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2-Hydroxy-2-(4-Methylphenyl)Acetic Acid

    • Product Name 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid
    • Alias Mandelic acid, p-tolyl-
    • Einecs 226-679-5
    • 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

    591568

    Chemical Name 2-Hydroxy-2-(4-Methylphenyl)acetic acid
    Molecular Formula C9H10O3
    Molecular Weight 166.18 g/mol
    Cas Number 4312-10-3
    Appearance White to off-white solid
    Melting Point 92-94°C
    Boiling Point 353.8°C at 760 mmHg
    Solubility Slightly soluble in water
    Pka 3.42 (carboxylic acid)
    Smiles CC1=CC=C(C=C1)C(C(=O)O)O
    Inchi InChI=1S/C9H10O3/c1-7-2-4-8(5-3-7)9(11)6-12/h2-5,9,11-12H,6H2,1H3
    Density 1.27 g/cm3
    Storage Temperature Store at room temperature
    Flash Point 168.5°C
    Synonyms 4-Methylmandelic acid

    As an accredited 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g amber glass bottle with tamper-evident cap, labeled "2-Hydroxy-2-(4-Methylphenyl)Acetic Acid, reagent grade," with hazard symbols.
    Shipping 2-Hydroxy-2-(4-Methylphenyl)acetic acid is shipped in sealed, chemical-resistant containers to prevent contamination and moisture absorption. It should be handled according to standard safety protocols, with clear labeling and proper documentation. During transit, it must be kept cool and dry, away from incompatible substances and direct sunlight.
    Storage Store 2-Hydroxy-2-(4-methylphenyl)acetic acid in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Ensure proper labeling, and avoid prolonged exposure to air. Use personal protective equipment when handling to prevent skin and eye contact.
    Application of 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid

    Applications of 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid in Industrial Manufacturing

    As an experienced manufacturer of 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid, we support key sectors utilizing its unique chemical properties for targeted industrial transformation. Here, we present proven downstream pathways focused on real production needs, ensuring process transparency for decision-makers and technical buyers.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

    Pharmaceutical firms incorporate this material as a critical intermediate during multi-step synthesis of specific NSAIDs, especially in proprietary arylacetic acid derivatives. Its reactive hydroxy group and substituted phenyl structure enable precise coupling and controlled aromatic substitutions, influencing pharmacokinetic characteristics in the final API. Production facilities operate stringent batch records and impurity profiles to satisfy international regulatory dossiers for eventual market registration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (API manufacture)
    • USP, EP monograph requirements for related pharmaceutical starting materials
    • FDA 21 CFR Part 211

    Typical usage ratio

    • 1.5–2.8 molar equivalents per target NSAID synthesis step, depending on side chain complexity; adjusted in process optimization based on conversion yield and impurity control

    Downstream process integration

    • Charged during controlled condensation or Grignard coupling steps in GMP reactor suites; involved in purification before downstream derivatization and salt formation

    Final product types

    • Pharmaceutical active ingredients in arylacetic acid NSAID categories (e.g., mefenamic acid structural analogs)
    • Regulated intermediates for further conversion into finished oral dosage NSAIDs

    2. Synthetic Building Block for Agrochemical Active Ingredients

    Leading agrochemical producers utilize this compound’s arylacetic acid core in constructing pre-emergent and selective herbicide actives, as well as specialized plant growth regulators. It supports high-specificity synthetic steps where maintaining aromatic ring integrity and precise carboxyl orientation critically affect herbicidal activity and crop safety. Process engineers monitor input quality to minimize trace contaminants impacting downstream plant trials and regulatory filings.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • ISO 17025-compliant QC for purity and residual solvents
    • U.S. EPA pesticide formulation requirements (40 CFR Part 158)
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • 8–15% by mass in pre-final herbicide intermediate stage; customized based on active ingredient type and target species selectivity

    Downstream process integration

    • Integrated in heterocyclic coupling or esterification reactors prior to crystallization and formulation into technical grade agrochemical powders or solutions

    Final product types

    • Technical herbicide actives for cereals, rice, and specialty crops
    • Plant growth regulator ingredients for horticultural use

    3. Monomer Precursor in Specialty Polymer Synthesis

    This raw material serves as an aromatic monomer unit in the production of high-performance specialty polymers where acid functionality and para-methylphenyl substitution deliver targeted thermal resistance and physical properties. Polymer chemists capitalize on its consistency and ease of processing, introducing it in step-growth polycondensation reactions for applications demanding strict batch traceability and reproducible mechanical strength across end uses.

    Industry compliance standards

    • ISO 9001:2015 quality management protocols
    • REACH Annex XVII—polymer safety limits regarding monomer and additive input
    • ASTM D638/D790 for mechanical property evaluation of finished polymers
    • RoHS-2 Directive compliance for polymer content in electronic/electrical applications

    Typical usage ratio

    • 18–30% by monomer mole ratio in copolyester or polyamide production; selected to meet precise Tg or modulus targets specified by downstream clients

    Downstream process integration

    • Added to bulk polymerization reactors during condensation, with reaction temperature and monomer feed adjusted to control polymer molecular weight and branching

    Final product types

    • Heat-resistant polymer pellets for molded automotive or electronic housings
    • High-gloss engineering films and sheets for optical, display, and specialty packaging sectors

    4. Fine Chemical Intermediate for Fragrance and Aroma Compounds

    Manufacturers of synthetic fragrances employ this acid in the multi-stage synthesis of advanced aromatic esters and alcohols, supporting the production of stable, high-purity components for finished perfumes and flavorings. Sourcing teams and process chemists rely on well-defined impurity control of this precursor, as trace residuals can distort olfactory profiles or impact food safety in end products intended for regulated markets.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice and purity specifications
    • EU Regulation (EC) No 1334/2008—flavoring substances in food
    • US FDA 21 CFR 172.515—synthetic flavoring substances
    • ISO 9235:2013 for aroma chemical classification

    Typical usage ratio

    • 3–12% by mass in aromatic esterification or alcohol reduction stages; optimized according to flavor/aroma intensity and retention requirements

    Downstream process integration

    • Fed into batch reactors for acid-catalyzed esterification; downstream purification steps ensure removal of starting acid prior to blending into fragrance bases or food-grade flavors

    Final product types

    • Complex perfume bases for personal care and luxury hygiene goods
    • Flavor additives for beverages and confectionery complying with global regulatory frameworks
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    Certification & Compliance
    More Introduction

    2-Hydroxy-2-(4-Methylphenyl)Acetic Acid: Precision at the Core of Modern Synthesis

    Introducing 2-Hydroxy-2-(4-Methylphenyl)Acetic Acid

    Manufacturing 2-Hydroxy-2-(4-methylphenyl)acetic acid is a blend of science and reliability. Through years of upscaling organic synthesis, we’ve built a process that produces this compound at high purity with consistent physical characteristics, making it a dependable ingredient for downstream innovators. Known in the field for its molecular precision and tailored reactivity, this compound functions as a linchpin for specialty chemistry, especially where accuracy in molecular structure matters. Every step in its creation—from initial feedstock selection to careful recrystallization—factors into the consistency end users expect.

    Product Details and Physical Characteristics

    This compound typically presents as a white to off-white crystalline powder, showcasing its high level of refinement. The model most clients request maintains strict boundaries on melting point and residue content because our experience shows that even minor impurities can cause major downstream unpredictability. Batch quality ties directly into analytical standards, so each lot undergoes testing using high-performance liquid chromatography and other established methods. Monitoring trace metals and organic byproducts throughout production keeps us on course for applications that cannot tolerate contamination.

    Molecular formula C9H10O3 and a molecular weight in line with the theoretical calculation—these specifics reflect the skill it takes to produce a reliable intermediate for advanced chemistry. Our process operates under strictly controlled temperature and atmosphere, using reagents free of excess water and pre-screened for reactivity with the acid’s unique functional groups. Over years of feedback from pharmaceutical and materials science partners, we have refined particle size distributions and moisture content so that integration into solid-phase or solution-phase processes proceeds seamlessly.

    Frontline Role in Synthesis and Applications

    Specialty organics thrive on small differences in structure or configuration. 2-Hydroxy-2-(4-methylphenyl)acetic acid stands apart for its balance of reactivity and selectivity. We’ve seen firsthand how the para-methyl group on the aromatic ring gently shifts electron density, which gives this acid favorable properties in reactions such as esterification, amidation, and other catalytic transformations. This small shift means researchers and process chemists can achieve higher selectivity when introducing functional groups compared to unsubstituted or ortho-substituted analogs.

    In our own labs and those of our long-term partners, this molecule unlocks new synthetic approaches for active pharmaceutical ingredients, agrochemical intermediates, performance dyes, and specialty polymers. Because we’ve tailored our workflows for scalability, both R&D teams and production chemists benefit from lots that behave predictably in chlorination, acylation, and condensation reactions. The hydroxyl group at the alpha position makes it a valuable synthon for building blocks with stereochemical complexity, a demand that keeps growing as targeted therapies and advanced materials become more precise.

    Why Purity and Batch Control Matter

    Even small contaminants trigger major headaches in multi-step synthesis. Based on feedback from customers and our own troubleshooting, we emphasize rigorous removal of starting material traces, isomeric byproducts, and moisture. These can deactivate catalysts or even poison whole reaction streams, leading to costly purification or failed batches down the line. Every batch receives spectral fingerprinting so any deviation from baseline triggers immediate corrective action.

    Refining the process for this acid isn’t purely an academic exercise. One of our clients experienced inconsistent yields when using material sourced from a general supplier. Our material replaced it and downstream variability fell to trace levels, cutting repeated testing costs. That’s the difference a manufacturer makes—instead of treating purity as a number on a certificate, we treat it as daily practice on the equipment and in the mindset of the team.

    Batch traceability helps us isolate improvements. Any production change, from reactor jacket temperature to minor pH tweaks in the final wash, goes into our records. Clients with tight compliance requirements, especially those in regulated industries, look to these records before qualifying our lots for production. Over time, detailed traceability reinforces both compliance and a climate for continuous learning and improvement. Trust builds not just from consistency, but from open documentation about how we got there.

    Comparing with More Common Analogs

    Close relatives to 2-Hydroxy-2-(4-methylphenyl)acetic acid, such as 2-hydroxy-2-phenylacetic acid or its ortho- and meta-methyl isomers, respond differently under laboratory conditions. From handling their physical forms to reactivity in complex synthesis, we see measurable distinctions. The para-methyl group in our compound reduces side reactions due to less steric hindrance near the reactive center. In practical terms, processes using this acid waste less material on byproduct remediation, saving both time and chemical resources.

    Some users might assume that omitting the methyl group or moving it to another position causes no substantial difference. Our technical support team, after examining end-stage yields and impurity profiles, can show how subtle changes alter reaction rates, selectivity, and even safety during scale-up. For instance, the parent compound sometimes delivers unacceptably high levels of aromatic ring chlorination in halogenation steps, while the para-methyl protects against these side products enough to make downstream purification and regulatory testing less burdensome. These are not theoretical differences—they turn up as improvements on project timelines and lower raw material spending.

    Handling, Storage, and Sustainability Footprint

    Long-term storage of 2-Hydroxy-2-(4-methylphenyl)acetic acid calls for dryness and cool temperatures. Every package ships from our site in lined, airtight containers because we have seen how exposure to humidity or UV light degrades both the monochromatic look of the product and its chemical reliability. Local regulations dictate final storage requirements for many end users, especially those near food or sensitive aquifers. To accommodate different set-ups, we coordinate with customers on batch sizes to minimize onsite storage time and avoid excess stock that can degrade over time.

    Sustainability has become a visible part of our workflow. Early on, waste acid streams created disposal challenges, so synthesis routes shifted to minimize chlorinated byproduct formation and reclaim organic solvents. We’ve set up joint studies with disposal providers to develop new neutralization pathways. These moves not only shrink the environmental impact but also lower disposal costs for us and our customers. Our internal metrics include solvent recovery rate and total chemical oxygen demand, pushing operations toward a smaller and cleaner footprint.

    Practical Lessons from Scale-Up

    Scaling specialty organic molecules reveals issues textbook processes gloss over. In the early days, we found large-scale batches of 2-Hydroxy-2-(4-methylphenyl)acetic acid susceptible to local heating and incomplete conversion, which led to color changes and unexpected byproducts. Fixing these issues required tweaking agitation speeds, feedstock addition rates, and installing inline sampling points. Now, our best batches look the same from flask to tote, so customers never see a difference whether they’re buying one kilogram or a full drum.

    During one scale-up cycle, variable moisture content from a reagent caused hydrolysis and the formation of an intractable gel. Simple incoming inspections using Karl Fischer titration stopped this problem at the door, sparing months of troubleshooting and customer follow-up. Learning from trouble isn’t just about fixing mistakes. It means analyzing root causes and feeding them back into procurement and operator training, so the same issue never repeats. Lessons like these have raised our standards and slashed rework rates over the years.

    Safety and Risk Management from a Manufacturer’s Perspective

    Organic acids demand respect in handling, particularly when moving from bench to plant scale. Early batches of this product once exhibited trace exotherms in the neutralization step; we needed to adjust both rate and method for base addition. These tweaks sound minor but avoid temperature spikes that can threaten both operator safety and yield. Our team reviews every incident and near-miss, training new operators under experienced staff. Strong internal culture around safety preserves both our people and the confidence our customers place in us as a supplier of specialty chemicals.

    Worker exposure to dust or vapors stays tightly controlled with closed handling and local extraction. Extended exposure to even low vapor levels prompted investment in additional exhaust filtration. By logging uptakes at every batch, we support operators with rotating responsibilities to limit total exposure time. The tangible results turn up not simply as cleaner air readings in the plant, but as long-term job satisfaction and lower absenteeism among our team.

    Challenges and Solutions in Process Optimization

    Process improvement never ends, no matter how many batches ship out that meet target specs. As customer demands tighten and regulatory requirements add complexity, we constantly look for both incremental advances and step changes. Case in point: clients in pharma recently asked for ever-sharper control over heavy metal levels. Routine inductively coupled plasma testing identified minor contamination from gasket wear inside reaction vessels. Changing seals and altering cleaning cycle frequency quickly pushed our readings below the new analytical limits. Other industries called for more granular particle size to aid slurry processing. Piloting new milling methods and screening protocols fixed this, without compromising product integrity.

    Open communication with users helps steer R&D priorities. On-field feedback about solubility problems in non-aqueous media triggered a solvent compatibility review. We responded by refining the final washing stage so residues don’t interfere with solvation in demanding conditions. It’s not just about adaptation, but anticipating issues and working directly with downstream chemists to solve them before they multiply.

    Working Collaboratively with Downstream Users

    Our relationship with users of 2-Hydroxy-2-(4-methylphenyl)acetic acid isn’t arm’s length. We see firsthand how chemists, engineers, and QA experts in pharmaceuticals, materials science, and fine chemicals handle this molecule. Their insights have changed our operations, from packaging improvements—moving toward antistatic liners for dry climates—to adjusting delivery schedules for “just in time” inventory management. Field visits keep our teams sharp and demonstrate our commitment to practical troubleshooting.

    Joint research projects push development further. Several of our most impactful leaps have stemmed from user case studies, especially where process failures or unusual byproducts surfaced. Each success reinforces a collaborative view of progress. Our staff learns how to speak the same language as our users and proactively suggest modifications that improve results. These relationships keep us tuned to new needs and emerging challenges.

    Quality Assurance for Regulatory Compliance

    As scrutiny grows in pharmaceuticals and electronics, having strong documentation and repeatable analytics proves more valuable than ever. Rather than treat external audits as an occasional inconvenience, we use them as basis for continuous self-inspection. Over the years, we have built a documentation structure that covers chain of custody, production batch data, raw material quality metrics, and environmental controls. These tools provide assurance both for our own staff and outside inspectors.

    Our internal standards don’t just mirror regulatory checklists—they extend beyond them. Regular reviews flag emerging compliance shifts that might reshape acceptance criteria. New impurity limits prompt updates to testing protocols before customers ask. Documenting these changes in clear, accessible language serves anyone relying on our material for high-compliance end uses. This mutual trust circles back, with users more likely to share concerns and work with us when surprises do appear.

    Staying Ahead through Continuous Learning

    Sourcing technology, regulatory frameworks, and downstream requirements never stand still in specialty chemical manufacturing. To deliver 2-Hydroxy-2-(4-methylphenyl)acetic acid that matches real-world expectations, we encourage cross-training and ongoing education for our teams. Analytical staff rotate through process operations, developing firsthand knowledge of what influences product quality. Troubleshooting groups run regular post-mortems on any batch deviations, seeing anomalies as signals of where systems or training can evolve.

    We’ve sent staff to seminars and user facilities, gaining appreciation for how our material fits into broad and shifting contexts. Technical advances in related fields—such as new catalytic routes or rising purity standards for next-generation applications—feed back into our R&D cycle. The process centers not only about chemistry, but about building organizational habits that push our standards higher and let us adapt with confidence and insight.

    The Manufacturer’s Perspective: A Commitment Beyond Product

    Our work making 2-Hydroxy-2-(4-methylphenyl)acetic acid is about far more than producing drumloads of refined chemical. It’s an ongoing commitment to detail, a willingness to learn from both setbacks and advances, and an ambition to drive improvement across the value chain. Each kilogram we ship reflects thousands of microdecisions about sourcing, handling, testing, and recordkeeping. Every success story shared by a partner using our material encourages us to double down on quality, responsiveness, and collaboration.

    Customers aren’t just buyers. They are participants in the journey to make molecular-level complexity practical and reliable across industrial and research landscapes. By keeping communication open, standards high, and learning constant, we strengthen the wider field of specialty chemical manufacturing. Our experience manufacturing 2-Hydroxy-2-(4-methylphenyl)acetic acid shows how attention to detail and pride in craftsmanship improve outcomes for everyone—from the frontline operator to the final user innovating at the edge of what is chemically possible.