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(S)-5-Bromomethyl-2-Pyrrolidone

    • Product Name (S)-5-Bromomethyl-2-Pyrrolidone
    • Alias (R)-5-(Bromomethyl)dihydro-2(3H)-pyrrolone
    • Einecs 629-733-4
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    304517

    Product Name (S)-5-Bromomethyl-2-Pyrrolidone
    Cas Number 1186125-76-5
    Molecular Formula C5H8BrNO
    Molecular Weight 178.03 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥ 98%
    Solubility Soluble in water and polar organic solvents
    Optical Activity S (Sinister) configuration; chiral compound
    Density Approx. 1.6 g/cm³ (estimated)
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms (S)-5-(Bromomethyl)pyrrolidin-2-one
    Hazard Information May cause irritation; handle with care

    As an accredited (S)-5-Bromomethyl-2-Pyrrolidone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of (S)-5-Bromomethyl-2-Pyrrolidone

    Applications of (S)-5-Bromomethyl-2-Pyrrolidone in Industrial Manufacturing

    As an established manufacturer of (S)-5-Bromomethyl-2-Pyrrolidone, we supply high-purity raw material to advanced industries that demand strict process control and traceability. This compound supports diverse sectors across synthesis, specialty chemicals, and pharmaceutical intermediates. Below we present key downstream applications with detailed compliance, usage, and integration profiles.

    1. Chiral Pharmaceutical Intermediate Production

    Pharmaceutical manufacturers use (S)-5-Bromomethyl-2-Pyrrolidone as a critical chiral intermediate in the synthesis of several non-racemic active pharmaceutical ingredients. The bromomethyl group enables functionalization at controlled positions in complex heterocycle scaffolds, including selective nucleophilic substitutions. Process chemists integrate this intermediate into multi-step batch and flow processes, often under cGMP conditions, where the enantiomeric purity and trace impurity profile are tightly monitored. The compound’s reactivity profile allows regioselective modifications without racemization, contributing directly to enantiospecific drug candidate pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. guidelines on impurities and residual solvents for APIs
    • 21 CFR Parts 210 & 211 (FDA cGMP for finished pharmaceuticals)
    • ISO 9001:2015 Quality Management System for supplier qualification

    Typical usage ratio

    • Applied at 0.5–5.0 molar equivalents relative to primary amine or nucleophile depending on target molecule structure
    • Stoichiometry adjusted according to yield and chromatography recovery optimization

    Downstream process integration

    • Introduced as a starting material or intermediate during lead diversification in multistep synthesis
    • Undergoes alkylation, substitution, or condensation steps in jacketed reactors under controlled temperature and inert atmosphere
    • Feeds directly into purification/isolations by preparative HPLC or recrystallization after transformation

    Final product types

    • Chiral antiviral agents
    • Optically pure pyrrolidone-based CNS drugs
    • Small-molecule enzyme inhibitors in oncology research

    2. Agrochemical Intermediate Synthesis

    Producers of crop protection compounds utilize (S)-5-Bromomethyl-2-Pyrrolidone as a structural building block for the preparation of bioactive heterocyclic agrochemicals. The compound serves in the construction of pyrrolidone-based scaffolds with substituted amines or organometallic nucleophiles, especially for selective herbicide and fungicide leads. Quality control ensures absence of by-products and robust batch reproducibility, as regulatory scrutiny on agro inputs remains high. The use of enantiomerically pure material can influence the eventual activity and selectivity of the formulated agrochemical.

    Industry compliance standards

    • EPA 40 CFR Part 174—Plant-Incorporated Protectants; Tolerances and Exemptions
    • OECD Guidelines for the Testing of Chemicals (Residues and Environmental Fate sections)
    • ISO 17025 accreditation for process testing laboratories
    • EFSA Guidance on Chemicals Used in Plant Protection Products (EU Regulation No 1107/2009)

    Typical usage ratio

    • 0.2–1.2 equivalents based on desired substitution pattern and final molecule complexity
    • Ratio fine-tuned during medicinal chemistry scale-up for process efficiency and cost containment

    Downstream process integration

    • Incorporated into synthetic sequence during heterocyclic ring assembly or throughout late-stage modifications
    • Applied in reactors compatible with halogenated intermediates and stringent containment
    • Followed by quenching and organic extraction; further purification by flash column chromatography

    Final product types

    • Selective pre-emergent herbicides
    • Chiral fungicide actives
    • Non-systemic insecticide precursors

    3. Specialty Polymer Additive Preparation

    Polymer material formulators turn to (S)-5-Bromomethyl-2-Pyrrolidone as a functional monomer for advanced polymer modification, offering improved thermal resistance and controlled crosslinking. It is employed to graft enantiomerically pure pendant groups onto polymer backbones, particularly polyamide and polyurethane systems where enhanced chiral recognition, solubility, and biocompatibility are required. The compound’s controlled introduction supports fine-tuning of polymer physical properties, with attention to removal of residual bromide species post-functionalization.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for new monomer registration and usage
    • ISO 9001 with materials traceability per polymer additive sector requirements
    • FDA CFR 21 177.1680 (for indirect food-contact polymers, where applicable)
    • EN ISO 11357 for Differential Scanning Calorimetry QC in modified polymers

    Typical usage ratio

    • 0.1–0.6% by weight of total monomer feed for specialty polymer applications
    • Loading level determined by target degree of functionalization and end-use specification

    Downstream process integration

    • Added during polymer melt or solution phase prior to initiation of chain propagation
    • Functionalized via nucleophilic substitution or radical copolymerization with base monomers
    • Processed in closed-system polymerization vessels, followed by devolatilization and pelletization

    Final product types

    • High-performance chiral recognition membranes
    • Medical-grade hydrogels
    • Functionalized copolyamides for electronics encapsulation

    4. Fine Chemical Synthesis for Research Reagents

    Producers of analytical and synthetic research reagents employ (S)-5-Bromomethyl-2-Pyrrolidone as an alkylating agent for introducing chiral pyrrolidone units into specialty molecules. Its defined stereochemistry is critical for the creation of calibration standards, chiral selectors, and lead compounds in preclinical screening campaigns. The compound’s reactivity profile allows for site-selective transformations under mild conditions, minimizing racemization and degradation of sensitive functional groups. Batch records maintain stringent documentation for research-grade supply.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • Good Laboratory Practice (GLP) for intermediate quality control and shipment
    • Hazardous chemical management per 29 CFR 1910.1200 (OSHA HCS, for US labs)
    • REACH Annex XVII restriction conformance for laboratory distribution in the EU

    Typical usage ratio

    • Applied from 0.05 to 0.5 equivalents per synthetic step depending on intended reagent quantity and reaction selectivity
    • Batchwise or semi-continuous dosage based on multi-parallel synthesizer scale

    Downstream process integration

    • Introduced post-core assembly during final derivatization of analytical standards
    • Processed in glove-box or dry-box conditions to prevent degradation
    • Purified using semi-preparative chromatography and lyophilization where necessary

    Final product types

    • Analytical chiral calibration reagents
    • Preclinical lead compound libraries
    • Chiral auxiliary building blocks for asymmetric catalysis kits
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    More Introduction

    Unlocking Value in the Lab: An Editorial Introduction to (S)-5-Bromomethyl-2-Pyrrolidone

    Looking Beyond the Label

    Step into a modern lab or a specialty R&D center, and there are a handful of tools and building blocks that drive innovation. Sometimes, a molecule with a modest name quietly ends up right in the middle of a big breakthrough. (S)-5-Bromomethyl-2-Pyrrolidone sometimes fits that bill. Chemists and researchers use this compound less for the headline-grabbing traits than for its reliability and function as a stepping stone. Sure, naming conventions make these molecules sound like something far removed from daily life, but the work behind the scenes reveals a much more hands-on role.

    Model and Quality Matter

    Researchers tend to notice pretty fast that not all versions of (S)-5-Bromomethyl-2-Pyrrolidone are built the same. For those who have ever run a reaction that failed because of inconsistent purity or a mystery contaminant, the significance of quality control becomes clear. The best supply comes from lots produced under strictly managed conditions, with high enantiomeric purity and controlled moisture levels. Scientific literature and patent filings point toward effectiveness increases when the right enantiomer is used, especially in chiral syntheses. That (S)-version in the name signals a specific spatial arrangement, often making all the difference for researchers pushing toward new pharmaceutical agents or specialty materials. A high level of purity, say, above 98 percent, means less time wasted troubleshooting reactions, fewer surprises in downstream steps, and better reproducibility. That isn’t a bullet point on a sheet—it becomes a lived experience across months of experimental work.

    Application: More Than a Niche

    Most colleagues who have tackled challenging synthesis pathways will recognize (S)-5-Bromomethyl-2-Pyrrolidone as a handy intermediate. In medicinal chemistry, it is a familiar building block for introducing chiral centers and fine-tuning molecular properties. There is a certain sense of satisfaction watching a reaction progress when that bromo group reacts as predicted, making connections without excessive side products. I’ve seen it play a critical role in setting up the basic skeletons for more advanced targets, sometimes pharmaceuticals, sometimes agrochemicals. This molecule often works as a vital pivot point for further modifications; the bromomethyl group almost behaves like a molecular handle, letting chemists attach what they need, where they need it.

    Standing Apart from the Crowd

    Ask a synthetic chemist about bromination of a pyrrolidone, and you’ll probably get a rundown of pitfalls. Some starting materials require harsh conditions just to introduce the bromo group. Earlier attempts, often using racemic mixtures or non-specific isomers, can generate a frustrating mix of products, tough to separate and even tougher to scale. The (S)-5-Bromomethyl-2-Pyrrolidone showcases why stereochemistry matters: the selectivity and predictability it brings have rescued projects that might have otherwise ended up on the shelf. In a world where regulatory requirements get stricter every year, having a defined enantiomer doesn’t just save time; it reduces the guesswork and potential for regulatory headaches. Compared with more generic intermediates, this compound lets a team move from idea to result with fewer detours and distractions.

    Direct Experiences: From Bottlenecks to Breakthroughs

    Anyone working in a research environment knows the frustration that follows a failed synthesis. In one project focused on CNS-active compounds, our group kept running into trouble with inconsistent yields. Switching to a higher standard of (S)-5-Bromomethyl-2-Pyrrolidone—one with traceable certification and a documented synthetic pathway—cut the noise down considerably. Our chromatograms actually lined up. Batch-to-batch headaches faded. The value in sourcing reliable chemical intermediates doesn’t lie in the bottle on a shelf, but in all the post-doc hours saved and papers published without having to defend away unexplained byproducts. Published studies echo these outcomes: greater control over enantiomeric excess leads to improved biological profiles, fewer off-target interactions, and better patentability for pharmaceutical leads.

    Importance in Drug Discovery

    Drug development—especially for targeted therapies—has evolved. Chiral purity can no longer be sidelined or approached as an afterthought. Many diseases rely on treatments designed at a molecular level, and that often means fine-tuning each element in a synthesis. The presence of a pure (S)-enantiomer makes a tangible difference in pharmacokinetics, impacting how the body absorbs, distributes, and clears a compound. Scientific reviews and regulatory reports have documented increased success rates for candidates synthesized from high-purity asymmetric intermediates. (S)-5-Bromomethyl-2-Pyrrolidone holds an established position here as a reliable entry point for elaborating into bioactive agents.

    Meeting Researcher Demands: Flexibility and Compatibility

    Every laboratory operates with slightly different protocols and objectives. Some need intermediates amenable to solid-phase synthesis, while others optimize for liquid-phase work. (S)-5-Bromomethyl-2-Pyrrolidone displays a notable solubility profile in polar aprotic solvents such as DMF and DMSO. This property removes bottlenecks in both manual and automated reactions. Colleagues who fine-tune their reactions find fewer obstacles when starting from a well-characterized intermediate like this. Its tolerability with commonly used protective group strategies matters, letting chemists try new routes without tearing up old playbooks.

    Minimizing Risk in Complex Syntheses

    Failures in multistep synthesis don’t just waste time; they eat into budgets and can derail whole projects. A reliable starting point like (S)-5-Bromomethyl-2-Pyrrolidone helps take out unnecessary risk. Teams can trace problems to their roots more readily, without worrying that minor, batch-to-batch variations in starting materials caused the trouble. In the hands of a skilled chemist, this molecule’s functionality leads to higher yields, fewer purification steps, and less reliance on heavy metal catalysts. These factors not only streamline the workflow but also align with responsible chemical stewardship, reducing environmental and safety impacts.

    Benefits for Scale-Up and Commercialization

    Transitioning from a proof-of-concept synthesis to pilot or commercial scale often reveals hidden issues overlooked during small-scale runs. Many intermediates behave unpredictably out of the flask and into a reactor. (S)-5-Bromomethyl-2-Pyrrolidone, when manufactured with stringent controls, stays reliable both in the hood and at scale. Documentation, chain-of-custody, and reproducibility become more than nice-to-have qualities, they enable technology transfer between groups and support compliance with international regulatory expectations. Groups transitioning into manufacture for regulated spaces often cite the key role played by trustworthy starting materials—and this compound features prominently in such discussions.

    How It Compares to Other Building Blocks

    Other related intermediates—whether alternative brominated pyrrolidones or less specialized bromoalkyl compounds—often lack the fine-tuned properties that come from precise stereochemistry. They may be less selective, leading to more time spent purifying diastereomeric mixtures and chasing elusive targets. By contrast, (S)-5-Bromomethyl-2-Pyrrolidone acts as a springboard for modern medicinal chemistry, offering cleaner conversions and a more straightforward road toward target molecules. This difference becomes clear in time- and cost-to-hit statistics routinely cited in published case studies. Even outside the pharmaceutical domain, industries involved in advanced materials or specialty chemicals see similar benefits—stronger starting points mean fewer headaches downstream.

    Quality, Traceability, and Reputation

    As much as technical details matter, those who have worked through procurement cycles and regulatory reviews learn to respect suppliers who back up claims with transparent data. Genuine analytical certificates showing NMR spectra, chiral HPLC traces, and residual solvent analysis speak louder than any datasheet boilerplate. In one instance, our team narrowed down a persistent source of variability to subtly different batches from unverified sources—something that resolved only after making the switch to tracked, certified lots. The value of this transparency shows up again and again in peer-reviewed publications and process validation efforts, shaping everything from grant funding outcomes to intellectual property strength.

    Challenges and the Road Ahead

    Procurement teams and researchers alike face the ongoing tension between cost and quality. Cheaper, lower-grade versions of (S)-5-Bromomethyl-2-Pyrrolidone sometimes circulate, tempting with baseline functionality but hiding upstream liabilities. Skipping the vetting process to save on initial costs nearly always leads to higher expenditures later, whether through failed runs, wasted time, or missed milestones. Addressing this challenge requires ongoing communication between suppliers and end users, setting shared expectations for purity levels, analytical verification, and packaging standards appropriate for sensitive chiral compounds. Many research groups have adopted more thorough onboarding checks, requiring side-by-side analytical comparisons before adopting new lots into their workflows.

    Practical Points: Storage and Handling

    In a bustling lab environment, the smallest oversights—like leaving a bottle uncapped or letting humidity sneak past a stopper—can ruin a batch. Solid entries like (S)-5-Bromomethyl-2-Pyrrolidone benefit from cool, dry storage conditions, as even trace moisture affects its stability and reactivity. For anyone new to advanced synthetic work, paying attention to these details can be the difference between a productive week and a lost opportunity. Practical experience beats theory here: handling it with gloves, sealing containers promptly, and keeping it away from incompatible reagents removes variables from experiments where control is already a premium.

    Ethics and Environmental Responsibility

    With tighter regulations and rising expectations around laboratory safety and sustainability, each new starting material comes under greater scrutiny. (S)-5-Bromomethyl-2-Pyrrolidone, when produced and handled according to best practices, presents a manageable risk profile. Responsible suppliers document their processes, reduce waste, and ensure proper disposal guidelines. Researchers play their role by following established protocols and supporting choices that reduce unnecessary releases or exposures. The net effect isn’t just personal safety—it contributes to a larger culture of stewardship where the right tools support both innovative outcomes and a safer laboratory landscape.

    Looking to the Future

    The pressures on scientific teams grow heavier each year—more data, faster turnaround, stricter regulatory scrutiny. From personal experience and field-wide trends, the consensus leans toward sourcing intermediates like (S)-5-Bromomethyl-2-Pyrrolidone from partners who prioritize traceability, purity, and open communication. That shift pays dividends not only in more robust experimental pipelines but in the increased trust grant agencies and clinical reviewers place in the outcomes. As chemistry continues to move towards sustainable and green practices, compounds like these—when properly managed—fit neatly within a new paradigm: maximize utility, minimize headache, and always keep an eye on the bigger picture.

    Making Smart Choices

    Having spent years in both academic and industrial chemistry roles, it becomes clear that reliance on trusted starting materials holds the key to consistent breakthroughs. Every new synthesis project brings lessons in the value of preparation, reliable sourcing, and the importance of details that easily slip through the cracks at the start. For working teams, adopting a deliberate approach to selecting and validating (S)-5-Bromomethyl-2-Pyrrolidone often marks the difference between a promising lead compound and a string of dead ends. A focus on quality pays off, not just in laboratory metrics but across entire project timelines and budgets.

    Final Thoughts on the Path Forward

    For researchers and teams shaping solutions in pharmaceuticals, advanced materials, or specialty chemicals, the building blocks always matter as much as the end result. Smart selection and diligent stewardship of intermediates like (S)-5-Bromomethyl-2-Pyrrolidone allow science to move from bench to impact with fewer roadblocks. From my own journey through the process of sourcing, validating, and using such compounds, the takeaway rings clear: better materials drive better science, and good choices here multiply across every result yet to come.