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4-(Hydroxymethyl)Phenoxyacetic Acid

    • Product Name 4-(Hydroxymethyl)Phenoxyacetic Acid
    • Alias Paracoumaric acid
    • Einecs 287-608-9
    • 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

    588865

    Productname 4-(Hydroxymethyl)Phenoxyacetic Acid
    Casnumber 104-82-5
    Molecularformula C9H10O4
    Molecularweight 182.18
    Appearance White to off-white solid
    Meltingpoint 150-153°C
    Solubility Soluble in water and polar organic solvents
    Boilingpoint Decomposes before boiling
    Density 1.36 g/cm³
    Ph 4.0-5.0 (1% aqueous solution)
    Smiles C1=CC(=CC=C1CO)OCC(=O)O
    Inchi InChI=1S/C9H10O4/c10-6-7-2-1-3-8(4-7)13-5-9(11)12/h1-4,10H,5-6H2,(H,11,12)

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-(Hydroxymethyl)phenoxyacetic acid; labeled with chemical details and safety information.
    Shipping 4-(Hydroxymethyl)phenoxyacetic acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be packed according to chemical safety regulations, typically in amber glass bottles and cushioned within secondary packaging. The package is clearly labeled with hazard and handling precautions, ensuring protection during transit under controlled temperature conditions.
    Storage 4-(Hydroxymethyl)Phenoxyacetic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat and moisture. Protect from direct sunlight and incompatible materials such as strong oxidizing agents. For prolonged storage, refrigeration (2–8°C) is recommended. Always label the container clearly and follow all relevant safety and handling guidelines.
    Application of 4-(Hydroxymethyl)Phenoxyacetic Acid

    Applications of 4-(Hydroxymethyl)Phenoxyacetic Acid in Industrial Manufacturing

    As an experienced manufacturer of 4-(Hydroxymethyl)phenoxyacetic acid, we supply this intermediate to a select range of advanced industrial sectors. Below, we detail its principal downstream application fields, compliance aspects, technical formulation parameters, critical process integration steps, and finished product categories as established in the international market.

    1. Pharmaceutical Intermediate for Beta-blocker Synthesis

    Pharmaceutical manufacturers use this compound primarily as a key building block in the synthesis of certain beta-blockers, where its phenoxy group enables precise functionalization in active molecule assembly. Production involves strictly defined aseptic and reaction conditions to maintain purity and prevent cross-contamination, meeting regulatory demands for human medicinal products.

    Industry compliance standards

    • Complies with ICH Q7A for Good Manufacturing Practice (GMP) of Active Pharmaceutical Ingredients
    • Meets requirements under US FDA 21 CFR 210/211 and EU EudraLex Volume 4
    • Traceability under USP/NF and EP monograph systems for pharmaceutical impurities
    • Relevant Hazard Analysis Critical Control Points (HACCP) for process safety

    Typical usage ratio

    • Employed at 0.2–0.7 molar equivalents relative to final API backbone, with ratio adjusted according to target substitution step and desired yield; higher ratios ensure complete conversion in high-purity syntheses.

    Downstream process integration

    • Input after initial aromatic ring formation; undergoes etherification and side-chain functionalization steps prior to chiral separation or salt formation stages.

    Final product types

    • Beta-blocker APIs for hypertension and cardiovascular therapeutics (e.g., metoprolol analogues)
    • Intermediate bulk pharmaceuticals intended for licensed formulation houses

    2. Herbicide Selective Growth Regulator Intermediate

    Agrichemical formulators incorporate the molecule as a regulated precursor in the synthesis of aryloxyacetic acid-based herbicides and plant growth regulators. Here, formulation consistency and residue control are mandated, and the acid group is critical for conjugation reactions that dictate herbicidal spectrum.

    Industry compliance standards

    • Registration under OECD guidelines and REACH Annex IX procedures
    • GLP certification for all synthesis and residue field studies
    • Compliance with FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • Maximum Residue Limit (MRL) settings according to Codex Alimentarius

    Typical usage ratio

    • Used at 5–12% by weight in herbicide active ingredient synthesis, depending on target ester or amide substitution.

    Downstream process integration

    • Employed in the early alkylation or condensation stages prior to acid chlorination, followed by formulation into technical concentrates or emulsifiable bases.

    Final product types

    • Selectivity-modifying herbicides for cereal or broadleaf crop applications
    • Finished plant growth regulators for agronomic dispersion

    3. Monomer Precursor in Advanced Polymer Synthesis

    In specialty polymer manufacturing, this raw material serves as a nucleophilic agent for the creation of high-performance polyesters and polyarylethers. Its dual functional groups enable precise control of molecular weight, chain architecture, and polymer end properties, matching technical requirements in high-temperature and corrosion-resistant plastics.

    Industry compliance standards

    • Manufactured and handled under ISO 9001:2015 quality management systems
    • Composition disclosure compliant with EU REACH registration
    • Polymer grade assessment by ASTM D638 for mechanical testing
    • RoHS Directive 2011/65/EU for environmental safety in electrical/electronic end-uses

    Typical usage ratio

    • Feeds at 10–25 mole% of total diol/diacid monomers in polymerization blend, determined by chain-length target and desired flexibility or crystallinity.

    Downstream process integration

    • Added during melt-stage or solution polycondensation, with timing and concentration optimized to control degree of polymerization and incorporation of hydroxy-functional side chains.

    Final product types

    • High-performance polyarylether polymers
    • Engineering plastics used in electronics, automotive, and chemical processing equipment

    4. Cosmetic Ingredient Stabilizer and Intermediate

    Personal care product manufacturers employ this compound as a stabilizing and delivery system precursor for advanced cosmetic actives, particularly where hydrophilic modification is required for improved skin absorption. Formulation must meet stringent non-toxicity and allergy safety tests as mandated in major cosmetics markets.

    Industry compliance standards

    • Complies with EU Cosmetics Regulation (EC) 1223/2009 for ingredient safety and labeling
    • Conforms to US FDA Voluntary Cosmetic Registration Program (VCRP) and CIR Expert Panel reviews
    • Follows ISO 22716 for Good Manufacturing Practices in cosmetic raw materials
    • Prohibition of animal testing as per international regulations

    Typical usage ratio

    • Utilized at 0.1–1.5% w/w in cosmetic emulsions and up to 2.8% in intermediate surfactant blends, customized for product matrix and stability.

    Downstream process integration

    • Introduced during primary emulsion or microemulsion blending; also employed in pre-functionalized delivery vehicles prior to final mixing and packaging.

    Final product types

    • Skin serums with controlled-release actives
    • Moisturizing creams requiring hydrophilic enhancer ingredients
    • Intermediate surfactant and emollient concentrates

    5. Laboratory Reagent for Analytical and Biochemical Research

    Chemical R&D laboratories and analytical service providers use this compound for controlled conjugation reactions, derivatization of phenolic compounds, and assay development. High purity and trace contaminant control are required to ensure data reproducibility and integrity in regulated environments.

    Industry compliance standards

    • Conforms to ISO/IEC 17025 for calibration laboratory quality
    • Meets ACS Reagent Grade or analytical standards relevant for biochemical research
    • Proper documentation for traceability and certificate of analysis (COA) issuance
    • Storage and handling per Chemical Hygiene Plan (CHP) and local safety standards

    Typical usage ratio

    • Dosed at 10–300 μmol per reaction, scaled as needed for batch or microplate scale; users adjust based on assay sensitivity and substrate amount.

    Downstream process integration

    • Added in the derivatization or sample preparation step prior to analytical measurement (HPLC, GC, LC-MS); also serves as a molecular probe or linker in synthetic biology protocols.

    Final product types

    • Research-use-only analytical test kits
    • Labeled conjugates for immunoassays and enzyme analysis
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    Certification & Compliance
    More Introduction

    4-(Hydroxymethyl)Phenoxyacetic Acid: From Laboratory Synthesis to Industry Application

    Introduction

    As manufacturers, we walk a fine line each day between creative synthesis and practical demands. 4-(Hydroxymethyl)Phenoxyacetic Acid, which carries the formula C9H10O4, represents the kind of molecule that sparks fresh conversation between chemists and production teams alike. Its role as an intermediate in fine chemicals and pharmaceuticals continues to expand. Quite a few clients who once sought more familiar building blocks have grown curious about its possibilities. Bringing this product to scale isn’t just about process know-how—it's about trust, responsibility, and noticing the way small structural changes can open unexpected doors.

    Understanding the Structure and Its Implications

    This molecule draws attention because its scaffold offers both stability and targeted reactivity. The phenoxyacetic acid backbone has served many in fields like agrochemicals, but adding a hydroxymethyl group at the para position influences how it takes part in further transformations. Many derivatives follow similar core patterns, yet their practical uses can differ sharply. Our experience shows that the introduction of a hydroxymethyl group—essentially transforming a basic aromatic system—affects solubility, reactivity for downstream coupling, and alters the way the compound interacts with other raw materials. The acid group promotes water solubility, and that opens up safe, predictable handling for various reaction pathways. Our chemists appreciate how this balance between hydrophilic and hydrophobic features makes it more accessible in certain synthesis routes.

    Production Challenges and Ingenuity

    To deliver a reliable product, we’ve poured hours into safe, scalable synthesis. Several older processes relied on multi-step protection and deprotection of functional groups, often sacrificing yield and requiring hazardous reagents. Our production philosophy centers on reducing bottlenecks and controlling impurities at every stage. The hydroxymethyl group, reactive by nature, demanded clever solutions to avoid unwanted side products. We leaned into improvements by investing in better catalysts, tracking each stage with modern chromatography, and documenting every deviation closely. Lower batch variability doesn’t just reduce headaches for us. It gives end users confidence that downstream conversions won’t be tripped up by batch-to-batch quirks. We’ve noticed that even small shifts in purification methods leave a notable fingerprint on reproducibility for customers working at scale.

    Purity, Documentation, and Confidence in Supply

    No lab team appreciates a material with ambiguity. Our standard offering of 4-(Hydroxymethyl)Phenoxyacetic Acid comes with certificates of analysis that detail spectral data rather than ticking off generic box checks. HPLC purity commonly surpasses 98 percent. We don’t stop at dry numbers; our staff cross-checks melting point ranges and follows up on reported anomalies. Customers sometimes assume small-volume purchases don't need the same scrutiny as ton-scale output, but our QC standards stay consistent, regardless of order size. Out-of-spec shipments eat away at productivity, and we aim to do our part in minimizing interruptions, especially for clients running tightly scheduled campaigns.

    Regulatory Familiarity and Responsible Handling

    As international customers grow more vigilant about compliance, producers like us have a duty to provide transparent information about trace impurities and documentation for regulatory filings. Over the last decade, authorities have placed more focus on the source and control of starting materials, especially those used in pharma. Our history working with global partners ensures we shape batches to meet both established and emerging regulatory needs. This means not only meeting spec on physical quality, but documenting batch genealogy, process parameters, and stability data. The acid’s clean toxicological profile also gives peace of mind to formulators compared to some halogenated or nitro derivatives that raise red flags. Every shipment leaves our plant with a clear chain of custody, so customers in tightly regulated territories don’t have to untangle compliance questions later on.

    Application Versatility: Pharmaceuticals, Agrochemicals, and Beyond

    Many first encounter 4-(Hydroxymethyl)Phenoxyacetic Acid in early-phased pharma synthesis, where it proves valuable as both a precursor and a linker. Our records show that its structure is prized for building blocks in active pharmaceutical ingredients—especially those seeking improved metabolic stability and predictable reactivity. Its dual functional groups lend themselves to esterification, alkylation, and amidation. Colleagues from the agrochemical sector appreciate its adaptability as a template for herbicide and fungicide candidates. One distinct feature is the acid’s performance in coupling reactions, often improving yields and product isolation thanks to the selective reactivity of the hydroxymethyl moiety. Unlike related acids with bulkier substituents, the product’s moderate steric profile allows for cleaner downstream chemistry.

    Specialty polymer manufacturers tap its unique balance between rigidity and modifiability. We’ve supported teams incorporating it into novel resins and plasticizers. Its predictable melting profile and thermal stability suit resin synthesis where performance and longevity matter. Feedback from partners in the fragrance and flavor industry pointed to its aromatic core as a base for new ingredients, especially where a subtle hydrophilic handle provides a performance edge.

    Distinguishing from Related Materials

    We routinely get questions about the differences between our 4-(Hydroxymethyl)Phenoxyacetic Acid and older phenoxyacetic acid analogues. The main distinction lies in its functional group density. Where a basic phenoxyacetic acid falls short in further modification, the hydroxymethyl group at the four-position quickly stands out as a gateway to more complex derivatives, whether protective groups or advanced branching are required. Our process ensures that the product stays free from over-alkylated or oxidized by-products—a challenge commonly seen when less experienced hands handle this chemistry. We’ve also evaluated parallel materials that include ortho- or meta-substituents, but these often fall short in either solubility or reactivity during parallel reactions.

    We sometimes address comparisons with related compounds like 2-(Hydroxymethyl)phenoxyacetic acid and its meta-isomer. The para arrangement in our material brings both practical and theoretical advantages. Solubility, melting behavior, and reactivity under catalytic conditions show more predictable outcomes, reducing surprises during multi-step synthesis. Some have looked to simpler para-substituted acids, but efforts to attach hydroxymethyl groups post-synthesis often result in low yields and messy purification.

    Insights Gained from Real-World Collaboration

    Too often, manufacturers and users talk past each other. Our own best lessons came through hands-on trials with pharmaceutical and agrochemical companies. We’ve observed that early conversations about solvent choices or acceptable particulate load can prevent frustration later. For example, one customer’s formulation would fail with residual water content above 0.3 percent. We modified our final drying regimen to ensure product delivered always came comfortably below this threshold. Other partners needed custom particle sizes for process efficiency. We responded by refining our milling and sieving steps and provided real-world samples rather than relying on theoretical distributions. These iterative refinements paid off not only for them but also raised the bar for our next batches.

    The product’s popularity grew not merely through catalog listing but through the careful tailoring to very real project constraints. We found value in sharing our own troubleshooting diaries—highlighting times when new impurities cropped up or yields dipped during scale-up. Relaying those stories proved more useful than sterile graphs or spectra. This candidness built mutual respect—especially in regulated fields where reproducibility isn’t negotiable.

    Anticipating Supply Chain Demands

    The past few years tested every chemical supplier’s agility. Shortages in raw materials, as well as shifting energy costs, forced adaptation. Our location let us cultivate stable supplier relationships. Knowing how far ahead to secure key reagents proved critical—especially since some upstream chemicals face regulatory scrutiny or sudden export restrictions. Price volatility had to be managed thoughtfully. We shared cost projections openly with customers to help them plan, sometimes offering feasible alternatives for projects with sensitive cost parameters.

    We devote constant attention to packaging and logistics. Some partners require tailored drum sizes or vacuum-sealed containers to prevent moisture uptake. For global shipments, clear labeling in accordance with destination regulations keeps transfers through customs as hassle-free as possible. We invest in transport partnerships who understand our customers’ expectations for prompt, damage-free delivery. Success means not just leaving our facility on time, but ensuring materials reach their final destinations in usable condition. Our shipping team routinely monitors transit temperatures and transit times, flagging any disruptions before they become customer pain points.

    Long-Term Storage and Shelf Life Insights

    Many compounds storing a free hydroxyl group face stability issues. Our in-house trials show that 4-(Hydroxymethyl)Phenoxyacetic Acid resists significant degradation under cool, dry conditions. We encourage customers to store the compound in sealed, opaque containers, as even moderate humidity and sunlight can encourage slow discoloration or acid value drift. Some partners request formal stability reports to meet internal QA requirements. We provide these alongside change logs describing every process tweak, right down to filter material. Over the years, we observed that improper storage, especially exposure to cyclic temperature swings, diminished purity. Recognizing storage realities in both warehouse and laboratory settings, we fine-tuned our default packaging and documented optimal environmental settings.

    Environmental and Safety Considerations

    Chemical manufacturing carries a heavy duty to community health and the environment. Throughout our production, we designed waste streams to minimize impact. Recovering solvents, reducing aqueous waste, and capturing airborne by-products means less material leaves our site. Process emissions are measured with calibrated equipment; reports are shared with regulatory authorities and, when requested, with customers keen on green credentials. Product residuals show low aquatic toxicity compared to halogenated equivalents—an important distinction for partners seeking to minimize their environmental reporting burden.

    Handling within the plant prioritizes ventilation and personal protective measures. While 4-(Hydroxymethyl)Phenoxyacetic Acid doesn’t present acute hazards, every kilogram earns our respect. Staff receive updated training annually; incidents or near-misses are debriefed openly. The learning loop here means safer production runs and fewer surprises downstream.

    Future Opportunities and Research Directions

    We monitor the literature and our own collaborations for new application ideas. More groups experiment with its inclusion in drug conjugate research, linking to peptide or sugar moieties for targeted delivery. Some materials engineers are exploring its performance as a crosslinking agent in next-generation composites. Our technical group welcomes dialogue with research teams tackling bold projects. Many advances come from shared mistakes just as much as from unqualified successes.

    Production methods aren’t static. We trial greener reducing agents, minimize hazardous intermediates, and incrementally adjust for process intensification. Some suppliers handled this acid as merely a checklist item; we see each lot as a chance to build on what’s been learned before. Fielding customer suggestions drives many of our best improvements, from batch size adaptation to custom labeling practices.

    Conclusion

    From a manufacturer’s vantage point, 4-(Hydroxymethyl)Phenoxyacetic Acid stands as a testament to the ongoing conversation between bench chemistry and industrial reality. Real value emerges not from sameness, but from attention to the subtle differences in each batch, each application, and each partnership. As demands shift and projects scale, continuing to ask tough questions—and listening to feedback—lets us keep pace with both innovation and regulation. At root, every drum shipped doesn’t just contain a chemical; it represents years of growing expertise, practical adjustment, and genuine collaboration across the supply chain.