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Beta-Hydroxyisovaleric Acid

    • Product Name Beta-Hydroxyisovaleric Acid
    • Alias HMB
    • Einecs 211-519-9
    • 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

    854105

    Chemical Name Beta-Hydroxyisovaleric Acid
    Molecular Formula C5H10O3
    Molar Mass 118.13 g/mol
    Synonyms 3-Hydroxyisovaleric acid
    Appearance White crystalline solid
    Melting Point 50-54°C
    Solubility In Water Soluble
    Cas Number 625-08-1
    Chemical Structure CH3CH(OH)CH2COOH
    Pka 4.34
    Boiling Point 240°C (decomposes)
    Odor Odorless
    Storage Conditions Store in a cool, dry place
    Uses Intermediate in organic synthesis
    Stability Stable under recommended conditions

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

    Packing & Storage
    Packing 250g of Beta-Hydroxyisovaleric Acid comes in a sealed amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping Beta-Hydroxyisovaleric Acid is shipped in tightly sealed containers to prevent moisture exposure and contamination. It should be stored in a cool, dry place, away from direct sunlight and incompatible substances. Transport complies with relevant regulations, and all containers are clearly labeled with hazard and handling information to ensure safety during shipping.
    Storage Beta-Hydroxyisovaleric Acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature or as specified on the product label. Ensure proper chemical labeling, and store away from strong oxidizing agents and sources of ignition. Follow all regulatory and safety guidelines.
    Application of Beta-Hydroxyisovaleric Acid

    Applications of Beta-Hydroxyisovaleric Acid in Industrial Manufacturing

    Beta-Hydroxyisovaleric Acid serves as a precise intermediate for complex synthesis in specialty chemical production. As a direct manufacturer, we supply high-purity material tailored for integration in advanced industrial workflows, supporting strict regulatory and process requirements across multiple manufacturing sectors.

    1. Pharmaceutical Intermediate for Brivaracetam Synthesis

    This material is a key intermediate in the multistep synthesis of anticonvulsant active pharmaceutical ingredients such as Brivaracetam. Manufacturers implement controlled reactions under cGMP environments to ensure batch consistency and compliance. Our quality-controlled, impurity-profiled product meets the stringent thresholds required for regulated pharmaceutical production, with traceability and supporting documentation included for regulatory submission and customer audits.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API Manufacturing
    • USP <797> and EP monograph references (as to relevant APIs)
    • US FDA Drug Master File (chemical intermediate section)

    Typical usage ratio

    • Reaction input at molar equivalence (1.0 – 1.2 molar ratio to coupled reagents); final ratio adjusted according to yield and purity goals in the manufacturing route.

    Downstream process integration

    • Introduced during the key ketone-to-amide transformation step in Brivaracetam synthesis.
    • Purified by crystallization or preparative chromatography before downstream reactions.
    • Subject to in-process HPLC/GC purity testing prior to API coupling.

    Final product types

    • Brivaracetam API
    • Related chiral pharmaceutical intermediates
    • Small-molecule neurological drug intermediates
    • Active pharmaceutical ingredient precursors

    2. Amino Acid Derivative Production for Sports Nutrition

    Industry formulators utilize our product for the synthesis of research-grade branched-chain amino acid derivatives. Processing facilities employ carefully managed esterification and hydrolysis steps, ensuring food safety and purity. Precise lot segregation and compliance with international food ingredient regulations protect end-user safety and brand reputation, especially when importing into North American and EU markets.

    Industry compliance standards

    • FSSC 22000: Food Safety System Certification
    • 21 CFR Part 117: FDA Food Safety Modernization Act (FSMA)
    • EFSA Guidance on Novel Foods and Food Additives
    • ISO 22000:2018 for food ingredient manufacturers

    Typical usage ratio

    • Blending at 0.1% – 2% by dry weight in amino acid precursor routes; adjusted based on target conversion and analytical footprint in finished products.

    Downstream process integration

    • Converted via selective condensation and esterification to produce BCAA esters or analogues.
    • Monitored by QMS-controlled batch records and analytical verification of residuals prior to formulation.
    • Further processed to isolate pure L-valine analogues for direct use in sports nutrition supplements.

    Final product types

    • Branched-Chain Amino Acid (BCAA) supplements
    • Functional sports nutrition blends
    • Amino acid derivative tablets and capsules
    • Powdered protein enrichment formulations

    3. Fine Chemical Synthesis for Agrochemical R&D

    Research and pilot plants leverage our material as a building block for the synthesis of specialty agrochemical agents. Controlled application in esterification, amidation, or precursor coupling enables target molecule elaboration with consistent molecular purity, supporting new product registration trials. Documentation and analytical support comply with industry and regional chemical management laws for safe handling and regulatory acceptance.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (EC 1907/2006) registration for intermediates
    • OECD Good Laboratory Practice (GLP) Guidelines
    • EPA TSCA Inventory Status (for US R&D facilities)

    Typical usage ratio

    • Input as 0.5% – 5% by mol in multi-step trial batch synthesis; adapted based on stoichiometric yields and side-product screening.

    Downstream process integration

    • Reacted in the initial condensation or esterification stage of herbicide prototype synthesis.
    • Analytical verification by NMR and HPLC during scale-up.
    • Integrated into route scouting protocols to assess synthetic flexibility.

    Final product types

    • Experimental pesticide intermediates
    • Trial agrochemical active ingredient scaffolds
    • New herbicide lead compounds for regulatory registration
    • Fine chemical research samples for field efficacy studies

    4. Chemical Synthesis in Flavor and Fragrance Precursors

    Our high-purity acid functions as a controlled precursor in the synthesis of specialty flavor and fragrance building blocks. Producers emphasize safe handling and compliance throughout manufacturing in accordance with food and cosmetic law. Reliable consistency in odor and analytical profile after reduction, coupling, and distillation steps supports both boutique and mass-market end use.

    Industry compliance standards

    • IFRA Code of Practice for Fragrance Materials
    • 21 CFR 172 Food Additives Permitted for Direct Addition (US FDA)
    • EU Regulation 1223/2009 (Cosmetics Safety)
    • ISO 9001 for flavor and fragrance intermediate manufacturing

    Typical usage ratio

    • Supplemented at 0.2% – 1.5% by weight in precursor production; ratio tailored to target aroma notes and analytical control during distillation.

    Downstream process integration

    • Reacted with alcohols or aldehydes under mild catalytic conditions as an intermediate step for desired aroma compound creation.
    • Material enters the workflow during precursor batch preparation before final purification.
    • Subject to organoleptic testing and GC/MS validation prior to finished batch release.

    Final product types

    • Niche flavor intermediates for beverage formulation
    • Specialty fragrance compounds for perfumery
    • Cosmetic aroma additives
    • Fine chemicals for aroma chemistry libraries
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    Competitive Beta-Hydroxyisovaleric Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Beta-Hydroxyisovaleric Acid: Our Experience, Value, and Practical Insight

    Real-World Production and What Sets Our Beta-Hydroxyisovaleric Acid Apart

    Working over the years with branched-chain carboxylic acids, one compound always stands out for us as practical, reliable, and straightforward to handle — Beta-Hydroxyisovaleric Acid (HIBA). Also known as 3-hydroxy-3-methylbutyric acid, it’s a specialty chemical that requires both technical precision and real working familiarity with controlled fermentation, precise separation, and careful purification. We’ve refined every stage, not just to meet a specification, but because every batch and application require us to stand behind our product, not just on paper, but in the field and on the factory floor.

    Physical and Chemical Profile

    Beta-Hydroxyisovaleric Acid comes as a white crystalline solid, easy to handle for those accustomed to carboxylic acids of this class. Melting point sits comfortably between 56 and 58°C; most labs or plants already have everything needed for safe and reliable storage. Solubility in water and polar organics opens up several process routes, both in large-scale manufacturing and in finer specialty work. Odor is nearly nil, which makes handling in closed rooms more manageable compared to some other acids of similar structure.

    Chemical stability stays high so long as temperatures stay below the melting point and storage containers keep dry. From direct observation, you won’t see much if any browning or off-gassing in well-sealed drums kept away from direct light. The structure (C5H10O3) — a beta-hydroxy acid with a methyl branch — gives it a reliable identity in both IR and NMR profiles, and we regularly verify both our incoming raw materials and outgoing batches with these tools.

    Purity and Lot-to-Lot Consistency

    Too many people overlook the trouble of lot variation, especially when sourcing intermediates. Several customers have come to us after seeing inconsistent performance with lesser grade material. Our standard purity lands over 99% by HPLC, and we've settled on a careful selection of raw vendors, plus a tailor-made crystallization step, to ensure there’s no residual solvent or unreacted precursor. In our labs, we keep a reference standard at hand to compare every batch, sidestepping subtle yield fluctuations that may show up as ghost peaks in LC or changes in end-use bioassays.

    We monitor moisture content by Karl Fischer titration — this method gives us practical assurance since even trace water can alter acid strength and cause headache downstream for those formulating sensitive blends. By working directly with the compound in-house, the operation also means we catch odd impurities that wouldn’t show up at low levels on a COA but can break a formulation or set off a customer’s QC alarm.

    How Beta-Hydroxyisovaleric Acid Actually Performs

    Beta-Hydroxyisovaleric Acid isn’t just another entry in the catalog. We’ve seen its effect as a metabolic intermediate, especially in research on protein turnover, muscle preservation, or nitrogen loss in specialized medical nutrition formulas. Many sports supplement brands know of HMB (the calcium salt), but if your R&D or formulation group needs the unesterified acid, you need the real thing, not a salt or an analog that might complicate downstream synthesis.

    We sell our HIBA primarily to advanced contract manufacturers, research centers, and downstream synthesis groups working with amino acid derivatives. Some are using it for metabolic tracing in stable isotope studies; others need it for synthetic building blocks used in peptide chemistry, especially where retention of the hydroxy acid and methyl group are central to the pharmacophore.

    If you’re tasked with making dietetic drugs or specialty animal feeds, you’ll run across regulations and stability requirements that only pure acids — not partially neutralized salts or solvent-rich stocks — can tolerate. We’ve gotten calls from customers who tried to cut costs with impure or ill-suited material and wound up with regulatory recalls or process shutdowns. Having HIBA made from scratch on a dedicated line is the only way we trust our own name with end-use manufacturers.

    Typical Applications by Industry

    Our direct experience supporting industry projects informs how HIBA slots into those fields. In medical nutrition and sport supplementation, HIBA acts as a necessary precursor or reference compound for the more common calcium HMB. It’s essential not just for its direct physiological role but for its value in method development, baseline studies, and control samples. With regulatory rigor tightening for everything that touches human nutrition, a reliable source with open documentation and batch history goes further than just a high purity number.

    Research chemical synthesis sees Beta-Hydroxyisovaleric Acid in the production of enhanced amino acids, certain peptidomimetics, and as a branching point for bioactive molecule discovery. Chemists value the accessible hydroxy and methyl groups — they leave room for further substitutions or oxidative modifications without long protecting group steps.

    Agricultural sectors explore HIBA’s inclusion as a metabolic adjunct in certain specialty animal feed formulas, especially where maximizing lean mass or minimizing viral muscle breakdown matters. We supply these projects with full trace documents and stability data, since repeatability drives margins on such tight formulations.

    Our Process: Beyond Standard Synthesis

    Making Beta-Hydroxyisovaleric Acid at any appreciable scale involves careful process order: starting with safe, well-tested fermentation or catalytic hydrolysis, keeping contamination low, and controlling final crystallization parameters. Raw material handling makes a big difference here — just small slips in storage humidity or a misunderstanding about supplier purity have forced shutdowns for other plants we’ve seen.

    Water quality impacts the final acid as much as any fancy step at the end. The difference between chemically pure and genuinely uncontaminated HIBA comes down to time spent running pilot batches and troubleshooting odd color or odor events. Our technicians and operators work from real notebooks, not just batch cards, flagging any subtle changes in yield or product quality so we catch problems at the root.

    After crystallization and drying, the finished acid runs through a final visual inspection before packing, eliminating off-color material and any contaminated particles. This saves resource and customer time lost on re-testing or complaint investigations. Containers are chosen for real work environments: no ultra-delicate packages, just sturdy, lined drums that keep HIBA ready for use months, not days.

    Quality Control & Analysis in Practice

    Having our own lab on-site lets us handle quick turns on analytical requests. We back every lot with batch chromatograms, NMR traces, and titration curves, and if a customer ever sees something unexpected in their own lab, we investigate immediately with them, not just send a new COA. Instead of relying on outside reports, in-house staff check against our validated reference samples — and this hands-on approach catches even subtle process drifts.

    One critical check for HIBA comes with residual solvent or unreacted precursor analysis. We use GC-MS in parallel with HPLC to shut out not just regulatory trouble, but real-world headache — solvents can sneak through even the best crystallization if you aren’t tracking every phase. Potentiometric titration and thermogravimetric analysis follow, since even sub-percent levels of residual water cause lot-to-lot variation for customers working in exacting synthesis or animal nutrition blends. Drying, not over-drying, keeps the acid at the right consistency and avoids the brittleness or clumping that can throw off batch work downstream.

    We use a long-term batch retention program for all HIBA produced here. This means that if a customer comes back months or even years later with a stability concern or question about an old order, our samples show the full history, not just lab paperwork. Trust and transparency matter more in these cases than any quick sale; it’s how we’ve kept recurring contracts and trust with clients for the long haul.

    Comparing Beta-Hydroxyisovaleric Acid to Other Related Products

    A question that often comes up revolves around differences between HIBA and its more widely marketed cousin, beta-hydroxy-beta-methylbutyrate (HMB). HMB, usually supplied as the calcium salt, finds popularity in sport nutrition, but the research side and specialty synthesis demand the acid form for flexibility and custom derivatization. Using the raw acid can allow direct coupling, esterification, or salt formation, expanding possible downstream modifications while avoiding extra processing steps.

    Compared to other beta-hydroxy acids such as beta-hydroxybutyric acid or standard isovaleric acid, HIBA’s methyl branching and hydroxy placement offer unique steric and chemical properties. Isovaleric acid, by contrast, brings tougher odor and lower hydroxy activity. Hydroxybutyric acid lacks the methyl branch, changing solubility and reactivity. Those differences show up transaction after transaction, affecting not only yield or ease of synthesis, but safety and regulatory check-ins downstream.

    Several research groups have also found that using HIBA instead of similar branched chain intermediates speeds up derivatization steps and cuts time spent on protection/deprotection sequences. This shaves man-hours off multi-step synthesis and broadens the types of analogs you can reach without introducing residual metals or tricky chromatographic separations. In nutritional and biochemical studies, the pure acid represents metabolic reality more directly, helping eliminate ambiguity in tracer studies or biological effect tracking.

    Safety, Handling, and Practical User Notes

    No matter where it’s used, Beta-Hydroxyisovaleric Acid brings safety needs common to organic acids. Gloves, lab coats, and goggles remain basic requirements. For plant-scale transfers, good ventilation, dry conditions, and careful bulk handling prevent clumping or accidental slips. We use lined drums and tamper-evident closures to keep the acid dry and protected from ambient air. Each time you open a drum, you’ll find the solid material ready for weighing or dissolving — not stuck together or compromised by moisture intrusion.

    Cleanliness at transfer is more than a habit — any trace carryover from earlier batches in your weigh booths can lead to cross contamination. We recommend dedicated scoopers, dust masks, and immediate clean-up of spills; the acid sweeps up easily, but wet conditions turn it slippery, so extra attention never hurts.

    Waste generation isn’t high, thanks to the acid’s easy disposal in most regulated waste streams, but always check local handling requirements. In our experience, storing backup stock in climate-controlled lockers prevents rare issues with caking. Full traceability and lot reporting go with every shipment, so every customer can align incoming material with their own process records.

    Problems We’ve Helped Customers Solve with Our Beta-Hydroxyisovaleric Acid

    Over the years, some issues come up time after time — all solvable with a frank look at process detail. One recent case involved a supplement manufacturer running into solubility trouble and off-odors when using a low-end non-standard HIBA. Our in-house acid, rendered without residual fermentation byproducts, solved the problem outright, allowing their formula to pass both shelf life and taste tests. Another time, a research organization struggled with untraceable side peaks during NMR analysis. Once we supplied them high-purity acid with open batch documentation, they could repeat their experiments cleanly and submit for publication.

    For a specialty chemical group, process impurities in HIBA from alternate suppliers led to roadblocks in peptide synthesis. The group reported poor yield, unexplained side products, and lot inconsistency. After reviewing their workflow and running their samples against ours, we pinpointed the impurity to a specific synthetic route used by another vendor. Supplying material made with a different, more controlled process eliminated those artifacts, saving their downstream yield and cutting time spent in troubleshooting.

    No batch ever leaves our lines without a deliberate check and a signoff by someone who has handled the product directly and fielded questions in real time. That feedback loop, not just paperwork, keeps our process sharp and our customers out of trouble.

    Collaborating and Improving — Lessons Learned

    Feedback from the field always trumps theory in the chemical plant. We keep tight communication with formulating partners, informing even tweaks in drying or lot selection if they tell us about a new process upstream or a tighter regulatory basket. Every time a customer crosses a hurdle — whether in animal testing, formulation, or first scale-up — we check in and see how our acid measured up. These lessons filter back through our process, letting us adjust and sharpen. If a customer learns something new about end-use or downstream stability, we roll that detail into future production — feedback is valued, not disregarded.

    Ethical Sourcing and Transparency

    There’s no cutting corners on source transparency. Our operation, from receipt of raw materials to final shipment, stays auditable and open to review by qualified partners. Certificates represent real, reviewed results — not autoprinted records. Each case of Beta-Hydroxyisovaleric Acid carries a chain of custody and an attached analytic history. If a client ever has questions, one of our chemists or plant managers explains directly, not an answering service.

    That approach keeps trust both ways: downstream users get what they order, and we take pride in every batch of HIBA. We do not bulk out shipments or blend lots for convenience; each shipment arrives from one traceable batch. We keep long-term records on every delivery, allowing full backtrack in the event of a problem, so users never get left holding the bag for a supplier’s shortcut.

    Contributing to Progress in Applied Chemistry

    Each container of Beta-Hydroxyisovaleric Acid that leaves the plant supports not just routine work, but advances in nutrition, analytical chemistry, and even pharmaceuticals. Over several years, our batches have traveled from protein metabolism research labs to formulation specialists seeking better shelf stability or reduced process downtime. One thing learned from close contact with academic and industrial partners: open, run-ready acids free of side impurities speed up everything from documentation to scale up. The more open the supply, the fewer obstacles users find in regulatory filings, product launches, or research studies.

    Having boots on the ground at both pilot and full-scale production facilities built up our know-how when troubleshooting new synthesis streams or user requests for tailored blends. Direct technical Q&A, fast user feedback loops, and a willingness to adapt production schedules for urgent needs have let us turn occasional first-time users into repeat partners who value a transparent source.

    What You Can Count On with Our Beta-Hydroxyisovaleric Acid

    Throughout every process, from bench to drum, we pay close attention to feedback from those who use Beta-Hydroxyisovaleric Acid not as a catalog entry, but as a building block or control substance in real trials and production. Purity alone means little unless it comes with batch traceability, fast response to user questions, and the ability to adapt run size and lot packaging to match requirements. That’s why our full process remains both open to customer inspection and subject to constant improvement.

    We stake our name each time a drum ships, reflecting not only years of process effort but ongoing practical lessons about what matters most: dependability, technical integrity, and honest feedback from every link in the chain.