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2-Benzyloxyphenylacetic Acid

    • Product Name 2-Benzyloxyphenylacetic Acid
    • Alias (BPAc)
    • Einecs 629-668-0
    • 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

    996909

    Iupac Name 2-(benzyloxy)phenylacetic acid
    Molecular Formula C15H14O3
    Molecular Weight 242.27 g/mol
    Cas Number 16652-77-0
    Appearance White to off-white solid
    Melting Point 78-80°C
    Boiling Point No data available (decomposes)
    Solubility In Water Slightly soluble
    Density 1.25 g/cm³ (approximate)
    Smiles O=C(O)Cc1ccccc1OCC2=CC=CC=C2
    Inchi InChI=1S/C15H14O3/c16-15(17)10-12-7-6-8-14(11-12)18-13-4-2-1-3-5-13/h1-8,11H,9-10H2,(H,16,17)
    Refractive Index No data available
    Storage Temperature Store at room temperature
    Purity Typically ≥98% (supplier-dependent)
    Use Chemical intermediate in organic synthesis

    As an accredited 2-Benzyloxyphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Benzyloxyphenylacetic Acid, 25g. Supplied in a sealed, amber glass bottle with printed label including chemical name, quantity, and safety information.
    Shipping 2-Benzyloxyphenylacetic Acid is shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. Packaging complies with relevant safety regulations to prevent leaks or contamination. The product is typically dispatched via ground or air transport, accompanied by appropriate documentation and labeling for identification and hazard communication. Store in a cool, dry place.
    Storage 2-Benzyloxyphenylacetic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Store away from incompatible substances such as strong oxidizers and bases. Always ensure containers are clearly labeled and follow relevant safety and chemical handling protocols.
    Application of 2-Benzyloxyphenylacetic Acid

    Applications of 2-Benzyloxyphenylacetic Acid in Industrial Manufacturing

    As a direct manufacturer of 2-Benzyloxyphenylacetic Acid, we supply this specialty intermediate to customers across several niche but well-established downstream sectors. Our quality systems, batch documentation, and technical support focus on supporting demanding industry-specific production environments. Explore below for sector-specific insights on compliance requirements, recommended formulation ratios, process integration points in manufacturing, and representative end-use product categories.

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

    2-Benzyloxyphenylacetic Acid functions as a crucial intermediate during multi-step synthesis of certain emerging benzylic-acetic acid NSAIDs. Pharmaceutical manufacturers use this raw material in preparatory alkylation or hydrolysis phases after initial coupling, due to its functional group compatibility and reactivity profile suitable for later deprotection or further acylation under GMP-controlled conditions. Handling specifications and traceability must address residual solvents, enantiomeric purity, and trace impurities due to downstream regulatory scrutiny.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 5.0
    • Chinese Pharmacopoeia (ChP) for bulk drug intermediates

    Typical usage ratio

    • 0.65–1.00 molar equivalent relative to final target NSAID (adjusted per synthetic step and side product formation limits)

    Downstream process integration

    • Charged into the main reactor post-coupling or phenol protection stages; follows controlled temperature addition and subsequent work-up for product isolation prior to final API condensation

    Final product types

    • Pharmaceutical-grade NSAID intermediates and finished active pharmaceutical ingredients (APIs)
    • Precursor substances for generic or proprietary anti-inflammatory tablets and capsules
    • Key building blocks supplied for contract API synthesis plants

    2. Aromatic Ester Pesticide Intermediate Synthesis

    Crop protection formulation plants use 2-Benzyloxyphenylacetic Acid for in-process generation of phenylacetic acid esters within multi-step manufacturing of specialty aromatic ester pesticides. This material enters as a substrate for subsequent esterification and O-debenzylation steps under controlled acidic or basic catalysis, allowing tailored substitution patterns needed in new-generation, selective insecticides. Site-specific batch records link to safety evaluation dossiers and pre-registration requirements for agrochemical actives.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • China ICAMA Product Registration (Agrochemicals)
    • ISO 9001:2015 Quality Management System for pesticides
    • REACH Regulation (EC 1907/2006) for intermediate registration

    Typical usage ratio

    • 10–18% by weight of total batch input mass during ester forming step, adjusted by required molecular excess to drive conversion while minimizing unreacted starting material

    Downstream process integration

    • Added as a feedstock at esterification reactor inlet, usually following solvent charge but prior to catalyst dosing; proceeds directly to acyl chloride activation and then purification before final active ingredient isolation

    Final product types

    • Aromatic ester pesticide active ingredients
    • Formulated insecticide technical concentrates
    • Key intermediates for selective herbicide synthesis

    3. Specialty Fragrance Ingredient Manufacturing

    Within the fine fragrance industry, downstream producers employ 2-Benzyloxyphenylacetic Acid as a custom intermediate for lactone-ring closure and subsequent hydrogenation operations, generating musk-like or floral olfactory profiles not replicable by simpler aromatic acids. Its unique substitution pattern allows for controlled benzyl removal and precision cyclization, supporting narrow-specification aroma ingredients for luxury perfumery. Compliance with IFRA and adherence to trace contaminant limits are essential for downstream blending.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards and Amendments
    • EU Cosmetics Regulation (EC) No 1223/2009
    • Global Fragrance Ingredient Transparency Guidelines
    • ISO 9001-certified fragrance production protocols

    Typical usage ratio

    • 5–12% by weight in base reaction mixture; further reduced in post-synthesis fractionation depending on targeted fragrance intensity and purity profile

    Downstream process integration

    • Introduced during intermediate lactone synthesis or musk precursor stage; followed by careful hydrogenation, phase separation, and vacuum distillation prior to blending into the perfume base

    Final product types

    • Fine fragrance core aroma intermediates
    • Luxury market perfume base blends
    • Musk and floral note fragrance compounds

    4. Advanced Liquid Crystal Precursors for Display Materials

    Manufacturers of advanced display technology source 2-Benzyloxyphenylacetic Acid for conversion into functionalized aromatic intermediates essential for high-stability liquid crystal monomers. The rigid phenylacetic backbone and selective oxygen substituents ensure precise coordination with core cyanobiphenyl or ester-based mesogen systems, enhancing electro-optical performance in LCD/LED modules. Process design requires meticulous control of purity and is aligned with proprietary panel manufacturing protocols and electronics material regulations.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances, EU 2011/65/EU)
    • REACH Regulation (EC 1907/2006) for polymer and electronics chemicals
    • ISO 14001 Environmental Management Systems (for display panel production)
    • IEC 61249-2-21 for halogen-free laminate materials

    Typical usage ratio

    • 3–8 mole% of total monomeric feed for liquid crystal formulation, adjusted based on dialkylation or crosslinking requirements in final display matrix

    Downstream process integration

    • Feeds directly into high-temperature bulk polymerization units during liquid crystal monomer synthesis; subsequent purification via preparative chromatography, then blended into eutectic mixtures for display cell alignment

    Final product types

    • High-performance liquid crystal monomer concentrates
    • Custom display material blends for advanced LCD and LED screen panels
    • Electro-optic alignment layer additives for electronics

    5. Custom Chiral Ligand Synthesis for Fine Chemicals

    Fine chemical plants and contract synthesis labs utilize 2-Benzyloxyphenylacetic Acid as a precursor for constructing chiral ligand scaffolds in asymmetric catalysis protocols. Its molecular framework supports regioselective functionalization, facilitating precise development of homochiral auxiliaries used in complex synthesis. Entry sequence typically involves O-debenzylation followed by conversion to amino acid or phosphine derivatives; batch manufacturing must satisfy trace impurity and metal content specifications aligned with chiral synthesis quality requirements.

    Industry compliance standards

    • GMP for Manufacturing of Non-API Fine Chemical Intermediates (as required by end-user)
    • ISO 9001:2015 Quality Management System
    • Specialty chiral ligand supplier audit protocols
    • OECD Good Laboratory Practice (GLP) for R&D processes

    Typical usage ratio

    • 0.8–1.2 molar equivalent in target ligand synthesis; scaled per final chirality requirement and depending on auxiliary pathway

    Downstream process integration

    • Used in initial ligand backbone assembly before functional group exchange and derivatization; integrated into protected/deprotected workflow stages with batch QC release before use in catalytic cycles

    Final product types

    • Chiral ligand intermediates and custom auxiliaries
    • Functionalized ligands for asymmetric transition-metal catalysis
    • Specialty organocatalytic agents for enantioselective reactions
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    Certification & Compliance
    More Introduction

    2-Benzyloxyphenylacetic Acid: A Manufacturer’s Perspective

    What We Produce: Focused on Quality

    Every time we weigh, mix, react, or recrystallize in our facility, we draw from years of commitment to high-quality chemistry. With 2-Benzyloxyphenylacetic acid, our team releases a specialty building block for custom synthesis, differentiated by batch-to-batch consistency, color clarity, and measured purity. Our chemists work on the floor that brings out each lot, not from a distance but right alongside technicians who watch for the smallest changes in crystalline texture or slight variations in melting range. The acid’s defining feature lies in its benzyloxy moiety connected to the phenylacetic core, which sets it apart from classic phenylacetic acid derivatives. As a team, we have learned the details that separate high-value material from generic stock: moisture level, residual solvents, and visual appearance matter as much as composition on a COA.

    The product arrives as a white or nearly white crystalline powder, with melting behavior and solubility closely monitored. Chemically, 2-Benzyloxyphenylacetic acid carries a phenylacetic acid backbone with a benzyloxy group at the ortho position. Chemists value this structure for its versatility. Whether applied in the synthesis of pharmaceutical intermediates, or leveraged in fine chemicals, it often serves as a starting point for further modifications and specialty compound development. From repeated reactions and purifications, we have refined steps to minimize side products like benzyl alcohol or unreacted O-benzylphenol, delivering a cleaner compound.

    The Importance of In-House Synthesis

    Our industry experience tells us that every synthetic step counts. Using direct benzylation and careful control of reaction temperature, we avoid excessive byproducts and produce reproducible yields, closely watching both reagent ratios and timings. Early in our history, we tried contract manufacturing routes but found that off-site batches rarely lived up to claims. Residual metals, broad melting points, or color issues would appear. Today, any batch labeled with our name is handled on our own reactors and monitored by our own chemists.

    It is not only about making acid that matches specification – we build in steps to prevent cross-contamination and monitor for degradation. No batch leaves our plant without confirming purity by HPLC, and we back that up with NMR and mass spectrometry checks. Our QC lab maintains standards above commonly accepted benchmarks, because we have worked downstream and know how even minor impurities can cause headaches later in synthesis. This down-to-earth approach avoids fancy terms and focuses on one central principle: what leaves our facility must work without complication for the next chemist, whether in research or scale-up.

    Defining the Model and Its Relevant Specifications

    Our 2-Benzyloxyphenylacetic acid follows a straightforward production model: direct benzylation of phenol, careful control of side reactions, and extraction to remove organic impurities. We do not chase marketing buzzwords or overhyped branding. What matters on our floor is the actual chemical sitting in the drum. Typical lots carry an assay above 99% by HPLC. Moisture content sits at low single-digit ppm, and appearance gives a gauge for any possible oxidation or polymerization. We always run additional identification beyond the bare minimum, running both proton and carbon NMR for every batch, and maintain archived samples for future reference.

    One of the most relevant differentiators in our process comes from how we handle purification. We worked for years with different solvent systems before developing one that preserves the full benzyloxy moiety while minimizing colored byproduct formation. This empirical refinement sets our product apart from many market alternatives, where yellowish tints or oily residues suggest incomplete removal of aromatic contaminants. Our batches show tight melting point windows, which means the lot will behave as expected, with no tackiness or late-melting residues common to incompletely purified material.

    Experiences From Production: Meeting Practical Challenges

    Scaling organic synthesis brings practical headaches rarely talked about in textbooks. Benzylic ethers invite both oxidative degradation and sometimes require gentle handling to avoid benzyl cleavage. Through many campaigns, we learned to maintain a slightly inert atmosphere in our reactors and process vessels, protecting the acid during both formation and storage. Between laboratory and 500-liter scale, subtle shifts in agitation speeds or solvent ratios led to a handful of lessons about crystallization and filtration – some of those early fouling events led us to switch to custom filters and set up additional drying capacity. Each challenge, from lumping to unexpected color shifts, forced us to improve process robustness.

    Customers in the pharmaceutical sector expect full traceability. Every drum coming from our lines can be traced back to a specific synthesis day, origin of raw material, and operator who signed off on batch records. This level of transparency, built up over years of GMP and ISO audits, protects both us and downstream developers. Returns or performance complaints get a prompt, clear investigation.

    Why This Product Matters: Not Just Another Phenylacetic Acid

    Chemists working across drug discovery, agrochemical research, or materials development know that small structural shifts can change everything. The benzyloxy group at the ortho position provides unique reactivity. It can serve as a masked phenol that gets unveiled during hydrogenolysis, enabling stepwise complexity without premature side reactions. On our end, we receive requests for both multigram and multi-kilo lots, supporting a range of applications: active pharmaceutical ingredient intermediates, specialty ligands, and even some polymer additives where structure specificity drives property profiles. Our repeated, close collaboration with R&D partners has helped us spot the subtle differences that matter — for example, the rate of side-chain deprotection under palladium-catalyzed conditions, or compatibility with particular coupling reagents.

    Other suppliers might offer a 'similar' molecule but fail to guarantee the absence of contaminants like benzylic ethers or overalkylated byproducts. Cutting corners in benzylation leaves material that, under real synthesis conditions, releases unexpected compounds. Our attention to detail — from raw input validation through to validated clean-up — prevents these tripwires for researchers. It has become second nature for us to supply supporting analytical data on request, providing more than just a generic COA. We have learned, through closeout reviews and batch release meetings, that customers value not only consistent supply but also fast answers to technical questions.

    Taking Responsibility for Supply Chain Reliability

    Secure sourcing and reliable batch homogeneity count as real deliverables. We operate our own raw material evaluation, analyzing each drum of benzyl chloride and phenylacetic acid for both purity and trace metal content before it ever reaches our reactors. These early steps matter far more than slick marketing materials. If the base chemicals lack quality, nothing downstream can fix the result. From supplier vetting to ongoing audits, we aim to minimize variables.

    No manufacturer in our field avoids every hiccup forever. We focus on transparent communication as soon as any issue arises. In our experience, even a day lost to an equipment failure can affect three customer timelines. Fast notification and risk assessments have built a reservoir of trust that keeps partners across Europe, North America, and Asia closely engaged. Production scheduling, inventory buffers, and emergency response drills receive the same care as our laboratory analytics — and from years in the industry, we know how quickly a single weak link ruins good work elsewhere.

    Product Handling and Use Cases: Insights from the Factory Floor

    2-Benzyloxyphenylacetic acid stores well in cool, dry facilities with low light, but we still recommend limiting exposure to air and especially to open flames, given the sensitivity of the benzylic ether. Recrystallized material rarely puts off any odor, and its physical handling raises no particular red flags with standard laboratory PPE. Out of the numerous acids, this one rarely triggers reagent incompatibilities during routine use — a testament to both chemical stability and process cleanliness.

    Researchers talk to us frequently about downstream workups. The ortho-benzyloxy group shows reliable removal under catalytic hydrogenation, allowing for clean conversion to the phenolic acid without scrambling protected groups elsewhere in the molecule. Some use our product in Suzuki coupling routes, others in Friedel-Crafts or alkylation tasks, and many in sequence assemblies where orthogonality in protecting group strategies determines project progress. Because we engage directly with these users, their feedback cycles back to us, helping us update process notes or suggest best practices for solvent handling, storage temperatures, and workup procedures.

    Standing Out From Other Phenylacetic Acid Variants

    Chemically, the distinction between 2-Benzyloxyphenylacetic acid and para- or meta-substituted isomers matters. Our synthetic method selects for the ortho isomer, which offers unique synthetic handles for subsequent functionalization. The benzyloxy group, as configured, resists migration or rearrangement under most conditions researchers apply, making synthesis step planning more reliable for complex compound assembly.

    Commercially, most bulk phenylacetic acid derivatives lean toward generic use, but our product finds its niche in demanding synthesis. Other offerings frequently lack a reliable supply chain audit trail or rely on outsourcing that introduces hidden variables. By holding our entire process in-house, we cut out surprise contamination issues. Chemists often tell us about projects delayed by inferior feedstock or unstable intermediates from third-party sources. Our history shows that prompt supply, paired with batches that match analytical claims, enables research teams to focus on the experiments that matter.

    Supporting Customers: Our Role Beyond Simple Supply

    Sales and support personnel here do not operate from distant call centers; they work within steps of the laboratory, communicating directly with the process development team. Most customer inquiries reach someone who has worked with the actual material, sometimes even running their own reactions as proof of performance before making recommendations. This immediacy shortens feedback loops and helps us keep technical support closely tied to real-world conditions.

    Custom adaptation matters. Over the past few years, several partners have asked for specific particle size distributions, for tightly defined moisture tolerances, or for new solvent residuals analysis. Our team does not shy away from special requests, and ongoing collaborations have led to new purification steps or alternative packaging options tailored to sensitive materials. Whether the acid needs to ship across continents or to a university next door, our logistics crew tracks each step, from dry room packing to customs paperwork.

    Sustainability and Safety: Learning Over Time

    Sustainable chemical manufacture means more than handling waste coupons or ticking regulatory boxes. Daylight in the plant falls on solvent recovery systems, scrubbers, and staff safety meetings held every week. From direct experience, we know that good solvent management, efficient benzylation practices, and real attention to waste minimization deliver both environmental and bottom-line benefits. A minor improvement in reaction yields or reduction in side-products translates into real reductions in disposal loads and lower cost per batch — a lesson learned over decades, not in a single turn of the calendar.

    Safety drives every improvement. Benzylic ether precursors can cause irritation or, if handled carelessly, fire hazards. Our in-house safety trainers walk through every new process campaign, retraining not just for regulatory reasons but because we have seen the alternative. The stories we tell new staff — spilled drums, poorly ventilated transfer rooms, missed MSDS updates — reinforce a culture defined by real consequences and real responsibility.

    Future Directions: Building on a Track Record

    Developing new grades or adapting to research customer demand means constantly refining both process chemistry and logistics. We keep ongoing research efforts tuned to trends we notice in the downstream industry: demand for even higher purity lots, expanded NMR libraries, tighter control of metallic impurities, and customized documentation for patent filings. Recent expansions to our QC instrumentation bring both speed and confidence to release testing, shortening lead times for customers putting projects under time pressure.

    No batch ever represents the end of our learning curve. Occasional surprises in crystallization habits or shifts in input quality prompt both troubleshooting and innovation. By bringing troubleshooting and improvement together under the same roof, we maintain an edge in both reliability and adaptability. Customers in regulated markets find value in this record of traceable, defensible processes. Experienced staff who have seen full project lifecycles ensure that knowledge is not lost, training the next generation with the same hands-on detail that protects quality every day.

    Direct Voices, Real Trust

    The value of 2-Benzyloxyphenylacetic acid does not stop at a line on a specification sheet. From the initial synthetic plan to the final shipment, every step we take embodies the lessons and standards forged in real chemical manufacturing. Consistency, transparency, and a focus on doing things right drive our work. Customers and partners return because they find not only a product that performs, but a relationship with a supplier that stands accountable for every kilo delivered. The acid, in our hands, becomes more than a commodity; it becomes a foundation for new molecules, a testament to craftsmanlike care, and a story of chemical progress rooted in experience.