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Methyl 2-Bromo-3-Methylbutanoate

    • Product Name Methyl 2-Bromo-3-Methylbutanoate
    • Alias Methyl 2-bromo-3-methylbutyrate
    • Einecs 252-347-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    701275

    Chemical Name Methyl 2-Bromo-3-Methylbutanoate
    Molecular Formula C6H11BrO2
    Molecular Weight 195.06 g/mol
    Cas Number 6963-31-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 65-68°C (18 mmHg)
    Density 1.382 g/mL at 25°C
    Refractive Index 1.454-1.456
    Purity Typically ≥97%
    Smiles CC(C)C(Br)C(=O)OC
    Storage Temperature Store at 2-8°C
    Synonyms Methyl 2-bromo-3-methylbutyrate

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

    Packing & Storage
    Packing Brown glass bottle with secure screw cap, labeled "Methyl 2-Bromo-3-Methylbutanoate, 25g," includes hazard warnings and storage instructions.
    Shipping Methyl 2-Bromo-3-Methylbutanoate is shipped in tightly sealed containers to prevent leakage or contamination, in compliance with chemical transport regulations. It should be packed with adequate cushioning and labeled as a hazardous material. Avoid exposure to heat, direct sunlight, and incompatible substances. Appropriate documentation and safety data sheets accompany all shipments.
    Storage **Methyl 2-Bromo-3-methylbutanoate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible materials such as strong oxidizers and bases. Store at room temperature or as specified by supplier instructions. Ensure proper labeling and restrict access to trained personnel only.
    Application of Methyl 2-Bromo-3-Methylbutanoate

    Applications of Methyl 2-Bromo-3-Methylbutanoate in Industrial Manufacturing

    Methyl 2-Bromo-3-Methylbutanoate serves as a key intermediate in several specialized chemical manufacturing sectors. Our production, quality control, and application support address industry-specific needs across multiple regulated fields, ensuring high purity and consistent performance in demanding downstream environments.

    1. Pharmaceutical Intermediate for Statin Synthesis

    This material is an essential building block in the preparation of intermediates for HMG-CoA reductase inhibitors, particularly in the industrial synthesis routes for certain statin pharmaceuticals. Downstream pharmaceutical producers rely on its functional groups to introduce chirality or structural complexity through alkylation or halogen exchange steps. The reactivity profile demands close attention to process control, especially under GMP or regulatory inspection environments. Integration typically occurs during mid-stage API synthesis under controlled temperature and solvent conditions, contributing to the desired configuration for the statin molecule. End products manufactured with this intermediate include high-value cholesterol-lowering medications supplied to regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Pharmacopeia monographs: USP, EP, JP (as applicable to downstream API)
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • EU GMP Part II Compliance

    Typical usage ratio

    • 10–20 mol% relative to key coupling partners, adjusted per target pharmacophore complexity
    • Applied stoichiometrically in step-growth or combinatorial reaction protocols

    Downstream process integration

    • Mid-stream intermediate incorporation during API synthesis under anhydrous and controlled pH conditions
    • Purification through crystallization or chromatography
    • Routine in-process controls for residual solvent and halide testing

    Final product types

    • Atorvastatin calcium (bulk API and formulated tablets)
    • Rosuvastatin intermediates
    • Other branded and generic statin drugs
    • Research-stage cholesterol-lowering molecules

    2. Agrochemical Active Ingredient Intermediate

    Downstream agrochemical manufacturers use Methyl 2-Bromo-3-Methylbutanoate as a precursor for specialized herbicide and insecticide synthesis. Its bromoalkyl moiety allows for precise halogen exchange and esterification steps, supporting the production of bioactive molecules with targeted activity. Compliance with national pesticide regulations and environmental quality systems governs production and application, particularly in formulations requiring high-purity intermediates. Industrial-scale usage averages depend on campaign batch size and desired product load, with direct integration into multi-step synthetic blocks leading to further functionalization or ring closure. Major outputs include active pesticides registered for broadacre crop protection and horticultural uses.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management Systems
    • Regulation (EC) No 1107/2009 (EU PPP authorization)
    • EPA 40 CFR Part 158 Data Requirements for Pesticides

    Typical usage ratio

    • 12–28% by moles in synthetic sequence, adjusted by target active and scale
    • Batch-specific calculation based on reaction efficiency and target conversion

    Downstream process integration

    • Added during early-to-mid synthetic routes as a brominated building block
    • Used in direct halogenation or amidation steps under inert conditions
    • Integrated with standard purification and waste handling protocols

    Final product types

    • Pre-emergent herbicides (e.g., β-keto ester-based actives)
    • Insecticide intermediates for pyrethroid analogues
    • Seed treatment actives
    • Broad-spectrum crop protection agents

    3. Synthesis of Flavors and Fragrances Precursors

    This compound serves as a regioselective intermediate in the flavor and fragrance sector, enabling the construction of ester-functionalized molecules for artificial and natural product synthesis. Flavors and fragrance houses utilize it under food additive or cosmetic-grade regulatory frameworks. The material enters controlled esterification or hydrolysis steps, often in the presence of specific catalysts or under vacuum distillation protocols. Application levels are tightly regulated depending on end-use in trace-level aroma or taste compounds. Resultant outputs are incorporated in consumer formulations such as perfumes, food flavors, and specialty essence blends.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EC Regulation 1223/2009 on Cosmetic Products (EU)
    • 21 CFR Part 172 (US FDA Food Additives Permitted)
    • ISO 9001:2015 and ISO 22716:2007 (GMP for Cosmetics)

    Typical usage ratio

    • 0.2–1.5% by mass in precursor blend, adjusted for target yield and organoleptic intensity
    • Trace levels for high-potency aroma chemicals, higher for synthetic musks or macrocycles

    Downstream process integration

    • Input as a key ester source in fractional distillation or selective hydrolysis
    • Used in micro-reactor and batch mixing protocols for aroma synthesis
    • Removed by column chromatography to achieve high purity for end-blending

    Final product types

    • Synthetic musk and fruity esters
    • Flavoring agents for beverages and confectionery
    • Essential oil analogues
    • Cosmetic base notes in perfumes

    4. Fine Chemical Synthesis for Chiral Building Blocks

    Organic synthesis laboratories and specialty chemical manufacturers employ this material as a precursor for enantioselective synthesis of advanced building blocks. The molecule’s reactivity in asymmetric alkylations, nucleophilic substitution, and homologation reactions allows tailored design of chiral products for pharmaceuticals, crop protection, and advanced material monomers. Process chemists use specific catalysts and bases to control stereochemistry and yield, incorporating rigorous analytics such as HPLC or NMR for isomer purity assurance. It is incorporated at well-defined stages in custom synthesis contracts requiring traceability and batch control, with adjustments based on specific downstream target molecules.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Control Protocols
    • REACH (EC No. 1907/2006) Registration for Substances in the EU
    • GMP protocols for pharmaceutical-use chiral synthons
    • Local hazardous substance controls as per OSHA or EU CLP

    Typical usage ratio

    • 1.0–10.0 equivalents per desired chiral product, determined by scale and transformation efficiency
    • Fine-tuned to minimize waste and maximize selectivity in catalytic cycles

    Downstream process integration

    • Enters at key transformation steps in custom synthesis service workflows
    • Used with chiral ligands in asymmetric hydrogenation or alkylation
    • Monitored through in-process analytical technologies for isomer ratio tracking

    Final product types

    • Enantiopure pharmaceutical intermediates
    • Custom chiral auxiliaries for fine chemical catalogues
    • Specialty polymers with chiral monomer units
    • Research-grade building blocks for R&D screening
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    Certification & Compliance
    More Introduction

    Methyl 2-Bromo-3-Methylbutanoate: An Experienced Manufacturer’s Perspective

    Introduction to a Trusted Intermediate

    We have spent years navigating the world of esters and halogenated intermediates. Among the many fine-tuned chemicals in our portfolio, Methyl 2-Bromo-3-Methylbutanoate has carved out its own share of practical value. The product often draws attention from pharmaceutical and agrochemical firms working at the edge of specialty synthesis. Not every ester with a halogen tag behaves as cooperatively on the bench or in scale-up, and our process reflects the experience built through repeat production, variable conditions, and customer-driven troubleshooting.

    This compound, categorized under methyl esters and known for its bromo substitution, regularly serves as a building block for a variety of chemical transformations. In our facility, we maintain the CAS registry number and molecular structure as our standard reference, but behind these data points lies an established track record from repeated batch runs and tight quality control. A well-constructed intermediate makes life easier in the next synthetic stage, and the feedback from our partners reflects that reality. Satisfied chemists appreciate the improved yields and reliable workups, a direct result of an intermediate that behaves consistently between lots.

    Practical Production Considerations—Model and Specifications

    Our manufacturing approach keeps quality and reliability at the core and avoids shortcuts. The material comes as a clear to slightly pale yellow liquid, with a boiling point and refractive index that align with published data. Purity typically stands no lower than 98% based on gas chromatography, something we routinely verify across every drum that leaves the plant. Moisture and residual solvents, especially those used during bromination, are kept well below levels that would impede the next reaction step.

    Customers running reactions on pilot or kilo scales routinely ask about solvent compatibility and storage needs. Methyl 2-Bromo-3-Methylbutanoate travels in sealed HDPE containers or glass, depending on batch size and specific order. We store it under nitrogen, away from strong bases, to prevent hydrolysis and side product formation. Since shelf life matters to our partners, we monitor chemical integrity with regular retests, even when the product sits for months before use.

    Why Application Knowledge Matters

    Methyl 2-Bromo-3-Methylbutanoate enters pharmaceutical projects primarily as a versatile alkylating agent, usually for installing branched methylbutanoate chains or introducing the bromo group for further nucleophilic substitution steps. Not all laboratories treat the subsequent transformation the same way, so a one-size-fits-all mentality would have let us down years ago. We have seen synthetic challenges in gram-scale settings turn into problems with pounds of intermediate—overbromination, color issues, or inconsistent assay values. By tracking impurities, even those present at low levels, we make sure that nobody receives material hiding unseen problems.

    In the agrochemical sector, this ester often moves into the synthesis of specialty molecules, sometimes with unusual heterocyclic structures or multiple functional groups. Small agricultural biotech firms ask for our input on solubility in less polar solvents or look for solutions to crystallization troubles that appear during post-reaction workup. Our technical team shares sample handling tips, crystallization protocols, and filtration hints, all learned through direct trial, pilot errors, and modern analytical methods.

    Production Approach Versus Commodity Sourcing

    Bespoke chemicals like this don’t benefit from mass-market commodity approaches. In a world full of traders and resellers, product consistency too often takes a back seat to price pressures. Our facility controls bromination step parameters to minimize side reactions and color formation. By thoroughly drying the end material and filtering out residual salts, we sidestep the contamination issues that dog less diligent sources.

    We have faced clients frustrated by failed syntheses using material from secondary suppliers or brokers. The concerns range from batch-to-batch changes in purity to unexplained color or odor, both of which trace back to uncontrolled side reactions or shortcut purification. All it takes is a subtle byproduct or a fraction of a percent water to ruin downstream NMR or mass spec confirmation. Our manufacturing process reflects those lessons—not just for appearance, but for deep chemical quality. The end user spends less time troubleshooting and more time developing target molecules.

    Comparisons With Similar Brominated Esters

    Methyl 2-Bromo-3-Methylbutanoate stands apart from its simpler analogs such as methyl bromoacetate, due to its increased steric hindrance and alkyl substitution. That extra branching has practical consequences in reactivity. End users often tell us that methyl bromoacetate’s small size can encourage unwanted side reactions or overalkylation, while the 3-methylbutanoate structure delivers better selectivity in stepwise synthesis. We followed several customers moving between these two esters; they noticed the difference immediately in lab and pilot runs.

    On the other hand, ethyl esters in the same class might seem interchangeable, but the methyl version often gives superior solubility profiles in certain reaction setups. This matters for teams focused on small volume, high-purity transformations. The bromo group itself can cause different reaction rates for nucleophilic displacement or for Grignard reagent introduction compared to chloro or iodo analogs. Experience has shown catalytic processes can act more smoothly with the methyl-2-bromo-3-methylbutanoate variant, especially under conditions demanding precise temperature control or minimal side chain formation.

    Real-World Challenges and Lessons Learned

    The path from raw material to finished intermediate rarely runs smooth. Early batches of this brominated ester showed us the risks of insufficient agitation during bromination, and the tendency of side reactions to introduce colored impurities. Direct feedback from the bench inspired adjustments to our addition rates, better cooling protocols, and the introduction of in-line drying agents. These practical measures allowed us to cut down on polar byproducts and improve overall purity without the need for re-distillation.

    We have also encountered repeated questions about handling and storage. Shipments that transit long distances in warm climates sometimes see increased color or small changes in the assay. Our experience taught us to pre-treat storage vessels, use argon blanketing when possible, and reinforce container seals before long transits. One northbound shipment delayed on a summer dock led to enough decomposition that we began proactively stabilizing batches for overseas orders, an innovation prompted by a single customer complaint and addressed in every subsequent lot.

    Safety, too, factors into our approach. Bromine-containing esters deserve industrial respect—either in their volatility or in their interaction with nucleophiles. We train staff to manage accidental spills using standard sodium thiosulfate neutralization. Lessons from process incidents help shape our containment policies for both small packaged shipments and in-plant bulk storage.

    Impact on Downstream Synthesis

    Pharma and agrochemical R&D teams often find that success in a multistep sequence depends on the behavior of a single early intermediate. Methyl 2-Bromo-3-Methylbutanoate has proven itself a robust choice for generating diverse motifs, whether making key intermediates for enzyme inhibitors, agricultural herbicides, or test compounds for lead optimization. Our repeat clients see smaller impurity loads during scale-up and fewer issues during regulatory submission, both of which can be traced back to the intermediate’s quality.

    On more than one occasion, chemists pushing project timelines contacted us with questions about late-stage reaction bottlenecks that traced back to material from generic supply sources. By offering batch-specific data, NMR scans, and retention samples, we smoothed the path back to consistent batches and restored momentum to stalled development. Such support springs directly from years of experience, both successful and hard-won.

    Technical Support: Beyond Just Raw Materials

    We spend as much time consulting with technical teams as we do running reactors. Many inquiries start with a molecule specification but quickly turn into a conversation about compatibility, side reactions, or crystallization failures. Best practices don’t result from theory alone. Our technical staff have run the same reactions, filtered the same residues, and dried the same intermediates our customers deal with daily. Questions about leaving groups, handling residual acids, or recycled solvent usage draw directly from plant-floor experience.

    Feedback circles back into our process design. For example, a North American contract research group needed a tighter upper limit for residual bromine than our standard. Rather than forcing a generic fix, we developed an additional purification and validation step. That new protocol now benefits all downstream clients working under similarly sensitive regulatory regimes, especially in projects where residual halides pose a concern for later product purity or safety.

    Continuous Improvement Based on Industry Needs

    Just as product requirements shift, our process evolves with feedback from repeat users. Higher throughput campaigns triggered an evaluation of our production scale, solvent handling, and in-line filtration systems. After noticing purification challenges among research-scale users, we invested in better distillation columns and more robust chromatography techniques, both tagged to impurity profiles and final purity targets.

    Collaborative pilot projects sometimes expose new variables, such as differing rates of ester hydrolysis under acid or base catalysis. Rather than shield ourselves from this feedback, we invite it into our process meetings. Every story, from reactions gone sideways to successful time-savings in workup, adds to our library of technical knowledge. The more we share those tips, the more valuable the partnership becomes for new adopters of the product.

    Environmental and Regulatory Experience

    Modern chemical manufacturing must answer more than technical questions. Regulatory standards for API intermediates and agrochemical actives lead us to document every aspect of production from incoming raw materials through outgoing shipments. We maintain full traceability and supply certificates of analysis that extend beyond basic purity—covering impurities, solvent residues, and the origin of critical reagents.

    We maintain compliance with local and international chemical safety guidelines. All handling and shipping procedures reflect lessons from both regulatory inspections and third-party audits, especially for hazardous materials. Material sourced from our reactors arrives pre-labeled with the necessary GHS hazard statements, and our documentation ships alongside every container for straightforward regulatory clearance.

    Market and Supply Chain Realities

    Global supply chains have grown complicated, especially for specialty intermediates. We manage procurement by cultivating long-term relationships with bromine and methyl precursor suppliers. Disruptions—like recent port delays or raw material shortages—can trigger production bottlenecks, so we build buffer inventories. The chemical market rewards those prepared to weather such storms, and end users benefit from a partner willing to coordinate shipments, keep stock, and communicate honestly about challenges as they arise.

    Some customers request just-in-time orders or anticipate phased delivery over months. Our planning system reflects the realities of customization, frequent retesting, and last-minute adjustments. Large fractions of our output supply contract manufacturing organizations (CMOs) who need flexibility in both quantity and delivery. Direct experience has taught us to prefer firm collaboration over arms-length transactions.

    What Sets Our Methyl 2-Bromo-3-Methylbutanoate Apart

    Differences in production approach, quality control, and technical support shape outcomes for the end user. By mastering small-batch and bulk manufacturing, and documenting every refinement, we ensure the product remains free of unpredictable byproducts. Purity matters—but equally important are insights from real synthesis campaigns: whether a residue lingers, a yield drops, or an unexplained color taints the end product.

    Close cooperation with distributors and direct end users allows us to anticipate evolving formulation trends. If a process route changes to require lower levels of a certain impurity, our technical department investigates and adapts the plant workflow. Feedback loops from customers to process engineers to quality control guarantee that changes don’t just happen in theory—they appear in every container we ship. Our flexibility and willingness to invest in better instrumentation, new glassware, and safer protocols make a difference that clients see firsthand.

    The Path Forward for Reliable Specialty Building Blocks

    Synthesizing complex molecules demands building blocks that perform as expected. We believe in a transparent process—one that welcomes scrutiny and embraces challenges. By keeping an open dialogue with end users, documenting every change, and taking care of quality from lab bench to loading dock, we support better science and more efficient chemical production. Methyl 2-Bromo-3-Methylbutanoate carries our experience in every lot; in each drum or flask, our standards match those of the people using it for tomorrow’s breakthroughs.