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Methyl 2,5-Dibromovalerate

    • Product Name Methyl 2,5-Dibromovalerate
    • Alias Methyl 2,5-dibromopentanoate
    • Einecs 252-381-8
    • 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

    927832

    Chemical Name Methyl 2,5-Dibromovalerate
    Cas Number 5118-13-8
    Molecular Formula C6H10Br2O2
    Molecular Weight 273.96 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 110-112°C at 15 mmHg
    Density 1.759 g/cm³
    Refractive Index 1.494
    Purity Typically ≥97%
    Solubility Soluble in organic solvents (e.g., ether, chloroform)

    As an accredited Methyl 2,5-Dibromovalerate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of Methyl 2,5-Dibromovalerate

    Applications of Methyl 2,5-Dibromovalerate in Industrial Manufacturing

    Methyl 2,5-dibromovalerate plays a critical role in several niche chemical synthesis sectors where selective reactivity and halogenated functionalities are vital. As a direct manufacturer, we serve industries that require this intermediate for precision synthesis processes supporting crop protection, pharmaceuticals, advanced materials, and specialty fragrance precursors. The applications below represent verified downstream use cases, each operating under specific industrial and regulatory frameworks to ensure process integrity and product quality.

    1. Agrochemical Synthesis: Intermediate for Herbicide Active Ingredients

    Methyl 2,5-dibromovalerate is used in the agrochemical industry primarily as a chain-elongation intermediate for constructing halogen-containing herbicide molecules, enabling the synthesis of actives for selective weed control. It enters the process as a key building block for certain pyridine and triazine derivative herbicides demanded in high-value crop segments where targeted application and resistance management are critical. Precision in bromination degree allows consistent downstream yields and product purity, essential for regulatory registrations and field performance.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 (Quality Management Systems for chemical manufacturing)
    • Registrations per Regulation (EC) No 1107/2009 (EU Plant Protection Product regulation)
    • US EPA active ingredient registration requirements (40 CFR 158)

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target molecule backbone, typically 8–14% of total finished active mass basis; adjusted based on target compound stoichiometry and process yield.

    Downstream process integration

    • Charged during the initial C5 chain assembly or bromoalkylation step, then subjected to nucleophilic substitution or cyclization, depending on the herbicide scaffold. Used in batch or semi-continuous stirred tank reactors with inert gas blanketing for safety.

    Final product types

    • Brominated pyridine-based herbicides
    • Selective triazine derivatives for pre-emergent weed control
    • Herbicide technical concentrates
    • Formulated emulsifiable concentrate herbicide preparations

    2. Pharmaceutical Synthesis: Precursor for Anticonvulsant and Antiviral Intermediates

    Chemical process development in the pharmaceutical sector uses methyl 2,5-dibromovalerate as an alkylating or functionalization agent for complex molecule synthesis, where the two bromines serve as active handles for key step transformations. Pharmaceutical R&D groups and API manufacturers rely on its reactivity for synthesizing specialized intermediates, notably in the synthesis of substituted valeric acids and lactam rings found in anticonvulsant and antiviral drug candidates. Purity and traceability are monitored closely to comply with cGMP and ICH guidelines throughout the multi-stage route.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)
    • European Pharmacopoeia Purity Requirements (current edition)
    • US DMF (Drug Master File) for starting material registration

    Typical usage ratio

    • 1.0–1.3 molar equivalents per step, 4–10% of reaction mass depending on target route; higher equivalence employed in convergent syntheses to ensure full conversion and minimize side reactions.

    Downstream process integration

    • Dosed at the controlled alkylation or bromination stage under inert conditions, followed by hydrolysis, reduction, or lactamization. Applied in closed-system glass-lined reactors, with continuous isolation and purification steps for intermediate handling.

    Final product types

    • Substituted gamma-valerolactone intermediates
    • API precursors for next-generation anticonvulsants
    • Halogenated cyclopentane derivatives for antiviral drugs
    • Key intermediates for pharmaceutical contract synthesis (CDMO platforms)

    3. Specialty Flavors and Fragrances: Synthesis of Halogenated Fragrance Intermediates

    In the specialty fragrance and flavor compound sector, methyl 2,5-dibromovalerate enables the stepwise construction of halogenated ketones and esters that serve as building blocks for marine, green, or exotic accords. Its reactivity drives chain modification reactions essential to forming molecules with unique odor profiles, valued for their persistence and impact in fine fragrance blends. QMS and food safety guidelines govern its use, with rigorous supplier documentation trails for downstream audits and IFRA standards compliance.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for restricted substances
    • ISO 22000 (Food Safety Management System) for food-grade fragrance intermediates
    • AISE Charter (Detergent and fragrance formulation safety)
    • Material Safety Data Sheet (MSDS) requirements per EU REACH

    Typical usage ratio

    • 3–7% by weight in key intermediate synthesis steps, modifiable based on fragrance molecule backbone and required odor intensity/persistence of the final accord.

    Downstream process integration

    • Entered into the halogenation or acylation sequence where chain extension and ring closure are then followed by downstream distillation and solvent exchange to preserve odor integrity. Small to medium batch scale with dedicated glass equipment preferred for aromatic chain building.

    Final product types

    • Halogenated ester-based aroma chemicals
    • Marine note fragrance intermediates
    • Specialty green accord enhancers for fine fragrances
    • Perfume oils for luxury home and personal care sectors

    4. Advanced Materials: Precursor for Functionalized Polymeric Additives

    Methyl 2,5-dibromovalerate functions as a reactive initiator or chain extender in advanced polymer applications, enabling the creation of functionalized copolymers or specialty additives with flame-retardant or unique solubility profiles. Polymer compounders integrate it into precise synthesis schemes to impart targeted halogen content, critical for electronics encapsulation and performance coatings. Its dual bromine groups provide sites for further derivatization, tightly controlled under materials compliance audits and batch traceability.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics Materials)
    • RoHS (Restriction of Hazardous Substances Directive, EU 2011/65/EU)
    • EN ISO 9001:2015 (Quality Management in material manufacturing)
    • REACH Annex XVII SVHC (Substance of Very High Concern tracking)

    Typical usage ratio

    • 0.2–1.5% by polymer/resin weight, depending on desired halogen load and final application flammability rating; exact ratio optimized during compounding QA trials or customer-specific formulations.

    Downstream process integration

    • Added during copolymerization or end-capping step in polymer melt reactors or solvent-based synthesis. Follows through to compounding, extrusion, or masterbatch preparation, with post-polymerization QA analytics to confirm additive integration.

    Final product types

    • Brominated polymeric flame-retardant additives
    • Functionalized acrylate copolymers for electronics
    • High-performance coatings with improved chemical resistance
    • Polymer masterbatches for specialty plastics
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    More Introduction

    Methyl 2,5-Dibromovalerate: Shaping Modern Organic Synthesis

    In the world of fine chemicals, Methyl 2,5-Dibromovalerate stands out for its reliable performance in building blocks aimed at pharmaceutical, agricultural, and advanced materials research. Speaking from experience, sourcing raw materials with strict purity levels and reliable batch-to-batch reproducibility can feel like squeezing water from a stone. It’s refreshing to come across a compound like Methyl 2,5-Dibromovalerate that puts consistency front and center, meeting the expectations of both bench chemists and scaled-up production teams.

    The Details That Make a Difference

    The chemical makeup reveals a five-carbon backbone, esterified at one end, and brominated at the 2 and 5 positions. In practical lab work, this arrangement brings both reactivity and flexibility. As methyl esters go, most folks in synthetic chemistry will nod at the uses—either as a precursor for subsequent hydrolysis or straightforward transesterification. Brominated chains bring their own value to the table, acting as handles for nucleophilic substitution, Grignard chemistry, and cross-coupling reactions. This extra bit of control in the structure means researchers can design syntheses with fewer side steps, avoiding problems like unwanted rearrangements or tedious purifications found with more complex, less predictable intermediates.

    The purity issue cannot be dodged. For complex chemical syntheses, trace impurities and variable yields can stall progress in preclinical research or materials development. Speaking from the perspective of someone who has spent weeks troubleshooting just one reaction due to questionable reagents, every percentage point in purity matters. Technical data commonly list purities approaching or exceeding 98%, which gives professionals peace of mind when accuracy and safety are on the line. Analytical details—infrared spectra, nuclear magnetic resonance, chromatography traces—make it much easier to validate before the first gram is used in synthesis. This transparency supports the reliability users need to trust new suppliers.

    Predictable Results Backed by Careful Design

    Lab timesaving comes not only from chemical reactivity but from how easy a material is to handle. Methyl 2,5-Dibromovalerate appears as a clear, colorless to pale yellow liquid, and from accounts in research group meetings, it pours and measures without trouble. No worrying about clumps or unstable powders. Storage in a cool, moisture-proof space keeps it ready for use into long project timelines. In my own experience, I appreciate compounds that don't require complicated handling or specialized storage, which lets newcomers and experienced professionals alike focus more on their projects and less on fussy logistics.

    The model and specs often focus on the molecule’s weight—around 287.96 g/mol—along with high-grade purity and minimal moisture. These are more than numbers for purchasing forms. They influence every downstream application, whether used at gram scale or for multi-kilo production runs. Tighter moisture limits, for instance, mean less variation during base-sensitive steps, which is a big help for anyone taking a project from discovery through to pilot manufacture.

    Setting It Apart from Everyday Brominated Esters

    Not every brominated ester delivers the same bang for your buck. Most folks familiar with methyl esters know that single bromination gives some flexibility, but double bromination—at specific points like the 2 and 5 carbons—opens new synthetic doors. This lets users construct intermediates that simply aren’t accessible from single-site brominated versions or from other unbranched alkyl esters. If you’ve ever dealt with positional isomer headaches, separating out mixtures post-reaction, the advantage here becomes obvious quickly.

    Competing products might add substitution at a single site, or they might swap the methyl group for a bulkier ester—choices that impact not just the chemistry but safety, volatility, and downstream environmental controls. What stands out in this compound is the symmetry and the unhindered ester end. I recall one project that demanded strict regioselectivity for a medicinal chemistry application; relying on Methyl 2,5-Dibromovalerate meant cleaner conversions, which means less chromatography and less waste.

    Versatility Across Research and Industry

    For those in medicinal chemistry, the trajectory from idea to biological testing needs reliable intermediates. Methyl 2,5-Dibromovalerate offers a foothold for constructing molecules where bromoalkyl handles act as points for amination, ether formation, or even cyclization. Drug discovery teams look for clean intermediates that can undergo high-yield transformation, and this compound meets that need based on its track record. In agricultural research, building new active ingredients sometimes means finding new routes to chlorinated or brominated rings and macrocycles. Years ago, colleagues pointed out how switching to a dibromo substrate meant a 30% bump in yield over a drawn-out sequence using conventionally substituted esters. The time savings and fewer purification steps genuinely matter for both progress and bottom lines.

    Polymers and advanced materials researchers chase innovations for specialty coatings, resins, and electronic materials. Here, the dibrominated structure enters step-growth or chain-transfer polymerizations, helping incorporate functional halogens into polymer backbones. I’ve seen collaboration groups use this compound as a monomer precursor, tuning the spacing of reactive sites within the final polymer. The flexibility lets development labs tweak product properties without sending costs through the roof, as alternative starting points might.

    Challenges and the Value of High-Quality Reagents

    Challenges still crop up—cost, availability, regulatory pressures—yet high-quality raw materials provide a buffer against many surprises. Large-batch variability and spotty documentation can send projects off the rails, especially when one batch behaves differently from the next. Many chemical companies have learned to insist on transparent sourcing data, reproducible spectra, and fair lead times. Personally, I have seen too many projects delayed by poorly labeled supplies or ambiguous certificates of analysis. Having a history of reliable performance builds trust between vendors and researchers, which is absolutely not something to take for granted in today’s global economy.

    Sustainability is creeping up the list of user concerns. Brominated organics sometimes raise eyebrows due to environmental fates and toxicity concerns, especially when used in scale or disposed of improperly. Forward-thinking manufacturers are gradually adopting cleaner production methods—closed-loop processes, improved waste capture, and process chemistry innovations that minimize hazardous byproducts. Though these improvements may add a tick to the purchase cost, experience suggests that spending the extra dollar up front saves many more down the road by dodging environmental headaches and compliance violations.

    In research settings, safety data sheets recommend standard personal protective equipment—lab coat, goggles, gloves—but anyone who has splashed concentrated chemicals in a hurry knows the true value in clear labeling and secure packaging. Methyl 2,5-Dibromovalerate typically comes packed in sturdy amber bottles, minimizing UV breakdown and reducing user exposure. Spill cleanup is straightforward with standard solvents and absorbents for organics, though always best handled with care, especially at scale. Labs that have adopted rigorous micro-scale handling and immediate decontamination routines rarely see incidents escalate, so best practices count for far more than regulatory minimums.

    What Sets Methyl 2,5-Dibromovalerate Apart

    Unlike some more sensitive halogenated reagents, Methyl 2,5-Dibromovalerate stores well for extended periods under the right conditions. Labs can bank supplies over project phases, a rarity with some more volatile or light-sensitive counterparts. I have known projects that kept drums in controlled storerooms for over six months with no perceptible degradation or shift in reactivity. Stability, while sometimes overlooked during initial planning, can become the difference between a smooth project and a logistical train wreck. Chemistry professionals know to check real-world experiences and supplier records before purchasing in volume, and this compound rarely disappoints in those checks.

    Comparing methyl esters, the dibromo version covers a swath of applications broader than single analogs. Single brominated esters, for instance, give fewer reaction vectors and slower rate enhancements in nucleophilic reactions. Attempts to compensate with stronger bases or higher temperatures can lead to side-reactions, rearrangement, or loss of product during purification. The 2,5-dibromo arrangement encourages high regioselectivity without resorting to harsh or dangerous conditions. That alone explains its regular appearance in new methodologies published in major organic synthesis journals.

    The Human Side: Practical Lessons from the Lab

    Day-to-day, technical staff and research chemists care about more than structure diagrams and lot numbers. Time spent contending with unreliable materials comes at a real cost. Nobody wants to rerun reactions or chase phantom impurities. Methyl 2,5-Dibromovalerate earns a solid reputation for reliability precisely because those problems rarely arise when its batch is sourced from a diligent supplier. Colleagues share stories about scaling syntheses up thanks to inputs behaving as advertised, and that level of predictability becomes a selling point all its own. Students and postdocs often make the mistake of shopping only on price, only to find themselves fighting strange results. My advice: invest in a well-characterized intermediate at the outset—it saves headaches, money, and lost time over the course of a project.

    Professional organizations and trade groups now pay close attention to the paper trail that accompanies every intermediate. From my seat, real traceability comes from a combination of supplier transparency, robust analytics, and the willingness to listen to end-users’ feedback when problems arise. I have seen batch numbers logged alongside reaction yields in company databases, so it’s easy to trace issues if something goes sideways. This adds an extra layer of security when moving a project toward a regulatory approval milestone, or simply keeping track of where each gram has gone. Methyl 2,5-Dibromovalerate continues to find favor where transparency isn’t just appreciated—it’s mandatory.

    Looking Ahead: Research, Reformulation, and Responsible Use

    Exciting directions are opening up in catalysis, biomolecule modification, and new reaction methodologies. The dibromo motif on a relatively simple aliphatic chain keeps things approachable for a broad range of transformations while pushing the boundaries of what’s possible. At several conferences, I’ve seen research teams share updates on cross-coupling approaches that pivot off dibrominated esters, enabling faster routes to libraries of analog compounds. Speeding up medicinal chemistry cycles means faster access to drug candidates, which is as crucial for startups as it is for established multinationals. Colleagues in green chemistry have started examining how to use less energy and more benign solvents in routes involving this reagent, driving broader conversations about sustainability throughout the chemical pipeline.

    Personally, as someone who has worked both at the bench and in project management, I see real value in reagents that serve as stepping stones to greater innovation. Methyl 2,5-Dibromovalerate empowers teams to work smarter with fewer surprises. Its performance rarely disappoints at both research and production scales. As attention grows on responsible chemical innovation, its track record sets a solid example for what reliable supply, robust analytics, and real customer support can look like for specialty reagents.

    Quality matters anywhere chemistry is used to build something important—from drugs to crop protection, smart materials, and the next generation of polymers. The difference between a promising idea and a real-world product can come down to the properties of a single intermediate. Methyl 2,5-Dibromovalerate, with its thoughtful structure and consistently high performance, continues to earn its place on lab benches and factory floors alike.

    Finding the Right Fit in a Crowded Marketplace

    The specialty chemicals market is crowded and competitive. New products come and go, flashy marketing abounds, and overwhelmed buyers have to cut through layers of information to spot genuine value. My advice—learn from fellow practitioners, look closely at published data, and weigh actual batch records. Few compounds manage to merge ease of use, high reactivity, clear documentation, and dependable shipping protocols as effectively as Methyl 2,5-Dibromovalerate. If a new synthesis needs a versatile, robust building block, this compound merits a hard look—whether for a niche research effort or the ramp-up to full-scale manufacturing.

    The devil is always in the details. Projects falter due to inconsistent starting points more often than dramatic missteps during the core chemistry. Running a smooth operation, whether in a startup or a global conglomerate, depends on reliable partners and predictable workflows. The compound in focus fits this bill and stands ready to meet demands as chemistry evolves with global needs and local ambitions. Smart purchasing, solid training, and ongoing research ensure the best results while keeping eyes on future opportunities for more sustainable, efficient synthesis.