Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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D-Cystine

    • Product Name D-Cystine
    • Alias Cystine
    • Einecs 222-048-3
    • 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
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    Specifications

    HS Code

    594388

    Product Name D-Cystine
    Chemical Formula C6H12N2O4S2
    Molecular Weight 240.30 g/mol
    Cas Number 56-89-3
    Appearance White crystalline powder
    Solubility In Water Slightly soluble
    Melting Point 247-249 °C (dec.)
    Optical Activity [α]D20 -224° (c=1, 6M HCl)
    Purity ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed

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

    Packing & Storage
    Packing White, sealed plastic bottle labeled "D-Cystine, 25g" with hazard symbols, batch number, product code, and storage instructions printed clearly.
    Shipping D-Cystine is shipped in tightly sealed containers to ensure product integrity and prevent contamination. It is stored and transported at ambient temperature, away from moisture and incompatible substances. Proper labeling and documentation accompany the shipment to comply with regulatory standards and safety guidelines. Handle with care using appropriate protective equipment.
    Storage D-Cystine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at room temperature (15–25°C), and away from incompatible materials such as strong oxidizers. Ensure proper labeling of the storage container, and follow all relevant laboratory safety protocols when handling the chemical to maintain its stability and prevent contamination.
    Application of D-Cystine

    Applications of D-Cystine in Industrial Manufacturing

    As the direct manufacturer, we supply D-Cystine to a range of specialized industrial sectors that demand high standards of raw material quality, traceability, and batch-to-batch consistency. Below, we detail its most prevalent applications, unique compliance requirements, processing integration points, recommended formulation ratios, and the nature of finished products in each sector.

    1. Active Pharmaceutical Ingredient (API) Manufacturing – Chiral Intermediate for Synthesis

    Pharmaceutical process chemists incorporate D-Cystine as a critical chiral precursor in the stereospecific synthesis of certain APIs, including d-enantiomer based peptidomimetics and protected cysteine analogs for advanced small molecule drugs. Stringent industry documentation, handling, and traceability requirements apply due to the role this material plays in controlled regulatory environments.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • USP-NF monographs (when D-Cystine is referenced as impurity profile ingredient)
    • European Pharmacopoeia (Ph. Eur.)
    • FDA Drug Master File (DMF) submissions where applicable

    Typical usage ratio

    • 0.1% to 2% of overall reaction mass, proportion varies according to target chiral purity; adjusted based on process yield and enantiomeric excess requirements.

    Downstream process integration

    • Enters synthesis workflow as a protected amino acid for intermediate stages in API assembly; subjected to reduction, salt formation, or derivatization before final isolation.

    Final product types

    • Chiral APIs for generic and branded pharmaceuticals
    • D-Peptide therapeutics and modified peptide actives
    • Small molecule intermediates for oncology and CNS drugs

    2. Peptide and Oligonucleotide Synthesis – Peptide Chain Construction

    Custom peptide synthesis operations rely on D-Cystine for constructing D-form disulfide linkages, enhancing structural resistance to proteolysis and extending peptide half-life for research-grade and, increasingly, clinical peptide modalities. Trace impurity control and precise stereochemistry are prioritized for this downstream scenario.

    Industry compliance standards

    • ISO 9001:2015 for quality management in custom synthesis
    • Shanghai Institute of Biological Sciences Peptide Synthesis Norms
    • IFSET (International Federation of Synthetic Peptide Producers) guidelines
    • Contract Analytical Testing for enantiomeric purity (HPLC/Chiral LC-MS)

    Typical usage ratio

    • 0.5 to 2.2 equivalents per mole of target peptide, modified per sequence design for cyclization or terminal D-cysteine incorporation.

    Downstream process integration

    • Fed into solid-phase or solution-phase peptide assembly cycles after initial Fmoc/Boc protection; undergoes subsequent deprotection and controlled oxidative folding steps to establish disulfide bridges.

    Final product types

    • Peptide research tools and reference standards
    • D-form stabilized peptide drugs and vaccine candidates
    • Labelled peptides for proteomics and metabolic research

    3. Cosmetic Active Ingredient – Functional Additive for Hair Treatment Formulations

    Personal care and hair cosmetic manufacturers introduce D-Cystine to premium formulations aimed at promoting hair strength, structural repair, and unique claims for keratin reinforcement. Its role as a bioactive amino acid supports specific claims in damage repair and anti-breakage lines, requiring careful compliance checks in each target market.

    Industry compliance standards

    • EU Cosmetic Regulation (EC) No. 1223/2009
    • U.S. FDA Voluntary Cosmetic Registration Program (VCRP)
    • China National Medical Products Administration (NMPA) filing
    • IFSCC Microbiological and Quality Guidelines for peptides and amino acids in cosmetics

    Typical usage ratio

    • 0.01% to 0.10% by weight in finished hair serums, masks, or conditioners, with adjustments based on local pre-market safety studies and formulation compatibility.

    Downstream process integration

    • Added post-emulsion as a water-phase ingredient; typically combined with reducing/oxidizing agents to control disulfide content before final blending and packaging.

    Final product types

    • Repairing and anti-breakage hair masks
    • Professional salon keratin treatments
    • Nutricosmetic hair care lines

    4. Food Amino Acid Additive – Nutritional Supplement Manufacturing

    Functional food and dietary supplement producers utilize D-Cystine in specialized formulations that require enantiomeric purity, including research products and limited-use nutritional blends. Careful adherence to food additive regulations and ongoing monitoring of global ingredient approval lists remains essential.

    Industry compliance standards

    • Food Chemicals Codex (FCC)
    • Codex Alimentarius INS Additive Listings
    • China GB 2760 Food Additive Standards (as permitted ingredient or functional analog)
    • EU Novel Food Regulation (EC) No. 258/97 where D-form amino acids are classified as novel

    Typical usage ratio

    • 0.01% to 0.05% by weight in finished blend; fraction is set by total daily intake recommendations and cumulative amino acid profile constraints per national health authority limits.

    Downstream process integration

    • Blended into premix powders prior to granulation or encapsulation; validated with homogeneity testing and monitored for racemization and residual solvent content prior to packaging.

    Final product types

    • Nutritional premixes for clinical research
    • Amino acid supplement capsules and tablets
    • Medical food blends for metabolic studies
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    Certification & Compliance
    More Introduction

    D-Cystine: Quality and Reliability from a Direct Manufacturer

    Deep Roots in Amino Acid Chemistry

    Working with amino acids for decades, I have witnessed the ever-increasing demand for precise, high-purity ingredients in food, pharmaceutical, and personal care industries. D-Cystine, the product of careful engineering and efficient process control, stands as one of the most essential building blocks in our line-up. Each batch of D-Cystine comes from a finely tuned fermentation and purification process, designed to meet the stringent requirements our customers face in their regulated industries. With our roots firmly planted in the science—steadfast production management, skilled technicians, rigorous testing on every run—our D-Cystine keeps delivering the consistency and purity that end users need, year after year.

    Understanding D-Cystine: Model, Appearance, Specification

    D-Cystine, chemically known as the d-enantiomer of cystine, offers a unique profile. As a white or off-white crystalline powder, it carries the molecular formula C6H12N2O4S2 with a molecular weight of 240.3 g/mol. Our standard material, Model D-Cys-99, features an assay (HPLC, anhydrous basis) no less than 99%. Moisture content holds under 0.5%. Specific optical rotation falls in the range of -222° to -229°. We watch for impurities, keeping heavy metals below 10 ppm and residues of solvents or organic volatiles under defined thresholds set by international monographs and client needs.

    Each customer appreciates a tightly controlled product, so we invest heavily in systems that guarantee traceability, documentation, and real-time quality checks at every stage. That’s not a claim; it’s how we operate, stemming from hard lessons about what happens when oversight slips. Not all D-Cystine is equal, and we keep ours sharp, with regular method validations and cross-lab verification of analytical methods to avoid drift in specifications.

    The Unique Characteristics of D-Cystine

    Down on the production line, staff recognize the peculiarities of D-Cystine’s crystallization and its distinct sulfur-containing odor. Quality is never a theoretical discussion here—it manifests in how easily the compound dissolves, how strongly it resists contamination, and how little batch-to-batch variation you’ll encounter. Sometimes, new buyers expect D-Cystine to behave like L-Cystine or DL-Cystine due simply to the shared root of the name; in practical use, D-Cystine’s stereochemistry lends it unique reactivity and selectivity in both chemical synthesis and biological applications.

    We never take surface appearance or certificate data at face value without thorough verification. Years ago, receiving lots from other vendors, we ran into issues—unstable color, pockets of insoluble material, off-spec impurity peaks. Now, every incoming raw material, every batch of finished product, undergoes a stepwise evaluation protocol. If we spot differences in crystal habit, discoloration, or even a faint change in odor, we dig deeper to prevent downstream failures.

    Why D-Cystine Matters: Real-World Uses

    Our customers rarely buy D-Cystine in isolation; they select it for a very specific role—supporting peptide synthesis, providing a sulfur bridge in custom pharmaceuticals, or acting as a chirality source in research laboratories. Formulators in the drug industry rely on the unambiguous stereochemistry for targeted reactions. D-Cystine appears in some novel peptide APIs, injectables, and occasionally as a specialty supplement intermediate, tracing the link between sulfur metabolism and metabolic pathways. Our bulk shipments typically go to peptide manufacturers, contract research organizations, and campus-based research teams, all demanding a pure, defined molecule with minimal variability.

    Food technologists use D-Cystine less often than its L-form cousin, but some niche fermentation blends and function-specific additives—especially in high-concept sports nutrition and scientific diets—employ the D-enantiomer for its interaction with enzymes and metabolic modifiers. Academic teams studying enantioselectivity in biochemical pathways ask us to customize D-Cystine for challenging reaction schemes. In personal care, select brands commission D-Cystine for hair and skin products—although L-form finds broader acceptance, a few formulations specify D-Cystine for its distinctive contribution.

    From Manufacturing Perspective: Delivering Beyond the Standard

    Years in the business have shown me that speed and transparency in manufacturing make all the difference. We process D-Cystine at our own facility, so adjustments—whether to particle size, dryness, or even packaging—start and finish under our roof. That means data doesn’t get lost in translation and end users get the clarity they need on identity, batch history, and safety.

    During scale-up, handling sulfur dioxide and controlling pH are real-world concerns that manufacturers, not resellers, intimately understand. We monitor temperature and time at crystallization, then employ repeated washing for salt-free product. Final lot release includes a chromatographic fingerprint cross-checked with reference standards and historical lots. Any deviation triggers a full-scale review—no exceptions, no “close enough” mentality.

    Clients sometimes bring challenging requests: higher solubility, ultralow endotoxin levels, specific granule size for advanced formulations. Thanks to our direct control, we can revalidate process steps, invest in new equipment, or run pilot-scale experiments to deliver on those requirements. When major API or cosmetic ingredient houses audit our facility, we prepare real-time data access—full electronic batch history, in-process controls, and real sample remnants. That level of transparency fosters trust far more than a polished brochure or wordy certificate of analysis.

    Facing the Challenges: Why Quality Matters

    The world of amino acid manufacturing has shifted. Legal thresholds on trace solvents, elemental impurities, and genetic provenance continue rising. Meanwhile, demand from clinical trial sponsors and regulatory agencies means no room for shortcuts. Some competitors cut corners, offering “D-Cystine” sourced by blending DL-Cystine and claiming D-purity by calculation. We insist on genuine enantiomeric purity—confirmed by chiral HPLC—since subtle stereochemical contaminants can derail advanced syntheses or biological systems, rendering a costly project useless.

    A few years back, an industry customer suffered an expensive product recall. We dissected the issue—off-ratio D/L content, missed during incoming quality checks from a third-party supplier. Subsequent syntheses failed, and correcting the problem took not just product replacement but months of rebuilding trust. Cases like this remind us why direct manufacturing, with unbroken chain of custody and constant oversight, pays long-term dividends. As regulations and customer expectations continue rising, slack manufacturing approaches stand out quickly—and rarely in a good way.

    How Our D-Cystine Stands Apart from Market Alternatives

    Many products look identical on a spec sheet. In practice, D-Cystine produced through controlled fermentation and gentle crystallization runs circles around bulk commodity material. We refuse to buy from zone-refined, poorly characterized intermediates. The difference reveals itself in sharp melting points, reliable chromatographic runs, and almost zero off-odor—traits that downstream partners in the pharma and biotech spheres recognize instantly.

    What sets ours apart isn’t a proprietary label or licensing trick—it’s the commitment to eliminating the sources of process drift and impurity creep. Small particles, trace metal content, and solvent residues, imperceptible to most, manifest in skipped reactions and slow regulatory reviews. Our in-house controls, multi-stage washing protocol, and regularly audited downstream handling help us avoid those pitfalls. Without those processes, “commodity” D-Cystine often tops allowable impurity limits or shows up with inconsistent chirality, leading to slowdowns in synthesis or rejected lots at the client’s end.

    Direct feedback from repeat buyers often mentions not just purity, but how batches match each other—reaction times stay steady, yields go up, failures all but disappear. We keep a detailed record of client outcomes and use those data to tighten our own process—iteratively, not through grand gestures but steady, relentless improvement. That’s how a direct manufacturer keeps D-Cystine competitive.

    Industry Trends: Why Manufacturers Must Stay Engaged

    Looking at the broader landscape, demand for amino acids continues trending upwards, with a sharper focus on molecular chirality. Synthetic biologists, pharmaceutical formulators, and advanced material researchers are driving this demand. A few years ago, high purity D-Cystine sold in kilograms; now, some clients need hundreds of kilograms monthly for clinical programs, research, and new product launches. The need for process rigor and traceability grows, and we see regulators pushing for even stricter control on all chiral intermediates in medical and nutritional manufacturing.

    Switches in manufacturing methods influence everything—fermentation-based systems save energy and reduce reliance on petrochemical feedstocks, but they introduce new process variables to control. Only manufacturers with integrated process management, real-time data monitoring, and staff who know amino acid chemistry from the inside keep up the pace and keep delivering to the expectations of a changing market. We invest in staff development, not just compliance checklists, because hands-on understanding prevents mistakes better than rules alone.

    Our R&D team stays engaged, watching client use-cases and shifting internal targets as soon as new regulatory guidance appears or a customer application surfaces something new. Experimentation stays grounded in client feedback and real-world results—not wishful thinking, but persistent iteration. That approach keeps our D-Cystine aligned with not just standards, but the demands of tomorrow’s peptide developers and life science innovators.

    Supporting the Next Generation of Researchers and Innovators

    Our onsite support team fields questions every week from startups, academic labs, and emerging pharma companies trying D-Cystine in new ways. We provide detailed product histories and batch characteristics, not a generic fact sheet. Those conversations point us to new applications—such as protein refolding experiments or metabolic labeling studies. While not all those ideas turn into large-scale projects, they push us to adapt equipment, scale, or documentation practices so even the most demanding clients get what they need.

    By handling our own manufacturing, we can give researchers full visibility into where their D-Cystine comes from and how it matches up with both industry-leading standards and their internal requirements. That transparency and willingness to listen help us attract and keep clients through multiple research cycles. Their breakthroughs drive us to refine our process—a positive feedback loop built on expertise, not commoditization.

    How Packaging, Delivery, and Traceability Aid Quality Assurance

    At our plant, packaging is more than just a container—it’s a final product characteristic. We monitor every packing run for tight moisture seals, proper liner type, and correct batch labeling. Shipping partners change as needed, but our own internal team controls product handoff and final destination checks. For critical GMP lots, we track material throughout the supply chain, ensuring verified arrival with all COAs, shipping manifests, and safety information intact.

    Clients ask about trace elements, allergens, and origin, especially those exporting finished goods to North America, Europe, or other regulated markets. Our team provides this information readily, supported by full-lifecycle data. A mislabel or mistaken origin can stop an export in its tracks or trigger costly requalifications. Internal traceability systems, designed years ago, now form the backbone of our compliance and client assurance programs. That, in itself, differentiates a responsible manufacturer from those trading on short-term margin.

    Building Relationships in Chemical Manufacturing: Trust Through Actions

    Day in, day out, chemical manufacturing’s not about selling the shiniest pitch—it's about being a reliable, clear-eyed partner. We know researchers and product formulators placing an order measure value through successful experiments, seamless pilot lots, compliant documentation, and products that don’t surprise them with unwanted deviations. Our team still handles every major client with direct communication, offering not only technical assurance but the ability to explain why a batch might slightly differ, and how those adjustments tie back to improved process controls or better performance in application.

    Food, pharma, and personal care deliverables all rest on supply that people can count on—not just for what they’re making today, but for the next formulation or product launch. Our reputation as a direct manufacturer working in the open means that we listen to feedback, own up to rare missteps, and push improvements through quickly. Over time, that accountability earns more business than the lowest price ever did.

    Looking Ahead: The Evolving Landscape for D-Cystine

    The next few years will see new production technologies, tighter audit standards, and more discerning buyers. We see advances in fermentation biology—potential for greener, higher yielding routes to D-Cystine that don’t add regulatory risk. At the same time, medical device, nutraceutical, and pharmaceutical firms plan launches depending on chirally pure intermediates. D-Cystine, with its tight niche but broadening appeal, isn’t likely to become a commodity ingredient, no matter the scaling innovations. Each market application carries different risks, and we keep investing in our analytics, people, and facilities to stay ahead.

    Operating as the direct manufacturer, our focus stays on improvement and clear communication. Uncertainty doesn’t help anyone when you’re working with sensitive projects or new molecule launches. By keeping manufacturing local, well-controlled, and expertly managed, we provide D-Cystine as clients expect it—precise, clean, reliable, and free from the ambiguity that often drags progress down.

    In sum, D-Cystine forms just one part of our amino acid catalog, but it stands out as a benchmark for what chemical manufacturing can achieve: deeply technical, shaped by decades of boots-on-the-floor experience, and trusted by sophisticated partners who recognize the value of expertise. As uses expand and market demands evolve, D-Cystine’s track record as a reliable, traceable, and precisely manufactured ingredient keeps it essential to both traditional and next-generation applications.