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Ethyl 4-Hydroxy-3-Methoxybenzoate

    • Product Name Ethyl 4-Hydroxy-3-Methoxybenzoate
    • Alias Ethyl vanillate
    • Einecs 243-266-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    579944

    Chemical Name Ethyl 4-Hydroxy-3-Methoxybenzoate
    Synonyms Ethyl vanillate
    Molecular Formula C10H12O4
    Molecular Weight 196.20 g/mol
    Cas Number 826-99-1
    Appearance White to off-white crystalline powder
    Melting Point 72-76°C
    Solubility Slightly soluble in water, soluble in organic solvents such as ethanol and methanol
    Boiling Point 329.4°C at 760 mmHg
    Density 1.202 g/cm³
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed container
    Smiles CCOC(=O)C1=CC(=C(C=C1)O)OC

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

    Packing & Storage
    Packing Ethyl 4-Hydroxy-3-Methoxybenzoate, 100g, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping Ethyl 4-Hydroxy-3-Methoxybenzoate is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Standard shipping practices for laboratory chemicals apply, with labels indicating chemical identity and hazard information. The product should be handled and transported by authorized personnel in compliance with regulatory and safety guidelines.
    Storage Ethyl 4-Hydroxy-3-Methoxybenzoate should be stored in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store at room temperature and avoid moisture. Ensure proper labeling and follow standard chemical storage practices to prevent contamination and degradation.
    Application of Ethyl 4-Hydroxy-3-Methoxybenzoate

    Applications of Ethyl 4-Hydroxy-3-Methoxybenzoate in Industrial Manufacturing

    Ethyl 4-Hydroxy-3-Methoxybenzoate serves as a specialty functional ingredient in several regulated industrial sectors. As an original manufacturer, we supply this material meeting strict quality and consistency requirements. Below we detail primary downstream applications, compliance frameworks, validated formulation usage, integration points in customer production lines, and the typical end products incorporating this ingredient.

    1. Pharmaceutical Intermediate Synthesis

    This raw material is widely selected as a key intermediate in manufacturing certain APIs, especially within antipyretic and analgesic drug classes. Downstream pharmaceutical manufacturers introduce this compound during the advanced intermediate formation stage, ensuring the presence of the hydroxy and methoxybenzoate moiety crucial for molecular diversification before target molecule coupling. Process engineers adjust input concentration based on targeted end-product impurity profile control, typically after initial condensation and prior to final coupling or protective group removal. Major pharmaceutical manufacturers rely on consistent quality to maintain reproducibility in batch records.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Parts 210/211 (cGMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monograph standards for intermediates
    • China Pharmacopoeia (ChP) process intermediate guidelines

    Typical usage ratio

    • Employed at 0.6–1.5 molar equivalents relative to the target API precursor; specific loadings vary depending on route and impurity control strategy

    Downstream process integration

    • Added during advanced intermediate coupling in multi-step synthesis lines, usually after esterification or alkylation, and prior to final API formation and purification

    Final product types

    • Pharmaceutical actives for paracetamol and similar antipyretic drugs
    • Intermediate isolates for anti-inflammatory and analgesic agents
    • Bulk intermediates supplied to global API producers

    2. Food Additive Preservative Manufacturing

    Food-grade processing units utilize this compound as a synthesis feedstock for downstream production of certain benzoate-based preservatives. It supports the formation of molecular structures that meet strict migration and purity protocols required in food and beverage applications. Operators integrate the material during the transesterification process where the hydroxy and methoxy groups are essential for yielding aroma-preserving entities or functional preservatives with paediatric beverage compatibility. Addition levels align with end-use tolerance to avoid off-flavor and comply with national food safety frameworks.

    Industry compliance standards

    • GB 2760 National Food Safety Standard for Food Additive Use (China)
    • EU Regulation (EC) No 1333/2008 on food additives
    • FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • HACCP and FSSC 22000 for controlled production environments

    Typical usage ratio

    • Typically 0.1%–0.4% w/w in precursor formulation, adjusted to comply with maximum residue and taste threshold for beverage and syrup bases

    Downstream process integration

    • Introduced during transesterification or direct esterification, prior to distillation and blending into bulk preservative concentrates or flavor bases for food-contact products

    Final product types

    • Benzoate-based preservative concentrates
    • Shelf-life enhancers for soft drinks and juices
    • Flavor-protecting additives for syrups and canned goods

    3. Personal Care and Cosmetics Ingredient Production

    Downstream specialty chemical formulators employ this benzoate derivative as a masking and stabilizing agent during synthesis of personal care ingredient bases. Its functional group compatibility allows for mild antioxidant action and fragrance stability when processed in cream, lotion, or rinse-off surfactant systems. Cosmetic manufacturing teams dose this raw material post-emulsification and before final fragrance or vitamin additive blending to modulate stability and maintain sensory profiles over product shelf-life. All usage and manufacturing steps comply with international safety dossiers and labeling frameworks.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • ASEAN Cosmetic Directive (ACD) guidelines
    • ISO 22716 GMP for Cosmetics
    • US FDA Voluntary Cosmetic Registration Program (VCRP)

    Typical usage ratio

    • Standard formulations contain 0.2–0.8% w/w, with precise levels tuned according to end-product skin compatibility and functional claim validation testing

    Downstream process integration

    • Dosed after oil phase emulsification, before cooling and fragrance addition in continuous mixers or batch tanks

    Final product types

    • Hand and body creams targeting long-term stability
    • Fragrance-masked surfactant blends for shampoos and washes
    • Emulsion-based leave-on conditioners

    4. Polymer Stabilizer and UV Absorber Precursor

    Industrial polymer manufacturers process this compound during masterbatch and stabilizer concentrate production, exploiting its hydroxy and methoxy substitutions for downstream transformation into UV absorber and antioxidant functional agents. Compounders accurately portion the material into the stabilization additive line, where it undergoes reaction with benzotriazole or other aromatic building blocks during extrusion. Personnel monitor input ratios according to polymer matrix type and durability requirements, adhering to extensive consumer safety and packaging contact material standards.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on plastic materials and articles intended to come into contact with food
    • US FDA 21 CFR 177.1520 for olefin polymers
    • REACH Regulation (EC) No 1907/2006—Annex XVII for restricted substances
    • ISO 9001 quality management for industrial additives

    Typical usage ratio

    • Polymer masterbatch formulations typically incorporate 0.05%–0.3% by weight; final dosage refined based on desired photo-stability and migration control in the finished plastic

    Downstream process integration

    • Pre-blended with resin pellets or liquid stabilizer precursor mix prior to extrusion and pelletization; reacted or compounded during twin-screw or high-shear mixing operations

    Final product types

    • UV-stabilized films, bottles, and packaging materials
    • Photo-protection additive concentrates
    • Antioxidant-extended service life polymer components
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    Certification & Compliance
    More Introduction

    Ethyl 4-Hydroxy-3-Methoxybenzoate: Perspective from the Manufacturer’s Floor

    Insight Into Production and Quality

    Ethyl 4-Hydroxy-3-Methoxybenzoate, better recognized by many researchers and industry veterans as ethyl vanillate, has a unique way of connecting practical chemistry with usable solutions. On the plant floor, you can feel its aromatic signature even before you read the batch label—a gentle hint of vanilla, earthier compared to the raw sharpness of straight vanillin. This compound forms when you take vanillic acid and give it an ethyl ester shoulder, making it more soluble in certain organic media and less prone to rapid hydrolysis under ambient conditions.

    From our experience, a tight grip on both the moisture and residual solvent levels during synthesis goes a long way toward achieving a pure, crystalline form. Our batches go through repeated purification until they reach bright white or off-white powder consistency. The model that leaves our warehouse consistently features a purity at or above 99%. Trace impurities, mostly from the starting vanillic acid, never exit the production line without confirmation from chromatographic purity checks. Each kilogram tells its own story on the certificate of analysis.

    Spotlight on Specifications and Process Nuances

    The lab grade we supply fits the complex demands of pharmaceutical intermediates and food fragrance formulators. Molecular weight sits close to 196.18 g/mol. With a melting range typically registering from 76°C to 78°C, you know you’re looking at the right material when the crystals remain solid and reliable in storage, without caking or breakdown under controlled temperature and humidity. Each run keeps a close watch for trace metal contamination, since organic synthesis can drag along unwanted companions if reactor surfaces lose their passivation or if water sources shift seasonally. We install in-line detection for heavy metals and follow up with periodic third-party spectral scans to maintain customer confidence.

    Solubility data stand clear: insoluble in water but freely soluble in ethanol, ether, and chloroform. Some clients drift toward ethyl 4-hydroxy-3-methoxybenzoate expecting it to mix easily into aqueous systems. The unadorned truth—this isn’t its strong suit. Where it shines is in organic phase formulations, oil-based flavor applications, or as a modifier in the synthesis of pharmaceutical derivatives that call for greater lipophilicity.

    Functionality Across Industries: Use Cases On the Ground

    R&D teams favor this ester in the early synthesis stages for active pharmaceutical ingredients. We’ve supported several process scale-ups where its stable ester group resists hydrolytic cleavage during prolonged reactions, outlasting simple vanillic acid derivatives exposed to open air and intermediate washes. In flavors, it brings a subtler profile than bulk vanillin—think of it as lending structure and rounded notes to perfumes and high-end flavoring bases rather than dominating the aroma. Ethyl vanillate has earned a steady place in our specialty chemicals catalog, never reaching the volume of mass-market additives, but consistently attracting orders from customers who seek performance over quantity.

    Cosmetic formulators choose this molecule during trials focused on antioxidants and stabilizers. Working directly with formulation labs, we often walk through stability data, especially as it relates to ester bond integrity in the presence of mild acidifiers or alcohol carriers. Creams and serums with ethyl vanillate keep their olfactory tones more evenly across their shelf life. Function aside, the compound’s gentle aromatic presence improves consumer experience and reduces the need for harsher synthetic perfumes.

    Some customers choose ethyl vanillate as a reference standard in chromatography due to its sharp, reliable peak and minimal tailing. We've learned over years that this molecule holds true in trace analysis, dependable batch-to-batch when synthesized under careful temperature and time monitoring. Many specialty labs reach beyond its common uses to exploit its ester moiety, tweaking the molecule for next-generation antioxidants and anti-microbial agents.

    Putting It Side-By-Side With Other Products

    Molecular tweaks bring choices—our production history spans not just ethyl vanillate, but methyl, propyl, and butyl analogs. These differences matter more in real-world application than on any data sheet. Methyl vanillate might melt at a slightly lower temperature and is often discussed as slightly more volatile. For industries like food flavoring or perfumery, the volatility profile steers the decision. Ethyl vanillate’s extra carbon in the side chain brings a slower evaporation rate, which translates into a longer-lasting aromatic influence and more controlled release.

    Vanillic acid itself, the precursor, dissolves much better in polar solvent bases, but it tends to break down under basic or strong acidic conditions during extended processing. Customers drawing up plans for multilayer formulations or long-reacting synthetic steps have told us they now favor the stability edge of the ethyl ester. For strictly water-based projects, vanillic acid often remains the front-runner—but in everything else, including oil-based systems, ethyl vanillate outpaces it. These fine differences save headaches in mixing, streamline process controls, and support the long-term stability of finished products.

    Vanillin, the well-known cousin, costs less and dominates the sweet or edible aroma segment. Yet, it acts as a strong, rather than nuanced, contributor. Ethyl vanillate answers calls for depth and roundness—where a customer asked us to tune a food-grade chocolate base that didn’t overpower the product, ethyl vanillate performed reliably. Manufacturers working in gourmet or specialty ingredients increasingly return to this molecule based on its performance over time, with fewer product recalls linked to odor fade or instability than with some alternatives.

    Direct Feedback and Onsite Experience

    No webpage or catalog entry can fully transmit the feel you get producing and handling ethyl 4-hydroxy-3-methoxybenzoate in real life. Weight, texture, and aroma tell their own story. Chemists in our facility value its consistency: a lot that clumps or darkens on the shelf rings alarms immediately and prompts a full audit. Anything less than a bright white or slightly cream-colored result gets rerun or adjusted before packaging. These field habits, built over decades, matter more to end-users than lab numbers alone.

    The logistics crew moves it in sealed, food-grade containers with tight nitrogen blankets wherever long storage or ocean freight gets involved. This practice grew out of lessons learned the hard way—on one occasion, improper sealing led to a faint sour undertone in a high-value batch, which failed a critical sensory inspection and never left our warehouse. Since then, even single-batch shipments from small-lot orders use the same protective atmosphere as bulk material. It's not a requirement from local regulations, but the customer feedback has made it a perpetual part of our SOP.

    We invest in training for QC staff about the subtle signs of degradation or contamination—ethereal off-notes, textural differences, or even a faint yellowing under harsh warehouse lighting. Manuals and batch training incorporate these experiential cues, recognizing the skill set required at every step from synthesis to shipment. Many of our repeat clients—some family-run flavor houses, some large-scale contract manufacturers—reference our product by experience, not just code, saying “the ester from your last run kept our chocolate stable through summer storage.”

    Addressing the Demands for Consistency and Safety

    Safety and compliance drive every batch. The team calibrates handling procedures to keep losses below the international average, and nobody relaxes on PPE or ventilation in the plant. While ethyl vanillate generally shows low toxicity, our incoming orders for pharmaceutical or cosmetic grades prompt even tighter control. Dust exposure and cross-contamination risks, especially when switching tank feeds from food- to pharma-grade, require deliberate cleaning cycles and batch labeling, all based on direct process experience facing multi-industry clients.

    We bring traceability to the centerpiece of our supply chain approach. Every drum, from the first weigh-in to the final check before shipment, receives a barcode for instant lot recall and digital access to full QA data going back ten years. Situations have called for investigation of a product’s entire chain of custody, especially where a customer needed to troubleshoot an unexpected odor shift. Our system, built by the operations crew with continuous input from floor staff and IT, allows transparent visibility that builds trust, not just compliance.

    Solutions to Ongoing Challenges and Customer Questions

    Making a stable, high-purity ester at scale means balancing yield with process safety. Over the years, exothermic runaways on esterification lines taught us that temperature must follow the reaction rather than the schedule on paper. Our reactors use dynamic temperature monitoring, logging every spike and dip, creating a knowledge base that shortens future troubleshooting cycles. Clients in pharmaceutical synthesis, working with highly sensitive intermediates, have appreciated our willingness to disclose historical production quirks, transparency that heads off surprises on their end.

    Packaging grows more important as global regulations tighten. We adopt higher-barrier liner materials and design reusable drums for clients with green goals—a move sparked by direct feedback. Food and fragrance manufacturers pressured for tighter environmental controls now prefer our returnable container solutions, which we clean and refill after independent verification. Real progress didn’t come from white papers, but from steady discussion between our logistics and the receiving teams at customer sites, reviewing what failed and what held up across continents and through customs.

    As regulatory lines shift, especially on permitted food additives across different regions, our regulatory affairs team works hand-in-hand with chemists on pilot-scale reformulations. Labels, trace heavy metal levels, and even aroma profiles change at the request of new audits. The documentation process, built into our workflow, responds to the evolving landscape, ensuring nothing gets missed in the translation between paperwork and physical product. Sometimes a minor item on a change control log leads to a reformulation that benefits all downstream users, making compliance less reactive and more proactive.

    Long-Term Value for Formulators and Supply Partners

    The most successful applications for ethyl 4-hydroxy-3-methoxybenzoate come when formulators tap its nuanced properties rather than treat it as a mere substitute. For long-release flavor bases, the slower volatilization stands out. Surveying feedback from gourmet food houses, we see consistent praise for lingering aroma profiles not easily matched by shorter-chain esters. Over the past ten years, bulk buyers from the confectionery industry and functional beverage brands have described extended shelf lives and improved “true-to-formula” flavor delivery weeks after opening.

    In fine fragrance work, creators exploit its stability. Rather than fading or morphing unpleasantly in high-alcohol blends, ethyl vanillate weathers temperature swings and light exposure with more grace than vanillin or its methylated analogs. We run continuous shelf-life assays to keep up with evolving demands and refine additives to suit even more challenging perfumery standards. These hands-on tests produce more meaningful guidance than recycled laboratory data, serving both innovators and legacy producers under the same roof.

    Contract manufacturers, facing unpredictable order sizes and shifting compliance rules, value the predictability from our stable lots. Smaller runs—tailored for specialty labs or regional suppliers—call for a degree of flexibility uncommon among commodity chemical producers. Rather than cut corners, our team tweaks reactor loadings, storage cycles, or even packaging based on direct conversations with client site engineers. This give-and-take drives the continuous improvement loop, ultimately making the compound more useful and reliable year after year.

    Supporting Innovation and Responsible Manufacturing

    Our culture rewards small innovations. When less-experienced operators spot an emerging issue—an unusual color drift, condensation on container walls, aroma change in a sample—management listens, investigates, and shares findings openly with both internal teams and external partners. Over time, this habit reduces near-misses and positions our product as dependable, not just by analysis but by living up to the stories passed along by those who handle it daily.

    Environmental control remains a moving target. We update our solvent recovery and emissions control quarterly, in part because raw material providers rotate their process solvents or change filtration aids. We test new scrubbing technologies and review post-condensation treatments every batch cycle, tracking residual solvent drops where new capture sequences yield cleaner waste streams. These adjustments contribute subtly but significantly to batch purity and lower downstream contamination. In this area, change doesn’t happen for compliance alone, but because experienced hands in production see improvements firsthand.

    Beyond process, we look to incoming material selection to optimize consistency. Building supplier networks that share our standards for quality and traceability makes a difference over the long term. A shift in starting vanillic acid quality can ripple through the process, showing up as solubility differences, mild discoloration, or altered melting points. We invest in direct audits of vendor processes, forging relationships that deliver better starting material batch over batch.

    Customer-Led Adjustments and Shared Learning

    No single use case defines ethyl 4-hydroxy-3-methoxybenzoate entirely. We handle requests ranging from kilogram-scale for reference standards to tons for seasonal flavor cycles. Through direct dialogue, we learn more every season: a batch deemed “perfect” for a European bakery may prove too subtle for an Asian beverage bottler. We hold technical workshops, physically bringing together QC and production teams from both sides to exchange lessons learned, aroma comparison, and application tests under real conditions.

    Adjusting to the needs of food safety regulations keeps everyone on their toes. Not all regions accept the same solvent residues; not every end-user values the same aromatic thresholds. Our routine now includes dual pathways—one for pharmaceutical grades with clinical trial support, another for food-grade that weather multiple state- or country-specific audits. This complexity requires hands-on management, reaffirmed by positive feedback from customers whose products reach shelves with fewer reformulations or regulatory holds.

    We adapt our product based on these shared journeys. An example—years ago, a single batch went out with a barely detectable off-note only detected months later in finished beverage testing. Pulling together the QA, synthesis, and distribution teams, the source traced back to an unexpected shift in a single filtration aid. Rather than cover or reroute, the team updated the entire on-site training sequence and supplier specifications. These real-world learnings inform ongoing improvement, ensuring our ethyl vanillate reaches users at high purity and with the consistent performance we seek in our own formulations.

    Final Thoughts From the Production Line

    Ethyl 4-hydroxy-3-methoxybenzoate serves a broad array of industries, but its true value shows up where attention meets applied experience. From the batch reactor’s hum to the careful analysis in our QC suites, every step reflects a dedication to quality, safety, and adaptability built over years of change. For formulators and technical buyers, this product stands as more than a raw material. It’s a result of collaboration, continuous tuning, and thoughtful feedback from those who rely on consistency, subtlety, and stability—not only on paper, but in every real-world result.