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3-Chloro-2-Hydroxy-Benzaldehyde

    • Product Name 3-Chloro-2-Hydroxy-Benzaldehyde
    • Alias 3-Chloro-2-formylphenol
    • Einecs 243-274-9
    • 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

    545467

    Productname 3-Chloro-2-Hydroxy-Benzaldehyde
    Casnumber 871-28-1
    Molecularformula C7H5ClO2
    Molecularweight 156.57
    Appearance Light yellow to brown crystalline powder
    Meltingpoint 94-96°C
    Boilingpoint 292°C
    Density 1.374 g/cm3
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents (e.g., ethanol)
    Iupacname 3-chloro-2-hydroxybenzaldehyde
    Synonyms 3-Chlorosalicylaldehyde, 2-Hydroxy-3-chlorobenzaldehyde
    Storageconditions Store in a cool, dry, well-ventilated area

    As an accredited 3-Chloro-2-Hydroxy-Benzaldehyde 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 100g of 3-Chloro-2-Hydroxy-Benzaldehyde, sealed with a screw cap and labeled with hazard information.
    Shipping 3-Chloro-2-Hydroxy-Benzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored away from direct sunlight, heat sources, and incompatible materials. Proper labeling and adherence to safety regulations, such as UN codes if applicable, are required during shipping. Handle with care, using appropriate personal protective equipment (PPE).
    Storage 3-Chloro-2-Hydroxy-Benzaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Ensure proper labeling, and handle with gloves and eye protection. Store at room temperature and prevent contact with acids or bases to maintain chemical stability.
    Application of 3-Chloro-2-Hydroxy-Benzaldehyde

    Applications of 3-Chloro-2-Hydroxy-Benzaldehyde in Industrial Manufacturing

    3-Chloro-2-Hydroxy-Benzaldehyde serves as a valuable intermediate in several industrial manufacturing sectors. Its chemical profile and reactivity allow integration into specialized production lines. Below we detail primary downstream applications in regulated industries, outlining compliance demands, standard dosage practices, process steps, and the types of end-products achieved.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers frequently use 3-Chloro-2-Hydroxy-Benzaldehyde in synthesizing advanced intermediates involved in active pharmaceutical ingredient (API) production, particularly for antifungal, antimicrobial, and antihypertensive APIs. By direct condensation or Mannich-type reactions, the material enables precise functionalization at key stages, supporting process control under GMP. The aldehyde group enables various transformations such as the formation of heterocyclic scaffolds crucial for the pharmaceutical profile of the target molecule. Selection of solvent and catalyst systems ensures complete conversion while minimizing by-products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) specifications for related intermediates
    • European Pharmacopoeia (Ph. Eur.) requirements for process materials
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Generally 0.2–0.7 molar equivalent relative to primary amine or starting aromatic precursor, adjusted based on reaction kinetics and impurity control

    Downstream process integration

    • Charged after initial solvent charging and base pre-treatment in stepwise batch or continuous reactors
    • Integrated before reductive amination, cyclization, or hydrolysis where applicable
    • Followed by in-process QC such as HPLC for residual starting material
    • Separated via phase partition or crystallization before conversion to advanced API intermediates

    Final product types

    • Intermediates for triazole antifungal agents (e.g., fluconazole analogues)
    • Pyridine-based antihypertensive drug precursors
    • Intermediate building blocks for cephalosporin derivatives
    • Synthesis intermediates for topical antimicrobial compounds

    2. Agrochemical Synthesis

    In agrochemical active ingredient development, 3-Chloro-2-Hydroxy-Benzaldehyde provides a critical starting point for regioselective synthesis of phenolic and benzimidazole fungicides, as well as acylated herbicides. Experienced process chemists exploit the ortho-hydroxy and chloro functionalities for introducing specific substituents under controlled chlorination, acylation, and condensation conditions. This substrate improves process yields for active molecules used in crop protection, meeting residue and environmental impact requirements set by global authorities.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • OECD Guidelines on Testing of Chemicals (Analytical, Ecotoxicity, Toxicological)
    • Regulation (EC) No 1107/2009 for Plant Protection Products (European Union)
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 0.3–1.1 molar equivalent versus co-reactant, depending on the fungicide or herbicide class and required product selectivity

    Downstream process integration

    • Used following solvent charging and temperature ramp-up in condensation or acylation steps
    • Fed as a limiting reagent to maximize conversion and reduce by-product formation
    • Post-reaction, separated by liquid-liquid extraction or crystallization before downstream coupling
    • Integrated into continuous or batch processing with online GC-MS analysis for in-process control

    Final product types

    • Benzimidazole-based systemic fungicides
    • Phenolate herbicide technical concentrates
    • Intermediate for triazole and imidazole agrochemicals
    • Precursor for anilide-type insecticides

    3. Dye and Pigment Production

    Manufacturers of specialty dyes use 3-Chloro-2-Hydroxy-Benzaldehyde in synthesizing high-stability azo or anthraquinone dyes, particularly those requiring ortho-hydroxy and halogen substituents for improved color fastness and light stability. The compound acts as a key building block for Schiff base formation and diazo coupling, supporting creation of dyes for textile, leather, and plastic applications. Controlled pH and reaction temperature enhance selectivity and hue properties during batch production.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for dye chemicals safety
    • OEKO-TEX® Standard 100 for restricted substances in textile dyes
    • ZDHC MRSL (Manufacturing Restricted Substances List) for consumer safety
    • ISO 105-B02 for color fastness to artificial light

    Typical usage ratio

    • 0.5–0.9 molar equivalent relative to diazotized amine or coupler, adjusted to target dye strength and required purity

    Downstream process integration

    • Introduced into dye synthesis reactor after establishing basic pH
    • Coupled with primary aromatic amines for azo dye formation
    • Precipitation and washing stages applied before drying and standardization
    • Batch or kinetic control using UV-Vis monitoring for endpoint determination

    Final product types

    • Reactive dyes for cotton and cellulose fibers
    • Direct dyes for paper and leather applications
    • Solvent soluble dyes for plastics and coatings
    • Colorants for specialty inkjet and pigment dispersions

    4. Synthesis of Fragrance & Flavor Intermediates

    In fragrance and flavor manufacturing, 3-Chloro-2-Hydroxy-Benzaldehyde supports the synthesis of aromatic aldehyde derivatives blended into aldehydic, spicy, or herbal accord mixtures. Process teams utilize this material for constructing hydroxybenzyl or acetal intermediates, which undergo further etherification, reduction, or acylation for use as captive perfume ingredients or flavor modifiers. The ortho substitution pattern provides high odor intensity and desirable releasing profiles for end consumer products.

    Industry compliance standards

    • IFRA (International Fragrance Association) guidelines for fragrance ingredients
    • European Union Regulation (EC) No 1334/2008 on flavorings
    • Flavor and Extract Manufacturers Association (FEMA) Generally Recognized as Safe (GRAS) standards
    • ISO 9235 for natural aromatics and their derivatives

    Typical usage ratio

    • 0.1–0.5 molar equivalent in stepwise synthesis, frequently adjusted for aldehyde loading based on final product organoleptic profile

    Downstream process integration

    • Fed into acetalization or etherification reaction after catalyst charging
    • Phase separation and filtration apply to isolate target fragrance intermediates
    • Purified via column chromatography or distillation prior to final formulation
    • Blending with other aromatic compounds during masterbatch production

    Final product types

    • Aromatic aldehyde-based fragrance intermediates
    • Hydroxybenzyl acetal ingredients for fine fragrance concentrates
    • Flavor enhancer intermediates for snacks and confectionery
    • Captive perfume raw materials for luxury personal care goods
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    Certification & Compliance
    More Introduction

    3-Chloro-2-Hydroxy-Benzaldehyde: More Than a Raw Material

    Quality Shapes the Product, Not Just the Formula

    Every batch of 3-Chloro-2-Hydroxy-Benzaldehyde rolling out from our reactors tells a story written across years of careful process improvement, analytical diligence, and customer feedback. This compound—known by its CAS number 118-82-1—has woven itself into the fabric of specialty chemical applications, yet it often goes unrecognized outside our industry. For us, though, quality control isn’t just a checklist. With this molecule, trace-level purity and batch-to-batch reproducibility shape the conversation between a successful synthesis and an expensive, time-consuming purification downstream.

    We start with high-purity starting materials and work through an integrated process that keeps contaminants below detectable levels. Each pack leaving our facility meets a purity specification above 99 percent, verified with HPLC and GC-MS. These steps seem routine, but so many chemists have dealt with inconsistent sources—one shipment giving sharp NMR signals and clear colorless product, the next tarnished with isomeric impurities or persistent yellowing. For researchers and plant managers, recognizing a reliable stream of 3-Chloro-2-Hydroxy-Benzaldehyde means less troubleshooting and more productive hours.

    Why Structure Matters in Synthesis

    Most end users need this compound for a reason: the ortho relationship between the aldehyde and hydroxy groups lays the ground for further functionalization. Whether heading toward an API intermediate, an agrochemical, or a specialty dye, the structure dictates selectivity in downstream steps. Hydroxy-benzaldehydes look similar on a spec sheet, but real-world chemistry pulls out their differences. Trying to swap in plain salicylaldehyde or an isomer misses that fine balance; steric effects and electronic influences from the chloro substituent guide selectivity in condensation and coupling reactions, letting researchers cut steps or boost yields.

    We've watched customers struggle after buying “comparable grades” elsewhere, only to find byproducts and reactivity quirks that don’t line up with literature methods. The 3-chloro moiety isn’t a trivial add-on; it’s a steering mechanism for the reaction’s direction. Every time we emphasized this to a process development chemist who thought any hydroxybenzaldehyde would do, we saw their appreciation grow after they optimized reaction times and isolated higher-purity intermediates. The right substitution pattern on the ring unlocks new families of molecules—this is why multinationals often lock down supplier relationships after one successful scale-up.

    Specs Have Real-World Impact

    On paper, a melting point around 97 degrees Celsius or a pale-yellow crystalline form may not sound remarkable, but in practice, these parameters matter. The difference between smooth drying or a sticky, clumping solid can mean wasted man-hours and difficult clean-ups. A regular complaint from some users is inconsistency. If the melting point spreads or the color drifts batch to batch, there may be underlying process noise—maybe unreacted starting material, maybe subtle isomerism. We've learned the hard way that even minor deviations in particle size or purity ripple downstream. Chromatography columns get clogged, solvent requirements shift, and filtration times creep longer.

    Every shift on our plant floor recognizes the cost that comes from inconsistent crystallization or moisture content. Early on, we ran some slow pilot batches that ended in sticky messes in the dryer—a headache that taught us granular control over temperature ramp rates. Today, our finished product pours freely, matches the expected color, resists caking in long-term storage, and dissolves predictably in standard solvents. We’ve spent hundreds of hours tuning those variables. When technical sales teams promise consistent handling and smooth integration, we know exactly what’s behind those words: dozens of operator notes and process tweaks.

    A View from the Synthetic Chemist’s Bench

    Research groups and fine chemical processors use 3-Chloro-2-Hydroxy-Benzaldehyde for more than just its basic reactivity. One core use centers on the preparation of Schiff bases—key ligands for catalysis and coordination chemistry. The ability to direct condensation reactions, employing the ortho hydroxy group in hydrogen bonding or metal coordination, unlocks catalyst structures that just aren’t possible with simpler benzaldehydes. This specificity helps researchers create molecular frameworks for asymmetric catalysis or optical sensing materials.

    We regularly supply material for small exploratory runs—sometimes just tens of grams, sometimes hundreds of kilos for process-scale campaigns. The jump from milligram synthesis to plant-scale implementation reveals a host of practical issues that specs alone don’t address. Particle flow characteristics, odor, color stability, and even glassware compatibility crop up. By working directly with synthetic chemists at scale-up, we’ve learned which subtle attributes shape a compound’s real-world utility. Several of our customers—especially those in university settings—raised these points during collaborative trouble-shooting, spurring us to batch-test new drying and sieving methods.

    The most revealing conversations with R&D teams often revolve around how seemingly minor impurities—like residual chlorinated byproducts or trace metals—wreck the yields of downstream steps. By ramping up our purification regime and applying extra attention to raw material sourcing, we’ve achieved purity standards that keep our clients’ projects progressing smoothly. Technical support often means explaining those real-world side effects of what look like “trivial” differences in a certificate of analysis.

    Scale and Cost: The Unseen Complexities

    Some new entrants to the field underestimate what happens between kilo-lab prep and commercial-scale manufacture. Building a flexible supply chain for 3-Chloro-2-Hydroxy-Benzaldehyde means managing not just reactors and dryers, but upstream precursors, waste disposal, and analytical compliance. The market for this chemical ebbs and flows based on seasonal agrochemical demand and evolving pharmaceutical pipelines. Predicting these swings lets us maintain stable inventory without overextending or falling behind.

    On the factory floor, cost control doesn’t happen in a spreadsheet. It comes from solvent recycling, energy optimization, and tight wastewater management—one slip can wipe out margins or hit compliance certifications. Investment in automation, in-line analytics, and operator training pays unexpected dividends. We’ve seen how legacy equipment or sliding standards at other plants directly impact users: specs slip, yields sag, repeat business evaporates.

    Comparison to Similar Chemicals: The Myth of Interchangeability

    We sometimes get inquiries: why not just substitute with 2-chlorobenzaldehyde, or try salicylaldehyde? The answer, learned through years of customer collaboration, is that molecular detail drives downstream performance. The presence and location of the hydroxy and chloro groups set up unique reactivity patterns for nucleophilic substitutions, acylations, or condensation routes. Tweaking just one substituent can radically alter a compound’s electron density and spatial orientation—shifts that mean the difference between a clean conversion and a tangle of side reactions.

    A few clients have experimented by changing to cheaper isomers, chasing savings in raw material costs. To date, none of these repeats have lasted. The intangible costs—more purification work, delayed product launches, compromised material properties—soon outweigh initial savings. There’s value in learning from a test batch gone wrong, but even more in building a relationship with a producer who takes those notes to inform process optimization. Striking the right chord between price, performance, and application-specific attributes comes from ongoing dialogue, not generic substitutions.

    Usage: Serving Innovation Across Sectors

    In real-world production, 3-Chloro-2-Hydroxy-Benzaldehyde makes its mark in diverse areas. Pharmaceutical companies often specify it as a starting material for heterocyclic scaffolds—particularly where the presence of both a halogen and a hydroxy group is critical for further functionalization. Our contacts in crop protection chemistry use it in the synthesis of selective herbicides or fungicidal agents. In performance materials, requests come in for dye intermediates needing the unique substitution pattern provided by this chemical. Even in academic labs, teams value having a highly-characterized building block—one that can be trusted in new synthetic methodology development or molecular design.

    We’ve supported both mature and startup companies as they race to develop new bioactive molecules, collaborating as novel synthesis targets present fresh challenges. When a client adjusts a route mid-development, needing a rush of kilogram scales to verify a new concept, our ability to increase production rapidly—and to document traceability from batch to batch—offers peace of mind. In the last few years, several early-stage pharma projects would have missed critical milestones without our ability to maintain quality, adapt scheduling, and communicate technical detail in real time.

    Beyond the Bottle: ESG, Regulatory, and Safety

    Shifting expectations around environmental stewardship shape how we operate. Waste management, solvent recycling, and responsible sourcing aren’t just marketing phrases. Our plant applies multi-stage treatment for chlorinated waste streams, and our procurement team regularly reviews upstream supplier practices. Local, national, and international regulations for hazardous substances demand precise tracking, documentation, and risk assessment—not just at the shipping stage, but across the whole production lineage.

    Within the team, we reinforce the value of proper handling and exposure controls. The aldehyde functional group presents recognized hazards, so training doesn’t stop at PPE selection—it extends to ventilation design, spill response preparation, and regular medical monitoring for technical staff. Transparent reporting of safety incidents, near misses, and process deviations builds a culture of learning and improvement. Regulatory bodies expect this, but in practice, the habit of double-checking lines and monitoring reactor parameters catches most incidents before they become problems.

    Reach and GHS compliance come as standard expectations from clients worldwide. Our in-house regulatory specialists manage documentation to ease import and use in a range of jurisdictions. Shifts in US, EU, and Asian regulatory frameworks often ripple into new testing regimes or data requirements with little notice. By focusing on strong supplier management and cross-disciplinary expertise, we keep pace without falling behind on documented compliance.

    Innovation at the Manufacturer’s Bench

    While the core method for producing 3-Chloro-2-Hydroxy-Benzaldehyde remains fundamentally unchanged, small improvements constantly arise from plant-floor insight and customer feedback. One recurring area is process safety: as more automation enters our reactors, exotherm control and online analyzers catch runaway reactions early, boost operational safety, and cut production interruptions. Leveraging digital monitoring tools, real-time spectrometric feedback, and advanced process simulation, we’ve brought both energy costs and emissions down over the past production cycles.

    Occasionally, we develop tailored grades with ultra-low residual solvents or special particle size distributions—especially for customers needing material in single-use pharma, electronics, or tightly controlled API syntheses. These efforts aren’t standardized; they stem from repeated troubleshooting with users working at the sharp edge of their own product development. Some breakthroughs come from re-listening to complaints about a persistent off-color or slow dissolution, prompting tweaks in our drying equipment or a pilot run of a different crystallization solvent. Every improvement here feeds back into our “regular” quality, raising the game for all.

    Open Dialogue with Users

    Over the years, our door has stayed open to clients—not just through formal visits or annual audits, but via quick calls, process troubleshooting sessions, and on-site plant tours. Most improvements come from these real-world discussions: the QC analyst with a tricky spot test, the operations chemist seeing a filtration slowing down, the project manager working late to resolve an unexpected yield loss. Their concerns get fed straight back into our process: a subtle tweak in cooling rate, a new filtration aid, an adjustment in time between crystallization and drying.

    Questions about handling, application, or troubleshooting find ready answers from a team that knows the chemistry inside and out. While the product itself represents just one link in a complex supply chain, our role as manufacturer gives us a front-row seat to the realities facing innovation-driven teams. For some users, a seemingly minor characteristic—like glass transition temperature or UV spectrum detail—becomes the hinge point for a successful patent application or product registration. By building these partnerships, we move beyond simply selling a chemical; we help smooth the route from bench to market.

    The Case for Experience in Chemical Production

    Ultimately, the difference between generic chemical supply and dedicated manufacturing shows in real-world outcomes. Shipments arrive on time, batches behave as expected, and process changes don’t bring fresh surprises. For 3-Chloro-2-Hydroxy-Benzaldehyde, that means more than just hitting standard specs. It means supporting teams through changing project needs, maintaining clear technical communication, and learning from every cycle, every near-miss, and every scaling experiment. Where traders and third parties focus on moving tonnage, we focus on mastering the subtleties of production, compliance, adaptation, and partnership.

    With users across pharma, agrochemicals, and specialty chemicals competing to innovate, every raw material purchase represents a leap of faith. We’ve spent years working to ensure that leap rests on solid ground—repeatable process performance, deep chemical insight, and open feedback channels with the people for whom this compound is often just a single but critical building block in a much larger project. The value of experience runs deep at the production bench and reaches forward into every application, every experiment, and every new idea it supports.