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Chloroacetyl-DL-Phenylalanine

    • Product Name Chloroacetyl-DL-Phenylalanine
    • Alias DL-2-(Chloroacetyl)amino-3-phenylpropanoic acid
    • Einecs 252-914-7
    • 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

    763785

    Product Name Chloroacetyl-DL-Phenylalanine
    Cas Number 95770-68-8
    Molecular Formula C11H12ClNO3
    Molecular Weight 241.67
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Storage Temperature 2-8°C
    Boiling Point Decomposes before boiling
    Iupac Name 2-chloro-N-(1-oxo-3-phenylpropan-2-yl)acetamide
    Smiles ClCC(=O)N[C@@H](C(=O)O)Cc1ccccc1

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

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of Chloroacetyl-DL-Phenylalanine, with secure screw cap and tamper-evident seal, labeled with hazard information.
    Shipping Chloroacetyl-DL-Phenylalanine is shipped in tightly sealed containers, protected from moisture and light. It should be labeled as a chemical substance and handled according to safety regulations, including proper documentation. During transit, the package must be cushioned and kept at ambient temperature, avoiding exposure to extreme heat or cold to ensure stability and integrity.
    Storage Chloroacetyl-DL-Phenylalanine should be stored in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated conditions). Store separately from incompatible substances such as strong oxidizing agents. Properly label the container and follow laboratory safety protocols for handling and storage of chemicals.
    Application of Chloroacetyl-DL-Phenylalanine

    Applications of Chloroacetyl-DL-Phenylalanine in Industrial Manufacturing

    Chloroacetyl-DL-Phenylalanine serves as a specialized intermediate within several regulated industrial segments, where its reactivity and functional group structure support downstream synthesis of value-added compounds. We manufacture this raw material for use by direct processors in tightly controlled environments, where consistent quality is essential for yield and compliance.

    1. Peptide Pharmaceutical Synthesis

    In peptide API production, Chloroacetyl-DL-Phenylalanine operates as an N-terminal protected amino acid building block. Our manufacturing customers employ this material in the synthesis of custom therapeutic peptides, targeting research and clinical pipeline molecules. The unique chloroacetyl group offers selective reactivity in stepwise acylation during solid-phase peptide synthesis, minimizing racemization while allowing precise chain elongation. Reliable traceability, batch-to-batch purity, and impurity profiles are critical for process validation and registration documentation.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • USP <797> (Pharmaceutical Compounding—Sterile Preparations, where applicable)
    • 21 CFR Part 210/211 (Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General)
    • European Pharmacopoeia (Ph. Eur.) monographs for amino acid derivatives

    Typical usage ratio

    • Used at 1 molar equivalent per N-terminal acylation event; adjusted by peptide length and sequence complexity
    • Integrated into resin-coupling stages at concentrations of 0.1 to 0.5 mmol/g resin

    Downstream process integration

    • Introduced during initial resin loading or post-cleavage acyl protection step in SPPS (solid-phase peptide synthesis)
    • Sometimes used in solution-phase elongation for special frameworks
    • Critical for functionalization ahead of side-chain deprotection and global peptide cleavage

    Final product types

    • Generic peptide APIs for clinical research and preclinical studies
    • Specialty peptide drugs under IND or EU IMPD classification
    • Peptides used in diagnostic kits and imaging agents

    2. Protected Amino Acid Synthesis for Research Chemicals

    Academic and industrial R&D labs use the material to generate selectively protected amino acid derivatives for combinatorial chemistry and probe design. In this segment, the requirement centers on process reproducibility and compatibility with orthogonal protection schemes. Materials undergo characterization protocols for spectral identity, chiral purity (where verified), and minimal cross-contamination. Our scale-up batches minimize residual solvents and meet QC parameters suited for analytical and preparative synthesis laboratories.

    Industry compliance standards

    • GLP (Good Laboratory Practice) principles
    • Purity and analytical requirements according to Sigma-Aldrich/Aldrich/Acros in-house monographs
    • Traceability supporting Material Transfer Agreements (MTA) in collaborative research

    Typical usage ratio

    • Scaled by batch size: 0.5–5 mmol per synthesis run, adapted for microplate or small-parallel setups
    • Used as limiting reagent or as protecting agent, often in excess if complete modification required

    Downstream process integration

    • First introduced during protection of sensitive functional moieties
    • Utilized in N-alkylation, amidation, or acyl transfer reactions
    • Followed by chromatographic purification and characterization

    Final product types

    • Building blocks for combinatorial peptide libraries
    • Labeled amino acids for mechanistic and labeling studies
    • Protected chemical probes for receptor binding and functional assays

    3. Chemical API Intermediate Production

    Custom synthesis providers and large-scale pharmaceutical manufacturers use this intermediate in multi-step transformations. Its chlorinated acyl moiety acts as a precursor in the elaboration of chiral building blocks for active pharmaceutical ingredient (API) candidates. In these routes, strict impurity controls and audit trails for quality assurance are maintained. Regulatory documentation references the origin and batch data from our certified manufacturing site, enabling end users to support DMF submissions or equivalent regulatory filings.

    Industry compliance standards

    • EU GMP (Part II, applicable to intermediates)
    • ICH Q11 (Development and Manufacture of Drug Substances)
    • ISO 9001:2015 for quality system and documentation management

    Typical usage ratio

    • Standard input of 1:1 molar ratio with targeted amines or alcohols; can be loaded in excess in downstream steps to drive conversion
    • Process-specific, typically 10–80 g/L in batch reactors

    Downstream process integration

    • Stagewise fed into condensation, substitution, or hydrolysis processes
    • Used before or after chiral separation steps, depending on threo/dl requirements
    • Subjected to in-process GC/MS or HPLC monitoring to confirm conversion and impurity profile

    Final product types

    • Key advanced intermediates for small-molecule drug candidates
    • Specialty amino acid derivatives for custom customers’ process development
    • Precursor compounds for regulatory-submitted APIs

    4. Specialty Fine Chemical Manufacturing

    Producers in the fine chemicals segment rely on this material to synthesize functionally customized amino acids for flavor, cosmetic, or specialty additives. Its utility extends to creating rare protected analogues that impart specific activity modifications in performance materials. Quality documentation supports full batch traceability, and our supply is engineered for integration into large or pilot-scale batch reactors where control of exposure and reactivity is crucial.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for substance registrations in Europe
    • ISO 14001:2015 for environmental management during chemical synthesis
    • FSSC 22000 or ISO 22000:2018 if final use involves food-related applications (customer-dependent)

    Typical usage ratio

    • Dosing determined by targeted functionalization level, typically 0.2–1.0 molar equivalent per batch
    • Adjusted for end-use properties (e.g., retention time, sensoric attributes), confirmed by customer trials

    Downstream process integration

    • Employed during acylation and protection phases for downstream derivative preparation
    • Added at monitored intervals to control reaction rate and minimize by-product formation
    • Quality-checked before downstream hydrolysis or transamidation

    Final product types

    • Functionalized amino acids incorporated in specialty flavors or aroma compounds
    • Customized cosmetic peptide fragments
    • Performance chemicals for advanced material modification
    Free Quote

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    Certification & Compliance
    More Introduction

    Understanding Chloroacetyl-DL-Phenylalanine from the Manufacturer's View

    Innovation Begins with Reliable Raw Materials

    Our daily work revolves around mastering process control and ensuring that each batch lives up to demanding standards. Today, I want to turn our attention to Chloroacetyl-DL-Phenylalanine, a fine chemical that captures both the complexity of organic synthesis and the discipline of careful engineering.

    From Plant Floor to Finished Product

    Every kilogram of Chloroacetyl-DL-Phenylalanine speaks to the effort of exacting synthesis. This product, unlike simple amino acids, requires precise conditions to introduce a chloroacetyl moiety onto phenylalanine’s backbone. The DL form offers both enantiomers, giving chemists flexibility for different research and production applications.

    I’ve seen the difference that controlled reaction temperatures, steady feeding, and measured pH adjustments make for product purity. Diligence in raw material selection ensures contaminants don’t creep in, which is why we source our starting materials from vetted, long-term suppliers. The average batch we produce ranges in the tens of kilograms, not hundreds, because specialty chemicals have a tighter market and require more oversight.

    The Character of Our Material

    Production quality matters more than a certificate. A lot of what we do isn’t visible in a single number on a specification sheet. Sure, we set an assay usually over 98% by HPLC, and we watch water content closely, but hands-on experience tells us that meticulous washing and drying yields better handling properties and longer shelf stability.

    Our Chloroacetyl-DL-Phenylalanine is manufactured as a white crystalline powder, easily distinguished by its clarity and flow. The chemical structure includes an activated chloroacetyl group, which increases its synthetic utility for peptide coupling and functional group installations. It generally stores well if sealed, but we always remind partners to keep their stock in a dry, cool area, as moisture can promote hydrolysis over time.

    Bulk density, melt point—these are the things you notice when scaling up. We pack it in lined drums or HDPE bags to protect it from humidity and light, because any discoloration or clumping can hint at underlying issues. We don’t take shortcuts here: every lot gets a full identity match and purity screen before it leaves our floor.

    Applications in Real-World Chemistry

    Chloroacetyl-DL-Phenylalanine’s main use comes in synthetic peptide work, especially where site-specific modifications or protective groups matter. The chloroacetyl moiety reacts efficiently with nucleophiles, which lets researchers introduce the phenylalanine backbone in various chemical scaffolds. Pharmaceutical projects use it as a starting point for peptidomimetics aimed at protease inhibitors and other small-molecule therapeutics. In my experience, reaction time is generally swift, and yields remain high compared to non-activated derivatives.

    Academic labs value its availability for developing new ligands and catalysts. The DL mix simplifies purchasing for those not needing optical purity at the outset, reducing cost and lead time. At our scale, we’re able to customize pack sizes, helping reduce wastage and inventory obsolescence for smaller users.

    Quality of the starting material determines how much trouble you’ll have downstream. We’ve had feedback from development chemists noting that our Chloroacetyl-DL-Phenylalanine delivers reliable reactivity without excessive byproducts, which saves time in demanding workups. We've seen it applied in proteomics studies, linker design for targeted drug delivery, and constructing bioactive scaffold libraries.

    Setting Apart from Similar Compounds

    A common question from partners concerns the distinction between our product and other modified phenylalanine derivatives. Non-chlorinated forms, like acetyl-phenylalanine, offer less reactivity and more limited coupling options. The extra reactivity of the chloroacetyl group opens up synthetic strategies not possible otherwise, enabling the creation of stable bonds under milder conditions.

    The DL blend ensures broader applicability compared to single-enantiomer products, which find use in chiral-selective syntheses. For applications where chirality does not dictate biological activity, the racemic form streamlines sourcing and reduces costs. When compared with O-acyl derivatives, we find the chloroacetyl group offers higher selectivity and greater resistance to unwanted side reactions.

    On purity, we have seen some manufacturers tolerate lower HPLC thresholds or moisture content, which for us invites risk downstream. We prioritize higher assay and tighter moisture specs because trace impurities—like residual solvents—can trigger issues in scale-up or formulation.

    Manufacturing Experience Shapes Every Gram

    Long years handling challenging chemicals have shown us that details matter at every step. The reaction between phenylalanine and chloroacetyl chloride needs thorough monitoring, as high exothermicity can cause localized overheating and product discoloration. We employ jacketed reactors with internal cooling coils, keeping temperatures in check, and have invested in real-time analytics to keep impurity formation to a minimum.

    Once synthesis completes, we follow a multi-step recrystallization and filtration process, using solvent mixtures carefully optimized for yield and purity. Operators routinely test intermediate samples for identity and purity before dismissing each batch as finished. Our dryers run at controlled temperatures to prevent thermal degradation—one of the less obvious, but frequent, causes of color change and assay drift.

    Packaging follows strict procedures to avoid cross-contamination. Before every transfer, cleaning validation is performed, especially since our equipment also handles other amino acid derivatives. Experience has taught us that minor residues carry over into finished product if overlooked.

    Every shipment leaves our plant with full analytical documentation, but true confidence comes from repeat partners returning cycle after cycle. Reliability in manufacture translates directly to fewer surprises for everyone down the value chain.

    Navigating Industry Trends and Challenges

    The growing spread of peptide therapeutics drives consistent demand for activated amino acids. Sourcing pressure on base chemicals occasionally impacts timelines, but we manage that risk through a mix of advance contracting and local buffer stocks. Despite tight supply, we never cut corners for cycle time; every order is subject to QC, and no batch moves forward unless all specs are met.

    Regulatory scrutiny has grown in recent years, with authorities seeking tighter impurity profiles and traceability. In our facility, we maintain full batch traceability from raw input to finished product, both to answer partner audits and to support registration dossiers. The reality is, cutting-edge therapeutics require building blocks that meet higher purity benchmarks and documented histories.

    Sustainability also figures into production decisions. We recently switched from a high-energy drying method to a more efficient alternative, trimming energy usage and product loss. While Chloroacetyl-DL-Phenylalanine is not produced on a large commodity scale, every bit of resource saved reduces overhead and environmental footprint—something both our team and our partners care about.

    Supporting Research and Scale-Up

    Research teams face enough uncertainty without supply headaches. Our model as a manufacturer is to provide batch consistency and responsive technical support. Sometimes, process chemists ask for solvent-residual data or elemental analysis beyond standard COA limits. We don’t treat those as bothers; sharing practical process knowledge improves everyone’s results.

    On a handful of occasions, partners have scaled up to multi-kilogram quantities and needed help optimizing their downstream chemistry. Our team has spent days on the phone troubleshooting purification steps, recommending compatible solvents or scavenging strategies, and advising on safe reaction temperatures. Customization sometimes means minor tweaks in drying time or pack sizes, but the long-term partnerships these efforts foster matter more than transactional sales.

    Differences You Can Feel in Daily Use

    End users often mention handling as a concern. Sticky or clumpy amino acid derivatives slow production and complicate weighing. We invest in both process optimization and storage stability testing to keep our material flowing smoothly. Good particle size distribution helps ensure consistent sampling, which translates into reliable, predictable downstream reactions.

    In the early days, moisture pickup created issues during warmer, humid months. Our response was to upgrade packaging and monitor environmental controls, so today’s product stays dry through transit and long-term storage. These changes come from customer feedback, and each improvement we make reflects user experience as much as analytical data.

    Over time, labs comment that the color of our Chloroacetyl-DL-Phenylalanine remains bright, which helps in visual inspection and avoids unnecessary troubleshooting during reaction set-up. Consistency reduces process deviations and helps minimize downtime—a hidden cost in any research environment.

    Quality Control Anchored in Experience

    Everything we ship faces multi-point inspection: HPLC for purity, TLC for spot check, Karl-Fischer titration for water, targeted GC for solvents. We’ve set thresholds based on knowledge of what causes reaction failures downstream, not simply what meets regulatory targets. That means retaining tighter controls than strictly required, because reliable production is only as good as its weakest link.

    Impurities like chlorinated byproducts can escape notice without vigilant screening, so we’ve invested in method development to catch them at trace level. Regular instrument calibration and split-sample comparisons between operators avoid human error. Our team goes beyond minimum requirements because reputational loss from a single bad lot far outweighs short-term savings.

    Future Developments and Continuous Improvement

    We believe product quality improves through daily discipline and learning from every batch. Batch records get reviewed after each run, with anomalies flagged and discussed in regular team meetings. Process changes—no matter how minor—are only made after small-scale validation. This culture of review avoids the pitfalls of overconfident shortcuts.

    Every few cycles, partners ask for chiral-selective material or modifications to the chloroacetyl moiety. We’re able to produce related derivatives on request, but our core strength remains in delivering reliable, well-characterized DL grade suited for diverse development work.

    Our R&D team is exploring solvent reduction and greener chlorination routes to trim waste and environmental impact. These projects can take months to reach fruition, but steady incremental progress pays off over the long term. We’re always open to feedback from synthetic chemists and end users; the practical insights from daily use far outstrip any specification alone.

    Shaping Chemistry with Consistent Building Blocks

    Chloroacetyl-DL-Phenylalanine stands as a versatile component for innovative synthesis. Its controlled reactivity, durability in storage, and broad-minded approach to customization ensure that industrial and research partners spend less time with troubleshooting and more time unlocking results. Our manufacturing philosophy—rooted in direct, hands-on experience—believes good chemistry is more about careful practice than shortcuts.

    Listening closely to partners, keeping up with changing needs, and never compromising on traceability or purity allows us to support projects beyond a simple transaction. As new applications for activated amino acids arise, our confidence continues—grounded in every drum, every bag, and every gram we ship.