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2-Hydroxy-3-Methylbutyric Acid

    • Product Name 2-Hydroxy-3-Methylbutyric Acid
    • Alias HMBA
    • Einecs 210-155-6
    • 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

    781773

    Chemical Name 2-Hydroxy-3-Methylbutyric Acid
    Molecular Formula C5H10O3
    Molecular Weight 118.13 g/mol
    Cas Number 600-38-0
    Appearance White to off-white crystalline solid
    Melting Point 72-74°C
    Boiling Point 228-229°C at 760 mmHg
    Solubility In Water Soluble
    Iupac Name 2-Hydroxy-3-methylbutanoic acid
    Density 1.088 g/cm3
    Smiles CC(C)C(C(=O)O)O
    Pka 3.54
    Storage Conditions Store at 2-8°C in a tightly closed container
    Synonyms Atrolactic acid; 2-Hydroxy-3-methylbutanoic acid
    Pubchem Cid 95865

    As an accredited 2-Hydroxy-3-Methylbutyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Hydroxy-3-Methylbutyric Acid is supplied in a 25g amber glass bottle with a secure, tamper-evident screw cap.
    Shipping 2-Hydroxy-3-Methylbutyric Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored at room temperature, away from direct sunlight and incompatible substances. Proper hazard labeling and documentation are required. Shipping must comply with local, national, and international regulations for handling and transporting chemicals.
    Storage 2-Hydroxy-3-methylbutyric acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store at a cool temperature, preferably between 2-8°C (refrigerated). Ensure proper ventilation in the storage area and avoid contact with incompatible materials such as strong oxidizing agents. Clearly label the container and keep it away from food and drink products.
    Application of 2-Hydroxy-3-Methylbutyric Acid

    Applications of 2-Hydroxy-3-Methylbutyric Acid in Industrial Manufacturing

    2-Hydroxy-3-methylbutyric acid serves as a specialized intermediate in various industrial sectors. As a chemical manufacturer, we directly supply this raw material to partners who require high purity and stable supply for precise downstream applications. Each target industry employs this compound for specific technical formats, integration points, and performance requirements. Below, we detail key industrial use scenarios with focus on actual compliance, standard formulation ratios, direct process roles, and the types of finished products our customers manufacture.

    1. Chiral Intermediate for Pharmaceutical Synthesis

    Major pharmaceutical companies use this compound as a chiral building block, especially for the synthesis of statins, anti-inflammatory drugs, and select amino acid derivatives. The acid enables enantioselective synthesis and high-yield routes to active pharmaceutical ingredients. Integration typically occurs at the stage of asymmetric catalysis or as a precursor in multi-step synthesis. Strict controls on residual solvents, contamination, and trace impurities are observed throughout production.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF and EP monograph requirements for chiral intermediates
    • FDA 21 CFR Part 210/211 for drug substance manufacturing
    • REACH (EC No 1907/2006) registration for intermediates

    Typical usage ratio

    • 2-10 mol% relative to final API yield, adjusted per target molecule’s reaction pathway

    Downstream process integration

    • Introduced in initial or mid-stage synthetic operations for chiral center construction
    • Often coupled in direct esterification or amide coupling reactions
    • Final purification is followed by chromatographic separation or crystallization

    Final product types

    • Statin intermediates (e.g., synthesis of atorvastatin side chain)
    • Nonsteroidal anti-inflammatory drug intermediates
    • Enantiomerically pure amino acid derivatives
    • Custom research molecules for pharma discovery

    2. Flavor and Fragrance Esterification

    Manufacturers in the food and fragrance sector utilize this acid as a precursor in enzymatic and chemical esterification to produce branched esters exhibiting fruity, creamy, or buttery notes. These esters impart key sensory profiles in dairy flavors, confectionery, and certain alcoholic beverages. Regulatory compliance involves strict GRAS evaluations, residual analysis, and sensory stability trials prior to end-use authorization.

    Industry compliance standards

    • FCC Food Chemicals Codex specifications
    • 21 CFR 172.515 (US FDA) for flavoring agents
    • EU Regulation (EC) No 1334/2008 for food flavorings
    • IFRA Standards for fragrance components

    Typical usage ratio

    • 0.02–0.3% in finished ester flavor formulations, subject to sensory panel results and local regulatory limits

    Downstream process integration

    • Acid introduced to batch or continuous esterification reactors with specific alcohols
    • Catalyst selection (acid/base/enzyme) and process time optimized for conversion and odor profile
    • Post-reaction distillation and fractionation yield target flavor esters

    Final product types

    • Creamy or fruity flavoring agents for dairy products
    • Confectionery flavor concentrates
    • Alcoholic beverage aroma enhancers
    • Perfume and fine fragrance ester bases

    3. Biochemical Research and Diagnostic Reagents

    Producers of life science reagents employ 2-hydroxy-3-methylbutyric acid as a specific substrate for metabolic and enzymatic assays. The compound participates in in vitro detection kits, oxidative stress measurements, and research quantification of hydroxy acid metabolism. High purity and batch traceability are mandatory due to the analytical sensitivity of these applications.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic reagent manufacturing
    • OECD GLP guidelines for analytical reference materials
    • Certificate of Analysis (CoA) including HPLC purity and trace element testing

    Typical usage ratio

    • Prepared as 0.1–100 mM stock solutions for use in assay kits and calibrators, according to detection sensitivity requirements

    Downstream process integration

    • Reconstituted as a substrate in enzyme assays (e.g., dehydrogenase activity measurement)
    • Combined with buffer systems and calibrants for ready-to-use kits
    • Supplied as lyophilized or stabilized aqueous solutions for distributed reagent panels

    Final product types

    • Clinical diagnostic test kits for metabolic markers
    • Biochemical assay reagents for academic and industrial research
    • Reference standards for calibration of analytical instruments
    • Enzyme substrate mixes for laboratory automation

    4. Specialty Polymer Synthesis Additive

    In performance materials manufacturing, specialty resin and polymer producers use this compound as a co-monomer or chain modification agent. Its branched structure influences glass transition temperature, flexibility, and processability in polyesters and acrylic systems. Stringent control over residual content and migration potential is required in consumer-facing finished polymers.

    Industry compliance standards

    • ISO 9001:2015 for industrial production quality control
    • EU REACH Annex IV/V applicable to monomer registration and polymer use
    • RoHS and EN 71-3 where polymers target electronics or children’s articles

    Typical usage ratio

    • 0.5–5% by weight relative to primary monomers; precise percentage determined by property optimization targets

    Downstream process integration

    • Fed into melt or solution polymerization reactors during monomer blending
    • Reaction temperature, catalyst type, and addition rate closely monitored for molecular weight control
    • Incorporation confirmed by FTIR or NMR analysis before compounding or extrusion

    Final product types

    • Functional polyesters for engineering plastics
    • Acrylic copolymers for coatings and adhesives
    • Flexible packaging films with tailored mechanical profiles
    • Specialty thermoplastics for consumer and industrial components

    5. Precursor for Fine Chemical Synthesis

    Chemical companies specializing in agricultural and specialty fine chemicals select this material for use as a key intermediate in the synthesis of select herbicides, plant growth regulators, and surfactants. The molecule’s functional groups allow straightforward derivatization and integration into higher-value chemical scaffolds. Adherence to chemical handling and environmental safety regimes is essential throughout all stages.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in chemical operations
    • GHS/CLP classification for labelling and safe transport
    • National inventories (TSCA, IECSC) for raw materials in synthetic protocols

    Typical usage ratio

    • 5–15% by molar input depending on the target molecule’s backbone and functional loading

    Downstream process integration

    • Used in condensation, alkylation, or amide coupling steps for building specialty molecules
    • Process involves phase separation, intermediate purification, and analytic confirmation
    • Residue control and batch sampling occur prior to moving to multi-ton production scale

    Final product types

    • Agrochemical formulation intermediates
    • Biocide precursor compounds
    • Surfactant additive bases
    • Fine chemicals for custom synthesis markets
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    Certification & Compliance
    More Introduction

    2-Hydroxy-3-Methylbutyric Acid: From Synthesis to Industry Solutions

    Experience from the Manufacturer’s Floor

    Crafting 2-Hydroxy-3-Methylbutyric Acid isn’t about following a recipe off the internet. Our teams operate from the ground up, from sourcing quality raw materials to tuning fermentation conditions, to handling the challenging purification steps unique to branched hydroxy acids. We’ve run countless batches, each carrying its own fingerprint. We know how trace impurities, undetectable by the casual eye, can change the end-use suitability, especially in pharmaceutical intermediate applications.

    Unlike big commodity chemicals, this compound calls for precise control, starting at raw input and including choice of fermenting microorganisms or catalysts, and tailing out with purification that won’t leave color, odor, or reactive contaminants behind. We investigate every shipment closely and keep records predictable and transparent, because—frankly—a failed batch shows up everywhere, from high performance coatings to clinical intermediates. There’s nothing theoretical about quality loss; customers notice, and so do we.

    Clarity on What Sets 2-Hydroxy-3-Methylbutyric Acid Apart

    At the molecular level, this acid features a hydroxy group at the second carbon and a methyl group at the third. This gives it some non-obvious properties compared to the more common butyric or lactic acids. It’s not a widely traded commodity but a product with a niche—customers specifically request it for applications where acidity, steric hindrance, or chirality matter.

    As a manufacturer, what stands out is how the hydroxy and methyl combination influences solubility, reactivity, and biological compatibility. In our own pilot studies, substitution at the third carbon alters the metabolic route in biological systems compared to straight-chain analogs, making it valuable in biochemistry research and synthesis of bioactive molecules. Some customers source this acid for use as a reference material in clinical biochemistry, especially in metabolic pathway studies dealing with branched-chain amino acid catabolism.

    We see distinct behavior during distillation and crystallization. The molecule resists some of the easy separation tricks that work with simpler carboxylic acids. We’ve learned that temperature gradients and pH have to be optimized not just by calculation but by hands-on monitoring to achieve a clear, odor-free final product. Residual solvent, off-odors, or yellowing can ruin whole lots, especially when the end use demands a stable, high-purity chemical.

    About Our Process and Product Range

    We manufacture primarily in crystalline and aqueous solution forms, depending on destination. Through years of process improvements, we’ve achieved reliable purity levels above 99%, with water content monitored batch-wise and organic residue documented. It’s not just about running a column or rotary evaporator; we run each batch through our analytics suite, including NMR and HPLC, to confirm the molecule’s structure and ensure batch-to-batch reproducibility.

    Specification sheets, based on both in-line monitoring and finished product assessment, typically highlight melting points, specific rotation, and enantiomeric excess. Modifications are possible for custom runs targeting isotopically labeled versions or alternative salt forms, but we stick with standards that meet most application needs. Customers working in analytical chemistry, for instance, often request higher purity thresholds and additional documentation, which we support through archived batch chromatograms and certificates of analysis.

    Bulk production scale sits squarely in the kilo to multi-ton range. For those in research and specialty chemical synthesis, we cater to gram and sub-kilo quantities. This flexibility allows labs to test concepts before scaling up without sinking major capital into untried intermediates. Production lead times are updated based on supply chain realities; raw input disruption translates quickly into scheduling delays, and we communicate changes early to our customers.

    Breadth of Use Cases and Field Experience

    Our product makes its way to pharmaceutical synthesis labs, polymer additive specialists, and research groups studying metabolic disorders. Each market segment demands different things. In pharma, for example, 2-Hydroxy-3-Methylbutyric Acid serves as an intermediate for certain statin drugs, antiviral compounds, or building blocks for new peptide-based molecules. Early on, we saw uptake from groups working on rare branched-chain organic acidemias, who rely on high-purity reference standards for biomarker analysis.

    We’ve been approached by companies exploring biodegradable plastics and specialty copolymers, where minor deviations in the hydroxy acid ratio can shift everything from mechanical strength to the degradation timeline. One group developed an antimicrobial surface by blending it at specific loading levels, counting on the branched side group to disrupt bacterial adhesion. They brought us in to confirm the chemical stability across a range of pH and temperature cycles, knowing off-spec product would show up as inconsistent field results.

    In flavor and fragrance chemistry, our experience shows most formulators prefer straight-chain acids, but a handful of perfumers and flavorists need the unique profile that 2-Hydroxy-3-Methylbutyric Acid offers. Slight differences in volatility and hydrolysis products, compared to lactic or isobutyric acids, have inspired some custom flavor profiles. While the market volume is niche, these users have a low tolerance for off-notes—another reason attention to product purity makes a real impact.

    Differences from Neighboring Acids: A Practitioner’s Perspective

    Customers occasionally ask if lactic acid, 2-hydroxybutyric acid, or simple isobutyric acid could substitute for 2-Hydroxy-3-Methylbutyric Acid in their protocols. Hands-on trials prove the answer is usually no. The methyl group on the third carbon is not just a trivial branch; it changes the acid's chemical reactivity, especially in coupling reactions and amidation processes. Mixing up these molecules can sabotage an entire synthetic scheme, leading to unwanted byproducts or low yields.

    In our facility, side-by-side stability testing makes the differences clear. 2-Hydroxy-3-Methylbutyric Acid shows better shelf life under controlled storage than some of its isomeric siblings. Its branched structure lowers susceptibility to microbial attack compared with straight-chain analogs—a fact valued by those storing solutions at room temperature for extended periods. There’s an uptick in requests from customers focused on in vitro diagnostics, where the stability of small molecules can determine the reliability of a year’s worth of controls.

    We have also seen that this compound resists non-specific oxidation better than lactic acid or simple hydroxybutyrate under ambient exposure. There’s a practical side—less off-odor, improved batch homogeneity, and tighter results for those relying on analytical precision. In applications tied to metabolic fingerprinting, for instance, users notice differences immediately: the wrong acid throws off calibration curves and leads to spotty results.

    The Realities of Manufacturing at Scale

    Scaling the process requires more than bench-top optimization. There’s unglamorous work—tank cleaning, filter changeouts, packing columns with fresh resin—that separates a reliable batch from a problematic one. Our teams share what works: pH control is critical, as is careful ramping of feed concentrations. We document reactor temperatures, residence time, agitation rate, all the routine steps that only matter when practiced with consistency across dozens of campaigns.

    Solvent recovery and waste treatment deserve special mention. 2-Hydroxy-3-Methylbutyric Acid poses specific wastewater handling challenges, especially versus regular hydroxy acids. We run pilot tests on new waste streams before committing to major synthesis campaigns. Lessons come hard when scaled-up batches produce side streams that don’t match small-scale chemistry. By investing in detailed material balances and contingency planning, we avoid shutdowns from failed environmental tests or local compliance headaches.

    Every employee at our plant knows the value of traceability. If a batch number ties to questionable analytical results, we pull it and provide supporting documentation. No one likes product recalls, but we stand behind every ton shipped; we’ve grown by solving problems directly instead of passing blame. This approach builds trust and keeps our production lines running smoothly, despite outside supply chain pressures.

    Market Signals and Quality Expectations

    Demand for 2-Hydroxy-3-Methylbutyric Acid waxes and wanes. Early in the decade, pharma customer R&D drove volume upward; lately, polymer additive startups make up a bigger slice. Market swings sharpen our need for real-time batch documentation, so we maintain lot records, archived QC data, and sample reserves. Spot testing for acetic acid, residue solvent, and enantiomeric purity is part of routine release practices.

    Walk around our loading docks and you’ll hear discussion of storage conditions and logistics. Cold-chain shipments, required for select biochemistry clients, make logistics expensive, but skimping on controls leads to failure at the customer site. We act on field feedback: if a batch arrives darkened or with excessive water content, we immediately review process logs and update procedures.

    Working with specialty acids means living with tight expectations and quick turnaround times. We’ve learned to update SOPs with each new order spec. Our technical sales staff have chemical process backgrounds and work closely with production—no disconnect between lab claims and what gets filled into drums and bottles.

    Troubleshooting: What Experience Has Taught Us

    Problems arise in every plant. What helps is a culture of reporting and learning, not hiding issues. We’ve had to rework batches that topped the specification limit for color or trace solvent. Sometimes, moisture from humid weather changes the outcome of purification stages; other times, a subtle mistake in feedstock blending shows up three steps down the process chain.

    To solve these, we rely on hands-on knowledge. Our shift leads track pH drift, monitor for off-gassing, and inspect every vessel for carryover from previous campaigns. Harmonizing manual checks with digital logging tools closes the gap between theory and real-world operations. We invest in internal audits and actively support suggestions from the line, whether it’s a simple equipment tweak or an overhaul to the documentation flow.

    Product quality never rests on a single analytical measurement. We run regular cross-validation with independent labs, and trace outcomes back to earlier steps if results deviate from internal controls. This multi-source quality monitoring has cut down on customer complaints and streamlined resolution times when issues occur.

    Looking Forward: Future Directions and Customer Solutions

    Some customers have begun to ask for greener synthesis options and reduced solvent footprints. Adapting to more sustainable synthesis methods isn’t easy, especially with the specificity this molecule demands. We’ve trialed biocatalytic processes and green oxidants, but tradeoffs in cost and reproducibility slow full-scale adoption. Our teams keep exploring, sampling new fermentation strains, adjusting for better yields, and seeking new separation techniques to cut down on solvent use.

    Clients concerned with trace contaminants drive us to continually refine housekeeping and validation procedures. More than once, a customer in medical research flagged a compound with background ion peaks at trace levels—feedback we welcome, knowing it pushes us toward even higher standards. We respond by sharing process transparency, opening up process logs and sample data for customer audits. These partnerships often lead to improved processes and stronger relationships.

    Some industries push for customization. We’ve produced isotopically-labeled versions in limited runs, for use in metabolic tracer studies. On other projects, we’ve developed salt forms for easier handling in high-throughput assays. We treat these requests not as one-off headaches but as learning opportunities, tuning equipment and retraining operators to meet unique demands without disrupting standard product lines.

    Knowledge Sharing and Industry Standards

    We field regular calls from research scientists and production chemists asking about downstream compatibility or synthetic work-ups involving 2-Hydroxy-3-Methylbutyric Acid. Over the years, our application notes and shared field results have set unofficial best practices—sometimes even influencing peer-reviewed research or cross-company standards. Too often, we see avoidable mistakes with poorly characterized batches or confusion over isomers.

    Our staff participate in technical meetings and submit findings to journals when new process insights emerge. We’ve helped troubleshoot scale-up failures for external labs and shared anonymized data on impurity control. Each exchange builds industry knowledge. It’s a two-way street, and we learn just as much from the challenges brought by our customers as we do from internal R&D.

    Concluding Thoughts from a Manufacturer’s Viewpoint

    We produce 2-Hydroxy-3-Methylbutyric Acid by marrying proven groundwork with curiosity and continued feedback from the field. Each lot we ship travels down the chain into labs, pilot plants, and production floors, impacting research, health, and industry in visible ways. Years of hands-on problem-solving and ongoing technical conversations have shown us that success isn’t just about reaching a purity number but about listening, responding, and being prepared for next year’s needs.

    From our vantage point, real-world manufacturing is measured not only in kilos and drums but by the usefulness of each shipment as seen by end-users. Data, experience, reliable documentation, and plain hard work build products that deliver benefits in every batch.