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4-Benzyloxyphenylacetic Acid Methyl Ester

    • Product Name 4-Benzyloxyphenylacetic Acid Methyl Ester
    • Alias Methyl (4-(benzyloxy)phenyl)acetate
    • 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

    289896

    Chemical Name 4-Benzyloxyphenylacetic Acid Methyl Ester
    Cas Number 116042-23-4
    Molecular Formula C16H16O3
    Molecular Weight 256.3 g/mol
    Appearance White to off-white crystalline solid
    Purity Typically >98%
    Boiling Point 410.6°C at 760 mmHg
    Melting Point 53-57°C
    Solubility Soluble in organic solvents such as dichloromethane and ethanol
    Storage Temperature Store at 2-8°C
    Smiles COC(=O)Cc1ccc(OCC2=CC=CC=C2)cc1

    As an accredited 4-Benzyloxyphenylacetic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White crystalline powder packaged in a 25-gram amber glass bottle, sealed with a screw cap, labeled with chemical name and safety information.
    Shipping 4-Benzyloxyphenylacetic Acid Methyl Ester is shipped in tightly sealed containers, protected from moisture, heat, and light. It is typically transported as a solid packed in chemical-safe packaging, following standard hazardous material handling protocols. Shipping complies with local and international regulations for laboratory and research chemicals to ensure safe delivery.
    Storage **4-Benzyloxyphenylacetic Acid Methyl Ester** should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry place, ideally at 2-8°C (refrigerator), away from incompatible substances such as strong acids or oxidizers. Ensure the storage area is well-ventilated, and follow all safety guidelines for handling organic esters.
    Application of 4-Benzyloxyphenylacetic Acid Methyl Ester

    Applications of 4-Benzyloxyphenylacetic Acid Methyl Ester in Industrial Manufacturing

    As a specialized manufacturer of 4-Benzyloxyphenylacetic Acid Methyl Ester, we supply this intermediate to selected sectors where it addresses targeted synthesis and functionalization challenges. Below we detail real, downstream industrial applications where our product demonstrates unique value in production flow, compliance, and formulation.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis

    In non-steroidal anti-inflammatory drug manufacturing, this ester serves as a protected precursor in the multi-step construction of complex arylacetic acid frameworks. Downstream processing teams introduce it during the early-stage side chain assembly, taking advantage of its stability for selective deprotection and subsequent functionalization. The methyl ester group allows for mild hydrolysis, minimizing degradation of sensitive moieties and ensuring batch reproducibility according to pharmaceutical GMP requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF monographs for starting material control
    • European Pharmacopoeia Section 5.2.6 (Starting Materials, Intermediates)
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.75–1.4 mol per mol of target arylacetic acid intermediate; strictly adjusted based on the target NSAID structure and total process yield targets

    Downstream process integration

    • Reacts after initial aryl halide activation, during nucleophilic substitution or Friedel–Crafts acylation steps; ester group hydrolyzed in late-stage deprotection before active ingredient isolation

    Final product types

    • Branded and generic NSAID APIs (e.g., derivatives of ibuprofen and analogs)
    • Intermediate blocks for further conversion into anti-inflammatory formulations

    2. Fine Chemicals: Synthesis of Custom Arylacetic Acids for Research Reagents

    Within fine chemicals manufacturing, research institutes and custom synthesis labs use the methyl ester as a modular building block in arylacetic acid derivatization. Its structure supports regioselective reaction schemes, minimizing byproducts and offering controlled hydrolysis options. Laboratories select this material to maintain high purity profiles necessary for analytical and screening reagents, and to enable specific substitution positions critical to bioactive compound library development.

    Industry compliance standards

    • ISO 9001:2015 certified QC and lot traceability
    • Good Laboratory Practice (GLP) for starting material management (OECD/US EPA)
    • Internal purity standards — HPLC ≥99% for research critical reagents
    • Material Safety Data Sheet (MSDS) registration for university research procurement

    Typical usage ratio

    • 10–25 mmol per 100 mmol batch in research synthesis; ratios customized based on desired substitution pattern and downstream conversion route

    Downstream process integration

    • First charged in substituted benzylation or Grignard reactions, followed by methyl ester hydrolysis under basic or acidic conditions to yield research-grade arylacetic acids

    Final product types

    • Custom arylacetic acids for pharmaceutical screening
    • Small molecules for chemical biology and academic research
    • Reference standards for analytical HPLC and mass spectrometry

    3. Agrochemical Intermediate: Precursor for Selective Herbicide Synthesis

    Agrochemical companies incorporate this raw material into the active ingredient synthesis chain for selective herbicides. Its protected ester format ensures controlled reactivity during aryl group modifications and prevents unwanted hydrolysis before the final acylation step. Production teams prioritize this intermediate when high selectivity is required for arylacetic acid-based herbicide APIs, particularly in the selective modification of aryl groups to generate crop safe products.

    Industry compliance standards

    • FAO/WHO specifications for technical materials and pesticide active ingredients
    • ISO 9001:2015 integrated production quality management
    • REACH registration as a chemical intermediate (EC 1907/2006)
    • ISO 14001:2015 environmental management for hazardous process residues

    Typical usage ratio

    • 3–10% by weight as a protected intermediate in total batch mass, depending on target herbicide molecule complexity and downstream hydrolysis yield

    Downstream process integration

    • Charged after main aromatic functionalization; methyl ester hydrolyzed during final API conversion; downstream purification follows before formulation blending

    Final product types

    • Selectivity-enhanced herbicide active ingredients
    • Agrochemical technical concentrates for further formulation

    4. Fragrance Intermediate: Precursor in Synthesis of Aromatic Ester Components

    Specialty fragrance manufacturers turn to 4-benzyloxyphenylacetic acid methyl ester for custom transformation into complex aromatic esters, providing signature notes in high-end perfumery. The methyl ester protection permits selective modification by catalytic hydrogenation followed by controlled ester hydrolysis. This pathway optimizes both the olfactory profile and the shelf stability of the resulting fragrance base materials for luxury applications.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety and Usage Standards
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9235:2013 for aromatic raw material definitions
    • Good Manufacturing Practices (GMPs) for fragrance ingredient production

    Typical usage ratio

    • 2–6 mol% in aromatic ester synthesis step, depending on target molecular profile of the fragrance concentrate

    Downstream process integration

    • Introduced after preliminary aromatic ring functionalization; undergoes selective hydrogenolysis, then ester group is hydrolyzed with mild acidic catalysts, generating aromatic acids for subsequent esterification

    Final product types

    • Complex fragrance base esters (e.g., for niche fine fragrance houses)
    • Perfumery components for high-value aroma compositions

    5. Specialty Polymers: Functional Monomer Synthesis for High-Performance Polymers

    Manufacturers in specialty polymers utilize the methyl ester to introduce pendant arylacetic acid motifs into polymer chains, improving material flexibility and processability. It enters the synthesis during prepolymer functionalization, protecting sensitive acid groups until final deprotection just prior to polymerization. This offers precise control over copolymer structure and supports batch-to-batch consistency in technical polymer applications.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • REACH compliance for specialty monomers (EU Regulation 1907/2006)
    • ASTM D256 (Standard Test Methods for Polymers and Plastics upon request)
    • GHS (Globally Harmonized System) compliant labeling and transport

    Typical usage ratio

    • 1.5–5 mol% monomer incorporation rate per mol of total monomer mix, based on the desired degree of pendant group functionalization

    Downstream process integration

    • Added in prepolymer reactive blending; methyl ester group is hydrolyzed under controlled conditions immediately before final polymerization, yielding activated monomer ready for chain extension

    Final product types

    • High-performance specialty polymers with arylacetic acid side chains
    • Polymer intermediates for electronics, coatings, and MEMS substrates
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    Certification & Compliance
    More Introduction

    4-Benzyloxyphenylacetic Acid Methyl Ester: Experience From the Manufacturer’s Lab

    Shaped by Years at the Bench

    Making 4-Benzyloxyphenylacetic Acid Methyl Ester in our facility has taught us a few hard lessons about consistency, reliability, and the fine points of organic synthesis. Delivering quality every batch isn’t only about recipes on paper—it grows from tweaking reaction conditions, spotting impurities early, tuning crystallization temperatures, and never assuming a previous success guarantees the same next time. We’ve fielded questions from research chemists, pharmaceutical process groups, and scale-up teams who push beyond basic catalog data, looking for small details that matter during downstream synthesis. Over time, we’ve realized that meaningful support starts on our own production floor, paying attention to the difference between textbook chemistry and what actually comes out of the reactor.

    Getting Down to the Chemistry

    4-Benzyloxyphenylacetic Acid Methyl Ester doesn’t simply appear. Preparing each batch involves benzylating phenylacetic acid, using clean catalysts, and controlling moisture levels throughout. We usually target a product with a purity above 99%. Residual solvents, trace metals, and minor isomers remain stubbornly persistent without careful monitoring. It’s not unusual for analysts to catch faint benzyl ether impurities from incomplete separations, or methyl ester hydrolysis if the workup drifts off temperature. We chase these down, not only for regulatory comfort but to prevent headaches later in our customers’ routes.

    Our product’s white, crystalline form gives visual clues about batch health. Yellowing hints at over-exposed intermediates; sticky residues sometimes point to incomplete esterification. Consistency from lot to lot isn’t a checkbox in a spreadsheet—it’s seen in the way the crystals pour, their dryness, the way they dissolve in standard solvents. Only by standing at the discharge, collecting samples, and matching them to reference runs do we control these outward signs of what’s going on at the molecular level.

    Beyond the Data Sheet: How We Use It and See Others Use It

    Research groups turn to 4-Benzyloxyphenylacetic Acid Methyl Ester for making various aromatic compounds and related drugs. The methyl ester’s reactivity makes it a flexible entry point for further functionalization—saponification, reduction, and more. Medicinal chemists often need this compound to serve as an anchor for attaching new functional groups or rings in the pursuit of selective bioactivity. Small-scale labs might synthesize a few grams, but we’ve handled requests for multi-kilogram lots for pilot work and full manufacturing. The challenges don’t stop at the bench; scaling means washing, filtering, drying, and packaging each batch so that it holds up under months of storage without caking or degrading.

    Some customers approached us after trouble with off-brand suppliers: batch-to-batch variation, unknown byproducts, suspicious odors that derailed their analytical data. We learned early not to dismiss these reports as “user error.” More often, the supply chain lacked robust quality checks, with the assumption that a white powder always equals high purity. We keep our process paper trail open to those who ask—the HPLC traces, residual solvent results, and stability data. Trust grows not from claims but from showing the product’s journey, right down to the last point of inspection.

    How It Compares to Similar Products

    We have manufactured both 4-Benzyloxyphenylacetic Acid Methyl Ester and its close relatives: phenylacetic acid derivatives bearing other ether protections or different ester groups. Swapping out the methyl ester for ethyl, tert-butyl, or even direct acid forms changes solubility and reactivity profiles. Methyl ester typically offers a good balance—easily converted with sodium hydroxide, stable enough for routine storage, and compatible with chromatographic methods.

    Benzyl protection at the para position brings selective stability against oxidation or over-reaction in multi-step syntheses. It can be removed under hydrogenolysis without disturbing more acid- or base-sensitive moieties, unlike alkyl ethers or unprotected acids. That’s made 4-Benzyloxyphenylacetic Acid Methyl Ester attractive in complex pharmaceutical and agrochemical research, where selectivity saves waste and rework.

    You’ll sometimes find suppliers offering the parent acids or different esters. Unprotected acids absorb water quickly and cake up or clump in storage, complicating weigh-outs and filtration later. Some labs prefer ethyl or isopropyl esters for slower hydrolysis, but methyl remains a staple for ease of deprotection at room temperature.

    Attention to Details That Shape Real-World Performance

    Quality does not depend on meeting a spec sheet once. True performance comes after sitting in warehouses through seasonal swings, after shipment in containers crossing oceans, and after exposure to varied lab atmospheres. Over time, we’ve built up a record of stability—how the product’s moisture stays within target, how the melting point moves only within a degree or two, how the filtration finishes clear even after months of storage. Customers notice these differences not in the first few grams, but after opening the fiftieth bottle from a single lot.

    Cost-conscious buyers sometimes waver between different esters, different protections, or starting with unprotected phenylacetic acids. We provide honest assessments—not every project gets value from the benzyloxy group. Early-process steps, high-heat reactions, or strong acid conditions may demand other protections. We do not push a one-size-fits-all answer. Instead, we offer hands-on advice, visibility into our own process journey, and samples that truly reflect bulk supply, not cherry-picked grams from a single good day.

    Shipment and packaging play a quiet but important role. We’ve seen what can go wrong: paper-lined drums failing in high humidity, plastic bags leaching unwanted additives, residue from container seals ending up in fine-particle lots. Every container and liner has been personally tested in our own labs, with attention to ease of resealing, powder flow, and avoidance of static charge buildup.

    Meeting the Needs of Diverse Research and Manufacturing Environments

    Over the years, buyers’ questions shifted from just “what is the purity?” to “what else could be lurking in the bottle?” Some research projects demand trace metal analysis down to low ppm, especially for catalyst-heavy downstream processes. We’ve developed individual batch data for hard-to-detect contaminants—Fe, Cu, Zn—because a missed impurity can disrupt sensitive catalytic reactions or bioprocesses. Even the batch's residual solvents matter when evaporative losses impact fine analytical endpoints. Our QC team records these runs and shares the data for every inquiry, mindful that transparency gives confidence, not just reassurance.

    Some clients introduced precise requests about particle size, though most advanced small molecule chemistry doesn't require fine milling. We control particle range during crystallization and avoid unnecessary grinding, as overworked product can generate dust and process loss. Larger scale buyers, especially those moving toward GMP-grade work, ask about cross-contamination; we dedicate lines and double-check cleaning records to meet their thresholds.

    Staying Ahead With Continuous Process Improvement

    Process drift is always a risk. We have seen a single change of solvent grade translate into a spike in byproduct levels. A few years back, a supplier changed their benzyl chloride pre-treatment, which subtly shifted our product’s GC trace. Learning this lesson convinced us to requalify every raw material, update in-process controls, and regularly revisit impurity profiles even when regulatory standards haven’t shifted. We treat our own process as a living system—never immune from surprise.

    Technology pushes us farther each year. NMR, GC-MS, and advanced HPLC methods now let us catch byproducts early that once passed unnoticed. During one tech transfer, we discovered an impurity forming under slightly different temperature holds. We adjusted crystal seeding, extended drying times, and brought the impurity back below detection. This constant feedback loop—between bench chemistry, analytical review, and customer outcome—drives our routine.

    Reliability Beyond the Catalog: Earning Trust Repeatedly

    It’s not enough that 4-Benzyloxyphenylacetic Acid Methyl Ester appears on a catalog web page. Buyers remember if the bottle matched their expectations, if the powder flowed evenly, and especially if projects ran smoothly without headaches from rework or troubleshooting. Trust is built over time—through records shared, problems discussed openly, surprises avoided, and results delivered batch after batch. We keep learning from customer returns and feedback. Questions about trace contaminants or requests for alternate packaging pushed us to innovate on details that traditional run sheets might overlook.

    Today, our conversations may center on regulatory compliance, sustainability of sourcing, and readiness for process audits. Customers ask us for full traceability: where were those feedstocks sourced, what solvents were recycled, what are the waste profiles. Instead of passing these questions up the line, we dig into our own operations, working with suppliers to trace back each flask and drum. We share this data, warts and all, because confidence grows from real transparency, not just promises.

    The Broader Value: Building Real Connections With End Users

    Many researchers depend on the quiet reliability of starting materials like 4-Benzyloxyphenylacetic Acid Methyl Ester. Few papers mention these building blocks by name, but every project that advances depends on their quality. We’ve learned to measure success not just in sales but in the stories that come back: a new synthetic route that worked because of cleaner material, a reduced waste stream from more consistent reactivity profiles, a pilot batch scaled quickly because requalifications weren’t needed.

    Our role extends beyond our own walls. When a client asks about reusability of drums, preferences for less dense powder, or questions regarding regulatory filings, our experience with this product, forged over years of consistent supply and careful improvement, makes us a reliable voice in their process chain.

    Working Together: Sharing Challenges, Finding Better Solutions

    Some of our best improvements arose from customer challenges. One process chemist flagged increased static buildup in a summer shipment, which led to powder clumping and difficult transfers. We traced the problem to increased ambient humidity and shifted packaging to lower-static liners, retesting in simulated transport conditions. Feedback like this shapes how we ship and store today—not only for ourselves, but now as a supplier who advises others in avoiding the same pitfalls.

    Another time, a veterinary pharmaceutical pipeline ran into trouble with downstream hydrogenation because a trace byproduct from an earlier batch proved resistant to reduction. Our technical team joined the troubleshooting, adjusting purification and identifying the culprit by matching chromatograms. The next campaign succeeded, saving weeks of lost work. These partnerships, grounded in shared trial and honest dialogue, drive every decision we make to improve—not just on paper but where it truly counts.

    A Product Maturing Alongside Methodologies

    Synthetic methodologies rarely stand still. As coupling chemistries, protecting group protocols, and scale-up technologies change, the requirements for building block quality move alongside. We keep tabs on evolving literature, patent developments, and feedback from conference presentations. A request last year for a “carbon-free” process rerouted us to explore alternatives to benzyl protection—yet for many transformations, the traditional methyl ester form still performs as the reliable, workable choice.

    Over time, project managers look for ways to streamline, reduce purification steps, and boost sustainability. Our experience shows that cleaner, consistently produced starting materials cut down on rework, labor, and hazardous solvent use downstream. Even as greener protections and catalytic alternatives appear, users report that solid data, predictable behavior, and deep batch record support still separate success from setbacks.

    Final Thoughts From the Manufacturing Line

    We manufacture 4-Benzyloxyphenylacetic Acid Methyl Ester not just to fill a sales line—but because we’ve seen its importance in practical chemical research, pilot-scale development, and ongoing pharmaceutical and agrochemical manufacturing. Every lot tells its own story, shaped by the care and attention given along the way, from raw material sampling to final packaging. Our goal remains unchanged: deliver trust you can see, backed by real experience, open records, and a willingness to listen and adapt to what’s needed next.

    As end users demand greater transparency and deeper partnership, we stand ready to support not just sales, but shared success across the evolving landscape of chemical research and industry.