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6-Chloro-2-Fluoro-3-Methylbenzaldehyde

    • Product Name 6-Chloro-2-Fluoro-3-Methylbenzaldehyde
    • Alias 6-Chloro-2-fluoro-m-tolualdehyde
    • Einecs 857041-78-2
    • 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
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    Specifications

    HS Code

    340024

    Product Name 6-Chloro-2-Fluoro-3-Methylbenzaldehyde
    Cas Number 189628-66-0
    Molecular Formula C8H6ClFO
    Molecular Weight 172.59 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Smiles CC1=C(C=CC(=C1Cl)F)C=O
    Inchi InChI=1S/C8H6ClFO/c1-5-7(4-11)2-3-8(10)6(5)9
    Solubility Soluble in most organic solvents
    Synonyms 2-Fluoro-6-chloro-3-methylbenzaldehyde
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited 6-Chloro-2-Fluoro-3-Methylbenzaldehyde 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 25 grams of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde, tightly sealed with a red screw cap and labeled clearly.
    Shipping **Shipping for 6-Chloro-2-Fluoro-3-Methylbenzaldehyde:** This chemical is shipped in sealed, chemical-resistant containers, in compliance with relevant hazardous material transport regulations. It is typically shipped at ambient temperature, with appropriate labeling and documentation. Ensure storage away from heat sources and direct sunlight during transit. Handle according to safety and regulatory guidelines.
    Storage 6-Chloro-2-Fluoro-3-Methylbenzaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container protected from light and moisture. Appropriate labeling and secondary containment are recommended to prevent spills or leaks. Use personal protective equipment when handling.
    Application of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde

    Applications of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde in Industrial Manufacturing

    As a specialized producer of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde, we support multiple advanced manufacturing fields that require high-purity aromatic aldehydes for their unique physicochemical properties. The following application scenarios detail how our material integrates into key downstream sectors, highlighting precise compliance, formulation, processing steps, and typical end products.

    1. Pharmaceutical Intermediate Synthesis (API Manufacture)

    Pharmaceutical manufacturers rely on this compound as a building block for synthesizing active pharmaceutical ingredients, particularly heterocyclic compounds and complex drug candidates. The controlled introduction of both chloro and fluoro functional groups enables downstream chemists to direct selectivity in multi-step organic synthesis, especially in the preparation of novel anti-infective agents and CNS-modulating compounds. Our product integrates in the initial condensation or coupling reactions, downstream from primary aromatic functionalization, where high isomeric purity is essential to ensure reliable yield and minimal side reactions.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • USP 43–NF 38 (as applicable to intermediates)
    • EMA Guidelines on Impurities in New Drug Substances (ICH Q3A)
    • ISO 9001:2015 for quality management in pharmaceutical materials

    Typical usage ratio

    • 5–20% by molar ratio relative to the final API molecular base, adjusted for route efficiency and step yield
    • Optimization based on targeted impurity profile and structural complexity

    Downstream process integration

    • Purified through vacuum distillation prior to use
    • Condensation with amines, hydrazines, or enolates in batch reactors, under nitrogen atmosphere
    • Multistep reactions proceeding to functional moiety protection/deprotection, hydrogenation, or cyclization

    Final product types

    • Small molecule APIs (e.g., neuroleptic agents, anti-infective APIs)
    • Secondary intermediates for contract research organizations (CROs)
    • Reference compounds for structural libraries
    • Final APIs after additional downstream transformations

    2. Agrochemical Active Ingredient Production

    Leading crop protection formulators select 6-Chloro-2-Fluoro-3-Methylbenzaldehyde for designing selective herbicides and insecticide active substances. Its electron-deficient aromatic ring supports site-specific building of functionalized benzene derivatives via nucleophilic substitution and Suzuki coupling, critical in the production of modern selective herbicides. Use of our material meets the strictest requirements on trace contaminants for field application to edible crops, entering after synthesis of the benzaldehyde core and before conversion to functional pesticide moieties.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals, EU
    • ISO 17025 for analytical testing and impurity analysis
    • EPA Pesticide Registration Standard (40 CFR Part 158)

    Typical usage ratio

    • 2–8% of total reactant mass in the synthesis of specific herbicide active substances
    • Adjusted according to crop residue analysis and active substance target concentration

    Downstream process integration

    • Enters after construction of base benzaldehyde ring, prior to halogenation or coupling reactions
    • Processed in stainless steel jacketed reactors under anhydrous conditions
    • Undergoes derivatization to form ester, amide, or nitrile intermediates in subsequent steps

    Final product types

    • Selective herbicides for broadleaf weed control
    • Systemic fungicide intermediates
    • Prototype insecticidal actives for regulatory dossier studies
    • Crop protection formulations registered for cereal and vegetable markets

    3. Advanced Dye and Pigment Manufacturing

    Commercial dye manufacturers rely on chloro- and fluoro-substituted benzaldehydes as key linkers for synthesizing high-performance azo and anthraquinone dyes. Our product offers strong electron-withdrawing effects, supporting stable color fastness and tailored shade properties during diazotization and coupling reactions. Integration typically occurs after the initial benzaldehyde condensation phase, progressing to the introduction of chromophore-forming groups under strictly controlled pH and temperature regimes.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restricted substances in textiles)
    • EU REACH Annex XVII SVHC restriction compliance
    • ISO 105-B02 (Colorfastness to artificial light: Xenon arc fading lamp test)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)

    Typical usage ratio

    • 6–12% weight of total dye intermediate batch, adjusted by target molar extinction coefficient and color depth requirements

    Downstream process integration

    • Charged into glass-lined or enamel reactors post-alkali fusion
    • Dissolved with controlled solvents to regulate substitution rates during azo coupling
    • Formed isomers purified for final coupling sequence with amino or hydroxy aromatics

    Final product types

    • Azo dyes for synthetic and natural fibers
    • Fluorinated pigment dispersions for industrial coatings
    • Specialty colorants for high-performance plastics
    • Textile printing ink intermediates

    4. Electronic Chemical Intermediates (Liquid Crystal Precursor Synthesis)

    Manufacturers in the electronics industry use chlorofluoro-methyl benzaldehyde derivatives as precision intermediates for synthesizing liquid crystal compounds and functional organic semiconductors. The specific regiochemistry allows precise control of dipole moment orientation, essential for high-contrast liquid crystal displays and photonic materials. The compound is introduced during the aldehyde derivatization stage, leading to the formation of fluorinated biphenyls or terphenyl intermediates, under rigorous anhydrous and ultra-clean manufacturing conditions.

    Industry compliance standards

    • IEC 61249-2-21 (Requirements for halogen-free base materials in electronics)
    • RoHS Directive (2011/65/EU) for hazardous substance management
    • ISO 14001:2015 Environmental Management
    • JEITA Guidelines for Electronic Chemical Purity

    Typical usage ratio

    • 3–10% by mole, dependent on the specific structure and target dipole alignment in end-use liquid crystal modules
    • Control of dose is reviewed per batch via in-line analytical quantification

    Downstream process integration

    • Stepwise introduction after protection of aldehyde group, followed by selective halogen exchange reactions
    • Batch and flow-reactor processing under cleanroom conditions
    • Intermediate purification through chromatography and vacuum stripping

    Final product types

    • Mono- and di-fluorinated biphenyl liquid crystals
    • TFT-LCD display panel materials
    • Organic electronic functional layers (semiconductor films)
    • Photonic device precursor compounds

    5. Fragrance Intermediate for Fine Chemicals

    Specialty aroma chemical producers select chloro-fluoro-substituted benzaldehydes as intermediates for producing unique alicyclic and aldehydic perfume ingredients. The compound’s defined electronic environment supports selectivity in aldol and Wittig reactions, making it suitable for integrating specific odor notes found in luxury fragrances. Our material enters downstream after initial benzylic modifications, often followed by hydrogenation and esterification steps under carefully monitored reaction conditions to preserve olfactory signature.

    Industry compliance standards

    • IFRA Code of Practice and Amendment Guides
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • Food Chemicals Codex (FCC) for flavor intermediates (as applicable)
    • FEMA GRAS (Generally Recognized as Safe) guidelines for aroma materials

    Typical usage ratio

    • 0.5–3.5% of finished aroma compound mass, with adjustments for intensity and stability in complex formulations

    Downstream process integration

    • Sequential use in controlled aldol condensations, followed by reductive workup
    • Esterification or acylation to build long-chain aroma molecules
    • Fractional distillation and purification to meet odor threshold specifications

    Final product types

    • Aldehydic fragrance bases for luxury perfumes
    • Floral and citrus-inspired aroma ingredients for fine fragrance blends
    • Long-lasting fixatives for personal care products
    • Complex perfume accords in niche scent lines

    6. Specialty Polymer Additive Production

    Producers of high-value specialty polymers utilize halogenated benzaldehydes to functionalize polymer chains, enhance thermal stability, or introduce reactive sites for cross-linking. The incorporation of this raw material typically occurs in the pre-polymerization additive phase, where precise dosing influences polymer microstructure and end-use properties such as flame retardancy and optical clarity. Compatibility testing and batch adjustment remain critical at this stage to meet specific polycondensation or copolymerization requirements.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastic Materials
    • ASTM D256 for Polymer Impact Strength Testing
    • FDA CFR 21 177.1520 (as applicable to food contact polymer grades)
    • ISO 9001:2015 for quality assurance in specialty polymer production

    Typical usage ratio

    • 0.8–2.5% by weight during additive blending, based on resin molecular weight and desired functionalization level
    • Optimized via small-scale extrusion assays before scale-up

    Downstream process integration

    • Mixing with pre-polymer or base resin in heated kneaders or extruders
    • Covalent binding or in situ reaction during monomer activation stage
    • Quality control testing for chain architecture and dispersibility

    Final product types

    • Flame-retardant engineering plastics
    • Optical grade copolymers for film and sheet applications
    • High-impact thermoplastic compounds
    • Functionalized bead polymers for specialty coatings
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    Certification & Compliance
    More Introduction

    Introducing 6-Chloro-2-Fluoro-3-Methylbenzaldehyde: Experience, Reliability, and Application

    Overview of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde

    On the production floor and in the development lab, precision and quality speak louder than glossy brochures. 6-Chloro-2-Fluoro-3-Methylbenzaldehyde, with CAS number 1072952-86-3, came to our attention after the continued growth of fine chemicals in both pharmaceuticals and advanced materials. As a direct manufacturer, not a distributor passing unopened drums between hands, we've watched this molecule streamline several synthesis routes once considered tricky or inefficient.

    How We Manufacture 6-Chloro-2-Fluoro-3-Methylbenzaldehyde

    We synthesize each batch using controlled halogenation and selective fluorination. Technical staff anchor our processes in sound science, without skipping steps to shave a few hours off turnaround. The result is a product with high chemical purity, typically exceeding 98%, accompanied by a measured and reproducible impurity profile. Each lot undergoes GC-MS and HPLC analysis. Consistency isn’t abstract or aspirational – these numbers come from deliberate procedural planning and clear accountability. Every kilo that leaves our facility represents hours of careful work and record keeping by chemists and operators who track the process at every stage.

    Physical Specifications and Testing

    At ambient temperatures, 6-Chloro-2-Fluoro-3-Methylbenzaldehyde forms a pale yellow liquid or low-melting solid, depending on residual moisture and cooling speed. The aldehyde group creates a distinctive, sweet but sharp odor in our pilot lot rooms. We package this product in tightly sealed high-density polyethylene containers that can withstand material handling stress and the occasional bump on loading docks.

    Actual specifications matter most to colleagues and customers who must trust the material in chromatographs and glassware. GC purity regularly hovers above 98%. Water content sits under 0.3%, based on Karl Fischer titration. We keep chloride and fluoride byproducts under strict limits, backed by titration and ion chromatography. Each certificate of analysis tells the honest story of that day’s production.

    Where 6-Chloro-2-Fluoro-3-Methylbenzaldehyde Fits in Industrial Chemistry

    Instead of a catch-all chemical, this compound serves a focused purpose. Pharmaceutical companies often select halogenated and fluorinated aromatics while developing intermediates for active drug molecules. The electron-withdrawing nature of both halogen groups — plus the methyl group’s steric push — creates a scaffold difficult to substitute with more common benzaldehydes. We have seen several customers use it directly in Suzuki and Heck couplings, forming biaryl systems bound for anticancer or antiviral screening.

    For agrochemical research, our product’s ability to deliver clean conversions during further functionalization steps— such as amination or cyanation — saves chemists time that used to be spent debugging side reactions. As producers ourselves, setting up a clean chlorination while preserving the methyl group demands steady control of temperature and reagents. These details add up to fewer production interruptions later.

    In materials science, this benzaldehyde variant appears in syntheses that require the controlled introduction of both chlorine and fluorine atoms, such as in intermediates for specialty polymers or advanced coatings. While this field is less publicized, customer visits and batch feedback confirm that these chemical motifs remain hard to mimic with cheaper or older aromatic building blocks.

    Real-World Use Cases and Feedback

    Researchers in pharmaceutical development come to us with stories of failed batches and wasted time from unreliable sources. They ask for documentation at every step: raw material origin, process notes, small fluctuations in process parameters. Over the years, trust builds by matching results with documentation. One R&D director from a mid-sized European pharma group shared that switching to our directly supplied 6-Chloro-2-Fluoro-3-Methylbenzaldehyde eliminated 4 hours per week of sample retesting. With fewer by-products and a narrow melting range, their downstream palladium-catalyzed coupling reactions reached 90% yield, compared to the mid-70s on materials sourced from general resellers.

    Agrochemical partners notice the value in controlled substitution patterns. Leaving the multi-step build-up of their complex targets in the hands of untested vendors never pays off. With clearly assigned lab technicians in charge of every batch and immediate technical support, our partners move faster than their competitors in pilot plant scale-ups. This matters during early season product launches or when preparing dossiers for regulatory submission.

    For academic chemists, reproducibility and documentation are key. Theses and grant-funded research projects can derail quickly when a batch varies from expectation. We supply full chromatographic datasets, not simply summaries or marketing sheets. As a result, several academic publications have included our lab reports as supplementary files, meeting the reviewing standards of top-tier journals.

    What Sets Our Product Apart From Generic Options

    Manufacturing batches ourselves gives us immediate control over what goes in and out, limiting contamination risks and ensuring single-lot traceability. By contrast, traders and general resellers often lack direct knowledge of how a compound was made or what by-products it might contain. Small overlooked differences in crystal habit, residual solvents, or unreacted precursors commonly translate to large headaches in research and scale-up.

    Feedback from global clients highlights the peace of mind that comes from clear communication. They do not want generic apologetic emails attached to shipments when something looks off; they want proactive updates and root-cause analysis described in detail. Operating our own reactors and purification systems, we observe these variables firsthand and make targeted adjustments based on historical process data.

    Another point worth noting is our approach to regulatory compliance and safety testing. As a manufacturing site with regular local inspections, we regularly review both our internal handling protocols and the downstream environmental profile of each lot. This attention to real-world risks—such as detecting trace polychlorinated by-products—sets our batches apart from generics origin traced only through shipping stickers.

    Scale, Batch Sizes, and Supply Reliability

    Customers ask us about scale, delivery timelines, and inventory planning more often than molecular weight tables. We produce 6-Chloro-2-Fluoro-3-Methylbenzaldehyde year-round, with production runs ranging from pilot-scale (less than 20 kg) to several hundred kilo campaigns for ongoing clients. By keeping our own stocks and adjusting scheduling based on up-to-date demand, delivery times remain responsive.

    Supply interruptions damage trust. Real manufacturing means standing by each committed delivery, even if an order lands right before a holiday or during raw material crunches. Our direct involvement in every production phase lets us respond to urgent requests and communicate clear delivery expectations, not just pass along lead times from a distant upstream supplier.

    Technical Support, Documentation, and Collaboration

    Seasoned technical teams are present from quotation through shipment and post-delivery questions. Researchers and process chemists often ask about side reactions, compatibility with their hydrogenation or cross-coupling catalysts, or purity thresholds affecting downstream synthesis. By controlling the production lab and testing in-house, our chemists speak with practical, firsthand experience instead of passing around generic safety data sheets.

    Complete analytical documents, including NMR, MS, IR, and chromatograms, are provided for each lot. This transparency stems from decades working with partners who cannot afford to troubleshoot with incomplete data. We also support custom specification requests for water content, specific impurity limits, packaging configuration or bespoke labeling, helping customers optimize their workflows instead of forcing one-size-fits-all batches.

    Environmental and Regulatory Considerations

    It’s not enough to only look inward at process improvements and yields. Organizations working with halogenated aromatics face increasing scrutiny about waste handling, emissions, and worker safety. As a chemical manufacturer in regular communication with regulatory authorities and environmental auditors, we practice closed-system handling of reagents and manage solvent recycling to reduce impact. Routine monitoring via spot checks and external analysis demonstrates compliance with the latest local and regional standards.

    Our focus on minimizing chlorinated and fluorinated by-product content directly reflects these priorities. Downstream customers avoid unexpected regulatory questions or costly waste disposal issues when their intermediate arrives with a full impurity profile and clear material origin. Selecting a directly accountable supplier pays dividends in regulatory audits — something we have weathered and passed without incident several years running.

    Continuous Process Improvement and Employee Expertise

    Every new production campaign brings lessons learned — either to be recorded and repeated or re-examined for improvement. Tracking exact stepwise temperatures, reaction times, and purification cycles forms the foundation of reliable delivery. In our experience, improving a synthesis route or tightening an impurity cutoff usually traces to input from experienced operators who’ve spent years at the same production site, not from outsiders reciting theory.

    Regular in-house workshops focus on technique improvement and safety. Operators and quality analysts contribute data from previous runs to refine reactor profiles or update workflow diagrams. This tradition of knowledge sharing cuts down on repeated errors and builds a core of experience visible in the consistency and performance of the chemicals we supply.

    Economic Considerations and Real Costs

    Long-term partners repeatedly stress the value in reliable, direct sourcing over chasing the lowest price. While lab managers always monitor budgets, they’ve shared stories of multimillion-dollar research programs held back by single-batch inconsistencies from non-manufacturing suppliers. Making cost effective decisions requires more than comparing price sheets — the risks of re-processing, impurity-driven failure, or documentation gaps outweigh any short-term savings.

    Manufacturing chemicals at scale draws on more than just the operator’s attention. Raw materials, safety controls, lab analysis, and trained staff form fixed costs that traders or brokers rarely shoulder. Clients appreciate the difference once they handle material that behaves as described in reaction set-ups or analytical runs. Many have shared they would rather receive candid feedback about real production lead times or temporary shortages than risk hidden supply chain delays introduced by third parties.

    Quality Assurance, Traceability, and Trust

    Buyers of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde often mention prior troubles with traceability or inconsistent performance in key reactions. Our direct manufacturing model tackles this problem head-on through controlled batch production and robust data archiving. Each outgoing lot includes reference samples stored on-site, digital production records, and explicit operator sign-offs. If a question about performance or impurity profile arises months later, anyone from the technical team can pull the original records — data backed by timestamps and retained control samples.

    Long-term customers share project-specific details with us, relying on our confidentiality and institutional memory. By keeping consistent technical teams handling both R&D and production, we provide input that helps clients adapt in real time rather than sending unrelated sales contacts or form responses.

    Comparisons to Related Products and Precise Advantages

    Practically, 6-Chloro-2-Fluoro-3-Methylbenzaldehyde differs from more commonly available benzaldehyde derivatives in reactivity, selectivity, and downstream compatibility. The combined presence of the chlorine at the 6-position and fluorine at the 2-position resists many standard transformations, allowing for predictable functionalization at other positions — a property leveraged in both medicinal chemistry and electronic material research. This molecular backbone often withstands conditions that would cause overreaction or side product formation in less substituted analogs.

    For developers who have tried unsubstituted or mono-substituted benzaldehydes, the difference in yields, especially in palladium-catalyzed couplings or nucleophilic substitutions, can be dramatic. Tests in our partner labs show as much as a 15% improvement in desired product purity after switching to our precisely characterized material, highlighting the value of tailored substitution patterns.

    While some producers offer similar-sounding compounds, such as 2-Chloro-3-Fluoro-4-Methylbenzaldehyde or 3-Fluoro-4-Methylbenzaldehyde, these variants do not match the reactivity profile required by modern synthetic routes. Subtle placement of halogens on the ring matters; misplacement changes the vector of electron density, altering catalyst compatibility in ways often missed by high-level theoretical descriptions. Uninitiated traders rarely understand how these nuanced differences can derail a synthesis or force process chemists to redesign protection strategies from scratch.

    Insights From Direct Manufacturer Experience

    Working at scale shows quickly that minor production changes ripple throughout an organization. Issues like reactor fouling, unexpected exotherms, or solvent carry-over in purification get solved only with hands-on attention. Every operator and process chemist who works with 6-Chloro-2-Fluoro-3-Methylbenzaldehyde gains practical insight into what consistently delivers the required performance. We know every shortcut in the literature and have evaluated many under real-world conditions, often confirming their limits. This is not armchair chemistry: each improvement or deviation is debated, documented, and validated on the same equipment customers depend on for their own synthesis reliability.

    Supporting incoming customer projects becomes smoother when we’ve already piloted custom variants or adjusted specifications in our own facilities. We have partnered with several clients to adapt impurity cut-offs or packaging configurations to support tricky launches. This direct collaboration, paired with the willingness to share mistakes and suggestions, sets the stage for success in even the most time-sensitive R&D projects.

    Senior process engineers regularly brief junior staff on recurring pitfalls, such as distinguishing real process deviations from harmless day-to-day fluctuations. These internal feedback loops prevent overcorrection and ensure that every production run meets a standard measured by experienced eyes rather than one-size-fits-all checklists.

    Commitment to Long-Term Partnership

    Supplying 6-Chloro-2-Fluoro-3-Methylbenzaldehyde represents more than a single invoice or shipment. Trust, built on real and tested performance, matters at every stage of manufacturing, shipping, and customer support. Our ongoing investment in technical competence, updated equipment, and supply resilience creates an environment where customer challenges are treated as shared problems, not separate burdens. Feedback from partners informs process updates and shapes internal improvement efforts.

    Chemists and procurement teams searching for a supply partner recognize the difference immediately. Direct access to analytical documentation, real point-to-point technical support, and the ability to accommodate changes all reflect the experience gained through years of direct manufacturing. Our focus on complete transparency and readiness to engage with specialized requirements continues to distinguish our product from both generics and resold alternatives.

    In the end, every batch of 6-Chloro-2-Fluoro-3-Methylbenzaldehyde that we produce carries the practical knowledge, careful documentation, and long-term responsibility that comes from manufacturing, not just trading. Customers see this difference — not in marketing claims, but in every step of their research and production workflow.