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4-Methoxyphenylacetic Acid

    • Product Name 4-Methoxyphenylacetic Acid
    • Alias 4-Methoxybenzeneacetic acid
    • Einecs 211-980-8
    • 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

    564000

    Name 4-Methoxyphenylacetic Acid
    Synonyms p-Methoxyphenylacetic acid, 4-Anisylacetic acid
    Molecular Formula C9H10O3
    Molecular Weight 166.18 g/mol
    Cas Number 104-01-8
    Appearance White to off-white crystalline powder
    Melting Point 105-107°C
    Boiling Point 334.2°C at 760 mmHg
    Solubility In Water Slightly soluble
    Density 1.20 g/cm³
    Smiles COC1=CC=C(C=C1)CC(=O)O
    Inchi InChI=1S/C9H10O3/c1-12-8-4-2-7(3-5-8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11)

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

    Packing & Storage
    Packing Packaging for 4-Methoxyphenylacetic Acid, 100g: Supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping 4-Methoxyphenylacetic Acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It should be packed and labeled according to relevant regulations, handled with care, and transported at ambient temperature. All shipments comply with safety guidelines for shipping non-hazardous organic chemicals. Suitable documentation accompanies each shipment.
    Storage 4-Methoxyphenylacetic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Proper labeling and secure shelving are recommended to prevent accidental spillage or misuse. Store at room temperature for optimal stability.
    Application of 4-Methoxyphenylacetic Acid

    Applications of 4-Methoxyphenylacetic Acid in Industrial Manufacturing

    We produce 4-Methoxyphenylacetic Acid for industrial partners across specialized downstream markets, supporting processes in pharmaceutical, fine chemical, fragrance, and agrochemical synthesis. Our material meets stringent quality and regulatory requirements for critical intermediate and additive roles in each application.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    4-Methoxyphenylacetic Acid serves as a critical building block in manufacturing active pharmaceutical ingredients, such as β-blockers and specific angiotensin receptor antagonists. Pharmaceutical manufacturers apply it in the synthetic sequence where the methoxy-substituted benzyl moiety is required for target molecule construction. Its high purity supports consistent batch quality and process control through crucial condensation and amidation stages prior to final API crystallization.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient intermediates
    • 21 CFR Part 211 (US FDA current Good Manufacturing Practice)
    • European Pharmacopeia (Ph.Eur.) monographs for API synthesis
    • USP General Chapter <795>

    Typical usage ratio

    • 0.5–2.5 molar equivalents per core API target, adjusted based on reaction selectivity and expected yields in the synthetic route

    Downstream process integration

    • Introduced at early-to-mid-stage condensation or amidation reactions, often coupled with activating agents (e.g., EDC, DCC), followed by purification by recrystallization or chromatography

    Final product types

    • Bulk antihypertensive APIs (e.g., certain β-blockers, ARBs)
    • Pharmaceutical intermediates for further side chain modification
    • Contract manufactured custom drug substance blocks

    2. Synthesis of Aroma Compounds for Fine Fragrance Manufacturing

    Key fragrance houses utilize 4-Methoxyphenylacetic Acid in multi-step syntheses of musky and floral aroma molecules, notably in the construction of macrocyclic musks and anisic esters. Its aromatic and ether functionalities deliver structural elements essential for fragrance profile consistency, ensuring reproducibility in olfactive blends after downstream esterification and acylation processes.

    Industry compliance standards

    • IFRA (International Fragrance Association) Codes of Practice
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • ISO 9235:2013 (definition of natural, aromatic raw materials)
    • REACH registration for import and use in blends

    Typical usage ratio

    • 3–10% by weight of reaction batch depending on target ester or alcohol and desired olfactive strength in final product formulation

    Downstream process integration

    • Esterification or acylation with alcohols or acid chlorides, followed by distillation and quality fractionation to separate targeted aroma compounds for blending

    Final product types

    • Perfume base aroma chemicals
    • Fine fragrance concentrates
    • Personal care formulations (eau de toilette, lotion fragrances)
    • Home care scent bases (candles, diffusers)

    3. Agrochmical Intermediate for Herbicide Synthesis

    Major agrochemical formulators employ this acid as a strategic intermediate in synthesizing specific phenoxyalkanoic acid herbicides. Its consistent quality underpins reproducible condensation and cyclization steps, enabling targeted modifications for improved herbicide selectivity on broadleaf crops while maintaining environmental stewardship in downstream application.

    Industry compliance standards

    • ISO 9001:2015 for agrochemical production
    • FAO/WHO Specifications for Agricultural Pesticides
    • China GB 2763/2764 MRLs for crop protection chemicals
    • REACH and CLP (Classification, Labelling and Packaging) European regulations

    Typical usage ratio

    • 5–15% by mass in active ingredient precursor synthesis, with actual ratio determined by desired substitution pattern and downstream coupling efficiency

    Downstream process integration

    • Participates in etherification or haloalkylation, followed by ring closure and neutralization prior to formulation into technical concentrate

    Final product types

    • Phenoxyalkanoic acid-based herbicides
    • Technical-grade agrochemical intermediates
    • Ready-to-use crop protection solutions for broadleaf weed control

    4. Raw Material for Fine Chemical Synthesis in Dye and Pigment Intermediates

    Leading dye and pigment manufacturers integrate this acid in tailored aromatic coupling reactions, particularly for functionalized azo and anthraquinone intermediates requiring high-purity para-methoxybenzyl units. The material supports both laboratory-scale and continuous production, facilitating reliable color performance in textile, ink, and plastics coloration systems through robust downstream controls.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (certification for textile and leather chemicals)
    • EN 71-3:2019 (safety of colorants in toys and plastics)
    • ISO 9001:2015 for pigment production
    • ZDHC MRSL v3.1 (Restricted Substances List for manufacturing)

    Typical usage ratio

    • 1–8% weight basis in coupling stages, adjusted according to the targeted chromophoric group and batch scale

    Downstream process integration

    • Introduced during diazotization or Friedel–Crafts acylation, followed by oxidative coupling for chromophore extension and finishing post-treatment for dispersion quality

    Final product types

    • Azo dye intermediates
    • Anthraquinone pigment precursors
    • High-performance textile and polymer colorants
    • Industrial ink color bases
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    Certification & Compliance
    More Introduction

    4-Methoxyphenylacetic Acid: Insights from a Chemical Manufacturer

    Understanding 4-Methoxyphenylacetic Acid from Our Daily Work

    4-Methoxyphenylacetic acid, a compound that rolls off the tongue a bit easier in the lab as PAA-OMe, forms a crucial part of our product lineup. We have been manufacturing this aromatic carboxylic acid for years, watching different sectors pull it into diverse applications. In our experience, the identity of this molecule—CAS number 104-01-8, chemical formula C9H10O3—revolves around its methoxy substituent, which transforms basic phenylacetic acid into something more selective, versatile, and valuable for organic syntheses and downstream applications.

    From Raw Materials to Final Product: Our Manufacturing Approach

    Our production starts with strict sourcing of raw phenols and reagents. We use catalytic and controlled etherification for placing the methoxy group onto the aromatic ring. Monitoring stepwise purification allows us to hit purity benchmarks above 99%, important for pharmaceutical and agrochemical partners who cannot tolerate even trace contaminants. Each time we isolate a batch of 4-methoxyphenylacetic acid, our QC team documents parameters like melting point, residue on ignition, and total organic content.

    Special attention goes into managing by-products. Years ago, internal testing led us to tune our recrystallization protocol with solvents that minimize carryover of halogenated impurities and tautomeric isomers. These changes were not mandated by regulation but saved customers countless hours in downstream HPLC clean-up. Small approaches like this keep our quality reputation strong, more so than certifications stapled to batch records.

    Specifications We Hold Ourselves To

    Most customers order crystalline 4-methoxyphenylacetic acid, ranging from 25 kg drums up to metric ton lots. Granular, free-flowing powder makes dispensing and measuring possible even in humid climates. Every lot leaves our facility meeting a minimum purity threshold of 99% based on area normalization with reference standards by HPLC. Moisture content sits below 0.2%, and we rarely encounter requests for extra drying, since our packaging proves robust during ocean freight and warehousing.

    Besides basic purity, we also control for residual solvents. Any remaining methanol, dichloromethane, or toluene clocks in at levels far below ICH guidelines, mostly because our reactors and washing protocols are tuned for rapid changeovers and minimal cross-contamination. Our technical team coordinates with buyers who need tighter specifications—some drug discovery settings demand even narrower impurity profiles, and we have test records on hand for heavy metal screening through ICP-MS.

    Where Real-World Use Shows Value

    Chemists across research institutes, pharma labs, and agrochemical plants see something unique in 4-methoxyphenylacetic acid. Its structural motif—the methoxy group ortho to the acetic acid side chain—unlocks selective reaction pathways that the parent phenylacetic acid cannot deliver. For example, when used as a starting material for amide couplings, this acid feeds into potent central nervous system agents or antispasmodic intermediates that demand electronic fine-tuning across the aromatic ring.

    One noticeable advantage in synthesis arises during methylation, bromination, or lithiation reactions. The electron-donating methoxy group stabilizes intermediates, letting reaction temperatures stay moderate, so process engineers face fewer runaway exotherms and scale-up headaches. Having manufactured both methoxy- and non-methoxy variants at scale, we see first-hand how the para substituent impacts color stability and by-product profiles. The end result means less effort poured into cumbersome purifications, which resonates with chemists balancing tight budgets and unforgiving timelines.

    Customers have approached us seeking alternative acids, but every time, the absence of the methoxy group led to issues—higher melting point, altered solubility, slower reaction rates, or simply more expensive pathways. From our vantage point behind the reactor glass, 4-methoxyphenylacetic acid consistently streamlines synthetic steps for new molecules in the CNS, anti-inflammatory, and even fragrance sectors.

    Direct Contrasts with Related Acids

    Compared to unsubstituted phenylacetic acid, our methoxy derivative behaves gently in Schotten–Baumann reactions or amidation protocols. Manufacturers try both variants during process development. Only the methoxy product gives the right balance between yield, reproducibility, and downstream workup ease.

    4-Hydroxyphenylacetic acid sometimes pops up as a potential substitute in the lab, yet the hydroxyl group installs additional hydrogen-bonding complications, raising issues around crystallization or formulation. With 4-methoxyphenylacetic acid, the blocked ring station grants chemists a tool for fine-tuning polarity and lipophilicity at later synthetic steps. Unlike bulkier alkoxy or halogen derivatives, the methoxy group offers a compact, electron-donating boost without knocking off reactivity or causing isomeric splitting under common conditions.

    On the environmental front, the methoxy group on our acid exhibits lower volatility and a favorable partition coefficient for aqueous and organic extractions compared to fluorinated or chlorinated alternatives. That difference matters when dealing with in-plant emissions and regulatory checks. Years of pilot work showed the methoxy variant delivers on both performance and compliance fronts.

    Supporting Innovation in Downstream Synthesis

    Every development chemist we talk to values predictability. In customer labs, 4-methoxyphenylacetic acid shows reliable batch-to-batch performance. It handles well during milling, slurry mixing, and solvent switching. The fine, crystalline material disperses easily in methanol, ethanol, and DMF, common process solvents for peptide syntheses and selective reductions. By working closely with process engineers, we optimized particle size distribution to eliminate dusting but retained reactive surface area.

    Our long-standing partnerships with academic chemists and formulation scientists push us to trace even minute variations between lots. Once, a customer flagged higher-than-usual titration endpoints with one batch, leading our team to review microbalance calibrations and holding room temperatures. We pinpointed minor solvent interactions as the root cause, adjusted our post-drying schedule, and returned results that satisfied the most exacting HPLC assays. Experiences like this shape how we adapt process controls before specifications drift from what researchers need.

    Highlighting What Sets Our Material Apart

    Seasoned procurement teams increasingly request data on raw material origin, trace analytics, and batch reproducibility. Years of fielding technical audits and compliance checks means we assemble data packages that answer the questions buyers wish their previous suppliers had anticipated. Geared for the regulated sectors, our 4-methoxyphenylacetic acid never draws red flags on trace residual solvents, heavy metals, or unlisted by-products.

    Rather than relying on generic COA templates, we keep retention samples and support lot genealogies that map back to synthesis dates, operators on duty, and every change in technical SOPs. Visiting labs and regulatory agencies see more than a simple certificate—they see an unbroken paper and analytical trail that builds trust batch after batch.

    Another detail often overlooked is the mechanical behavior of our crystalline acid under warehouse and process conditions. Some suppliers push out overly fine or agglomerated material, which clogs feeders or resists dispersion. Years of feedback refine how we regulate drying, sifting, and drum sealing for safe, dependable handling across scales.

    Impact on Scale-Up and Commercial Manufacturing

    We watch what happens as smaller R&D orders ramp up to pilot and commercial quantities. A recent customer moved from flask-scale trials to a multi-ton synthesis campaign; they found other vendors’ acids caused color instability during high-temperature steps, traced to poorly controlled methoxy group migration and peroxide contamination. Our controlled etherification and stabilization steps shield batches from this issue, helping customers avoid rework, downtime, and batch failure.

    By investing in real-world trials with partners at different plant scales, our team bridges gaps between theoretical specifications and reality on the plant floor. Customers find that proper packaging and consistent particle size make large-scale material flows behave predictably, saving them from unplanned down days or costly cleanup cycles.

    Ensuring Long-Term Supply and Consistency

    In the chemical industry, a dependable source often means as much as the molecule itself. We built inventory buffers and dual extraction/production lines, so plant outages, supply chain disruptions, or regulatory updates do not choke off deliveries. More than once, this approach let global pharma partners hit critical timelines for pilot batches and market launches. Experience from cold chain logistics and extreme humidity climates factored into our moisture barrier drum liners and labeling—details that only come from fielding repeated issues in the real world.

    Long-term supply contracts gave us a window to track seasonal variations in raw material cost, batch reproducibility, and transport losses. From these lessons, we budget production cycles to avoid seasonal price hikes and track transit times for key customers. Adjusting drum sizes and double sealing for ocean export cut product loss complaints by more than half last year—a small change that earned longer commitments from our core buyers.

    Across years and multiple regulatory audits, our methods produced a consistent track record for quality, compliance, and timely supply. We do not rewrite specifications after every revision cycle or regulatory notification—instead, our technical sales and production engineers adjust process variables within validated limits, saving buyers from sudden surprises.

    Product Safety and Environmental Performance

    Being both manufacturer and steward means treating product safety as more than a regulatory checkbox. Because 4-methoxyphenylacetic acid shows relatively low volatility and aquatic toxicity, we support partners in managing safe handling during synthesis campaigns. Bulk containers remain sealed under nitrogen until use, and our on-site environmental engineers monitor any losses or leaks with standard sampling protocols.

    Our approach to waste minimization pushes us to recover any filtrates or mother liquors where feasible, minimizing impact on municipal treatment systems. Years ago, we adjusted purification and solvent recovery to curtail halogenated emissions and reduce hazardous waste loads. This discipline helps us stay ahead of regulatory changes and appeals to buyers focused on green chemistry.

    By maintaining full documentation and traceability on residual content and by-product recovery, we stay ready for changing document demands, certifications, and downstream audits. Sharing our environmental stewardship practices with customers helps them comply with frameworks like REACH and support their own sustainability initiatives.

    Why Experience Matters

    Today’s market brings no shortage of traders and relabelers eager to sell bulk 4-methoxyphenylacetic acid based on price alone. Our work as a manufacturer means real accountability—when a batch lands, it carries our technical history, not a mystery chain of intermediaries. We monitor each shipment with a stake in its safe arrival, and our technical staff remain available for troubleshooting, change control, and coordination well beyond delivery.

    Frequent site visits, process walk-downs, and shared troubleshooting with customers set us apart in a market crowded by opportunistic sellers. Each year, process chemists and plant engineers reach out with new problems or ideas—batch inconsistencies, solvent switching, or optimization for lower-energy processes. These exchanges drive us to update process protocols and batch controls, feeding back improvements that make future batches more reliable and easier to use at the plant or bench scale.

    We go beyond filling orders and look to the next phase—whether that means more sustainable manufacturing or better downstream technical support. Our commitment springs from plenty of lessons learned: batch losses, equipment upgrades, staff training cycles, and plenty of direct conversations with end-users. Those lessons deepen our understanding of this compound and shape our ability to serve a tighter, more responsive supply chain year by year.

    Enabling Growth for New Chemical Pathways

    The road from a kilo-lab sample to continuous commercial production is rarely straight or simple. By providing not only 4-methoxyphenylacetic acid but also direct know-how about its real-world handling, we give industry partners confidence as they translate ideas to finished products. Whether their goal centers around new drug candidates or fine chemicals for consumer use, reliability and deep technical support tip the balance between delay and success.

    We welcome technical challenges and real feedback—be it improving regulatory support, troubleshooting melt behavior for a new API, or solving packing and storage needs for a large-volume consumer campaign. Each engagement, each learning cycle, pushes our own methods ahead, so we can deliver ever more practical, responsive chemical products. Amid rapid change and tighter scrutiny, years of manufacturing have shown us how small improvements often matter more than sweeping changes. This steady, forward-looking approach lets us supply 4-methoxyphenylacetic acid and similar critical intermediates with a level of transparency, support, and reliability that our partners count on.