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D-3,4-Dichlorophenylalanine

    • Product Name D-3,4-Dichlorophenylalanine
    • Alias D-3,4-Dichloro-D-phenylalanine
    • Einecs 253-855-0
    • 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
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    Specifications

    HS Code

    314306

    Chemical Name D-3,4-Dichlorophenylalanine
    Molecular Formula C9H9Cl2NO2
    Molecular Weight 234.08 g/mol
    Cas Number 30029-31-7
    Iupac Name (2R)-2-Amino-3-(3,4-dichlorophenyl)propanoic acid
    Appearance White to off-white crystalline powder
    Solubility Soluble in water and most polar organic solvents
    Optical Rotation [α]D ≈ -
    Purity >98% (typical)
    Melting Point 185-190°C
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited D-3,4-Dichlorophenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 10-gram amber glass bottle with a screw cap, labeled "D-3,4-Dichlorophenylalanine," features hazard, purity, and handling information.
    Shipping D-3,4-Dichlorophenylalanine is shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged according to chemical safety regulations, labeled appropriately, and transported under cool, dry conditions. Handling and shipping must comply with local, national, and international chemical safety and hazardous materials guidelines.
    Storage D-3,4-Dichlorophenylalanine should be stored in a tightly closed container, in a cool, dry, and well-ventilated place, away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Ideally, store at 2–8°C (refrigerated) unless otherwise specified. Proper labeling and secure storage are essential to avoid contamination and ensure safe handling.
    Application of D-3,4-Dichlorophenylalanine

    Applications of D-3,4-Dichlorophenylalanine in Industrial Manufacturing

    As the original manufacturer with dedicated expertise in specialty raw materials, we supply D-3,4-Dichlorophenylalanine to sectors relying on high-spec amino acid derivatives for advanced synthesis. Our material is incorporated in demanding downstream applications where strict compliance, precision in formulation, and consistent supply are essential for quality and regulatory needs. Below we detail principal use cases, referencing real integration points, validation protocols, and final output types for our global industrial clients.

    1. Chiral Intermediate for Non-Proteinogenic Peptide Synthesis

    Peptide API manufacturers use our D-3,4-Dichlorophenylalanine as a key building block to introduce protected, non-natural amino acid residues into complex peptide sequences, enhancing molecular stability or activity. The raw material is specified in research and multi-ton commercial routes for the synthesis of peptidomimetic drug substances, where chiral purity and consistent halogenation are required by regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • Certificate of Suitability (CEP) for European submissions
    • DMF referencing as required by FDA and EMA

    Typical usage ratio

    • 5–18 mol% of total protected amino acids in synthetic peptide segment, determined by target peptide sequence and desired functional group incorporation

    Downstream process integration

    • Integrated during solid-phase peptide assembly or liquid-phase fragment coupling, following Fmoc/Boc protection-deprotection strategy
    • Monitored at loading, coupling, and cleaving stages for chiral retention and residue uniformity

    Final product types

    • Investigational and commercial peptide APIs containing halogenated side chains
    • Non-natural peptide reference standards
    • Peptidomimetic research compounds for pharmaceutical development

    2. Starting Material for Agrochemical Intermediate Synthesis

    Multinational agrochemical producers utilize this raw material as a chiral starting point for developing phenylalanine-derived herbicide and insecticide intermediates through precision halogenation and chain extension processes. Strict purity and halide pattern are required to ensure downstream catalytic specificity and environmental safety in regulated crop protection agents.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006 for intermediates registration
    • EPA 40 CFR Part 158 Data Requirements for Pesticides (USA)

    Typical usage ratio

    • 2–9% by mol in microgram-to-kilogram scale syntheses, according to targeted intermediate’s molar requirements and subsequent conversion efficiency

    Downstream process integration

    • Charged to the first step in amide coupling or esterification, prior to cyclization or chain modification steps for final active structure creation
    • Monitored for chlorine retention and by-product minimization during each catalytic step

    Final product types

    • Phenylalanine-derived pesticide intermediates
    • Key units in herbicide active ingredient synthesis chains
    • Specialty chiral auxiliaries for agrochemical research

    3. Advanced Intermediate for Small-Molecule API Synthesis

    Pharmaceutical fine chemical companies incorporate this molecule as a pivotal intermediate when synthesizing small-molecule active ingredients that demand precisely positioned halogen substituents on aromatic amino acid scaffolds, supporting enzyme inhibition or heightened receptor selectivity in late-stage drug candidates.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as defined in 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) monographs for starting materials
    • ICH Q11 Development and Manufacture of Drug Substances
    • ISO 15378:2017 Primary Packaging Materials for Medicinal Products

    Typical usage ratio

    • 5–15 mol% of the total synthetic route, based on final active ingredient structure and degree of halogenated residue required by the pharmacophore

    Downstream process integration

    • Added at targeted aromatic substitution or amidation steps; frequently enters after initial ring functionalization
    • Subject to in-process QC for chiral integrity and residual solvent levels

    Final product types

    • Clinical and pre-clinical pharmaceutical candidates featuring dichlorinated residues
    • Patent-protected small-molecule APIs for specialty therapeutics
    • Investigational compounds for combinatorial chemistry research

    4. Component in Diagnostic Amino Acid Reagent Kits

    Manufacturers of clinical and research diagnostic kits formulate D-3,4-Dichlorophenylalanine into analytical reagents for use as standards, enzyme activity markers, or labeled analogs in metabolic assays where halogenated D-amino acids are needed for substrate specificity or traceability.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management Systems
    • ISO 17511:2020 In vitro diagnostic medical devices—Requirements for reference measurement procedures
    • CLSI EP25-A Evaluation of Stability of In Vitro Diagnostic Reagents
    • Regional regulatory approval as required by FDA 21 CFR Part 820 (USA) or MDR (EU)

    Typical usage ratio

    • 0.02–0.2% w/v in diagnostic reagent formulations; precisely measured during calibration based on assay detection limits and analytical method validation

    Downstream process integration

    • Incorporated at reference standard blending or conjugation stage in lyophilized or liquid reagent manufacturing
    • Subjected to batch release QC by HPLC and stability testing for analytical performance

    Final product types

    • Reference standards for amino acid quantitative analysis
    • D-amino acid enzyme activity diagnostic kits
    • Custom amino acid marker panels for metabolic profiling
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    More Introduction

    D-3,4-Dichlorophenylalanine: Production Insights and Value in Advanced Synthesis

    Genuine Manufacturer Perspective: Why We Emphasize Purity And Consistency

    Our experience with D-3,4-dichlorophenylalanine stretches back many years and informs every batch that leaves our reactors. This specialty amino acid does not attract the same attention as common proteinogenic compounds, but for research groups and industrial partners requiring halogenated intermediates, the stakes remain high with every kilogram. In our manufacturing lines, D-3,4-dichlorophenylalanine stands as a benchmark for advanced process control.

    Chlorinated aromatic amino acids pose a challenge in both synthesis and purification. We have watched unsatisfactory yields, ambiguous isomer profiles, and color impurities turn up in commercial material from sources less committed to the exacting control we follow. D-3,4-dichlorophenylalanine, manufactured in our facility, achieves an HPLC purity of not less than 98%. Observed melting points track published values, avoiding the several-degree deviations evident in hastily prepared lots.

    We respond to batch-to-batch consistency through a tightly managed route of protection, halogenation, and deprotection. Each process pivot emerges from hands-on troubleshooting, not just from the textbooks. Transition metals and oxidants introduce risk of side reactions, and we switched from oxidative to electrophilic chlorination routes after we saw trace polychlorination via high-field NMR. Our team closely monitors both intermediate and final product for residual solvents, controlling for the acetonitrile content to below 0.05%. This detailed attention shows up in every specification sheet—every gram gives researchers an interpretable baseline.

    Applications: From Enzyme Mechanism Probes to Fine Chemical Synthesis

    Industries exploring enzyme active sites or structure-activity relationships turn to D-3,4-dichlorophenylalanine as a non-canonical amino acid for both in vitro and in vivo exploration. We have watched its application in peptide engineering, probing selectivity in halogen bonding and conformational effects in peptides. Medicinal chemistry groups have incorporated the 3,4-dichloro aromatic side chain, hunting for improved receptor binding, metabolic stability, or adjusted pKa. Chiral intermediates derived from this building block have appeared in patent disclosures for enzyme inhibitors and imaging probes.

    A major advantage in synthesizing D-3,4-dichlorophenylalanine lies in its compatibility with modern peptide synthesis protocols. The D-configuration sidesteps proteolytic degradation and enables researchers to focus on backbone modifications without interfering with side chain chemistry. The selectivity we engineer into our material helps researchers distinguish analytical signals from common impurities in HPLC or LC-MS, removing ambiguities in downstream analysis.

    D-3,4-dichlorophenylalanine earns its way into unusual roles, too. Some of our synthetic biology partners feed this compound to cell cultures that incorporate non-canonical amino acids into proteins. This opens possibilities for protein engineering, creating novel bond types through metal coordination or halogen bonding. Precise stereochemistry brings researchers consistent biophysical properties. In asymmetric synthesis, our product serves as a reliable starting point for chiral ligands and specialty polymers.

    Understanding the Features That Make a Difference

    Compared to unsubstituted phenylalanine or even mono-chlorinated derivatives, 3,4-dichlorination changes the molecule’s reactivity. Double substitution impacts electronic distribution in the ring, suppressing some common side reactions in acid-catalyzed peptide couplings. In our hands, yields run higher during Fmoc protection and subsequent coupling steps, especially when using hybrid resins or constrained secondary structures.

    We have collaborated on projects with both small and large research groups. Bigger labs and commercial customers find increased value in our bulk scale, where homogeneity between packs keeps research consistent over long campaigns. We keep a tight eye on optical rotation, running measurements both before and after shipment. This is not only a regulatory necessity, but also a way to catch racemization or degradation missed in rushed lots elsewhere. Over the years, we have learned the hard way that skipping this control step exposes scientists to results that do not replicate—which in chemistry can burn through months of effort.

    D-3,4-dichlorophenylalanine does not share the same supply pipeline as standard amino acids. Availability can become a bottleneck when larger synthetic schemes require multi-kilogram lots. By keeping both pilot and commercial-scale reactors ready, we have managed to respond to needs from universities and growing biotechs alike. Storing larger lots under nitrogen, we guard against slow oxidative discoloration that creeps in as the material sits exposed on a shelf. We do not over-process; instead, we match shelf life to real demand, minimizing overexposure to oversized warehouse environments.

    How D-3,4-Dichlorophenylalanine Differs From Other Amino Acid Products

    Chemical properties set this compound apart. Its melting point runs higher and the dichlorophenyl side chain makes it less soluble in aqueous buffers than standard phenylalanine. Some research protocols demand careful dissolution, often relying on heated solvents or chosen salt forms. Early customers taught us that a lot that clumps or fails to dissolve quickly can stall an entire project. We responded by optimizing particle size and moisture content, targeting specifications that encourage both long storage and rapid reconstitution. Our team avoids milling techniques that risk introducing fine iron particulates—a persistent issue with less rigorous workflows.

    Chlorination chemistry is not trivial. Mono-halogenation often yields a mixture of ortho and para isomers; selective 3,4-dichloro substitution requires carefully tuned conditions. In our process, we measure the ortho/meta/para content not just in finished product but throughout the intermediate stages. Customers from institutions with high analytical standards come to us because our chromatographic profiles remain clean, with side product content below 0.5%. Internal QC records track each deviation for five years. We openly publish impurity profiles for our top-selling batches so that partners can build analytical models with full confidence in their starting material.

    Our D-3,4-dichlorophenylalanine does not carry over the unpleasant odor or tan coloration sometimes reported with crude lots from bulk suppliers. It features a crystalline white appearance that flows easily, unaffected by the residual toluene or acetic acid sometimes encountered during synthesis. Years ago, we encountered an entire shipment of off-color material that turned out to have hydrolyzed intermediates. Since then, we have required double verification on all crude isolation and final washes.

    Most importantly, the D-configuration of our material guarantees chirality necessary for specialist applications. While L-3,4-dichlorophenylalanine can come from natural sources or even microbial syntheses, the D-form is strictly synthetic. This sharpens the edge for our pharmaceutical partners, who cannot risk cross-contamination with natural isomers. Side-by-side, the D- and L-forms behave differently even in routine biophysical tests; only strict adherence to enantioselective routes satisfies these exacting customers.

    Addressing Safety, Handling, and Regulatory Standards in Production

    True chemical manufacturing demands close attention to safety, both for the people making the product and for the users who handle it downstream. D-3,4-dichlorophenylalanine synthesis takes place under contained conditions with real-time monitoring of chlorinating agent concentrations. We make no compromises with PPE and training. There have been near misses—once a reagent batch arrived with lower purity than expected, and our pre-screening triggered a halt, sparing the operators from an uncontrolled side reaction. Having these experiences changes a shop’s approach—realistic risk management beats theoretical compliance every time.

    Global distribution for this kind of specialty intermediate requires tracking each regulatory update. Our documentation follows both domestic and overseas standards, staying current with REACH, TSCA, and regional requirements regardless of where the shipment travels. We assign a full analytical profile to each lot, meeting drug master file demands where customers request it. This access to transparency has narrowed the trust gap between manufacturer and user—direct supply chain management helps partners avoid delays caused by documentation mismatches that plague traders or unregistered sources.

    Solutions to Scaling, Lead Time, and Integration in Research

    Changes in demand often highlight weaknesses in upstream production planning. Early on, we faced surges in orders from projects that had underestimated ramp-up requirements. Our solution grew from direct engagement with customers. We share forecasts with trusted R&D partners, facilitating pre-reservation of capacity. For emergency projects, our site keeps reserve lots of material on hand, preventing researchers from stalling at critical junctions. We moved away from just-in-time models for these products—a move that paid off as supply shocks hit global logistics in recent years.

    We work closely with peptide synthesis teams, pharmacology labs, and material science researchers. Their feedback feeds directly into incremental process improvements. Some require custom salt forms or special packaging to maintain stability during long transit. By keeping these lines of communication strong, we have eliminated common complaints about caking, slow shipment, or unpredictable particle size. Our facility runs pilot batches of new variants prior to full-scale launch, based on utility, not marketing trends.

    Researchers sometimes ask about the utility of the product in enantioselective enzymatic reactions or as a probe for new biosynthetic pathways. From our experience, D-3,4-dichlorophenylalanine holds its own as a probe for structure-function relationships in enzymes engineered for halide binding or C-H activation. We support such academic-industry partnerships with both material supply and data sharing, aiming for more than just routine sales. Advancing the chemistry matters as much to our team as meeting sales targets.

    Technical Details Rooted in Production Reality

    D-3,4-dichlorophenylalanine is prepared through protection of the amino and carboxyl groups before chlorination, a stepwise approach that helps us avoid over-chlorination and unwanted ring substitutions. Our technicians routinely track intermediate conversion by both TLC and NMR, making on-the-fly adjustments to reagent concentrations. Each isolation proceeds with aqueous acidic workup and solvent washes, followed by crystallization when the structure demands.

    We have seen, over time, that the dichloro group’s influence on reactivity extends to coupling protocols: yields run higher in automated peptide synthesizers because the ring halogens stabilize activated esters. Researchers experimenting with new ligands or chiral auxiliaries often cite our lot numbers in their publications—reproducibility depends on reliability in the chiral pool. Analytical data for each shipment includes HPLC, NMR, mass spectrometry, optical rotation, and elemental analysis. We never release product that sits on the fence of these benchmarks.

    Handling advice comes from direct lab practice. D-3,4-dichlorophenylalanine resists hygroscopicity but does best when stored under dry nitrogen. On open benchtops, mechanical stresses are more likely to affect particle shape than moisture. We pack all lots in tamper-evident, low static containers that survive both temperature extremes and rough handling, because we have seen the results of accidental in-transit compression punctures. For large orders delivered to pilot facilities, we work with packaging suppliers to test pre-shipment resilience in simulated warehouse conditions.

    Industry Experience—Real Differences for Customers

    Our journey with D-3,4-dichlorophenylalanine has not followed a straight path. The production challenges, chemical nuances, and evolving applications have built a hard-won knowledge that no distributor or trading agent can match. Our team has walked the line between chemistry and engineering, always looking for the best balance between capacity growth and product integrity. Customers know—when the project’s success rides on a specialized non-canonical amino acid, the closer to the source, the less risk for both purity and documentation.

    Relying on our production means fewer surprises, shorter lead times, and direct access to the analytical data that matters. Over the years, we have watched deals fall apart because a link in the distribution chain could not answer for a contamination incident or missing regulatory form. Our choice to keep all steps in-house—protection, halogenation, deprotection, and final QC—has meant direct accountability. It’s not uncommon for a customer to call about variant specifications or to troubleshoot an application concern; our technical team, not a sales desk, picks up. Those conversations feed back into real improvements for future lots.

    Large-scale orders have shaped our approach to production infrastructure. Expanding reactor size without sacrificing process safety or cleaning validation became a cornerstone objective. Our in-plant monitoring adapts to both process upsets and scale-related thermal gradients, because repeatability matters more than theory in these scenarios. Each success here adds to the practical, on-the-floor experience that our customers rely on rather than marketing claims.

    Fostering Collaboration, Not Just Sales

    Collaboration with leading research groups has refined our outlook. Not every project needs boutique-grade D-3,4-dichlorophenylalanine; sometimes smaller pilot batches address novel ideas before the full-scale commitment. We support researchers by adjusting quantities, documentation, and shipment terms to match the unpredictable pace of discovery. Some breakthroughs in enzyme engineering and synthetic methodology would not have been possible without this kind of agile supply.

    Environmental responsibility factors into all our scale-up decisions. Organochlorine chemistry carries unique waste management challenges. We have invested in integrated scrubbers and solvent recovery systems, maintaining output quality without trading away sustainability. Safe handling protocols developed through accident investigation have led us to over-engineer in favor of safety, always favoring personnel and community well-being over production speed.

    Our team remains committed to transparency. Customers regularly receive full analytical records and manufacturing histories with each shipment. Technical reports on impurity retention, batch-specific reviews, and troubleshooting bulletins accompany every large delivery. No diluted promises—just backing up our claims with the kind of detail that makes scientific progress possible.

    Future-Proofing Production for Evolving Research

    Demand for D-3,4-dichlorophenylalanine continues to grow as protein engineering, medical imaging, and advanced synthetic methodologies broaden their horizons. We stay engaged with front-line users, updating processes and controls in response to changing analytical requirements. Routine monitoring of new regulations and environmental guidance shifts the way we approach both raw material qualification and emissions control.

    As scientific applications expand, so do our avenues for improvement. We engage with both legacy and new-customer feedback, considering pilot batch changes and scale-out strategies before locking production cycles. No two inquiries are the same; some projects need high-throughput small packs delivered with exacting COA and shelf-life guarantees. Other customers ask for kilogram-scale lots with added documentation for investigational new drug filings. Adapting to this diversity has become a manufacturing strength.

    By keeping one foot in the laboratory and the other in the plant, we continue to build real value into every lot of D-3,4-dichlorophenylalanine we ship. The result: operational confidence for the teams that rely on our product in their most sensitive and ambitious research.