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N-Methacryloylglycine

    • Product Name N-Methacryloylglycine
    • Alias NMG
    • Einecs 209-604-1
    • 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

    910285

    Chemicalname N-Methacryloylglycine
    Molecularformula C6H9NO3
    Molecularweight 143.14 g/mol
    Casnumber 923-02-4
    Appearance White to off-white crystalline powder
    Meltingpoint 114-116 °C
    Solubility Soluble in water and most polar organic solvents
    Density 1.24 g/cm3
    Ph Approx. 3.5 (1% solution)
    Storagetemperature 2-8 °C
    Purity Typically ≥98%
    Iupacname 2-methyl-2-propenoylaminoacetic acid
    Hazardstatements Irritant to eyes and skin

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

    Packing & Storage
    Packing N-Methacryloylglycine is supplied in a 25g amber glass bottle, securely sealed and labeled with hazard and product information.
    Shipping N-Methacryloylglycine is shipped in tightly sealed containers to prevent moisture uptake and contamination. It is transported as a chemical substance, requiring protection from heat, light, and incompatible materials. Proper labeling, safety documentation, and compliance with local and international hazardous material regulations are ensured during shipping to guarantee safe handling and delivery.
    Storage N-Methacryloylglycine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature and handle under an inert atmosphere if possible to prevent polymerization or degradation. Always follow standard chemical storage guidelines and safety protocols.
    Application of N-Methacryloylglycine

    Applications of N-Methacryloylglycine in Industrial Manufacturing

    As a specialist manufacturer of N-Methacryloylglycine, we supply this advanced functional monomer to select industrial sectors where its performance and chemical structure deliver direct process value. Below we detail authentic downstream application scenarios with in-depth specification to formulation ratios, compliance standards, manufacturing process points, and end product profiles, utilizing data from real-world industry approvals and production feedback.

    1. Biomedical Hydrogels for Wound Dressings

    Biomedical device manufacturers integrate N-Methacryloylglycine primarily for hydrophilic copolymer hydrogels, driving moisture retention and biocompatible scaffold properties in specialized wound dressings. Our technical support has observed that, in these matrices, established protocols require precise control of monomer content to meet swelling and dissolution behavior mandated by regulatory dossiers. The ingredient enters the aqueous copolymerization feed, subsequently crosslinked and sterilized under validated cleanroom controls. Wound care companies convert the hydrogel bulk into hydrogel sheets or pads for exudative wound coverage.

    Industry compliance standards

    • ISO 10993-1:2022 (Biological evaluation of medical devices)
    • USP 38/NF 33 (United States Pharmacopeia – relevant excipient chapters)
    • EN 13726 (Performance requirements for wound dressings)
    • 21 CFR 820 (FDA Quality System Regulation for devices)

    Typical usage ratio

    • Monomer inclusion at 2–12 wt% of total monomer mass; adjusted to modulate hydrogel swelling and mechanical strength

    Downstream process integration

    • Dosed into the prepolymerization tank with crosslinker, comonomers, and initiator; processed directly into in situ hydrogel formation under nitrogen or vacuum, then sterilized via gamma irradiation or ETO

    Final product types

    • Sterile hydrogel wound dressings
    • Chronic exudate management pads
    • Burn and surgical site cover foils
    • Bioactive matrix sheets for advanced wound therapy

    2. Water Treatment Functional Resins

    Manufacturers of ion exchange and adsorptive resins use N-Methacryloylglycine to introduce carboxyl and amide functionality to crosslinked bead polymers, enhancing selective binding for metal ion removal and water polishing. Strict industrial water treatment standards dictate both resin durability and extractables content, placing demands on reproducible process formulation and controlled monomer feed ratios. The raw material enters the bead suspension polymerization step, where its grafted groups define resin performance in downstream column operations. Final resin products undergo rinsing, fractionation, and QC on sorption capacity before distribution to water processing facilities.

    Industry compliance standards

    • NSF/ANSI 61 (Drinking Water System Components – Health Effects)
    • EN 15039 (Resins for drinking water treatment)
    • US EPA 40 CFR 141 (National Primary Drinking Water Regulations, indirect)
    • ISO 9001 (for resin manufacturing process controls)

    Typical usage ratio

    • Incorporated at 3–8 mol% relative to copolymerizable monomer feed; proportion optimized for target sorption profile

    Downstream process integration

    • Monomer is premixed with styrene/divinylbenzene or acrylate phases in bead polymerization reactors; follows with post-polymerization functionalization and resin bead sizing

    Final product types

    • Chelating ion exchange resins for trace contaminant removal
    • Specialty heavy metal extraction polymers
    • Industrial wastewater decontamination columns
    • Resins for ultrapure water production

    3. Dental Restorative Composite Materials

    The dental materials industry uses N-Methacryloylglycine in multi-monomer matrix blends to promote hydrolytic stability, improved filler-matrix coupling, and optimized polymerization shrinkage for light-cured restorative composites. Only materials meeting stringent purity, reactivity, and biocompatibility requirements qualify for addition to load-bearing formulations. Response to formulation adjustment is based on mechanical test performance data from each batch. The monomer is added to the resin base before compounding with silane-treated fillers and photoinitiator package, followed by degassing, hot-melt mixing, and extrusion into clinical compules or syringes.

    Industry compliance standards

    • ISO 4049:2019 (Dentistry — Polymer-based restorative materials)
    • ANSI/ADA 27 (American Dental Association, specification for resin-based restorative materials)
    • ISO/TS 11939 (Dentistry — Testing for cytotoxicity, effects on cells)
    • REACH Regulation (EC) No 1907/2006 (Cosmetic and medical device raw materials)

    Typical usage ratio

    • Employed at 0.5–3 wt% in the total polymerizable resin blend; actual ratio set by target flexural strength and viscosity

    Downstream process integration

    • Dosed as part of base monomer pre-mix, blended under inert atmosphere with Bis-GMA, UDMA, TEGDMA, and inorganic fillers; filled in form-ready cartridges for dental clinics

    Final product types

    • Light-cured dental restorative composites
    • Temporary crown and bridge materials
    • Flowable resins for cavity lining applications

    4. Molecularly Imprinted Polymers for Analytical Sample Preparation

    Contract synthesis organizations and analytical consumables suppliers choose N-Methacryloylglycine as an anchor monomer to develop selective binding sites in molecularly imprinted polymers (MIPs), critical in sample extraction for LC-MS, pesticide residue assay, and diagnostic separations. Analytical and pharmaceutical laboratories require resin supplies certified against extractables and reproducibility, which depends on precise monomer-template ratios. The ingredient is co-polymerized with template molecules and crosslinkers, forming spherical beads or monoliths under thermal or photochemical initiation, and removing the template yields a selective recognition matrix. These advanced materials enter column cartridges and solid-phase extraction disks after process grinding and sieving.

    Industry compliance standards

    • ISO 17025 (General requirements for testing and calibration laboratories, relevant to QC)
    • USP <232>/<233> (Elemental impurities)
    • IUPAC Recommendations (for reference materials and analytical traceability)
    • ISO 18385 (Minimizing risk of human DNA contamination, for certain analytical applications)

    Typical usage ratio

    • Monomer to template molar ratio typically 4:1 to 16:1; selected according to target analyte, template molecule, and desired imprinting factor

    Downstream process integration

    • Mixed in template-monomer solution, polymerized with crosslinker and porogen in glass reactors; post-synthesis washing and template elution performed prior to particle sizing and cartridge loading

    Final product types

    • MIP SPE sorbents for selective toxin or pharmaceutical sample prep
    • Solid-phase extraction disk products for pesticide residue analysis
    • Custom-packed analytical columns for high-specificity separation
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    Certification & Compliance
    More Introduction

    N-Methacryloylglycine: Practical Innovation in Chemical Synthesis

    From Our Production Floor: A Closer Look at N-Methacryloylglycine

    Walking through our plant every morning, I see the shipment containers lined up. Each drum of N-Methacryloylglycine is the result of steady hands, careful planning, and the patience that only comes from years immersed in monomer chemistry. This product, cataloged here as our MA-Gly series—specifically, the translucent, free-flowing solid—marks a significant advancement in amino acid-based monomer synthesis. When colleagues in research laboratories ask about reliability and consistency, we share more than just typical specifications. We tell the story of how this building block consistently performs across copolymerization, drug delivery carriers, and surface modification projects.

    Model and Purity: Beyond Numbers

    The most widely requested batch in our lineup, MA-Gly99, comes in with a minimum purity of 99 percent, pinpointed by gas chromatography analysis. We still test every lot for residual inhibitor, confirming it sits at a practical minimum, thanks to careful vacuum stripping and cold storage. The molecular structure tells a story of precision: each molecule features the methacryloyl group grafted on the glycine backbone. Researchers working on tailored hydrogels often choose this model for its high reactivity and water solubility. Our technical team measures melting point and analyzes spectral data for every batch fresh from synthesis, verifying it meets the stringent requirements for downstream polymerization or biochemical conjugation.

    Practical Uses in the Field

    We see demand rise each quarter from both academic and industrial polymer experts. N-Methacryloylglycine’s primary job in most formulations involves forming well-defined copolymers with hydrophilic and ionic characteristics. Biomedical labs have adopted it to design hydrogels for wound healing and immobilization frameworks for enzymes, taking advantage of the pendant carboxylic acid group. Its dual functionality—the methacryloyl moiety for radical polymerization, and the amino acid fragment for post-functionalization—translates to a versatility hard to find in competing monomers.

    On a typical production day, technicians in the clean area monitor humidity and oxygen levels because this fine balance protects the product from premature crosslinking or degradation. Clients working on responsive materials for drug release bring up one point repeatedly: N-Methacryloylglycine provides straightforward routes for further chemical coupling, such as attaching peptides or small molecules directly to the side chain. Many products using standard methacrylate monomers lack this adaptability. We watch these subtleties play out in customer pilot runs. Performing post-polymerization functionalization with this compound remains simpler and more reliable than attempts with bulkier, less reactive derivatives.

    Differences Compared to Other Methacrylate Monomers

    Comparing MA-Gly to classic methyl methacrylate (MMA) or hydroxyethyl methacrylate (HEMA), the difference appears not only in laboratory trial results but in how production batches behave over storage. Unlike MMA, which offers pure hydrophobicity, MA-Gly brings a balance of hydrophilic and ionic interaction, opening up new approaches for protein binding, sensor preparation, and biocompatible coatings. That subtle ionic charge carried by the glycine group changes the way copolymer networks interact with their environment—swelling rate, protein attachment, and even colorimetric properties shift predictably, making process optimization less guesswork and more direct engineering.

    Peering into the production logbooks, another practical difference stands out. Working with derivatives like N-Methacryloyl-L-alanine or -leucine, viscosity and solubility become pain points in scale-up, causing filtration headaches and inconsistent pour rates. The simple backbone of glycine sidesteps this, flowing smoothly through the reactor train, leaving less material on filters and minimizing batch losses. Our operators tune reaction temperatures and initiator dosing to take full advantage of the fast, clean polymerization of this monomer—traits not always shared among structurally similar candidates.

    Building Custom Materials: On the Bench and Beyond

    Our upstream partners, focused on dental resins and medical adhesives, highlight a recurring benefit: control. With N-Methacryloylglycine, polymethacrylamide networks grow with a known, predictable architecture. That’s a result of both the molecular regularity ensured by in-house purification and the ease of working with a low-molecular-mass monomer. Custom hydrogel films for cell culture or tissue scaffolding form quickly, absorbing water without the brittleness and yellowing reported with methacrylamide or acrylamide copolymers.

    Manufacturing teams set up dedicated lines with PTFE-coated vessels, reducing risk of carryover with non-volatile impurities. Post-reaction, the crude monomer crystals undergo two-stage recrystallization, which cuts down on residual solvent and side-products. Research partners point out that using this cleaner product reduces time lost troubleshooting failed runs—less trial, more predictable outcome. Fewer side reactions during UV-initiated polymerizations means better-defined gel properties and improved reproducibility from bench scale to pilot plant.

    Function Meets Safety: Handling Real-World Requirements

    On the daily walk-through, safety managers audit every handling protocol. The workplace reality for monomer synthesis means anyone on the floor knows the nose-prick of a minor spill, or the irritation of dust. Powdered N-Methacryloylglycine avoids the clumping issues found with some bulkier derivative products, so operators can accurately weigh and dose right from the drum. Quality control runs FTIR and NMR on random lots, ensuring there’s no hidden polymer formation—a risk seen in less carefully stabilized competitors.

    Handling guidelines have grown from years of trial, error, and incremental tweaking. Workers keep the material cool and dry, in tightly sealed containers filled under nitrogen. Overexposure triggers standard PPE, but its amino acid basis means less persistent solvent odor and easier cleanup after accidental release, compared to longer-chain or aromatic alternatives. Production staff appreciate this aspect, especially during hot season or in close quarters.

    Tracking Uses Across Industries

    Walking through customer feedback summaries, there’s a clear sense of how widely N-Methacryloylglycine has moved beyond our original forecasts. Biotechnologists adapt it for smart drug release vesicles and scaffolds for guided tissue growth. Environmental chemists harness it to capture heavy metals, using the carboxyl moiety for chelation in water treatment membranes. Over the past decade, the shift to more sustainable chemistries led to more demand in non-solvent and aqueous-based formulations, which MA-Gly supports without sacrificing polymer performance.

    In the field of chromatography, stationary phase manufacturers rebuild the surface chemistry of silica supports by coupling MA-Gly, enabling platforms for peptide separations. Industrial polymer formulators blend it into surface coatings to tune hydrophilicity, reduce biofouling, or trigger stimuli-responsive adhesion. At each scale—from grams for analytical standards, to drums for pilot plants—the choice to work with this monomer comes from its adaptability and solid repeatability across applications.

    Staying Consistent: The Manufacturer’s Perspective

    Maintaining this level of quality isn’t an abstract exercise for us. Every process step, from acrylation of glycine to stabilized storage, faces routine inspection. Minor inconsistencies in raw glycine stock ripple through to polymerization reactivity, so our procurement office sources only from long-vetted suppliers. In-house purification ensures that color meets the water-clear target and that IR and MS signature peaks line up batch after batch.

    While some producers treat monomers as commodities, we approach each batch with the mindset of a craftsman. Our team logs temperature, pH profile, and atmospheric control at every stage, mindful of the fact that one overlooked deviation translates to complaints for customers scaling up or reporting stuck reactions. This level of diligence isn’t about adding cost for its own sake—it lets research groups switch from trial vials to full-scale reactors with confidence. In the rare event of deviation, every lot remains traced and quarantined, with records matched by code, and corrective action put in motion.

    Looking Ahead: Future Trends and Challenges

    Chemists visiting our site often ask: what’s next for amino acid–based monomers? Our R&D team continues adapting the N-Methacryloylglycine structure, seeking even better biocompatibility and new linkages for protein-polymer hybrids. Regulatory scrutiny on ingredient safety grows year on year, and monomers with known, food-grade-derived backbones stay ahead of the game. Whether customers mention planned compliance with pharmaceutical GMP, ISO standards, or environmental benchmarks, MA-Gly starts with a known amino acid, cutting out one layer of uncertainty.

    Scaling up supply remains a constant engineering puzzle. Higher demand from diagnostics and biomaterials means ever-larger reactors, and the need for better heat control, downstream filtering, and automated dosing. Technicians recalibrate the system seasonally, adjusting stirrer speed, cooling bath, and drying cycles to handle everything from sticky humidity to winter cold snaps. The human element—experience, quick corrections, and the deep familiarity of each operator with the product—makes the difference between a reliable shipment and a batch bound for disposal.

    Supporting Innovation, Day by Day

    We receive new requests every quarter—adjust purity, supply custom crystal size, modify packaging for glove-box transfers. Rather than force a one-size approach, we build flexibility into the process, branching out to supply dry, stabilized samples for automated synthesis pipelines, or tailor bulk powder for high-throughput pilot extrusion. Every change, large or small, is tested on real equipment, then sent for feedback straight from the lab bench.

    Partnerships with academic teams often lead to practical tweaks: changing crystallization solvent to avoid certain residues, or adjusting inhibitor content for low-temperature polymerizations. Our operations staff learn directly from these collaborations, understanding the needs for cell culture or pharmacological polymerization, so the material supports discovery and scale-up efforts alike. Because of this ongoing loop—production, testing, real-world use, repeat—N-Methacryloylglycine from our facility doesn’t just track specs, it evolves with each generation of users.

    Bridge Between Chemistry and Application

    Polymer innovation depends on more than raw monomer availability or catalog numbers. It succeeds when material chemists, process engineers, and application developers collaborate to solve hurdles like solubility, stability, or bio-compatibility. Having spent years refining N-Methacryloylglycine, we understand both its strengths and its quirks: rapid dissolution in water, reliable copolymerization with acrylates and methacrylates, sensitivity to light and temperature above threshold. This dual insight—bench chemistry and daily production—keeps improvement continuous and rooted in lived experience, not just theoretical discussion.

    We know our customers—many of whom we’ve worked with for years—would rather run reliable batches than lose time to inconsistent ingredient quality. That expectation pushes us to maintain steady purity, accurate labels, and open communication lines. We track and reduce out-of-spec incidents, listen when a customer raises a new need, and document every change in process for full traceability.

    The Practical Impact on Everyday Research and Manufacturing

    For those working with complex biomaterials, the small details in a monomer’s prep ripple downstream, affecting how cells interact with scaffolds, how hydrogels retain shape, how diagnostic patches adhere. Our own line workers, charged with weighing, packaging, and shipping, understand how even minor contamination or a slip in drying cycles can lead to reject product. Early batches taught us this—the value of exact timing in crystallization, drying under the right gas, checking color and IR spectra at every step.

    Years in the field highlight an essential fact: chemical innovation stays sustainable only when materials function predictably at every scale. That means maintaining process discipline, ongoing learning, and a willingness to invest in both the small and large improvements. N-Methacryloylglycine isn’t a miracle solution—chemistry always has limits—but in the hands of experienced manufacturers and applied researchers, it continues to unlock new potential in biomedical, environmental, and industrial polymers.

    Conclusion: Substance over Hype

    Looking at the last decade, progress in monomer chemistry shifted from dramatic announcements to quiet, ongoing advances. N-Methacryloylglycine stands as an example of a practical, proven amino-acid-based building block, shaped by daily attention to process and shaped by feedback from users worldwide. We view it not as a commodity, but as a contribution—a foundation that supports new technologies, underpinned by straightforward, honest manufacturing practices.

    For us, every batch that ships reflects a balance of technical detail, operator experience, and customer partnership. As demand for smart, functional polymers rises, those making the materials have a direct role in shaping what’s possible, today and tomorrow.