|
HS Code |
919568 |
| Cas Number | 1188-38-1 |
| Molecular Formula | C6H10N2O5 |
| Molecular Weight | 190.16 g/mol |
| Synonyms | Carbamylglutamate, NCG, N-Carbamoylglutamic acid |
| Appearance | White to off-white powder |
| Solubility | Soluble in water |
| Melting Point | 170-172°C (dec.) |
| Ph 1 Solution | Approximately 2.0–3.0 |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C (refrigerated) |
| Chemical Structure | Contains a carbamoyl group attached to the alpha amino group of L-glutamic acid |
| Iupac Name | 2-[(Aminocarbonyl)amino]pentanedioic acid |
As an accredited N-Carbamoyl-L-Glutamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g N-Carbamoyl-L-Glutamic Acid is packaged in a sealed, high-density polyethylene bottle with a clear, tamper-evident label. |
| Shipping | N-Carbamoyl-L-Glutamic Acid is shipped in tightly sealed containers to protect against moisture and contamination. The packaging complies with relevant safety and chemical transport regulations. It is typically stored and transported at room temperature, away from incompatible substances, and includes proper labeling and documentation for safe and compliant handling during transit. |
| Storage | N-Carbamoyl-L-Glutamic Acid should be stored in a tightly sealed container at 2-8°C, protected from light and moisture. Keep the storage area well ventilated and away from incompatible substances such as strong acids and bases. Ensure the chemical is kept in a dry place to prevent degradation and maintain its stability over time. Always follow standard laboratory safety protocols. |
Competitive N-Carbamoyl-L-Glutamic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
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Tel: +8615365186327
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Every day on our site, we see demand steadily climbing for N-Carbamoyl-L-Glutamic Acid, a product people in biochemistry circles call NCGA for short. This compound doesn’t grab headlines like some novel enzymes or blockbuster pharmaceuticals, but for production engineers and R&D managers who want reliable, traceable building blocks for their work, NCGA stands out.
Many operations still rely on legacy glutamic acid derivatives, and there’s a longstanding loyalty to those tried-and-true options. Standing at our centrifuge controls and talking to seasoned chemists by the reactors, we see the same challenges again and again—boosting yields, cutting out contaminants, and keeping everything HPLC-clean without introducing extra risks downstream. NCGA has shifted conversations in our labs, mostly because its use keeps the core reactions running cleaner, cuts out common bottlenecks, and reduces the rework that comes with older forms.
We produce NCGA using a fermentation approach that hits precise points for purity and consistency batch after batch. Our standard grade offers a purity of over 99% (as determined by HPLC analysis), with moisture and ash content kept below 0.5%. In our shop, this matters because strict material profiles mean technicians spend less time hunting down causes for off-target results in their process control logs.
NCGA leaves our plant as a white crystalline powder with a neutral taste and mild, characteristic odor. We avoid binders, flow agents, and excipients to limit unknowns that could throw off final applications. Each lot comes as a free-flowing powder, stored in polyethylene-lined drums to keep it bone-dry and uncontaminated. Handling the material is straightforward for our teams; it dissolves easily into water and standard buffers, freeing up vessel time and sidestepping the headaches of inconsistent dissolution or caking that sometimes happen with older derivatives.
Our customers put NCGA straight to work in enzyme production lines, cell culture media, and high-purity amino acid synthesis. During fermentation processes for arginine biosynthesis, this material enables regulatory bypass at the carbamoyl phosphate stage, which is critical in engineered strains of bacteria and fungi. Our process managers have seen outfits using regular L-glutamic acid running into feedback inhibition, slowing yields or compromising end-product profiles. We run side-by-side trials, and the difference stands out: NCGA pushes the conversion forward, leading to higher titers, especially in strains prone to stalling under traditional protocols.
On protein refolding lines, we watch teams turning to NCGA for its ability to stabilize intermediate forms and cut down misfolded fractions that complicate purification. The compound integrates smoothly with other amino acids and chaperones, without the oddball residues that creep in from less pure glutamates or synthetic cainoids. In-house testing sees our product consistently meeting trace impurity specs, saving downstream labor at quality checkpoints.
Many industry veterans have worked with monopotassium and monosodium glutamates for years. Those products are plentiful and relatively cheap, with a long safety record. For applications that need regulatory bypass, especially in non-animal-derived media, these salt derivatives lose their punch. In our batch logs, the switch to NCGA means fewer corrective interventions and improved stability of the resulting amino acid pools.
The difference comes through most sharply in GMP production, where trace contaminants can torpedo product release. Our chromatography runs on NCGA batches show a single dominant peak with residuals well below European Pharmacopoeia thresholds. No buffering cations, no unnecessary salt load—just the carbamoyl-protected form exactly where you want it. On a practical level, that helps plant managers cut out the routine tank rinses or membrane replacements that sodium- or potassium-heavy media can require.
Our business spends a lot of time tracking the pain points of process development teams. Too often, substitutions introduce risks that ripple through entire production runs. Somebody in the formulation group tweaks a recipe, and suddenly there’s a spike in by-product peaks or a jump in endotoxin readings.
We have watched this story play out across multiple commercial platforms: a team runs one batch on legacy materials, faces weeks tracking contamination hits, swaps in NCGA, and records fewer deviations. This flow of data drove us to scale up our NCGA line—not as a replacement for older chemicals, but as a way to offer reliability that lets production supervisors sleep at night.
QC staff in our plant run triple checks on every lot, not just for the regulatory tick-box but because tracking IC, HPLC, and micro profiles against our baseline keeps surprises out of the customer pipeline. Our experience with older impurity-prone compounds guided us to tighten up every cleaning step, making sure the final NCGA batches come out as close to theoretical spec as possible. We keep a full chain of custody so every drum in the plant can be traced back through decades of plant history and all the tweaks that got us here.
From our vantage in manufacturing, we see the energy sector eyeing NCGA for bio-catalysis optimization. The food sector checks our trace records for cGMP and GRAS alignment. Biopharmas come looking for a solution to batch variability in enzyme expression and find NCGA delivers on both purity and price. Our feedback loops go both ways: on-site technical teams bring their results back to us, we adjust processing accordingly, and the product gets better year after year.
Supply chain pressures have gotten intense since the pandemic years. Where traders chase substitute lots overseas and roll the dice on quality, we hold tighter controls, minimizing wobble in each drum. Our raw material sources lock us into stable pricing and let us protect customer timelines, which—talking with lab managers—matters more than shaving cents per kilo. Consistent NCGA output lets them plan future work with confidence, not dread another recall or investigation.
It’s easy to put high-purity or GMP-compliant on a drum. In our experience, what comes after matters most. We run NCGA through stability testing at three and six months, exposing it to temperature and moisture gradients found in real-world warehouses and shipping docks. Data from these tests flows to our customers in unrestricted COAs, with chromatograms posted for each batch.
The greatest value comes from direct factory-to-lab and factory-to-plant relationships. Customer analysts don’t field calls shuffling between middlemen—they talk directly to our QC staff who know the production lines inside and out. If one of our partners spots an anomaly, transparency takes center stage. We can replicate the exact conditions and find solutions without long, uncertain chains of custody.
NCGA’s biggest strength shows in modern, multi-product plants. With batch records running back decades and validation logs for every molecule produced, a stable input like NCGA helps keep those records clear. We’ve worked with operations scaling from pilot tens of kilos up to metric-ton levels—NCGA slides into most reactors with no change to existing lines. The ease of transition wins points from validation and EH&S teams, especially compared to legacy compounds that need redocumentation or new PPE protocols.
On visits out to customer sites, we see the payoffs: less downtime for line cleaning, fewer unplanned stoppages for root-cause investigations, lower rates of final product discards blamed on input impurity. All of these details matter for the plant managers, regulatory submissions, and the bottom line. That may not excite marketers or distributors, but the difference shows up in cleaner audit trails and tighter batch yields.
The pressure on chemical producers only climbs—environmental standards tighten, shipping issues add complexity, customers expect full transparency. Our philosophy puts every stage of NCGA production directly under our roof. Operating under ISO protocols and quarterly third-party audits means we face the same rigor as our largest customers. We absorb those costs and logistical headaches on the factory side, so customer teams focus on what matters inside their own operations.
We learned early on not to promote new compounds until all in-plant validation checks out. This approach ensures that when partners come to us, NCGA’s record reflects years of uninterrupted, real-world process results. No generic repackaging or random sources—just one material, always made on the same lines, documented every step. It’s an approach built for trust, not flash.
Technical service plays just as big a role as manufacturing in seeing NCGA succeed for our industry partners. In our experience, real learning begins when plant teams ask for root-cause analysis on new yields or side products, and we get on calls with their scientists to run through logs, compare samples, and solve tough process puzzles together. Data coming from end-use testing in customer fermenters lets us fine-tune our process, improving future lots.
Our technical staff work directly with end users, sharing experience on optimal concentrations, real-world pH control, and line cleanouts. We offer assays and in-process checks to help customers avoid trial-and-error runs. By cutting years of duplicate development, everyone on the floor sees actual improvements—quicker setup, steadier output, and fewer late surprises. The comfort that comes from working with a known manufacturer, rather than random suppliers, pays off in plant-wide reductions in risk.
Chemical plants carry a heavy responsibility. We see reports around the world about poor handling, shortcuts taken at the expense of safety or the environment. Our process design for NCGA stands as a response to those concerns. Solvent recovery systems, close-cycle water usage, and full endotoxin screening remain non-negotiable on our site. All waste gets documented and routed to proper handling from start to finish.
Our record stands up to inspection—no off-book emissions, zero tolerance for adulteration, and full compliance with all current REACH, EPA, and State-level requirements for process chemicals. We built in third-party testing where our own audits could miss and encourage full customer reviews on every site visit. Trust is a two-way street, and it comes from sharing more than just certificates—open factory tours, full sample packages, and transparent production runs matter far more than glossy data sheets or anonymous lot codes.
Over three decades manufacturing specialty chemicals, we have seen products quietly transform entire industries. NCGA may look unremarkable as a powder on a shelf, but for those grappling with plant-scale bioprocess and quality pressures, its availability, reliability, and trace purity drive forward progress. Lab teams get better repeatability, production staff work with a cleaner and more predictable material, and leadership avoid sleepless nights worried about recalls or missed audits.
We remain committed to steady production, tighter quality specs, and open partnerships. Our factory floors blend traditional craftsmanship with the newest controls, and our teams work shoulder-to-shoulder with users solving practical problems. Supporting growth in enzyme, pharmaceutical, and industrial biocatalysis continues to motivate our craft—NCGA offers not just another compound, but a proven foundation for those who need to run at industrial scale without uncertainty holding them back.