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Methyl 3-(4-Hydroxyphenyl)Propionate

    • Product Name Methyl 3-(4-Hydroxyphenyl)Propionate
    • Alias MHPP
    • Einecs 241-777-0
    • 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

    368285

    Productname Methyl 3-(4-Hydroxyphenyl)Propionate
    Casnumber 3795-52-2
    Molecularformula C10H12O3
    Molecularweight 180.20 g/mol
    Appearance White to off-white solid
    Meltingpoint 73-77 °C
    Boilingpoint 338.6 °C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC(=O)CCc1ccc(O)cc1
    Inchi InChI=1S/C10H12O3/c1-13-10(12)6-5-8-2-4-9(11)7-3-8/h2-4,7,11H,5-6H2,1H3
    Refractiveindex 1.523 (predicted)
    Storageconditions Store at 2-8 °C, keep container tightly closed

    As an accredited Methyl 3-(4-Hydroxyphenyl)Propionate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, with tamper-evident screw cap; white label detailing chemical name, formula, batch number, hazards, and supplier.
    Shipping Methyl 3-(4-Hydroxyphenyl)propionate is shipped in tightly sealed containers to prevent moisture and air exposure. It should be transported at ambient temperature, away from direct sunlight and incompatible materials. Proper labeling and documentation are required, adhering to local and international regulations for chemical handling and transportation to ensure safety and compliance.
    Storage Methyl 3-(4-Hydroxyphenyl)propionate should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15-25°C). Store away from oxidizing agents and strong acids. Ensure proper labeling and limit exposure to air to prevent degradation or contamination.
    Application of Methyl 3-(4-Hydroxyphenyl)Propionate

    Applications of Methyl 3-(4-Hydroxyphenyl)Propionate in Industrial Manufacturing

    Methyl 3-(4-Hydroxyphenyl)propionate serves as a critical intermediate in a variety of specialized sectors, enabling high-value manufacturing across pharmaceutical, fine chemical, fragrance, and specialty polymer industries. As an integrated producer, we focus on strict process control and compliance at every step, supporting advanced formulations by leading global companies.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

    Major pharmaceutical manufacturers use this compound for synthesis of selective NSAID actives, especially compounds built on hydroxyphenylpropionic acid frameworks. Controlled process conditions ensure the stability and purity required for downstream ester hydrolysis, amide coupling, and cyclization steps. Batch traceability and impurity profiling comply with health authority requirements from raw material intake to finished API output.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (for finished dose-drug manufacturing)
    • European Pharmacopoeia (Ph. Eur.) raw material monographs
    • Chinese Pharmacopoeia (ChP) relevant raw material specifications

    Typical usage ratio

    • Typically 0.95 to 1.1 molar equivalents in initial coupling reactions; precise ratio set according to the target API molecule and side-reaction controls

    Downstream process integration

    • Introduced during early-stage intermediate synthesis, followed by hydrolysis or amidation
    • Subject to in-line chromatography and QC for purity before further transformations
    • Supports subsequent cyclization and functional group modifications in multi-step API synthesis

    Final product types

    • Non-steroidal anti-inflammatory drug APIs (e.g., Flurbiprofen analogs)
    • Metabolite reference standards
    • Pharmaceutical research intermediates

    2. Fragrance Ester Precursor in Fine Aroma Chemicals

    Fragrance compound producers employ this material as a building block for synthesis of specialty esters in fine aroma applications. Its hydroxy functional group enables selective etherification and oxidation steps, leading to fruity, floral, or green note esters. Process steps require tight feedstock qualification to support reproducible product aroma profiles and batch consistency for global fragrance market requirements.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards and Guidelines
    • EU Regulation (EC) No. 1223/2009 (cosmetics and fragrance compositions)
    • IFRA Transparency List for Ingredients
    • US Food Chemicals Codex (FCC) – for relevant aroma ingredient purity

    Typical usage ratio

    • Ranges between 2% and 20% by mass in esterification batches, depending on the target ester’s volatility and olfactory intensity

    Downstream process integration

    • Fed into batch reactors with alcohol or acid co-reactants under controlled catalytic conditions
    • Purified via vacuum distillation prior to blending in fragrance bases
    • QC sampling by GC-MS to verify aroma profile at each step

    Final product types

    • Specialty aroma esters for perfumery
    • Flavor ingredients for luxury personal care and home care
    • Custom fragrance intermediates for premium scented consumer goods

    3. Polymer Additive for High-Performance Polyesters

    Advanced polymer compounders use this product as a functional monomer or chain modifier when formulating specialty polyesters with improved mechanical and thermal properties. Its phenolic content enhances polymer stability and provides opportunities for tailored polymer architectures in demanding industrial or electronic applications. Analytical controls verify monomer reactivity before melt or solution polymerization steps.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for industrial raw materials
    • RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU for electronics applications
    • EN 15343:2007 (plastics traceability and chain of custody) for recycled content compliance where applicable

    Typical usage ratio

    • Typically 0.5% to 5% by weight as a comonomer; rationing adjusted to achieve targeted glass transition temperature or hydrolytic stability

    Downstream process integration

    • Added directly to melt-phase or solution-phase polyesterification lines
    • Incorporated during chain extension or end-capping stages in copolymer design
    • Ensures compatibility with flame retardant or antistatic masterbatches

    Final product types

    • Engineering polyesters for automotive or electronic housings
    • Modified PET for specialty film and fiber applications
    • Polymer resins used in composite laminates or 3D printing

    4. Intermediate for Synthesis of Light Stabilizers in Coatings

    Producers of advanced coating additives select this hydroxyphenyl compound as a precursor in manufacturing ultraviolet (UV) light stabilizers, particularly hindered amine light stabilizers (HALS) and related phenolic antioxidants. Carefully monitored reaction conditions determine the structure-property outcomes needed to meet weathering resistance criteria in architectural, automotive, and industrial coatings.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical processing
    • ASTM D5201: Standard Practice for UV Degradation of Coating Additives
    • REACH (EC 1907/2006) registration for downstream additive safety
    • EPA TSCA Inventory Listing for US market entry

    Typical usage ratio

    • Usually 3% to 12% relative to total additive batch mass, adjusted to achieve desired lightfastness in target coatings formulation

    Downstream process integration

    • Introduced during multi-step synthesis of HALS compounds via ester-amide formation and subsequent functionalization
    • Subjected to thermal stress tests and UV exposure in formulated coatings
    • Ensures constant impurity profiles with every production lot

    Final product types

    • Light stabilizer concentrates for automotive OEM topcoats
    • Additive masterbatches for exterior architectural paints
    • UV-resistant clear and pigmented industrial coatings
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    Certification & Compliance
    More Introduction

    Methyl 3-(4-Hydroxyphenyl)Propionate: Reliable Quality Rooted in Real Production

    The Manufacturer’s Perspective on Consistency, Function, and Value

    Every batch of Methyl 3-(4-Hydroxyphenyl)Propionate coming off our production line reflects thousands of hours of team fine-tuning and decades working with the subtle differences that shape chemical outcomes. Down on the plant floor, you quickly learn that real quality stands in the small details—how clean your reactors run, how much solvent you recover, how carefully you segment reaction stages. These things matter more than the bold claims sketched on most datasheets.

    This compound, sometimes called MHPP, delivers far more than numbers on a table. Its backbone—a propionate side chain attached to a hydroxy-substituted phenyl ring—gives it a profile prized by fragrance chemists, pharmaceutical developers, and resin formulating teams alike. The presence of both an ester and a para-hydroxy group opens up routes for further derivatization, letting clients steer it toward the specific end-uses they need. But real-world usability rarely rests only with a chemical’s paperwork; consistency and purity set the tone for a manufacturer’s reputation.

    Batch Quality: Batch After Batch

    We live inside our reactors as much as in our offices. Temperature ramp rates, solvent recovery, and cleaning routines decide how a batch will turn out. Minor shifts—say, a five-minute difference in acid quench or a modest uptick in water content—show up later as yield losses or impurity levels that nag even before QC checks flag them. That’s why our process doesn’t rely just on final analytics. We measure in-process at every key stage, not to chase an abstract ideal, but because it makes the difference between a gram and a kilogram scaling smoothly.

    Say a client tunes their process to take a certain melting point and color index. If a batch wanders from the set route, that’s not just paperwork out of spec—someone wastes time, labor, and raw material having to troubleshoot. Modern pharmaceutical and specialty chemical plants work on tight windows. Out-of-range MHPP cascades downstream, tying up filtration lines, causing off-odors, or changing reaction times for the next step. Reliable production rests on not letting those little things pile up.

    Product Model and Practical Specifications

    Over the years, we developed several process routes using different catalysts and solvents to produce MHPP. The route we stick with uses a Friedel-Crafts alkylation, followed by specific purification stages and careful esterification. Some manufacturers shortcut these, leading to colored product or hard-to-remove side-reactants. We patrol for those, since a slightly yellow product signals trace iron or oxidized byproduct, which throws off downstream hydrogenations or coupling reactions.

    Our typical MHPP comes as a white crystalline powder. Purity on a dry, as-is basis stays above 99.5%, confirmed by HPLC and NMR. The melting range needs to aim narrow, usually centered near 104–106°C; a wider or lower range reports unreacted starting material or moisture taken up in storage. We don’t just shoot for SOP targets—we compare batch-to-batch using archived samples, so shifts in spectral purity or particle size distribution tell us if the process drifts.

    Aromatic contaminants and trace metal levels stay low, since high-purity MHPP supports sensitive reactions. Water content runs below 0.2% as checked by Karl Fischer titration. Any higher, and clients using it in moisture-sensitive couplings quickly notice inconsistent performance and may even see precipitates or sticky residues.

    Applications Shaped by End-User Feedback

    Clients approach us from different walks—fragrance houses seeking musky, sweet-woody nuances; pharmaceutical labs tailoring it as a key intermediate for beta-blocker synthesis; coating specialists looking for tough, flexible resins. Each group brings its own pain points. Fragrance chemists tell us even slight impurities show up as off-notes. Drug researchers highlight how variability in melting behavior throws off precise reaction times. Resin producers, often working in bulk, hunt for consistent batch size and flow—clogged lines cost them days, not hours.

    By talking directly with these teams, we learn what matters most. Some require MHPP with particle size cut tight, free of fines, to avoid dusting and loss during transfer. Others want the lowest odorous impurities, since some ester traces carry forward into finished fragrance bases. Feedback here drives our continuous process tweaks—topping up vacuum during drying, adjusting solvent cut points, and cleaning reactors to ensure residue from previous products never contaminates the next batch.

    Standing Apart from Blended or Repacked Material

    In today’s market, too many players resell blended or imported MHPP, sometimes after sitting in warehouses for months exposed to variable humidity, temp swings, and subpar packaging. We see problems from those sources all the time: product caked up, yellowed from light and air, burdened with unexpected hydrolysis. The cost in rework and rejection adds up, and the chemical never performs quite as expected.

    There’s a real difference when you buy direct from the plant making the product—no wasted time tracking lots or questioning storage conditions. With us, clients get MHPP shipped quick from controlled warehouses, within the same city as the main reactor blocks. Feedback and complaints cycle fast, so we find and fix issues before they ripple through months of supply.

    Some try to cut corners with blends, particularly on large-scale commodity contracts. MHPP mixed from multiple sources might pass simple identity checks, but subtle differences show up under close inspection. Non-uniform particle size means inconsistent feeding into reactors or hoppers. Variable water content saps yields in moisture-critical steps. Lax packaging gives clients clumpy product that won’t dissolve smoothly. Our team spends hours in QC to stamp out those problems before finished stock ever leaves the plant.

    Meeting Pharma and Fragrance Requirements

    In pharma, traceability counts for everything. We document not just each batch, but every raw material, operator, maintenance event, and test. That’s not bureaucracy; it cuts through confusion if a customer notices odd NMR or strange IR signals during their syntheses. For those developing beta-blockers and similar actives, a known history from synthesis to drying means they don’t need to chase down ghost peaks or worry overrunning impurity limits.

    In fragrance and flavor, where sensory outcomes mean more than black-and-white numbers, performance under real throughput matters most. Pure MHPP translates directly to crisp, consistent notes in finished bases, and we’ve learned through repeated customer dialogues how a contaminant under 0.5% can change perceptions. Down this path, we collaborate closely, adjusting dryness, particle fineness, or packaging barriers to keep the product as close to “just made” as possible on arrival.

    Handling and Transport Insights

    Our teams know MHPP doesn’t tolerate poor packaging. We use double-layer sacks with desiccant sachets. Every drum gets sealed under nitrogen soon after drying. Trucks and containers avoid direct sunlight, and warehouse racking keeps drums off the floor—even during summer’s worst humidity. Every time a client receives product outside ideal quality due to transit handling, we track back not to the shipper, but to what we can change in storage and prep.

    Bulk users benefit from our tight scheduling. We ship MHPP within days of QC release, not weeks. Clients order fresh, avoiding stale stock with the faint acid odor or color changes that signal slow breakdown. Shelf life bears out in real-world use, not just in theory—a lesson heavy-batch users taught us after one humid summer led to more caked product returns than any spec sheet could explain.

    Practical Differences from Similar Aromatic Esters

    Methyl 3-(4-Hydroxyphenyl)Propionate gets compared with p-hydroxyphenylacetic acid methyl ester and methyl p-hydroxybenzoate. In practice, the extra -CH2- in the propionate tail expands uses, especially where flexibility or reactivity down the side chain gives added value. Shorter esters tend toward higher volatility and sharper odors, which some fragrance clients avoid. MHPP hits that middle ground—rich enough for lasting notes without overwhelming top ends.

    Compared with methyl p-hydroxybenzoate, our compound offers lower volatility, higher melting point, and greater stability in base-catalyzed reactions. Formulators in plastics and resins report better performance due to enhanced flexibility and toughness, especially at cool temperatures. Pharmaceutical applications succeed since the extra propionate length positions functional groups for chemistry not accessible to the benzoate version.

    We’ve seen customers try substituting related compounds due to tight markets or pricing squeezes. Results rarely match predictions, especially for late-stage drug routes. Methoxy, ethoxy, or benzoic esters might save some cost, but in cyclization, hydrogenation, or selective acylation, the downstream waste or required rework ends up erasing any short-term gains.

    Contamination and Storage: What Years of Experience Teaches

    We test for residual solvents well below allowable limits, since modern downstream applications—including injectables—tolerate nearly nothing above trace levels. Our analytics team checks not just for leftover methanol but also chlorinated, aromatic, and heavy hydrocarbons. Our dryers vent under reduced pressure, and the process equipment changes get documented thoroughly, so any new gasket or valve doesn’t introduce contamination.

    Moisture ruins good MHPP quickly. Any absorbance beyond standard limits triggers a full cleaning, not just a reblend. We store only in lined, sealed containers, turned over fast enough that lab staff can always say which batch is in what location, and what conditions it saw. Our warehouse team runs hourly temperature and humidity logs, not just for show, but to spot problems before clients do.

    Once, an overlooked shipping misfire forced a lot to sit in a non-climate-controlled warehouse. When recovered, even unopened, the powder showed slight tackiness and lost flow—it taught us moving stock quickly and monitoring environment matters more than any theoretical best practice written in an office. Each of these lessons gets reinforced in our SOPs, not for show, but so new staff avoid the basic mistakes that eat margins.

    Continuous Improvement: Driven by Feedback and Hard Data

    Trends in the market shift fast. Ten years back, MHPP demand leaned heavy into fragrances; today, pharma drives the majority. Clients want lower limits on metals, lower water, and stricter impurity thresholds. Each of these needs specific changes—higher purity starts with carefully sourced raw material, followed by investment in new dryers, tighter reactor cleaning, and improved sealing.

    We run root cause analyses whenever complaints come in, inviting clients to check our logs and see where issues began. Root stock grade, not just end-of-the-line QC, sets the limit on quality. Our shift supervisors and QC chemists sit at the same table weekly, scouring for outliers in moisture stats, melting points, or impurity spectra. Data matters, but hands-on experience with what customers see in the field counts just as much. Smart clients know to judge this through repeated interaction, not a single spec sheet or phone call.

    Environmental and Safety Considerations: A Manufacturer’s Take

    Regulatory pressure and client scrutiny only grow. We don’t discard process solvents or byproducts on a whim. All waste gets cataloged and channeled back for recovery or safe destruction, tracked through digital logs. Regional authorities sit in on audits; our team prepares as if every month will bring another visit. MHPP itself poses low acute hazard, but storage, packaging, and dust control prevent incidents—techs all wear local monitors and full PPE during filling, not just because protocols say so, but because we’ve seen what happens when steps go skipped.

    Production performance aligns tightly with good stewardship. Solvent losses, dust emissions, and energy waste all get tracked down to the shift level. From improved agitation designs—to limit dust—and new magnetic seals—to halt leaks—every uptick in production emerges from someone on the plant floor finding, not just reading, the next improvement. Clients care, and regulators care, but real change starts months before a new law takes effect.

    Looking Forward: True Value from Dedicated Manufacturing

    Methyl 3-(4-Hydroxyphenyl)Propionate isn’t just another line item for us. Years of small improvements, daily syncs between shift leads and QC, and tough lessons taught by unexpected recalls all shape how we build, document, ship, and support this compound. Product value comes not just from batch purity, but from knowing exactly what went into every lot, and seeing firsthand the difference that makes to chemists, formulators, and operations managers farther down the line.

    We defend our reputation with every kilogram, every day. Each order draws on our lessons, from how to keep product flowing in humid summers, to how to troubleshoot client complaints in winter’s slow ports. Our entire operation strives to save clients not only on paperwork and logistics, but through reliable, repeatable manufacturing rooted in experience no lab report alone can capture.