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(S)-(-)-2-Methyl-2-Propanesulfinamide

    • Product Name (S)-(-)-2-Methyl-2-Propanesulfinamide
    • Alias Ellman's Reagent
    • Einecs 629-674-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    422022

    Chemical Name (S)-(-)-2-Methyl-2-Propanesulfinamide
    Cas Number 82508-12-5
    Molecular Formula C4H11NOS
    Molecular Weight 121.20
    Appearance White to off-white solid
    Melting Point 110-114°C
    Optical Rotation [α]D20 -54° (c=1, CHCl3)
    Purity Typically >98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Inchi Key CTPPEJXAWCKTSB-SCSAIBSYSA-N
    Smiles CC(C)(C)S(=O)N

    As an accredited (S)-(-)-2-Methyl-2-Propanesulfinamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (S)-(-)-2-Methyl-2-Propanesulfinamide is supplied as a white solid in a tightly sealed amber glass bottle, 5 grams.
    Shipping (S)-(-)-2-Methyl-2-Propanesulfinamide is shipped in a tightly sealed container, protected from moisture and light. It is handled according to standard regulations for transporting chemicals, ensuring stability and safety during transit. Proper labeling, documentation, and, if required, temperature control are maintained to prevent contamination or degradation throughout shipping.
    Storage (S)-(-)-2-Methyl-2-Propanesulfinamide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, moisture, and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and store at room temperature or as specified on the product label to maintain stability and prevent degradation.
    Application of (S)-(-)-2-Methyl-2-Propanesulfinamide

    Applications of (S)-(-)-2-Methyl-2-Propanesulfinamide in Industrial Manufacturing

    (S)-(-)-2-Methyl-2-propanesulfinamide serves as a key chiral auxiliary in asymmetric synthesis across several specialized chemical sectors. As a manufacturer, we provide this material with consistent optical purity and tight batch control. Below, we detail core application segments based on current industrial practices.

    1. Chiral API Intermediate Production in Pharmaceutical Synthesis

    Pharmaceutical manufacturers use (S)-(-)-2-methyl-2-propanesulfinamide as a chiral auxiliary to prepare enantiomerically pure intermediates, particularly for active pharmaceutical ingredients (APIs) targeting CNS, cardiovascular, and oncology drugs. The sulfinamide ensures precise stereochemistry during asymmetric synthesis, especially for amine building blocks, beta-amino acids, and macrocyclic structures. QC departments rigorously monitor enantiomeric excess and residual levels in intermediates. Production teams integrate the material into early or mid-stage synthetic steps demanding controlled stereoselectivity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for chiral purity
    • USP/NF Synthesis of chiral amines guidance sections
    • FDA 21 CFR Part 211 cGMP for finished pharmaceuticals

    Typical usage ratio

    • Ranges from 1.0 to 1.2 molar equivalents relative to the target substrate
    • Potential excess of up to 10% by moles to ensure full conversion in cases of competing side reactions
    • Adjusted based on yield and recovery efficiency of chiral auxiliary

    Downstream process integration

    • Introduced during reductive amination, alkylation, or cyclization steps
    • Removed post-reaction via acid/base extraction or chromatographic purification
    • Monitored using chiral HPLC for residual auxiliary and product purity

    Final product types

    • Chiral amino acid building blocks
    • Optically pure amine API intermediates
    • Non-racemic small-molecule drug precursors
    • Chiral auxiliaries for further multistep syntheses

    2. Agrochemical Active Ingredient Synthesis

    Leading agrochemical producers utilize (S)-(-)-2-methyl-2-propanesulfinamide to establish stereocenters in the synthesis of biologically active compounds for crop protection. The material facilitates the generation of chiral amines and heterocycles required for selective herbicides and fungicides. Technical teams validate the process through regular GC and NMR analysis to confirm stereoselectivity and minimize formation of undesired enantiomers.

    Industry compliance standards

    • ISO 9001 Quality Management System for chemical manufacturing
    • REACH registration for chemical raw materials in agrochemical applications (EU)
    • OECD Guidelines for the Testing of Chemicals
    • National agrochemical regulatory authority requirements (China, EPA-US, EFSA-EU)

    Typical usage ratio

    • 0.8–1.2 molar equivalents, depending on target molecule and batch yield
    • Process optimization may reduce ratio by recycling recovered auxiliary

    Downstream process integration

    • Added at chiral synthesis stage of precursor assembly
    • Excised after introduction of target chirality via acid/base extraction
    • Integrated with inline monitoring for residual chiral auxiliary

    Final product types

    • Chiral pyridyl compounds
    • Amine-substituted triazoles
    • Optically active heterocyclic intermediates for selective herbicides
    • Building blocks for fungicide actives

    3. Fine Chemical Synthesis for Specialty Materials

    Producers of specialty chemicals—especially those manufacturing advanced polymers and electronic chemicals—apply (S)-(-)-2-methyl-2-propanesulfinamide to obtain optically pure amines and nitrogen heterocycles. These intermediates play essential roles in liquid crystal material production, optoelectronic polymer synthesis, and custom advanced materials. Close management of enantiomeric ratios is key for downstream performance specifications.

    Industry compliance standards

    • ISO 14001 Environmental Management for specialty chemical production
    • ISO 9001 Quality Management systems
    • Custom supply chain audit requirements for semiconductors and display sector

    Typical usage ratio

    • 0.9–1.1 molar equivalents, calculated relative to the key functionalized substrate
    • Modified in high-complexity syntheses based on impurity profile

    Downstream process integration

    • Added during key amination and heterocyclization steps
    • Subsequently cleaved to yield chiral amine intermediates
    • Recovered or removed by selective extraction or crystallization

    Final product types

    • Advanced liquid crystal intermediates
    • Chiral additives in optoelectronic materials
    • Specialized polymers with chiral side chains
    • Precursor molecules for electronic chemical synthesis

    4. Contract Manufacturing of Research-Grade Chiral Compounds

    Contract research and manufacturing organizations (CROs and CMOs) depend on (S)-(-)-2-methyl-2-propanesulfinamide for pilot and small-scale production of custom chiral amines. These clients require precise control over stereochemistry for evaluation in biomedical, flavor, fragrance, and catalyst research programs. Reliable batch traceability and full document support form part of supply agreements.

    Industry compliance standards

    • ISO 9001 certified Quality Management processes
    • Project-driven documentation and material traceability (as per customer contract)
    • GLP (Good Laboratory Practice) compliance for research materials
    • Regular supplier audits as per CMO/CRO protocols

    Typical usage ratio

    • 1.0 molar equivalent for core synthesis
    • Adjustable between 0.95–1.1 based on analytical confirmation and customer requirements

    Downstream process integration

    • Utilized in small-batch asymmetric syntheses, often with full analytical workup
    • Recovery and purification protocols established per compound
    • Batch-level certification and COA provided for each order

    Final product types

    • Research-scale chiral amines and amino alcohols
    • Building blocks for catalyst evaluation
    • Intermediates for fragrance and flavor research
    • Specialty ligands for chemical development
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    Certification & Compliance
    More Introduction

    (S)-(-)-2-Methyl-2-Propanesulfinamide: Supporting Precision in Modern Synthesis

    Product Introduction

    Our daily focus at the production site commonly revolves around meeting the strict demands of pharmaceutical manufacturing, and few fine chemicals have reshaped our thought process as much as (S)-(-)-2-Methyl-2-Propanesulfinamide. The molecule—sometimes referenced as (S)-t-Butanesulfinamide by researchers and synthetic chemists—offers not just a core for imine synthesis, but also a reliable foundation in the pursuit of single-enantiomer products. We recognize the ongoing challenge of balancing purity with scale, especially when process chemists demand precise stereochemistry. Our role goes beyond producing a chemical to ensuring that the integrity of each batch supports reliable outcomes throughout development pipelines.

    In our hands, consistent manufacture of (S)-(-)-2-Methyl-2-Propanesulfinamide means maintaining not only high enantiomeric excess—often exceeding 99% ee—but also offering material with a minimal residual solvent fingerprint and low levels of trace impurities. Since early 2000s, our plant has continually improved both optical resolution steps and final purification sequences for this sulfinamide, leveraging both chromatographic and crystallization methods to avoid racemization.

    Model and Specifications: Built for Demanding Applications

    This chiral auxiliary has carved out an essential role in establishing stereocenters within pharmaceutical candidates and agrochemicals. Our standard specification delivers crystalline white powder, typically at 99% chemical purity with controlled moisture content and confirmed by both HPLC and chiral analysis. GC-MS and FTIR verification augment our release process, reflecting our work ethic shaped by countless hours resolving production bottlenecks. Based on years of user feedback, we took deliberate steps to optimize the batch filtration system, which lets us minimize fine particulates that sometimes hampered downstream synthetic yields.

    Each production lot receives thorough identity checks including specific optical rotation measurements, which help chemists confirm that they are indeed working with the desired (S)-enantiomer rather than the racemate or the (R)-isomer. Our team runs additional tests on select lots to verify trace metals and residual base, so that end-users face fewer complications in multistep transformations, particularly in Grignard additions to the resulting sulfinimines.

    Usage in Synthesis: Ground-Level Problem Solving

    Reflecting on our own experience, (S)-(-)-2-Methyl-2-Propanesulfinamide has come to represent a practical solution for asymmetric amine construction. Chemists regularly employ it as a nitrogen source, first condensing with aldehydes or ketones to yield chiral N-sulfinyl imines. What looks straightforward on paper often turns into a juggling act at scale, as these condensation steps demand dry conditions and carefully controlled pH. During early development, we modified our drying protocols and solvent swap approaches to anticipate these challenges—cutting out pre-drying inefficiencies to help users jump straight into their synthetic work.

    When handed over to the hands of a skilled chemist, this sulfinamide can impart a chiral auxiliary effect, steering the approach of organometallic nucleophiles. We’ve seen our customers in pharmaceutical R&D, both local generics manufacturers and global innovators, leverage our product in multi-kilogram scale syntheses, using it to push asymmetric induction as far as possible before cleaving off the auxiliary. The cleavage step itself underscores several essential features: our batches allow for mild acidic or basic deprotection, and the process produces no toxic byproducts, supporting green chemistry priorities.

    The success stories and troubleshooting calls we’ve handled over the years taught us which solvent systems work best, and which purification strategies make sense with our specific product quality. Some customers want consistent melting points for direct crystallization from the reaction mix, while others emphasize ultra-low water content to avoid hydrolysis. We adapt both product and documentation support to these points rather than applying a one-size-fits-all philosophy.

    Differences from Other Chiral Sulfinamides and Auxiliaries

    The global market offers several chiral auxiliaries designed for imine synthesis, yet (S)-(-)-2-Methyl-2-Propanesulfinamide finds favor in large part because of its unique steric and electronic properties. Compared with (R)- or (S)-tert-butylsulfinamides from other suppliers, our route delivers not just high enantiopurity but also robust physical stability during shipping and storage. We learned field testing matters a great deal: products meant to travel great distances, sometimes through climates ranging from sub-zero container shipping to equatorial heat, need a crystalline form that resists caking and degradation.

    In practice, other chiral auxiliaries like Ellman’s sulfinamide analogs, camphorsulfonic imines, or even enzymatically derived auxiliaries may offer niche advantages in particular transformations, but the high bulk stability and relatively simple deprotection protocols of our product have reduced supply headaches for both academic and industrial customers. Unlike some chiral diamines, which require complex handling or produce hazardous byproducts, the process friendly nature of 2-methyl-2-propanesulfinamide helps a wider user base stick to their project timelines.

    Alongside differences in stereochemical outcome control, we've also noted practical cost savings through reduced waste in neutralization and workup steps—directly tied to the solubility profile and mechanical filtration characteristics of our batches. Each time we adjust for customer feedback, such as shifting to different sieve grades or fine-tuning the crystallization solvent, we put those learnings back into regular process adjustments.

    Understanding Customer Challenges: Batch Reliability and Documentation

    Our years at the reactors have convinced us that reliability at kilo and multi-kilo scale hinges on more than analytical results. Reliable batch-to-batch consistency cannot be separated from proper documentation, robust deviation handling, and tight process control on every shift. What often separates manufacturers from resellers or brokers is the day-to-day hands-on work of isolating and characterizing off-spec lots long before delivery.

    We’ve built our operation to meet GMP-relevant standards, making full use of electronic batch records, trained QA chemists, and a responsive support team. For customers in regulated industries, we stand ready with full product dossiers, audit trail data, and regulatory support statements on request. Regulatory inspections have helped us refine both the manufacturing process and the internal culture of openness that lets us present accurate, timely information to customers facing stringent internal reviews.

    It is this immersion in the details—often long after the last shift has gone home—that keeps our product relevant in fast-moving areas like medicinal chemistry, where a single out-of-spec batch can delay entire clinical development timelines.

    Environmental Responsibility and Process Safety

    Operating as a chemical manufacturer in today’s world brings with it the responsibility not only to customers but also to our staff and surrounding community. Our production plant operates under ISO-based environmental guidelines, and we have invested in solvent recovery and filtration improvements specifically for the (S)-(-)-2-Methyl-2-Propanesulfinamide campaign. Our efforts to optimize chromatography columns, reduce fugitive dust, and manage container rinsates stem from the real-world challenges faced by plant operators.

    Minimizing waste solvent streams—particularly hazardous organics—sits alongside our efforts to raise staff safety awareness. Training covers not only material handling and emergency response but also real situations that arise in drum transfers, day tank operations, and quality control labs. Supporting sustainability means working with auditors to track improvements in energy use per kilogram produced and investing in technologies that make both people and product flows safer.

    Building Ingredients for Innovation

    We recognize our place within a supply chain driven by both the needs of today's researchers and the shifting requirements of regulatory authorities. Feedback from end users in Europe, North America, and Asia has shaped our ongoing improvements not just in manufacturing robustness but also in support for customer troubleshooting. Every month, our technical support team reviews production notes, new analytical results, stability trends, and field queries to identify areas needing further research or process refinement.

    Pharmaceutical and agrochemical innovators depend on access to starting materials with well-documented origins, low impurity profiles, and the resilience not to break down in unplanned hands-on use. We’ve tailored our shipping packs to support those needs with moisture-barrier protection and tamper-evident seals. These measures deliver predictability and reduce downtime for development labs that cannot afford material shortages.

    In developing our version of (S)-(-)-2-Methyl-2-Propanesulfinamide, we make continual use of real customer case studies—sometimes working with clients to co-develop new applications or solve bottlenecks in asymmetric synthesis. This collaborative process often yields stronger technical bulletins, faster troubleshooting, and in several cases, joint publications within the scientific community. The mutual exchange of experience, both at the benchtop and at scale, enriches our capacity to respond quickly and efficiently to evolving user needs.

    Navigating Supply Chain Volatility

    Producers today face unexpected challenges caused by global shipping disruptions, raw material shortages, and shifting regulatory landscapes. Our internal supply chain team tracks the availability of key starting materials, carefully evaluating alternative sources in the event of geopolitical instability. For (S)-(-)-2-Methyl-2-Propanesulfinamide, this also means periodically reassessing our upstream partnerships for supply security, while strengthening our own inventory management know-how.

    From the beginning, we avoid speculative buying or stockpiling that can introduce risk. Instead, our forecasting relies on real purchase orders from both recurring clients and new buyers scaling up synthetic campaigns. Batch reservation options, advance scheduling, and multi-month delivery planning all rely on clear communication—both ways—in a market where a delayed precursor shipment might set production back by weeks or months.

    In tight markets, smaller users can lose out to larger procurement offices. We take steps to reserve dedicated lots for long-standing clients and honor framework agreements—helping R&D projects stay on schedule in sectors where a missed deadline can affect patient enrollment or regulatory submissions.

    Technical Support: Bridging the Gap Between Bench and Plant

    Providing high-quality chemicals by itself only solves part of the challenge for our users. Many of our customers value real-time technical feedback and troubleshooting beyond standard datasheets. We pride ourselves on maintaining a full-time team with bench and plant experience, equipped to answer questions on reaction optimization, scale-up bottlenecks, and even custom packaging needs.

    Requests often range from solvent series recommendations for imine formation, to optimal conditions for storage or recovery of unreacted sulfinamide. Our archives include years’s worth of field case studies, which inform present-day practice and help us identify patterns that can indicate a need for process adjustments—not only for our product, but also for user campaigns where a minor change in physical properties can cascade into workflow delays.

    Setting Quality Standards Through Direct Production

    By retaining full control of our process from raw material intake through final packaging, we built up a deeper understanding of molecular consistency and reliability. Every cycle in our reactors tells us something about process drift, unintended byproduct risk, or the potential for a better workup method. Where other market participants source material from brokers or indirect vendors, we track improvements and incidents directly on the plant floor—closing the loop between synthesis, QC, and customer outcomes.

    Our documentation includes in-process photos, batch logs, environmental monitoring results, and deviation reports. We maintain a practice of batch retention so that we can reference each production campaign, and regularly participate in proficiency testing to benchmark our analytics against leading laboratories worldwide.

    We regularly review feedback from both small startups and large multinational clients, using it to drive corrective actions, retrain staff, or adapt our process. This open loop, hands-on approach distinguishes direct manufacturers from hands-off traders or distributors.

    Continuous Improvement and Staying Ahead

    Our culture prizes ongoing learning, both at the production line and in technical support. Manufacturing (S)-(-)-2-Methyl-2-Propanesulfinamide teaches the value of process discipline, detail orientation, and direct dialogue between chemists, site engineers, and analysts. By fostering this environment, we reduce both defect rates and the risk of unanticipated problems at the user end.

    Improvements are often driven by direct plant observations—like noting the impact of agitation speed on crystallite size, or identifying a solvent blend that optimizes both purity and yield. These changes appear small, but over time they drive notable gains in product quality and user satisfaction.

    We monitor trends both in scientific literature and in industry best practices, making time in our annual schedule for staff development, site audits, and technology upgrades. Each learning feed—whether from an operator's report, a failed batch, or a success story from an international customer—acts as fuel for the next round of process optimization.

    Conclusion: Trust Born of Attention to Detail

    Delivering (S)-(-)-2-Methyl-2-Propanesulfinamide to users across the globe means understanding the chemical, the process, and the people counting on both. Every kilo departs our gates as the sum of lessons, not the result of formulaic batch execution. The highest purity, consistent crystalline structure, and reliable chiral induction properties reflect more than technical capability; they emerge from direct manufacturing experience and an ongoing commitment to safety, transparency, and practical customer service.

    Our aim is consistent: provide a dependable foundation for asymmetric synthesis, anticipating—not just responding to—the issues that matter most to practitioners. Whether the goal is a new pharmaceutical candidate, an agrochemical innovation, or another application requiring asymmetric amine synthesis, our product reflects the reality of manufacturing in a world that prizes precision, responsiveness, and demonstrated trustworthiness.