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HS Code |
913597 |
| Product Name | N-Acetylneuraminic Acid Methyl Ester |
| Cas Number | 107204-35-7 |
| Molecular Formula | C12H19NO9 |
| Molecular Weight | 321.28 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 175-180°C |
| Solubility | Soluble in water and methanol |
| Purity | Typically ≥98% |
| Storage Condition | Store at -20°C, protected from light and moisture |
| Iupac Name | 2-(Acetamido)-2-deoxy-3,5,6,7,8,9-hexahydroxy-4-[(methoxycarbonyl)oxy]nonanoic acid |
| Synonyms | Neu5Ac methyl ester, Methyl N-acetylneuraminate |
| Density | 1.6 g/cm³ (approximate) |
| Ph Aqueous Solution | Around 5-6 |
As an accredited N-Acetylneuraminic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-Acetylneuraminic Acid Methyl Ester, 1g, is supplied in a tightly sealed amber glass vial with clear labeling and safety information. |
| Shipping | N-Acetylneuraminic Acid Methyl Ester is shipped in tightly sealed containers under cool, dry conditions to protect it from moisture and degradation. Due to its sensitivity, it is typically transported with refrigerant packs or on dry ice for long-distance deliveries. Proper labeling and handling in accordance with chemical safety regulations are strictly adhered to. |
| Storage | N-Acetylneuraminic Acid Methyl Ester should be stored tightly sealed in a cool, dry, and well-ventilated area, away from moisture, light, and incompatible substances. Ideally, it should be kept at 2-8°C (refrigerated conditions). Protect from strong oxidizing agents and ensure containers are properly labeled to prevent contamination or degradation. Follow standard laboratory safety and storage protocols. |
Applications of N-Acetylneuraminic Acid Methyl Ester in Industrial ManufacturingN-Acetylneuraminic Acid Methyl Ester serves specialized roles across multiple high-value sectors. As a direct manufacturer of pharmaceutical and biopharmaceutical raw materials, we supply this compound to downstream users in disciplines that demand precise quality, strict regulatory compliance, and controlled process integration. The following application scenarios outline the main industrial routes, industry standards, usage parameters, production steps, and the resulting end products. 1. Active Pharmaceutical Ingredient Synthesis for NeuromedicineMajor pharmaceutical processors use N-Acetylneuraminic Acid Methyl Ester as a critical building block in the semi-synthetic fabrication of advanced neuromedicine molecules, particularly for small-molecule CNS (central nervous system) actives and investigational sialic acid analog drugs. Leading innovators reference monographs from the major pharmacopoeias, and demand high purity and validated traceability at each batch level. For ISO and GMP-manufactured neuromolecule APIs, tight specification of impurity content and chiral integrity during ester introduction remains essential. Downstream API production lines use in-situ methyl esterification and chemical conversion, usually following validated process analytical control (PAT) steps, to integrate this intermediate before final purification and formulation. Finished drugs reach the final market after tablet, capsule, or injectable product formation. Industry compliance standards
Typical usage ratio
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2. Glycobiology Reagents and Biotech Research ToolsBiotechnology firms utilize N-Acetylneuraminic Acid Methyl Ester as a reference standard and as a key precursor for labeling, derivatization, and conjugation reactions targeting glycan analysis. During bioprocess research and analytical kit development, accurate methyl ester introduction ensures defined reactivity and stability, meeting requirements for LC-MS, HPLC, capillary electrophoresis, and ELISA workflows. The manufacturing process in this sector employs the compound at the pre-derivatization step, where tight moisture and impurity control is mandated by internal QC systems and ISO 13485 or ISO 9001 traceability demands. The final reagent kits and standards must match industry traceability and stability specifications for worldwide distribution. Industry compliance standards
Typical usage ratio
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3. Intermediate for Antiviral Oligosaccharide SynthesisProducers of synthetic oligosaccharide-based antivirals require N-Acetylneuraminic Acid Methyl Ester as an activated sialic acid source for controlled glycosylation. The raw material enters glycosylation process lines where protection/deprotection strategies and stereospecific linkage formation are essential for producing pharmacologically active sugar chains. Compliance with regulatory expectations for multi-step chemical syntheses intended for clinical candidates or pre-market assessment is strictly monitored by downstream client QA teams. The integration of methyl ester intermediates under inert and moisture-controlled conditions maintains product yield and purity. Final oligosaccharide drug candidates undergo downstream formulation and stringent QC for pharmaceutical applications. Industry compliance standards
Typical usage ratio
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4. Nutritional and Infant Formula Additive PrecursorFood industry manufacturers and specialized infant nutrition producers use N-Acetylneuraminic Acid Methyl Ester as a controlled precursor in enzymatic or chemical synthesis of functional sialic acids for nutritional fortification. Standard infant formula processes require precise substrate ratios and robust monitoring of purification to meet global food safety standards, particularly for use in regulated markets. Ingredient suppliers work under HACCP-compliant food plant regimes and use the material in the pre-hydrolysis or conversion stage, often followed by downstream ion-exchange and crystallization processing prior to final blending with other permitted nutritional additives. Industry compliance standards
Typical usage ratio
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Chemical manufacturing feels like a long conversation with nature, just with more glassware and patience. In our facility, we work with rare sugars, amino acids, chiral intermediates, and a host of custom organics that drive discovery in academic and industrial labs worldwide. Among these, N-Acetylneuraminic Acid Methyl Ester has become a staple for researchers looking to push the boundaries in glycobiology and pharmaceutical synthesis.
This methyl ester is a derivative of N-acetylneuraminic acid, better known in many circles as sialic acid. Over years, we've watched it evolve from a barely known glycan into a molecule that gets requested by name for work in protein glycosylation, diagnostic kit development, and antiviral research.
We produce N-Acetylneuraminic Acid Methyl Ester following repeated rounds of practical feedback from chemists and formulators. Researchers told us about the bottlenecks caused by impure esters or variable solubility. After several process upgrades, we manufacture this product with a typical purity above 98% by HPLC, confirmed batch by batch. We make it available as a white to off-white powder, with the molecular formula C12H19NO9 and a molecular weight of 321.27. Every lot comes with a clear, traceable COA so no one has to guess at what’s in the jar.
Producing N-Acetylneuraminic Acid Methyl Ester in-house means every kilo starts at our own preparation of N-acetylneuraminic acid. We never have to guess about residual contaminants introduced upstream, since the crystallization and esterification all occur under our roof, monitored by our staff chemists. That single-site approach adds cost during setup, but it’s paid back many times over in product consistency.
Many have tried sourcing this ester from generic suppliers and found odd batches that dissolve poorly in methanol or chloroform, or show impurities that interfere during downstream reactions. Our experience shows that these headaches usually grow out of cut corners on purification or careless recrystallization. We’ve eliminated those steps from our own work. Every production run ends with comprehensive NMR, mass spec, and HPLC verification. If the spectroscopy doesn’t match, it doesn’t ship.
In biochemistry and cell biology labs, sialic acid derivatives form essential tools for studying how sugars decorate proteins and how viruses bind their hosts. The methyl ester form has proven especially useful in synthesizing sialylated oligosaccharides because its methyl group offers a convenient handle for further reactions, or for selective deprotection. Over the last decade, more researchers have been requesting the methyl ester as a starting scaffold for analog synthesis, including fluorescent tags for imaging studies and probes for cell-surface recognition.
What makes the methyl ester shine is its compatibility with mild deprotection conditions. Classic approaches for peptide or oligosaccharide assembly often require orthogonal protection: a group that shields the carboxyl end during synthesis but leaves the rest of the molecule available for modification. While the free acid or its sodium salt can hydrolyze or degrade under these synthetic conditions, the methyl ester resists breakdown, staying intact until the final deprotection step.
Our customers in academia often work on projects involving the chemical or enzymatic sialylation of glycoproteins. Purity here isn’t optional — a single percent of unknown impurities can change the way a sialyltransferase enzyme handles the donor molecule. With our product, labs have reported greater reproducibility and sharper LC peaks during analytical workup. We have heard about dozens of successful reactions forming sialylated linkages, as well as efficient labeling of cell-surface glycans.
Anyone searching for N-Acetylneuraminic Acid Methyl Ester might find a confusing list of vendors, each rolling up product under near-identical names. As the producer, we face decisions about equipment cleaning, raw material traceability, and employee training that no intermediary ever gets to see. Meeting tight impurity specs means committing to in-house analytical testing — HPLC, NMR, and even optical rotation checks — for every lot.
What we see on the other side of the market? Plenty of samples shipped with ambiguous documentation and faint residue from leachable plasticizers. Some brands blend small lots or relabel imports. Our batches never get mixed. With each run, we date and code jars so researchers can trace exactly which reactor, crew, and purification column prepared the batch. It sounds obsessive, but these habits cut out a lot of troubleshooting at the bench.
Pharmaceutical partners sometimes mention the difference in appearance between ours and re-bottled imports: a free-flowing crystalline powder, without fine dust clumps or the kind of static charge you get from double handling. This makes accurate weighing easier and results in cleaner transfers when moving product to solution. Researchers working with microgram quantities find this eliminates a source of dose error.
Running our own plant for rare sugar chemistry means we worry about things that rarely cross a distributor’s mind. We start with N-acetylneuraminic acid isolated using a fermentation method that ends with a high-purity product. The subsequent esterification step in methanol is optimized for minimal byproduct formation, using a carefully monitored temperature profile. To flush out any traces of moisture or unreacted acid, we use a sequence of drying cycles in vacuum rotors, followed by crystallization from cold ethanol.
Each of these steps comes from years spent optimizing what textbook chemistry misses. During one project, trace iron in the glassware threw off the color of the ester, and it took weeks to isolate the source. We still catch those details — every batch gets checked for trace metals because one customer lost a week to a purple byproduct caused by an upstream vendor. Over time, these lessons get written into our process steps and double-checked by real people, not just QC signatures.
Across hundreds of shipments, we've tracked that labs using our N-Acetylneuraminic Acid Methyl Ester report fewer issues with reaction byproducts and observe more predictable coupling yields when compared head-to-head with rebranded stock. Published literature from our customers shows successful applications in chemoenzymatic synthesis, viral receptor research, and the construction of trisaccharide sialosides for vaccine candidates.
This isn’t just about patting ourselves on the back. We’ve handled urgent calls for technical support on Friday afternoons, walked through troubleshooting steps when an enzyme reaction failed, and even tested retained samples from earlier lots to see if storage handled by others introduced moisture or contamination. That’s why our documentation for storage recommends a desiccator below -20°C, not a bench-top cabinet. Those details make real differences in yield and experimental repeatability.
Our customers put N-Acetylneuraminic Acid Methyl Ester to work as a core building block in synthesizing complex carbohydrates, especially where precise stereoselectivity matters. The methyl ester group prevents unwanted reactions at the carboxyl, unlocking selective glycosylation strategies. We’ve supplied it for enzymatic sialylation studies, ganglioside synthesis, cell labeling projects, and as an intermediate for incorporating sialic acid into bioactive peptides and glycopeptides. Some labs leverage its solubility in polar organics to prepare custom tracer molecules for imaging or diagnostic kits.
Each time a team at a research institute struggles with scale-up or gets inconsistent results with a commercial sample, we invite a sample of our lot for trial testing. Several customers have published protocols based on our material, proving that fine-tuning purity and process detail actually delivers better reproducibility. Our QC covers more than just nominal purity — we screen for residual methanol, check for consistent melting points (between 85-89°C), and cross-check every run for hydrolysis products.
Demand for specialty glycochemicals like this ester has soared alongside the growth of biopharma research. In one conversation, a customer recounted how a major catalog vendor shipped two different lots labeled identically but showed different TLC behavior and color under UV. Our approach fixes this problem at the root — nothing leaves our site without full LC and NMR matching both the reference compound and company archive spectra.
We’ve also heard frustration around ambiguous documentation from batch relabelers. When you buy from the actual manufacturer, you can trace back every step from the fermentation tank through purification, solvent drying, and packing. Each container leaves with the signed analytical data and storage recommendations, plus a named chemist who prepared and checked the batch. That kind of transparency has become a benchmark for quality assurance in the research chemical world.
It’s tempting for price-conscious buyers to pick up the cheapest offering on the web. In our experience, low-ball material often comes with invisible costs — lost time, repeated syntheses, or irreproducible data. Hidden by the per-gram cost are factors like poor lot uniformity, solvent residue, or incomplete reactions, each of which adds noise to critical research.
Our material rarely wins the race to the absolute bottom on price, but what we see from repeat customers is that reliable quality winds up cheaper after adding up the true costs of failed experiments or lost biological material. Whenever a team scales from milligram to multi-gram runs, or shifts from test-tube work toward pilot production, they find out whether their supplier is actually a manufacturer or just an importer with a nice label printer.
We accept that not every researcher will look for the stories behind their chemicals — but those who have struggled often do. When it comes to sialic acid chemistry, we hear the same themes: demand for paired analytical data, clean documentation and predictable product.
Carbohydrate chemistry leaves very little room for error. Small contaminants, water traces, or side products can derail months of synthetic work or create false positives in assays. Our team learned this lesson more than once, when a batch with slightly higher residual solvent content gave inconsistent glycosylation yields. Since those early days, our process has evolved — each batch gets vacuum dried in a cleanroom suite, we pack with pre-weighed desiccant, and customer feedback loops directly back into our SOPs.
For research on sialyltransferase enzymes, cell adhesion, or viral entry, scientists can’t afford off-spec building blocks. Researchers also tell us about the headaches they face with non-uniform melt points or hygroscopic powders. Those issues come from careless handling or aging stock. Our material is batch dated, with analytical runs immediately after packaging to guarantee the powder they see matches the spectra we've stored.
Manufacturing specialty chemicals for research involves a relationship with the entire supply chain. We source raw sugars from audited suppliers, maintain end-to-end documentation, and never pool batches from different runs. This policy comes from direct experience: pooled batches in the past led to variable purity and retention times, compromising customer results. We maintain dedicated equipment for rare sugar esters and segregate cleaning processes to avoid cross-contamination with unrelated organics or acids.
We go beyond the basics, offering technical support from the people who actually manage the process. Our staff handle requests for lower moisture content or special grind sizes, processing each request with the tools and institutional memory built over years. In several cases, customer feedback led us to adjust our drying and packaging routines, for instance by adding additional sieving or inert gas blanketing for moisture-sensitive projects.
When something isn’t right, real-time answers beat emails bouncing between non-chemist front desks. One particular case: a customer called about a faint, off-color tinge in a batch shipped during summer. Our chemist, who supervised the preparation, reviewed the archived sample, checked the temperature record during shipping, and guided the researcher on simple re-crystallization steps that solved the problem. Traders and resellers simply can’t offer this level of support.
Understanding the challenges faced by users comes from years of walking the same halls. Many of our chemists come from academic research backgrounds or process development roles, so they know what it feels like to chase down the reason an NMR spectrum looks off or a glycosylation doesn’t take. We log all issues reported by users and fold customer suggestions directly back into production and QC checklists.
Manufacturing rare chemicals like N-Acetylneuraminic Acid Methyl Ester carries responsibility for both safety and environmental compliance. We follow strict internal controls on solvent use, waste management, and emissions. Each batch is produced in compliance with the latest chemical handling protocols, minimizing residual toxic byproducts. Our process water and waste solvents get neutralized and recycled wherever possible.
We regularly audit our environmental impact, reporting usage and recovery statistics for solvents like methanol and ethanol. Routine reviews cover not just cost savings but occupational safety and reduction in chemical footprint. This connects to actual operator safety — training in proper PPE and spill containment — rather than just checklists for auditors. It's a philosophy learned in real working conditions, not just regulatory binders.
The competitive landscape demands we do things better each year, but the most valuable ideas often come from users in the field. Feedback on solubility, color, handling, and storage drives incremental changes. One example: researchers working with automated liquid handlers said static charge in the powder sometimes led to weighing errors. We adjusted our packaging and sieving process, adding a few milligrams per jar to allow for residue loss and using slightly antistatic containers. It’s small, but it makes a difference for precision users.
Our analytical team responds to requests for details sometimes omitted from catalog certifications — reporting optical rotation, enantiomeric excess, multiple chromatography traces, or expanded impurity profiles. Documented feedback from peer-reviewed publications using our product gets fed into our QC reference library to cross-validate future batches.
In the changing world of glycoscience, matching advances in synthetic biology and diagnostics means suppliers must stay closely attuned to the needs of researchers. For us, it means continuous process tuning, tighter analytical controls, and rapid response to requests. Whether it’s a gram for a pilot project or several hundred grams for preclinical development, we apply the same process care, analytic rigor, and transparency to each order.
From the choice of raw materials onward, every aspect of preparation reflects the day-to-day experience of working chemists, not just catalog marketing. With N-Acetylneuraminic Acid Methyl Ester, the difference real manufacturing makes can be measured in purity, reliability, time saved, and new results unlocked. That’s not just talk — it’s built into every lot we ship, batch after batch.