Products

4-Bromo-γ-Butyrolactone (97%)

    • Product Name: 4-Bromo-γ-Butyrolactone (97%)
    • Chemical Name (IUPAC): 4-Bromooxolan-2-one
    • CAS No.: 20730-46-9
    • Chemical Formula: C4H5BrO2
    • Form/Physical State: Liquid
    • Factroy Site: Gulei Port Economic Development Zone, Zhangzhou, Fujian
    • Price Inquiry: sales3@ascent-chem.com
    • Manufacturer: Fujian Gulei Petrochemical Company Limited
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    Specifications

    HS Code

    446321

    Product Name 4-Bromo-γ-Butyrolactone
    Purity 97%
    Cas Number 20708-53-4
    Molecular Formula C4H5BrO2
    Molecular Weight 180.99 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 103-105°C at 17 mmHg
    Density 1.624 g/mL at 25°C
    Refractive Index n20/D 1.487
    Smiles C1C(=O)OC(C1)Br
    Storage Temperature 2-8°C
    Synonyms 4-Bromobutyrolactone

    As an accredited 4-Bromo-γ-Butyrolactone (97%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Bromo-γ-Butyrolactone (97%) is packaged in a 25-gram amber glass bottle with a tightly sealed screw cap for safety.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 16000 kgs of 4-Bromo-γ-Butyrolactone (97%) packed in drums, securely stowed for export shipment.
    Shipping 4-Bromo-γ-Butyrolactone (97%) is shipped in secure, airtight containers to prevent leakage and contamination. The packaging complies with chemical safety regulations and includes proper labeling. It is transported as a hazardous material, adhering to international shipping guidelines, with all necessary documentation to ensure safe and legal delivery.
    Storage 4-Bromo-γ-Butyrolactone (97%) should be stored in a tightly closed container, in a cool, dry, and well-ventilated place, away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at controlled room temperature, ideally between 2–8°C, and ensure the chemical is properly labeled. Use appropriate safety precautions when handling.
    Shelf Life 4-Bromo-γ-Butyrolactone (97%) should be stored tightly sealed, protected from moisture and light; typical shelf life is 1-2 years.
    Application of 4-Bromo-γ-Butyrolactone (97%)

    Synthesis Intermediate: 4-Bromo-γ-Butyrolactone (97%) with high purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurities.

    Reactivity: 4-Bromo-γ-Butyrolactone (97%) with a bromine functional group is used in organic coupling reactions, where it provides increased reactivity and selectivity.

    Purity: 4-Bromo-γ-Butyrolactone (97%) with 97% purity is used in advanced chemical research applications, where consistency and reproducibility of results are critical.

    Stability: 4-Bromo-γ-Butyrolactone (97%) with a stability temperature of up to 50°C is used in storage under controlled laboratory conditions, where it maintains structural integrity over extended periods.

    Molecular Weight: 4-Bromo-γ-Butyrolactone (97%) with a molecular weight of 177.01 g/mol is used in mass-sensitive syntheses, where accuracy in stoichiometry is essential for process optimization.

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    Certification & Compliance
    More Introduction

    4-Bromo-γ-Butyrolactone (97%): Manufacturer’s Editorial Perspective

    A Thoughtful Introduction to 4-Bromo-γ-Butyrolactone (97%)

    Years amid reactors and analytical labs have taught us a great deal about specialty lactone compounds, particularly 4-Bromo-γ-Butyrolactone, which often appears in R&D wish lists. As manufacturers, our perspective differs from that of distributors and commercial resellers. We see the raw demands of process chemistry, the hurdles in scaling up a niche molecule, and the small details that make or break a research batch. At over 97% purity, our 4-Bromo-γ-Butyrolactone stands as a testament to batch control and solvent discipline. The path from brominated butyrolactone intermediates to an industrial-grade product is never simple. Small adjustments ripple into stability, shelf life, reproducibility, and safety, which are the pillars that researchers and formulators depend upon.

    Understanding the Product’s Identity

    There’s something distinctive about working with heterocycles that feature a halogen motif. Gamma-butyrolactone rings are already popular in organic synthesis for their reactivity and manageable properties, but once a bromine enters the ring, you gain both reactivity and selectivity not found in the parent compound. Our process for 4-Bromo-γ-Butyrolactone uses a controlled bromination step – avoiding over-halogenation or ring cleavage – and we keep purification tight so that chemists receive a genuinely usable reagent.

    Our typical lot comes in at 97% minimum purity by GC, with impurities held low through distillation and careful solvent removal. Appearance is usually a colorless to pale yellow liquid, not far off standard butyrolactone, but with a distinctive faint odor. Moisture content is tracked down to the ppm level, since a little water can introduce ring-opened acids or hydrolyze product during storage.

    Why Purity Matters in 4-Bromo-γ-Butyrolactone

    Many believe high purity is simply about numbers on a certificate. Anyone who’s run scale-up or analytical method development for halogenated lactones knows otherwise. A percent or two of unknowns translates directly into noise, side products, misassignments in spectroscopic work, and nasty surprises during scale-up. Process hazard assessments flag these unknowns as possible sources of HBr gas or corrosive byproducts. In some students’ hands, material bought from generic channels can smell faintly sour or display unexpected coloration from old stock or recycled solvent, tainting results even before the flask warms up.

    We maintain a clarity in our manufacturing not just for compliance, but because we see the faces of scientists relying on material batch-to-batch. PhD candidates years ahead from today will print our lot numbers in their theses, so there’s an ethical pressure behind our batch sign-off.

    Making Sense of Usage: Genuine Field Experience

    We often hear researchers ask about the scope of 4-Bromo-γ-Butyrolactone. Its most respected role appears in synthetic organic chemistry, where it acts as a masked 4-hydroxybutanoic acid source, or as a versatile alkylating and acylating agent. That bromo group at the 4-position makes nucleophilic substitution both possible and selective, which opens the door to pipelining advanced intermediates for pharmaceuticals, crop protection agents, and specialty polymers.

    Some pharmaceutical inventors favor the molecular scaffold for beta-lactam analog design, while others use it for building blocks in CNS-active small molecules. Polymer specialists mention the controlled ring-opening properties, which introduce bromo functionality onto growing chains. As producers, we receive feedback on the product’s behavior in continuous flow regimes, catalyzed reactions, and the oddities of base-promoted rearrangement chemistry.

    Those who have worked with other halogenated butyrolactones, such as 4-Chloro-γ-Butyrolactone, notice the difference immediately. The bromo version ushers in more sluggish but much cleaner nucleophilic aromatic substitution, which matters in route scouting. Bromine is a heavier, less volatile leaving group than chlorine – a benefit in batch reactors where tight control is crucial. Side reactions stemming from over-reactivity or unwanted elimination take a back seat with the bromo format. As a manufacturer, seeing operators reporting lower volatile organic components and fewer system alarms from corrosive gas is a welcome quality marker.

    Differences from Other Related Lactones

    It’s easy to conflate 4-Bromo-γ-Butyrolactone with its cousins. Commercially, we see demand for γ-Butyrolactone itself, 4-Hydroxybutyric acid, and 4-Chloro-γ-Butyrolactone, each with their own quirks. Unbrominated butyrolactone has broader legal uses in cleaning, polymer solvent, and as an intermediate for safer commodity chemicals. It’s abundant and much less troublesome during transport. But it doesn’t provide the direct entry to more elaborate molecules that the brominated version does.

    In the lab, 4-Chloro-γ-Butyrolactone is easier to store and less likely to trigger strict regulatory scrutiny or hazardous waste management headaches. Still, the bromo derivative delivers in selectivity and enables transformations that chlorinated or unfunctionalized lactones simply can’t manage. The activation energy for nucleophilic substitution follows the leaving group hierarchy: Br > Cl > OH, so chemists find the bromo variant a more potent tool.

    We’ve processed 4-Iodo-γ-Butyrolactone on small scale, but commercial realities – cost, instability, ineffective purification – mean bromo remains the best compromise between reactivity and manageability.

    Constraints and Realities of Scale

    From a purely manufacturing viewpoint, producing 4-Bromo-γ-Butyrolactone at scales suited to labs and pilot plants is no minor undertaking. The precursors demand careful sourcing so that bromine isotopic purity and background halide contamination don’t compromise downstream processes. Batch sizes must match order profiles; producing more risks storage complications (the product, even in good drums, can slowly evolve corrosive vapors over many months), while producing less fails to achieve cost efficiency.

    Process bottlenecks arise at the purification and packaging stages. Small mistakes in distillation temperature or vacuum conditions yield off-spec lots, which either loop back for rework or go to incineration. Paperwork follows the product at each step, including environmental and safety documentation – a fact that rarely gets mentioned in distributor websites but lands squarely with us, the producers.

    Waste streams from halogenated solvents, off-gas scrubbing, and still bottoms require real capital expenditure. Avoiding cross-contamination – especially with other bromo- or lactone-based products in the facility – keeps batch reproducibility on track and supports credibility in the eyes of auditors and regulatory agencies.

    Practical Risks and Handling Insights

    Laboratory users rarely see the full risk picture. We enforce robust controls around moisture and ambient light in our packaging bays, as the product can slowly decompose or polymerize under poor conditions. Operators wear specialized PPE and monitor for HBr emissions in closed areas. Each incident of careless handling – spills, drips, mislabeling – echoes in lost productivity and sharp decreases in batch quality.

    Tracking down the origins of batch-to-batch variations takes time. Sources typically include upstream solvent residues, unmatched glassware, or peroxides lingering in feedstocks. Localized overheating during distillation can darken the product and catalyze ring opening, leading to poor shelf-life for downstream customers. Each of these risks receives a mitigation strategy before a drum leaves our facility.

    Feedback from real users taught us to avoid over-designing packaging. Too complex, and lab techs fumble opening procedures. Too simple, and the liquids leak or draw in humidity. We use tamper-evident closures with compatible interior coatings, based on failure data from years of shipping to both city labs and rural process plants.

    Quality Beyond the COA

    Lab managers and technical buyers sometimes believe that a COA and an SDS cover every question about product quality. Direct conversations with method developers have shown us otherwise. Even levels of residual solvent – at parts per million – disrupt NMR readings, gas chromatograms, and high-throughput screens. Not all regulatory bodies treat residual bromo-containing solvents or butyric acid contaminants equally. As a manufacturer delivering into North America, Europe, and APAC, it’s our task to anticipate variances in expectations and build in process flexibility accordingly.

    We’ve hosted site visits for senior pharma scientists who audit upstream controls for potential genotoxic impurities. As a rule, reporting full impurity profiles (within the limits of modern LC-MS and GC-MS) reassures customers that nothing unexpected can creep in. Over the years, we’ve matched process documentation from batch records to customer journals, closing the loop on traceability. Reliability means more than hitting a number, it means anticipating outliers and handling contamination with transparency.

    Support for Research and Industry

    Decades of experience serving both academic and industrial labs have taught us two truths: researchers innovate fastest with reliable reagents, and regulatory hurdles are growing steeper each year. Our 4-Bromo-γ-Butyrolactone batches tie into workflows that don’t tolerate missed deliveries or hidden impurities. Consistency in boiling point, color, titratable acid number, and impurity profile means less troubleshooting and more productive hours at the bench.

    Feedback loops from pilot plants sometimes reach us months after delivery. A batch that failed downstream led to an internal root cause investigation, ultimately traced to a seasonal shift in solvent quality. Without firsthand process control, these issues could persist for years, eroding trust and impacting whole supply chains. Such feedback shapes every revision in our production SOPs.

    Comparative Experience: Other Sources Versus Manufacturer Direct

    We hear plenty about the uneven quality of products passed through resellers and repackagers. Labs complain of unlabeled impurities, inconsistent performance, and even improper storage leading to high acidity or degradants. These complaints aren’t aimed at any particular actor, but they highlight the growing need for vertically integrated manufacturing of chemically sensitive products like 4-Bromo-γ-Butyrolactone.

    Direct purchase from the source means a transparent line of accountability. Any deviation can be traced back through the batch record, and remediation starts immediately – without sending emails into the void or waiting for third party approvals. Years of working alongside QC chemists and plant operators sharpened our response times. A genuine manufacturing origin brings unmatched traceability and control.

    Looking Ahead: Innovation and Production Challenges

    New applications for 4-Bromo-γ-Butyrolactone continue to arise in advanced materials and niche biochemistry. Each new demand tests plant design and process robustness. Automation and real-time analytics now monitor batch outcomes, reducing human error and capturing subtle changes that weren’t detected a decade ago. Data from our own reactors now drive process improvements, not hearsay.

    On the regulatory front, evolving limits on halogenated waste, workplace exposure, and transport require constant adaptation. As a manufacturer, we see laws not as hurdles to skirt, but as opportunities to streamline and improve safety. Customers pursuing green chemistry demand minimized tox profiles, smarter waste handling, and the ability to trace every molecule’s journey. Lean process design and improved worker training help square these requests.

    Conclusion: Manufacturer’s Pledge to Quality and Usability

    Years in the field have taught us that users don’t just value molecules in isolation. They seek assurance that every facet – from synthetic route to packaging to transparency in impurity disclosure – is handled with care and accountability. As direct manufacturers of 4-Bromo-γ-Butyrolactone (97%), our work supports breakthroughs across the chemistry landscape. The lessons we learn from milligram to metric ton echo back through our processes, making every new batch an opportunity for cumulative improvement. Past batches, user data, and customer conversations shape every drum, vial, and bottle that leaves our site. Real, day-to-day practice, and continual feedback, ensure that this isn’t just another specialty chemical, but a vital collaborator in others’ success stories.