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N-Hydroxymaleimide

    • Product Name N-Hydroxymaleimide
    • Alias NHMI
    • Einecs 226-333-7
    • 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
    VTB
    Specifications

    HS Code

    437653

    Chemicalname N-Hydroxymaleimide
    Casnumber 668-86-0
    Molecularformula C4H3NO3
    Molecularweight 113.07 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 129-132°C
    Solubility Soluble in water, ethanol, and acetone
    Boilingpoint Decomposes before boiling
    Density 1.561 g/cm³
    Purity Typically ≥98%
    Flashpoint Non-flammable
    Storagetemperature Store at 2-8°C
    Synonyms NHM, Hydroxymaleimide

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

    Packing & Storage
    Packing N-Hydroxymaleimide is packaged in a sealed 25 g amber glass bottle, labeled with hazard information and chemical identification.
    Shipping N-Hydroxymaleimide should be shipped in a tightly sealed container, away from moisture and incompatible substances. It must be handled as a hazardous chemical, following standard safety protocols. Use appropriate labeling, and ensure shipment complies with local regulations for hazardous materials. Store in a cool, dry place during transit.
    Storage N-Hydroxymaleimide should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from light. Store at room temperature or as specified by the manufacturer, and ensure appropriate labeling and containment to prevent accidental exposure or release.
    Application of N-Hydroxymaleimide

    Applications of N-Hydroxymaleimide in Industrial Manufacturing

    N-Hydroxymaleimide serves as a precision functional intermediate in multiple advanced manufacturing sectors, supporting efficient reaction control, targeted modification, and process consistency in specialized industrial workflows. As a direct manufacturer with audited supply chains, we detail several downstream applications with relevant compliance features, realistic formulation guidance, process roles, and end-use profiles.

    1. Pharmaceutical Active Ingredient Synthesis

    N-Hydroxymaleimide plays a targeted role in the preparation of active pharmaceutical ingredients via selective oxidation and functional group introduction. Research-driven pharmaceutical plants apply the material as a phase-transfer catalyst or oxygen donor when building heterocyclic scaffolds, optimizing process yields and reducing by-product contamination through controlled addition. Chemists select it for specific steps, such as N-oxidation or cyclization, where mild reaction conditions and predictable conversion rates are critical for regulatory clearance and batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 cGMP requirements
    • EU-GMP Guidelines EudraLex Volume 4
    • US and EU Pharmacopeial Monographs (USP/EP) for relevant APIs

    Typical usage ratio

    • 0.05–0.3 equivalents relative to target functional group; optimized by stoichiometry for reaction completeness and impurity profile

    Downstream process integration

    • Added to the core reaction vessel during the oxidation or cyclization stage, before or after temperature adjustments
    • Monitored in-process by HPLC to ensure conversion and acceptable by-product threshold

    Final product types

    • Synthetic antihypertensive drug intermediates
    • API building blocks for antiviral agents
    • Chiral heterocyclic scaffolds for R&D libraries
    • Targeted metabolic pathway inhibitors

    2. Polymer Crosslinking and Curing Enhancement

    Here, industrial polymerization lines utilize N-Hydroxymaleimide for controlled crosslinking in high-performance thermoset resins such as polyimides and epoxies. It reacts preferentially with amines and other nucleophilic groups to form stable linkages, which harden the polymer matrix and improve heat and chemical resistance. Engineers incorporate the additive at the resin precursor stage to modulate curing kinetics and obtain dimensional stability in specialty electronics, aerospace, and automotive composites.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • UL94 Flammability Classification for polymeric materials
    • ISO 9001:2015 certified manufacturing for traceability

    Typical usage ratio

    • 0.5–2.0 wt% relative to total resin solids; adjusted for targeted crosslink density and mechanical specifications

    Downstream process integration

    • Homogeneously blended with resin and curing agent in the premixing tank under nitrogen
    • In-situ monitoring for gel time and exotherm using rheometry or DSC

    Final product types

    • High temperature circuit board laminates
    • Aerospace structural composite matrices
    • Automotive under-the-hood molded components
    • Specialty adhesives for electronics assembly

    3. Specialty Chemical Reagent Manufacturing

    Producers of custom reagents employ N-Hydroxymaleimide as a building block for synthesizing maleimide derivatives, which act as versatile intermediates in chemical R&D and process scale-up. Its selective reactivity enables stepwise modification, facilitating high-purity production through minimal side reactions. Quality departments confirm batch consistency and adherence to declared purity specifications as required by downstream reagent suppliers and specialty catalog houses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for traceable synthesis
    • Hazardous Substances Regulations for reagent storage and transportation
    • GHS Classification and labelling for chemical catalogs
    • Analytical Certificate of Analysis (COA) as per customer contract

    Typical usage ratio

    • 1.0 equivalent in stoichiometric reactions; excess up to 5 mol% for full conversion in scale-up

    Downstream process integration

    • Reacted in batch or semi-batch reactors during synthesis and post-modification of fine chemical intermediates
    • QC testing for NMR, HPLC, and elemental analysis post-purification

    Final product types

    • Activated maleimide tagging agents for bioconjugation
    • Functionalized crosslinkers for specialty research
    • Analytical standards for assay validation
    • Molecular biology labeling reagents

    4. Surface Modification for Biomedical Devices

    Advanced coating lines use N-Hydroxymaleimide as a reactive linker in surface modification, especially on polymer and metal substrates requiring biofunctional groups. Its activation of exposed surfaces allows the grafting of targeting motifs such as peptides or polyethylene glycol, enhancing biocompatibility and reducing fouling for medical devices. Process control focuses on uniform coating thickness and grafting density, as verified by analytical surface testing, to meet device release criteria.

    Industry compliance standards

    • ISO 10993 Biocompatibility standards for medical devices
    • ISO 13485:2016 for medical device quality management
    • FDA 21 CFR 820 Quality System Regulation (QSR)
    • ISO 11135 for sterilization process compatibility

    Typical usage ratio

    • 0.1–1.0 wt% in surface coating solutions; customized by substrate material and intended functionalization

    Downstream process integration

    • Introduced during thin-film formation or dip-coating prior to functional molecule coupling
    • Surface activation step monitored by contact angle measurement or FTIR

    Final product types

    • Drug-eluting stent coatings
    • Blood-contacting catheter and tubing surfaces
    • Diagnostic microarray slides
    • Implantable device surface modifications

    5. Advanced Agrochemical Formulation

    Agrochemical producers adopt N-Hydroxymaleimide as an auxiliary reactant for the synthesis of select maleimide-based herbicide, pesticide, and plant growth regulator intermediates. Its efficient ring activation allows chemists to introduce or modify functional groups under cost-sensitive, high-concentration processes. Application rates and reaction times are tailored to minimize environmental residues and align with tight impurity control governed by agrochemical approval standards.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • ISO 9001 certified batch manufacturing with traceability
    • REACH Regulation (EC) No 1907/2006 for agrochemical ingredients
    • National pesticide registration laws (e.g., EPA FIFRA, EU Regulation (EC) No 1107/2009)

    Typical usage ratio

    • 0.1–0.5 equivalents per key functional group; varies by downstream synthetic step and required activity profile

    Downstream process integration

    • Added during intermediate-stage functionalization or ring-opening reactions in concentrated batch reactors
    • Monitored in-process by HPLC and LC-MS for target compound formation and impurity profile

    Final product types

    • Precursor intermediates for selective herbicides
    • Building blocks for systemic insecticides
    • Fine chemicals for plant growth regulator synthesis
    • Pesticide active compound intermediates
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    Certification & Compliance
    More Introduction

    Introducing Our N-Hydroxymaleimide: A Practical Perspective

    The Product from a Chemist’s Bench

    N-Hydroxymaleimide doesn’t get much attention outside synthetic labs, but behind each lot of white crystalline powder, there’s a lot of decision-making and fine-tuning. Let’s strip away the jargon: at our plant, we manufacture N-Hydroxymaleimide to meet the real expectations of research chemists, process engineers, and scale-up specialists who turn ideas into value.

    Model and Specifications Grounded in Experience

    Over years of managing kilos of N-Hydroxymaleimide out of reactors, our model focuses on minimizing impurities that matter for downstream reactions. The benchmark, for us, isn’t a theoretical purity: it’s the repeatability and cleanliness of end-use reactions. Each batch follows strict controls for moisture, trace maleic anhydride, and phthalic byproducts, monitored continuously in our QC lab. We have learned that solvent residues — particularly chlorinated organics — linger and bite if not kept in check, so our process design eliminates those risks and the headaches that follow.

    Our material runs at a consistent 99%+ purity by HPLC, with water content capped below 0.3% as measured by Karl Fischer titration. In customer feedback, color matters more than anyone admits—offwhites, yellows, or gray tinges trigger questions, so we set an internal standard to keep visual appearance as crisp as possible, without chasing the unicorn of “absolute white.” Every kilogram is packed to guard against moisture ingress, and we can fill drums, fiberboard kegs, and double-lined bags depending on what fits the job.

    How We Use It Ourselves – and Why It Matters to Others

    N-Hydroxymaleimide’s value shows up in its reactivity. Years ago, we noticed new requests popping up from researchers working on protein modification and functional polymer development. They all needed something that takes a maleimide double bond and makes it available for further coupling, without dragging along unpredictable byproducts. The N-hydroxy group does this by activating the ring for precise substitution reactions.

    If you’re attaching labels or other cargos to thiol-containing molecules, this compound beats most alternatives on cleanliness. Our own lab teams leaned on N-Hydroxymaleimide during earlier antibody-drug conjugate feasibility studies because it forms stable linkages, with none of the persistent side reactions that dog some older ester approaches. We’ve seen contract manufacturers choose it for surface functionalization, site-selective modification, and click-chemistry routes, because these jobs can’t afford wildcards or trace contaminants.

    Not everyone in purchasing or operations sees the difference right away, so here’s how it has played out on the floor: batches built with clean N-Hydroxymaleimide reach full conversion with fewer filtration steps and less time in the dryer. Waste reduction matters, both for regulatory reporting and warehouse efficiency. Down the line, that clearer throughput drives down batch errors—anyone who’s spent an overtime weekend in production appreciates that.

    Standing Apart from Other Options

    People often ask how N-Hydroxymaleimide compares with its relatives—the succinimide and phthalimide analogs, for instance. Over time, we’ve seen that these molecules don’t behave the same during scale-up, even if lab protocols make them sound interchangeable. N-Hydroxysuccinimide, for example, forms good leaving groups for peptide chemistry, but its higher solubility comes at the price of tricky crystallization. In aqueous processes, it leaches and complicates downstream separation. Phthalimide derivatives, while handy in some syntheses, lag in reactivity and often drag along heavier colored impurities in final steps.

    In our own synthesis runs, we mapped out the reactivity profile for each cousin. N-Hydroxymaleimide provides the tightest band for coupling yields, with less interference in polar or nonpolar solvents. It also avoids some of the oxidation and hydrolysis risks we saw early in scale-up with N-hydroxyphthalimide, particularly with aggressive reagents under pressure. In applications where preserving delicate functional groups is crucial—bioconjugates, surface modification, crosslinker prep—N-Hydroxymaleimide wins out on both selectivity and byproduct simplicity.

    Behind the Manufacturing Curtain

    Our process for building N-Hydroxymaleimide isn’t proprietary magic; it comes from years of stubborn problem solving. Early batches wrestled with runaway exotherms and sticky intermediates that refused to crystallize. We adapted our purification protocols step by step, switching between solvent systems and dialing up to kilo scale only when we could chart a clean path from start to finish.

    We invested in closed-system reactors to eliminate atmospheric oxygen, which can degrade product during key stages. Temperature control—down to the circulation bath—made all the difference in avoiding byproduct formation. In the drying phase, we shifted away from vacuum ovens that stripped subtle qualities out of the product and moved to nitrogen-purged tray dryers, giving us more control and fewer surprises.

    Our technical staff have the freedom to stop a batch and troubleshoot, rather than force it through and cross their fingers on cost recovery. Each anomaly gets logged, tested, and—if it’s a genuine improvement—adopted across the plant. Operators and chemists run weekly audits with a clear mandate: if anything seems off, even if it meets the numbers, don’t release it. This approach has paid back in customer satisfaction and lack of returned product.

    QC Beyond Specifications: What We Learned From Our Clients

    Official certificates of analysis only scratch the surface of quality. Some of our early adopters flagged an odd spike on mass spec that didn’t show up on HPLC; this led us to add LC-MS profiling as a routine step. A few researchers in bioconjugates noticed micro-particles that slipped through standard filters, guiding us to revise our sieve mesh and in-line trap inspection. Chemists working on pilot batches caught occasional trace metal contamination traced to an older batch of glassware—prompting us to swap everything out for borosilicate lines and revalidate.

    Each of these stories forced us to move past “meets spec” thinking and focus on use-case-driven quality. For example, supplying to oligonucleotide couplings demanded ultra-low iron levels; our standard process now tests for ppm metals far below typical industrial thresholds. Customers scaling up surface modification projects preferred larger, easier-to-handle granules, so we tuned our crystallization process for a slightly coarser grade when requested. These lessons came straight from real-world feedback, not from any sales seminar or standard playbook.

    Practical Uses Seen in Industry

    A lot of N-Hydroxymaleimide goes into custom chemistry at the cutting edge. We’ve shipped to startups building targeted delivery agents, established firms working on sensor arrays, and academic groups probing site-directed bioconjugation. On the industrial scale, most volumes head for specialty crosslinkers or tie-in units for adhesives and coatings. Each end-use brings its quirks.

    Polymers using N-Hydroxymaleimide benefit from its ability to graft with precision—driving up efficiency and cutting down off-ratio component waste. In surface modification, activation steps that use our product tend to see smoother layer formation and less fouling on the reactor wall. Some electrochemical applications use it as a stable, redox-active intermediate in electrode fabrication, boosting uniformity and longevity in high-value cells.

    Our recordkeeping tracks not just what leaves our loading dock, but how it performs. We’ve logged cases where customers cut coupling times by half or reduced post-reaction cleanup from hours to minutes, especially where side-product formation can derail a project. It’s the applications nobody anticipated—ones where a small batch turns into a key step in a larger process—that usually bring the most insight. Production managers tell us downtime drops when purity stays high and granule flow matches their feeders; every minor improvement at the source gains leverage at scale.

    Safety—Lessons Learned and Process Improvements

    Manufacturers live with the risks of their own chemicals, so we don’t write safety paragraphs from a distance. Even seasoned operators respect the hazards of powder handling and dust control; we put in full enclosure for charging stations and use local exhaust ventilation at every unloading bay. Reactive hot-spot monitoring became standard after one too many “small” incidents turned into headaches.

    Systems flag high temperatures or runaway acid formation in the vessels, with operators cross-checking before each run. We follow a policy where any “unknown peak” in raw material checks automatically triggers retesting. Even though N-Hydroxymaleimide itself doesn’t carry notorious acute toxicity, we train for worst-case scenarios, from spills to accidental ignition. Weekly drills and ongoing retraining keep everyone honest.

    Environmental Responsibility—From Theory to Practice

    Disposal of spent solvents and purge streams remains a big item on our compliance list. Each upgrade in our process design aims to shrink the waste pool, whether by moving from chlorinated to greener solvents or reclaiming N-Hydroxymaleimide residues for reprocessing. Years back, we tracked our effluent to a nearby stream and added a third layer of filtration—no regulatory push required—after spotting traces that didn’t belong. Field checks on water, soil, and air keep us accountable, motivated by actual impact, not just ticking off legal boxes.

    Recent shifts in greenhouse gas reporting prompted us to switch a chunk of our heated-vessel utilities to solar and closed-loop reboilers. Every bit we cut in energy or raw material use reinvests in keeping our product available and our community relationships strong. If we save on utilities, the end-user feels it in both delivery reliability and price consistency.

    Supporting Innovation, Not Just Supply

    The research specialists who call about N-Hydroxymaleimide aren’t looking for volume alone; they want clarity on what the product will really do downstream. We spend time troubleshooting application hiccups with their teams, sharing failures as well as wins. If their process throws a curveball—thermal sensitivity, unexpected crosslinking, off-scale impurity formation—we dig through our own pilot logs and suggest alternatives, sometimes tweaking a parameter that never made it into the published protocols.

    Joint pilot runs with selected partners let us chart new solvent compatibility ranges or develop custom particle sizes, aimed at actual user challenges rather than theoretical advantages. One scale-up project needed a phase-separated intermediate to avoid column chromatography; our process engineers mapped a solvent switch sequence, pulling N-Hydroxymaleimide into the right phase and recovering better than 90% yield, knocking days off the schedule. None of this would come from a catalog listing.

    Real Challenges We Still Face

    No product run happens in a vacuum. Sourcing pressure on maleic anhydride, freight disruptions, and shifts in utility pricing all cut into predictability. We stay nimble by qualifying more than one raw material vendor and running side-by-side validations before making any supply change. Occasionally, a new impurity shows up unannounced and requires rapid troubleshooting—a process that draws everyone from production, QA, and tech support into the room until root cause is nailed down.

    Batch-to-batch reproducibility remains both an art and a science. On-the-fly adjustments—slowing an addition, switching the order of reagent charging—can spell the difference between a bland “spec-compliant” lot and a batch that users remember for all the right reasons. Sometimes, a simple tweak like adjusting seeding temperature improves the entire downstream handling profile. We don’t wait for problems to hit the market before acting.

    Staying Open to Customer-Driven Change

    The more feedback we get, the better our product gets. Major process tweaks often originate with persistent customer requests; switching to higher-capacity airlocks, automating bag handling, or redesigning labels for hazard visibility all came from those on the front lines, not our office desks. Plant staff visit major clients’ sites, swapping tips and learning best practices on handling, storage, and dosing.

    It’s not unusual for a customer to ask for a tailored solution—maybe a specific average particle size, tamper-resistant packaging, or pre-dried batches for critical water-sensitive work. These requests challenge our tech teams and ultimately strengthen our base process. Many project managers at client firms emphasize not just “what’s in the drum” but how it arrives and integrates with their systems. Small changes—extra humidity indicators, double-bagged units, drop-tested drums—start as experiments and often become new standards.

    Closing Thoughts from a Manufacturer’s View

    The story of N-Hydroxymaleimide in our plant is built from problem solving, practical know-how, and learning from mistakes. This isn’t just a reagent: it’s a piece of countless innovations, and its quality comes from the everyday care of the people making it. Anyone can supply a chemical; few dig into the details until they see how much difference the right batch in the right form makes on the bench and in the plant. That’s where long-term trust is earned.

    As a manufacturer, we see ourselves as partners to those driving new research, tackling large-scale production, or hunting for cleaner, safer, more effective processes. N-Hydroxymaleimide may not be the headline act, but in fields from bioconjugate design to high-performance materials, its well-made presence creates fewer headaches, better yields, and unexpected opportunities for those with the skill to use it well.