularly for single-brominated, acetyl-functionalized thiophenes to keep material costs and handling manageable while still allowing highly tailored synthetic approaches.

    Specifications and Quality: Lessons from the Plant

    Demand for 2-Acetyl-5-Bromothiophene now pulls samples out of our stockroom weekly, not just on special order. The market expects tight color standards, free-flowing powder, and packaging that supports both small-batch and bulk procurement. Years monitoring process parameters led us to tighten both HPLC and GC limits for residual raw materials and byproducts. Regular titrations, Karl Fischer analyses, and IR checks don’t simply serve as QC hurdles; feedback from users pointed to smoother operations and fewer surprises in scaling or reactivity.

    Moisture remains one of those ever-present headaches. Even a small uptick in ambient humidity rewards us with clumping and harder weighing. Our packaging team evolved its habits, spending extra attention on double-seal bags and low-permeability cartons. These details rarely make it onto brochures, but customers notice the difference as soon as they open a fresh shipment. On the back end, we track return rates, caked material, or broken seals; as producers, these metrics tell us how to adjust storage climate, shift blending times, or consider new desiccant types.

    For researchers driving sensitive Pd- or Ni-catalyzed couplings, the sulfur content and low halide contaminants in the material mean cleaner products in less time. Early on, we learned that unfiltered or unpolished product slowed chromatography and wasted precious column volumes. Today, we refine post-reaction filtration and crystallization to support rapid, efficient research programs.

    Heavy Use in API and Advanced Materials

    Not all organic intermediates see wide-ranging demand, but 2-Acetyl-5-Bromothiophene now stands as one of the mainstays for combinatorial libraries, fragment-based medicinal chemistry, and polymer development. Many active pharmaceutical ingredient projects require this intermediate somewhere along their synthetic pathway. We often see requests for custom packing, expedited orders, or certificates catering to regulatory gatekeepers, since production managers and purchasing officers count on fast turnarounds when screening new candidates.

    Material scientists working on organic electronics show renewed interest. The push for flexible displays, new battery electrodes, or advanced sensors hinges on bench-tested molecules where tuning electronic and steric properties matters. Bromothiophene derivatives consistently turn up as central scaffolds in preclinical candidates and experimental conductive polymers. We maintain direct talks with researchers, learning that purity, particle size, and ease of dissolution help or hinder their screening. Collaborative pilot projects in our own facility connect our technical team with PhDs from multinational labs. Together, we work out custom lots or adjusted syntheses to fit their protocols.

    Several years back, an OLED startup needed kilogram quantities on short notice, after a trial project scaled up unexpectedly. Because we keep manageable safety stock, production didn’t stall. Their chemists fed back that they could avoid revalidating dozens of synthetic steps based on our batch records and consistency. Timely, direct support for end users is rarely highlighted in specifications, but our day-to-day customer interactions revolve around it.

    Making and Handling: Our Viewpoint from the Production Line

    Producing 2-Acetyl-5-Bromothiophene depends on deep familiarity with the quirks of heterocyclic chemistry. From the first days we started preparing it, we knew that controlling exothermicity and handling corrosive reagents present unavoidable technical challenges. Our reactors reflect regular improvement, from upgraded agitation and sealing systems to constant monitoring of in-process temperatures. Standard procedures alone never guaranteed top product; steady iterations came from reading near-misses in the production records, plus blunt conversations between operators and process engineers.

    Recovery and waste handling grew into a focus for us. Early on, yield losses to over-bromination or byproduct formation climbed higher than expected. Tweaking feed rates, streamlining quench protocols, and building better extraction towers meant delivering higher output per shift. Waste stream neutralization also saved disposal costs. Neighbors in the industrial park care as much about effluent quality as contained reaction vessels. Every time customer audits took a close look, we benefited from detailed logs, batch history, and process documentation.

    Packaging lines keep up closely with production. The most frequent packaging form for 2-Acetyl-5-Bromothiophene is the fiber drum lined with antistatic bags for bulk, while kilo-scale customers lean toward double-layered foil pouches. Exposure to light and air affects visual quality over time. Shipping room practices now always double check sealing, package labeling, and documents before anything leaves our gates.

    Shipping logistics matter more than many assume. One lost airfreight shipment or customs hold-up costs not just time but downstream disruption for entire laboratories. Our logistics staff fine-tunes export papers for different markets, watches weather, and checks with local agencies regularly on hazardous cargo rules. A mix of local and international transport keeps our delivery schedules steady. End users want predictability, so we schedule backup routes, test out alternative suppliers for drums and liners, and maintain an open channel with customs brokers.

    Key Differences and Specialist Feedback

    Among thienyl derivatives, we witness certain trends. Chemists in medicinal discovery programs order 2-Acetyl-5-Bromothiophene for targeted functionalizations, often because competing products fall short in site selectivity or end-group compatibility. Material scientists seeking conjugated building blocks for optoelectronic devices choose our compound based on physical consistency and narrower impurity spots, which they say helps reduce background noise in device prototypes.

    In larger commercial syntheses, alternative products with multiple reactive bromines introduce mixing and heat management headaches, plus more costly purification steps. Laboratories that tried 2-acetylthiophene without the bromine group told us their routes required extra steps and produced lower overall yield. High-throughput screening teams trying similar sulfur heterocycles often revert to our product for its reliable behavior – clear melting onset, consistent solubility in common polar and nonpolar solvents, and lack of interfering side-products.

    We field questions on compound traceability and sourcing. Each order traces to batch numbers and archived QC records. This approach did more than solve audit worries; it arms our chemical engineers with the ability to troubleshoot user issues at the molecular or logistical level. If packaging materials or processing assistants ever vary, we identify trends and update procedures to align with what researchers expect in their daily work.

    Adaptation, Trends, and the Road Forward

    The field keeps moving. Just a few years ago, only small teams focused on organic conductors or OLED device platforms; now, large institutional research budgets rely on products like ours. We adapted by cross-training our staff to troubleshoot both organic synthesis and application-specific concerns. It takes more than supplying a chemical: we partner, in effect, by testing small-lot modifications or exploring new purification regimes as soon as clients surface an issue.

    Sustainability matters for the segment using 2-Acetyl-5-Bromothiophene as a building block. Many European and North American partners ask about lifecycle analysis, solvent choice, and post-synthesis waste. Our purchasing group works closely with feedstock suppliers to verify sources, while the process engineering team reviews solvent use for improved recovery each year. Risk mitigation came up during site visits, as visiting safety officers asked how we balance halogen inventory and flammability precautions. One of our ongoing projects involves solvent recycling and improved containment of halide residues, informed by industry consortium workshops and our own plant data.

    A few emerging research groups began exploring bio-based synthetic routes, hoping to cut dependency on traditional petrochemical feedstocks for key precursors. We keep an open ear to these potential shifts; several academic collaborators checked in regarding early-stage alternative syntheses. The cost, throughput, and reliability still lag conventional chemical manufacturing, so our production team is tracking developments and running bench-scale experiments in parallel.

    Challenges and Collaboration: Our Continuous Learning Curve

    Every step in manufacturing 2-Acetyl-5-Bromothiophene carries inherited complexity. Strict temperature controls, safe reagent handling, and efficient crystallization all demand focus. Each improvement cycle comes from concrete setbacks – a bad batch, a process stall, or an unexpected analytical quirk. QC failures introduce immediate adjustments, not just paperwork. This learning-by-doing built a resilient team capable of handling new requests, unplanned delays, or regulatory updates.

    Much of what distinguishes us from traders or resellers is living with these materials every day. Problems with clumping, inconsistent shipment weights, or regulatory delays push direct feedback into our next run. End users whose projects hinge on timely, pure intermediates trust us to recognize when tiny adjustments in drying or packaging influence their next stage of research.

    Direct dialogue with universities, startups, and manufacturer R&D groups shapes our own roadmap. We know from daily calls and plant walk-throughs that industries will keep innovating around molecules like 2-Acetyl-5-Bromothiophene. Whether used in drug discovery or display technologies, its versatility and approachable handling set it apart from legacy thiophene analogs. As process chemists and application specialists ourselves, we view every shipment not just as a commodity, but as an enabler for real progress in chemical research and industrial development.

    Conclusion

    Our experience with 2-Acetyl-5-Bromothiophene spans countless product lots, pilot plant adjustments, and customer collaborations. The market relies on it for its defined balance of reactivity, ease of functionalization, and manageable handling. Through trial, adaptation, and continuous communication, our production team crafts an intermediate that enables researchers to move from concepts in the lab to leading-edge applications in health care, electronics, and materials science. Each parcel leaving our warehouse reflects not just a specification sheet, but years of accumulated expertise at the junction of chemistry and industry.