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Ethyl 3,5-Dichloro-4-Hydroxybenzoate

    • Product Name Ethyl 3,5-Dichloro-4-Hydroxybenzoate
    • Alias Ethyl 3,5-dichloro-4-hydroxybenzoate
    • Einecs 259-451-5
    • 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

    409280

    Chemical Name Ethyl 3,5-Dichloro-4-Hydroxybenzoate
    Molecular Formula C9H8Cl2O3
    Molecular Weight 235.07 g/mol
    Cas Number 19748-63-5
    Appearance White to off-white crystalline powder
    Melting Point 123-126 °C
    Solubility In Water Low
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms Ethyl 3,5-dichloro-4-hydroxybenzoate; 3,5-Dichloro-4-Hydroxybenzoic Acid Ethyl Ester
    Smiles CCOC(=O)C1=CC(=C(C=C1Cl)O)Cl

    As an accredited Ethyl 3,5-Dichloro-4-Hydroxybenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical Ethyl 3,5-Dichloro-4-Hydroxybenzoate is packaged in a 100g amber glass bottle with a secure screw cap.
    Shipping Ethyl 3,5-Dichloro-4-Hydroxybenzoate is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazard regulations. It is handled as a chemical substance and typically transported by ground or air with standard safety precautions, ensuring compliance with relevant shipping and handling guidelines for laboratory chemicals.
    Storage **Ethyl 3,5-Dichloro-4-Hydroxybenzoate** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from light and moisture. Ensure proper labeling and keep away from food and drink. Only trained personnel should handle and access the storage area.
    Application of Ethyl 3,5-Dichloro-4-Hydroxybenzoate

    Applications of Ethyl 3,5-Dichloro-4-Hydroxybenzoate in Industrial Manufacturing

    Ethyl 3,5-Dichloro-4-Hydroxybenzoate supports several specialized segments of chemical manufacturing, serving as a vital intermediate for the synthesis of sophisticated products in pharmaceuticals, agrochemicals, and polymer additives. As an original manufacturer, we ensure that raw material integration aligns with stringent industry demands, detailed compliance parameters, and precise application protocols in downstream operations.

    1. Pharmaceutical Synthesis: Intermediate for Antimicrobial APIs

    This compound functions as a core building block in the synthesis of certain antimicrobial active pharmaceutical ingredients (APIs), particularly for developing narrow-spectrum agents targeting resistant bacterial strains. Process chemists use it in multi-step synthesis routes, typically for downstream sulfonation or further aromatic substitution. Material integrity and trace impurities directly influence final API purity and compliance with drug regulations.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) relevant monographs
    • European Pharmacopoeia (Ph. Eur.) general chapters
    • FDA cGMP CFR21 parts 210/211 for finished drugs

    Typical usage ratio

    • Applied at 1.2–1.6 molar equivalents relative to the downstream core structure, commonly 8–20% w/w by step depending on reaction yield and target batch size; stoichiometry is adjusted to minimize byproduct formation.

    Downstream process integration

    • Material is introduced as a key intermediate during the early-stage condensation or acylation reaction in the API synthesis train, subjected to further derivatization (e.g., ester hydrolysis, halogenation).

    Final product types

    • Bulk antimicrobial intermediates
    • Narrow-spectrum antibacterial APIs
    • Controlled-release pharmaceutical actives

    2. Agrochemical Active Ingredient Building Block

    Ethyl 3,5-Dichloro-4-Hydroxybenzoate serves as a targeted intermediate in the synthesis of selective herbicide ingredients and fungicide scaffolds. Its dichloro-phenol framework enables specific binding affinity and improved photostability in downstream molecules. Agrochemical formulators depend on its purity profile to meet regional pesticide regulations and product registration guidelines.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • European Regulation (EC) No 1107/2009 on plant protection products
    • US EPA FIFRA regulations for pesticide actives
    • ISO 9001:2015 for agrochemical manufacturing

    Typical usage ratio

    • Incorporation in the range of 5–12% w/w in the synthesis batch, adjusted according to the desired active ingredient’s substitution pattern and downstream coupling efficiency.

    Downstream process integration

    • Material enters as a coupling substrate in the targeted chlorination and ring modification processes, followed by formulation into technical concentrate or finished bulk active.

    Final product types

    • Selectivity-driven herbicide technicals
    • Broad-spectrum fungicide precursors
    • Seed treatment compositions

    3. Polymer Additives: UV-Absorber and Stabilizer Intermediate

    The compound acts as an intermediate in producing UV-absorbing stabilizers incorporated into high-performance engineering plastics. Its chlorinated hydroxybenzoate motif contributes to multi-wavelength UV stabilization when introduced into aryl ester-based additives. Manufacturers rely on this input for masterbatch and direct compounding processes to preserve material durability and meet regulatory standards for consumer or electrical products.

    Industry compliance standards

    • REACH (EC No 1907/2006) registration for polymer additives
    • RoHS compliance for electrical and electronic applications
    • Food Contact Regulation (EU) No 10/2011 for plastics (if applicable to the downstream product)
    • ISO 14001 for environmental management in chemical processing

    Typical usage ratio

    • Typically introduced at 0.1–1.5% w/w in stabilizer additive synthesis; the exact level is defined by polymer matrix compatibility and required UV protection threshold.

    Downstream process integration

    • Enters at the intermediate synthesis stage of UV-absorber production, with subsequent integration into compounding or extrusion steps for final polymer formulations.

    Final product types

    • UV-protective masterbatch pellets
    • Modified engineering thermoplastics
    • Weather-resistant outdoor polymer components

    4. Specialty Chemical Synthesis: Laboratory Reagent Production

    This molecule is employed in synthesizing reference reagents for chemical analysis and custom standards for regulatory laboratories. Its distinctive substitution enables precise analytical calibration, particularly for quality control in pharmaceutical and environmental testing laboratories. Traceability and batch homogeneity are priority considerations in downstream blending.

    Industry compliance standards

    • ISO/IEC 17025 for calibration laboratory competence
    • OECD guidelines for chemical testing standards
    • USP Reference Standards applicable to analytical reagents
    • ISO 9001 for reagent production quality systems

    Typical usage ratio

    • Precision formulation at 0.05–0.30% w/w in reference blend solutions or as specified by analytical protocol, with adjustment based on instrument performance characteristics.

    Downstream process integration

    • Incorporation at the blending and calibration stage, followed by aliquoting, packaging, and validation for laboratory use.

    Final product types

    • Chemical reference standards
    • Custom analytical reagent kits
    • QC bench solutions for pharmaceutical and environmental testing
    Free Quote

    Competitive Ethyl 3,5-Dichloro-4-Hydroxybenzoate prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Ethyl 3,5-Dichloro-4-Hydroxybenzoate: A Closer Look from the Manufacturer’s Bench

    At our plant, every batch of Ethyl 3,5-Dichloro-4-Hydroxybenzoate passes through a hands-on journey. We’ve watched this compound earn appreciation from researchers and industrial groups, thanks to its sturdy structure and versatile chemistry. Over years of production, the feedback from formulation teams and lab users has guided our understanding well beyond chemistry handbooks.

    What We Produce: Reliable Chemistry, Every Batch

    Ethyl 3,5-Dichloro-4-Hydroxybenzoate, which some know under alternate names in literature, delivers a balance of two chlorine atoms and a hydroxy group on a benzoate scaffold. Our most requested grade comes in crystalline form, clear and free-flowing, built for consistent performance in downstream synthesis and formulation work. We keep tight reins on purity, driving it up to 99% or better, and offer our standard lot size based on direct communication with many regular clients.

    From the ground up, we’ve built our process to avoid batch-to-batch surprises. Every worker knows that even a slight shift in temperature or solvent choice changes how the product crystallizes. Over time, our shifts have learned to rely less on automation’s promises and more on a keen set of eyes and simple spot checks. When our customer calls about an off-color or faint impurity, our teams huddle at the reactor, retrace each prep step, and solve the root cause. Some see chemistry as a black box; we open ours wide and get our hands dirty.

    How This Molecule Fits

    We understand that not every lab project needs the same benzoate derivative. Ethyl 3,5-Dichloro-4-Hydroxybenzoate holds a particular niche in synthesis work, especially for those exploring the boundaries of antimicrobial and pharmaceutical research. Our clients often highlight how its substitution pattern enables them to build out libraries of analogues—targets their screens demand—and our role becomes making enough, with enough clarity, to let their science move without slowdown.

    Production teams sometimes field questions about why chemists favor this variant over, say, a methyl or propyl ester or a version with only single chlorine substitution. The answer lies in how those chlorines at the 3 and 5 positions alter reactivity. They change electron density, impacting how the molecule reacts with nucleophiles or forms further bond linkages. Our own R&D explored the difference in reaction rates, finding the dichloro pattern boosts selectivity in some acylation and alkylation steps where single substitutions falter.

    What We See in Customer Use

    Pharmaceutical researchers come to us with a need: a consistent intermediate or starting point for their own molecule-building, often for lead discovery or advanced screening. One group from an overseas lab described how slight changes in the impurity profile—barely 0.2% by HPLC—could throw off their cellular assay. Direct feedback like this has prompted us to upgrade our purification steps, adding an extra charcoal polish before the final recrystallization. We learned early on that what remains unseen in the product matters as much as the main component.

    Other customers operate outside pharma: agrochemical development, protective coatings, or even specialty plastics. Here, Ethyl 3,5-Dichloro-4-Hydroxybenzoate becomes a building block rather than an end product. In these settings, process engineers tend to care about particle size, flowability, or insoluble residues. We once had a complaint about batch clumping in high summer humidity; this drove us to test new drying regimes and anti-caking measures. Not all improvements start on paper—many rise from real pouring, blending, and shipping.

    Differences That Matter: Comparing Benzoate Options

    Why do research teams select this compound over comparable esters or derivatives? Much comes down to the unique interplay of reactivity and solubility. The ethyl chain is long enough to help with organic solubility, yet not so bulky as to hinder reactivity at the aromatic core. Over dozens of application feedback sessions, research chemists shared that going longer—say, to n-propyl or butyl—reduces the ease with which they can react the compound in polar aprotic solvents. On the flip side, many claimed methyl esters sometimes introduce volatility or hydrolysis issues they don’t see with the ethyl ester.

    Beyond the ester tail, the arrangement of chlorines makes a difference. A mono-chlorinated hydroxybenzoate misses out on the precise electron-withdrawing pattern. Chemists advise that the dichloro version enables specific site-selective reactions, opening up pathways in complex molecule synthesis that single-chlorine analogues cannot match.

    For users stuck between methyl, ethyl, and higher esters or considering halogen patterns, our advice always flows from real-world stories and collaborative troubleshooting. Some customers run parallel tests, report back yields and product cleanliness, then lock in their choice for scale-up. This back-and-forth improves our process too, as we note which reaction steps most benefit from our molecule’s specific substitution.

    Manufacturing Benchmarks and Quality Metrics

    Over years at the reactor line, we’ve pushed to build-in reliability, not just chase after it. Our NMR and chromatographic data draw a consistent signature: the dichloro peaks on the aromatic ring and a single sharp hydroxy resonance. We scan for trace related compounds after each batch, running regular checks with liquid chromatography and confirming identity by matching against authenticated standards.

    The biggest production hurdle came early on: de-chlorination side reactions, which could creep in with sloppy timing or oxygen exposure. After much trial and error, we identified reliable conditions and trained our operators to spot telltale color changes or faint off-odors that forecast a problematic run. The result: fewer lost yields, fewer returns, and happier end users.

    Safe Handling from Experience

    Safe plant operation requires more than compliance. Those who handle kilos all day prefer easy-to-transfer material, low dust, and clear odor signals. We tested several packaging types to ensure the product leaves our gate in stable condition, resisting caking or powdering during storage and transport—no small feat in tropical or arid regions. Some clients store for months prior to use; we share real shelf-life data drawn from retention studies, not just numbers from literature. This transparency means fewer headaches downstream.

    Operators and users ask about compatibility with standard solvents, acids, and bases. Over time we’ve seen Ethyl 3,5-Dichloro-4-Hydroxybenzoate stand up well in most organic solvents, but not every lot behaves the same in aggressive alkaline conditions. We keep a catalog of solvent-resistance notes, updated after batch failures or unexpected precipitation in client trials. Sharing these details shortens problem-solving cycles for those who rely on us.

    Supporting the Whole R&D Pathway

    Our experience shows this isn’t a one-and-done product: it moves alongside users through ideation, pilot, and scale. Projects often pivot midway, needing extra supply at short notice or slightly altered specifications. One year we tweaked the drying protocol for a veterinary research group, then re-tuned the recrystallization for a cosmetic developer running high-resolution purity checks. By staying flexible, we keep up with shifting project goals, and by keeping records of these modifications, we support repeatable success.

    Communication with formulation chemists matters as much as HPLC data. One user group reported a problem with downstream dimer formation affecting their analytics. A few phone calls with their quality team brought the issue to our attention, and we jointly identified a trace fatty acid impurity as the culprit. Collaborative problem-solving like this does more to build lasting partnerships than flashy marketing.

    Adaptation: Not Just a Buzzword

    Spring and fall bring different challenges in our region. Humidity shifts, power flickers, and raw material quality can all intrude on what should be a smooth campaign. When purification steps falter, we retrain operators in real time and adjust timelines up front. Working in close tandem with end users, we often maintain a buffer supply to absorb sudden project surges or seasonal delays. Real relationships sustain us through market cycles and supply hiccups.

    Supply chains move faster today, but that increases risk of mishandled cargo or improper storage. We track weather on transport routes and update packaging as real-world problems crop up—sometimes with a simple liner switch, sometimes with reinforced drums. Client stories filter back, fueling our next round of process tweaks.

    Transparency Over Hype

    We skip the glossy claims; our clients want hard numbers, root-cause discussions, and fast information flow. When a product outperforms others, it’s usually because of specific synthons, impurity management, or a tweak in drying conditions. Our teams engage directly with clients, not through layers of distributors, so questions get honest answers from those who stand by the product every day.

    Mistakes happen—a missed timeline, a specification gap, an unflagged trace impurity. Real accountability means facing issues, learning from them, and rolling improvements into the next batch, never hiding behind paperwork or industry jargon. Over years, it’s the willingness to discuss problems openly that keeps projects on track and relationships productive.

    Why Buyers Return

    Once users gain confidence in a chemical’s performance and in the reliability of the supplier, they rarely switch unless forced. We spend as much effort building trust as we do refining production. Our support teams handle nuanced questions daily, drawing not on scripts but on hard-won experience from our own batches.

    The most loyal clients learn over time how we respond under pressure. Those who switched after testing cheaper substitutes found their work slowed by purity drifts or shipping lags. We earned our place not by chasing every contract, but by supporting researchers, procurement officers, and plant teams through thick and thin.

    What Changes: New Projects and Next Steps

    Demand for Ethyl 3,5-Dichloro-4-Hydroxybenzoate keeps us alert to changes outside our gates. Clients push into new applications—sometimes combining it with novel catalysts, sometimes folding it into large molecule libraries for industrial screening campaigns. We receive regular requests for slightly modified grades: higher or lower moisture, narrower particle size, or customized impurity profiles. Each request triggers a joint review with our technical group, balancing costs, feasibility, and client needs.

    Emerging regulations have prompted tighter tracking and stricter quality confirmation. We’ve updated protocols for documentation, traceability, and rapid response to compliance inquiries. By staying transparent about changes and rapid to share updated safety or analysis data, we keep our products moving confidently across borders and application sectors.

    Summing Up the Manufacturer’s Perspective

    Ethyl 3,5-Dichloro-4-Hydroxybenzoate occupies a precise, valuable spot in chemical production—not because of a magic formula or lucky branding, but for tangible, verifiable reasons. Its substitution pattern lines up with real-world application needs, and year after year, our approach to cleanliness, communication, and process flexibility brings new clients and keeps old ones close.

    Every improvement reflects collaboration with those who use our chemicals every day. Whether solving a bench-scale bottleneck or scaling up a commercial campaign, we treat every lot like it will end up in our partner’s critical path. Through steady adaptation and open dialogue, we deliver a product line that bears out our commitment in performance, delivery, and support.