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Ethyl 2-Bromovalerate

    • Product Name Ethyl 2-Bromovalerate
    • Alias Ethyl 2-bromopentanoate
    • Einecs 209-806-4
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    700970

    Cas Number 35691-65-7
    Molecular Formula C7H13BrO2
    Molecular Weight 209.08 g/mol
    Appearance Colorless to yellowish liquid
    Boiling Point 196-198 °C
    Melting Point -50 °C
    Density 1.309 g/cm3 at 25 °C
    Refractive Index 1.439
    Flash Point 85 °C
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Synonyms Ethyl 2-bromopentanoate
    Ec Number 609-118-3
    Smiles CCOC(=O)CC(Br)CC

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

    Packing & Storage
    Packing Ethyl 2-Bromovalerate is packaged in a 100g amber glass bottle, sealed with a screw cap and labeled with hazard warnings.
    Shipping Ethyl 2-Bromovalerate is shipped in tightly sealed containers to prevent leaks and contamination. Containers are clearly labeled and handled with appropriate safety measures. The chemical is kept away from heat, sparks, and strong oxidizers during transport. All shipping complies with regional and international hazardous materials regulations to ensure safety.
    Storage Ethyl 2-bromovalerate should be stored in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and bases. Keep the container tightly closed when not in use. Store in a chemical-resistant, appropriately labeled container. Avoid exposure to heat, moisture, and ignition sources, and follow all relevant safety and regulatory guidelines for hazardous materials.
    Application of Ethyl 2-Bromovalerate

    Applications of Ethyl 2-Bromovalerate in Industrial Manufacturing

    As the dedicated manufacturer of Ethyl 2-Bromovalerate, we support high-value industrial clients with direct integration of our raw material in their core production sectors. Below we detail verified downstream applications, providing comprehensive information on standards, dosage parameters, process steps, and finished goods for each scenario to ensure compliance, consistency, and actionable insights for procurement and technical teams.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Intermediate for Anticonvulsants

    Ethyl 2-Bromovalerate acts as an essential halogenated building block in the multi-step synthesis of certain anticonvulsant APIs, particularly within the valproic acid derivatives segment. Its molecular structure facilitates nucleophilic substitution and elongation reactions during the framework assembly of key actives. Pharmaceutical manufacturers employ it in controlled, closed systems under high-purity protocols and traceability requirements, where batch-to-batch consistency and full documentation remain mandatory for international registration and audit purposes.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Ph. Eur., JP, USP monographs (reference for finished actives)

    Typical usage ratio

    • Added at 1.5–8 mol% relative to target API backbone (precise ratio varies based on synthesis route and scale)
    • Adjusted to align with stoichiometry in stepwise alkylation or Grignard reactions; lab/scale-up runs may use slight excess to ensure complete consumption

    Downstream process integration

    • Inserted post-initial carbonyl precursor activation during chain extension sequence
    • Introduced as neat liquid or solution into pre-determined reaction vessels under inert gas with controlled temperature ramping
    • Monitored for residual bromide and validated for conversion yield via analytical QC (HPLC, GC-MS)

    Final product types

    • Pharmaceutical-grade valproic acid derivatives
    • Bespoke active pharmaceutical intermediates destined for in-house or contract API finishing

    2. Agrochemical Synthesis: Intermediate for Pesticide Actives

    In agrochemical manufacturing, Ethyl 2-Bromovalerate serves as a function-specific intermediate for synthesizing select herbicidal and insecticidal actives based on valerolactone frameworks. Leading pesticide producers rely on its halogenated side-chain to facilitate selective cyclization and alkylation steps, maximizing yield and minimizing side-product contamination under regulated process conditions. Its reproducible purity profile ensures downstream compliance for both export and domestic crop protection approvals.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for process controls in active synthesis
    • REACH Registration (EU) for chemical intermediates
    • Chinese GB2763-2021 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Typical addition of 3–12% w/w versus final batch mass, tailored to target molecule and process conversion
    • Adjusted based on cyclization efficiency and precursor concentration in pilot trials

    Downstream process integration

    • Dosed during second or third synthetic step post-basic condensation
    • Staged addition under continuous monitoring in jacketed reactors with controlled agitation
    • Used as an alkyl donor with subsequent in-line phase separation and initial crude purification

    Final product types

    • Technical-grade herbicide actives for blending into commercial formulations
    • Insecticidal agents for row crop seed treatments and field applications

    3. Specialty Polymer Initiator Chemistry

    For specialty polymer production, Ethyl 2-Bromovalerate functions as a well-characterized atom transfer radical polymerization (ATRP) initiator, supporting architectural control in block copolymer and grafted macromolecule synthesis. Industrial polymerization lines exploit its clean reactivity, optimizing molecular weights and dispersity profiles for niche engineering resins, adhesives, and elastomers, while maintaining compliance with product stewardship and environmental safety frameworks.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems in Polymer Manufacturing)
    • RoHS Directive (2011/65/EU) for material content mapping
    • ISO 14001:2015 (Environmental Management for Emissions Abatement)
    • REACH (EC 1907/2006) Registration as monomeric initiator

    Typical usage ratio

    • 0.2–2.5 mol% relative to monomer loading, based on degree of polymerization control desired
    • Dosage adjusted for macroinitiator chain-length targets and block length specifications

    Downstream process integration

    • Added directly to monomer solution prior to catalyst and ligand coupling in the ATRP process
    • Maintained under inert or reduced-oxygen atmospheres to ensure narrow molecular cut-off and low polydispersity
    • Sampled for residual initiator by NMR or SEC as part of batch release protocols

    Final product types

    • Engineering resins for membrane casting and performance films
    • Block copolymers and polymeric surfactants
    • Thermoset adhesives and sealants with controlled architecture

    4. Aroma Chemical and Fragrance Intermediate

    Within the flavors & fragrances industry, this compound operates as a substrate in the creation of specialty aroma molecules—such as saturated and unsaturated lactones—critical to fine fragrance, personal care, and flavoring applications. Downstream processors value its clean chain-branched profile to execute reductive ring closures and selective etherification under food-grade or cosmetic-grade process controls, contributing to consistent olfactory and sensorial profiles in finished compounds.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • FDA 21 CFR 172.515 (Flavoring Substances and Adjuvants, US Food-Use GRAS List)
    • ISO 22716:2007 (GMP for Cosmetics)
    • EU Regulation (EC) No 1223/2009 for Cosmetic Ingredients

    Typical usage ratio

    • 4–9% relative to main reactant mass in aroma intermediate synthesis
    • Refined up or down based on lactonization kinetics, fragrance strength targets, and desired batch concentration

    Downstream process integration

    • Added early as a starting ester in ring-closing reactions or side-chain alkylation
    • Processed under batch or semi-continuous synthesis in stainless steel reactors with food/cosmetic-grade cleaning validation
    • Resulting intermediates typically undergo vacuum distillation and gas-chromatographic aroma evaluation

    Final product types

    • Specialty fragrance lactones for fine fragrances and personal care
    • Flavor compounds for food and beverage formulations (subject to local market approvals)
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    Certification & Compliance
    More Introduction

    Ethyl 2-Bromovalerate: A Direct Approach to Chemical Synthesis

    Introduction to Practical Experience

    At our plant, every liter of Ethyl 2-Bromovalerate reflects a real shift that starts at the bench and ends with barrels rolling out the door. This compound stands out in the family of bromoalkanoic esters. Our technicians handle flasks and drums daily, keeping track of subtleties a textbook might not bother to mention. Over years watching countless batches, we adjust columns, confirm vapor temperatures, check color against calibrated standards—never trusting just one instrument or a spec sheet. Consistency comes from this hands-on scrutiny.

    Ethyl 2-Bromovalerate offers more than a chemical name. Its C7H13BrO2 backbone combines the reactivity of a bromine atom with the solubility and handling ease typical for small esters. We see chemists reach for it in active pharmaceutical ingredient (API) work, custom synthesis, flavors, agrochemical intermediates, and academic research. Every season brings custom orders with different specs—sometimes a tight GC purity, other times a particular color threshold or residual acid requirement. Flexibility in the plant, attention to isolation steps and crude pre-treatment, shapes how we deliver what the process chemists need downstream.

    Understanding the Product: What Makes it Reliable

    Our Ethyl 2-Bromovalerate never leaves the plant until it’s checked for assay by gas chromatography, water by Karl Fischer, and color by Hazen. Standard batch purity runs above 98%, but if a customer needs 99% for a sensitive route—particularly those after chiral downstream targets—our purification team circles up, tweaks fraction cuts, and keeps impurities in check. We produce this ester in volumes from pilot to multi-ton scale, shifting batch strategies in real time to balance yield and impurity profile.

    Origin matters: we start with ethyl valerate and brominating agents sourced directly, skipping intermediate trade layers. We minimize contamination risks, and continuous improvement meetings in the plant keep side reactions—particularly dibromo and higher boiling side products—on the radar. Experience has taught us that small changes in bromine feed rates or solvent pre-treatment can tip a batch from passing to rework, so veteran operators keep their eyes on the telltale signs during runs.

    Handling Ethyl 2-Bromovalerate gives you a clear, slightly heavier-than-water liquid with a faint characteristic odor. The real insight comes from correlating smell, color, and analysis from tank to bottle—off-specs never hide for long. Even outside of routine checks, we carry out extra headspace GC runs if something doesn’t look or smell normal.

    Specifications Rooted in Practice

    In practice, demands fall into a few main categories. Most customers require clear, colorless liquid, with chromaticity below 50 Hazen units. GC purity stays at or above 98% for routine applications, but for lab or pharma supply, higher grades run up to 99.5%. Water level below 0.2% is typical—going drier if crystallization or further transformations need it. Hydrolyzable bromide and acid number stay low, as high residual values increase byproduct risks in coupling reactions.

    We do not rely on theory alone. Every deviation—be it odor, unexpected boiling point, or GC flag—gets tracked down. Combining instrument data with operator instinct, the result is a product that stays in specification because people know what right looks like at each stage. Customers often comment they can tell ours from others by its clarity and minimal residue when evaporated.

    Key Uses from First-Person Perspective

    Chemists in pharmaceutical research request Ethyl 2-Bromovalerate as a go-to alkylating agent. At the plant, we often prepare special lots for those scaling a synthesis from milligrams to kilograms. They want reliable reactivity—bromine atoms ready for substitution or cross-coupling. In flavor and fragrance, mixer tanks draw from drums for the quick installation of five-carbon chains. Agricultural intermediates call for good batch consistency, as their final products must meet tight regulatory standards and avoid accumulative impurities.

    We see diverse reactivity after the product leaves our tanks. Its bromine site, placed at the 2-position of the valerate backbone, triggers efficient nucleophilic substitutions—particularly enolate alkylations and amino modifications. Peptide chemists lean on its clean conversion profile. Compared to three-carbon or longer six- and seven-carbon homologues, the valerate structure offers a balance of volatility and solid chemical handle. Lower carbon analogues give more volatility and handling hazards; higher ones are less reactive and harder to purify. Our in-house assays confirm that 2-substitution gives the best mix of reactivity and shelf stability for diverse organic transformations.

    Fine chemical producers and lab researchers have specific asks that shape our production design. Larger pharmaceutical companies sometimes request packs under nitrogen or with extra filtration. We gear up for these with product stability studies, confirming resistance to slow decomposition or color formation over many months. Knowing their reaction vessels hold high-value intermediates, we go the extra step to avoid trace metals or polymeric residues from plant equipment.

    Comparisons with Other Halogenated Esters

    In our portfolio, Ethyl 2-Bromovalerate sits beside a lineup of brominated and chlorinated esters: ethyl 2-bromobutyrate, ethyl 2-chlorovalerate, and their longer-chained siblings. Each has its following among synthetic chemists. Our teams routinely compare batches to spot cross-contamination or mixing errors. Ethyl 2-Bromovalerate stands out for reliable selectivity in alkylations. Its five-carbon chain proves just right for many transformations that fail or give unwanted side products with shorter or longer esters.

    Compared to ethyl 2-bromobutyrate, this product brings a slightly higher boiling point, easing separation from volatile solvents. Differences in physical handling, like reduced evaporation losses and easier containment, lower wastage and environmental exposure. In substitution reactions, the extra methylene gives a more forgiving platform for many nucleophiles, improving yields for certain pharmaceutically relevant side chains.

    We worked with several clients who initially used lower-cost chlorinated analogues—like ethyl 2-chlorovalerate—only to find their reactions slowed or gave lower conversion. Our technical support staff often ends up walking through kinetic and mechanistic points that favor the bromo derivates, especially when working up sensitive products. Even under similar purity specs, a clean Ethyl 2-Bromovalerate batch offers greater selectivity with less risk for unwanted elimination or rearrangement than chlorinated esters.

    Direct Feedback from the Plant

    Genuine process experience matters. Sometimes a batch seems analytically fine but behaves unpredictably for the end user. Between analytical reports and real-use cases, we balance improvements that work on both the numbers and hands-on application. In one case, a customer’s yield dropped unexpectedly; our staff found a trace byproduct downstream by re-examining HPLC data and tweaking solvent pre-wash on subsequent lots. Fast feedback loops make a difference.

    Storage and shelf life also play a role. Practical chemistry rarely leaves time for elaborate prep: customers want bottles ready to pour, with no phase separation, haze, or color drift. We store in light-resistant drums, tightly sealed under dry air, shipping promptly to minimize aging or decomposition. In one shipment, we detected slight pressure buildup; changing the sealing protocol solved future events. These lessons show up in every new batch.

    This day-to-day problem-solving shapes quality more than glossy brochures or abstract promises ever could. Our batches build on the collective know-how of operators who notice when a transfer line runs just a bit differently, or when a color shift signals a potential off-grade.

    Future Challenges and Opportunities

    From the manufacturer’s view, challenges are ever-present. Environmental regulations continue to tighten, particularly concerning brominated intermediates. We have modified production note cycles over the years, investing in closed system handling to reduce operator exposure and venting. Less waste, less loss, tighter mass balances—plant upgrades stem from real regulatory pressure and a long-term commitment to responsible chemical stewardship.

    We track global trends in pharmaceuticals and fine chemicals. Demand can spike suddenly as new targets emerge, forcing rapid scale-up or new packaging solutions to support project timelines. At these inflection points, our plant engineers rework schedules, re-validate cleaning processes, and adapt layouts. The result is a product that remains available and consistent when competition stumbles. Several companies have called us mid-campaign when other sources ran dry or batches failed specification; our ability to pivot makes a tangible difference for production chemists with pressing deadlines.

    On the opportunity side, Ethyl 2-Bromovalerate empowers creative chemistry. Every year brings new synthetic routes and process patents using this material as a backbone. Our relationship with customers—the feedback, the troubleshooting, the mutual commitments—pushes us to continuous improvement. We hold regular meetings, trade application data, and tweak lots to best fit the route envisioned by the user. Standard solutions rarely fit every application, so we respond in real time, dialing in purity, residual solvents, or packaging to make downstream handling easier and safer.

    Practical Recommendations for Users

    Hands-on handling, not mere paperwork, secures results when working with Ethyl 2-Bromovalerate. We recommend storing unopened drums in cool, dry, and well-ventilated areas—a lesson learned from several summer batches where temperature spikes accelerated shelf degradation. In laboratory settings, minimizing air and moisture exposure, combined with careful dispensing, maximizes shelf life and reactivity. Our on-the-ground knowledge says: never overlook odor or clarity checks, even if the analysis of record comes back clear.

    Users working with automated or pilot plant equipment benefit from pre-testing for material compatibility, since the ester can sometimes soften seals or gaskets after extended contact. Regular sampling and visual inspection prevent scale-up surprises. Process engineers appreciate our habit of double-sealing all drums and affixing batch history directly to the packaging—a practice standard in our warehouse but not always matched by outside suppliers.

    Waste reduction and sustainability increasingly motivate customer decisions. We have run side-by-side tests with both our drums and bulk totes to identify leakage, waste, and cleaning issues. Results get fed back into filling lines and packing protocols, lowering losses and giving customers full visibility from loading dock to end user bay.

    Building Confidence Through Consistency

    Ethyl 2-Bromovalerate’s real value shows up batch after batch, customer after customer, process after process. Our reputation—built on years of consistent delivery—rests on operator vigilance, plant upgrades, regular training, and customer feedback. The plant never stands still; quality is a moving target, and every shipment teaches us something new.

    By producing and handling this product at source, we catch and correct deviations before they reach the loading dock. Our staff’s cumulative experience and willingness to admit and solve problems head-on ensure users receive material matching real-world requirements. Customers trust us not only for specs on paper but for batches that work in practice, support critical syntheses, and stay reliable over years of repeat orders.

    This is how Ethyl 2-Bromovalerate earns its reputation—not through claims, but through the practical, measured, and consistent effort of everyone from reactor operators to loading dock supervisors. Our investments in people, plant, and partnerships put us reliably at the table whenever chemists require this crucial intermediate. The bond between manufacturer and user sets the standard, shaping every process from raw material arrival to finished product leaving the gate.