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3-Bromo-5-Chlorosalicylaldehyde

    • Product Name 3-Bromo-5-Chlorosalicylaldehyde
    • Alias 5-Chloro-3-bromo-2-hydroxybenzaldehyde
    • Einecs 629-505-7
    • 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
    VTB
    Specifications

    HS Code

    970750

    Chemical Name 3-Bromo-5-Chlorosalicylaldehyde
    Molecular Formula C7H4BrClO2
    Molecular Weight 235.46 g/mol
    Cas Number 185137-53-7
    Appearance White to off-white solid
    Melting Point 87-90°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles C1=C(C=C(C(=C1Cl)Br)O)C=O
    Inchi InChI=1S/C7H4BrClO2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H
    Synonyms 5-Chloro-3-bromosalicylaldehyde
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 3-Bromo-5-Chlorosalicylaldehyde 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 3-Bromo-5-Chlorosalicylaldehyde, tightly sealed, with hazard labels and product identification details.
    Shipping 3-Bromo-5-Chlorosalicylaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It is transported in compliance with chemical regulations, labeled as a hazardous material if required. All packaging ensures protection from physical and temperature damage, accompanied by safety documentation and handled by trained personnel during transit.
    Storage 3-Bromo-5-Chlorosalicylaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents and bases. Proper labeling and secure storage are essential to prevent accidental contact, spills, or contamination. Handle under inert atmosphere if recommended by the manufacturer.
    Application of 3-Bromo-5-Chlorosalicylaldehyde

    Applications of 3-Bromo-5-Chlorosalicylaldehyde in Industrial Manufacturing

    3-Bromo-5-Chlorosalicylaldehyde serves as a specialty chlorinated aromatic intermediate with key functionality for targeted synthesis in regulated industrial chemistry. As a direct manufacturer, we supply this active raw material exclusively to global B2B customers for precise integration in select downstream production lines, following validated industry protocols.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Manufacturers incorporate this compound as a building block for complex heterocyclic and halogenated pharmaceutical intermediates. It often enters stepwise Grignard, Suzuki, or palladium/copper-catalyzed arylation sequences, where the selectivity of its substituents supports the formation of target molecules including kinase inhibitors and selective aromatics for central nervous system drug candidates. Formulators determine integration based on required purity, and the compound's reactivity profile reduces the risk of side products, supporting GMP-compliant batch runs for both pilot and full-scale production.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) raw material chapters
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Chinese Pharmacopoeia Material Specifications

    Typical usage ratio

    • 5–20% w/w in intermediate synthesis steps; exact ratio determined by target yield and route selectivity

    Downstream process integration

    • Charged during initial or secondary halogenation/aromatic substitution stage
    • Integrated in multi-step synthesis streams before isolation/purification of API precursor

    Final product types

    • Kinase inhibitor precursors
    • Neuroprotective heteroaromatic scaffolds
    • Custom small-molecule intermediate blocks for contract synthesis

    2. Crop Protection Chemical Synthesis (Agrochemical Intermediates)

    Agrochemical formulators use this material as a halogenated precursor when producing selective fungicides and bactericides via condensation and copper-mediated coupling. The compound supplies a stable core structure for further derivatization such as oxime formation or etherification, supporting the creation of highly specific actives with controlled environmental fate. Quality control ensures the resultant intermediates meet established impurity thresholds for safe use in food chain applications. Material lots undergo residual solvent and halogen balance testing prior to downstream conversion.

    Industry compliance standards

    • FAO/WHO Specification and Evaluations for Plant Protection Products
    • ISO 17025 Laboratory Testing for Agrochemical Intermediates
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products

    Typical usage ratio

    • 8–16% w/w in primary condensation or coupling steps; ratio varies by crop protection molecule synthesis path

    Downstream process integration

    • Initial halogenated aromatic basis for further substitution or coupling
    • Added to reaction vessel prior to introduction of secondary reagents

    Final product types

    • Triazole fungicide intermediates
    • Heteroaromatic bactericide scaffolds
    • Seed treatment precursor compounds

    3. Specialty Dye and Pigment Manufacturing

    Advanced dye manufacturing utilizes this compound for the targeted synthesis of halogenated azo dye intermediates. It enables high chromatic purity via controlled aldehyde reactivity, promoting precise introduction of dye linkages in diazotization or condensation stages. As batch purity and color fastness rely on input consistency, formulation teams monitor the integration of each lot through QA-driven sampling, in keeping with hazard labeling and effluent permit restrictions specific to specialty dye plants.

    Industry compliance standards

    • OEKO-TEX Standard 100 (chemical input requirements)
    • REACH Registration for dye intermediates in the EU
    • Clean Water Act (40 CFR Subchapter N, Textile Mills)

    Typical usage ratio

    • 6–15% w/w relative to target chromophore during condensation reactions; adjusted for shade intensity and tone

    Downstream process integration

    • Fed into aromatic condensation lines for early-stage pigment intermediate synthesis
    • Participates in etherification/diazotization stages for azo or anthraquinone pigment development

    Final product types

    • Halogenated azo dye intermediates
    • Specialty fabric pigment precursors
    • Fiber-reactive dye building blocks

    4. Fluorescent and UV-Active Materials Production

    Producers of specialty fluorescent compounds introduce this raw material during the synthesis of halogenated salicylaldehyde-based dyes for use in analytical labeling, biological staining, or photochemical applications. The bromine and chlorine functional groups provide electronic modulation required for tailored excitation profiles used in high-precision industry contexts. Production lines require validated in-process control to prevent cross-contamination and maintain spectral properties to specification, with compliance verified through trace analytical batch release.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • RoHS Directive 2011/65/EU for restricted hazardous substances in electrical/electronic applications
    • Spectroscopy and fluorescence reference standards (ASTM E975, related QC)

    Typical usage ratio

    • 10–25% w/w, typically higher than in classical dye routes, based on molar absorption coefficient goals

    Downstream process integration

    • Charged at aromatic backbone formation and directly involved in subsequent etherification or Schiff base reactions
    • Incorporated before purification/crystallization of fluorescent or UV marker substances

    Final product types

    • Salicylaldehyde-derived fluorescent probes
    • Diagnostic reagent components
    • Light-activated labeling agents for biological research and process monitoring
    Free Quote

    Competitive 3-Bromo-5-Chlorosalicylaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Quality Matters: A Closer Look at 3-Bromo-5-Chlorosalicylaldehyde

    From Synthesis to Final Application

    Each product that leaves our facility tells part of a larger story. For years, working directly with chemists, we have seen firsthand the reliance on specialty intermediates such as 3-Bromo-5-Chlorosalicylaldehyde. As manufacturers, we recognize the weight behind each specification and the way a single impurity can stall an entire research project or commercial batch. When developing this compound, we chose methods that emphasize purity and stability, knowing these details determine whether the end user meets their goals—or faces frustration.

    Model, Form, and Physical Qualities

    We produce our 3-Bromo-5-Chlorosalicylaldehyde under batch numbers traceable to the original synthesis date, ensuring accountability at every step. The product arrives as a pale-yellow crystalline solid, with a melting point typically between 98 and 102°C, matching reference values in synthetic literature. With its molecular formula C7H4BrClO2, each lot undergoes full chromatographic and spectroscopic confirmation. After years of operator training and equipment refinement, our lines maintain levels of organic impurities far below the 0.5% mark—no shortcuts, just repeated verification. Chemists from small labs and multinational companies often ask about stability under ambient conditions. While hydroscopicity is minimal, we suggest airtight packaging only to prevent surface oxidation—something our team monitors in retained quality samples as part of internal audits.

    Beyond Purity—Consistency That Counts

    Making 3-Bromo-5-Chlorosalicylaldehyde is more than running a recipe. Variability often creeps in through temperature swings, raw material deviation, or even subtle changes in solvent quality. Early in our practice, we learned the hard way that consistency means controlling everything from the halogenation step to precipitation rates. Unlike generic sources, we refuse to accept deviations from HPLC and NMR patterns observed in reference spectra archived by our R&D team. Any batch showing unexplained minor components stops right there. It’s not about regulatory pressure—it’s about the years of feedback received from synthetic chemists who depend on a predictable performance in the lab and at scale.

    Application Realities

    3-Bromo-5-Chlorosalicylaldehyde often acts as a starting material for pharmaceuticals, agrochemicals, dyes, and advanced materials. Through ongoing conversations with formulators and process engineers, we notice an increasing shift toward efficiency—where every reaction step needs to deliver the highest yield and minimal unwanted byproducts. The ortho position of both halogen atoms in this molecule gives it a unique reactivity profile. It’s been used for synthesizing heterocyclic building blocks, fine-tuning functional groups in medicinal chemistry, and constructing ligands for metal complexes. Chemists have shown us how substitution patterns directly influence selectivity in downstream transformations—something impossible to achieve with off-grade intermediates or material not tightly controlled for contaminant levels.

    What Sets Our Product Apart

    Competition in chemical supply hinges on more than pricing or central distribution. Direct manufacturing gives us control over process choice. For 3-Bromo-5-Chlorosalicylaldehyde, we built custom, closed vessels engineered to handle bromination steps in a contained environment. This both protects our operators and improves batch reproducibility. Unlike traders, we crosscheck each batch against long-term stored reference lots and share full analytical data with each shipment—chromatograms, spectroscopic scans, and results from accelerated stability trials. Materials from bulk consolidators or third-party re-packers often tell a different story. We have accepted returned samples from disappointed clients who lost weeks to unexplained NMR peaks or slow crystallization due to hidden contamination. Unlike these uncertain supplies, our product supports seamless integration into GMP processes or research campaigns, anchored by full documentation and a transparent production chain.

    Lessons from the Factory Floor

    We learned early that making this aldehyde is unforgiving. Every raw material, from halide sources to organic acids, arrives with its own set of surprises. We stopped treating the supply chain as a secondary concern, shifting to trusted long-term partners for core reagents. Each barrel gets sampled and analyzed before a single drop enters production. Operators gauge reaction endpoints by both real-time analytics and experience. Too much heat in the introduction stage, and byproducts multiply; too little, and conversion lags. Teams log conditions down to the minute, passing hard-earned knowledge to the next shift.

    Quality control isn't just paperwork for us—it’s lived experience. After every batch, staff review visual color, TLC patterns, NMR spectra, and even particle size under the microscope. One morning, a junior chemist noticed a faint color change. Investigation traced it to minor contamination in washing solvent—preventable with a new filtration cartridge. Every instance like this reinforces a culture of attention, not just compliance. We move forward by asking ourselves after every cycle how we might avoid that issue next time. The goal remains steadfast: deliver exactly what the scientists and process engineers expect, batch after batch.

    Different by Design—Not by Accident

    Chemically, 3-Bromo-5-Chlorosalicylaldehyde looks a lot like its cousins—4-Chlorosalicylaldehyde, 5-Bromo-2-hydroxybenzaldehyde, and parent salicylaldehyde. The differences, though, run deeper than headspace on the chromatograph. We listen to researchers who explain their need for specific halogen placements, which affect electronic character and sterics in ring transformations. The dual halogenation at positions 3 and 5, with an aldehyde ortho to the hydroxy group, gives this molecule an edge in constructing more sophisticated heterocycles or preparing novel coupling partners for cross-coupling reactions. The right starting material makes all the difference, especially in medicinal chemistry, where a positional isomer could set a project back weeks.

    Many alternative suppliers try to push multipurpose “salicylaldehydes” without flagged substitutions, but for critical R&D or routine manufacturing, small changes translate to big problems—lower selectivity, lower yields, and higher purification costs. We engineer our production so that the final aldehyde meets both structure and purity requirements, documented down to trace residual solvents and halide content, as demanded by seasoned professionals.

    Documented, Traceable, Reliable

    From the first order to the tenth, project managers and QC teams ask for reliable paperwork. Manufacturing in-house, we generate a complete record for every lot number, detailing full route of synthesis, analytical confirmation, and all raw material sources. Each drum or small-sample bottle leaves our facility with certifications matching international expectations. Over the years, we have encountered many scenarios—urgent requests for non-standard batches, clarifications required by regulatory agencies, questions about potential impurities in downstream processes. Each situation drives us to clarify, record, and openly communicate every step. When a new team member joins, part of their orientation emphasizes both technical skill and communication, as our clients deserve direct insight into their supply.

    Why End Users Come Back

    Experience shapes our process. Chemists working in scale-up have shown us how a slight impurity in an intermediate like this can dissolve projected savings or even threaten product registration. Analytical chemists have sat with us in our lab, reviewing run-by-run chromatograms and confirming the reproducibility they rely on. It’s humbling to see experienced professionals trust our material for their proprietary syntheses or confidential explorations. Word travels quickly in the chemical world, and we’ve had more than one project leader come to us after burned experiences with unreliable trading partners.

    Some manufacturers focus on making their products look good on paper—impressive “spec sheets” or marketing claims about high yields that fall apart under scrutiny. We take pride not in advertising but in lasting relationships. More than once, a customer’s in-house testing revealed a minute issue with unexpected reactivity; our response always includes root cause analysis, a transparent test report, and if needed, process adjustment downstream. For us, these aren’t setbacks; they are learning moments that push us closer to our own standards.

    Looking Ahead—Continuous Improvement and Innovation

    Chemistry never stands still. New analytical techniques, tighter controls on impurities, and updated environmental guidelines all change how intermediates like 3-Bromo-5-Chlorosalicylaldehyde get made and used. We invest in ongoing R&D with our partners, testing greener halogenation routes and more efficient solvent recovery. Facing regulatory changes in waste handling, our teams experiment with reagent recovery systems and alternative base selection to minimize solvent and byproduct load. Some of the best ideas come not from external consultants, but from line operators and lead chemists responding to tangible needs day by day.

    In the last year, we have expanded automation in batch tracking and sample archiving, making it possible to search for past batches by analytical fingerprints. This has already paid dividends, allowing us to provide rapid support for technical inquiries as well as fast-track responses to customer process optimization requests.

    Safety—A Foundation, Not an Add-on

    Producing halogenated salicylaldehydes brings inherent risks. We built our process from the ground up with risk management as a foundation. Closed feeding, cascade ventilation, and mandatory health monitoring protect our team. We passed up expansion opportunities that would have compromised operator safety or product purity. All waste streams run through onsite removal protocols before outside shipment. Each batch gets flagged not just for performance but for safe handling and minimal environmental impact—because mistakes on either front hurt people and erode trust in the industry.

    Troubleshooting—Serving the Chemist, Not the Invoice

    Problems happen. Sometimes a user calls about unexpected reactivity or a shift in crystal habit. Our technical support links developers directly to production chemists, not just a customer service desk. More than once, feedback from client labs has informed tweaks to purification or packaging—creating better outcomes for those doing the hard work of synthesis instead of simply shifting responsibility. We don’t believe in “acceptable error rates”—quality means every drum or bottle coming off the line meets expectations learned through years of dialogue, not generic targets.

    Service That Complements Chemistry

    A well-made intermediate like 3-Bromo-5-Chlorosalicylaldehyde never works in a vacuum. Project managers often order multiple intermediates for a single research pathway. We coordinate to ensure compatible packaging, batch numbering, and logistics, so nothing slows down the progression from bench to production. As we see more demand for just-in-time delivery or specialized lot customization, our manufacturing flexibility meets these challenges. Direct lines of communication and proximity to key transport routes let us meet timeline demands—eliminating headaches and delays common with split shipments or slow third-party consolidator response times.

    Environmental Responsibility and Compliance

    Salicylaldehyde derivatives face increasing scrutiny from environmental and safety authorities. While meeting these guidelines takes time and investment, we view them as baseline. From solvent recovery to monitoring air emissions, every step leans on the latest technology and operator input. For each kilo of product, we track the associated waste, recovery yield, and emissions. If periodic review reveals an opportunity to reduce water use, switch energy sources, or reclaim additional solvents, we act.

    Our management regularly participates in risk assessment reviews and updates training so that factory practice matches evolving requirements—not just today, but in anticipation of future regulatory shifts. These policies add real cost, but they shield our customers from surprises and align us with those pushing chemistry forward responsibly.

    Feedback and Community—Strengthening Our Practice

    Underlying each success and setback remains one reality: chemistry moves forward through exchange. We never lose sight of the fact that most process improvements, yield upticks, or troubleshooting breakthroughs come after open dialogue with our customers or inspection agencies. We run regular feedback sessions, both with laboratory teams and senior management, to ensure every change is grounded in both technical merit and realized end-user benefit.

    We see our job as ongoing—delivering 3-Bromo-5-Chlorosalicylaldehyde to precise standards and supporting end users before, during, and after each batch moves from our warehouse. Each new application informs how we approach the next production run, the next innovation in purification, and the next round of raw material analysis. Our history with this molecule has shown that quality, flexibility, and transparent technical support remain valued across the entire chemical marketplace.