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HS Code |
646282 |
| Chemical Name | 2-Hydroxy-2-Methylbutyric Acid |
| Molecular Formula | C5H10O3 |
| Molecular Weight | 118.13 g/mol |
| Cas Number | 598-97-4 |
| Appearance | White solid |
| Melting Point | 49-51°C |
| Solubility In Water | Soluble |
| Density | 1.14 g/cm³ |
| Pka | 3.6 |
| Iupac Name | 2-hydroxy-2-methylbutanoic acid |
| Smiles | CC(C)(CO)C(=O)O |
| Storage Conditions | Store at room temperature in a tightly closed container |
| Hazard Statements | May cause eye, skin, and respiratory irritation |
| Usage | Intermediate in organic synthesis |
As an accredited 2-Hydroxy-2-Methylbutyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Hydroxy-2-Methylbutyric Acid, sealed with a tamper-evident cap and detailed labeling. |
| Shipping | 2-Hydroxy-2-Methylbutyric Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be stored at room temperature, away from heat and incompatible substances. Appropriate labeling and documentation, including safety data sheets, must accompany the shipment in accordance with regulatory requirements for chemical transport. |
| Storage | 2-Hydroxy-2-methylbutyric acid should be stored in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and store separately from oxidizing agents and strong bases. Use appropriate, chemical-resistant containers. Ensure storage area is equipped for spill containment and clearly labeled. Handle with suitable personal protective equipment to avoid contact and inhalation. |
Applications of 2-Hydroxy-2-Methylbutyric Acid in Industrial ManufacturingAs a direct industrial manufacturer, we supply 2-Hydroxy-2-Methylbutyric Acid for critical transformation steps across specialty chemical and biochemical sectors. The following sections detail key downstream markets that adopt this raw material into standardized, high-value manufacturing processes. 1. API Intermediate Synthesis for Chiral Pharmaceutical CompoundsOur production partners in API manufacturing use 2-Hydroxy-2-Methylbutyric Acid as a vital building block to construct specific chiral centers, especially in the synthesis of statins and other complex molecules. It enters asymmetric synthesis routes as a precursor to optically active intermediates and fine-tunes stereochemical outcomes by incorporation within Grignard and esterification sequences. Strict traceability in chiral purity is required at each batch, as pharmaceutical makers later purify and crystallize target actives for downstream formulation. Industry compliance standards
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2. Enzyme Substrate for Biocatalysis and Chiral ResolutionBiotechnology companies employ this acid as a substrate in enantioselective biocatalytic transformations. Its secondary alcohol group serves as a target for specific alcohol dehydrogenases or oxidases, facilitating kinetic resolution and biotransformation to produce single-enantiomer hydroxy acids and derivatives. We supply this raw material with tailored impurity control for compatibility with immobilized enzyme reactors, ensuring high conversion rates and minimal enzyme inhibition. Industry compliance standards
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3. Custom Polymer Additive in High-Performance PolyestersProducers of specialty polyesters introduce controlled quantities of 2-Hydroxy-2-Methylbutyric Acid as a functional co-monomer to adjust polymer flexibility, hydrophilicity, and degradation rates. The compound’s branching enables modification of chain architecture, impacting melt-processability and long-term thermal stability. Material selection teams routinely monitor input ratios to regulate final ester content within required performance brackets for end-user specifications in film or molded part applications. Industry compliance standards
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4. Sourcing Agent in Metal Surface Treatment for ElectronicsManufacturers in precision electronics use 2-Hydroxy-2-Methylbutyric Acid in metal pre-treatment solutions to adjust surface oxide and micropatterning prior to circuit deposition. The acid acts as a mild chelating agent, selectively removing trace contaminants and controlling etch rates for high-purity copper and aluminum substrates. Process engineers optimize dosing to establish microetch depth, ensuring reliable adhesion and conductivity in printed circuit board (PCB) fabrication. Industry compliance standards
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Manufacturing 2-Hydroxy-2-Methylbutyric Acid draws on years of hands-on work with carboxylic acids and α-hydroxy acids. The process involves the careful handling of isobutyraldehyde and glyoxylic acid under controlled temperatures, catalyst selection, and precise pH regulation. We observe every reaction’s nuance, knowing that real chemical behavior works outside a theoretical textbook. This acid, recognized under CAS number 594-61-6, presents itself as a colorless to pale yellow liquid or crystalline powder depending on temperature and storage conditions. The molecular formula, C5H10O3, fits into workflows where purity and structural reliability really count.
Each batch’s purity tells a story. By gas chromatography, we regularly achieve purity levels above 98% w/w – clear, sharp peaks, minimal impurities. For acid value and water content, we check every load before shipping. Shortcuts have consequences in downstream reactivity, so consistency matters more than anything. From weighing the raw isobutyraldehyde for the reactor, to adjusting the final product's crystallization, small changes affect the yield and clarity. A slight dip in storage temperature or a trace of ionic contamination can throw off the whole equilibrium, and we have learned to build robust quality tracking into every lot.
In the market, talk often centers on where 2-Hydroxy-2-Methylbutyric Acid fits into broader chemical routes. The real answer comes from feedback after years supplying research and manufacturing labs. Often, it acts as a chiral building block in pharmaceutical synthesis. Its non-aromatic, branched structure allows it to unlock certain catalytic reactions, especially for those pursuing optically pure intermediates in chiral drug development. Our chromatography data shows that even small improvements in stereochemical purity make a difference for these customers.
Researchers come to us for this compound when they face tough selectivity problems. Substituting more common α-hydroxy acids can alter both reaction rates and byproduct profiles in asymmetric synthesis. Some give lactic acid or 2-hydroxybutyric acid a try, but these carry straight side chains or form more predictable esters and salts. 2-Hydroxy-2-Methylbutyric Acid’s extra methyl group on the alpha-carbon throws a wrench into the usual reaction selectivity, which opens up unique pathways in fine chemical synthesis.
On the industrial side, coatings manufacturers tap our acid to serve as a modifier in alkyd resin formulations. Its branched structure increases flexibility and toughness compared to straight-chain acids. We've worked with polymer chemists who report more resilient films and better flow in aqueous varnishes thanks to the unique backbone it brings. These industry insights determine our process parameters; we keep water levels low and monitor for color shifts because certain customers need ultra-pure, low-odor compounds for coatings exposed to demanding environments.
Some stand back and ask what really sets 2-Hydroxy-2-Methylbutyric Acid apart from more standard hydroxy acids, like lactic or glycolic. Standardized chemical listings don't tell the full story. Taking the molecular structure apart, we see the additional methyl group at the second carbon disrupts hydrogen bonding compared to its analogs. That shift causes altered crystallization points, melting behavior, and subtle differences in acid strength. The acid dissolves freely in water and a broad range of alcohols, but its branched form means it will show slower reactivity in some esterification reactions—something our long-term manufacturing customers exploit for controlled-release or specialty resin work.
We've been asked if this molecule acts as a substitute in medical diagnostics, such as in analytical standards or clinical assays. Based on customer use, we know 2-Hydroxy-2-Methylbutyric Acid shows up in high-performance liquid chromatography for monitoring organic acidurias, especially in labs tracking inherited metabolic disorders. Our HPLC reference standards leave minimal residue and come with clean baseline separation—a benchmark hard to achieve with less refined analogues. Over the years, biomedical researchers report fewer interference peaks and more consistent calibration curves, which means less troubleshooting and re-running assays.
Chemical manufacturers who sit down with end-users long enough learn the practical headaches in formulation. Laboratories and production managers often face tank-to-tank differences in viscosity, color, or solubility. The sample request stage uncovers these variables, as some resins fail to fully dissolve, or oils develop opacity over time. With 2-Hydroxy-2-Methylbutyric Acid, our in-factory controls aim to minimize these issues before the product ever leaves our site.
Product stability depends on moisture and trace-metal content. Overly dry material can clump and slow downstream blending, while too much moisture triggers unwanted hydrolysis. We modify drying and blending steps accordingly. For customers manufacturing flavors, fragrances, or active pharmaceutical intermediates, our batches maintain volatile impurity contents below specified limits. Each load gets documented with in-house FTIR, NMR, and Karl Fischer titration results.
A decade ago, few buyers worried about environmental impact at the level they do today. Now, sustainability enters every purchase inquiry. Our plant reuses water in the synthesis stage, scrubs acid vapors, and treats wastewater before discharge. We minimize energy use with heat recovery systems on the hydroxy acid reactor, and we monitor raw material selection for both cost and environmental footprint. The process retains more starting material in the final product, so yields remain high and minimize waste.
Many clients working on “greener” coatings and biocompatible polymers ask about the bio-derived origin of our acid. At present, our main route uses petrochemical feedstocks, but we continue running pilot batches from fermentation-sourced intermediates. Discussions with R&D partners point to promising advances in microbial synthesis, though cost and scale-up hurdles remain. We offer technical guidance to teams interested in lower-carbon routes, whether for regulatory compliance or new product lines.
Practical feedback makes labs better. Our largest customers bring back data and stories from the trenches of their production lines. Teams working with chiral pharmaceutical building blocks report smooth scaling from gram to multi-kilogram levels, provided moisture and light exposure stay tightly controlled. Inconsistent storage leads to irregular melting, so we added desiccant-packing and UV-blocking drums for all export shipments. These fine details prevent unwanted degradation and keep the acid in spec.
A coatings manufacturer came to us after seeing shifts in hardness when switching to a lower-cost hydroxy acid from another supplier. The unique branched structure of 2-Hydroxy-2-Methylbutyric Acid, which they had originally overlooked for cost reasons, restored the desired physical properties in their finish. End-user reports on flow, viscosity, and impact resistance pushed us to upgrade the downstream purification process to reduce trace aldehyde impurities.
Some clients in academia share chromatograms from trials that swap lactic acid for our product in metabolic research—often leading to clearer separation and more reliable quantification of analytes in biological samples. Several customers in Asian markets, known for rapidly scaling pharmaceutical R&D, asked us to invest in supply security and batch traceability. In response, we expanded our lot control systems and provided more detail in certificates of analysis, enabling them to meet auditing and compliance demands.
Scaling up synthesis comes with its own challenges. We’ve run into unexpected exotherms and batch-to-batch impurity spikes when increasing reactor size. In response, engineers took time to analyze intermediate build-up and adopted semi-batch feed protocols. Slower feed rates and more robust temperature sensors limit hot spots, which in turn keeps side products from building up. It's rarely about finding a magic formula; it’s the incremental adjustments that matter. We periodically retrofit equipment for better agitation and automated dosing, which save endless hours in manual oversight.
Manual purification steps used to be a common bottleneck. Chromatography and distillation at small scale are straightforward, but they slow down at multi-ton volumes. By moving to continuous crystallization and inline filtration, our plant cuts cycle times and reduces labor needs. Energy usage stays lower, and we pass on lower costs and lead times to buyers, especially those operating on just-in-time schedules.
Odor control once caused customer complaints. Early batches of 2-Hydroxy-2-Methylbutyric Acid sometimes held residual aldehyde aromas or faint solvent notes. We responded with activated carbon bed technology and invested in upgraded vent systems for the reactor suites. Continuous microdistillation also guaranteed removal of light volatiles. Our sensory panel now logs routine batch odor profiles and provides direct feedback to operators.
Too often the feedback loop ends after a sale. Over the years, we made it a habit to hold direct conversations with researchers and factory floor staff who use our acid in projects. Those project leaders often call out limitations in batch-to-batch color or solubility that standardized specs alone don’t always reveal. Actionable criticism led to invest in additional purification steps and calibration routines.
European and North American clients working on clinical diagnostics place huge importance on purity, as their HPLC and LC-MS results hinge on eliminating trace contaminants. Hearing that a customer lost hours troubleshooting a baseline drift in their instrument was enough reason for us to tighten our quality targets even further, introducing tighter controls for chloride and sulfate levels.
Polymer and resin specialists, who often face high temperatures during synthesis, advised us to look deeper into our acid’s thermal stability. We ran detailed DSC and TGA studies and now supply technical guidance on optimal storage and transfer methods for those running continuous reactors.
End users recognize that identical specification numbers on paper can hide major performance and handling differences. Through routine manufacturing, we see that two lots with similar purity and acid values might behave differently due to subtle trace contaminants. Real-world observations count for more than a certificate’s numbers—the best performing batches sometimes have a slight visual distinction, such as clarity or absence of particulate.
Small changes in side-product content, missed by less sensitive analysis, end up causing major headaches for precision formulators. Years spent adjusting process steps, sampling across production tanks, and following feedback from. multinational customers have toughened our standards. For example, a resin formulator noticed recurring cloudiness traced back not to the main acid content, but to parts-per-million levels of an estery impurity. In response, new process modifications eliminated the culprit, improving downstream clarity without any costly additive change.
Colleagues sometimes ask how this acid behaves compared to better-known players like lactic or 2-hydroxybutyric acid. Those two compounds, found all over both pharmaceuticals and food chemicals, offer good miscibility and reactivity but lack the steric bulk that the 2-methyl group brings. The presence of an extra methyl shifts solubility, reactivity in esterification, and even the way it modifies polymer chains. In metabolic research, this subtle structure allows for more distinct detection markers in rare organic acidemia diagnosis.
Functionally, other hydroxy acids may suit routine buffering or flavor creation, but the unique chiral properties of 2-Hydroxy-2-Methylbutyric Acid find favor in nuanced synthesis. As chemists ourselves, we've seen how swapping to a branched acid prevents unwanted side-reactions in specialty resins, which helps cut scrap rates and improves consistency in reactive extrusion. That’s tough to replicate with linear or less bulky analogues.
The future for 2-Hydroxy-2-Methylbutyric Acid involves both incremental improvements and the willingness to rethink core processes. On the sustainability front, downstream users expect disclosure about traceability. We're conducting in-house studies on renewable feedstocks, pilot fermentation, and catalyst recycling. Regulatory changes in different markets keep us vigilant — updated REACH or TSCA rules across regions mean new challenges and strict documentation.
In the pharmaceutical and analytical sectors, the push for higher stereoselectivity drives continuous improvements to our purification methods, supporting new chiral chromatography and intermediate syntheses. Polymer and coatings manufacturers want ever tighter control over physical properties in their end products, so our plant continues to refine particle size, color, and odor specs beyond the industry standard.
Open discussion remains a priority. Our teams attend sector-specific conferences not only to present, but to sit with users and hear about the hurdles they face. It’s not just about talking up the latest product dimension—real trust forms in the give-and-take across the supply chain, from synthesis bench to final application.
Over years dedicated to the manufacture of 2-Hydroxy-2-Methylbutyric Acid, every challenge, every customer complaint, and every lab result shapes the way we work. Achieving reliable, reproducible acid is one part fine-tuned process control, one part open communication, and one part learning from each unique use-case in industries ranging from pharmaceuticals to advanced coatings. Every improvement, whether it’s tighter reaction monitoring, better purification, or deeper engagement with end users, brings about tangible benefits in chemical performance. These day-to-day lessons keep us committed to pushing the boundaries, aiming for products that consistently support the next wave of innovation in chemical manufacturing.