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2,6-Dichlorobenzaldehyde

    • Product Name 2,6-Dichlorobenzaldehyde
    • Alias 2,6-Dichlorobenzal
    • Einecs 203-934-2
    • 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
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    Specifications

    HS Code

    958751

    Chemical Name 2,6-Dichlorobenzaldehyde
    Cas Number 83-38-5
    Molecular Formula C7H4Cl2O
    Molecular Weight 175.01 g/mol
    Appearance White to off-white crystalline solid
    Melting Point 46-48°C
    Boiling Point 255-257°C
    Density 1.41 g/cm³
    Solubility In Water Slightly soluble
    Smiles C1=CC(=C(C(=C1)Cl)C=O)Cl
    Iupac Name 2,6-dichlorobenzaldehyde
    Refractive Index 1.597
    Storage Conditions Store in a cool, dry, well-ventilated place

    As an accredited 2,6-Dichlorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 2,6-Dichlorobenzaldehyde is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 2,6-Dichlorobenzaldehyde is shipped in tightly sealed containers, protected from light and moisture, and kept at room temperature. It is classified as a hazardous material and must comply with local, national, and international transport regulations. Proper labeling and safety documentation are required to ensure safe handling and transit.
    Storage 2,6-Dichlorobenzaldehyde should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. The storage area should have chemical-resistant shelving and be clearly labeled. Avoid exposure to moisture and sources of ignition. Proper safety measures, including secondary containment and access controls, are recommended to prevent spills or accidental exposure.
    Application of 2,6-Dichlorobenzaldehyde

    Purity 99%: 2,6-Dichlorobenzaldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures maximum yield and reduced by-product formation.

    Melting Point 44°C: 2,6-Dichlorobenzaldehyde with melting point 44°C is used in organic synthesis processes, where precise melting facilitates controlled reaction conditions.

    Molecular Weight 175.01 g/mol: 2,6-Dichlorobenzaldehyde with molecular weight 175.01 g/mol is used in fine chemical production, where accurate stoichiometric calculations improve process efficiency.

    Stability Temperature up to 80°C: 2,6-Dichlorobenzaldehyde with stability temperature up to 80°C is used in agrochemical formulation, where thermal stability ensures consistent active ingredient quality during processing.

    Particle Size <100 μm: 2,6-Dichlorobenzaldehyde with particle size less than 100 μm is used in pigment manufacturing, where fine particles enhance color dispersion and uniformity.

    Water Content <0.2%: 2,6-Dichlorobenzaldehyde with water content below 0.2% is used in polymer synthesis, where low moisture minimizes hydrolysis and maximizes polymer chain length.

    UV Absorption λmax 260 nm: 2,6-Dichlorobenzaldehyde with UV absorption maximum at 260 nm is used in analytical chemistry standards, where precise absorbance allows accurate calibration.

    Assay ≥98%: 2,6-Dichlorobenzaldehyde with assay not less than 98% is used in chemical research, where high assay values assure experimental reproducibility and reliability.

    Volatility Low: 2,6-Dichlorobenzaldehyde with low volatility is used in industrial resins production, where reduced evaporation losses increase process safety and cost-efficiency.

    Storage Stability 12 Months: 2,6-Dichlorobenzaldehyde with storage stability for 12 months is used in raw material inventory management, where extended shelf-life supports continuous operations.

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    Certification & Compliance
    More Introduction

    Exploring 2,6-Dichlorobenzaldehyde: A Closer Look at an Important Chemical Building Block

    What Makes 2,6-Dichlorobenzaldehyde Stand Out?

    2,6-Dichlorobenzaldehyde draws plenty of attention among chemical intermediates for good reason. Its structure—two chlorine atoms on the benzene ring at positions 2 and 6, plus an aldehyde group—creates a unique profile compared to other chlorinated benzaldehydes. Because of this, manufacturers and researchers often turn to it when looking to synthesize specialty dyes, agrochemicals, pharmaceuticals, or advanced polymers. I've seen labs choose this compound for its reliable performance where selectivity and consistency in reactions prove essential. Attempts to substitute other benzaldehydes often lead to different reactivities or unwanted byproducts. In practice, 2,6-Dichlorobenzaldehyde works as a dependable stepping-stone toward more specialized molecules.

    Understanding the Product's Specifications

    From what I've observed, high-purity 2,6-Dichlorobenzaldehyde—identified by the CAS number 83-38-5—typically comes as an off-white to pale-yellow crystalline solid. Its molecular formula (C7H4Cl2O) reflects the core structure that grants it those sought-after properties. Samples with purities above 98% serve the needs of most research and industrial labs, although pharmaceutical projects often tighten the spec even further. Melting points hover in the 45–49°C range, which makes it relatively easy to handle at room temperature without specialized equipment. Because moisture or prolonged exposure to air can affect its quality, most suppliers package it in well-sealed containers—something any chemist would appreciate to prevent loss or contamination.

    Why Users Turn to This Compound

    Demand for 2,6-Dichlorobenzaldehyde grows out of its versatility. In my own experience working on custom synthesis, this compound played a central role in the synthesis of complex aromatic aldehydes and acids that required substitution patterns not possible from conventional benzaldehyde starting materials. Recent years have seen applications in:

    Several routes can access this compound, but selecting those with milder conditions and higher atom economy helps cut waste and reduce costs. The reactivity of the aldehyde group and the electron-withdrawing effect of the two chlorine atoms make it attractive for selective functionalization—something not all benzaldehyde derivatives manage.

    Comparing With Other Benzaldehyde Derivatives

    Every chemist who has tackled aromatic syntheses has weighed the difference between isomeric dichlorobenzaldehydes. This variant—by virtue of the dueling chlorines at adjacent meta positions—stands apart. Take 3,4-dichlorobenzaldehyde or 2,4-dichlorobenzaldehyde, for example: both activate the benzene ring in different ways, affecting the outcome of downstream reactions. I recall running parallel syntheses with each isomer, only to see dramatic differences in reaction rates and product yields. The 2,6-isomer often resists unwanted ortho reactions, due to the blocking effect of the two chlorines, giving cleaner product profiles.

    It’s also worth noting the impact on solubility and handling. Some researchers report that 2,6-Dichlorobenzaldehyde dissolves more readily in polar organic solvents—think acetone, ethanol, or DMSO—compared to its counterparts. This comes in handy for preparative chromatography or solution-phase transformations, since it means fewer headaches when it comes to recovery and purification.

    Environmental and Safety Considerations

    Chlorinated aromatic compounds often spark a conversation around environmental persistence. Independent studies agree: careful management makes a difference. In research settings, I’ve watched protocols evolve over time—labs now emphasize secondary containment, careful labeling, and proper solvent disposal. Material Safety Data Sheets flag it as an irritant, so the advice stays straightforward: work with gloves, use local exhaust ventilation, wear goggles. Breathing dust or vapors never bodes well, so fume hoods become standard for weighing or transferring. Accidental spills are rare, but standardized cleanup kits help prevent environmental release.

    Long-term, reducing waste and capturing chlorinated emissions factors into sustainability goals for most chemical operations. Thanks to growing regulatory pressure, modern production sites favor greener synthetic routes and employ advanced purification processes to minimize harmful byproducts. I've seen suppliers respond by improving batch-processing controls to keep residual solvents and impurities low—helping companies meet both quality and environmental standards.

    Role in Innovation and Development

    It’s hard to ignore the importance of 2,6-Dichlorobenzaldehyde in the bigger picture. Chemistry pushes boundaries by combining building blocks like this with creative design. During consulting work, I've seen innovation teams revisit their raw material lists, searching for intermediates offering new reaction pathways or improved yields. This compound finds its way into research pipelines developing next-generation agrochemicals. University groups tap into it for the development of new ligands and catalysts. Pharmaceutical R&D leans on its defined substitution pattern to prototype novel APIs, particularly anti-infective and anti-inflammatory agents. The simple act of having high-purity starting material empowers faster bench-to-pilot scale transitions.

    On an industrial scale, improved access to reliable intermediates means shorter development cycles. I’ve witnessed firsthand how delays at the sourcing stage can cascade through a project, so ready availability of cornerstone materials such as 2,6-Dichlorobenzaldehyde pays dividends throughout the chain. As supply networks globalize, the emphasis on traceability and transparency intensifies, too. Batch-level documentation and certificates of analysis reassure downstream partners that material integrity meets expectation—this matters when the end product lands in consumer goods, medicines, or agrochemical formulations.

    Addressing Common Sourcing Challenges

    Sourcing specialty chemicals rarely feels straightforward. In the case of 2,6-Dichlorobenzaldehyde, buyers often weigh several factors: purity, batch size, turnaround time, and regulatory compliance. I’ve seen technical teams invest time validating new sources only to run into variability in crystal color or unexpected trace impurities. Most major suppliers now publish full analytical profiles before shipping. Whether you’re running a hundred-gram trial batch or ordering at multi-kilo scale for a pilot plant, transparency builds trust in the process.

    Questions sometimes arise around the handling of regulated substances, especially with customs scrutiny tightening around chlorinated aromatics. Experience shows that partnering with reputable providers streamlines logistics—ensuring the correct declarations support smooth import and export. Personally, I advocate for keeping open lines between end-users and suppliers, since rapid response to specification changes (such as updated impurity thresholds) can keep projects on schedule.

    Trends Shaping the Future

    Chlorinated intermediates often get re-examined as regulatory standards evolve. Across the industry, I’ve noticed a steady uptick in efforts to optimize production routes for both safety and sustainability. Catalysts with higher selectivity reduce unwanted chlorinated byproducts. Green solvents and continuous-flow processing cut waste, lower energy use, and improve process reliability. Clearer regulatory frameworks help everyone—manufacturers, importers, and end-users—know what's expected for registration, labeling, and safety documentation.

    With innovation comes opportunity. Demand for specialty agrochemicals and targeted pharmaceuticals keeps rising as global population and disease-resistance issues drive new R&D. Substituted aldehydes like 2,6-Dichlorobenzaldehyde serve as reliable backbones for such innovation. More recently, I’ve observed startups and research consortia exploring biodegradability and lower-chlorine alternatives, but for many applications this compound remains indispensable because of its well-documented performance and consistent manufacturing standards.

    Potential Solutions to Current Issues

    Running into challenges is the rule, not the exception, in specialty chemical supply. Looking at persistent obstacles—volatility in raw material pricing, environmental restrictions, and quality assurance—it's clear that a multifaceted approach works best. Direct engagement between users and manufacturers can pre-empt material shortages, especially for pharma and agrochemical sectors where interruptions delay revenue. Trusted distribution networks with redundant inventory alleviate localized disruptions from supply chain hiccups.

    Quality control stands as another pillar. Implementation of digital tracking—blockchain ledgers, advanced barcoding—offers a way forward to guarantee origin and history throughout the supply chain. For environmentally conscious buyers, supplier audits and updated certifications (such as ISO 14001 for environmental management) carry real weight in sourcing decisions. Meanwhile, joint industry initiatives to pool technical data and hazard studies help smaller companies keep up with evolving compliance rules.

    Education remains critical. I’ve seen tangible improvements after companies invested in updated training for handlers, including best practices for storage and waste minimization. Close collaboration with academic labs and start-ups can seed improved synthetic routes, lowering the environmental footprint of each kilogram produced. At the same time, institutions that encourage feedback from the end-user community foster incremental improvements—better packaging, more convenient volumes, clearer labeling—which ease bench work and scale-ups alike.

    A Responsible Path Forward

    Stakeholders from every corner—R&D, manufacturing, safety compliance, logistics—shape the landscape for chemicals like 2,6-Dichlorobenzaldehyde. From my years in the lab and in support roles, it’s clear that proactive engagement beats reactive troubleshooting. Early dialogue about anticipated changes in demand, regulatory rules, or technical requirements makes pivoting smoother and more cost-effective. I encourage open forums and transparent communication throughout the chain—that’s where creative solutions and collective problem-solving thrive.

    The next generation of specialty chemicals won’t spring from one corner alone. By investing in cleaner processes, improved data integrity, and collaborative innovation, producers and users of 2,6-Dichlorobenzaldehyde will continue to play a vital role in shaping smarter, safer industries. As a mainstay in chemical synthesis, this compound stands as both a testament to past achievements and a springboard for future breakthroughs.

    Useful Reminders for Users and Buyers

    A few points are worth repeating based on direct experience: always review analytical data before receiving material. Verify supplier credentials and quality standards. Store the solid in tightly sealed containers, away from heat and humidity, to avoid unnecessary degradation. Plan for responsible waste management and make sure anyone handling the compound receives appropriate training. These practices not only protect those working directly with the material but also reinforce responsible stewardship throughout the product’s life cycle.

    Thanks to advances in process chemistry and deliberate cooperation across research and manufacturing channels, users of 2,6-Dichlorobenzaldehyde can expect ongoing improvements in reliability and performance. Looking at how this compound continues to drive development in fine chemicals, specialty agriculture, and pharmaceuticals, there’s no question of its significance on both small and large scales. My experience suggests that, with continued vigilance and shared learning, the path forward remains bright for those tapping into the power of well-crafted intermediates like this one.