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2,6-Dichlorobenzaldehyde Oxime

    • Product Name 2,6-Dichlorobenzaldehyde Oxime
    • Alias 2,6-DCBO
    • Einecs 249-412-7
    • 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
    Specifications

    HS Code

    116825

    Name 2,6-Dichlorobenzaldehyde Oxime
    Cas Number 39078-59-8
    Molecular Formula C7H5Cl2NO
    Molecular Weight 190.03 g/mol
    Appearance White to off-white solid
    Melting Point 111-115°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 2,6-Dichlorobenzaldoxime, Benzaldehyde, 2,6-dichloro-, oxime
    Smiles C1=CC(=C(C(=C1)Cl)C=NO)Cl
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Brown glass bottle containing 25 grams of 2,6-Dichlorobenzaldehyde Oxime, sealed with a screw cap and labeled with safety information.
    Shipping 2,6-Dichlorobenzaldehyde Oxime should be shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. It must be clearly labeled as a laboratory chemical and handled according to local regulations. Store and transport at room temperature, avoid exposure to incompatible substances, and follow all hazardous material shipping guidelines.
    Storage 2,6-Dichlorobenzaldehyde Oxime should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. The storage environment should be shielded from light and moisture. Use proper labeling, avoid prolonged exposure, and ensure containers remain sealed when not in use to maintain stability and safety.
    Application of 2,6-Dichlorobenzaldehyde Oxime

    Purity 98%: 2,6-Dichlorobenzaldehyde Oxime with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced side-product formation.

    Melting Point 120°C: 2,6-Dichlorobenzaldehyde Oxime with a melting point of 120°C is used in organic reaction setups, where it provides thermal stability during process heating.

    Particle Size <50 μm: 2,6-Dichlorobenzaldehyde Oxime with particle size less than 50 micrometers is used in fine chemical formulation, where it allows for faster dissolution and homogenous mixing.

    Stability Temperature 70°C: 2,6-Dichlorobenzaldehyde Oxime stable up to 70°C is used in storage of chemical stock, where it prevents degradation in ambient conditions.

    Moisture Content <0.2%: 2,6-Dichlorobenzaldehyde Oxime with moisture content below 0.2% is used in agrochemical synthesis, where it minimizes hydrolytic decomposition during processing.

    Assay 99%: 2,6-Dichlorobenzaldehyde Oxime of 99% assay is used in analytical reference standards, where it guarantees consistent and reliable analytical results.

    Solubility in Ethanol: 2,6-Dichlorobenzaldehyde Oxime soluble in ethanol is used in solution-phase reactions, where it enables homogeneous reaction environments.

    Refractive Index nD25 1.570: 2,6-Dichlorobenzaldehyde Oxime with refractive index nD25 of 1.570 is used in optical material research, where it provides predictable light interaction properties.

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    Certification & Compliance
    More Introduction

    Understanding the Role of 2,6-Dichlorobenzaldehyde Oxime in Industrial Applications

    Shining a Light on a Specialized Intermediate

    Chemists have always appreciated the way a slight change in structure can redefine the purpose of a compound. 2,6-Dichlorobenzaldehyde oxime offers a good example of this idea in practice. Holding two chlorine atoms on the benzene ring at the 2 and 6 positions, paired with an oxime group bound to the aldehyde, this compound brings a nuanced profile that stands apart from the dozens of other benzaldehyde derivatives available on the market.

    From my time in chemical development, I’ve seen how an apparently subtle structural twist can make all the difference on the synthesis floor. This oxime isn’t just a shelf curiosity – it matters for people working at the bench, especially in pharmaceutical and agrochemical labs. Lab teams trust 2,6-dichlorobenzaldehyde oxime because it delivers consistent results in multi-step syntheses. Consistency means reliability, and in industries where process hiccups can cost thousands, even a single impurity can make an ordinary day a frustrating one.

    Exploring Specifications That Impact Real Work

    Let’s get into what defines this product beyond its tongue-twisting name. In production, most high-quality 2,6-dichlorobenzaldehyde oxime comes as an off-white solid, and I’ve found it stores well under normal conditions without caking or breaking down before it hits the reaction flask. Typical purity specs often exceed 98%, which speaks to the extra purification steps taken by careful suppliers. Moisture can ruin some batches – even a little can affect yields or the color of finished products. I’ve seen colleagues run HPLC or GC-MS checks for this reason alone.

    What does the molecular formula tell us? C7H5Cl2NO summarizes a weight just above 190 grams per mole. This relatively modest molecular mass makes weighing and solution prep straightforward for a broad set of extraction and synthesis tasks. In my experience, a workable melting point sits near 130-133°C, so you aren’t left with powdery or oily mystery if the lab thermometer reads within that range. Not every supplier gets it right – inconsistent melting points can point to contamination and shouldn’t be ignored.

    Why It Actually Matters in a Real Lab

    What distinguishes 2,6-dichlorobenzaldehyde oxime from the crowd is not just its reactive positions, but the knock-on effects for downstream chemistry. Many unsung intermediates float through the industry, but few anchor as many crucial transition steps. In my work with organic synthesis, replacing just one hydrogen atom with a chlorine can be the difference between a successful coupling or a failed one. With both ortho positions chlorinated, this oxime stands out for its resistance to over-oxidation, which translates to steadier outputs in scale-up runs.

    This compound pops up often in pharmaceutical research. It can function as a key building block for active pharmaceutical ingredient (API) candidates, such as certain antihistamines and central nervous system agents. For anyone developing molecules in fields like crop protection, this oxime is also attractive, where it feeds into frameworks found in novel fungicides or insecticides. Its signature lies in that balance: The oxime group shields the benzaldehyde core from hasty reduction or oxidation, yet readily undergoes transformation under controlled conditions. That's the kind of versatility synthetic chemists hunt for.

    The Everyday Reality of Using This Compound

    It’s one thing to have a product that works great in theory. The practical angle – how it behaves in a flask or a kilo-scale reactor – keeps researchers up at night. Process engineers in my circle usually ask about residue formation, filtration, and solubility before they sign off on a purchase. This oxime dissolves in polar organic solvents like acetone, acetonitrile, or DMSO. Solubility in water stays low, which can be convenient for some purification steps. For teams scaling up or conducting longer synthesis runs, knowing a compound will filter cleanly or crystallize out without mess is more valuable than a glowing catalog description.

    Some technical data helps answer these questions. For example, 2,6-dichlorobenzaldehyde oxime doesn’t give off any overpowering or hazardous fumes under normal use, unlike some lower-weight aliphatic oximes. Its stability under ambient conditions means it keeps on the shelf for a season, so researchers are not stuck worrying about fresh supply between synthetic campaigns. Hazards still exist – as with any aromatic chlorinated product, gloves and goggles should be routine – but it’s the kind of compound that fits easily into standard lab safety protocols. I’ve seen some manufacturers highlight low dust formation, which lines up with safer weighing and less risk of inhalation exposure.

    Comparing Alternatives and Understanding What Sets It Apart

    People often wonder if another oxime or chlorinated benzaldehyde might do the same job. I’ve seen experiments where other isomers – say, 3,4-dichlorobenzaldehyde oxime or non-chlorinated analogs – have been tried as substitutes. It’s tempting to swap, especially if there’s a price advantage or if procurement issues make the original compound hard to find. Substituting generally cuts into yield or changes the selectivity of a reaction route. That hinges on physical properties: the ortho-chlorination pattern creates specific electronic effects, which influence reactivity in steps like nucleophilic substitution, and that sets this candidate apart.

    From site visits and discussions with researchers, I’ve heard plenty about supply bottlenecks and quality discrepancies from less-verified suppliers. Buyers are right to be cautious – a lot rides on lot-to-lot consistency. Oximes, in general, can present isomeric impurities, and for this compound, that translates to unexpected spots on TLC plates or splits in NMR spectra. Reputable suppliers publish batch-level analytics and stand behind claims, which gives teams backup if documentation issues come up during audits. From years in the trenches, I can say: If your supplier isn’t showing their GC trace or HPLC chromatogram, keep searching.

    Applications That Keep Researchers Interested

    Talking with chemists across pharma and agro, I keep seeing 2,6-dichlorobenzaldehyde oxime show up in projects that aim to build new heterocyclic cores. The oxime group plays a key role as a selective nucleophile in cyclization reactions, which help form complex ring systems used in exploratory drug design. You also see it in the protection and deprotection of sensitive carbonyl intermediates, a core chapter in anyone’s synthetic playbook. For chemists hunting for ligands or specialty reagents, this compound serves as a launchpad for further custom synthesis, thanks to its defined positions and safety profile compared to bulkier, more reactive halogenated options.

    Beyond API work, it finds use in developing specialized dyes and optical brighteners. The presence of strong electron-withdrawing chlorine atoms leads to unique photophysical properties when the molecule is locked into larger conjugated systems. I’ve seen collaborations where this oxime-based intermediate was preferred in pilot runs, as opposed to more common para-substituted derivatives, purely for its improved performance under thermal stress or its easier purification routes.

    What Users Are Really Looking For

    In my discussions with purchasing and formulation teams, few questions matter more than “How does this product behave in my process?” Beyond purity and moisture, people ask about granule size, flow, or response to grinding. No one wants a compound that clogs a dosing valve or flies out of the jar the minute you open the lid. Skilled providers understand that customers want a uniform, pourable, and dust-reduced material; these qualities make day-to-day use more predictable and safer.

    Post-synthesis, cleanup and waste minimization gain importance. This oxime leaves behind a manageable residue profile in most systems, especially when compared with more heavily functionalized aromatic intermediates that leave behind halogenated tars or gums. Less mess means less cost for disposal and less time scrubbing glassware – a fact lab technicians and process engineers always appreciate. Having spent my share of weekends tracking down mystery residues, I can tell you firsthand: The right choice of intermediate matters.

    Addressing Challenges and Building Trust in the Supply Chain

    The chemical world doesn’t reward shortcuts, especially with regulated or high-purity intermediates. I’ve seen companies scramble over interrupted supplies or inconsistent batches. This is where a supplier’s credibility comes into play. Labs rely on trusted relationships, where production histories and certificates back up the label on the jar. Analytical data builds more trust than any marketing statement could. Regulatory registrations (like REACH in the EU) and transparent safety data sheets provide clarity about handling risks, and these documents should always be accessible.

    Sustainability is on everyone’s mind in recent years. The manufacture and downstream processing of products like 2,6-dichlorobenzaldehyde oxime should aim to avoid unnecessary waste and cut back on toxic byproducts. Some producers highlight more energy-efficient synthetic routes or closed-loop solvent recycling. Buyers, including those I work with, now ask about audits or third-party verifications for environmental compliance. The difference shows up not just in feel-good talking points but in tougher scrutiny from larger customers and regulators.

    Practical Improvements and Forward Thinking

    There’s still plenty of room to improve on sourcing and application. Some issues keep recurring – poor batch documentation, opaque impurity profiles, or last-minute shipments that push projects into overtime. Solutions come from suppliers who treat transparency as non-negotiable and respond to questions with meaningful detail, not just templated answers. For buyers, establishing a minimum expected documentation set (like batch COAs or recent HPLC traces) should come standard on technical-grade oximes.

    Process improvements make a difference as well. I’ve watched teams develop safer handling and packaging, like moisture-barrier containers, which keep this compound in top shape between delivery and first use. For plants or firms processing higher volumes, automating the weighing and addition steps goes a long way toward reducing human exposure and batch-to-batch deviation. These changes take investment and planning but pay off in fewer reworks and better resource management.

    Guiding Principles for Procurement and Safe Use

    People who work in labs or chemical production already know how crucial it is to pay attention to the source and handling of every intermediate. For 2,6-dichlorobenzaldehyde oxime, a combination of purity, detailed documentation, and responsive support usually tips the scale for informed buyers. Brand loyalty grows with suppliers who make no compromises on technical data and batch transparency, and who offer real-world troubleshooting.

    Safe handling remains a pillar. Follow practiced standards: Keep containers tightly closed, use appropriate PPE, avoid unnecessary exposure, and don’t skimp on disposal protocols. While regulations might shift by country or state, adopting international best practices for hazardous substances remains the smartest move – for employees, the community, and the company alike.

    Looking to the Future: Opportunities for Greater Impact

    With rapid advancements in process chemistry and automation, the way intermediates like 2,6-dichlorobenzaldehyde oxime get produced and used will keep evolving. Researchers and engineers push for smarter, cleaner, and safer process routes, not only to cut costs but to reduce environmental impact and boost regulatory compliance. Expanded analytics, like real-time process monitoring and impurity fingerprinting, help teams catch problems early and achieve higher quality standards.

    There’s a growing call from the industry for better information sharing. This means fuller traceability all the way back to raw materials, improved cross-border transparency, and honest discussions around both capabilities and limitations. Buyers want to know more than just the final batch numbers; they want assurances about worker safety and waste reduction along the supply chain. Laboratories and manufacturers have a real chance to set new examples by partnering for regular audits, data sharing, and co-development of greener production methods.

    Conclusion: Why It Matters to Choose Wisely

    For those working in chemical research, production, or application, selecting a specialty intermediate isn’t just a background choice – it shapes the whole project. 2,6-Dichlorobenzaldehyde oxime brings a combination of reactivity, selectivity, and day-to-day practicality that has earned it an important place in modern synthesis. A thoughtful approach to procurement, supported by strong technical data and open supplier dialogue, allows teams to achieve better outcomes, keep people safe, and build trust at every step. For anybody tasked with bridging the lab and production world, this kind of compound proves that small details really do make or break the big picture.