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N-Ethylmaleimide

    • Product Name N-Ethylmaleimide
    • Alias NEM
    • Einecs 202-713-4
    • 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

    404959

    Chemical Name N-Ethylmaleimide
    Cas Number 128-53-0
    Molecular Formula C6H7NO2
    Molecular Weight 125.13 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 42-44°C
    Boiling Point 110°C at 20 mmHg
    Solubility Soluble in water, ethanol, and acetone
    Storage Conditions Store at 2-8°C, protect from light
    Purity Typically ≥98%
    Hazard Statements Harmful if swallowed; causes skin and eye irritation
    Synonyms NEM; 1-Ethyl-1H-Pyrrole-2,5-dione
    Density 1.14 g/cm³
    Refractive Index 1.527
    Applications Thiol-blocking reagent in biochemistry

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

    Packing & Storage
    Packing N-Ethylmaleimide is packaged in a 5-gram amber glass bottle, sealed with a screw cap and warning labels for safe handling.
    Shipping N-Ethylmaleimide should be shipped in tightly sealed containers, under cool, dry conditions, and away from sources of heat or ignition. The chemical must be clearly labeled, packaged in accordance with relevant regulations (such as DOT or IATA), and transported as a hazardous material due to its toxic and irritant properties.
    Storage N-Ethylmaleimide should be stored in a tightly closed container, away from light, moisture, and incompatible substances such as strong oxidizers and bases. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical fume hood. Store at temperatures between 2–8°C (refrigerated), and avoid prolonged exposure to air as it is sensitive to hydrolysis.
    Application of N-Ethylmaleimide

    Applications of N-Ethylmaleimide in Industrial Manufacturing

    N-Ethylmaleimide is a key fine chemical intermediate with well-established roles in industrial manufacturing, particularly valued for its reactivity with thiol and amino groups in formulations. As a chemical manufacturer, we supply this material to downstream users in the biotechnology, pharmaceutical, polymer, and analytical reagent industries, ensuring rigorous compliance with international quality and safety regulations. Below we highlight specific application scenarios where its unique characteristics unlock performance in end-use products.

    1. Protein Modification in Biopharmaceutical Synthesis

    This compound plays a decisive role in the modification of protein and enzyme structures for downstream therapeutic and diagnostic uses. Biopharmaceutical enterprises employ its thiol-reactivity during protein engineering and PEGylation steps to improve drug properties and analytical reliability. Its precision in blocking cysteine residues supports controlled conjugation processes and formulation stability in active pharmaceutical ingredients.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211: US FDA cGMP requirements
    • EU EudraLex Volume 4: GMP for Medicinal Products
    • USP <1045>: Biotechnology-derived Articles

    Typical usage ratio

    • 0.5–5 molar equivalents relative to free thiol groups present in protein formulations; precise ratio depends on desired degree of modification and specific biological target.

    Downstream process integration

    • Added post-expression during protein purification and followed by dialyzation to remove excess reagent; employed before downstream conjugation (e.g., with PEG or fluorescent probes).

    Final product types

    • Monoclonal antibody-drug conjugates (ADCs)
    • PEGylated therapeutic proteins
    • Protein-based diagnostic reagents
    • Stabilized enzyme preparations for research and clinical diagnostics

    2. Crosslinking Agent in Specialty Polymer Manufacturing

    Industrial polymerization lines use N-Ethylmaleimide as a thiol-active crosslinker for advanced materials requiring tuned elasticity, strength, or chemical resistance. Its selectivity and compatibility make it suited for synthesizing high-performance resins or elastomers, especially where stability under harsh chemical environments is necessary. Custom polymer blends leverage its functional groups to engineer desired properties at varying crosslink densities.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006: Registration, Evaluation, Authorisation and Restriction of Chemicals (Europe)
    • RoHS Directive 2011/65/EU (for end-use in electronics encapsulation)

    Typical usage ratio

    • 0.1–3 wt% relative to base polymer in compound, depending on required crosslink density and compatibility with base matrix.

    Downstream process integration

    • Introduced during pre-polymer or masterbatch blending before heat-curing or UV-initiated crosslinking; dosage controlled based on viscosity and gelation profile development in batch reactors or continuous lines.

    Final product types

    • Chemical-resistant elastomer seals and gaskets
    • Specialty adhesives for electronics
    • Resin-encapsulated electrical components
    • High-durability protective coatings

    3. Sulfhydryl Group Inhibition in Analytical Reagent Formulations

    Analytical chemistry kit assemblers rely on N-Ethylmaleimide to block free sulfhydryl (–SH) groups, preventing unwanted side reactions during redox marker quantification and enzyme assays. The reagent’s selectivity for cysteine side chains ensures reproducibility in colorimetric and fluorometric detection, supporting stringent quality requirements for reference materials and QC kits delivered to laboratories worldwide.

    Industry compliance standards

    • ISO 13485:2016 for in vitro diagnostic (IVD) medical device manufacturing
    • CLSI document C24-A3 for quality assurance in analytical reagents
    • ISO/IEC 17025:2017 for chemical testing laboratories (applies to QC processes)

    Typical usage ratio

    • 0.2–2 mmol per liter of analytical working solution, adjusted based on sample matrix thiol concentration and detection system sensitivity.

    Downstream process integration

    • Added directly to buffer solutions or test kit concentrates before aliquoting and packaging; precise dosing monitored to avoid excess that could interfere with downstream signal detection.

    Final product types

    • Quantitative glutathione assay kits
    • Sulfhydryl group labeling reagents
    • Blood or plasma protein denaturation kits for research use
    • Stabilized enzyme substrates

    4. Blocking Reagent for Site-specific Peptide Synthesis

    Synthetic peptide manufacturers integrate N-Ethylmaleimide in the selective protection and modification of thiol groups within solid-phase peptide synthesis (SPPS) protocols. Its application enables precise blocking of cysteine residues, thereby regulating disulfide bridge formation or facilitating introduction of targeted modifications without random side reactions, allowing contract peptide synthesis plants to meet custom sequence requirements for biotech and pharmaceutical customers.

    Industry compliance standards

    • USP <1090>: Peptide Mapping
    • Japanese Pharmacopoeia (JP) for peptide APIs
    • Ph. Eur. general monographs for synthetic peptides
    • ICH Q11: Development and Manufacture of Drug Substances

    Typical usage ratio

    • 1–3 equivalents per cysteine residue, modified slightly depending on peptide chain length and resin loading capacity.

    Downstream process integration

    • Added during resin-coupling cycles following deprotection and prior to oxidative folding or cleavage; the blocked peptide subsequently purified via HPLC.

    Final product types

    • Synthetic therapeutic peptides
    • Peptide hormone analogs
    • Peptide-based diagnostic calibrators
    • Custom affinity-tagged peptides for proteomics

    5. Functionalization of Biosensor Surfaces

    Producers of biosensor devices employ N-Ethylmaleimide in the functionalization of gold and polymer surfaces destined for immobilizing biomolecule probes. Its reactive groups allow controlled covalent attachment of antibodies, enzymes, or oligonucleotides via cysteine linkages, leading to higher stability and reproducibility in sensor response characteristics for point-of-care, industrial, and laboratory platforms.

    Industry compliance standards

    • ISO 13485:2016 for medical device assembly
    • 21 CFR Part 820: FDA Quality System Regulation for device manufacturing
    • SQI Quality Standard for biosensor coatings (industry-specific)

    Typical usage ratio

    • 0.01–0.1 mg/cm2 of sensor surface, optimized according to surface area and intended probe density.

    Downstream process integration

    • Applied as a linker or pre-treatment activating agent following base substrate cleaning, followed by probe molecule attachment using controlled humidity and temperature protocols.

    Final product types

    • Electrochemical glucose sensors
    • Immunoassay biosensor chips
    • DNA microarray slides
    • Enzyme-linked optical sensors
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    Certification & Compliance
    More Introduction

    N-Ethylmaleimide: Chemical Precision for Advanced Synthesis

    A Closer Look at N-Ethylmaleimide Production

    At our facility, every batch of N-Ethylmaleimide goes through rigorous controls, from raw material handling to the purification stage. Careful temperature monitoring and reactant addition remain central throughout synthesis, especially during maleic anhydride transformation and subsequent ethylation. Our technical staff calibrates reaction timings and pH to keep by-product levels low. Because small contaminants can stall research, we’ve invested in analytical equipment to routinely check purity with HPLC and NMR. Each lot includes a record of analytical reports, reflecting a process built for chemists who cannot afford unreliable outputs.

    Years of direct feedback from academic labs and industrial R&D teams shaped our product specifications. Scientists rely on N-Ethylmaleimide for sensitive applications—bio-conjugation reactions, cysteine residue assays, and thiol group protection—so we ensure our crystalline material dissolves cleanly, showing minimal moisture and almost no colored impurities. We standardize crystalline size through controlled cooling and filtration, as too much fine powder or large crystals introduce inconsistencies in dissolution rates or weighing accuracy. Strict process discipline lets us guarantee N-Ethylmaleimide purity above 99.5%, never masking minor impurities through simple recrystallization. The final powder leaves our packaging room after checks for trace acids and phthalic by-products, two key risks introduced when shortcuts creep into maleimide synthesis.

    Specifications That Address Real-World Research Needs

    Our N-Ethylmaleimide bears the model KE-NEM202. Each sealed bottle contains pure white crystals, free from sticky residues, supporting efficient pipetting and storage. Technical users often ask for assurance on both content and trace-level impurities. Using in-house gas and liquid chromatography, our QA team quantifies organic and inorganic contaminants down to 0.1%, with every production run cross-referenced against prior years for trend monitoring. Loss during weighing and transfer drops significantly once the product hits that sweet spot in powder form—not too hygroscopic, not too dense.

    As a direct manufacturer, our access to intermediate streamlines the supply chain, cutting lead times for specialty quantities or custom packaging. Many customers request N-Ethylmaleimide in small vials to minimize air exposure, or ask for pre-portioned containers to speed up repetitive use. For researchers needing larger runs, we arrange direct shipment in vacuum-sealed formats to cut down on contact with atmospheric moisture, which can swiftly degrade maleimide derivatives. Each batch undergoes moisture content assessment by Karl Fischer titration, aiming for values below 0.05%. The difference appears during storage: high stability even after two months in ambient conditions.

    Key Applications: Advanced Biochemistry and Organic Synthesis

    N-Ethylmaleimide targets a niche once occupied by less selective alkylating agents, delivering superior reactivity when scientists want to block thiol groups in proteins or small molecules. Its mode of action is simple but effective—reacting efficiently with sulfhydryl moieties without attacking other amino acid side chains or destabilizing peptide bonds. This selectivity reduces background noise in protein workups and keeps target modifications predictable. Beyond protein chemistry, organic syntheses employ this product to mask reactive cysteines during multistep builds, improving yield consistency and downstream deprotection steps.

    The demand from biochemistry labs reflects increasing interest in cell signaling, protein trafficking, and redox biology. N-Ethylmaleimide helps dissect the role of cysteine in regulating protein structure. Researchers tell us they appreciate the clear, fast end-point of reactions, which enables precise identification of reaction completion without having to overuse harsh additives. This attribute proves essential in proteomic studies where incomplete modification skews mass spectrometry data.

    Outside of biochemistry, the product appears in organic synthesis for site-selective modification of complex molecules. Its high reactivity, relative stability, and manageable safety profile offer a route where alternatives like iodoacetamide introduce too much volatility or unwanted side reactions. Custom process development houses using N-Ethylmaleimide for pilot-scale transformations often come back with requests that highlight the need for fine-grained control over particle size and batch consistency to support reproducible scale-ups.

    Direct Insights from Manufacturing Practice

    Running maleimide lines for years, we see the subtle differences between N-Ethylmaleimide and its close relatives. Succinimide- and phthalimide-based modifiers share some chemical logic but fall short in terms of reactivity and selectivity. Maleic derivatives like N-Ethylmaleimide keep side reactions to a minimum, especially under aqueous buffer conditions. Overlooked points like the ease of stock solution preparation come up repeatedly: N-Ethylmaleimide dissolves smoothly in polar aprotic solvents and buffers, producing clear, stable solutions without excessive cloudiness—a major advantage when running sensitive kinetic measurements.

    Our technical team gets hands-on with every major batch, collecting representative samples and pushing them through simulated customer protocols. We chase after performance issues early, preferring to address them before full-scale rollout. Over multiple years, we’ve reduced residual acid content, a major source of protein denaturation and assay disruption. Internal trials confirmed that tweaking the ethylation timing cut unwanted side products. Delays of just five minutes in cooling shift reaction paths, something that shows up immediately in protein modification efficacy. This manufacturing experience gives direct insight into what makes for a reliable tool in molecular biology.

    Comparisons with Alternatives: More Than Just a Reagent

    Many labs, especially those focused on protein chemistry, once relied on N-Methylmaleimide or maleic anhydride derivatives. Initial results looked similar, but over time, subtle drawbacks appeared. N-Methylmaleimide, for instance, introduces slightly more hydrophilicity, leading to greater protein aggregation in certain assays. Other alkylating agents, such as iodoacetate, pose handling hazards and stricter regulatory controls, making logistics and lab safety harder to manage. Our N-Ethylmaleimide walks the line between chemical activity and operational safety—the ethyl group offers sufficient bulkiness to reduce off-target interactions, but not so much as to impede desired conjugation.

    Customers report that switching from less refined sources of N-Ethylmaleimide often impacts experimental reproducibility. Some off-brand products include too much undefined residue, causing cloudy preparations and inconsistent thiol blockades. This feedback pushed us to keep analytical rigor at the heart of our process and build out documentation that supports publication-ready research. When queries arise about stability, shelf life, and batch-to-batch reliability, our technical support references real data from retained samples, not marketing brochures.

    There’s a practical side, too—sourcing directly from the synthesis line supports custom requests. Certain medicinal chemistry workflows run best with slightly damp powder, while others prefer extra-dry, large crystals. Our process flexibility comes from owning the synthesis all the way from precursor to product, letting us adjust for these needs without long lead times or handoffs that add cost and risk.

    Addressing Common Issues with Hands-On Solutions

    Moisture-sensitivity remains the biggest challenge with N-Ethylmaleimide. Exposure to ambient air during weighing or transfer can jeopardize product stability and create downstream issues in buffer preparation. We always recommend minimizing air contact, but also package the powder in airtight, low-permeability materials. Our experience shows that glass vials, paired with induction-sealed caps, outperform plastic for long-term storage. Technicians who handle bulk packaging check for seal integrity every shift. Keeping storage and transit at low humidity avoids early product degradation.

    Product clumping occasionally comes up, particularly in tropical regions. To address this, we adapted our finishing steps to ensure the product leaves our site with a moisture content lower than most competitors. We monitor warehouse and loading area environments, and logistics works closely with shipping partners to avoid long transits under high humidity. During peak summer months, shipments include desiccant packs as a straightforward, proven safeguard.

    Another point: chemical hygiene. Our N-Ethylmaleimide synthesis never involves mercury, heavy metals, or problematic solvents, making downstream waste disposal easier for researchers. This makes our product more attractive for green chemistry labs and facilities with strict wastewater controls.

    Expertise Rooted in Daily Practice

    Rather than following textbook templates, our process comes from years of benchwork and direct feedback. Chemists testing each run notice even minor deviations in color, texture, or dissolvability, and quality assurance responds to these findings within days. Most adjustments to synthesis or packaging arise from solving real bottlenecks in customer workflows—not just chasing incremental purity digits but actually improving how the chemical performs in its intended environment.

    Good manufacturing practice means more than compliance for us: it’s a direct line to the performance biochemists and organic chemists expect. One missed temperature checkpoint or careless batch split turns up weeks later in customer complaints, so we double-source all raw materials and keep redundant process monitoring instruments online during every step of production. Our tech teams cross-train on reaction setup, purification, and packaging, so knowledge gaps rarely persist and suggestions carry straight from the line to product management.

    Supporting Scientific Progress with Reliable Chemicals

    Researchers tackling protein modification or small molecule conjugation projects operate within tight resource and time limits. Delays or inconsistencies from unreliable chemicals trigger costly reruns and hurt morale. Our N-Ethylmaleimide gives them one stable element amid complex protocols. Those who deal with precious biological samples or high-stakes synthetic campaigns can allocate their attention to experimental design and analysis, not quality control on reagents.

    We take seriously the feedback from scientists who get hands-on with every aspect of their projects. Their comments shape everything from batch size options to label clarity, even which languages appear on safety documentation. We invest in staff technical training to build teams who notice and care about small improvements, using data from customer returns, technical calls, and even negative feedback to keep pushing our standards higher.

    The broader field of biochemical modification grows more complex by the year, as techniques like CRISPR, proteomics, and post-translational modification profiling move mainstream. N-Ethylmaleimide, once a niche product, now takes a central role in enabling high-confidence characterization of protein structure and function. By keeping our manufacturing close to the demands of leading labs, we build practical value into each bottle—supporting real advances, not just meeting specifications.

    Final Thoughts: The Manufacturer’s Commitment

    Producing N-Ethylmaleimide at scale means more than running reactors and ticking checklists. Every lab order, every custom request, pushes us to maintain high standards across people, process, and materials. Across hundreds of batches, what sets reliable manufacturers apart is a culture that values accuracy and speed—delivering what working chemists need, in the format they request, with the transparency they expect. N-Ethylmaleimide serves as both a foundation for molecular discoveries and a test of a chemical manufacturer’s discipline and experience. By keeping product development grounded in hands-on chemistry, shaped by real user needs, and supported by robust analytical data, we don’t just sell a reagent. We deliver trust and enable scientific progress.