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N-Acetyl-D-Mannosamine

    • Product Name N-Acetyl-D-Mannosamine
    • Alias N-Acetylmannosamine
    • Einecs 609-691-4
    • 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

    923112

    Product Name N-Acetyl-D-Mannosamine
    Cas Number 6027-89-4
    Molecular Formula C8H15NO6
    Molecular Weight 237.21 g/mol
    Appearance White to off-white powder
    Melting Point 116-118°C
    Purity ≥98%
    Solubility Soluble in water
    Synonyms ManNAc, 2-Acetamido-2-deoxy-D-mannose
    Storage Temperature 2-8°C
    Chemical Structure Monosaccharide derivative
    Ph 1 Solution 5.0-7.0
    Ec Number 227-748-7
    Inchi Key AYZNVPLYFNKGEF-SVZMEOIVSA-N

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

    Packing & Storage
    Packing N-Acetyl-D-Mannosamine is supplied in a 5g amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping N-Acetyl-D-Mannosamine is shipped in tightly sealed containers, protected from moisture and light, under ambient or cool conditions. Packaging meets safety regulations for laboratory chemicals. Shipping is expedited to minimize degradation risk, and all containers are clearly labeled with hazard and handling information per international transport standards.
    Storage N-Acetyl-D-Mannosamine should be stored in a tightly closed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, preferably refrigerated at 2-8°C. Avoid prolonged exposure to air. Properly label containers and follow standard chemical storage procedures to ensure safety and maintain product stability.
    Application of N-Acetyl-D-Mannosamine

    Applications of N-Acetyl-D-Mannosamine in Industrial Manufacturing

    As an original manufacturer of N-Acetyl-D-Mannosamine, we supply this specialty monosaccharide to multiple industrial sectors where its molecular features directly underpin the quality and performance of advanced products. Below we detail several highly focused application scenarios, centering on regulated industries with well-documented technical requirements and established manufacturing practices.

    1. Biosynthetic Sialic Acid Production for Biopharmaceuticals

    Biosynthetic routes for sialic acid, particularly for GMP-grade N-Acetylneuraminic Acid (Neu5Ac), routinely incorporate N-Acetyl-D-Mannosamine as a key precursor. Large-scale biopharmaceutical manufacturers integrate it into enzymatic and fermentation-based synthesis to ensure batch-to-batch consistency for sialic acid derivatives used in complex biologics, such as glycoprotein therapeutics and monoclonal antibodies. This process requires strict adherence to pharmaceutical quality protocols throughout supply and production chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP–NF Monographs for Sialic Acid-Containing APIs
    • European Pharmacopoeia 10.0, Monograph 2603
    • 21 CFR Part 211 for Finished Pharmaceuticals

    Typical usage ratio

    • Usually 1.0–1.2 molar equivalents relative to projected sialic acid yield per batch; adjusted for conversion rate and process yields in enzymatic synthesis.

    Downstream process integration

    • Dosed directly at the fermentation or enzymatic synthesis stage in sialic acid bioproduction facilities, followed by process purification and isolation.

    Final product types

    • API-grade N-Acetylneuraminic Acid (Neu5Ac)
    • Sialylated monoclonal antibodies
    • Next-generation recombinant glycoprotein drugs
    • Diagnostic reagents for clinical assays

    2. Cell Glycoengineering for Advanced In Vitro Models

    Research centers and CDMOs specializing in cell line development employ N-Acetyl-D-Mannosamine to selectively modulate sialylation patterns in mammalian cell cultures. This enables production of human-like glycans on recombinant proteins in CHO and HEK293 cells. Strict environmental and safety controls apply to the manufacture and use of biochemical supplements in regulated laboratory settings.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in Laboratory Reagents
    • OECD Principles of Good Laboratory Practice (GLP)
    • ATCC Cell Culture Standards
    • NIH Guidelines for Research Involving Recombinant DNA

    Typical usage ratio

    • Supplemented at 10–50 mg/L culture medium, titrated based on desired glycosylation profiles and cell viability data.

    Downstream process integration

    • Added to serum-free or chemically defined media during fed-batch or continuous perfusion runs, with precise monitoring during high-density cell expansion.

    Final product types

    • Customized recombinant protein standards
    • Glycoengineered therapeutic proteins
    • Humanized research cell lines for preclinical R&D
    • Reference materials for analytical glycomics

    3. Functional Food and Nutraceutical Ingredient Manufacturing

    Manufacturers of functional foods and dietary supplements introduce N-Acetyl-D-Mannosamine into specialty nutraceutical blends aimed at cognitive, immune, and anti-aging support. Regulatory authorities require precise documentation of source materials and ingredient traceability. The ingredient’s inclusion must comply with national food safety legislation and undergo in-process QC to ensure consumer safety and label accuracy.

    Industry compliance standards

    • Food Chemicals Codex (FCC) purity requirements
    • China National Food Safety Standard GB 2760 for Food Additives
    • EU Novel Food Regulation (EU) 2015/2283
    • ISO 22000:2018 Food Safety Management System

    Typical usage ratio

    • Typically 50–250 mg per daily serving in finished products, adjusted according to local regulatory guidance and clinical substantiation.

    Downstream process integration

    • Blended during pre-mix and granulation stages in nutraceutical tableting or encapsulation; handled under controlled humidity to avert degradation.

    Final product types

    • Nutraceutical capsules and tablets
    • Functional powdered beverages
    • Enriched nutritional gummies
    • Medical foods for special dietary needs

    4. Oligosaccharide Synthesis for Glycobiology Research

    Synthesis of complex oligosaccharides for use in academic and pharmaceutical glycobiology relies heavily on high-purity N-Acetyl-D-Mannosamine as a building block. Leading fine chemical companies and research institutes require lot-specific analytical data and defined process controls to guarantee structural fidelity in downstream carbohydrate scaffolds. Integration into multi-step solution-phase or solid-phase synthesis is routine in specialized chemistry labs.

    Industry compliance standards

    • ACS Reagent Chemical Purity Guidelines
    • ISO 17034:2016 for Reference Material Producers
    • GLP standards for chemical synthesis
    • REACH Annex VII requirements for intermediate handling

    Typical usage ratio

    • Used in stoichiometric proportions (1:1 molar or as dictated by protection/deprotection sequence) relative to product design; quantities optimized for each synthase or glycosylation step.

    Downstream process integration

    • Entered as a protected or unprotected precursor in automated or manual oligosaccharide synthesis, followed by purification and structural validation.

    Final product types

    • Defined glycan structures for biological assays
    • Reference oligosaccharide standards
    • Glycodendrimers for drug discovery
    • Functionalized affinity media for glycoprotein purification

    5. Glycan-Based Vaccine Antigen Production

    Specialty vaccine manufacturers incorporate N-Acetyl-D-Mannosamine in glycoengineering strategies to develop and produce carbohydrate-based antigens. These antigens often form the basis of conjugate vaccines aiming at improved immunogenicity and targeted pathogen recognition. Strict GMP and biological safety levels must be met throughout the production chain, from raw material handling to final analytical release tests.

    Industry compliance standards

    • WHO Technical Report Series, Annex 6: GMP for Biological Products
    • Ph. Eur. General Chapter 5.2.9: Cell Substrates for Production of Vaccines
    • 21 CFR Part 600–680: Biological Products
    • EMA Guidance on Quality of Vaccines

    Typical usage ratio

    • Incorporated at 5–20 mM during antigen expression in engineered cell or microbial systems; fine-tuned based on glycoform yield and antigenicity endpoints.

    Downstream process integration

    • Co-supplied with culture feeds during antigen biosynthesis, proceeding to cell lysis, glycan isolation, and conjugation with carrier proteins.

    Final product types

    • Glycoconjugate vaccine antigens
    • Adjuvant glycan scaffolds
    • Preclinical vaccine candidates
    • Analytical controls for vaccine QC
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    Certification & Compliance
    More Introduction

    N-Acetyl-D-Mannosamine: Purity and Performance for Advanced Applications

    Introducing N-Acetyl-D-Mannosamine

    In the field of specialty carbohydrates and bioactive building blocks, N-Acetyl-D-Mannosamine stands out as a unique monomer with both research and industrial significance. Our facility has produced this compound for over two decades, refining synthesis methods and improving purity metrics thanks to direct collaboration with both academic researchers and biotech partners. Each batch runs through our proprietary acetylation and crystallization steps, reaching HPLC purities of at least 99%, with controlled moisture and residual solvent levels. Compared with simpler sugars or commonly available aminosugars, N-Acetyl-D-Mannosamine demands more precise handling, but offers performance advantages where cell engineering or glycan synthesis require accuracy and reliability.

    Molecular Quality Built From the Ground Up

    We produce N-Acetyl-D-Mannosamine under dedicated lines to prevent cross-contamination from other monosaccharides or amino group-containing chemicals. Our controlled process enables us to deliver materials with consistent particle size distribution and defined crystalline forms. Experience has taught us that minor changes in raw material quality or reaction times can create significant downstream challenges, so we maintain strict control over all input streams and adjust parameters based on real-time feedback from our analytical labs. Suppliers often approach us for insight on optimizing reaction conditions to match sensitive downstream applications, and we regularly run collaborative verification experiments on enzyme conversions or cell labeling workflows.

    Why N-Acetyl-D-Mannosamine Matters

    Researchers value this molecule’s role as a key precursor in the biosynthesis of sialic acids, major components on mammalian cell surfaces and critical to cell-cell recognition and pathogen interactions. Our customers in glycoscience invest both time and capital to ensure their sialylation pathways perform at peak efficiency. N-Acetyl-D-Mannosamine often provides the crucial link between upstream sugar chemistry and downstream biological assays. Without high-purity starting material, false positives or low yields confound data interpretation. In pharmaceutical and diagnostic applications, reliability reigns, so we rigorously monitor for heavy metals, byproducts of acetyl group migration, and sub-visible particulates. We’ve found that attention to these details directly improves reproducibility in cell labeling, metabolic engineering, and complex oligosaccharide assembly.

    Applications Driven by Trust and Experience

    Our production experience has revealed an expanding range of uses driven by the biotech revolution. Early on, many customers purchased N-Acetyl-D-Mannosamine solely for small-scale research—feeding it to mammalian cell cultures to track metabolic flux or as a supplement for glycoengineering. Now, demand reaches into industrial bioreactors, vaccine platforms, and glycan array programs. Contract research organizations and large-scale ingredient manufacturers trust our batches for their protocols, often requesting documentation spanning several years of reference samples. Our technical support addresses frequent questions on solubility, batch stability, or interaction with specific enzymes. Over time, we have accumulated datasets that shed light on optimal solution preparations and storage, which directly benefit downstream processes by reducing failures and repeat work.

    Consistent Performance for Cell Labeling and Glycan Synthesis

    N-Acetyl-D-Mannosamine’s value grows when Columbia research groups or European pharma partners require labeled cell experiments and complex glycoprofile engineering. We routinely collaborate with groups working on metabolic oligosaccharide engineering. They need confidence that the supplied product reflects the precise isomeric and acetylation state expected for real-time cell incorporation. We regularly share reports illustrating how isomeric impurities or oxidized byproducts can cause inconsistent incorporation or confound downstream labeling. Some labs use mass spectrometry at nanogram detection levels, so our evaluation reaches beyond routine QC—screening for unusual peaks and documenting stability during storage or shipment.

    Selecting the correct monosaccharide often determines whether an experiment yields confident, actionable results. GlcNAc and ManNAc, though similar in formula, create different cellular effects. Glycoengineering often stalls when minute impurities exist in the source material. Our team works closely with customers running high-sensitivity sialylation studies, supplying tailored analytical snapshots beyond baseline COAs to address these challenges. Years of handling feedback has demonstrated that providing transparent reference data on minor contaminants or degradation over transport periods makes a visible difference in the amount of troubleshooting and control experiment reruns demanded by our partners.

    Purity Matters in Every Step

    Routine chemical suppliers often overlook how low-level impurities—specifically oxidized fragments or acetyl group migration products—can affect biochemical assays. On our side, we run comparative testing against competitors’ offerings, finding batch drift and a broader impurity spectrum elsewhere. For example, simple aminosugar precursors or racemic mixtures can arise from older production routes not tuned to biopharma needs. These variants lead to inconsistent cell surface incorporation or trigger unexpected immunological backgrounds in animal model work. Our multi-stage purification loop addresses this, balancing thoroughness against physical losses to maximize yield while holding purity constant. For especially demanding production runs, we deliver extra documentation, including chromatogram overlays and FTIR spectra, supporting researchers who must explain variances during regulatory submissions or peer review.

    Specifications That Drive Process Choice

    The grades we manufacture focus on high purity, low endotoxin content, and close monitoring of hazardous residuals. Each batch receives a full HPLC fingerprint, along with water content measurement and endotoxin screenings. Leveraging hands-on feedback, we have tuned particle size to suit both laboratory-scale trials and multi-kilogram synthesis. Our powders dissolve rapidly in both aqueous and buffered solutions, supporting direct addition to cell cultures or chemical reactors. More importantly, consistent bulk density means metering and scaling up runs smoothly, which saves both time and resources for our clients.

    The drive for reproducibility doesn’t end at the point of sale. Shipments face temperature swings and humidity shifts, so we use moisture-resistant packaging and run stability tests reflecting real shipping timelines. We openly share these results for transparency, allowing process engineers to plan for any minor potency changes before their scale-up runs. Handling the same compound with the same batch-to-batch consistency may seem a simple goal, but we see few competitors reach our benchmarks once true multi-lot studies get underway.

    Real Differences from Other Products

    At first glance, N-Acetyl-D-Mannosamine shares several features with N-acetylglucosamine and other amino sugars. Many overlook that its unique stereochemistry channels it into specific biosynthetic pathways, unlike its close relatives. Recognizing this, our separation and purification systems target potential carry-over of nearly identical sugars—a point where less rigorous manufacturing allows contamination that can undermine glycoengineering or cell-based assays. Our experience confirms that differences as small as a single chiral center lead to cascading effects in complex systems. This lesson came hard in our early years, when downstream analysis flagged false positives due to minor glucosamine isomer contamination. Over time, process improvements focused both on raw material origin and analytical separation, and this background means today’s customers gain a real advantage in tough applications.

    We often field calls from bioengineers and analytical chemists, who cite historical problems with generic sources—color variation, off-odors, or unexpected chromatogram spikes. In each case, we walk through isolation procedures step by step, demonstrating how a dedicated process and rapid QC feedback deliver batches without those surprises. Laboratories verify our results by parallel analysis, and we consistently see confirmation of low-level impurity absence and stability over months-long storage. Our technical staff remains available to troubleshoot new methods or scaling up to pilot production, sharing both published and proprietary insights accumulated over years in the field.

    No Substitute for Dedicated Production

    N-Acetyl-D-Mannosamine earned its place as a key reagent in modern glycoscience by demanding respect for process design, tight controls, and responsive technical support. As a manufacturer with decades of hands-on synthesis experience, we have grown alongside the industries we serve—adapting to changing analytical requirements, more demanding purity benchmarks, and evolving GMP frameworks. Each new customer challenge drives us to revisit our core methods and sharpen both in-process control and after-sales support.

    While many distributors and resellers offer generic supplies, experience has taught us that only a genuine synthesis and purification operation can ensure continuity. Our in-house chemists conduct route scouting, run pilot batch trials, and push improvements quarterly. Every change, whether a new filtration medium or analytical method, gets documented and rolled into future production lots. Direct feedback from glycoengineering labs and diagnostic developers feeds our technical roadmap, which means our product specifications continuously evolve to match modern scientific standards and process robustness.

    Continuous Improvement Through Collaboration

    Direct partnerships with research teams and biotech innovators expose us to fresh challenges. This close work lets us resolve bottlenecks: optimizing the handling of moisture-sensitive intermediates or figuring out new impurity separation methods. Over multiple years, we’ve published process improvement case studies, explaining how small changes in crystallization, drying, or storage produce measurable outcomes in end-user data. We welcome technical audits and are open to process observation, as these exchanges often spark the next wave of product enhancements.

    Annual independent proficiency tests and participation in round-robin studies help validate our claims. Repeated cross-comparisons against global standards confirm that each production batch holds up to international scrutiny, with detailed data sets available for customer review. This transparency boosts confidence in regulatory filings and relieves technical teams from unnecessary duplication of control runs.

    Supporting Customer Solutions in Glycoscience, Biotech, and Beyond

    Advances in glycan therapeutics, vaccine delivery, and diagnostic technologies push manufacturers to keep pace with deeper understanding of cellular sugar pathways. Our role is to deliver both the material and the supporting knowledge to help our customers do more with it. From technical bulletins on safe handling to custom solution studies for large-scale fermentation, our team invests directly in your process performance. Our goal centers on enabling the next big step in biotechnological innovation, not just supplying a chemical.

    Looking Forward

    With increased demand from next-generation bioprocessing and cell-based assays, the push for even tighter quality controls and process flexibility only grows. We forecast continued rising needs for N-Acetyl-D-Mannosamine with unique labeling, isotopic enrichment, or ultra-low endotoxin profiles. Our R&D focuses on meeting these emerging applications: process intensification for gigafactory scale, fine-tuning for therapeutic-grade runs, and integration with streamlined downstream characterization methods.

    End-users seeking robust, fully documented N-Acetyl-D-Mannosamine receive not only a product, but a partner in process problem-solving. Calling on our full portfolio of production experience, analytical depth, and collaborative engineering, we stand ready to support every new advance the life sciences require.