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Dl-2-(4-Chlorophenyl)Glycine

    • Product Name Dl-2-(4-Chlorophenyl)Glycine
    • Alias Cpd46
    • Einecs 244-606-2
    • 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

    646601

    Product Name Dl-2-(4-Chlorophenyl)Glycine
    Chemical Formula C8H8ClNO2
    Molecular Weight 185.61 g/mol
    Cas Number 132047-03-9
    Appearance White to off-white crystalline powder
    Purity Typically ≥98%
    Melting Point 180-184°C
    Solubility In Water Slightly soluble
    Storage Temperature 2-8°C
    Synonyms DL-4-Chlorophenylglycine

    As an accredited Dl-2-(4-Chlorophenyl)Glycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for DL-2-(4-Chlorophenyl)Glycine contains 25 grams in a tightly sealed, amber glass bottle with hazard labeling.
    Shipping Dl-2-(4-Chlorophenyl)Glycine is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. The package includes appropriate hazard labeling and documentation, complying with relevant regulations for transport of chemicals. Temperature and handling instructions are provided to ensure safe delivery. Only authorized personnel should handle the shipment.
    Storage Dl-2-(4-Chlorophenyl)glycine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture, direct sunlight, and excessive heat. Store at room temperature or as specified by the manufacturer, ensuring proper chemical labeling and access only to trained personnel.
    Application of Dl-2-(4-Chlorophenyl)Glycine

    Applications of Dl-2-(4-Chlorophenyl)Glycine in Industrial Manufacturing

    As the direct manufacturer of Dl-2-(4-Chlorophenyl)Glycine, we have extensive experience supporting sector-specific downstream operations that leverage this raw material in core synthesis and formulation stages. The following sections outline its practical integration in several real-world industrial production contexts, strictly based on validated end-use scenarios and established technical standards.

    1. Pharmaceutical Intermediate for Nonsteroidal Anti-inflammatory Drug (NSAID) Synthesis

    Dl-2-(4-Chlorophenyl)Glycine frequently serves as a key intermediate in the synthesis of specific NSAIDs, where its unique structure enables the formation of arylglycine-derived active pharmaceutical ingredients. Its inclusion impacts yields and purity during the condensation reaction steps, which are tightly controlled to comply with regulatory filings. Inline QC during crystallization and purification stages ensures that residual chloride content, chiral purity, and impurities remain well within pharmacopoeial limits before downstream formulation into oral solid dosage forms.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) regulations (21 CFR Parts 210/211, US FDA)
    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP) monographs on intermediates and APIs
    • ICH Q3A/B for impurity profiles

    Typical usage ratio

    • Used as a building block at 1.05–1.15 molar equivalents relative to targeted API output, with molarity adjusted based on batch size and reaction yield

    Downstream process integration

    • Introduced during the initial condensation and coupling reaction with substituted benzoyl chlorides, followed by in-process monitoring of intermediate conversion

    Final product types

    • Tablet and capsule formulations of targeted NSAIDs (e.g., arylglycine-derivative pain relievers)
    • Bulk active pharmaceutical ingredients for contract manufacturers

    2. Building Block for Chiral Auxiliary Synthesis in Fine Chemicals

    In advanced organic synthesis, downstream manufacturers use this material for the construction of chiral auxiliaries, particularly in asymmetric hydrogenation and alkylation catalysis. The phenylglycine backbone facilitates the preparation of chiral ligands and auxiliary groups, aiding high-yield synthesis of enantiomerically pure compounds. Quality control relies on chiral HPLC and NMR spectrometry at each synthesis step, as industry standards require traceability and reproducibility in the resulting chiral synthesis pipelines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for batch reproducibility
    • REACH Regulation (EC) No 1907/2006 for chemical safety in the EU
    • Responsible Care program for process safety and stewardship

    Typical usage ratio

    • Added at 0.75–1.25 molar equivalents depending on the targeted stereochemical outcome and process scale

    Downstream process integration

    • Employed as a starting material during the chiral auxiliary assembly stage, before incorporation into catalytic or synthetic processes

    Final product types

    • Batch-scale chiral auxiliaries for pharmaceutical or agrochemical synthesis
    • Custom chiral ligand packages supplied to contract research organizations

    3. Intermediate for Agrochemical Active Ingredient Manufacturing

    Leading agrochemical producers utilize Dl-2-(4-Chlorophenyl)Glycine as an intermediate in the synthesis of certain herbicidal and fungicidal actives. It participates in amidation and ring-closing reactions that define the pharmacophore of the target molecules. The manufacturing process demands precise temperature and pH control to limit byproduct formation and maximize intermediate yield, ensuring compliance with agricultural chemical standards for residues and purity.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines (Joint Meeting on Pesticide Residues) for active ingredient purity
    • ISO 17025 for laboratory test accreditation and analytical methodologies
    • OECD principles of Good Laboratory Practice (GLP) for hazard and residue studies

    Typical usage ratio

    • Utilized at 0.8–1.2 molar equivalents, modulated according to final batch requirements and active ingredient recovery rate

    Downstream process integration

    • Inserted during nucleophilic aromatic substitution or selective reduction steps within the synthesis of the pesticide’s core structure

    Final product types

    • Technical concentrates of herbicides and fungicides
    • Finished agrochemical formulations (suspension concentrates, water-dispersible granules)

    4. Precursor in Specialty Dye and Pigment Synthesis

    Certain high-performance dye and pigment manufacturers incorporate Dl-2-(4-Chlorophenyl)Glycine to introduce targeted aromatic substitution patterns for chromophore modification. This intermediate supports the synthesis of specialty aniline-based dyes—useful for fiber, plastic, and ink coloration—by providing chlorine- and amino-functionalized motifs. Production batches rely on closed-loop reactors and filtration systems to prevent contamination, with full traceability to raw material sources as per sector-specific standards.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems (for waste management and emissions control)
    • EN 71-3 for safety of toy pigments and migration of certain elements
    • GHS (Globally Harmonized System) for hazard labeling and transport

    Typical usage ratio

    • Formulation ratio typically 0.65–0.95 molar equivalents, determined by the required color depth and batch synthesis yield

    Downstream process integration

    • Employed in the coupling reaction between aromatic amines and acid chlorides within dye synthesis lines, often followed by purification and concentration steps

    Final product types

    • High-purity dyes for synthetic fiber and engineering plastic coloration
    • Specialty pigment dispersions for ink, leather, and paper industries
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    Certification & Compliance
    More Introduction

    Dl-2-(4-Chlorophenyl)Glycine: A Manufacturer’s Perspective

    Understanding the Value of Dl-2-(4-Chlorophenyl)Glycine

    Real progress in chemical synthesis often relies on a handful of compounds that quietly but decisively shape research outcomes. Dl-2-(4-Chlorophenyl)Glycine is one of those products that has steadily earned a place in laboratories working on pharmaceutical and agrochemical innovations. Its robust molecular structure, featuring a chlorinated aromatic ring attached to a glycine backbone, offers solid building blocks for both early-stage discovery and process-scale manufacturing.

    As a manufacturer handling this product every day, developments in this compound’s use have never felt abstract. We have spent years refining the process—choosing the right raw materials, investing in precise control of each reaction parameter, and using analytical checks to confirm structural integrity. That focus pays off each time a sample performs as predicted in customer trials, whether they are synthesizing drug intermediates or optimizing herbicide leads.

    Practical Experience Shapes Product Excellence

    Our experience producing Dl-2-(4-Chlorophenyl)Glycine has shown that details matter, both in purity specification and consistency of supply. Maintaining a typical assay of no less than 98% for the main enantiomer, we reject anything less. The TLC profile is checked against verified standards, and we dedicate time to HPLC and NMR confirmations, not just as a regulatory exercise but as a real-world guarantee to our clients. Impurities, particularly unreacted starting materials or unintended isomers, can disrupt synthetic routes downstream. That risk is not theoretical; we have seen customers struggle with supply from sources that overlook these details. Our team willingly revisits purification protocol if even a single batch deviates toward the upper allowable limits for related substances.

    Moisture content makes a real difference in how well Dl-2-(4-Chlorophenyl)Glycine blends into solution phases. Even a percent or two above specification can lead to uneven dissolutions and poor downstream yields, especially when processes rely on precision scales. To mitigate this, we strictly control drying times and oven calibration, testing each run before certification.

    This ongoing vigilance contributes to every successful client synthesis. Our investment in strong material characterization and process tuning doesn’t simply keep regulatory boxes ticked—it adds tangible value on the bench and in the reactor.

    The Impact on Pharmaceutical Research

    Dl-2-(4-Chlorophenyl)Glycine stands out most of all in drug discovery pipelines. Its unique structure allows medicinal chemists to evaluate the effect of para-chloro substitution on biological activity. Analog development thrives on reliable access to such intermediates. Customers rely on our consistent quality for route scouting, SAR studies, and the late-phase optimization that often determines which compound moves forward.

    Pharmaceutical projects tend to require not only small amounts for screening but also multi-kilogram quantities for process development. That scale-up presents distinct challenges. Maintaining high-quality standards at tens or hundreds of kilograms per batch brings lessons fast—impurities and batch-to-batch variability are no longer minor annoyances but major project risks. Through hands-on production, we have found practical measures, from optimizing crystallization conditions to improving filtration and storage, that directly reduce variability. Meeting large project needs, we communicate directly with process chemists, sharing batch data and actively seeking feedback to shape the next run.

    Performance in Agrochemical Synthesis

    The use cases for Dl-2-(4-Chlorophenyl)Glycine in agrochemical research highlight different requirements. Where toxicity and persistence concerns drive innovation, researchers target new herbicides and fungicides using novel building blocks. Our compound provides a way to introduce electronic effects onto active cores via the 4-chlorophenyl group, often resulting in enhanced biological profiles. Early feedback from field R&D teams pointed to issues with process bottlenecks due to suboptimal purity from market alternatives. By refining our isolation techniques and controlling trace metals and organic byproducts, we have enabled these customers to overcome critical synthetic steps and reach trial quantities more swiftly.

    Comparing with Other Glycine Derivatives

    It helps to look at what sets Dl-2-(4-Chlorophenyl)Glycine apart from other glycine derivatives. Unsubstituted glycine finds use mainly as a buffer or simple synthetic precursor. Introduction of the 4-chlorophenyl moiety dramatically changes behavior—altering physical properties and opening up routes that aren’t possible with simpler amino acids. In contrast to alkyl-substituted analogs, the aromatic ring here delivers steric and electronic influences that help modulate activity in lead scaffolds. More electron-donating or electron-withdrawing groups at the para position further tune function, but the 4-chloro arrangement has proven itself as a sort of “goldilocks” substituent in both medicinal and crop science applications.

    As an example, researchers sometimes compare this product against 2-(4-fluorophenyl)glycine or 2-(4-methylphenyl)glycine while investigating SAR. The chlorinated variant generally gives a distinctive polarity and metabolic profile, supporting selection for both potency and stability. Our familiarity with the compound’s impact on reaction yields, solubility, and downstream purification means we can advise customers upfront on what to expect, reducing costly surprises. While other vendors simply deliver material, we offer insight developed through years of hands-on manufacturing and iterative improvement.

    From Process Chemistry to Product Assurance

    No batch rolls out the door untreated by our QA team. Control of both input and output has left us with data-backed confidence in what we ship. Process safety matters as well—chlorinated aromatics carry their own handling risks, and we’ve hardwired those lessons into our SOPs. Staff wear full PPE, detectors keep tabs on air quality, and regular drills ensure readiness for any event. This isn’t just ticking a box for compliance but the only way to keep operations moving day in and day out, protecting both workers and the surrounding community.

    Waste streams go directly into our on-site treatment facilities, which return clean effluent that passes independent third-party assays. Scrutiny of our environmental impact, especially around halogenated waste, shapes each production decision. Sustainable sourcing for starting materials, energy-efficient equipment, and batch tracking are all investments made because we manufacture day after day—cutting corners never pays in the long run.

    Collaborating with Customers

    Our customers range from small academic labs to some of the biggest pharmaceutical and agrochemical brands. Each has different priorities, but trust remains foundational. Some request additional documentation, such as custom COAs or more extensive impurity profiling. Others need lot reservation for long-term projects. We assign production liaisons and technical leads who communicate directly with client chemists, reducing translation errors and allowing rapid troubleshooting. Since we manufacture onsite, we make real-time adjustments: a moisture reduction run here, a custom particle size lot there. These tweaks often turn an off-the-shelf product into a problem solver for a specific synthesis or product platform.

    Occasionally, projects call for downstream modification—protected amino groups, isotopic labeling, or even custom salt forms. These requests are where manufacturing flexibility shows its worth. We have built side-stream labs to handle low-volume customization and dedicated reactors for special purifications, avoiding cross-contamination with larger, general-purpose lines. Flexibility like this is only possible for those who not only sell but also run their own facilities. Routine visitors—whether clients, auditors, or regulators—often remark on just how closely production, QA, and R&D collaborate under one roof. For us, this is simply how real manufacturing gets done.

    Methods and Lessons in Continuous Improvement

    Making Dl-2-(4-Chlorophenyl)Glycine for more than a decade has sharpened our focus on incremental process gains. We run side-by-side batch comparisons, tweak solvents, test out novel crystallization agents, and implement feedback from chemists on the ground. Some small changes—like shifting the sequence of addition or adjusting the cooling gradient—have led to big drops in impurity levels or shortened cycle times. Investments in upgraded filtration and automation deliver direct benefits for both small and large lots.

    We document every adjustment and run stability studies across temperature ranges. Some customers work in tropical climates and need assurance about product storage without cold chain solutions. That reality shapes how we package and test finished product. Packing in airtight, multi-layer containers has proven effective against both atmospheric moisture and light-induced degradation.

    Transparency and Traceability

    No synthetic route functions in a vacuum. Every order of Dl-2-(4-Chlorophenyl)Glycine is shipped with a full documentation package, including batch manufacturing records and certificates from QC. Clients get access to our stability and storage studies and can review real HPLC, MS, and NMR spectra alongside printed data. Open access to all the testing details reassures customers who must answer to their own QA systems or regulatory frameworks.

    Traceability means more than just ticking off boxes for GMP or ISO certification. We offer complete lot trace logs, linking raw material purchase, internal release, and all analytical checkpoints along the way. Few things derail a project like a missing or incomplete dataset at a critical project milestone. Through rigorous record-keeping, we give partners certainty that each molecule originates from a known place, has been checked at every stage, and can be tracked back through each link of the process.

    Customer-Driven Innovation

    Much of the development in how we produce Dl-2-(4-Chlorophenyl)Glycine has come from urgent challenges posed by downstream users. Difficulty in resolving isomers, inconsistent particle sizes, or loss of activity during storage—these issues reach us in direct feedback. We respond by shifting production, investing in new analytic tools, and sometimes rewriting entire purification workflows. The result is a product line that is shaped by the real needs of synthetic chemists and formulators, instead of by abstract marketing imperatives.

    Requests for alternative pack sizes or even nonstandard synthesis forms, like custom salts or derivatives, flow back to production and R&D. We view each request as a chance to improve not just for that client, but for the next one who uses this chemistry as leverage for new discovery.

    Building Trust: A Shared Commitment

    Partners stay with us because they see the practical difference in their processes. Early communication, transparent data sharing, and joint troubleshooting mean projects progress with fewer obstacles. Nobody enjoys delays caused by avoidable quality or fulfillment issues. Our clients have grown to depend on timely and accurate delivery, full transparency in test reports, and the kind of cross-functional attention that comes from real manufacturing depth.

    Each lot of Dl-2-(4-Chlorophenyl)Glycine leaves our facility with exactly the specifications agreed upon, and we stay available to address any concerns post-delivery. If questions arise about reactivity, shelf life, or unexpected side reactions, our staff are ready to dig into underlying root causes alongside the customer’s technical team. Rapid, evidence-based support often makes the difference between a successful synthesis and a stalled project.

    Moving Forward in the Chemical Industry

    As global regulatory and application demands grow, expectations for quality, transparency, and accountability continue to rise. Dl-2-(4-Chlorophenyl)Glycine stands as one example of how chemical manufacturers can meet these demands not through marketing, but through practical updates, constant learning, and a relentless focus on controllable variables in production and quality.

    Making this compound for many years, we see clear patterns: thoroughness in process design, investment in documentation and QA, technical adaptability, and responsiveness to market-driven needs. These are the measures that retain partners and improve outcomes for the research and product development teams depending on specialized materials.

    No amount of surface-level polish can substitute for authentic engagement with both chemistry and client. Year after year, Dl-2-(4-Chlorophenyl)Glycine challenges us to meet ever more exacting standards, and we rise to that challenge, informed by every kilo that leaves our floors and every feedback call we answer.