|
HS Code |
643246 |
| Cas Number | 2969-81-5 |
| Molecular Formula | C6H11BrO2 |
| Molecular Weight | 195.05 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 205-206 °C |
| Density | 1.375 g/mL at 25 °C |
| Refractive Index | n20/D 1.449 |
| Flash Point | 85 °C |
| Purity | Typically ≥98% |
| Melting Point | -47 °C |
As an accredited Ethyl 4-Bromobutyrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL of Ethyl 4-Bromobutyrate is packaged in an amber glass bottle, featuring a sealed screw cap and hazard labeling. |
| Shipping | Ethyl 4-Bromobutyrate is typically shipped in tightly sealed containers, away from heat and incompatible substances. It is classified as a hazardous chemical and should be transported according to local regulations for flammable liquids. Proper labeling and documentation are required, and handling should ensure protection from leaks and accidental exposure during transit. |
| Storage | Ethyl 4-Bromobutyrate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Use appropriate containment to prevent leaks or spills and avoid inhalation or skin contact. |
Applications of Ethyl 4-Bromobutyrate in Industrial ManufacturingEthyl 4-bromobutyrate is widely used as a specialty intermediate in several industrial chemical synthesis streams. As a direct manufacturer, we support global B2B clients with stable grade supplies for pharmaceutical building blocks, agricultural actives, advanced specialty polymers, functional flavors in fragrance blending, and high-value specialty solvents. Below, we break down representative downstream integration scenarios by market sector, focusing on key process stages and compliance frameworks. 1. Pharmaceutical API Synthesis – Anticonvulsant IntermediatesIn the pharmaceutical sector, this brominated ester serves as a high-purity intermediate for manufacturing various API key structures, notably in producing gamma-aminobutyric acid (GABA) analog drugs like gabapentin and pregabalin. Its role centers on supplying the bromoalkyl motif essential for subsequent nucleophilic substitution, cyclization, or amination steps under GMP guidelines. Manufacturers use the intermediate for batch or continuous synthesis, maintaining traceability and impurity control for regulated markets. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate – Herbicide and Insecticide SynthesisThis compound acts as a reactive linker for agrochemical synthesis, helping produce pyridine-based insecticides and butyric acid herbicide derivatives. The brominated ester group features as a nucleophilic substitution partner to introduce butyric side chains, with subsequent hydrolysis, amidation, or further ring modifications. Downstream manufacturers must meet strict residue and impurity thresholds for active formulation acceptance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Polymer and Resin Modification – Specialty Polyamides ProductionIn specialty polymers, the compound acts as a monomer precursor for producing modified polyamides and polyesters featuring bromine and butyric ester units. Manufacturers exploit its high reactivity in step-growth polymerizations, designing materials with altered solubility profiles, flame retardance, or specialty surface-tension attributes. Each delivery batch must meet polymerization-grade purity with validated absence of unsaturated by-products. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Flavor and Fragrance Synthesis – Building Block for Aroma ChemicalsWithin the flavor and fragrance sector, this ester acts as a key building block for manufacturing butyric ester derivatives, especially used in fruity or buttery note components. The raw material supports aroma compound production through controlled esterification and further modification reactions, where purity and trace contaminant absence are stringently regulated for food and personal care ingredient grades. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemical Synthesis – Custom Synthesis of Specialty Building BlocksMany downstream manufacturers employ this brominated ester as a flexible alkylating agent for synthesizing specialty fine chemicals, catalyst ligands, and functionalized heterocycles for research and industrial applications. Its reactivity profile allows precise control over substitution and chain extension steps in proprietary molecule production programs. Industry compliance standards
Typical usage ratio
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Ethyl 4-Bromobutyrate occupies an interesting niche among brominated intermediates. As manufacturers, we have worked with this colorless to pale yellow liquid to support the synthesis of a strikingly broad range of downstream chemicals. Ethyl 4-Bromobutyrate carries the chemical formula C6H11BrO2 and boasts a molecular weight of 195.06 g/mol. On the production floor and in the lab, one gets to know its faintly sweet, ester-like odor and its measured volatility, which helps during transfers and makes containment manageable with good ventilation.
Not all esters behave the same way in practical chemistry. What sets Ethyl 4-Bromobutyrate apart from similar esters like methyl or propyl bromobutyrates is the balance between molecular weight, handling ease, and reactivity. The ethyl group offers a middle ground—giving neither the excessive volatility seen with methyl derivatives nor the slow reaction rates found in larger esters. This particular balance makes it a dependable building block for fine chemicals, pharmaceuticals, and agrochemical intermediates. Its single bromine atom on the gamma carbon lends a predictable reactivity that is well understood and manageable for experienced process chemists.
We produce Ethyl 4-Bromobutyrate with purity levels often exceeding 98%, typically measured by gas chromatography as per industry protocols. Heavy metals, residual acidity, and bromide ion content remain controlled within strict thresholds. Technical personnel in our facilities monitor color and clarity since unwanted coloration can hint at instability or side reactions—a red flag for downstream processes. The product’s specific gravity, usually falling in the range of 1.35 to 1.38 at 20°C, signals material consistency. Boiling point checks, hovering between 98-100°C at 20 mmHg, further assure reliability since variations here tend to hint at off-spec batches.
We never underestimate the importance of odor and appearance checks, often handled right on the plant floor as part of early-stage QC routines before samples progress to full laboratory analysis. An off-odor might betray the presence of instabilities, unreacted starting material, or over-oxidized byproducts—all issues that complicate final applications, particularly in pharma syntheses. Our production team puts time into minimizing water content, knowing from experience that even small amounts of moisture can hydrolyze the ester over time, affecting both shelf life and downstream yield.
Ethyl 4-Bromobutyrate rarely stays on the shelf for long. Research organizations, pilot scale operations, and commercial pharmaceutical plants draw on a steady supply, and we see its main appeal as a versatile alkylating agent. It often plays a central part in synthesizing heterocycles—gamma-lactams, pyrrolidines, and similar structures. Our customers favor the ethyl ester because it can handle a wider range of reaction conditions without unwanted transesterification or excessive volatility, issues we see in methyl esters. Its chain length proves optimal for ring-forming reactions and for installing protected butyric acid units on larger molecules.
On large scales, many of our clients rely on this intermediate to synthesize compounds destined for anticonvulsant, antihypertensive, or musculoskeletal pharmaceuticals. In a laboratory context, researchers turn to Ethyl 4-Bromobutyrate for constructing libraries of molecular scaffolds. Compared to chlorinated or iodinated analogues, it brings a more manageable leaving group profile. Bromine’s intermediate reactivity smooths out the risk of overreaction or poor yields, and the companion ethyl group gives downstream chemistries a reasonable hydrolysis rate—critical for selective deprotection later in a synthesis.
Anyone who has run multi-step syntheses knows the frustration caused by an unstable or unreliable intermediate. Bromobutyrate with an ethyl ester rarely poses these headaches; you get consistency lot after lot, fewer side reactions, and reliable conversion rates for both nucleophilic substitutions and ester hydrolyses. Unwanted polymerization or oxidation, while always risks for brominated materials, seldom cause trouble here with appropriate storage and packaging. Tightly sealed, nitrogen-purged steel drums or coated glass bottles remain the trusted standard in our facility, with strict protocols that minimize oxygen ingress.
Decades in chemical manufacturing have taught us the realities of handling and storing reactive organobromines. Ethyl 4-Bromobutyrate, while more stable than its smaller cousins, has clear handling points that can make or break batch consistency. The ester functional group, because of its susceptibility to hydrolysis, draws our attention during all bulk transfers and storage. We train our operators to keep humidity under firm control, leaning on low-moisture nitrogen atmospheres during bottling and warehouse storage. Cross-contamination from water traces, or acids left from cleaning, shows up quickly as increased acidity or off-odors in outgoing QC checks.
Process safety is another major lesson. Though Ethyl 4-Bromobutyrate’s volatility is lower than ethyl acetate or methyl bromide, improper containment or poor fume control can still lead to operator discomfort, or worse, respiratory irritation in enclosed areas. We outfit all offloading and packaging lines with activated carbon filtration and maintain a culture of vigilance around organobromine exposure. Each batch processed undergoes final GC analysis; any deviation from the expected retention time and signal intensity triggers a full investigation—including a trace impurity screen for bromoacetic acid, a frequent unwanted byproduct if the reaction’s temperature spikes even briefly.
Much confusion arises from the menu of available bromobutyrate esters: methyl, ethyl, isopropyl, tert-butyl. The choice of alkyl group means a tremendous difference for practical users. Ethyl 4-Bromobutyrate strikes a distinctive balance: its volatility isn’t so high as to cause excessive loss during rotary evaporation or distillation, which keeps process yield higher. Its reaction rates with both soft and hard nucleophiles are easier to control, with fewer surprises during upscaling. We see fewer problems with unexpected ester cleavage, side-chain rearrangement, or elimination products—common headaches for bulk chemists working at high temperatures or under pressure.
Larger esters, such as tert-butyl 4-Bromobutyrate, offer improved stability under strong acid, which might suit certain protection strategies. Yet those larger groups often complicate downstream hydrolysis or increase process cost. Methyl 4-Bromobutyrate, sold for lower cost on the commodity market, creates evaporative and safety challenges on tonnage scales. Our clients usually settle on the ethyl variant because it splits the difference—easy enough to handle, with a reaction profile that supports both pilot and industrial runs.
We’ve seen growing demand for greener or more sustainable alternatives, but so far, no direct bio-based version offers the same performance at market scale. Ethyl 4-Bromobutyrate neither contributes extensively to process toxicity nor generates persistent byproducts, provided it is incinerated with modern scrubbers. Still, material handling and responsible end-of-life disposal always stay top of mind for us as manufacturers. Each year, we revise our MSDS (Material Safety Data Sheet) and environmental compliance reports to track changes in permitted emission levels and best practices for brominated waste.
Chemical manufacturing at any scale rewards attention to supply chain noise. We source raw 4-bromobutyric acid, ethyl alcohol, and sulfuric acid from verified partners, monitoring each for trace impurities. Reaction sequences rely on simple Fischer esterification, but careful temperature, agitation, and waste gas removal all shape outcomes. An under-reacted batch often means free acid persists, which in our experience triggers corrosion, reduces storage life, and can spoil entire tanks of downstream product. Skilled operators regularly run titration and GC checks—the last line of defense before we sign off on a tank or drum.
Any firm-based practitioner will agree—consistency means more than numbers on a datasheet. We put effort into cross-batch audits, shipping mild off-spec lots to internal use or redistillation, rather than risking a customer’s sensitive application. Documentation practices matter, not only for regulatory audits but for customer confidence. Our sales and technical teams field calls from formulators who want detailed impurity profiles, thermal stability checks, or Claudia chromatogram overlays showing five-batch comparison records. Years of aggregate data, not just a snapshot, give end users the trust to build multistep syntheses around our product.
During years of global logistics challenges, we’ve learned to adjust production volume proactively. Forecasting swings in demand from seasonal projects—new drug launches, research cycle peaks, or regulatory approval deadlines—keeps the material flowing. We also keep buffer stock, pre-tested and certified, for our larger contract partners. This approach helps with unexpected order spikes, and, as experience shows, head off delays brought on by supply chain interruptions in worldwide commodities.
Though pharmaceutical synthesis forms the backbone of Ethyl 4-Bromobutyrate demand, fields from agricultural chemistry to material science draw on this versatile ester. For active ingredient manufacture, where cost and waste streams matter immensely, the ethyl ester remains favored for scalable reactivity and manageable environmental footprint. University chemists turn to it for undergraduate labs and advanced technique demonstrations—making it familiar to future generations of synthetic scientists.
Some clients adapt Ethyl 4-Bromobutyrate for research in biodegradable polymers, such as specialty copolymers or as a precursor for modified polyesters. Niche applications in fragrance chemistry, flavor chemistry, or new energetic materials crop up on occasion, with small-scale users valuing predictable hydrolysis and substitution behavior. In our experience, the product’s chemical cleanliness—low content of unsaturated byproducts, residual acids, or halogenated impurities—proves essential for these high-value, low-volume efforts.
Chemical regulations rarely remain static, and brominated intermediates routinely face new scrutiny in international trade. Our site management works closely with compliance teams to verify export documents, REACH status, and the intricacies of dual-use classification. One recent trend we have responded to, as producers, is the growth of purity demands tied to new API (active pharmaceutical ingredient) approvals. Regulatory authorities now call for greater disclosure of impurity spectrums, background contaminants, and process byproducts.
We track candidate impurities—unreacted acids, esters, alcohols, or halogenated debris—using validated analytical methods. It’s now common to furnish comprehensive technical packages with lot-specific impurity breakdowns, and most of our contracts call for annual process revalidation. Our technical staff stays up-to-date with the latest pharmacopoeia requirements, adjusting cleanup steps to deliver the cleanest possible material. We retain reference samples from each ship-out batch, keeping three-year archives for troubleshooting or regulatory questions down the road.
For customers facing new regulatory landscapes, our team shares both regulatory documents and user-side best practices. Working together makes it possible to reduce project delays and complications, especially when projects move from R&D toward commercialization. We treat these exchanges as partnerships rather than transactional supplier-customer links.
As manufacturing practitioners, we always look for ways to improve yield, lower cost, or shrink our environmental impact. Most process advances have come from incremental adjustments—better catalysts for esterification, slower reagent addition curves, improved distillation columns for final purification. Less downtime and shorter cycle times allow us to keep lead times reasonable, with a knock-on effect for client schedules.
Solvent recovery and recycling form another priority. We recover more than 85% of the process solvents, and newer investments in fractional distillation improve the quality of returned feedstocks. Though full green chemistry replacement is not yet a reality for brominated chemicals at large scale, we continue to investigate biosourced alcohols and less energy-intensive recycling for reactor cleaning steps.
On the storage and transport front, we have moved away from single-use packaging. Rugged returnable steel drums, lined to prevent corrosion and guarantee inert contact, now make up most outgoing deliveries. For smaller quantities, specialized fluoropolymer jerrycans offer long-term stability and lower permeation losses—even during long ocean transit. By keeping shipment sizes flexible and lead times reliable, we help our customers plan for spikes in production demand and new product launches.
Persistent production challenges—like bromine volatility loss, cross contamination, or new purity thresholds—spur continuous improvement. Daily batch logs and root-cause tracking for any deviation furnish us with a rich source of improvement ideas. At the center of each process change lies user experience: we revise procedures after direct feedback, whether from complaints or from success stories told at customer technical visits.
Industrial chemists and research scientists consistently tell us that reliable supply supports innovation. We view every batch of Ethyl 4-Bromobutyrate not as a standalone commodity but as a tool that sustains long, risk-sensitive manufacturing chains. A subpar intermediate can derail an entire product line or slow a new drug launch. The ongoing challenge is to keep specification drift, environmental impact, and supply fluctuations low enough for today’s sophisticated end users.
Through years of dialogue with formulators, academics, and regulatory specialists, we’ve learned that transparency, technical documentation, and continuous quality audits matter just as much as price or delivery schedule. Each successful project delivered with Ethyl 4-Bromobutyrate reinforces our reputation, and we approach every improvement—be it in process yield, storage integrity, or shipment timing—with that in mind.
No chemical exists in isolation, and Ethyl 4-Bromobutyrate continues to evolve in the context of changing laboratory technique, process automation, and worldwide demand for new molecules. Our operations team aims to anticipate emerging needs—whether it means tightening impurity controls, developing custom blends, or collaborating on greener process developments. These challenges push us to innovate in daily routines, from the way we handle feedstock traceability to the adoption of digital batch control records.
Final production of Ethyl 4-Bromobutyrate stands on a foundation of chemical skill, historical learning, and respect for both client timelines and regulatory frameworks. We work to provide a reliable, practical, and well-documented building block for chemical engineers, medicinal chemists, and product developers alike. Our perspective as hands-on manufacturers frames every improvement, addressing current demands while preparing for tomorrow’s synthetic challenges.