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HS Code |
526698 |
| Cas Number | 2156-56-1 |
| Molecular Formula | C4H7NO2 |
| Molecular Weight | 101.10 g/mol |
| Iupac Name | 1,3-Oxazolidin-2-one |
| Appearance | White crystalline solid |
| Melting Point | 169-172 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.247 g/cm³ |
| Synonyms | N-Methylglycine anhydride |
| Chemical Structure | Five-membered oxazolidinone ring |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place |
As an accredited Sarcosine Anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sarcosine Anhydride, 100g: Sealed white plastic bottle with tamper-evident cap, labeled with chemical details, hazard warnings, and batch information. |
| Shipping | Sarcosine Anhydride should be shipped in tightly sealed containers, protected from moisture and heat. It must be labeled clearly as a chemical substance and transported in accordance with local and international regulations. Avoid exposure to incompatible materials, and use secondary containment to prevent spillage during transit. Handle with appropriate chemical safety precautions. |
| Storage | Sarcosine anhydride should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Protect it from moisture and incompatible substances such as strong acids and bases. Avoid exposure to humidity, as the compound may hydrolyze. Store away from sources of ignition or heat. Properly label containers and handle under an inert atmosphere if possible to maintain stability. |
Applications of Sarcosine Anhydride in Industrial ManufacturingSarcosine anhydride serves as a specialized intermediate in multiple industrial production routes. Our company supplies high-purity grades directly to manufacturers who require reliable consistency and traceability for downstream conversion processes. On this page, we outline its established roles within specific markets—each defined by the regulatory landscape, technical formulation requirements, integration points in manufacturing, and the kind of finished products realized by end producers. All scenarios provided reflect genuine industry practices based on current global regulations and supply chain feedback. 1. Active Pharmaceutical Ingredient (API) SynthesisThe compound sees primary use as a building block for synthesizing several oral and injectable APIs, particularly in peptide and small-molecule drug manufacturing. It functions as an activated amino acid derivative, facilitating peptide bond formation and enabling high-purity intermediates essential for regulated pharmaceutical production. The material requires strict documentation and analytical controls due to the sector’s focus on trace impurity and batch validation. Customers apply it in gram-to-multi-kilogram scales within GMP-validated assets. Industry compliance standards
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2. Industrial Surfactant & Detergent SynthesisProducers of specialty surfactants use this intermediate to create N-acyl sarcosinate classes of anionic surfactants, prized for their mildness in personal care as well as efficiency in technical cleaning products. The material’s reactivity supports direct acylation with fatty acid chlorides or acid anhydrides. Formulators value this raw material for its predictable reaction profile and the low residual by-products achievable in continuous and batch surfactant synthesis units. Industry compliance standards
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3. Glyphosate and Agrochemical Intermediate ManufactureIn the agrochemical sector, sarcosine anhydride acts as a core intermediate in glyphosate synthesis, the most globally utilized systemic herbicide. Producers leverage its high purity for consistent conversion during phosphonomethylation steps. Regulatory oversight focuses on batch purity, specific industrial hygiene controls, and minimization of residual organics and metals at each conversion stage. Continuous process units demand consistent supply and reproducibility to validate product fit for downstream registration and export. Industry compliance standards
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4. Biodegradable Lubricant Additive SynthesisManufacturers use sarcosine anhydride for the synthesis of biodegradable additives included in metalworking fluids and specialty lubricants. The material undergoes targeted chemical transformation to form licenced sarcosinate esters or amides. These additives address regulatory calls for lower aquatic toxicity and rapid environmental breakdown. Industrial users emphasize batch COA detail for amine, acid, and moisture levels due to downstream performance and emulsification characteristics in final lubricant formulations. Industry compliance standards
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5. Fine Chemical Intermediate for Polymer ModificationWithin performance polymer sectors, sarcosine anhydride acts as a customized end-group modifier for specialty polyamides and copolymers requiring precisely defined side-chain functionality. Reactive extrusion and solution modification processes benefit from its fast conversion, which enhances water solubility or biocompatibility properties of finished engineering plastics. Operators closely monitor process parameters to ensure consistent molecular weight and side-chain distribution, as the intermediate can impact final mechanical and chemical resistance profiles. Industry compliance standards
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In the chemical production industry, Sarcosine Anhydride often raises questions among chemists, formulators, and process engineers who look for specific amide reagents with dependable performance. Over years of synthesizing this material in our facility, we have seen up close the value that high-purity Sarcosine Anhydride delivers. We manufacture it not just to meet tight product specifications, but to support research and industrial processes that rely on clear, reproducible reaction pathways.
Sarcosine Anhydride, also known as 2,5-diketopiperazine or DKP, comes from a controlled cyclization of sarcosine or N-methylglycine. This white crystalline compound brings unique contributions to peptide synthesis, pharmaceutical intermediates, and advanced material development, where even minor impurities can derail entire syntheses. Over the years, we worked to refine our process so the final product meets rigorous standards — often to greater than 99% assay, measured by validated chromatography and titration.
Our production model for Sarcosine Anhydride focuses on batch synthesis with continuous monitoring, a process shaped by more than two decades of responding to customer feedback and hands-on lab research. Each batch includes a tight specification for melting point, ash content, and moisture, as excess water or trace minerals can impact polymerizations or hinder analytical accuracy. From the early stages, we saw how contamination with even low levels of amine byproducts can trigger unwanted side reactions in peptide coupling, so we dedicate resources to both analytical screening and in-line purification.
We standardize our Sarcosine Anhydride at a melting point of 237-240°C, a visual marker for batch consistency and identity. IR and NMR studies from our in-house laboratory confirm ring integrity and the absence of starting material. Over time, we observed that GC-MS and HPLC methods pick up residual solvents and organic contaminants far below visible limits, so our team samples every production run using these techniques before release. Ash and moisture levels stay well below 0.2%, guided by major pharmacopeia guidelines and customer assays in multi-step reactions.
We rely on decades of procedural refinement to keep our process consistent. Our synthesis starts with a high-grade sarcosine input, sourced from trusted suppliers with full traceability down to the lot. Through a carefully chosen catalytic cyclization and controlled temperature ramps, we maintain reaction integrity and prevent side reactions. Years ago, we tried switching solvents and catalysts based on theoretical predictions, but repeated testing led us back to our established process as the best balance between yield, purity, and waste minimization.
Throughout production, we dedicate significant resources to in-process checks rather than waiting until the end for product testing. Chemists sample intermediates at pre-set intervals, running rapid TLC and HPLC screens. This habit of early detection — learned from batches that failed when unchecked — dramatically cut our rework rates and gave us the confidence to stand by our material in both research and commercial supply.
Sarcosine Anhydride carries a unique position in the repertoire of amide-forming reagents. Its seasoned use finds roots in peptide chemistry, where researchers or production chemists exploit its ability to cyclize or open to controlled oligomers, bypassing pitfalls seen with other more reactive acyl donors. In our history collaborating with active pharmaceutical ingredient (API) companies, many prefer Sarcosine Anhydride for introducing N-methyl amino acids in their routes because it offers cleaner conversion and easier downstream purification than free sarcosine or open-chain derivatives.
Peptide chemists know that the diketopiperazine ring resists racemization, reducing scrambling of stereochemistry — an essential property for activity in biological molecules. During scale-ups for life sciences projects, our technical staff helps partners avoid harsh reagents that sometimes cause undesired side reactions or epimerization. Over time, repeat customers shared their NMR and chiral HPLC data, validating that our anhydride delivers protected peptide bonds without the need for extensive downstream clean-up.
We also watch Sarcosine Anhydride entering more advanced polymer and specialty material syntheses, often as a building block providing N-methylation in backbones with tailored flexibility. Our customers often discover that Sarcosine Anhydride brings more predictable opening reactions under basic or nucleophilic conditions versus other cyclic intermediates, especially where a clean N-methyl insertion is required without the risk of deamidation or decarboxylation seen in competitors.
In small-molecule synthesis, Sarcosine Anhydride offers a route to diketopiperazines — a family of compounds important in drug discovery for their biological activity and role as scaffolds. Over the years, we observed medicinal chemists choosing it for its stability on bench and shelf, which can be a risk with more labile peptide starting materials. We designed packaging to resist moisture ingress, based on customer feedback from humid environments that sometimes challenged product shelf-life.
Market conversations often raise comparisons between Sarcosine Anhydride and other amidation reagents or cyclic anhydrides. Right away, the distinction comes from the N-methyl group on sarcosine, a feature not found in classic glycine-based DKP or in many amino acid anhydrides. This methylation shifts both reactivity and stereoelectronic properties. In our labs, we find Sarcosine Anhydride noticeably less prone to unwanted polymerization than plain glycine anhydride. Customers working in controlled oligomerizations have shared that our product gives tighter distributions, a finding echoed in GPC results and batch reproducibility.
Some chemists look to alternatives like phosgene or mixed anhydrides for peptide syntheses. Unlike those routes, Sarcosine Anhydride gives a much safer handling profile and avoids issues of overactivation that sometimes encourage side reactions or hazardous byproduct formation. Our workers appreciate that engineering controls for Sarcosine Anhydride stay far simpler than for classic chlorinating reagents, helping both laboratory and pilot plant teams manage exposures and routine cleaning in a straightforward way.
Comparing with more reactive acylating agents, we observe that Sarcosine Anhydride often yields cleaner, more predictable transformations, especially under mild heating or with basic catalysis. Feedback from process chemists frequently highlights a reduction in side products, especially those that complicate chromatographic profiles or slow down API isolation. Our QC team tracks impurity trends batch by batch, improving purity by tweaking crystallization protocols in response to customer reports.
This N-methylated DKP also differs from open-chain sarcosine derivatives in its shelf stability, reduced hygroscopicity, and consistency in melting behavior. Open-chain salts or esters change physical form with environmental conditions, sometimes leading to material loss in transfer or unexpected dosing errors in reactors. We often hear from formulation chemists who struggled with other sarcosine forms, only to switch to our anhydride for better control in bulk or precision additions.
In specialty polymer uses, the ring structure of Sarcosine Anhydride introduces backbone rigidity and influences thermal behavior in ways pure open-chain sarcosine cannot match. We observed successful scale-ups in electronic material applications, where batch reproducibility directly impacted product performance. Our material sees use when polymer structure demands both N-methyl functionality and rigid conformational anchors, features not obtainable with glycine anhydride or sarcosine salts.
Feedback from our industrial and research clients shapes much of our ongoing process development. Over time, project chemists and engineers point out where single-lot consistency, handling ease, or spectral purity influences their own workflow. For research and small-batch customers, the white crystalline appearance and easy handling proved welcome after experience with sticky, impure, or variable material from other sources. We share validated spectral data for every batch — NMR, IR, melting point, GC, and HPLC — since seasoned chemists want to check for themselves.
On the large-scale manufacturing side, formulation engineers and project leads flag the origin and traceability of input materials. Many regulatory teams have come to view our documentation on input traceability and cross-contamination assessments as crucial for their own records. Years of coordinating stability and storage studies let us advise users on storage conditions that maintain the crystal character and keep degradation to a minimum, which prevents clumping and assay drift.
We have seen customers re-examine their entire process development after introducing Sarcosine Anhydride as a key intermediate, especially when switching from complex or multi-step amide bond-forming reagents. Pharmaceutical teams appreciate the reproducibility on multi-kilogram scales, especially when lot-to-lot assay results align tightly with prior qualification batches.
Producing high-purity Sarcosine Anhydride presents its share of practical challenges. We learned early that process bottlenecks often occur at the cyclization or during final purification. In the past, scaling up from bench chemistry to full reactor runs revealed crystallization inconsistencies and occasional color impurities, often related to small changes in solvent, temperature, or input quality. Troubleshooting those bottlenecks taught us to prioritize solvent water content, pre-drying of inputs, and low-temperature precipitation as part of routine batch controls.
The knowledge gained through decades of feedback and in-process reviews allows us to catch potential deviations early. Analytical chemists in our team routinely run both targeted and non-targeted screens, capturing low-level organics that creep in through less-obvious routes. For example, periodic customer complaints about minor off-odors or discoloration led our engineers to swap old reactor seals and update inert gas purging schedules, which improved product color and odor even before standard purification steps.
Moisture sensitivity remains an issue in rare cases, especially for users in tropical climates or settings where warehouse conditions fluctuate. We designed new packaging that balances cost and barrier effectiveness — dense poly-lined drums, double-sealed bags, and inclusion of desiccant pouches. Over years, we tracked customer storage success, incorporating their feedback into updated guidance that minimizes clumping or caking during extended storage. For those in high-humidity locations, we suggest rapid transfer protocols and prompt resealing, a practice that preserves assay stability up to the planned expiration.
We also invested in operator training for safe handling of both raw sarcosine and final anhydride. Remote or less-experienced users benefit from our guidance on dust control, handling tools, and transfer equipment. Those steps, straightforward once implemented, have virtually eliminated batch-to-batch cross-contamination and improved safety outcomes — building trust with both internal and partner project teams.
Our experience manufacturing and supplying Sarcosine Anhydride puts us in a good position to pursue product improvements as new application demands arise. On the technical side, our R&D team regularly collaborates with universities and customers developing next-generation peptides, pharmaceuticals, and specialty polymers. These interactions expose us to novel use cases, new reaction conditions, and analytical methods. Direct conversations with researchers have led us to develop lower-metal grades for metal-sensitive synthesis and finer particle cuts for applications needing rapid dissolution in non-aqueous media.
Environmental responsibility continues to hold priority on our agenda, especially as global customers raise questions about life-cycle impacts and solvent usage. Legacy processes used higher volumes of chlorinated solvents, but collaborative reviews of process analytics showed promising results with greener alternatives. We now prioritize less-persistent solvents in every possible phase, both upstream and downstream, and compress waste streams for easier post-processing.
Regulatory expectations evolve alongside new applications. To stay ahead in compliance, our quality team updates batch-release protocols, document retention, and process validation routines using the latest industry guidance. Whenever possible, we prepare for potential regulatory review by organizing reference standards and batch records in formats that align with both ICH and local agency requirements. This investment in documentation reassures our partners — particularly in pharmaceuticals — where batch consistency, impurity profiles, and handling safeguards come under close review.
Rarely does a year go by without a new request for a customized grade or packaging size. Whether for high-throughput libraries in research or multi-ton supply for chemical manufacturing, we find flexibility in logistics and batch splitting goes a long way to support emerging market needs. Real-world experience reminds us that keeping open channels with users, actively seeking feedback, and updating our offerings keeps our production aligned with the realities of bench and plant operations.
Years of firsthand experience in synthesizing, purifying, and distributing Sarcosine Anhydride have shaped our standards. Facing challenges on the lab bench and in full-scale production, we commit to maintaining high chemical purity, consistent physical characteristics, and honest technical support. This dedication comes from direct engagement with customers who rely on Sarcosine Anhydride for successful syntheses in numerous fields, from drug discovery and scale-up to advanced material science.
The stories and results from users help us evolve both the product and its supply. Whether for complex peptide assemblies, specialty intermediates, or tailored polymer syntheses, we harness a deep understanding of both technical demands and commercial realities. Our Sarcosine Anhydride reflects not just a chemical formula but a history of joint problem-solving and mutual growth with chemists and engineers worldwide.
We continue to invest in process control, analytical rigor, and open communication, ensuring that every shipment of Sarcosine Anhydride supports our customers’ goals for practical synthesis and reliable results — and builds trust, batch after batch, project after project.