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3,5-Dichlorosalicylaldehyde

    • Product Name 3,5-Dichlorosalicylaldehyde
    • Alias 3,5-Dichloro-2-hydroxybenzaldehyde
    • Einecs 249-412-1
    • 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

    710054

    Cas Number 609-19-8
    Molecular Formula C7H4Cl2O2
    Molecular Weight 191.01 g/mol
    Appearance White to pale yellow crystalline powder
    Melting Point 122-126 °C
    Boiling Point 333.4 °C at 760 mmHg
    Density 1.53 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 3,5-Dichloro-2-hydroxybenzaldehyde
    Smiles C1=C(C=C(C=C1Cl)Cl)C=O
    Inchikey LBAVZJFNZXEECU-UHFFFAOYSA-N
    Flash Point 155.6 °C

    As an accredited 3,5-Dichlorosalicylaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,5-Dichlorosalicylaldehyde is supplied in a 25g amber glass bottle with a screw cap, labeled with hazard and product information.
    Shipping 3,5-Dichlorosalicylaldehyde is shipped in tightly sealed containers to prevent moisture ingress and contamination. Packages are clearly labeled, comply with relevant hazardous material regulations, and are cushioned to avoid breakage. The chemical is handled by trained personnel, ensuring safe transport in accordance with international and local shipping guidelines for laboratory chemicals.
    Storage Store 3,5-Dichlorosalicylaldehyde in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition, moisture, and incompatible materials such as strong oxidizers. Protect from light and avoid prolonged exposure to air. Clearly label the container and ensure access is limited to trained personnel. Use appropriate chemical safety storage protocols at all times.
    Application of 3,5-Dichlorosalicylaldehyde

    Applications of 3,5-Dichlorosalicylaldehyde in Industrial Manufacturing

    As a certified chemical raw material producer, we supply 3,5-Dichlorosalicylaldehyde to specialized manufacturing clients across multiple regulated sectors. Below are detailed applications based on observed industry integration, including process technicalities, compliance criteria, and finished product categories.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers frequently use this compound as a core intermediate in the synthesis of anti-infective drugs and advanced intermediates for certain oncology therapeutics. Rigorous compliance with cGMP manufacturing controls is required for every batch used in regulated synthesis pathways. The raw material reacts with amine moieties during the construction of heterocyclic frameworks via condensation or cyclization reactions, such as in quinazoline or benzoxazole series. Batch formulation typically mandates narrow impurity cut-offs and tested residual content of chlorinated by-products. End product categories include registered APIs and key intermediates for patented therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <467> Organic Volatile Impurities Guidance
    • EU GMP Part II for Pharmaceutical Intermediates
    • FDA 21 CFR Part 211 for Finished Pharmaceuticals

    Typical usage ratio

    • 2–10% by weight of total reactant mass, depending on target heterocycle and process yield requirements; ratio adjusted according to stoichiometric demand and impurity filtration method

    Downstream process integration

    • Integrated in stepwise condensation or cyclization upstream; enters solvent phase with base or acid catalysts; followed by in-process chromatographic purification

    Final product types

    • Anti-tumor API intermediates
    • Antibacterial drug precursors
    • Specialty quinazoline derivatives
    • Benzoxazole-based pharmaceutical actives

    2. Agrochemical Synthesis: Fungicide Intermediate

    This material serves as a key building block in the manufacturing of selective fungicide actives. Agrochemical formulators employ it during multi-stage synthesis, often as a benzene ring precursor for substituted phenol or imine derivatives. Compliance with national pesticide regulations and agrochemical GMP protocols is necessary to meet downstream registration standards. Exact reactant ratios are selected to maximize target compound conversion and reduce process waste. Primary utilization resides in the construction of pyrimidine or triazole moieties, which serve as the basis for broad-spectrum crop protection agents.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Active Ingredients
    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • Chinese GB 2763-2023 Maximum Residue Limits for Pesticides
    • REACH Registration for Industrial Use

    Typical usage ratio

    • 5–15% by weight depending on the synthetic route and specific molecular target, with minor adjustment for solubility profile and target yield

    Downstream process integration

    • Employed in early-to-mid sequence organic synthesis; enters as a precursor during the coupling stage; typically followed by base-catalyzed cyclization or nitration

    Final product types

    • Pyrimidine fungicidal intermediates
    • Triazole agrochemical actives
    • Crop fungicide concentrate ingredients
    • Seed treatment active substances

    3. Dye and Pigment Intermediate Manufacturing

    3,5-Dichlorosalicylaldehyde is adopted in colorant manufacturing lines as a condensation partner for synthesizing high-purity azo and anthraquinone dyes. Quality control during integration focuses on color index requirements and limits for halogenated trace impurities. The compound enters as a key aldehyde reactant, supporting chromophore construction and providing improved thermal stability in the resulting dyes. Regulatory protocols dictate strict endpoint batch testing for nonylphenol, heavy metal, and chlorinated residuals to ensure compliance with global textile and plastics industry requirements. Output colorant grades are destined for plastics compounding, specialized coatings, and textile ink applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 for Textile Chemicals
    • REACH Regulation (EC) No 1907/2006
    • ZDHC MRSL (Zero Discharge Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 9001 Process Quality for Dye Manufacturing

    Typical usage ratio

    • 3–8% by formula weight in azo dye synthesis; ratio modified to tuning hue intensity and stabilization needs

    Downstream process integration

    • Incorporated during the condensation reaction with aromatic amines; follows sulfonation or chlorination stage; proceeds to crystallization and refining

    Final product types

    • Anthraquinone and azo dye intermediates
    • Thermally stable pigment colorants
    • High-performance textile inks
    • Specialty plastics masterbatch color additives

    4. Analytical Reagent and Ligand Production

    Chemical analysis reagent producers use this compound as a starting aldehyde in custom synthesis of chelating ligands and complex indicators. Batch production follows ISO-certified laboratory chemical manufacturing protocols with attention to near-zero metallic impurity thresholds and reagent functional group purity. The aldehyde functions in Schiff base formation, supporting the tailored development of analytical ligands for transition metal detection and process control markers. Compliance verification includes batchwise NMR and HPLC release testing. Finished goods supply both research chemical labs and in-process industrial quality control programs.

    Industry compliance standards

    • ISO 17034 General Requirements for Reference Material Producers
    • ACS Reagent Chemical Specifications
    • RoHS Requirements for Laboratory Chemicals
    • REACH Compliance for Analytical Reagents

    Typical usage ratio

    • 1–12% by final ligand batch weight, based on molecular design and metal-binding stoichiometry

    Downstream process integration

    • Initiates Schiff base or condensation phase; enters prior to metal complexation step; followed by intermediate purification and drying processes

    Final product types

    • Transition metal ion chelating ligands
    • Custom analytical indicator agents
    • Reference standards for laboratory QC
    • Organic synthetic research chemicals
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    Certification & Compliance
    More Introduction

    3,5-Dichlorosalicylaldehyde: Our Take as the Maker

    What We Know About 3,5-Dichlorosalicylaldehyde

    Producing 3,5-Dichlorosalicylaldehyde has kept us busy for years. From each batch, we see the direct impact of small choices in raw material purity, reaction timing, and equipment setup. Anyone interested in this compound has probably worked with its bright crystalline form or noticed its sharp aroma. Our facility puts out this aldehyde both for local labs and export customers looking for steady performance.

    Chemically, our 3,5-Dichlorosalicylaldehyde comes by the model identifier DCSA-98, reflecting our target for a minimum purity of 98 percent. Customers in fine chemicals, pharmaceuticals, and agrochemical research select this grade for its predictable behavior in synthesis. The controlled presence of 3,5-dichloro groups, paired with the aldehyde function, gives it higher stability in environmental tests compared to single-chloro alternatives. In reactivity studies, this stability carries through to downstream reactions. No matter if you're working on complex ligand construction or just need a reliable intermediate for active ingredient synthesis, the consistency counts.

    Why Purity and Handling Matter in Everyday Production

    In our workshop, the grade of input materials changes everything. We've used both 97-percent and 98-percent raw aldehyde, and the latter significantly reduces purification steps after the initial reaction with phenols or amines. Higher purity translates into less off-color byproduct, which saves time—no need to rerun chromatographs or loss more material during workup. Operating reactors with this aldehyde, we notice that too much water introduction or even a minor slip in temperature throws off yield. Years of hands-on experience taught us that process reliability matters more than flashy claims about "versatility" sometimes thrown around in datasheets.

    Distributors often don’t see what we see at the bench level. The difference between 3,5-Dichlorosalicylaldehyde made on-site, handled fresh, and what sits on a shelf for months is huge. Our product’s light color and clean melting point are results of robust isolation and short storage periods. Each shipment displays batch-to-batch consistency, thanks to controls at every stage, from chlorination through to crystallization and final packaging. These invisible details define the confidence our R&D partners have in our compound during method development.

    Understanding Usage Across Industries

    We made this aldehyde for seasoned chemists and formulation experts. In the pharmaceutical industry, its main value lies as a building block for heterocyclic synthesis and protecting group strategies. Project teams use it for making modified benzoic acid derivatives, focused on anti-microbial, anti-inflammatory, or enzyme inhibitory activity. The dichloro pattern resists oxidation and unwanted substitution, giving a wider synthetic window with electrophiles and nucleophiles.

    Custom agrochemical formulators rely on 3,5-Dichlorosalicylaldehyde to start new pesticide research. The unique structure directs bioactivity, particularly in early-stage lead identification work. Its specific capability to influence molecular electronics makes it suitable for ligands, dyes, and chelates—industrial users often choose our high-grade variant after struggling with less reproducible sources. Even in the dye and pigment sector, it acts as a core scaffold for color-intense and durable performance materials.

    Synthetic pathways involving this aldehyde often look straightforward on paper. In practice, we know that reaction rates, filtration ease, and precipitation steps depend on the precise composition and solvated ion content in each lot. Working side by side with pilot-scale users, we swapped stories about scale-up issues—material gumming, impurity retention, and unexpected polymorphism show up fast when starting with questionable intermediates. These are headaches we stamp out by managing every stage under strict in-process checks.

    Differences from Other Salicylaldehyde Derivatives

    Every structural tweak changes the game. Many have asked us about differences between our 3,5-Dichlorosalicylaldehyde and standard salicylaldehyde or its 3,5-dibromo analog. Through our own hands-on trials, 3,5-dichloro substituents yield an aldehyde less prone to over-reaction and hydrolysis under basic conditions. The bromo variant brings heavier atoms and higher reactivity but at the expense of stability and control in mild synthesis routes. Single-chloro versions, like 5-chlorosalicylaldehyde, have a wider reaction window but produce less defined products in couplings and condensations.

    Our compound also resists ambient light and moisture better than its non-chlorinated cousin. Lab workers who spent weeks tracking slow degradation appreciate not having to babysit bottles or handle repeated repurification. In custom synthesis, this aldehyde’s melting profile, clarity, and robust shelf stability stand out next to older, less refined grades. Users working in green chemistry routes—those requiring lower solvent load or fewer chromatographic purifications—noted faster workups thanks to our reliable batch-to-batch character.

    Having handled all three in bench experiments, the practical edge of the dichloro pattern shows when combining with strong bases, planning multi-step syntheses, or storing intermediates for scale-up. These facts have become clear through actual sample comparisons, not just raw literature references.

    What Sets Our Manufacturing Apart

    Tracing each gram from chlorination through separation takes more work than just following a standard protocol. Every few months, new suppliers approach us with slightly cheaper raw phenol, but our team sticks with trusted sources. In our daily operation, skipping these steps leads to off-color, inconsistent aldehyde, and customers notice any blip right away. Years of feedback pushed us toward tighter controls: small-batch testing, integrating fine particle filtration, and keeping nitrogen sweep lines active during isolation. All these decisions show up in each lot our partners open.

    A fresh batch always reveals its quality through odor, particle size, and purity by HPLC. We even test how well each batch dissolves in alcohols and acetonitrile—not just the basics like melting point or water content. Some users need microfiltered powder for solid-phase synthesis, others want coarser grades for solution preparation. It takes more effort during production to deliver both, but we prefer ensuring applications run without issue to risking downstream surprises.

    Any batch that falls short gets set aside for internal method development. This reduces headaches with end users and strengthens our internal standards every month. We share learnings with research partners, who in turn bring us into their projects at an earlier stage. Their feedback shaped our filtration, drying, and packaging methods, so that on arrival the aldehyde matches their exact usage needs.

    Improving Safety and Reliability at Scale

    Working with chlorinated organics forces daily attention to safety and waste. Direct exposure to vapors, even brief, leaves an impression—sharp smell, mild throat irritation, and the feeling of handling something that demands respect. Our team uses sealed handling lines, air scrubbers, and well-maintained PPE. Waste minimization and solvent recovery go hand in hand with efficient production; a small change in workup can halve the volume of chlorinated byproduct.

    Our relationships with downstream processors depend on this reliability. They must trust that our material won’t shift specifications mid-project. We regularly revisit storage protocols, adjusting for seasonal temperature swings and material transport distances. Keeping stability during long ocean transit or short-haul runs, and providing packaging tailored for local humidity, became part of our daily routine after feedback from users in tropical export markets.

    Feedback-Driven Changes and Real-World Experience

    Once, a key partner found micro-particles in delivered bottles, traced to a process line cleaning agent residue. This sparked a full review and doubled our batch release testing for common ions. Learning from these issues, we built more redundancy into our QA system. Now, a cloudier batch or one with trace yellowing never leaves the plant without extra checking.

    University researchers often reach out with detailed purity questions as they plan competing synthetic approaches—no one wants results confounded by trace halogen movement or aldehyde dimerization. We work with them during method setup, offering not only data but also practical tips on stirring, dissolution, and waste collection. This spirit of open dialogue led us to adjust bottle sizes, develop a sturdier closure, and launch a modular bulk-packing solution for volume buyers.

    Behind these surface details sits years of direct exchange between makers and users—continuous improvement, not marketing slogans, drives how our 3,5-Dichlorosalicylaldehyde lands in your hands. New requests, like ultra-low moisture content or special anti-static bottles for high-sensitivity synthesis, challenge us to move beyond just making a commodity and into real collaboration.

    Sourcing, Sustainability, and Supply Chain Lessons

    All chemicals start with basic building blocks, but repeated raw material shortages showed us nothing matters more than actual source reliability. When one year a global supply crunch for resorcinol hit, quality dropped across the market. We learned to pre-stock specialty chlorinating agents and maintain relationships with logistics partners. Through these steps, we cut interruptions and kept partners supplied even as others in the market had to pause shipments.

    Sustainability pressure grew, and we respond with ongoing solvent recycling, reduced water use, and recycling packaging wherever possible. Waste material now routes for regeneration or responsible treatment instead of dumping. Our on-site scrubbers reduce fugitive emissions—every kilogram saved in process translates into less environmental impact. Industry pressure pushes us to go further, but experience hands-on with process streams tells us which so-called "green" methods slow output or introduce new risks. Our goal is honest improvement, not compliance theater.

    Insights for Chemists: Working with 3,5-Dichlorosalicylaldehyde

    Seasoned users pay attention to subtle quality markers: crystal color, melting range, and ease of weighing. The best batches offer bright, snow-white powder, sharp melting points, and dissolve quickly with no floating debris. Handling this aldehyde in scale-up brings lessons every time. Careful weighing, rapid transfer to reaction vessels, and avoiding prolonged exposure to air improve results. In our production area, skilled staff shorten bottling time and ensure every container seals cleanly—not just to keep specs, but to give end users a trouble-free experience.

    On the technical side, the dichloro groups slow down air oxidation and resist color change better than plain analogs. In acid-catalyzed reactions, 3,5-Dichlorosalicylaldehyde stays smoother and resists forming heavy, sticky tar. Practicing these workflows, we document which batches work best under which solvent systems, and feed that knowledge back to our R&D allies as they develop next-generation syntheses.

    Each chemist brings their own approach and preferences. Some prioritize low dust levels for automated weighing stations; others want maximum solubility for rapid batch preparation. We compile feedback and adjust process parameters. These small changes accumulate—tighter specification, less work spent on purification, and more time spent on actual research.

    Emerging Trends and Market Shifts

    Demand patterns shift every year. Five years ago, most uses fell into small-scale pharmaceutical R&D. Growth now comes from electronics and smart materials: use as a ligand foundation, ionophore generator, or building block for advanced dyes. Electronics labs want extra assurance on elemental impurities, especially sodium and potassium content. In response, we run extra checks during final quality assessment. These details matter to partners wanting reliable dielectric properties or photoresist performance.

    In the agrochemical sector, firms cycle through libraries of substituted aromatics looking for new modes of action. 3,5-Dichlorosalicylaldehyde enables quick assembly of novel candidates with built-in persistence traits. By tracking usage data, listening to regulatory updates, and gathering field reports, we prepare both standard and enhanced grades. Transparency wins long-term trust more than aggressive pricing or hollow claims.

    Supporting Product Development and Custom Solutions

    Our engagement doesn’t end with the sale. Custom requests roll in for everything from non-metal-catalyzed synthesis to extra-low halide residue. We deploy parallel process trains for experiments and bulk runs—keeping research-grade and industrial-grade lots separate. By keeping close ties to key projects, we forecast demand, plan inventory, and support faster turnaround times.

    Some clients bring narrow requirements—a particular melting range for instrument calibration, or specific crystal habit for automated feeding systems. We respond with adjusted filtration, re-precipitation, or targeted grinding and screening. This readiness sets us apart: actual product, actual applications, tuned batch by batch, not just “off-the-shelf” or anonymous reselling.

    What We See for the Future

    New markets demand better data transparency, full traceability, and more support for rapid development. Automation, digital batch records, and predictive analysis on stability help us refine our work. Acceptance criteria grow tighter, but this challenge fits well with our capacity to grow, learn, and share what works. Out in the market, buzzwords fade quickly; real-world trial and error provide a steadier path.

    Customers want more than molecules. They seek partnership in overcoming obstacles, insight on problem-solving, and empathy for the stop-and-go rhythm of a project timeline. From sourcing to shipping, every step draws on real experience and direct user feedback. Our 3,5-Dichlorosalicylaldehyde reflects that approach—no shortcuts, no guesswork, just carefully made material ready for innovation.