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2-Bromo-3-Methylbutyric Acid

    • Product Name 2-Bromo-3-Methylbutyric Acid
    • Alias 2-bromo-3-methylbutanoic acid
    • Einecs 224-356-6
    • 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

    999977

    Productname 2-Bromo-3-Methylbutyric Acid
    Casnumber 31427-21-5
    Molecularformula C5H9BrO2
    Molecularweight 181.03 g/mol
    Appearance White to off-white solid
    Meltingpoint 51-54 °C
    Density 1.525 g/cm3 (estimated)
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Smiles CC(C)C(Br)C(=O)O
    Inchi InChI=1S/C5H9BrO2/c1-3(2)4(6)5(7)8/h3-4H,1-2H3,(H,7,8)
    Synonyms 2-Bromo-3-methylbutanoic acid
    Storagetemperature 2-8 °C

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with screw cap. Label clearly displays chemical name, hazard symbols, and safety information.
    Shipping 2-Bromo-3-Methylbutyric Acid is shipped in tightly sealed containers to prevent leakage and contamination. It should be kept in a cool, dry place, away from sources of ignition. The package must be clearly labeled with hazard information and handled according to relevant chemical safety regulations during transit.
    Storage 2-Bromo-3-Methylbutyric Acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents and bases. Protect from direct sunlight and moisture. Recommended storage temperature is typically 2–8°C (refrigerated). Always handle using appropriate personal protective equipment in accordance with safety guidelines.
    Application of 2-Bromo-3-Methylbutyric Acid

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

    2-Bromo-3-Methylbutyric Acid serves as a critical intermediate for various fine chemical and pharmaceutical synthesis routes. Our facility produces this raw material to meet stringent B2B quality and compliance requirements. The following are key downstream application areas where our product integrates into formulation and manufacturing processes.

    1. Pharmaceutical Synthesis: Statin Side Chain Intermediates

    Pharmaceutical manufacturers employ 2-Bromo-3-Methylbutyric Acid as a key intermediate in statin drug synthesis, particularly for the side chain elongation stages in atorvastatin and rosuvastatin production. This compound provides a bromoalkyl building block that allows for controlled alkylation and subsequent hydrolysis during active pharmaceutical ingredient (API) assembly. Precision in molar ratios and batch procedures drives the purity and yield of end products, while compliance with stringent pharmacopoeial standards is mandatory at every step.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) for API synthesis routes
    • EU GMP EudraLex Vol. 4 Part II for chemical intermediates
    • FDA 21 CFR Part 211 for process controls in pharmaceutical production

    Typical usage ratio

    • 0.95–1.10 molar equivalents relative to the core statin backbone, adjusted according to required isolation yield and impurity profile control

    Downstream process integration

    • Alkylation step during side chain assembly of HMG-CoA reductase inhibitor synthesis
    • Reacted under phase-transfer or polar aprotic solvent conditions using strong base catalysts
    • Followed by hydrolysis and purification prior to chiral resolution
    • Integrated into multi-step batch reactors with circulating solvent loops

    Final product types

    • Atorvastatin calcium API
    • Rosuvastatin calcium API
    • Generic statin pharmaceutical raw materials
    • Custom chiral drug intermediates for further derivatization

    2. Agrochemical Intermediate for Fungicide Synthesis

    Producers in the agrochemical sector utilize 2-Bromo-3-Methylbutyric Acid for the synthesis of various pyridine-based fungicides. The bromo acid moiety allows for regioselective introduction into heterocyclic scaffolds, facilitating further conversion into performance-enhancing crop protection agents. Chlorination, esterification, and amidation typically follow this initial integration. Agricultural chemical manufacturers depend on repeatable high-grade batches to ensure downstream biological activity and product registration approval.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • ISO 9001:2015 for chemical manufacturing
    • REACH registration with ECHA for European Union market entry
    • Chinese GB/T 19001-2016/ISO Quality Systems for pesticide intermediates

    Typical usage ratio

    • 10–18% by weight of total reactants during fungicide precursor synthesis; precise dosing monitored by HPLC analytics for optimal conversion

    Downstream process integration

    • Nucleophilic substitution to introduce bromoalkyl functionality onto pyridine ring
    • Followed by esterification or amidation, solvent-based continuous operations
    • Pilot to commercial scale reactors with in-line automated temperature profiling
    • Strict containment protocols during handling and transfer

    Final product types

    • Pyridine-based agricultural fungicides
    • High-value pesticide intermediates
    • Formulated crop protection agents marketed for fruit, nut, and cereal crops
    • Export-grade agrochemical technical concentrates

    3. Peptide Coupling Agent in Custom Peptide Manufacturing

    Custom peptide synthesis companies use this bromo acid as a coupling site modifier that enables selective blocking or extension within peptide chains. Its reactivity supports solid-phase and solution-phase peptide assembly, providing a strategic bromoalkyl intermediate that facilitates additional N-terminal derivatization or stable linkage for biomolecule construction. Stringent control of reaction stoichiometry and solvent conditions is required throughout the sequence coupling campaign.

    Industry compliance standards

    • ISO 13485 for medical-grade peptide synthesis
    • US FDA cGMP Guidelines for peptide Active Pharmaceutical Ingredients
    • EDQM Certificate of Suitability (CEP) for APIs in Europe
    • Japanese Pharmacopoeia (JP) for biopharmaceutical intermediates

    Typical usage ratio

    • 1.0 molar equivalent per target amino acid linkage, with minor deviation for sequence optimization or side-chain protection

    Downstream process integration

    • Pre-activation of bromo acid for coupling within automated peptide synthesizers
    • Incorporation into protected resin-bound chains under inert atmosphere
    • Removal of blocking groups under controlled acid/base wash sequences
    • Post-assembly deprotection and purification via preparative HPLC

    Final product types

    • Branched custom peptides for research and diagnostics
    • Therapeutic peptide APIs subject to clinical development
    • Peptide–drug conjugates for targeted medicine delivery
    • Peptide standards for pharmaceutical quality control

    4. Building Block for Chiral Auxiliary Synthesis

    Chiral chemical manufacturers select 2-Bromo-3-Methylbutyric Acid as a precursor for the production of chiral auxiliaries. Its structure allows for the construction of enantioselective catalysts used in asymmetric hydrogenation, aldol reaction, and other stereoselective conversions. Process engineers must fine-tune the stoichiometry and maintain solvent purity due to the high reactivity of the bromo group, ensuring both structural integrity and chirality transfer in downstream synthesis.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical production
    • ICH Q11 Development and Manufacture of Drug Substances for chiral intermediates
    • OECD Principles of Good Laboratory Practice for pilot production
    • Responsible Care Management System for environment and safety

    Typical usage ratio

    • 0.9–1.2 molar equivalents for each target chiral auxiliary, with ratio selected based on enantiomeric purity targets and catalyst loadings

    Downstream process integration

    • Bromination or alkylation to form oxazolidinone- and other imide-type chiral auxiliaries
    • Use in reflux or microwave-accelerated batch reactors
    • Final auxiliary isolated by crystallization or distillation under anhydrous conditions
    • Deployed directly in enantioselective synthesis workstreams

    Final product types

    • Evans-type chiral auxiliaries for stereoselective synthesis
    • Chiral catalysts for fine chemical manufacture
    • Intermediate-grade auxiliaries for research or scale-up R&D labs
    • Pre-formulated catalyst systems for contract synthesis
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    Certification & Compliance
    More Introduction

    2-Bromo-3-Methylbutyric Acid: Practical Experience from the Manufacturer’s Floor

    Understanding 2-Bromo-3-Methylbutyric Acid

    In the chemical production field, it’s common for customers to ask for specialty bromoacids. Among these, 2-Bromo-3-Methylbutyric Acid stands out because of its unique balance between reactivity and manageable handling. With the chemical formula C5H9BrO2 and CAS number 5118-13-8, this compound enters the scene for chemists working on active pharmaceutical intermediates, crop protection synthesis, and chiral building blocks.

    From my perspective as an actual manufacturer, not a trading middleman, every batch of 2-Bromo-3-Methylbutyric Acid tells a story of detail and steady process. We work directly with the raw inputs—starting from methylbutyric acid and carefully controlling the bromination reaction to get a consistent, high-purity product. There’s no substitute for seeing the reaction sequence with your own eyes and being able to adjust for every variable in real time. This hands-on production approach brings out the subtle differences between batches, which is where experience comes into play and quality can be protected.

    What Drives Demand for This Compound?

    Among various brominated acids, our clients come back for this one for how cleanly it reacts in the lab and in full-scale plant settings. During synthesis, the presence of a bromine atom and a methyl side group together creates a compound that toggles between being a functional group transformer and a synchronization point for more complex molecule construction. Our own chemists have used it as a key intermediate, especially when making β-amino acids, peptide derivatives, or certain anti-tumor and antiviral pharmaceutical candidates.

    There’s no need for a shelf full of stabilizers or extra purification steps when the core product leaves our plant at a minimum assay of 98%. Hydroxyl and acid numbers line up with the needs of downstream applications—direct from the reactor, with nothing hidden and no shortcuts.

    Specifications That Matter on the Shop Floor

    From the operator’s side, the batch records are full of results that highlight real production challenges: color must stay within a tight range—light yellow is typical—since darker product means uncontrolled side reactions. Acid value and melting point targets are consistently hit, making downstream processing smoother. Still, it isn’t just about numbers on paper. Put a sample in your hand, and the sharp odor and crystalline form make its identity unmistakable. Grain size has to be right for both lab and plant dissolution, since irregular chunks can jam up equipment or slow dissolving rates in continuous reactors.

    Stability in ambient storage is decent so long as moisture stays outside the drum. In our facility, humidity control and nitrogen purging help prevent hydrolysis and discoloration, especially for larger inventory turns. The lessons learned from years of making this material: even trace impurities—bromo-derivatives or unreacted acid—show up in end reactions. Our approach keeps these minimized with regular GC/IR checks on final and intermediate product.

    Real-World Applications and Why It Finds Its Way into Tough Syntheses

    Ask a synthetic chemist about a reliable, selective bromine source for side-chain functionalization or for forming chiral centers, and this compound often enters the conversation. We have shipped batches to pharmaceutical companies, agrochemical innovators, and scale-up projects targeting small molecules for biotech R&D. The carboxylic acid moiety clamps the compound to organic frameworks, while the bromine enables direct nucleophilic substitution. This gives formulators a direct, predictable reaction path, especially compared with more reactive and hazardous alternatives like bromoacetyl chloride.

    I often hear from project leads that alternatives—such as 2-Bromobutyric Acid or straight 3-Methylbutyric Acid—never quite fit the bill. The extra methyl branch in our product means increased steric hindrance. This subtle difference makes the compound less prone to overreaction or side chain scission in sensitive molecules. In peptide chemistry, selectivity matters; the right protecting group or chiral intermediate can save weeks of lab time. In recorded tests and customer feedback, products made with our acid have consistently higher yields and fewer impurity peaks in HPLC runs.

    How Our Production Differentiates This Acid from Others on the Market

    Small differences in raw material source and bromination technique show up later in analytical results and end-use performance. Unlike resellers who might just buy bulk and repack, we treat each batch as custom-made. Each run uses pharma-grade reactants, with batch-to-batch bromine content tracked and recorded. We maintain a closed-loop contamination check to stop unwanted halogens, heavy metals, or non-volatile residues from sneaking into product that ends up in a clinical or crop trial.

    Looking deeper, most competitors don’t control for trace organic byproducts—such as dibromo derivatives or residual solvents. This is a practical difference you can’t tell from a price sheet. Our direct control of the entire process chain, starting from bromine, to disposal of waste, and purification, allows tighter release specs on impurity levels—meaning less loss in downstream refining and less frustration during validation steps for our customers.

    We store and package every lot to withstand international shipping, temperature swings, and hold times during customs. Double-layer lined drums and desiccants extend shelf life. Whenever a coordinator on our team checks a returned sample or a customer sends a technical inquiry, we run extra tests in-house rather than sending the question upstream. For any issue—like color drift, crystal breakage, or stuck drums—we’re able to trace root causes without waiting for outside labs or approval.

    Environmental Safety and Worker Confidence

    Having handled and manufactured 2-Bromo-3-Methylbutyric Acid for over a decade, I’ve seen the small but persistent risks that come with halogenated carboxylic acids. We go beyond regulatory minimums with our facility controls and staff training. Workers use tailored PPE and real-time air monitors. Our waste bromine recovery system closed a decades-old compliance gap, meaning that both local and export customers can show positive sustainability records with this intermediate in their finished product.

    Transport sometimes makes other manufacturers nervous. Experience has taught us the forms this acid can take under rough shipping: caking, container corrosion, small leaks. To keep those headaches away, we double-seal our poly-lined containers, monitor humidity, and batch-produce to order, sending out product at its freshest. Our investment in safer transfer and packaging means less accidental release during transit and more confidence for the labs that receive it.

    Supporting Researchers and Process Scale-up Teams

    Most companies buying this acid aren’t making single test tubes of product—they’re building pilot plants or running kilo-scale syntheses that may end up in the next new drug or a field trial for a new pesticide. Shifts from gram to multi-kilo scale always reveal the hidden quality gaps. Our process chemists regularly consult with customers to solve scale-up headaches—like slow dissolution, unexpected residue, or new byproduct peaks in chromatography.

    Some research chemists still go through catalog suppliers only to find later that industrial scale batches don’t match the small-scale sample. The face-to-face relationship with customers who actually use our drum lots has shown how much production knowledge matters after the “specification” is met. Sometimes, even with matching numbers, a batch from a different line will show small surface area or wetting changes that ripple through a plant campaign. Direct feedback loops help us tweak cooling rates and drying steps until the product behaves the way real users want, not just what a third-party spec sheet says.

    Pushing the Limits of Bromoacid Chemistry

    As industrial chemists, we see quickly when a product opens up new synthesis options or brings efficiency to multi-step reactions. 2-Bromo-3-Methylbutyric Acid acts as a lynchpin in the build-up of carbon frameworks for both the pharma and agro-industry. Our collaboration with external R&D teams led to the identification of chiral auxiliaries and prodrugs not possible with related brominated acids. Instead of resting on tradition, we take customer process outputs and look for ways to redesign our own operation so that next year’s batches will be cleaner, easier to dissolve, or less prone to off-odors after a few weeks in the warehouse.

    Our technical team frequently reviews literature, supplier feedback, and internal pilot plant runs to spot new ways to improve. Recently, we experimented with increasing bromination selectivity using customized catalysts to bring down impurity tails in the final HPLC runs. This helps drug discovery teams avoid last-minute troubleshooting and keeps process validations on schedule.

    Comparison with Alternatives: Where Subtle Chemistry Shapes Outcomes

    2-Bromo-3-Methylbutyric Acid usually ends up compared with 2-Bromobutyric Acid, 2-Bromo-2-Methylpropionic Acid, and simple bromoacetic acid. The methyl substitution on the third carbon in our acid inserts a degree of steric control, reducing over-reaction with nucleophiles while conferring a slightly higher boiling point and less volatility. During in-house competition runs, synthesis steps using 2-Bromo-3-Methylbutyric Acid deliver higher selectivity for SN2 substitutions; background elimination or rearrangement reactions are less frequent, reflected in cleaner product streams and reduced need for post-reaction scrubbing.

    We have worked with contract manufacturing organizations around the globe who require predictable intermediate behavior, especially where certain enantiomeric outcomes must be maintained across tons of product. In these cases, switching from a standard straight-chain bromocarboxylic acid over to our branched acid cut down on side reactions, even at higher process temperatures. Direct comparisons from process records and customer post-reaction yields consistently show less waste and more recovery from distillation or crystallization steps.

    Practical Handling and Long-Term Value for Partners

    Labs and production units rely on reliable supply and consistent quality. When seasonal swings in humidity or shipping conditions risk throwing a wrench in process yields, we keep routine batch checks and send advance samples where necessary. This approach builds up a two-way trust with our partners, many of whom manage their own regulatory filings or GMP validations. If a formulation hiccup arises, our direct line of communication saves time and reduces material write-offs.

    It’s become clear that a hands-on manufacturing approach—backed with process analytics and real user feedback—separates real producers from bulk traders. Over thousands of kilograms produced across hundreds of lots, our commitment is demonstrated in the longevity of business relationships. Many of our earliest customers evolved from single kilo orders to daily plant shipments, thanks to small but critical upgrades made after analyzing process hiccups together.

    Day after day, the value of this compound for our partners hinges not only on purity and consistency but also on the reliability of our logistics and support teams. We routinely anticipate regulatory shifts, regional compliance issues, or transport disruptions, responding immediately by updating containment, labelling, or MSDS documentation—always tailored to real-world needs, not generic guideline checklists.

    Frequently Raised Issues—and How They Get Tackled Here

    Experience shows that even well-tested processes surprise users, especially as they scale up. Commonly reported issues are caking inside storage drums, slightly pink product after prolonged storage, or low but detectable levels of secondary bromination byproducts. We rotate inventory so customers always get freshly packed material. High humidity areas receive double desiccant pouches inside each drum, and our QC team checks random samples for both color and fines content before each shipment.

    Sometimes, customers worry about off-odors or acid fume releases during transfer. We address this by maintaining a closed system for both filling and cleanup. For users with automated feeders or flow reactors, we adjust our crystal drying regime during production and even modify particle size distribution if requested, so dust and static buildup issues drop away.

    How Direct Manufacturing Benefits You

    Working from raw acid to finished shipment within one facility gives us a line of sight into every stage of product life. This means product consistency over the years, traceable origin, and a clear adjustment path for the next project or production surge. Our chemists and operators care about end-user satisfaction because the impact comes back to our process in the form of clear, constructive feedback. Little details—like checking that each drum has an intact liner, or verifying IR spectra before release—set the difference between a batch that “just meets spec” and a drum that customers reorder for years.

    By being present from raw material selection through to shipment, we support our partners not just with a chemical, but with knowledge born from real-world production. It’s easy to offer a data sheet. It takes much more to offer the assurance that each order is backed by years of practical, roll-up-your-sleeves problem-solving, standing ready to help work through issues ranging from process troubleshooting to logistics, all built around this single, versatile intermediate.

    Conclusion: Why 2-Bromo-3-Methylbutyric Acid from the Source Moves Projects Forward

    2-Bromo-3-Methylbutyric Acid, with its reliable supply, tight specification, and well-managed downstream performance, brings projects in pharma, agro, and materials sectors closer to delivery. Seeing the material transform from a raw feedstock to a valuable intermediate, shipped securely and safely, gives us pride as manufacturers. The ongoing process improvements, direct communication, and hands-on troubleshooting reflect a dedication forged by experience, not just sales targets. For our team, and for those who depend on our compound, the difference is felt every day in real schedules, plant outputs, and new discoveries—proof that when chemistry and care combine at the source, every drum delivers real results.