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D-Dopa

    • Product Name D-Dopa
    • Alias 3,4-Dihydroxy-D-phenylalanine
    • Einecs 210-014-7
    • 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

    326208

    Product Name D-Dopa
    Alternative Names D-3,4-Dihydroxyphenylalanine
    Chemical Formula C9H11NO4
    Molecular Weight 197.19 g/mol
    Appearance White to off-white powder
    Solubility Slightly soluble in water
    Optical Isomerism D-enantiomer
    Storage Conditions Store at -20°C, dry and dark place
    Cas Number 352-06-5
    Purity Typically ≥98%
    Usage Research, reference standard
    Synonym D-(−)-DOPA
    Ph Neutral to slightly acidic in solution
    Shelf Life 2 years under recommended conditions

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

    Packing & Storage
    Packing White HDPE bottle with blue screw cap, labeled "D-Dopa, 10 grams," featuring hazard symbols and chemical information in black text.
    Shipping D-Dopa is shipped in tightly sealed containers, protected from light, moisture, and air to maintain stability. It is handled as a chemical substance, following standard regulatory guidelines for transport. Packaging ensures safe delivery, with appropriate labeling and documentation in compliance with local and international shipping regulations for laboratory chemicals.
    Storage D-Dopa should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it at 2–8°C (refrigerator temperature) and away from incompatible substances. Store it in a well-ventilated, cool, and dry area designated for chemicals. Proper storage minimizes degradation and ensures safety and stability. Always follow institutional or supplier-specific guidelines for handling and storage.
    Application of D-Dopa

    Applications of D-Dopa in Industrial Manufacturing

    D-Dopa, produced by our proprietary enzymatic synthesis, supports demanding processing environments in several specialized industrial sectors. Downstream users rely on its consistent purity profile and performance attributes within tightly regulated applications. Below we outline primary industrial scenarios utilizing D-Dopa as an essential intermediate or additive.

    1. Pharmaceutical API Synthesis for Dopaminergic Agents

    Pharmaceutical formulators incorporate D-Dopa as a precursor in manufacturing certain dopaminergic active pharmaceutical ingredients. During process scale-up, control of optical purity and impurity levels remains critical. D-Dopa undergoes conversion via hydrogenation or enzymatic transformation steps, forming APIs integrated in treatments for neurological disorders. Manufacturers conduct online chiral analysis throughout the synthesis train to ensure strict compliance. In addition, batch records document every raw material and conversion point according to industry cGMP guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and EP monographs (where applicable)
    • 21 CFR Part 210/211 (US FDA)
    • EMA Guidelines on process validation for APIs

    Typical usage ratio

    • D-Dopa to final API: 0.8 – 1.2 molar equivalents based on process selectivity; adjusted in each batch run according to yield and chromatographic purity instruments

    Downstream process integration

    • Introduced at the stage immediately preceding dopaminergic intermediate formation, typically in hydrogenation reactors or biocatalytic process modules
    • Flowed through in-situ conversion lines with automated pH and temperature control
    • Chromatographic purification and isolation of resulting API

    Final product types

    • Levodopa and related dopaminergic APIs for finished dosage formulations
    • Chiral pharmaceutical intermediates distributed to contract manufacturers
    • Bulk API shipments for further formulation downstream

    2. Nutraceutical Ingredient Manufacturing

    Within nutraceuticals, D-Dopa acts as a direct functional ingredient in specialty dietary supplements. Producers integrate pharmaceutical-grade D-Dopa into controlled blending systems to assure targeted release and bioavailability. Cleanroom handling and validated blending processes preserve material identity for later tableting or encapsulation. Each production lot traces back to specification through third-party testing and material audit trails in line with global nutraceutical regulations.

    Industry compliance standards

    • US FDA 21 CFR Part 111 Dietary Supplement cGMPs
    • EFSA food supplement ingredient guidelines
    • ISO 22000:2018 Food safety management systems
    • China GB 16740-2014 National Food Safety Standard for Health Foods

    Typical usage ratio

    • 0.5–5% w/w of total blend, depending on the final dosage strength and functional claims; formulation teams adjust ratio per regulatory maximums and end-user specifications

    Downstream process integration

    • Weighing and dosing into high-shear blenders fitted with dust extraction
    • Granulation as needed for direct compression or encapsulation
    • Stability tested for color, moisture, and ingredient content before packaging

    Final product types

    • Tablet and capsule supplements marketed for cognitive support and athletic performance
    • Direct-to-consumer raw powders with verified composition
    • Custom nutraceutical premixes for integrator brands

    3. Specialty Polymerization Initiator

    Chemical engineering teams use D-Dopa as a niche initiator and modifier for controlled polymerization of biomedical hydrogels. The catechol and amine groups participate in crosslinking reactions, especially for adhesives or scaffolds mimicking native tissue. Precision dosing automates the ingredient stream, requiring ROC-compliant input and analytical verification. Every lot receives QA approval against industrial material standards to ensure the final hydrogel meets medical device regulations.

    Industry compliance standards

    • ISO 13485:2016 Quality management for medical devices
    • FDA 21 CFR 820 Quality System Regulations
    • USP Class VI Biological Reactivity Tests (where applicable)
    • REACH Regulation (EC) No 1907/2006 for chemical safety

    Typical usage ratio

    • 0.1–2% w/w relative to monomer mass in hydrogel or biopolymer matrix; ratio subject to mechanical property targets and curing kinetics

    Downstream process integration

    • Metered addition into pre-polymer reaction vessel prior to crosslinking phase
    • Surface modification step for bioadhesive synthesis
    • Post-polymerization extraction and washing to remove residuals

    Final product types

    • Hydrogel wound dressings for clinical applications
    • Biocompatible adhesives used in surgical fields
    • Scaffold materials for regenerative medicine products

    4. Analytical Reference Standard Production

    Research organizations and analytical QC labs purchase D-Dopa for use as a reference material during chiral HPLC, LC-MS, and other high-sensitivity detection platforms. Material purity and traceability play a pivotal role here, as D-Dopa calibrates chromatographic response and supports instrument validation. Laboratories require documentation on lot-specific residual solvent, chiral excess, and potential isomeric breakdown products for regulatory submissions in pharmaceutical and food safety settings.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and calibration laboratory accreditation
    • USP General Chapter <621> Chromatography
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation
    • Chemical reference material guidelines (pharmacopeial and ISO)

    Typical usage ratio

    • 25–100 mg per validation run; quantity defined by instrument sensitivity, required response factor calibration, and regulatory method standards

    Downstream process integration

    • Portioned via analytical microbalance for solution preparation
    • Dissolved in certified analytical solvents for HPLC or LC-MS
    • Used as calibration and system suitability control during regulated compound assay development

    Final product types

    • Certified reference materials in ampoules or vials for laboratory calibrations
    • Calibration solutions for contract testing services
    • Regulatory method development kits for pharmaceutical QC labs
    Free Quote

    Competitive D-Dopa prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    D-Dopa: A Behind-the-Scenes Look From the Manufacturer

    Understanding D-Dopa From Experience

    For years on our production lines, we've watched D-Dopa move from raw material to finished product. Many in the industry use its chemical name—(S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid—but in our plant, everyone just calls it D-Dopa. Only a few manufacturers commit fully to the demanding protocols it takes to deliver this product at scale. We chose to specialize because we know what goes into every batch, right down to the humidity on a hot day in the packing rooms. That level of attention never comes across in a standard product listing or a third-party announcement.

    D-Dopa stands apart from the more commonly used L-Dopa. The L- isomer figures prominently in pharmaceutical therapies developed for neurodegenerative conditions—but D-Dopa carves out its own place, especially in research labs exploring enantiomeric selectivity, structure-activity relationships, or alternative synthesis routes for bioactivity assays. Large-volume producers rarely prioritize the seldom ordered enantiomer; most treat it as an occasional ask rather than a core output. That creates a gap, and over the past decade, we’ve filled it, turning out kilogram and multi-kilogram orders that don’t rely on third-party brokers or old warehouse stock.

    Product Details That Matter on the Ground

    Our standard offering brings forward D-Dopa with a purity typically above 99%. What does that high-specification truly mean? In daily shifts, we expect no sulfated or iron-based impurities, no stray peaks on a chromatogram. You hear feedback from synthetic chemists who demand those clear HPLC readings. Sometimes a fraction of a percent extra impurity sends a screening batch off the rails and weeks of effort wasted in a research pipeline. That’s the reason we push beyond minimum guidelines: each lot label includes in-house analytical data for your batch, not a recycled certificate or a generic specification sheet.

    Our D-Dopa comes in the stable, crystalline form—hygroscopic, so we pack under nitrogen with additional desiccants. Researchers using it for model reactions or biochemical assays don’t want degradation creeping in during transit or storage. Each container, whether 25 grams or a full 5-kilogram drum, leaves our facility triple-sealed after verified moisture testing. Even if a lab orders just a single small bottle, we ship using the same procedures as for a 50 kg consignment. Anyone working in process development, or scaling up from bench to pilot, can pull a sample and depend on consistent material throughout the batch.

    Real Uses for D-Dopa in the Lab and Beyond

    Some customers ask why D-Dopa draws attention at all. Its presence in nature is trace at best; it resists biological pathways that L-Dopa traverses easily. For most, it serves as a tool compound—to probe the mechanics of specific enzymes, test metabolic selectivity, or support studies that need a clear control versus the active therapeutic isomer. We’ve also shipped it to groups interested in asymmetric synthesis, university teams dissecting racemization, and industrial specialists running competitive inhibition trials. Feedback from buyers ranges from new methods for enzyme-catalyzed transformations to work on chiral resolution columns in analytical chemistry.

    In our own work, we see how D-Dopa’s differences enable science outside its pharmaceutical cousin. Because stereochemistry shapes bioactivity so sharply, access to high-purity D-Dopa lets chemists and biologists distinguish effects that standard L-Dopa can’t untangle alone. The demands for repeatability in modern research—especially with tighter funding and closer peer review—push everyone to source their materials directly, with no mixing or re-bottling in someone else’s hands. Researchers choosing D-Dopa this way make discoveries simpler to reproduce and publish with confidence.

    The Hard Facts: Manufacturing D-Dopa at Scale

    Many outside the plant assume D-Dopa simply mirrors the process for L-Dopa, just with inverted tanks or reactants. Real life, we know, isn’t so straightforward. Production pivots on stereoselective synthesis steps or adept use of chiral catalysts—options that demand skill and safe, reliable setups. Our teams rely on well-maintained glass reactors and scrupulous process controls. pH, temperature, and solvent ratios are logged daily and double-checked before scheduling. We rotate our reaction crews on a split shift: not just to keep up with demand, but to pull knowledge from those who watched last week’s run and tweak for next week’s optimization.

    Each production step—right from amino acid precursor selection to the isolation and washing of the crystalline product—happens under watchful eyes. Once, we found a supplier had changed their purification steps, sending us raw material with new trace impurities. Only years of routine analysis turned up the anomaly before final crystallization. That day, we canceled the lot, absorbed the cost, and charted a new supplier. A buyer scanning a product catalog might never see those disruptions, but from the manufacturing side, these moments decide the fate of your reliability in the long run.

    Customers alert us immediately when unusual test results surface. We support them directly, drawing on our own archived batch samples and full run history. Our own technicians, not distant third-party affiliates, handle every support inquiry. If any irregularity arises, it feeds straight back to R&D and QA for review. That culture, built over years, lets each client trust the D-Dopa crossing their facility’s threshold. It’s the only way our name has stayed at the top of preferred supplier lists for so many specialized accounts.

    How D-Dopa Differs From Other Products

    From a hands-on perspective, D-Dopa sets itself apart from both L-Dopa and broader classes of amino acid derivatives. Analytical chemists often use it to calibrate chiral detection equipment or as a test substrate in enzymatic transformations. In our lot release tests, we see its reactivity contrast sharply from racemic blends; the enantiomeric excess regularly surpasses 99%. This difference isn’t cosmetic—many reaction systems lose selectivity or yield side products if input material veers off specification. That steers synthetic teams toward source-grade D-Dopa, derived directly at the factory, not just repackaged from uncertain stocks.

    Some research teams attempt to racemize L-Dopa to produce D-Dopa as a shortcut, pushing yields using non-selective catalysts or driven temperature cycles. In our experience, these efforts often create contamination headaches and reproducibility issues. Having an authentic D-Dopa manufacturer ready with robust QA protocols saves projects weeks of cross-checking, re-purification, and method revisions. We’ve assisted partners in troubleshooting unexplained assay noise, which often traced back to minor L-isomer contamination in competitor samples.

    Unlike commodity amino acids, D-Dopa resists bulk synthesis. Its chiral specificity and lower demand drive up costs and complicate logistics. We’ve spent years perfecting routes that keep costs competitive without sacrificing purity or traceability. Our production logs show the evolution: earlier generations ran with broad pH ranges or inconsistent filtration, while current lots travel tight process specifications to hit both purity and yield targets.

    Perspective on Usage Trends and Request Patterns

    We track user requests in real time, not just from annual reviews but week to week across industries and research segments. Many buyers run specific screening platforms—biochemical, analytical, or metabolic profiling—where D-Dopa functions as a calibration or baseline standard. A growing number of orders now come from startup biotech labs, which rely on predictable supply chains for chiral synthons. These new entrants expect speed and guidance, especially when troubleshooting new protocols with expensive, time-sensitive trial windows.

    We’ve noticed a recent uptick from academic customers, reflecting a broader investment in chirality research for molecular biology and synthetic chemistry programs. Unlike pharmaceutical firms, campus labs tend to order in smaller quantities but with requests for tighter documentation, including batch chromatograms and in-house spectra. Years ago, these extras often seemed an afterthought; now they rank as essential, especially where grant-funded research faces rising scrutiny on material traceability.

    Industrial accounts differ in focus. Their priorities center on guaranteed re-orders and consistent shipment logistics. These users depend on our delivery track record—rarely missing a preferred dispatch date or failing to correct logistics before delays impact project schedules. More than once, we’ve moved up batch cycles to help a client avoid downtime at a pilot plant. Being directly responsible for each shipment, we know every day and every hour makes a difference.

    Quality, Traceability, and Supply Chain Transparency

    We operate out of a purpose-built site. Each barrel enters and exits by documented chain-of-custody, tracked down to the individual technician running the batch. Our internal training manuals cover handling and recordkeeping protocols for D-Dopa, training new hires in what goes wrong when care slips. We’ve learned firsthand—once, a shipment left with a missing batch certificate. Days later, the client’s data flagged anomalies. Our team spotted and rectified the shipment within hours, rerouting courier services at company expense, not pushing extra paperwork or blame elsewhere.

    Integrating new laboratories into our customer base often brings requests for longer paper trails and custom packaging. Our QA staff responds directly, providing scan copies of original paperwork, sequencing files of every run, and answering technical queries without funneling calls through sales agents. This transparency matters most to labs submitting work for regulatory review, or publishing in international journals, where data reproducibility turns on certified material origin.

    Conversations with end users keep us closely tied to quality standards. Instead of relying solely on outside audits, we invest in our own periodic review of plant procedures and analytical instruments. Every HPLC run, every IR spectrum, gets archived by both digital and paper record, stored for years after each batch. If a customer calls about a discrepancy months down the line, we access the exact vial data in minutes. This discipline—more than a certificate or document—forms the backbone of supply chain reliability.

    Meeting Challenges in D-Dopa Production

    Producing D-Dopa brings unique challenges. Unlike broad-market products with high-frequency runs, each campaign comes with less margin for error and fewer fallback suppliers for critical raw materials. Maintaining up-to-date reagents requires both good supplier relationships and frequent incoming QC. Anybody working in fine chemical manufacturing knows plant downtime spirals quickly into weeks lost, which is far costlier for a niche product such as D-Dopa.

    One problem we confronted was supply chain interruptions for chiral catalysts. Instead of waiting in line behind higher-profile clients, our procurement lead sought alternate synthesis approaches to avoid outages. Over two cycles, we built in redundancies, mapping every potential single point of failure. If a weather event or overseas shipping delay closes one route, our plant can start up another pathway within a week. This flexibility means clients can forecast long-term projects without dreading sudden market shortages or excessive price swings.

    Managing chemical risks safely, especially with compounds as reactive as D-Dopa intermediates, requires robust training and real-world experience. Every operator on our line undergoes practical hazard simulation drills; emergency shutoffs connect to local response teams. From solvents to temperature monitoring, nothing proceeds on autopilot. The benefit appears every month: high productivity, near-zero accident rates, and ongoing relationships with industrial safety auditors who know us by name.

    Our Role in Supporting Scientific Progress

    Manufacturing D-Dopa ties us into a network of creative, persistent scientists. Sometimes a customer shares their published assays or sends a sample back for shared analysis. Over the years, these partnerships have advanced both our technical toolkit and the broader field. Seeing our material mentioned in groundbreaking chirality studies or emerging analytical methodologies gives us pride and responsibility to keep improving. Each order shapes more than our bottom line—it feeds the progress of disciplines that solve larger-scale health and sustainability challenges.

    We often field requests from labs trialing new synthesis approaches or enzymatic screens. Drawing on production experience, we support these clients with practical tips on storage, handling, and optimal working concentrations. In turn, their feedback sharpens our internal methods and sometimes leads to product improvements. One research partner’s persistent feedback led us to refine desiccant ratios in packing, boosting long-term sample stability for climate-variable regions.

    Industry Trends Affecting D-Dopa Sourcing

    Recently, attention to supply chain transparency and analytical traceability has only grown. Regulators now request more detailed batch histories and supporting evidence. Labs and companies requiring absolute proof of source and handling—as well as consistent, fully documented production protocols—come directly to chemical manufacturers like us. We respond in kind, phasing in even more rigorous documentation and making datasets available on request. Every process tweak, every purification, every analytical result now supports not just our sales claims but independent, verifiable research outcomes.

    Customers once content with standard COAs now want original, itemized breakdowns—chromatograms, mass spectra, lot-by-lot impurity profiles. These detailed reports become part of their permanent research files. We prepare them as a routine step, so every shipment bundles transparent data with physical material, not just for major customers, but for every order.

    Another noticeable trend comes from acceleration in custom synthesis requests. Projects that once tolerated widely available intermediates now call for chirality-certified, origin-documented products—especially as enzyme and biocatalyst markets expand. Our plant is regularly approached for tailored D-Dopa batches, with lot sizes and purity targets set by client need, not just catalog convenience. This flexibility works both ways: enabling us to evolve processes, support diverse research, and adapt quickly to shifts in global demand.

    Future Directions for D-Dopa Manufacturing

    The road forward brings opportunities and new constraints. Chemical manufacturing rules continue to tighten, while methods for rapid analysis grow more powerful and less expensive. In our factory, we’re evaluating inline monitoring technology and investing in automation that preserves human oversight. Automation speeds up routine steps, but trained operators remain irreplaceable for troubleshooting and process nuance—especially with fine chiral compounds.

    From conversations with clients in pharma, biotech, and academia, we anticipate greater integration of D-Dopa in screen development, metabolic modeling, and asymmetric synthesis. Immediate access to well-documented, origin-certified materials enables ambitious projects with smaller teams, tighter schedules, and greater scrutiny. Our aim remains clear: produce the best D-Dopa available, support every customer directly, and adapt our production to science’s shifting demands.

    Every day our operators and chemists arrive onsite with the same focus: delivering high-quality D-Dopa, batch after batch, with no excuses. The real difference lies not in technical jargon but in knowing that every researcher opening a new bottle can trust the contents. In a world impatient for answers and breakthroughs, this trust continues to matter more with each passing year.