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Dl-4-Chlorophenylalanine

    • Product Name Dl-4-Chlorophenylalanine
    • Alias p-Chlorophenylalanine
    • Einecs 214-480-6
    • 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

    166554

    Chemicalname Dl-4-Chlorophenylalanine
    Casnumber 7424-00-2
    Molecularformula C9H10ClNO2
    Molecularweight 199.63 g/mol
    Appearance White to off-white powder
    Meltingpoint 247-249 °C
    Solubility Slightly soluble in water, soluble in ethanol
    Purity Typically ≥98%
    Storageconditions Store at 2-8 °C, protect from light and moisture

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

    Packing & Storage
    Packing The 25g Dl-4-Chlorophenylalanine is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping Dl-4-Chlorophenylalanine is shipped in sealed, secure containers, compliant with safety and regulatory standards. Chemical packaging ensures protection from moisture, light, and contamination. Handling and transportation follow hazardous material guidelines, including clear labeling and required documentation. Shipping typically utilizes express courier services with tracking to ensure timely and safe delivery.
    Storage Dl-4-Chlorophenylalanine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator temperature). Avoid exposure to incompatible substances such as strong oxidizing agents. Ensure appropriate labeling and access only to trained personnel. Follow all relevant safety guidelines for storage and handling of chemicals.
    Application of Dl-4-Chlorophenylalanine

    Applications of Dl-4-Chlorophenylalanine in Industrial Manufacturing

    As a dedicated manufacturer of Dl-4-Chlorophenylalanine, our material supports numerous critical industrial synthesis workflows. Below, we outline key application sectors utilizing this raw ingredient, with emphasis on genuine production settings, compliance frameworks, formulaic distinctions, integration procedures, and finished goods outputs across regulated markets worldwide.

    1. Pharmaceutical Intermediates for CNS-Active Drug Synthesis

    Pharmaceutical manufacturers employ Dl-4-Chlorophenylalanine extensively as a non-proteinogenic amino acid intermediate, facilitating step-growth synthesis in central nervous system (CNS)-targeting APIs, especially for agents modulating serotonin pathways. The material enters into acylation, resolution, and chiral transformation processes where its side-chain functionality is critical for achieving specific pharmacophores in psychoactive drugs under clinical development and generic manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 211–Manufacturing, Processing, Packing, or Holding of Drugs
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • Chinese Pharmacopoeia (ChP) Intermediates Guidelines

    Typical usage ratio

    • Batch formulations incorporate Dl-4-Chlorophenylalanine at 1.5%–4% molar equivalents in API intermediate synthesis steps, adjusted based on desired product yield, reaction scale, and structural complexity.

    Downstream process integration

    • Material introduced post-initial condensation or amidation stages, preceding enantiomeric separation or direct cyclization, and consumed fully during multi-step organic synthesis toward the final API scaffold.

    Final product types

    • Finished pharmaceutical ingredients for antidepressant and anxiolytic drugs
    • Precursors to selective serotonin synthesis inhibitors for neuropsychiatric disorders
    • API building blocks in generic CNS-active compound production
    • Intermediates for clinical drug candidate libraries

    2. Biochemical Reagent Manufacturing for Research Kits

    Dl-4-Chlorophenylalanine is a preferred substrate in biochemical reagent production, specifically for research kit manufacturers requiring serotonin biosynthesis inhibitors. Its ability to selectively block tryptophan hydroxylase activity makes it crucial for constructing diagnostic and neuroscience research tools. Strict traceability and batch-to-batch consistency are mandatory for satisfying research laboratory quality expectations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ISO 13485:2016 for Medical Device Reagent Kit Manufacturing
    • REACH Regulation (EC) No 1907/2006 – Laboratory Chemical Supply

    Typical usage ratio

    • Common reagent kit formulations incorporate 0.2–1 mg/mL of Dl-4-Chlorophenylalanine per solution or solid assay; calibration to experimental specificity and targeted enzymatic inhibition is essential for achieving intended biomarker responses.

    Downstream process integration

    • Supplied as a pure powder or pre-dissolved solution, the compound is aliquoted into kit vials during final QC filling under laminar flow and integrated directly before lyophilization or packaging for distribution to laboratories.

    Final product types

    • Non-clinical serotonin synthesis assay kits
    • Academic neuroscience research assay panels
    • Custom biosample preparation reagents for pharmaceutical R&D
    • Enzyme inhibition test kits for neurochemical analysis

    3. Fine Chemical Synthesis of Aromatic Amino Acids Derivatives

    Industrial fine chemical enterprises utilize Dl-4-Chlorophenylalanine as a precursor for a variety of substituted aromatic amino acid derivatives. These intermediates function as ligand scaffolds, polymer building blocks, and specialty reagents within high-purity organic synthesis workshops. Rigorous process controls and trace impurity reduction are monitored in compliance with chemical safety regulations.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
    • European Union CLP Regulation (EC) No 1272/2008
    • China National Standard GB 30000 Series—Chemicals Classification

    Typical usage ratio

    • Formulation processes apply 3–8% w/w of Dl-4-Chlorophenylalanine depending on target derivative molecular weight and intended downstream application, with proportion increased for multi-step aromatic substitution or chiral resolution.

    Downstream process integration

    • Material is added near the outset of synthetic routes, frequently subjected to halogenation, diazotization, or esterification before separation and purification steps.

    Final product types

    • Substituted aromatic amino acid derivatives
    • Advanced ligands for coordination chemistry and catalysis
    • Polymerizable monomers for engineering plastics or biopolymers
    • Specialty building blocks for custom chemical libraries

    4. Veterinary Drug Intermediate Production

    Veterinary pharmaceutical divisions make extensive use of Dl-4-Chlorophenylalanine as a foundation molecule for developing medications targeting animal serotonin pathways and related behavioral or metabolic interventions. Production focuses on scalable synthesis under feed and drug regulatory systems, ensuring safety and controlled residuals in final veterinary active substances.

    Industry compliance standards

    • Veterinary Drug Good Manufacturing Practices (GMP) – China, EU, US
    • VICH GL 3 – Stability Testing of New Veterinary Drug Substances and Medicinal Products
    • Pharmacopoeia of the People’s Republic of China (Veterinary Section)
    • European Union Directive 2001/82/EC on Veterinary Medicinal Products

    Typical usage ratio

    • Standard mixing ratios range from 1–3 mol% per synthetic stage depending on molecular target and interaction with other amino-acid-based intermediates; adjustment guided by animal species specificity and final product residue limits.

    Downstream process integration

    • Compound is introduced post-initial condensation, facilitating amidation or cyclization; followed by filtration and crystallization under GMP-compliant control measures to reduce cross-contaminants for veterinary substance formulation.

    Final product types

    • Veterinary anesthetic agent APIs
    • Feed-grade neurological balancer intermediates
    • Behavior-modifying agent precursors for livestock and companion animals
    • Research compounds for animal model pharmacology

    5. Chiral Resolution Agents in Analytical Chemistry

    Analytical chemistry suppliers deploy Dl-4-Chlorophenylalanine as both a test substrate and component of racemate resolution agents in chromatographic and electrophoretic applications. The molecule’s unique side-chain halogenation supports identification and quantitative analysis of optical purity in pharmaceuticals and specialty chemicals, where regulatory demands for chiral specification are stringent.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • USP <823> Radiopharmaceuticals—Analytical Procedures and Tests
    • FDA Analytical Procedures and Methods Validation Guidance
    • OECD Good Laboratory Practice (GLP) Principles

    Typical usage ratio

    • Chromatography resolutions utilize 0.5–2 mmol per analytical assay or mobile phase mixture, scaled to sample complexity and sensitivity requirements of downstream enantiomeric excess determination.

    Downstream process integration

    • Material is prepared into standardized racemate mixtures, blended with mobile phase buffers or stationary phase carriers before being loaded onto preparative columns or HPLC cartridges for rapid analytical workflows.

    Final product types

    • Chiral resolution stationary phases for HPLC/UPLC
    • Reference standards for enantiopurity assessment
    • Analytical quality control kits
    • Mobile phase additive blends for pharmaceutical QC laboratories
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    Certification & Compliance
    More Introduction

    Dl-4-Chlorophenylalanine: A Practical Look from the Manufacturer’s Floor

    Real-World Experience with Dl-4-Chlorophenylalanine

    Dl-4-Chlorophenylalanine belongs to the class of unnatural aromatic amino acids. It plays a unique role in modern chemical manufacturing, especially in research and pharmaceutical development labs. Many newcomers think it’s just a modification of phenylalanine, but subtle variations make all the difference in lab outcomes and downstream applications.

    Over years of hands-on batch production, workers and technical staff learn that this compound demands close control throughout synthesis and purification. Unlike common amino acids, the presence of the chlorine atom on the aromatic ring changes both its reactivity and safety handling parameters. The Dl-form means this version contains both D and L enantiomers, and we routinely see researchers request this racemic form when studying biochemical pathways that don’t depend on strict stereospecific effects. From our own process, everything from the initial chlorination of the phenylalanine substrate to final drying requires careful adjustment for yield and quality. During final QC checks, differences in color, odor, and melting point between batches have led us to make incremental changes on the shop floor that only seasoned operators can spot.

    Product Characteristics and Purity in Practice

    In our facility, Dl-4-Chlorophenylalanine is usually manufactured as a fine, off-white to pale yellow powder. Sometimes the product is a little darker, especially if left in humid air, so our team puts particular focus on environmental controls during storage. Analyses show the melting point near 160 degrees Celsius — a reliable indicator for confirming purity. The accepted assay and impurities profile, measured by HPLC and NMR, shows that detection of residual solvents and unreacted starting materials forms a key part of release testing. We’ve seen subtle shifts in chromatographic behavior if hydrogen chloride levels in the reactor fluctuate, so maintaining stable operating conditions matters for every batch.

    Over time, customer feedback has driven us to tighten particle size distribution, improve filtration steps, and adapt packaging to minimize caking during shipping. Labs seeking higher-purity grades receive additional recrystallization. Universities and core research labs sometimes ask for technical-grade material, where cost savings are more important than the highest purity achievable. On the other hand, major pharmaceutical houses always push for 99%+ by HPLC, and our experience with multi-kg batch scale production allows us to offer both choices without long lead times.

    Typical Usage: Research Drives the Demand

    Companies and academic groups use Dl-4-Chlorophenylalanine most often as a tool compound for studying tryptophan and serotonin metabolism. Through hands-on collaboration, we’ve learned that this material can interrupt the biosynthesis of serotonin by inhibiting tryptophan hydroxylase in animal models. One pharmacologist shared lab tests where they measured serotonin levels in rat brain tissue after administration; the results depended directly on the grade, particle size, and freshness of the Dl-4-Chlorophenylalanine they sourced from us.

    In other settings, chemical biologists use the compound as a probe for metabolic flux analysis or as an intermediate to make radiolabeled standards. We see some demand from the drug development sector, where the need for a chlorinated phenylalanine derivative comes up in synthetic peptide work. The presence of the para-chloro group not only alters the physicochemical properties but also unlocks opportunities to modify peptide function or stability. The molecule’s niche utility means most users require modest amounts, and accurate weighing on microbalances turns out to be more challenging than many expect, especially given its tendency to form static-charged fine dusts. Inside our filling rooms, strict humidity control and anti-static measures reduce both product loss and operator exposure.

    Key Differences Compared to Related Compounds

    Many ask what sets Dl-4-Chlorophenylalanine apart from regular phenylalanine, 4-chlorophenylalanine single isomers, and other aromatic amino acids. Having synthesized and handled tons of these over decades, some trends jump out. The addition of the chlorine atom at the para position changes reactivity and increases lipophilicity. In practice, solutions of this compound show different solubility in water and organic solvents compared to unmodified phenylalanine.

    Regarding the racemic versus single enantiomer forms, most biological studies involving enzyme inhibition don’t require a stereospecific version, and producing the Dl mixture allows for larger-scale, economical manufacturing. Producing pure L-4-chlorophenylalanine or D-4-chlorophenylalanine, on the other hand, involves added chiral resolution steps and results in higher prices and lower availability. Based on user feedback and our own knowledge, unless a specific chiral interaction is under investigation, the racemic material often proves to be a more practical choice.

    Our Take on Safety and Handling: Lessons from the Production Floor

    Anyone who’s spent years in a chemical plant knows that even stable, “ordinary” organic compounds come with hazards if mishandled. Dl-4-Chlorophenylalanine, while not among the most reactive or acutely toxic substances, still needs respect. Fine powder disperses easily and can irritate mucous membranes. Early on, a few operators learned the hard way that gloves must fit well and break rooms should be kept strictly separate from production areas, since transfer on work clothes proved all too easy. Today, the whole crew suits up in powder-tight PPE during packaging.

    We follow written SOPs and have trained dozens of technicians over the years. Emergency drills focus not only on direct exposures but on cleanup of spills, which is more common than big accidents. Old-style bags with twist ties used to leak dust; after a series of customer complaints, we shifted to heat-sealed foil pouches. Stacked drums now use desiccant packs, protecting the product for months against clumping and hydrolysis.

    Market Trends and Shifts We’ve Witnessed

    Decades ago, orders for Dl-4-Chlorophenylalanine mostly came from university researchers and government toxicology programs. Changes in neuroscience spurred more demand for animal studies on serotonin. We noticed a surge in global shipments to biotech startups exploring new mechanisms for neurotransmitter modulation. Some years bring requests for gram-scale samples, others bring multi-kg industrial-scale contracts when someone scales up production of specialty peptides.

    With tightening regulations for research chemicals, the need for reliable documentation and traceability now surpasses even purity requirements. Our compliance staff have introduced barcoded batch records for all B2B shipments, and packaging gets relabeled in additional languages on EU and Japanese orders. As markets evolve, our advantage comes from walking the balance between traditional batch preparation techniques and continuous improvement through customer feedback.

    Dl-4-Chlorophenylalanine’s Role in Syntheses: A Manufacturer’s Perspective

    On the chemical side, this amino acid serves as a building block for more complex molecules. We’ve seen it incorporated into peptide synthesis workflows, routed into the production of agricultural research agents, and even adapted for making radiolabeled tracers. Because it contains the chloro group, the molecule reacts differently in coupling reactions. We learned to adapt coupling agent concentrations and adjust pH during dissolutions to prevent undesirable byproducts.

    Sometimes the difference between a successful synthesis and a stalled reaction comes down to the batch source. A few of our large pharma partners run validation checks on each batch, looking not only at purity but also residual metals and byproduct profiles. Our team holds regular meetings to discuss customer feedback about solubility, moisture absorption, or filtration efficiency so we can modify operations as needed.

    Why Reliable Supply and Consistent Quality Matter to Our Customers

    In research and preclinical development, any interruption in supply can set back whole teams for weeks. Stories of delayed grant-funded projects arrive every year, usually caused by inconsistent raw material sourcing or unexpected regulatory delays. Our direct involvement in production, rather than just trading or relabeling, lets us follow material all the way from warehouse storage to final shipment. That level of control limits variability and builds trust through repeatable performance.

    We have seen how researchers can lose months troubleshooting odd results in animal or in vitro work, only to discover later that a subtle change in incoming material caused the trouble. That sort of problem can be avoided with honest conversations between manufacturer and user, as well as transparent traceability. We mark all our pouches, issue certificates with every lot, and keep an open channel with our technical sales team so that feedback comes back to production in real time.

    Cost, Scale, and Customization: Insights from Decades in the Industry

    Despite its niche application, requests for Dl-4-Chlorophenylalanine come with wide variation in scale — from 25-gram bottles up to 25 kg drums. Pricing depends on purity grade, packaging requirements, and special certifications. Over the years, some customers have needed extra testing for trace contaminants, while others want raw technical-grade product for screening work. Scaling batch size means rechecking the entire process for unexpected byproducts, and experienced process chemists watch for thermal runaway, incomplete reactions, or differences in filtration time when larger reactors are used.

    Some of the most challenging orders come from teams tweaking dosage forms or studying pharmacokinetics. They request adjusted particle size, low-metal content, or specific moisture levels. Each new request causes us to revisit the process, sometimes changing filter setups, drying cycles, and even the order of adding reagents. Existing relationships with chemical and equipment suppliers smooth the way, but process flexibility still matters most.

    Environmental Responsibility: Learning from the Past, Planning for the Future

    Manufacturing Dl-4-Chlorophenylalanine generates waste streams that require attention. Spent solvents, reactor rinse water, and filter cakes all need appropriate handling. In earlier decades, some companies were content to offload this waste without concern for long-term impact. Witnessing the aftermath of poor disposal drove us towards on-site solvent recovery, water treatment, and routine audits of waste haulers.

    Auditors and inspectors now show up more frequently, especially for export shipments. They examine records of how we minimize emissions, reduce waste, and prevent contamination. By adopting closed-system transfers and investing in modern scrubbers, the plant improved both its regulatory standing and local community relations. Younger staff now bring fresh perspective on green chemistry, helping us pilot new catalyst systems that cut down on byproducts. Customer agreements increasingly reflect shared commitments to lower-waste and higher-efficiency processes.

    Practical Advice for Selecting a Dl-4-Chlorophenylalanine Supplier

    From a manufacturer’s vantage point, choosing where to buy this product involves more than price shopping. Users should visit or audit plants where possible, ask questions about process changes, and request detailed batch records. Our customers who take the time to engage directly with technicians and managers rarely encounter unexpected problems. They get prompt answers about origin, impurity profiles, or regulatory acceptance that distributors simply cannot provide.

    Product recalls are rare when both sides communicate clearly and follow through on agreed testing and shipping protocols. Our staff work closely with clients to interpret COA data, troubleshoot inconsistencies, and propose alternative shipping or storage options when needed. Over the long haul, those relationships make a true difference in lab productivity.

    Quality Standards in Action: Not Just a Claim

    Throughout our workflow, quality control steps stay transparent and consistent. Our lab teams calibrate instruments daily, compare in-house reference standards with external benchmarks, and conduct trending analysis for all key product features. Actual user feedback closes the loop, as researchers tell us about unexpected outcomes, stability under different conditions, or issues in analytic detection. By tracking each batch from start to finish, the plant remains ready to address questions with substance rather than vague reassurances.

    Through years of problem-solving, product improvement becomes a cycle driven by practical experience — like switching filter media after noticing fine suspended solids showed up in some customer HPLC traces, or altering packaging based on transport stress tests. Our staff include some with two decades of experience at the plant, who have helped new hires spot the tiny color changes or odor differences that indicate something went awry during synthesis or drying.

    Research-Grade Product vs Technical Grade: What the Distinction Means Here

    In the real world, the difference between research-grade and technical-grade Dl-4-Chlorophenylalanine extends beyond numbers on a certificate. High-purity research lots command a premium, undergo more stringent testing, and come with more detailed documentation. Technical material, destined for initial screens or non-critical studies, trades off some attributes for cost savings. On our end, extra purification steps for research grades mean lower yields and longer production times — realities that pricing reflects.

    Some institutions have strict requirements for documentation, stability data, and trace analysis. Meeting those means investing in better equipment, extra training, or periodic external audits. Customers needing consistent quality for regulatory filings or published research benefit from clear, candid communication about what’s possible and which grade suits their application.

    Long-Term Commitments: Building Trust Through Transparency

    Manufacturing specialty compounds like Dl-4-Chlorophenylalanine rewards those willing to put in sustained effort. From iterative process improvements to open communication about challenges, our team’s history of delivering on promises builds goodwill with customers and auditors alike. Regular production reviews and plant tours help buyers learn what goes on behind the scenes and verify that claims match reality.

    In the end, consistent quality, operational transparency, and practical problem-solving set one manufacturer apart from another. Dl-4-Chlorophenylalanine may not be a blockbuster commodity, but its value in research and chemical development means every delivery counts.

    The Road Ahead: Anticipating Changes and Meeting New Needs

    Every year brings new questions about improved analytical testing, alternative synthetic routes, or regulatory acceptance in diverse markets. As customers explore new uses for Dl-4-Chlorophenylalanine, from metabolism research to custom syntheses, we keep adapting the process and refining our support. Our experience guiding clients through regulatory filings, storage and shipping, and technical troubleshooting ensures that research goals receive solid material support. The story of this compound, as seen from the manufacturer’s perspective, continues to evolve with every batch we make and every scientist we serve.