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3-Hydroxyphenylacetic Acid

    • Product Name 3-Hydroxyphenylacetic Acid
    • Alias 3-HPA
    • Einecs 221-432-0
    • 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

    930361

    Cas Number 621-37-4
    Molecular Formula C8H8O3
    Molecular Weight 152.15 g/mol
    Iupac Name 2-(3-hydroxyphenyl)acetic acid
    Appearance White to off-white crystalline powder
    Melting Point 149-153 °C
    Solubility In Water Slightly soluble
    Pka 4.31
    Smiles OC(=O)CC1=CC(=CC=C1)O
    Synonyms 3-Hydroxybenzeneacetic acid
    Density 1.34 g/cm³ (approximate)
    Pubchem Cid 7683
    Storage Temperature 2-8 °C

    As an accredited 3-Hydroxyphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g 3-Hydroxyphenylacetic Acid is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 3-Hydroxyphenylacetic Acid is typically shipped in tightly sealed containers to prevent moisture and air exposure. It should be packaged according to chemical safety regulations, labeled clearly, and protected from heat and incompatible substances. During transit, the package must be handled carefully to avoid breakage, leaks, or spills.
    Storage 3-Hydroxyphenylacetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect the container from moisture and direct sunlight, and keep it at room temperature or according to the manufacturer’s recommendations. Ensure the storage area is clearly labeled and accessible only to trained personnel.
    Application of 3-Hydroxyphenylacetic Acid

    Applications of 3-Hydroxyphenylacetic Acid in Industrial Manufacturing

    3-Hydroxyphenylacetic Acid serves as a key intermediate across specialized industrial sectors. Our manufacturing-grade material consistently supports processes that require high-purity aromatic acids for the synthesis of complex molecules, with downstream applications spanning pharmaceuticals, flavors and fragrances, specialty chemical synthesis, and advanced research reagents. Each scenario outlined below details its technical value chain, regulatory context, recommended inclusion levels, and integration into downstream production environments.

    1. Pharmaceutical API Intermediate Manufacturing

    Pharmaceutical companies use 3-Hydroxyphenylacetic Acid as a crucial intermediate in the multi-step synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), antipsychotics, and beta-blockers. The raw material enters validated chemical transformations, such as amide coupling, acylation, and selective halogenation, to construct active pharmaceutical ingredients. The purity and traceability of the input lot directly affect target compound yield and impurity profiles, falling under strict regulatory oversight.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) standards for pharmaceutical intermediates
    • US FDA cGMP (21 CFR Parts 210, 211) for drug substance manufacturing
    • ICH Q7 Good Manufacturing Practice Guidance
    • Japanese Ministry of Health, Labour and Welfare (MHLW) JP guidelines

    Typical usage ratio

    • 0.5–3.0 molar equivalents per step, depending on the synthetic pathway; adjusted case-by-case for stoichiometric or excess use to drive desired transformations

    Downstream process integration

    • Charged at the condensation, acylation, or electrophilic substitution step of small molecule synthesis
    • Often introduced following chlorination, methylation, or hydrolysis steps with quantitative in-process control

    Final product types

    • Ibuprofen and analogues (NSAIDs)
    • Beta-blocker precursors (e.g., atenolol intermediates)
    • Psychoactive drug intermediates (e.g., risperidone, paliperidone)

    2. Flavors and Fragrances Synthesis

    In the fine chemicals sector, formulators rely on this aromatic acid to construct synthetic notes and building blocks for flavor and fragrance compounds. Through controlled esterification, reduction, or cyclization reactions, it forms the foundation for crafting high-value aroma chemicals and taste enhancers, where purity and byproduct minimization are critical for compliance and traceability in global consumer markets.

    Industry compliance standards

    • IFRA (International Fragrance Association) safety standards
    • US FDA 21CFR Part 172 (Food additives permitted for direct addition to food for human consumption)
    • REACH (EC) No 1907/2006 for registered chemical substances
    • ISO 9001:2015 certification for process control

    Typical usage ratio

    • 1–5% of reaction batch, based on target ester or alcohol yield; formulators adjust the ratio according to desired aroma intensity and regulatory maximum inclusion levels

    Downstream process integration

    • Fed into batch reactors during the esterification or reduction stages of synthetic flavor/aroma production
    • Purified using fractional distillation or crystallization post-reaction to isolate desired derivatives

    Final product types

    • Phenolic esters for fruit and honey flavors
    • Aromatic alcohols for perfume and cologne blends
    • Complex flavor additives for confectionary and beverages

    3. Peptide Synthesis Reagents

    In peptide and oligonucleotide laboratory and industrial synthesis, 3-Hydroxyphenylacetic Acid provides a protected structural motif for the assembly of peptide fragments and side-chain modification. Its orthogonal functional groups enable selective coupling when building block libraries or analogues for drug discovery, ensuring reliable reaction outcomes in solid-phase peptide synthesis (SPPS) and solution-phase protocols.

    Industry compliance standards

    • US Pharmacopeia (USP/NF) guidelines for peptide APIs and intermediates
    • ISO 13485:2016 for medical device and reagent manufacturing
    • ICH Q11 Development and Manufacture of Drug Substances
    • GLP (Good Laboratory Practice) for process R&D

    Typical usage ratio

    • 0.2–1.0 molar equivalent per coupling step; optimized based on peptide length and side-chain modification frequency

    Downstream process integration

    • Loaded as a protected amino acid or side-chain functional group at the respective assembly stage
    • Follows deprotection and activation chemistry for peptide elongation or library screening

    Final product types

    • Custom peptide analogues for preclinical development
    • Pharmaceutical-grade peptide APIs
    • Peptide diagnostic kits for research and clinical use

    4. Advanced Research Reagents and Diagnostics

    Institutes and commercial labs integrate this compound as a metabolite standard, chromophore precursor, and reference substance for analytical method development. Its purity and precise spectral characteristics make it integral for calibration, quantitative analysis of catecholamine pathways, and the synthesis of labeled standards for mass spectrometry and high-performance liquid chromatography (HPLC) applications.

    Industry compliance standards

    • ISO 17025:2017 for laboratory quality management systems
    • USP Reference Standard specifications for calibration and validation
    • GLP adherence for analytical method validation
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Standard concentrations typically range 1–50 mg/L for HPLC/MS calibration; quantities tailored per method sensitivity and matrix complexity

    Downstream process integration

    • Dissolved and standardized as an analytical reference material prior to instrument calibration
    • Included as a precursor in the custom synthesis of isotopically labeled internal standards

    Final product types

    • HPLC and GC-MS reference materials for clinical analysis
    • Metabolite standards for neurotransmitter research
    • Calibrants and control materials in forensic and pharmaceutical testing
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    Competitive 3-Hydroxyphenylacetic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Hydroxyphenylacetic Acid: A Foundation for Advanced Chemistry

    What Sets Our Product Apart

    For those of us working in fine chemicals, quality makes all the difference. 3-Hydroxyphenylacetic acid, known by its chemical formula C8H8O3 and CAS number 614-75-5, holds a special place among organic intermediates. Our production line pushes for purity that consistently exceeds 99%. Through years of refining our synthesis and quality control, we have built up a product that researchers and manufacturers can use as a reliable component—not just as another bulk chemical. Watching this molecule move from raw input to final crystal, we keep a close eye on moisture, trace metals, and color, all of which affect downstream reactions.

    Depending on the manufacturing route, impurities like 2-hydroxyphenylacetic acid or residual starting materials can persist. For us, tight control over these allows our 3-hydroxyphenylacetic acid to perform predictably, limiting variability batch-to-batch. We source quality phenol and acetic acid. Our team adjusts each step on real-time feedback from in-house HPLC and GC-MS analyses, going beyond basic thin-layer chromatography. Every year, we invest in purification, bottle washing, and in-process sampling because these affect whether bench scientists or industrial operators can trust our product.

    The Product’s Physical Profile

    3-Hydroxyphenylacetic acid takes the form of a white to off-white crystalline powder at room temperature. Material consistency matters for weighing, mixing, and dissolving. Our process yields a narrow melting point range—typically between 146°C and 148°C—whereas lower-grade batches from shortcuts in synthesis often display a broader, slushy melt. Particle size distribution stays tight, falling primarily within the 80–200 mesh range, without excessive fines that cause dusting or caking in storage.

    Sensitive storage and transport help us maintain this profile. By drying, vacuum packaging, and nitrogen overlay, our drums reach customers free from hydrolysis or oxidation products. Some makers have trouble preventing discolored or lumpy material, especially after air exposure; this frustrates both chemists and production line staff. Promoting product integrity at every step lets us avoid surprises with solubility or reactivity.

    Applications in Synthesis and Beyond

    3-Hydroxyphenylacetic acid sees regular use in pharmaceutical, agrochemical, and material research. It’s often a starting point for manufacturing more complex molecules—anti-inflammatory agents, CNS drugs, certain herbicides, and specialty polymers all trace back to this fundamental acid. One of its defining features, the free phenolic hydroxyl next to the acetic acid group, opens up functionalization routes: acetylation, etherification, halogenation, and amide coupling reactions all proceed cleanly when the acid is pure enough.

    Unlike standard phenylacetic acid, which lacks the hydroxyl group, this compound allows for aromatic substitutions that unlock new series of analogs. Chemists looking for greater diversity in their lead structures lean on 3-hydroxyphenylacetic acid, especially with coupling strategies relying on its phenol reactivity. It’s a pivotal building block in the production of some newer antipsychotics, cardiovascular drugs, and growth regulators.

    Certain pigment and dye makers also rely on 3-hydroxyphenylacetic acid for colorants with improved light fastness and solubility. In these settings, consistency and minimal trace contaminants avoid batch-to-batch color drift, so they appreciate a source that stays vigilant with purification.

    Differences from Related Compounds

    On the surface, it might seem like phenylacetic acids are fungible, but real-world chemistry says differently. The hydroxy group at the 3 position (meta to the acetic acid) profoundly shifts electronic character, solubility, and acidity. Take 4-hydroxyphenylacetic acid, a close cousin; the difference in substitution pattern changes how it can interact with enzymes or catalysts. We routinely discuss these differences with customers scaling up or changing synthetic plans.

    Our 3-hydroxyphenylacetic acid is not simply a niche alternative. Its unique properties—higher reactivity under electrophilic aromatic substitution, greater solubility in polar solvents, and propensity to form stable salts—expand its usefulness across disciplines. The 2-isomer, in contrast, brings different sterics and hydrogen bonding, affecting biological and catalytic outcomes.

    Several resin and plastic manufacturers have run side-by-side process trials using both isomers in polyester synthesis; only the 3-hydroxy version provided the desired flexibility and clarity. These differences become critical in applications like pharmaceutical intermediate production, where off-target products or low yields from a poorly matched starting compound can cost months of work.

    The Importance of Sourcing Direct from Manufacture

    As manufacturers who have watched this sector for decades, we’ve seen how fragmented supply chains and resold product can introduce trouble. Traceable production, documented process controls, and real-world accountability matter immensely. Direct purchase from the source means transparent QA/QC, technical support that can track issues back to a batch process, and the ability to modify output for a customer’s specific downstream chemistry.

    In-house manufacturing means we control everything from the solvent purification to the final drum fill. If an academic lab needs trace-metal-free material for sensitive palladium-catalyzed cross-coupling, we can provide that certificate—not as a box-checking exercise, but because our plant layout and cleaning processes cut contamination risks at every turn. We don’t blend leftover lots or take shortcuts by outsourcing key purification steps overseas, which sometimes leads to batch variability or hidden impurities. 

    Safety and Environmental Focus

    Every modern chemical facility faces scrutiny about environmental responsibility. We take that seriously—both to comply with regulations and to deliver on the unwritten expectations of our partners. Sourcing sustainable raw materials, recycling solvents, and implementing low-emission reactor systems have been central to our production upgrades. Sulfur- and nitrogen-containing byproducts, sometimes present in less refined material, rarely make it out of our gate, and anything not used in bulk product goes straight to well-documented waste channels.

    Our packaging meets current regulatory requirements, using recyclable drums and clear labeling for safety in handling. We routinely work with logistics companies to keep transit as efficient as possible, and our warehouse team monitors temperature and humidity around the clock. Simple steps—fast sealing after final drying, aged stock rotation, and frequent QA audits—let us resolve quality and safety issues before they reach anyone else’s lab or plant.

    Customer Collaboration and Problem Solving

    Many customers reach out before switching a synthetic route or moving to scale. We answer directly, with chemists who’ve made and used this material themselves—not just salespeople reading from a sheet. Process chemists involved in scale-up get advice about solubility, compatibility with coupling agents, and downstream reactivity, all based on real batches and actual plant experience. Over-specification by third-party resellers sometimes causes headaches for buyers who end up with unusable or inconsistent material. We’ve solved more than one problem for companies caught with out-of-spec acid from other sources.

    Some clients working with automated synthesis platforms have pushed for powder form modifications to improve dosing accuracy. After rounds of discussion, we introduced a narrow particle-size-cut product line, milled and screened under nitrogen and immediately packaged. Others found value in our desiccated packaging and low-endotoxin versions built for bioconjugation work. Through ongoing collaboration, we tailor production not by theoretical specs but by addressing actual challenges reported on the ground.

    Pushing Quality Standards

    Regular reviews of analytical profiles ensure our acid stands up to the latest synthetic demands. We maintain in-house archives on each batch for long-term data tracking. Any deviation or trend, whether in melting range, color, or particle distribution, gets flagged for process improvement. Aware that some users perform their own incoming quality tests, we encourage feedback and welcome sent-back samples for joint analysis, allowing both sides to dig in and address unforeseen complications.

    Our plant embraced inline NMR and online IR-spectra adoption early to catch reaction-phase issues as they occur, improving yield, purity, and cost structure. Analysts cross-check HPLC peaks for side-products and possible oligomers, and microbalance moisture checks ensure stability for months, even in warm or humid climates. Investing at every stage in better monitoring means researchers don’t have to deal with the risk of impurity-related noise in sensitive syntheses.

    Real-World Results

    Clients have taken our acid into peptide synthesis, PET imaging precursor production, and combinatorial library work. Once, a biotech firm described how side-products in lower-purity versions led to reduced assay reliability, impacting the outcome of months-long animal studies. By switching to our batch, their results stabilized. Pharmaceutical co-development partners have engineered novel prodrugs using the unique profile of our 3-hydroxyphenylacetic acid, docking into molecules where the ordinary phenylacetic acid backbone simply couldn’t deliver.

    For one agrochemical pilot project, clean hydroxy acid made the difference between scalable esterification in water and a fouled batch that forced hours of cleanup and risked worker safety. Real chemistry in the real world rewards those who invest in starting materials—and penalizes shortcuts.

    Continuing to Drive Innovation

    Years of hands-on production teach a few hard truths: purity matters, minor details in crystal habit affect yield, and scalable synthesis always relies on quality raw material. Our teams discuss new applications with partners, including use of 3-hydroxyphenylacetic acid as scaffolds for polymer design and as modifiable handles for fluorescent dyes and bioactive compounds.

    Some customers are pushing for even tighter control on trace residuals—chlorides, sulfates, metal ions—especially as catalysis and enzyme-coupled reactions grow more sensitive. Through dialogue with these innovators, we map new purification streams and analytical methods, translating bench-level demands into plant-scale improvements.

    The feedback loop between practical use and manufacturing improvements keeps us moving forward. Each time a research team builds a patentable molecule or a process engineer scales a critical batch without complications, we see the benefit of careful, and sometimes painstaking, attention to our acid production.

    Looking Forward

    Markets for 3-hydroxyphenylacetic acid evolve with changing drug pipelines, material science lines, and regulatory backdrops. Our place stays the same: steady, traceable production, hands-on expertise, and ongoing flexibility to help new projects take root. Careful, science-driven manufacturing never goes out of style, even as industries shift and expand.

    Whether it’s a new compound library, a scale-up campaign at a specialty pharma site, or an R&D effort hunting clean starting acids, we work to supply the kind of material we would want to use ourselves—no compromises, no lost batches, and no surprises. That’s what years in this business have taught us, and it’s the outlook we bring to every kilogram that leaves our doors.