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2-Bromide Butyrate

    • Product Name 2-Bromide Butyrate
    • Alias Butyric acid, 2-bromo-
    • Einecs 211-254-4
    • 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
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    Specifications

    HS Code

    522416

    Product Name 2-Bromide Butyrate
    Cas Number 2032-11-9
    Molecular Formula C4H7BrO2
    Molecular Weight 167.00 g/mol
    Appearance Colorless to yellowish liquid
    Boiling Point 191-193°C
    Density 1.569 g/cm³ at 20°C
    Melting Point -53°C
    Refractive Index 1.449
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 70°C (closed cup)
    Smiles CCC(Br)C(=O)O
    Iupac Name 2-bromobutanoic acid
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C

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

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    Application of 2-Bromide Butyrate

    Applications of 2-Bromide Butyrate in Industrial Manufacturing

    2-Bromide Butyrate serves as a functional intermediate across multiple chemical production sectors. The following sectors detail specific technical uses, industry standards, application ratios, and downstream processes based on industrial-scale deployment of this material in advanced manufacturing.

    1. Pharmaceutical Active Ingredient Synthesis

    Specialty and generic pharmaceutical manufacturers employ 2-Bromide Butyrate primarily as an alkylating and functionalizing reagent within the synthesis of active pharmaceutical ingredients (APIs), especially for small-molecule drugs requiring butyrate- or brominated intermediates. Integration occurs in regulated GMP environments, where this material supports carbon-chain extension or specific structure modifications under controlled conditions to maintain pharmacopoeial quality for oral and parenteral medicines.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU Pharmacopoeia Monographs (Ph. Eur.)
    • US FDA 21 CFR Parts 210/211
    • Chinese Pharmacopoeia (CP) applicable standards

    Typical usage ratio

    • Ranges from 0.1 to 1.2 molar equivalents per reactant, adjusted by reaction yield optimization and regulatory impurity control requirements

    Downstream process integration

    • Incorporated during alkylation or bromination reaction step; conducts functionalization before purification and crystallization; monitored for residuals in QA/QC

    Final product types

    • Beta-blocker intermediates
    • Antiviral agent precursors
    • Bupropion hydrochloride related actives
    • Pyridine-based pharmaceutical compounds

    2. Agrochemical Intermediate Manufacturing

    Crop protection formulators use 2-Bromide Butyrate for synthesizing selective herbicide and insecticide intermediates. It participates as a halogen-source or chain-elongation agent within multi-step batch production under ISO 9001 and ISO 14001 environments, providing essential building blocks for next-generation active molecules. Application varies by the specific structure evolution desired for the target pesticide.

    Industry compliance standards

    • FAO/WHO specification for technical material purity
    • ISO 9001:2015 Quality Management System
    • REACH chemical safety registration (EU)
    • China Pesticide Registration Regulation (GB 2763)

    Typical usage ratio

    • Employed at 5–20% w/w of total reactant mass, customized for each process route and kinetic profile

    Downstream process integration

    • Dosed during pre-coupling steps in synthesis of butyrate- or halogenated side-chain pesticide molecules, then carried through extraction, drying, and formulation for technical grade output

    Final product types

    • Herbicide synthesis precursors (e.g. for amide or pyridine-based products)
    • Intermediate for pyrethroid insecticides
    • Branched carboxylic acid derivatives for fungicide precursors
    • Customized technical materials for patent-protected crop agents

    3. Flavor and Fragrance Ester Production

    Industrial-scale flavor and fragrance manufacturers integrate 2-Bromide Butyrate as a specialized acylation precursor for synthesizing esters critical to food, beverage, and fragrance compositions. Selective reactivity and predictable chain-length extension make it suitable for regulated processes targeting reproducibility and purity, for end use in consumer markets with compulsory food safety and labeling requirements.

    Industry compliance standards

    • Food Chemicals Codex (FCC) for allowed esters
    • EU Food Additive Regulation (EC) No 1333/2008
    • GRAS notice procedures (US FDA)
    • IFRA Code of Practice for fragrance ingredients

    Typical usage ratio

    • Applied at 0.3–1.5 molar equivalents relative to alcohol reactant, variable per final ester purity specification

    Downstream process integration

    • Fed into acidolysis or esterification reactors following precursor alcohol charging, purified by distillation, and quality-controlled for food- or fragrance-grade compliance

    Final product types

    • Ethyl butyrate flavoring agents
    • Branched butyrate esters for natural and artificial fruit bases
    • Synthetic fragrance building blocks for fine perfumery
    • Brominated ester intermediates for use in flavor encapsulation carriers

    4. Polymer Modifier and Plastic Additive Synthesis

    The polymer and plastics industry utilizes 2-Bromide Butyrate in functional group modification reactions for specialty polymer additives, especially in applications demanding enhanced flexibility, processability, or compatibilizer performance in co-polymer or thermoplastic materials. Process engineering departments control dosing to influence plasticizer or impact modifier efficiency and ensure full conversion during melt or solution-phase polymerization techniques.

    Industry compliance standards

    • ISO 9001 Quality Management for production lines
    • IEC 60296 purity requirements for insulating fluid intermediates
    • US EPA TSCA regulations on specialty additives
    • EU REACH registration on monomer substances

    Typical usage ratio

    • Routinely 1–15% by monomer mass, optimized by polymer matrix compatibility, desired end-use, and mechanical property targets

    Downstream process integration

    • Charged into polymerization reactors during synthesis of co-polymer backbones or graft-copolymerization steps, followed by compounding, extrusion, and pelletization for downstream processors

    Final product types

    • Plasticizer-modified PVC compounds
    • Impact additives for engineered thermoplastics
    • Brominated compatibilizers for advanced polymer blends
    • Insulating polymer intermediates for electrical and automotive use

    5. Specialty Chemical and Fine Organic Synthesis

    Producers of bespoke organic molecules use 2-Bromide Butyrate as a controlled-source of bromobutyrate for custom synthesis projects, including brominated acids, functionalized heterocycles, or as a starting point to access rare carboxylic moieties. These applications require precise material handling and documentation, with technical-grade purity or higher, meeting stringent customer feedstock specifications for contract or toll manufacturing scenarios.

    Industry compliance standards

    • ISO 17025 Laboratory Testing Accreditation
    • Custom supply agreements referencing customer specifications
    • REACH Authorization for downstream uses
    • SAFETY DATA SHEET (SDS) communication per GHS standards

    Typical usage ratio

    • Between 0.4 and 3.0 equivalents depending on product architecture and stepwise conversion yield, tuned for project-specific requirements

    Downstream process integration

    • Introduced at specific alkylation or bromination stages, or as the first-step reagent for compound diversification, leading to further derivatization, isolation, and final purification according to project design

    Final product types

    • Bromobutyric acid derivatives
    • Custom brominated heterocycle intermediates
    • Precursor molecules for research reagent supply
    • Intermediates for advanced materials R&D
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    Certification & Compliance
    More Introduction

    Meet 2-Bromide Butyrate: Bringing Reliability to Chemical Synthesis

    Today’s science-driven industries don’t just run on breakthroughs, but on the steady pulse of chemicals that quietly get things done. 2-Bromide Butyrate, though not a household name, earns respect where reliability in synthesis means everything. With the model designation of C4H7BrO2, this compound stands out for both its chemical versatility and its dependable performance in a toolkit full of specialty reagents.

    Understanding the Model and Specifications

    2-Bromide Butyrate packs structural integrity that makes it useful for a range of lab and industrial applications. With a butyric acid backbone and a bromine atom attached to the second carbon, this molecule falls in the category of bromo-carboxylic acids. The backbone gives it a predictable reactivity, and the bromo group opens doors for substitution and coupling reactions. What people often notice in practice is its stable liquid state under standard conditions, its clear or pale yellow appearance, and its signature odor. The boiling point tends to hover between 180°C and 200°C, marking it as manageable for distillation and separation steps.

    Attention to purity sits at the center of successful experiments. Commercial sources usually offer 2-Bromide Butyrate in grades above 98%, with trace impurities like dibromides or unsaturated byproducts screened out through rigorous filtration and quality control. Density hovers around 1.5 g/cm³, higher than most simple butyrates, a direct result of the heavier bromine. Such details matter because subtle changes in density or composition can alter rates of reaction or the efficiency of downstream processing.

    Hands-On Experience in Synthesis and Industrial Use

    Over the years, many of us working in pharmaceutical research and fine chemical production have run across 2-Bromide Butyrate during key steps in synthesis. Its true strength becomes clear during alkylation reactions, especially for introducing butyryloxy groups into target molecules. In my work, I've leaned on it as a reagent for esterification, converting alcohols into butyrate esters with a bromine 'hook' left for further substitution. The presence of the bromine atom allows for easy nucleophilic displacement, so chemists can introduce a wide range of substituents, tailoring molecular properties to meet a specific goal.

    In companies that build molecules for pharmaceuticals, fragrances, and agrochemicals, 2-Bromide Butyrate bridges the gap between raw feedstock and finished goods. Its role in the functionalization of aromatic compounds, for instance, often simplifies steps that would otherwise require clunky, less selective reagents. The molecule’s consistent reactivity also saves troubleshooting time during scale-up, where surprises can turn into expensive detours.

    Beyond the bench, safety and storage matter. 2-Bromide Butyrate isn’t as volatile as light ethers or simple chlorides, yet it’s not free from hazards either. Careful storage in a cool, well-ventilated area away from strong bases keeps accidental releases under control. Unlike some of the old-generation halogenated acids, it tends to cause fewer headaches related to corrosion or environmental persistence. Nevertheless, a good fume hood and protective gloves aren’t negotiable.

    Comparing to Other Brominated Butyrates and Analogues

    The butyrate family has grown with the arrival of various halogen-substituted versions, but not all bring the same balance of performance and manageability. In the lab, it’s common to see requests for both 2- and 4-bromide isomers. The 2-bromide structure, with the reactive site closer to the carboxylic acid, gives you more control over regioselectivity in complex syntheses. In contrast, 4-bromobutyrate tends to deliver cleaner results when long alkyl chains are essential, but it doesn’t provide as much leverage in activating aromatic rings or optimizing sterics.

    Chlorinated analogues always seem to get compared as well. While 2-chlorobutyrate can perform many of the same substitutions, the lower atomic weight of chlorine translates to less dramatic reactivity shifts. Bromine’s size and polarizability often help drive reactions at milder conditions, which matters if you’re working with sensitive substrates. I've experimented with both, and the brominated version stands out by cutting reaction times and boosting yields in cases where aldehydes or amines are prone to degradation.

    Some researchers ask about iodinated versions. Though possible to prepare, these are bulkier and much less common in commerce, mostly due to cost and less favorable safety profiles. In the plant or lab, bromide butyrates offer the sweet spot for folks seeking a balance between forcefulness in reaction and manageable hazards.

    Decoding Everyday Importance of 2-Bromide Butyrate

    You can find textbook discussions about functionalized carboxylic acids, but hands-on users care more about what happens day in and day out. In practical terms, 2-Bromide Butyrate smooths over routine bottlenecks. Where free acids can fall short—showing limited solubility or mixing poorly with solvents—this compound often blends in with a wide range of organic or polar media. As someone who has spent hours troubleshooting solubility and reactivity issues, I've learned to appreciate the flexibility this brings. Unexpected precipitation or emulsions can zap hours from a tight project schedule, but this reagent’s predictable solubility prevents such headaches.

    It shines in multi-step synthesis, where the choice of intermediate dictates the fate of the entire process. Specialty crop protection agents and APIs (active pharmaceutical ingredients) often require controlled and specific introduction of alkyl chains. Bromide butyrate offers chemists a reliable pathway to install those groups with fewer byproducts, leading to cleaner downstream profiles and easier final purification.

    Troubleshooting and Problem-Solving Experience

    No chemical, no matter how versatile, works for every scenario. There have been occasions where an unexpected side reaction or incomplete conversion popped up when using 2-Bromide Butyrate. Examining the reaction setup, one key factor always came up—moisture sneaking in through glass joints or pipettes rushed from the stockroom. Bromides are notorious for hydrolysis, generating hydrobromic acid, which doesn’t play well with sensitive amines or acid-labile groups.

    To counter that, a simple trick of oven-drying all glassware and flushing systems with inert gas has spared countless hours. In crowded labs where tools get recycled quickly, these habits are easy to forget. As a rule of thumb, personal vigilance is the surest defense. In teaching environments, passing on the lesson of “dry before you try” saves newcomers from avoidable setbacks with 2-Bromide Butyrate.

    Scaling up brings its own lessons. Handling liters instead of milliliters amplifies minor issues. I remember one instance where inconsistent stirring rate during large-batch alkylation translated into hot spots and uneven yields. After re-fitting the reactor with a more robust overhead stirrer and rebalancing reagent addition rates, yields climbed, and the process could be transferred to pilot scale without fuss. Feedback from production and analytical teams proved the value of treating process transfer as a chance to refine, not just repeat, what worked at bench scale.

    Environmental and Regulatory Considerations

    Awareness of the broader impact of chemical reagents has changed the way labs and plants operate. 2-Bromide Butyrate isn’t classified as environmentally persistent or bioaccumulative, which bodes well for its use in regulated settings. That said, safe handling releases and waste streams should always get top priority. In the companies I’ve worked with, dedicated waste disposal and spill response training have become standard, ensuring compliance and safety in everyday practice.

    Compared to some older halogenated solvents and acids, this compound brings an advantage by breaking down more efficiently in properly managed waste treatment systems. Still, that loosens no one’s obligation. Routine use of secondary containment and periodic waste audits reinforce team accountability.

    With global chemical regulations tightening—especially in regions following REACH and similar frameworks—supply chain documentation has improved. Certificates of analysis, batch traceability, and transport labels deliver peace of mind. They also allow rapid response if anything unusual happens.

    Opportunities to Improve and Streamline Workflows

    Working at the bench, it’s natural to look for ways to push productivity higher. One opportunity comes from better process integration. In pharmaceutical chemistry, bringing together nucleophilic substitution with hydrolysis or esterification in a one-pot protocol often shaves hours off the schedule. By judiciously matching 2-Bromide Butyrate to the solvent system and catalyst, teams can avoid isolating unstable intermediates. The payoff isn’t just speed, but higher overall yield with less waste.

    Digitalization and automation across labs have carved out another opportunity. With more data coming in faster—from reaction monitoring to chromatography—chemists can find optimal conditions sooner. For instance, high-throughput experiments can uncover where 2-Bromide Butyrate best matches reagents or substrates. Automation makes it easier to systematically address persistent bottlenecks, cutting down manual repetition and freeing up bandwidth for unexpected challenges.

    Market and Supply Chain Adaptability

    Anyone who’s worked through supply chain turbulence will know the value of a compound that consistently arrives to spec on time. In the specialty chemicals market, 2-Bromide Butyrate occupies a niche with just enough global demand to support steady production, without the volatility that hits rare or highly regulated intermediates. Manufacturers supplying industries from pharmaceuticals to agrochemicals, and even specialty flavors and fragrances, have maintained reliable logistics channels, giving process managers peace of mind.

    Economic pressures in recent years have tested the resilience of chemical supply on every continent. Companies sourcing 2-Bromide Butyrate have seen some increases in lead times during raw material disruptions. But its moderate production volume has kept it insulated from dramatic price swings. In my own experience shopping for unusual reagents, this stability lets teams plan research and scale-up projects with a clearer runway, knowing supplies won’t dry up unexpectedly.

    Training, Knowledge Sharing, and Skill Development

    Chemistry doesn’t stand still. As techniques evolve, more teams are using 2-Bromide Butyrate than ever before—not by rote, but with a deeper understanding of its quirks and strengths. In my years mentoring grad students and early-career chemists, I've seen how a solid introduction to this compound can save repeated troubleshooting. Demonstrations that walk through risk points—like hydrolysis, proper extraction, and safe neutralization—turn an unknown variable into a trusted part of the toolkit.

    Conferences and workshops have played a useful role, too. Presentations on best practices for using brominated reagents—covering everything from waste mitigation to tougher topics like scale-sensitive exotherms—give teams real-world tools for smoother experimentation. Sharing near-misses and lab victories helps chemists on both sides of the bench, and makes working with 2-Bromide Butyrate less a matter of trial and error, more a matter of skillful routine.

    Future Outlook and Responsible Innovation

    More attention is falling on green chemistry, and that shines a new light on how intermediates like 2-Bromide Butyrate contribute to sustainability targets. Developing recyclable systems for halide recovery, designing closed-loop processes, and collaborating with upstream suppliers who use renewable feedstocks—it all weaves together into a responsible practice. Teams working at the intersection of academic research and industry have started trial runs using alternative solvents and catalysts, aiming to slice the carbon and halide footprint down even further.

    The ongoing refinement of synthetic protocols, paired with continuous feedback between end-users and suppliers, keeps improvement on track. I’ve found that having an open channel to suppliers about batch composition, impurity profiles, and packaging options pays in the long run. Nobody wants to stall a process or re-validate a method due to an overlooked variable.

    What Sets 2-Bromide Butyrate Apart: My Take

    Working hands-on, 2-Bromide Butyrate stands out for three things—reliability, controllable reactivity, and a solid safety profile compared to less predictable alternatives. With enough data and anecdotal feedback stacked behind it, it’s earned a place in the workflow both for daily benchtop chemistry and for piloting the next big molecule. In a world where the difference between finished product and setback can hinge on the properties of a single reagent, it’s no exaggeration to say this compound earns trust with every successful batch.

    It doesn’t promise miracles; nobody expects it to solve problems beyond its reach. But it does deliver the kind of confidence that comes only with consistent, predictable behavior—from one bottle to the next, from micromole-scale trials to industrial-scale syntheses. For professionals who deal with the realities of budgets, yield targets, regulatory scrutiny, and deadline pressure, that kind of reliability counts for a lot more than a flashy new label or a theoretical best-case scenario.

    Conclusions and a Look Ahead

    The next time you see a bottle labeled 2-Bromide Butyrate on your shelf, it’s worth a moment to reflect not just on what it is, but what it lets you do better. Backed by years of dependable service, and by a worldwide community of chemists refining their methods, it sits in the toolkit not because it’s the newest or flashiest, but because it just works. The drive to innovate responsibly, train colleagues well, and keep one step ahead of changing regulations will keep this modest molecule at the center of meaningful progress for years to come. With each new discovery and every improvement in responsible handling, it’s clear that real value in chemistry lies not in the wild claims, but in the steady, reliable progress of compounds like 2-Bromide Butyrate.