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L-Methionine Sulfoxide

    • Product Name L-Methionine Sulfoxide
    • Alias methionine-sulfoxide
    • Einecs 259-222-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    940217

    Cas Number 2149-10-8
    Molecular Formula C5H11NO3S
    Molecular Weight 165.21
    Iupac Name 2-amino-4-(methylsulfinyl)butanoic acid
    Appearance White to off-white powder
    Solubility In Water Soluble
    Melting Point Decomposes above 226°C
    Ph Value 5.0 - 7.0 (1% solution in water)
    Optical Rotation [α]20/D +22° to +28° (c=1, H2O)
    Storage Temperature 2-8°C
    Synonyms L-Methionine S-oxide

    As an accredited L-Methionine Sulfoxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, tightly sealed plastic bottle containing 100 grams of L-Methionine Sulfoxide, labeled with product details, hazard symbols, and batch information.
    Shipping L-Methionine Sulfoxide should be shipped in a tightly sealed container, protected from light, moisture, and heat. Store and transport at room temperature, unless specified otherwise. Handle with standard laboratory safety protocols. Ensure proper labeling and documentation as per chemical shipping regulations. Avoid contact with incompatible substances during transit.
    Storage L-Methionine Sulfoxide should be stored in a tightly sealed container, away from light, moisture, and incompatible substances. Keep in a cool, dry place, ideally in a refrigerator at 2–8°C. Ensure good ventilation in the storage area and avoid sources of heat or ignition. Label the container clearly and follow local regulations for hazardous material storage.
    Application of L-Methionine Sulfoxide

    Applications of L-Methionine Sulfoxide in Industrial Manufacturing

    As a direct manufacturer of L-Methionine Sulfoxide, we supply this unique amino acid derivative to specialized industrial segments where controlled oxidation and targeted biochemical modification are critical. Below, we outline key application fields, compliance requirements, dosage parameters, production flow integration points, and end-product categories relevant to downstream industrial partners.

    1. Pharmaceutical Intermediate Synthesis

    L-Methionine Sulfoxide plays an important role in the synthesis of chiral pharmaceutical intermediates, particularly for APIs involving oxidation-sensitive moieties. Manufacturers use this compound during multi-step syntheses where sulfoxide functionality enhances intermediate reactivity and stereochemical control. Exact stoichiometry depends on downstream molecular modifications, but precise addition at designated steps ensures high yields and purity for targeted pharmaceutical actives.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) relevant monographs if used in API synthesis
    • European Pharmacopoeia (Ph. Eur.) and Japanese Pharmacopoeia for specific regional compliance
    • 21 CFR Part 211 for US finished drug manufacturing

    Typical usage ratio

    • 0.5–3 molar equivalents per batch, adjusted based on specific reaction chemistry and required conversion rate; ratio fine-tuned by HPLC/GC analysis of process intermediates.

    Downstream process integration

    • Added to stirred-tank reactors during chiral auxiliary stage or as a reactant in sulfoxidation procedures; monitored under inert atmosphere to avoid byproduct formation; followed by in-situ extraction and purification steps.

    Final product types

    • Enantiopure drug intermediates
    • Chiral sulfoxide building blocks
    • Precursor formulations for final API production

    2. Peptide Modification for Research Reagents

    This raw material is used by peptide synthesis laboratories and contract manufacturers to introduce site-specific oxidized methionine residues in custom peptides. Such chemical modification permits the study of protein oxidation, structural changes, and molecular signaling in biomedical research and proteomics projects. The compound is dosed according to sequence requirements and protected group strategies.

    Industry compliance standards

    • ISO 9001:2015 for laboratory chemical production
    • ISO/IEC 17025 for analytical confirmation of peptide sequence and modification
    • Relevant institutional animal research or clinical trial material regulations, if supplied for further study

    Typical usage ratio

    • 0.1–1 mmol per resin loading, determined by targeted methionine content and modification sites within peptide sequence.

    Downstream process integration

    • Integrated after solid-phase peptide chain assembly; used in selective oxidation protocols on resin or in solution, followed by cleavage and RP-HPLC purification to confirm correct oxidation state.

    Final product types

    • Oxidized peptide standards
    • Protein structure-function analysis reagents
    • Proteomic calibration kits
    • Research-only modified peptides

    3. Analytical Reference Material for Oxidative Stress Profiling

    Regulated laboratories utilize this compound as a primary or secondary reference standard for calibration in assays measuring protein and amino acid oxidation. The material ensures traceable, quantifiable benchmarking in LC-MS/MS and ELISA workflows. Handling and batch documentation must align with analytical laboratory accreditation protocols.

    Industry compliance standards

    • ISO 17034:2016 for production of reference materials
    • ISO/IEC 17025 compliance for analytical validation
    • US FDA GLP (21 CFR Part 58) for clinical diagnostic and research reagent production

    Typical usage ratio

    • 10–100 µg/mL in assay standard curves; concentration range set according to detection system sensitivity and linearity requirements for target matrices.

    Downstream process integration

    • Provided as a lyophilized solid or solution, reconstituted directly into calibration standards for chromatographic or immunological platforms used in hospital and core research labs.

    Final product types

    • Certified analytical standards
    • Reference panels for medical device QC
    • Calibration kits for biomarker quantification

    4. Functional Food Ingredient for Oxidative Marker Studies

    Specialized nutrition product developers incorporate oxidized amino acid sources as marker compounds to support food ingredient stability research and simulate oxidative degradation in protein-rich matrices. The compound is used in small, controlled amounts within research and pilot-scale batches to confirm antioxidant system performance and validate storage protocols.

    Industry compliance standards

    • ISO 22000:2018 Food Safety Management Systems
    • FAO/WHO Codex Alimentarius where applicable for food ingredient trialing
    • EU Regulation (EC) No 178/2002 for food safety and traceability
    • GB 2760-2017 (China Food Additive Use Standard) when trialing for Chinese applications (trial exceptions for research use only, not GRAS)

    Typical usage ratio

    • 5–30 ppm in protein matrices, chosen to model typical oxidative modification levels in food shelf-life and simulated digestion studies; not intended for retail finished food products but for R&D and pilot only.

    Downstream process integration

    • Added during bench-top formulation or microencapsulation studies; mixed into ready-to-drink nutritional beverages or protein-fortified food samples prior to storage or simulated preparation.

    Final product types

    • Experimental meal replacements for stability study
    • Research-prototype nutritional bars
    • Model protein hydrolysates for antioxidant screening
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    Certification & Compliance
    More Introduction

    L-Methionine Sulfoxide: Commitment to Quality and Applications in Modern Chemistry

    Introduction to L-Methionine Sulfoxide and Our Experience Manufacturing It

    Producing specialty amino acid derivatives calls for a careful approach, both in terms of process and quality assurance. Over the years, L-Methionine Sulfoxide has become one of those unique products we’ve learned to handle with exactness. Our focus on purity goes beyond standard batch testing; every lot gets full chromatographic scrutiny, which means we safeguard the molecular integrity and stereochemistry that matter throughout its supply line. That involves more than just technical box-checking. In our experience, even a slight slip in production conditions shows up downstream, especially when customers put this product to work in advanced peptide synthesis, oxidative stress biology studies, or custom pharmaceuticals.

    The Model of L-Methionine Sulfoxide We Offer

    Our L-Methionine Sulfoxide (CAS No. 2143-25-5) arrives as a white-to-off-white crystalline powder, offered at a purity grade of not less than 98% based on HPLC. Purity at this level doesn’t just look impressive on a certificate; it defines compatibility for research and production. Customers using our material in critical protein research applications and drug development regularly share results indicating how purity plays a direct role in repeatable synthetic yields.

    From upstream fermentation to final crystallization, every step remains under real-time control, because shortcuts quickly show up during end-use testing. We continuously tune filtration, monitor pH, and double-check lot homogeneity—lessons hard-won after catching minor deviations. By maintaining tight water content controls below 1%, we help labs and production facilities avoid inconsistent batch results.

    Specifications We Deliver and the Rationale Behind Them

    Over countless production runs, our specs have sharpened to fit both biochemical and industrial needs. Purity (HPLC): >98%, optical rotation consistently at [α]20/D = +24° to +27° (C=1, H2O), and moisture controlled below 1%. Total residue on ignition stays well under 0.5%. These details come out of feedback from analytical labs and process engineers who’ve flagged anything outside these limits as a source of unnecessary troubleshooting.

    We used to see higher tolerance for heavy metals and residual solvents in early years, but long-term customers explained the compounding headache in downstream enzyme assays and biological cultures. So, for heavy metals, we hold firm below 10 ppm (as Pb), and on solvents, we keep to pharmacopeial requirements, consistently reporting non-detects for common volatile organics. Our powder grinds easily, flows predictably, and dissolves quickly, making it amenable to small-scale peptide assembly, offline analytical work, and larger bioprocessing setups.

    Usage Experience: Real-World Insights from Our Facility to Your Application

    Those who’ve developed diagnostic kits, tested oxidative protein folding pathways, or fed proprietary fermentation blends with L-Methionine Sulfoxide bring us their stories often. One of our earliest challenges involved a pharmaceutical research partner who traced a bottleneck in peptide synthesis back to subtle batch impurities in sulfoxide derivatives. We altered our recrystallization step, adjusted temperature ramps, and within one production cycle, their peptide results stabilized. For us, this drove home that process discipline and real-world outcomes are tightly related.

    We craft L-Methionine Sulfoxide with stereopurity and trace element cleanliness front of mind, aiming for flexible use: as an intermediate in pharma R&D, as a marker of oxidative stress in cell culture models, or as a feed component in nutritional research. Peptide chemists frequently request targeted advice about solution stability or compatibility alongside reducing agents. In these cases, we’ve found that controlling even trace levels of precursor residues keeps sensitive downstream reactions in a predictable range. Model organism facilities, especially in oxidative stress research, report consistent response curves when using our product, feedback that doesn’t go unnoticed on the production floor.

    How L-Methionine Sulfoxide Differs from Other Methionine Derivatives

    Working hands-on with amino acid derivatives for years clarifies that L-Methionine Sulfoxide stands apart, both chemically and functionally. L-Methionine itself serves as a hydrophobic, sulfur-containing essential amino acid, vital for protein biosynthesis and methylation pathways. In contrast, its sulfoxide form comes after selective oxidation—an extra oxygen atom on the sulfur group creates distinct physicochemical characteristics.

    The altered sulfur center changes solubility, reactivity, and biological behavior. Enzymologists and structural biologists know this modification impacts how proteins fold, respond to stress, or get repaired inside living cells. Compared to the plain L-Methionine or its D-sulfoxide enantiomer, the L-sulfoxide is valuable in monitoring and manipulating oxidative processes, serving as a precise probe for methionine-oxidizing enzymes like methionine sulfoxide reductases. Pharmaceutically, L-Methionine Sulfoxide sometimes enters custom synthesis sequences where redox reactivity must be tightly regulated—something its parent amino acid can’t accomplish.

    Other suppliers often list generic “methionine derivatives” with little detail on configuration purity or trace impurities. In field use, we’ve seen that such generalization leads to unpredictable responses in cell lines, animal models, or enzyme assays. Our approach starts with verifying the L-configuration by optical assay and stacks that with full identification by NMR and mass spectrometry. Years of comparative runs against racemic or lower grade batches showed that maintaining optical and chemical purity isn’t a regulatory afterthought but a real technical need.

    Feedback Loop: Learning from End Users to Refine Our L-Methionine Sulfoxide

    Many modifications to our process began as direct responses to researchers and manufacturing chemists who found subtle flaws or performance differences that standard QC missed. The complexity of peptide assembly, enzyme kinetics, or in vivo applications means we often field questions about how our sulfoxide matches up with theoretical and practical expectations.

    A common request involves confirmation that L-Methionine Sulfoxide batches stay shelf-stable without yellowing or caking, especially when stored at room temperature. Years ago, we enhanced our drying phase by revisiting our choice of vacuum levels and final bleed gas, which kept the powder crisp and free-flowing—details gleaned from failed early batches that absorbed ambient moisture too aggressively. Since then, user complaints about clumping dropped off, and repeatability in solution preparation improved.

    Another subject that comes up involves compatibility with specific coupling reagents or buffer systems. For those assembling longer peptides or conjugates, we provide technical support on solubility, buffer pH, or suggested use concentrations, backed by practical lab testing alongside instrumentation partners. The feedback we gather helps us anticipate issues in advance, calibrate our lot release criteria, and keep open lines of communication as needs evolve.

    Genuine Production Know-How: Lessons from the Shop Floor

    Every kilogram of L-Methionine Sulfoxide starts with careful raw material screening. Even the smallest impurity in the methionine input feeds through the oxidation process, so we vet every supplier and build redundancy into analytical checks. In our facility, oxidation proceeds with specific oxidants under tightly regulated pH and temperature. A missed temperature inflection can lead to unwanted byproduct formation, and we monitor for trace overoxidation.

    Our operators run parallel analytical sampling, cross-checking both TLC and HPLC throughout crystallization. We noticed early on that holding times in intermediate steps affect homogeneity and downstream solubility, prompting us to reduce unnecessary standing time and to introduce real-time moisture sensors in drying ovens. This focus has translated into fewer customer queries about solubility consistency in aqueous and mixed organic systems.

    Routine finished-product release steps include three-point IR fingerprinting, color assessment, and independent chromatography. We keep close ties to our packaging suppliers, specifying food-grade liners and strict water-activity cutoffs. The extra steps in traceability and careful documentation mean we can respond to regulatory or scientific queries quickly, sending full analytical records to customers without delay.

    Quality Challenges and Practical Solutions

    Raw material variability remains a constant challenge. Not every methionine supplier meets our standards, and fluctuating supply has prompted us to develop a broader network of vetted partners. Some years, we’ve had to reject half of incoming lots to avoid uncertainty down the line, especially when human or animal research is involved. We maintain an audit program and rotate between preferred suppliers based on recent analytical quality.

    Oxidation control presents another key hurdle. Incomplete reactions leave unwanted starting material, while over-oxidation gives rise to sulfone byproducts that complicate downstream reactions. We fine-tuned oxidant addition protocols and monitor the reaction endpoint with quantitative HPLC spiking. Our continual investment in process control—using temperature feedback and inline analytics—helps maintain batch-to-batch uniformity even when environmental conditions fluctuate.

    We’ve also learned that storage conditions play a bigger role than anticipated. If product sits in suboptimal environments, hydrolysis or oxidation from air exposure can impact both shelf life and analytical test results. In response, we moved to moisture-barrier packaging and implemented controls on warehouse humidity. This led to sharp declines in customer-reported variance and allowed for longer guaranteed shelf lives.

    Why These Approaches Matter: Supporting Reliable Science and Industry Growth

    L-Methionine Sulfoxide isn’t a commodity chemical to us. It represents a connection between specialized production skills and real-world application in science and health. Our technical team stays directly engaged with university research groups, protein engineering teams, and diagnostics developers who see the subtle yet substantial differences in outcome tied to product quality.

    We’ve seen advances in protein oxidation research, neurodegenerative disease models, and synthetic biology workflows where even minor impurities or configuration inconsistencies disrupt months of experiments. Over the long term, investing in process control and direct feedback keeps us agile. As demand evolves, especially in redox biology and enzyme modulation research, continuous improvement protects the trust of everyone relying on our consistency.

    Continuous Learning and Forward Steps

    Experience has proven that even experts can miss new patterns of impurity or instability. That’s why we invest in ongoing analytical method development, cross-train staff for troubleshooting, and share insights with partners in both academia and industry. While we keep pace with regulatory shifts, we value hands-on know-how above all, since real improvements come from understanding how product behavior in your lab or facility relates to every tweak we make on the production line.

    Our approach to L-Methionine Sulfoxide manufacturing means never treating any production challenge as trivial. Direct discussion with users, continual data monitoring, and never settling for industry minimums shape how we operate and improve. If issues arise, we troubleshoot rapidly—sometimes in person, sometimes by running replicated scenarios in our QA lab—until we’ve pinned down the cause and found a fix.

    Looking Ahead: Meeting New Challenges in L-Methionine Sulfoxide Applications

    Fields such as proteomics, redox biochemistry, and precision fermentation show no signs of slowing. L-Methionine Sulfoxide finds new roles each year, from advanced protein folding studies to next-generation bioactive molecule design. We pay close attention to trends emerging in preclinical and diagnostic research, always asking what product enhancements would unlock better experimental outcomes or reduce hassle for our customers.

    Solubility, trace impurity control, and long-term storage stability remain the pillars of our continuous improvement efforts. Each feedback cycle adds a new layer of manufacturing discipline, data evaluation, or customer support expertise. Our dedication stems from a simple recognition: reliable specialty chemicals drive progress, and every batch reflects years of practical lessons carried forward.

    Closing Thoughts

    L-Methionine Sulfoxide remains a focal point in our specialty product portfolio, both for the technical challenge it presents and the impact it delivers downstream. By listening, adjusting, and investing in process and quality at every step, we aim to meet the evolving needs of everyone using this product. The lessons we’ve learned in production, quality improvement, and partnership don’t just stay within our factory doors—they travel along with each container we ship, ensuring that reliable chemistry supports reliable science.