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6-Chloro-3-Formylchromone

    • Product Name 6-Chloro-3-Formylchromone
    • Alias 6-Chloro-4-oxo-4H-1-benzopyran-3-carbaldehyde
    • Einecs 631-545-6
    • 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

    903983

    Product Name 6-Chloro-3-Formylchromone
    Molecular Formula C10H5ClO3
    Molecular Weight 208.6 g/mol
    Cas Number 13784-35-7
    Appearance Yellow to orange crystalline powder
    Melting Point 232-234°C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in ethanol
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles O=Cc1c(Cl)cc2oc(=O)ccc2c1
    Iupac Name 6-chloro-4-oxo-4H-chromene-3-carbaldehyde

    As an accredited 6-Chloro-3-Formylchromone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure cap, labeled "6-Chloro-3-Formylchromone," includes hazard warnings and chemical details.
    Shipping **Shipping Description for 6-Chloro-3-Formylchromone:** 6-Chloro-3-Formylchromone is shipped in tightly sealed containers, protected from light and moisture. The package complies with relevant chemical safety regulations. It is transported as a non-hazardous material under normal shipping conditions, with clear labeling and documentation to ensure safe handling during transit.
    Storage 6-Chloro-3-Formylchromone should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition or incompatible substances such as strong oxidizers. Store at room temperature or as specified by the supplier, and ensure proper chemical labeling and secure storage to prevent unauthorized access or accidental exposure.
    Application of 6-Chloro-3-Formylchromone

    Applications of 6-Chloro-3-Formylchromone in Industrial Manufacturing

    6-Chloro-3-Formylchromone serves as a high-purity chemical intermediate in several specific industrial applications. The following scenarios detail practical downstream use in professional manufacturing operations, addressing industry standards, real formulation guidelines, process chain integration, and resulting finished products.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    This material plays a role in the multi-step synthesis of advanced intermediates for select antiviral pharmaceuticals. Research-driven manufacturing utilizes 6-Chloro-3-Formylchromone to introduce heterocyclic aldehyde groups, forming key pharmacophores in non-nucleoside drug candidates. Processing facilities apply stringent GMP protocols throughout batch and continuous syntheses to meet international quality requirements for active pharmaceutical ingredient (API) production.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: US FDA Current Good Manufacturing Practice
    • EU GMP Volume 4 (APIs)
    • Chinese Pharmacopoeia API Standards (when supplying China)

    Typical usage ratio

    • 5-10 mol% relative to total starting material in target antiviral synthesis
    • Adjusted per route optimization and desired yield for scale-up batches

    Downstream process integration

    • Fed into Stage 2 or 3 of multi-step condensation or cyclization reactions
    • Subjected to high-purity solvent extraction followed by crystallization
    • Monitored for residual aldehyde and chromone content in purification steps

    Final product types

    • Intermediate for HIV-1 reverse transcriptase inhibitor APIs
    • Intermediate for hepatitis virus inhibitor candidates
    • Building block in pipeline of broad-spectrum antiviral small molecules

    2. Chemical Synthesis of Flavonoid Derivatives

    Manufacturers of specialty flavonoids incorporate 6-Chloro-3-Formylchromone as a precursor in the synthesis of bioactive chromone or flavone derivatives. The formyl group enables controlled condensation and functionalization for structure-activity research and targeted product development. Downstream processors handle the raw material in closed-system reactors to manage reactivity and ensure operator safety.

    Industry compliance standards

    • ISO 9001: Quality Management Systems for chemical synthesis
    • REACH Regulation (EC) No 1907/2006, for European downstream use
    • Chinese GB T 17513.2 for specialty intermediates
    • Material Safety Data Sheet (MSDS) compliance for occupational safety

    Typical usage ratio

    • 10–30 wt% based on overall reagent charge in flavonoid modification steps
    • Ratio refined according to structure of target chromone/flavone and reactivity

    Downstream process integration

    • Introduced at the condensation stage for selective C3 functionalization
    • Reacted in controlled temperature reactors (typically 60–90ºC)
    • Often followed by chromatographic separation for purity enhancement

    Final product types

    • Rare and custom-substituted flavone analogs for pharma research
    • Chemically engineered chromone derivatives for R&D
    • Precursors for aglycone and glycosylated flavonoid products

    3. Active Ingredient Precursor in Agrochemical R&D

    Agrochemical innovators in crop protection formulations rely on 6-Chloro-3-Formylchromone as a lead scaffold for discovering new fungicides and insecticides. Structure-activity optimization in the discovery stage requires reliable supply and predictable reactivity to efficiently generate compound libraries. Processing teams document all input lots and synthesize under ISO and GLP protocols, minimizing impurity carry-over into bioassay stages.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025:2017 for testing and calibration laboratories
    • Regulation (EC) No 1107/2009 for plant protection products
    • China Pesticide Registration Standard (GB 2763)

    Typical usage ratio

    • 2–6 mol% in early stage combinatorial synthesis of agrochemical candidates
    • Ratio adjusted to obtain regioselective substitution for analog screening

    Downstream process integration

    • Used in primary condensation or cyclization steps with heterocyclic nucleophiles
    • Intermediates purified then submitted for biological screening against target pests/fungi
    • Strict tracking of starting material batch numbers for regulatory compliance

    Final product types

    • Discovery-phase fungicide and insecticide screening samples
    • Synthesized scaffolds for mode-of-action study
    • Early phase agrochemical lead structures

    4. Intermediate in Dye and Pigment Laboratory Development

    Specialty dye manufacturers use 6-Chloro-3-Formylchromone in the elaboration of heterocyclic dyes for analytical and functional coloration applications. Its chromone core enables fine-tuned absorption spectra and allows subsequent attachment of auxochrome groups. All operations requiring this intermediate adhere to chemical hazard regulations and updated environmental management standards for colorant manufacturing.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes (applicability assessed case-by-case)
    • ISO 14001: Environmental Management for chemical sectors
    • EU Regulation (EC) 1907/2006 (REACH) for colorant raw materials
    • GHS HazCom for chemical labeling and worker safety

    Typical usage ratio

    • 5–15 wt% relative to chromogenic reactants
    • Optimized to control dye shade and light-fastness characteristics

    Downstream process integration

    • Added at condensation or azo-coupling stage in dye molecule assembly
    • Subjected to temperature-controlled reactions (70–110ºC) for structure formation
    • Subsequent purification by solvent extraction or preparative chromatography

    Final product types

    • Prototype analytical dyes for laboratory or diagnostic use
    • Chromone-based colorants for specialized industrial coatings
    • Functional dyes for electronics and sensor calibration fields
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    Certification & Compliance
    More Introduction

    Introducing 6-Chloro-3-Formylchromone: A Chemist’s Perspective

    Inside our plant each batch of 6-Chloro-3-Formylchromone reflects decades of skill, practical refinement, and uncompromising process control. This is not just another molecule; the path from raw materials to this fine crystalline substance tells a story about careful reaction management and attention to every trace of impurity. From our earliest attempts scaling up chromone chemistry, we came to appreciate the subtleties in the formation of its backbone, especially when introducing the chloro and formyl groups without excess byproducts. The chemical model stands as 6-chloro-4-oxo-4H-chromene-3-carbaldehyde, with our in-house protocols keeping purity benchmarks above 98% by HPLC for demanding downstream syntheses.

    Production Realities and Consistent Quality

    The laboratory and production floor communicate constantly, ensuring the translation from grams to multi-kilo batches doesn’t lose critical details. Not all chromone derivatives behave alike and 6-Chloro-3-Formylchromone demonstrates this quirkiness. Chloro substitution at the six-position offers more than a structural difference. Our team recognized early on that controlling chlorination—not over-chlorinating or introducing off-target isomers—required tight control over reagent grade, temperature ramps, and reaction time windows. Chromatographic purity and stable storage became talking points after every production run because we know how quickly minor impurities creep into seemingly straightforward output.

    Some buyers have noticed a faint color variation between our lots and competitors’ material: our batches hold a consistent pale yellow, the direct result of well-defined precipitation and drying procedures. We credit regular solvent recovery, not just for cost savings but for keeping the environmental profile clean and minimizing potential cross-contamination. Those who depend on high consistency in further transformations—like forming pharmaceutical intermediates—can trace that attention to real chemical facts, not just marketing statements. This consistency shapes the behavior of the molecule in later reactions and brings the confidence that no unwanted surprises will slip through downstream processes.

    What Sets 6-Chloro-3-Formylchromone Apart

    Our perspective comes from daily work with dozens of chromone and coumarin derivatives. The distinguishing features of 6-Chloro-3-Formylchromone revolve around reactivity and stability. While plain chromones display predictable behavior in cross-coupling or cyclization steps, this compound offers a unique transcription between electronic activation (from the formyl group) and sufficient steric anchoring (from the chlorine). For custom libraries or pilot series in pharmaceutical research, these two groups interact to channel the selectivity in post-derivatization appending, which saves time in purification and character isolation. Technically, the slightly increased polarity from the formyl group shifts handling conditions: the optimal solvent profile for dissolution and crystallization differs enough that switching to this compound from a regular chromone often requires a review of established methods—and this cannot be ignored if output and yield remain a concern.

    We’ve supplied this compound for academic and industrial researchers exploring bioactive compounds, especially those targeting kinase inhibition, anti-inflammatory, and anti-tumor activities. The presence of the 6-chloro group can enhance binding selectivity and stability in bioassays—something that pure 3-formylchromone lacks. It’s not uncommon for us to field technical calls about analog screening and mechanism elucidation, where our broader knowledge of the structure-activity relationship plays a role. Our field chemists track breakthroughs as much by lab notebook as by published patent disclosures. Customers who develop new heterocycles through condensation or fusion chemistry routinely cite cleaner reactions and fewer purification headaches with our 6-chloro-3-formyl analogue compared to unsubstituted variants.

    Process Safety and Environmental Management

    People sometimes ask about byproduct management—a valid concern. Our protocols keep chlorinated waste to a minimum, relying on modern in-line monitoring and small-footprint neutralization. We constantly optimize to minimize adverse worker exposure, especially during the final handling and packaging steps. Closed reactor systems and automated wash-downs have become standard in our plant architecture because we understand the lasting impact of even sub-ppm residues on both handler safety and product shelf life.

    Each drum or jar carries a story of measured steps: from reagent selection, through careful control at each synthesis stage, to exhaustive in-process analysis. Quality assurance isn’t a box we tick after the fact. During crystallization we monitor the subtle interplay of solvent evaporation rates and temperature drops, since minor deviations can lead to trapping solvent or producing mixed hydrates. Microscopic examination of the finished product helps us catch early signs of insoluble material or unintended polymorphs—defects that, over a big production campaign, can undermine repeatability.

    Comparative Performance in Downstream Applications

    In chemical manufacturing, not all derivatives serve the same purpose. Some clients use 6-Chloro-3-Formylchromone as a pivotal intermediate in building flavone-based frameworks or modified coumarins for next-generation pharmaceuticals. The distinguishing features here cannot be overstated: the concurrent presence of both chloro and aldehyde groups shifts how the molecule interacts with nucleophiles, directing substitution without excessive side products. In contrast, 3-formylchromone or unhalogenated chromones run higher risks of uncontrolled over-reactions when exposed to strong nucleophiles, leading to yield loss or prolonged clean-up work.

    Through hands-on process trials, we have seen the compatibility of our 6-chloro-3-formylchromone with a wide array of coupling reagents and catalysts, spanning Suzuki, Heck, and Sonogashira chemistries. The electrophilic carbon at the chromone three-position, paired with the electron-withdrawing chloro influence, makes for crisp, targeted reactivity—something process chemists value deeply, especially when working on time-sensitive or resource-intensive syntheses. In-house collaborations have demonstrated quantitative yields using our product in the Knoevenagel condensation and Michael addition sequences, allowing for direct scale-up without extensive route tweaking. Researchers keep coming back with requests for kilo lots not because of glossy brochures, but because they observe genuinely better reproducibility and downstream efficiency.

    Adapting to Customer Feedback and Technical Support

    We approach every inquiry as a technical dialogue instead of a sales pitch. Customers come to us with specific requests: variable particle size, alternative solvent finishes, flexible packing weights. Our chemists work alongside our tech support staff to address these demands, running pilot lots for customers who want tailored performance for their particular research or development needs. Each formulation tweak is tracked and performance logged, not just for regulatory compliance but to inform future development. We talk directly with users to bridge lab and production realities, recognizing that a seemingly minor adjustment in drying temperature or post-synthesis wash can shift the entire downstream workflow for a partner site.

    Some clients want to push beyond standard pharmaceutical research applications. There’s rising interest in 6-Chloro-3-Formylchromone for material sciences, especially for building blocks in dye intermediates and molecular electronics. Here, our hands-on knowledge of the compound’s behavior under different reaction atmospheres and its photostability shines. Where other manufacturers offer the standard certificate of analysis and generic chromatograms, we have a history of providing side-by-side process records, including particle micrographs, accelerated stability profiles, and tailored advice on storage routines. This sense of partnership keeps our researchers on their toes and pushes us to deliver more information than just “meets specification.”

    Integrating 6-Chloro-3-Formylchromone into Advanced Synthesis

    The leap from basic laboratory-scale chemistry to scalable manufacturing requires a specific mindset. Over time, we found that success with 6-Chloro-3-Formylchromone depends on a blend of detail orientation and flexibility. In fields like medicinal chemistry, the molecule often acts as a launching point for fused chemotypes or as a foundation for introducing further substituents. Researchers tell us about the cleaner mass spectra, sharper chromatographic peaks, and higher chiral selectivity in subsequent steps using our material versus competitors’ lots. Access to consistent, genuinely high-purity material can mean fewer failed reactions and less time spent troubleshooting unknown variables in the lab.

    Some high-throughput screening projects depend critically on reproducible batches. We record each lot’s spectral and physical parameters, inviting third-party audits and peer-to-peer review processes to keep standards braided with transparency. Individual methods for each use case—be it small-scale medicinal development or ton-scale preparation for advanced polymers—often need unique drying, micronization, or dissolution profiles. Our operators and support scientists collaborate directly with customer teams to test handling parameters, sometimes running sample splits or even in-person plant visits to witness real world conditions and reinforce mutual confidence. This level of support sets lasting relationships apart from one-time transactions, influencing the way new molecules get adopted by major R&D organizations.

    Why Specification Details Matter

    It’s tempting to judge chemical quality solely on basic metrics—purity, melting point, water content. While these numbers matter, ongoing lessons from the lab remind us that batch-to-batch reproducibility influences more than basic statistics. Impurity profiles, crystal habit, even batch age can affect reactivity and downstream stability. For this reason, we publish not just typical assay but side-by-side melting behavior, IR and NMR overlays, and detailed impurity breakdowns upon request. Many open-market sources struggle to maintain this level of analytical transparency; it only comes from treating production as a shared challenge with end-users rather than a one-way supply chain.

    Our internal QC procedures go beyond the usual: we routinely run stress tests to check hydrolytic and oxidative stability. Shelf-stable powders should not alter in color, odor, or flow even after prolonged exposure to ambient humidity or light. Material science users, in particular, require such stability for precise coating or formulation steps. Our real-world storage studies use ambient warehouse conditions rather than just climate chambers, so users receive truthful expectations for their stored inventories. That degree of validation only grows more important as global standards for chemical traceability and end-to-end transparency keep tightening year by year.

    Product Handling, Packaging, and Shipping Insights

    Handling 6-Chloro-3-Formylchromone starts with recognizing its subtle hygroscopicity. The molecule attracts ambient moisture if left unprotected, which can affect sensitive end-uses or create isolated clumping in long-term storage. For this reason, we take effort with inert gas flushing and sealed packaging. Our dedication to safe, traceable logistics means each batch gets double-bagged with silica desiccants and vacuum-sealed packaging for international freight. For high-volume clients, we’ve trialed lined drums to guard against atmospheric ingress and accidental rupture, reporting feedback and iteratively improving design with user input.

    Shipping logistics often go overlooked until a delay or accident occurs. Our warehouse protocols focus on temperature and humidity control, but equally on anti-tamper and anti-spill measures. Packing slips include full traceability to manufacture date and storage history, not just serial numbers. Over time, we’ve built relationships with logistics partners who understand that a shipment isn’t just another box, but integrally tied to someone’s R&D schedule, regulatory process, or product warranty promise. Each metric ton sent means hundreds of hours’ labor by plant operators, chemists, and compliance teams—all invested up front to keep the supply chain lean and disruption-free.

    Navigating Industry Trends and Compliance Pressures

    Year after year, tighter global regulations challenge chemical producers. Our approach to 6-Chloro-3-Formylchromone keeps compliance on the agenda, adapting to evolving registration needs and safety data demands in each target region. The European Union and various Asian jurisdictions keep raising documentation and batch testing standards. As direct manufacturers, we see this not as a burden, but a chance to prove our ability to maintain full traceability and deliver independent batch test records matched to each customer’s regulatory needs. Our compliance specialists consult with clients upfront, helping to anticipate future changes and remain proactive, rather than scrambling to supply new documentation after the fact.

    One visible trend is growing demand for sustainable production. We invested in solvent recycling units and run pilot studies to lower the carbon footprint of each batch. That means every drum of 6-Chloro-3-Formylchromone leaves a smaller environmental shadow than before, both in terms of raw material sourcing and waste reduction. Sustainability doesn’t end with manufacturing; it follows the product down the supply chain to final application. End-users increasingly ask about lifecycle analysis and environmental certifications, and our team stands ready with the real numbers.

    Collaborative Innovation and New Directions

    The story of 6-Chloro-3-Formylchromone is ongoing. Our earliest batches came from bench-scale flasks; now, automated reactors fill the order queue for partners across five continents. Some of our most innovative projects began with a technical challenge or product customization request from a long-time customer willing to share core data for mutual benefit. Over the years, we’ve contributed to academic collaborations, process optimizations, and new product introductions that owe their success to a transparent dialogue about this molecule’s unusual features. Our teams publish process improvements—not just to tick a corporate transparency box, but to share lessons that let the broader chemical community build smarter, safer syntheses and applications.

    We believe the real difference shows each time a partner reports higher throughput, lower waste, clearer analytical data, or simply fewer headaches handling our 6-Chloro-3-Formylchromone. That reflects a chain of decisions—on raw materials, process control, documentation, and support service—that turn an “off-the-shelf” product into a reliable foundation for discovery and scale-up.

    Conclusion: Why Chemists Return to the Right Source

    The track record hasn’t been built on marketing promises alone; it rests on daily technical exchanges and the relentless pursuit of process improvement. Each new request—whether for a different lot size, special packing, or analytical report—helps us refine further. By treating 6-Chloro-3-Formylchromone as more than a commodity, our team continues to set higher standards for what advanced intermediates should deliver. The dialogue between manufacturer and chemist keeps driving smarter chemistry, raising efficiency, and expanding what this distinctive compound can do in the hands of dedicated researchers around the world.