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HS Code |
732878 |
| Name | N-P-Tosylglycine |
| Cas Number | 97-09-6 |
| Molecular Formula | C9H11NO4S |
| Molecular Weight | 229.25 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 150-153°C |
| Solubility | Slightly soluble in water, soluble in methanol and ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, dry place |
| Synonyms | p-Toluenesulfonylglycine, Tosylglycine |
| Smiles | CC1=CC=C(C=C1)S(=O)(=O)NCC(=O)O |
As an accredited N-P-Tosylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-P-Tosylglycine is supplied in a sealed amber glass bottle containing 25 grams, labeled with product details and safety information. |
| Shipping | N-P-Tosylglycine is shipped in tightly sealed containers, protected from moisture and light. It should be transported at ambient temperature unless otherwise specified. Ensure compliance with local regulations for chemical shipping. Handle with appropriate precautions, including use of personal protective equipment, and store in a dry, well-ventilated area upon receipt. |
| Storage | N-P-Tosylglycine should be stored in a tightly sealed container, protected from light, moisture, and heat. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature or as specified by the manufacturer (usually 2-8 °C). Ensure that incompatible materials, such as strong oxidizers, are kept away. Label containers clearly and follow standard laboratory chemical storage protocols. |
Applications of N-P-Tosylglycine in Industrial ManufacturingN-P-Tosylglycine serves as a precision intermediate in several demanding chemical synthesis sectors. Its selective reactivity supports regulated downstream transformations, ensuring quality control and established standards adherence across pharmaceutical, agrochemical, specialty chemical, and peptide synthesis industries. Below are detailed industrial application scenarios, focused on actual end-use requirements and compliance environments. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisN-P-Tosylglycine acts as a chiral auxiliary and protected glycine source during the synthesis of peptide-based APIs and beta-lactam structures. Our production integrates full traceability and validated conversions for safe introduction into regulated pharmaceutical chains. Leading API producers incorporate this intermediate in the coupling phase, where N-protection prevents side reactions and ensures high-purity amino acid conjugates. Downstream, integrated deprotection and coupling strategies streamline multistep synthesis, supporting batch and continuous processing models. Our manufacturing ensures consistent impurity profiles, meeting strict pharmaceutical release criteria for subsequent formulation and sterile applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Peptide Synthesis for Diagnostic ReagentsIn the biotechnological manufacture of high-purity peptide reagents for clinical diagnostics and immunoassays, N-P-Tosylglycine contributes as a building block enabling controlled domain construction on automated synthesizers. Contract manufacturing labs leverage this protected glycine to prevent epimerization and sidechain modification during resin-bound coupling cycles, maintaining strict sequence fidelity. Subsequent steps include selective tosyl removal under monitored conditions, releasing functional peptides into downstream purification. We supply analytical-grade material, meeting stringent lot-to-lot consistency benchmarks demanded by diagnostic kit producers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate for Selective Herbicide SynthesisN-P-Tosylglycine plays a targeted role as a precursor in the synthesis of certain glycine-derivative selective herbicides. Large-scale agrochemical manufacturers utilize this intermediate in the formation of key molecular structures that require high purity and batch reproducibility. It enters the process during the condensation stage, ensuring correct backbone formation for downstream functionalization. Stringent impurity thresholds and process safety documentation support compliance with crop protection active ingredient regulations, critical for multinational agrochemical supply chains. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Chemical Intermediates for UV Absorber ManufacturingN-P-Tosylglycine is integrated into the production of high-value specialty UV absorber agents used in plastics, coatings, and industrial polymers. Chemical plants apply this raw material in synthesis routes where the protected glycine ensures uniform amino-functionalization prior to aromatic substitution. The process benefits from reduced by-product formation and enhanced light-stability characteristics of the resulting UV absorber. Producers meet demanding end-market requirements through validated reaction monitoring, high-purity input streams, and full compliance traceability for key downstream clients in the polymer protection segment. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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For more than a decade, our production floors have seen countless barrels and batches. Among them, N-P-Tosylglycine stands out, not just by its molecular formula but by the role it plays in fine chemical synthesis. This product has grown along with us, gradually transforming as new synthesis routes and starting materials became available and as colleagues tinkered with reaction conditions in pursuit of higher purity and yield. We manufacture it under model NG-101, using processes designed onsite and refined across dozens of trials, not handed down by outside partners or built for someone else’s facility.
N-P-Tosylglycine, chemically known as N-p-Toluenesulfonylglycine, brings a distinctive functional group—tosyl-protected glycine—that gives it a unique place among building-block chemicals for pharmaceutical and research applications. Glycine itself is simple; the tosyl group broadens its reactivity, shields the amino moiety, and allows for selective transformations down the line. Our team first adopted this product to meet our internal need for a selective, crystalline intermediate. Early on, we found commercial samples balled up with minor impurities or uneven melting points. This set off a mission in our lab to smooth out the process—starting with the quality of p-toluenesulfonyl chloride and extending to the choice of base and the temperature at which we add glycine. Over time, those efforts built the NG-101 model, a grade now known among chemists for its high-purity crystalline form, sharp melting point near 160°C, and freedom from yellowish byproducts that can play havoc in sensitive downstream reactions.
Our batch records fill rows and rows of logbooks, showing tweaks that matter: adjusting stoichiometry based on the season’s humidity, gauging the equivalence of water in reaction to suppress hydrolysis, even timing the addition of base to avoid lumping. Many off-the-shelf samples on the market come out clumpy or tacky because operators let acid-base reactions stall, or because the crystallization step isn’t closely watched. Our reactors run with in-line monitoring—conductivity, pH, temperature—so technicians catch even small deviations before they snowball into process disruptions or off-spec product. Every batch undergoes a full HPLC and NMR suite, not just spot checks. We learned the hard way that shortcutting this last step can introduce variable side products, like sulfonamide oligomers, which behave unpredictably during later synthetic steps.
Purity here is more than a number. Tighter purity allows faster and more reliable downstream coupling reactions—a boon whether working on peptide synthesis, specialty pharma intermediates, or high-value crop protection ingredients. We have seen customers frustrated by sluggish or incomplete coupling when using lower-grade alternatives. After switching to our material, they reported sharper endpoints, easier workups, and cleaner product separations. It saves time and cuts solvent costs, with less chance of puzzle-solving during process troubleshooting. That insight comes not from marketing pitches, but from sitting down with process chemists and seeing what matters on their end, then tuning our model accordingly.
N-P-Tosylglycine does not typically enjoy the same spotlight as active pharmaceutical ingredients or blockbuster solvents. Still, over many process runs, its importance becomes clearer. It acts as a well-behaved synthon in peptide bridge formation, coupling reactions, and as a precursor to protected amino acid derivatives. Its utility in selective N-alkylation or acylation comes from the balance between reactivity and protection. Unlike more volatile or sensitive reactants, it sits comfortably on the shelf at room temperature; our team has handled inventory over the years without dealing with stubborn caking or the need for elaborate refrigeration.
Several times, we debated expanding the catalog to include analogues or mixed tosyl-protected amino acids. Some bring similar strengths, but N-P-Tosylglycine frequently holds its ground due to its ease of handling, predictable solubility profile, and direct compatibility with many coupling reagents. Its crystalline form packs efficiently, allowing volumetric dosing and scale-up beyond what sticky oils or amorphous pastes permit. These practical advantages matter every day in a plant or a kilo-lab, not just on the page of a reference book.
The specification for our NG-101 model draws directly from field experience. Laboratory and pilot-plant teams have set cutoff levels for moisture, residual solvent, and inorganic byproducts stricter than most published monographs. We use a combination of gravimetric moisture analysis and Karl Fischer titration for water, ensuring levels comfortably below 0.5%. Sulfonate purity (measured by HPLC area percentage) routinely exceeds 99%, while the remaining fraction—trace byproducts, polymeric sulfonamides, or coloring agents—is squeezed out during final wash and recrystallization steps. We do not stop at the raw number; it is common for production supervisors to explain the logic to junior chemists, showing why a barely-passable number on HPLC is not good enough for a sensitive downstream process.
The market sees products sourced through many brokers, each offering various “lots” or “grades.” Our NG-101 model is not only designed for consistency—it is built on iterative improvements fed back from end users who shared the types of cleaning, coupling, and protection tasks they carry out. We keep strict hold of batch-to-batch traceability, linking every drum of finished product to a precise reaction log and analytical record. We have turned away labeled samples from resellers that did not match the real thing when checked by NMR or mass spectrometry, often finding discrepancies in impurity levels or the faint presence of unreacted tosyl chloride, which can ruin a scale-up.
Chemists sometimes ask us to compare N-P-Tosylglycine with other amino acid derivatives, especially those with alternative protecting groups like Boc or Fmoc. Our experience shows N-P-Tosylglycine is less prone to hydrolysis under mild aqueous workups and allows for easy deprotection under standardized reduction or acidic conditions. The tosyl group’s electron-withdrawing strength brings a selective, seldom-seen balance between stability during handling and reactivity at the desired step. We have watched our colleagues in scale-up skip purification steps that would be unavoidable with more labile protecting groups, reducing waste and maximizing yields. This brings both cost and operational advantages.
N-P-Tosylglycine rarely suffers from long-term degradation when stored properly. In contrast, more fragile amino acid derivatives, even when rated “high purity,” sometimes show spotty shelf-life. Some aminated derivatives tend to brown or suffer from slow hydrolysis if packaging is compromised for even a few hours. We have taken bags of N-P-Tosylglycine through multiple re-packagings—between vacuum sealer, PE liner, and fiber drum—without seeing significant change in content or performance even after months. This holds true under the standard warehouse conditions maintained at our site, subject to seasonal changes in temperature.
From a processing standpoint, the model NG-101 crystallizes as uniform, colorless needles or plates. In contrast, competitors’ materials often appear as powdery, slightly beige solid, signaling a minor presence of decomposition or impurities from uncontrolled pH in the last crystallization step. Operators on our team know how decisive even a faint smell of p-toluenesulfonic residue can be in predicting later reactivity or off-flavors in scale-up. Such attention to detail comes only after many cycles of both success and troubleshooting.
We have supplied NG-101 to users focused on high-throughput peptide synthesis, along with custom research teams who value its crystalline flow and measured reactivity. In coupling steps with carbodiimide reagents, its rate and purity matter greatly. Low-level impurities can increase side reactions, making HPLC cleanup trickier for delicate peptides. With our material, process teams report increased recovery and fewer chiral side products—one more sign that consistency from the outset saves time and headaches down the line.
Another field that leans on N-P-Tosylglycine is specialty agrochemical research. Researchers working up selective herbicide intermediates have shared with us how NG-101’s handling properties and high purity have reduced batch failures and simplified filtration. One team described how they shifted to our supply following months of yield setbacks linked to trace colored byproducts in competitors’ stocks. The result: tighter process control and improved product quality. That link between the small invisible factors in a starting chemical and outcomes in a multi-step process gets undersold in standard catalog listing—until someone experiences the difference in a later batch.
Safe production is no slogan; our operators are reminded of that every day, monitoring not just yield but also risks from exotherm or byproduct formation. N-P-Tosylglycine, in the NG-101 model, releases minimal volatile compounds at working temperatures. Before product leaves our plant, it has already passed handling trials in our own kilo-lab, where spills or contact can occur in practice and not just in a theoretical scenario. We provide our teams with effective PPE, robust cleaning protocols, and regular refresher training born from real incidents—not reworded industry checklists.
Batch records show that, over the past five years, production improvements have dropped waste byproducts by nearly 35% without resorting to expensive external treatment; instead, we optimize in situ during synthesis and keep a close eye on venting and quenching protocols. To reduce environmental impact, we constantly re-examine our water and solvent cycles. These are not marketable features on their own, but they mean something to the team working night shifts and to process chemists downstream who count on both performance and conscience.
We take pride, sometimes quietly, in the hands-on character of our N-P-Tosylglycine. Unlike distributed or relabelled material, ours carries the signature traits of real chemical know-how: documented process tuning, real feedback from users, and production floors that buzz with small talk about grain size, color, and batch features. Operators will tell you which kettles do better on early stages and who brings the most reliable analytical calibration. Every year, we pour time into comparing new raw materials and checking for subtle changes—sometimes traced back to shifts in suppliers’ routes far upstream. If even minor trace differences pop up in the FTIR or LCMS readout, we quarantine the whole batch until retesting validates the product. That vigilance carries through all our work, and refinements stack year over year, giving process chemists fewer worries and users a dependable, familiar supply.
For those who depend on quality, the difference between trader-sourced and manufacturer-made material is more than branding. Our warehouse only releases product after the final QA signoff, which takes place with at least two staffers cross-checking records and physical inspection. It is not rare for the same staff who filled the reactor to draw the final sample, bridging pride of workmanship with hard evidence. Over time, our regulars have come to expect not only fast delivery but also predictability—whether they work in R&D or run multi-hundred-kilo production lines.
Our commitment to N-P-Tosylglycine remains personal. No batch leaves the factory without approval by a team member who understands what the product will face downstream. We keep connected with end users—not only through sales, but also ongoing joint troubleshooting and method development. Every phone call asking about the impact of a ten-point difference in melting point, or the significance of an unlisted trace impurity, feeds back into our own process improvement. Conversation with users continues to shape the course of our production, adjustment of washing steps, and even the granule size coming out from the filter.
Chemical manufacturing can seem impersonal from the outside, but each improvement, minor adjustment, and feedback loop adds up to a better product. NG-101 stands as the result not just of chemistry, but a day-in, day-out process of trial and progress. Those who have worked with inconsistent, unpredictable starting materials before know the tangible benefits found in well-made, reliably performing N-P-Tosylglycine. That is what we deliver—and why we keep at it, one batch at a time.