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(S)-(+)-Alpha-Methoxyphenylacetic Acid

    • Product Name (S)-(+)-Alpha-Methoxyphenylacetic Acid
    • Alias (S)-(+)-MPA
    • Einecs 246-484-0
    • 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
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    Specifications

    HS Code

    311193

    Chemical Name (S)-(+)-Alpha-Methoxyphenylacetic Acid
    Cas Number 16356-11-9
    Molecular Formula C9H10O3
    Molecular Weight 166.18 g/mol
    Purity Typically ≥98%
    Appearance White to off-white crystalline powder
    Melting Point 87-89°C
    Optical Rotation [α]D20 +66° to +70° (c=1, CHCl3)
    Solubility Soluble in methanol, ethanol, and chloroform
    Boiling Point 360.6°C at 760 mmHg
    Density 1.2 g/cm³
    Storage Conditions Store at 2-8°C, protected from light and moisture

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

    Packing & Storage
    Packing (S)-(+)-Alpha-Methoxyphenylacetic Acid, 25g: Supplied in a sealed amber glass bottle with hazard labeling and a tamper-evident cap.
    Shipping (S)-(+)-Alpha-Methoxyphenylacetic Acid is shipped in secure, airtight containers to prevent moisture and contamination. Proper labeling and documentation are included, complying with relevant chemical shipping regulations. The package is handled with care, ensuring temperature and environmental stability, and is delivered promptly to guarantee product quality and integrity upon arrival.
    Storage (S)-(+)-Alpha-Methoxyphenylacetic Acid should be stored in a tightly sealed container, protected from light and moisture. Store at room temperature or below, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and avoid exposure to excess heat. Follow all relevant safety and chemical hygiene guidelines.
    Application of (S)-(+)-Alpha-Methoxyphenylacetic Acid

    Applications of (S)-(+)-Alpha-Methoxyphenylacetic Acid in Industrial Manufacturing

    (S)-(+)-Alpha-Methoxyphenylacetic Acid serves as a critical chiral intermediate across specialist chemical sectors. Its chemical stability, defined stereochemistry, and pure form make it essential in regulated synthesis of fine chemicals, pharmaceuticals, and agrochemical actives. As a direct manufacturer, we supply this raw material for precise integration into advanced downstream processes.

    1. Chiral Pharmaceutical Intermediates

    This material functions as a core building block for enantiopure drug synthesis, supporting the production of selective beta-blockers, anti-hypertensives, and CNS actives. Pharmaceutical processors use this compound for asymmetric synthesis, optimizing enantiomeric purity in active pharmaceutical ingredients (APIs). High-stakes protocols require tight process monitoring, given strict authority controls on chiral purity and traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) guidelines
    • European Pharmacopeia (Ph. Eur.) purity requirements
    • FDA 21 CFR Part 210 and 211 for process validation

    Typical usage ratio

    • 0.5 – 1.2 molar equivalents relative to target chiral amine/alcohol synthesis step
    • Adjusted based on desired enantiomeric excess and process scale
    • Tighter range for GMP final stage intermediates: 0.95 – 1.05 equivalents
    • Batch size typically ranges from 10 kg to 1 MT for API plants

    Downstream process integration

    • Introduced during chiral resolution or asymmetric synthesis step
    • Reacts with Grignard or amination reagents to provide single-enantiomer building block
    • Monitored by HPLC for enantiomeric excess and residual solvent levels
    • Downstream coupling yields API precursor ready for crystallization or purification

    Final product types

    • Enantiomerically pure beta-blocker APIs (e.g., (S)-Metoprolol intermediates)
    • Chiral anti-epileptic drug intermediates
    • Selective serotonin-norepinephrine reuptake inhibitor (SNRI) intermediates
    • CNS drug substances with strict regulatory profiles

    2. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers adopt this material as a key asymmetric intermediate for highly regulated crop protection products. It enters synthetic pathways of optically active herbicide and fungicide actives which require narrowly controlled stereochemistry for environmental and biological effectiveness. Compliance demands strong batch documentation and process reproducibility.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Material
    • ISO 9001:2015-certified process documentation
    • REACH Regulation (EC) No. 1907/2006 registration for import/use
    • OECD Good Laboratory Practice (GLP) for synthesis steps

    Typical usage ratio

    • 0.8 – 1.1 molar equivalents in chiral nucleus formation reactions
    • Adjusted per required isomeric purity and toxicological profile
    • Multi-ton scale for continuous technical material production
    • Single-use or recycle depending on product-specific pathways

    Downstream process integration

    • Feeds into early-to-mid stage of technical material synthesis
    • Couples with heterocyclic precursors to deliver optically active intermediates
    • Stereochemical purity confirmed by GC or chiral LC checkpoints
    • Subsequent formulation into granules, suspensions, or emulsifiable concentrates

    Final product types

    • Enantiomerically defined selective herbicides
    • Optically active systemic fungicide actives
    • Chiral precursor compounds for insect growth regulators
    • Intermediates for new generation bio-pesticides

    3. Flavour and Fragrance Chiral Synthons

    Leading aroma chemical manufacturers use (S)-(+)-Alpha-Methoxyphenylacetic Acid in production of high-value, chiral flavor and fragrance materials. Its defined enantiopurity supports controlled synthesis of specialty aldehydes and lactones needed for luxury and mass-market formulations. Sensory consistency and traceability are essential for compliance with global food and cosmetic safety regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No. 1334/2008 on flavourings and certain food ingredients
    • US FEMA GRAS for food-grade intermediates
    • ISO 22716 Good Manufacturing Practices for cosmetics ingredients

    Typical usage ratio

    • 0.15 – 0.8 equivalents for key aroma ingredient synthesis
    • Adjusted for batch vs. continuous synthesis (lower in high-volume reactors)
    • Concentration monitored to minimize off-odors and cross-contamination
    • Final product purity requirements drive tighter usage at luxury segment

    Downstream process integration

    • Incorporated at chiral alcohol or aldehyde formation step
    • Chemical conversion under mild conditions to preserve scent characteristics
    • Finished products undergo sensory and GC/MS testing prior to blending
    • QC documentation maintained for traceability to source material lots

    Final product types

    • Single-isomer musks and lactones for premium fragrance bases
    • Optically active aldehydes for use in food flavors
    • Chiral aroma chemicals in natural-identical formulations
    • Ethically sourced ingredients for certified natural fragrances

    4. Chiral Catalyst & Ligand Manufacture

    Chemical catalyst manufacturers deploy (S)-(+)-Alpha-Methoxyphenylacetic Acid in constructing advanced chiral ligands and organocatalysts. Its stereochemical integrity ensures high selectivity in catalytic reactions, particularly in fine chemical and polymerization processes. Downstream integrators require compliance with both chemical safety and function-specific standards, including trace stereochemical impurity controls.

    Industry compliance standards

    • ISO 9001:2015-certified production protocol
    • OECD guidelines for test chemicals purity
    • REACH pre-registered status (for supply in Europe)
    • SHE (Safety, Health, Environment) controls for catalyst manufacture

    Typical usage ratio

    • Determined by stoichiometry of ligand backbone, typically 1.0 – 1.3 equivalents
    • Increased ratio for multi-functional catalyst synthesis
    • Batch size ranging from grams for R&D to 100+ kg for commercial tonnage
    • QC based on residual acid and purity profile of ligand product

    Downstream process integration

    • Fed at initial condensation or amidation step in ligand synthesis
    • Purified intermediate forms installed onto target scaffold
    • Purity checked by NMR and chiral HPLC during intermediate and final steps
    • Subsequent packaging for multinational catalyst and chemical processors

    Final product types

    • Chiral phosphine and oxazoline ligands for enantioselective hydrogenation
    • Organocatalysts for asymmetric Diels–Alder and aldol reactions
    • Functionalized resin-bound catalysts for flow chemistry
    • Chiral auxiliaries used in flavor, pharma, and materials synthesis
    Free Quote

    Competitive (S)-(+)-Alpha-Methoxyphenylacetic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (S)-(+)-Alpha-Methoxyphenylacetic Acid: Our Perspective as Chemical Manufacturers

    Experience from Our Factory Floor

    Anyone working in fine chemicals knows the pressure to deliver both purity and consistency. We’ve been making (S)-(+)-Alpha-Methoxyphenylacetic Acid for years, using chiral synthesis that keeps stereochemistry tight and reproducibility high. In every batch, we see clear demand for crystal clarity, minimal impurities, and absolute repeatability. Nothing else satisfies clients in the pharmaceutical and agrochemical sectors, where even slight drifts can spark headaches down the line. Running these reactors ourselves, we see the impact of each parameter, from solvent to catalyst, affecting the outcome in tangible ways. Unlike simple resellers, we live through the dozens of steps, the pH adjustments, the challenges that crop up mid-reaction. We face the cleanups and quality checks first-hand, knowing customer projects depend on us getting all the way to >99% enantiomeric excess.

    Specifications Backed by Daily Reality

    On our production line, (S)-(+)-Alpha-Methoxyphenylacetic Acid emerges as a crystalline white powder, with a melting point that sits between 74°C and 76°C. We produce it using enantioselective methods, ensuring optical purity that meets or exceeds 99%. HPLC readings and optical rotation checks are part of our daily final quality checkpoints. Physical properties matter just as much—particle size, residual moisture, and color are all watched due to their effect on downstream reactions. Years of feedback led us to control the odor profile, so you don’t get faint, off-putting notes that can interfere in sensitive applications. Water and solvent residues are generally held below 0.2%, a target reached by slow, methodical drying and constant batch monitoring. We keep levels of related substances low by tuning reaction conditions and purification, as byproducts in chiral intermediates often spell trouble ahead for anyone seeking clean transformations.

    Usage: Precision for Stereocontrolled Applications

    From our hands-on perspective, (S)-(+)-Alpha-Methoxyphenylacetic Acid proves its value where stereochemical integrity is non-negotiable. Drug developers lean on it heavily as a chiral auxiliary or building block in synthesizing vital intermediates, especially for active pharmaceutical ingredients and peptide analogs. Custom peptide manufacturers ask us repeatedly for this acid, trusting its stability under mild to moderate coupling conditions. Researchers working on optically pure phenylglycines or beta-lactam derivatives find our product slashes steps since it incorporates the (S) configuration right from the first coupling. Agrochemical firms use it for synthesizing selective herbicide or fungicide precursors, preferring the cleaner, more predictable course this acid offers compared to starting from racemic substrates. On the academic side, post-docs and grad students rely on its robust reactivity in asymmetric synthesis, often reporting higher yields and easier purifications than with racemic or less pure alternatives.

    Differences Born from Hands-On Manufacturing

    We appreciate what makes (S)-(+)-Alpha-Methoxyphenylacetic Acid stand apart from the racemic and other chiral analogs we’ve produced over the years. Racemic alpha-methoxyphenylacetic acid has a place in research, but for anyone scaling production or looking for high stereo-selectivity, the pure (S)-enantiomer holds obvious advantages. Reactions deliver higher optical purity and require less downstream separation. By contrast, sourcing the racemic substance means later investment in costly chiral separation or risking stereochemical drift, something most pharma or fine chemical clients won’t accept. (S)-(+)-Alpha-Methoxyphenylacetic Acid offers that shortcut directly—delivering a molecule with the spatial arrangement needed in one shot. This shaves hours off process chemistry and reduces the waste inherent to post-synthesis resolution.

    Compared to its (R)-enantiomer, the (S)-form serves applications where the absolute configuration affects biological activity. We've fielded plenty of questions about substituting one for the other and have learned from long partnerships that the switch isn’t trivial. In the hands of a medicinal chemist, a misplaced chirality can crater a project’s value, leading to weaker bioactivity or entirely new byproducts upon further derivatization. Our choice to specialize in the (S)-form arose because industry engagement—especially in small-molecule drug synthesis—demands unwavering stereocontrol. Synthetic pathways using our product routinely eliminate extra steps otherwise spent correcting unwanted chiral centers formed from achiral or racemic inputs.

    Continuous Quality Through Direct Oversight

    Manufacturing (S)-(+)-Alpha-Methoxyphenylacetic Acid ourselves gives us tighter reins over process parameters. Each time we adjust temperature, change a workup solvent, or reinforce purity specs, the feedback reaches us instantly, not filtered through multiple hands. This direct control builds confidence into each lot, because laboratory staff, plant operators, and quality assurance are all under the same roof, holding each other to clear accountability. We see rapid feedback if something strays off-target. Spectra shift? Moisture rises? Off-flavor creeps in? Adjustments happen the next day, not after weeks of third-party investigation. This allows our technical team to innovate small tweaks—like more sensitive chromatography media or dedicated lines for avoiding cross-contamination—without outside compromise.

    Challenges and How We Tackle Them

    Making a chiral acid this clean brings constant hurdles. As with any asymmetric synthesis, batch variations can show up if reactant purity drops, or if catalysts lose their edge after a few cycles. Unlike those outsourcing their production, we learn where control matters most—tightening raw material sourcing, swapping out aging reactor gaskets, or extending dry-down times. Customers ask about scalability for clinical or pilot projects, and we answer by referencing the hundreds of kilograms we’ve produced in campaign runs, often doubling reactor size while holding purity steady. Every technician on our team knows the mistakes that can sabotage chiral purity, having seen the, spectral tails, or irregular melting points that can hint at a drift from the desired (S)-form. Our on-site R&D routinely chases new routes and purification tweaks, cutting down on energy consumption and streamlining workups to sustain both yield and quality.

    We also see persistent demand for documentation. Not a month goes by without a regulatory affairs or procurement manager asking for updated impurity profiles, batch traceability, or new certifications. Because our records come straight from our own floor and our own lab, we supply real numbers that match the bottles customers receive. There’s no guessing or third-party lag—clients get technical answers directly from the chemist who ran or signed off that particular sister batch. While sometimes this means admitting a batch needs retesting, it also fosters trust. People want to see chromatograms, not brand statements. This transparency represents a reliability that distributors rarely match.

    Why Industry Trusts Direct Manufacturers

    Having roots in the production of complex chiral building blocks, we’ve watched both researchers and process chemists shift away from intermediaries. Customers tell us they want to avoid the uncertainty that shadows products from traders who may resell, relabel, or lack product insight. They want to talk to the people tuning solvent ratios or swapping out crystallization protocols, not just someone quoting a spec sheet out of context. This expectation has grown as regulatory oversight tightens and as buyers learn to distinguish real manufacturers from those further removed from production.

    Direct feedback loops push us to address unique client specs—some demand enhanced drying for moisture-sensitive projects, some ask for custom batch sizes to fit pilot plant schedules. By keeping production under one roof, we notice batch-to-batch nuances faster. Lab staff troubleshoot at the bench, and if issues arise, they’re addressed before shipment, not after a container has crossed oceans. Our experience makes it clear: control remains strongest with those closest to the source. This means problems get solved before they become supply chain snarls.

    Supporting Innovation in Downstream R&D

    Over time, our (S)-(+)-Alpha-Methoxyphenylacetic Acid has become indispensable in research groups scaling asymmetric syntheses, especially as they transition from milligram to kilogram scale. Scientists relay that access to single-enantiomer acids reduces bottlenecks during process validation, as well as lowers the burden of extra purification. Academic publications increasingly cite our product for enabling stereocontrolled routes to complex molecules. This isn’t just marketing spin; we see the orders come in for follow-up projects, often with feedback on minor purity adjustments helping improve subsequent experiments. Larger pharma partners use this acid to launch clinical development batches where traceability and batch uniformity support straightforward regulatory filings.

    We also interface with custom synthesis houses that use (S)-(+)-Alpha-Methoxyphenylacetic Acid to produce advanced pharmaceutical ingredients for cancer, cardiovascular, or antiviral drugs. Their feedback shapes our specification improvements—requests for lower heavy metal content, finer particle sizing, or improved solubility help us refine process steps. These collaborations help ensure our product evolves with market needs rather than resting on outdated standards. Through dozens of scale-up projects, we’ve learned where adjustments deepen our value proposition for companies pushing into new chemical space or scale.

    Comparing with Other Chiral Compounds

    Plenty of chemists ask us how (S)-(+)-Alpha-Methoxyphenylacetic Acid stacks up against similar chiral carboxylic acids or auxiliaries. We’ve produced a range, from mandelic acid derivatives to substituted phenylalanines, but each brings its own quirks in reactivity and side-product profile. (S)-(+)-Alpha-Methoxyphenylacetic Acid proves more robust than many, standing up to both acidic and mildly basic conditions. It resists racemization under moderate heat, opening up wider application in condensation or amide-coupling chemistry. We’ve seen alternative products force users into extra protection or deprotection steps, or generate more waste in scale-up. For the right synthesis, ours offers a more straightforward entry to target molecules. Its substitution pattern and configuration grant higher selectivity in several known routes to beta-lactams, arylglycines, and related targets. Some competitors’ chiral acids bring extra functional groups that raise sensitivity or add preparation steps not always compatible with robust, scalable chemistry.

    Building on Transparency and Deliverable Results

    In a crowded market, we distinguish ourselves not just by producing (S)-(+)-Alpha-Methoxyphenylacetic Acid but by focusing on limit testing, detailed QC, and responsiveness. Customers engaged in patent filings or process development need more than reassurance—they want logs, audit trails, real-time batch analyses. We’re comfortable being closely scrutinized because we touch every step ourselves. Requests to tailor specs or adjust supply plans reach people empowered to make the call, not a go-between shuttling information back and forth.

    Our logistics support also comes from a place of experience. Shipping chiral acids requires careful control of temperature and humidity, and we know from practical mishaps how easily goods can degrade on a hot tarmac or in a leaky warehouse. All our supply chain decisions follow from the same sense of ownership we bring to manufacturing. We pack according to actual product stability, using tested materials and protocols derived from repeated, direct customer feedback. Each season teaches lessons—whether it’s improving desiccant choices or refining customs paperwork—to keep product arriving as it left our factory.

    Adapting to Evolving Industry Requirements

    Regulation never stands still, and synthetic intermediates like (S)-(+)-Alpha-Methoxyphenylacetic Acid face ever-stricter demands from both regulatory agencies and customer project managers. We’ve had to meet rising standards in impurity profiling, trace metals, and batch-to-batch consistency, which often means further investment in laboratory capabilities. Adding more sensitive LC-MS instruments, increasing frequency of out-of-spec batch reviews, or getting outside verification for optical purity all happen because we see changing customer audits. These adjustments impact our costs and workflow but deliver a product trusted in even the most tightly regulated projects. Our strategy always includes reinvestment in process control systems and documentation. Keeping clients and regulators satisfied only works when your information tracks truthfully from raw material to shipped drum.

    Researchers in both academia and industry tell us that the ability to trace bottle contents to exact production batches, with details on reagents and timepoints, sways their purchasing choices. We supply this granularity because we make everything in-house, not relying on intermediaries who might blend or obscure lot records. The resulting documentation travels with each shipment, providing certainty that the acid in the bottle matches the paperwork and will deliver in the synthesis it supports.

    Optimizing Solutions to Problems We Face

    Even with decades of experience, we never stop looking for smarter solutions. (S)-(+)-Alpha-Methoxyphenylacetic Acid synthesis can occasionally create byproducts during oxidation or methoxylation. Our technical team experiments regularly with improved catalysts and alternate protecting groups, searching for cleaner conversions and easier purifications. Sometimes the answer involves switching to more costly but purer inputs, other times it means slowing a reaction axis for thorough completeness. Each tweak produces learnings that benefit our customers and help keep projects moving forward without interruption.

    If we see recurring challenges—a rise in formaldehyde traces, a shift in melting point, or an uptick in customer complaints—we convene plant and quality teams to dig into root causes. We hold sample back-ups for years to aid in such trouble-shooting, enabling rapid retesting and comparison to historic benchmarks. Solutions arise from repeated process optimization, not from sidestepping underlying problems or masking outliers. Clients who’ve worked with us through years of multi-ton scale-ups recognize the depth of oversight and technical flexibility unique to manufacturers charting their own improvement course.

    Looking Ahead as Makers, Not Middlemen

    Our direct production of (S)-(+)-Alpha-Methoxyphenylacetic Acid places us alongside our customers. Each gram leaves our reactor as the result of deliberate choices—on reagent selection, purification approach, packaging quality, and logistical care. This allows us to guarantee and support the material far more thoroughly than those passing along intermediates from anonymous sources. Knowing the stakes tied to precise enantiomeric purity and clean spectra, we stand ready to solve problems and accommodate ever-changing customer needs. Whether you’re launching a new synthetic route, scaling up a pharmaceutical intermediate, or refining process validation samples, we appreciate the importance of having material from people who stake their daily reputation on what they produce, not just what they source.