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Boc-4-Methyl-D-Phenylalanine

    • Product Name Boc-4-Methyl-D-Phenylalanine
    • Alias Boc-4-Me-D-Phe
    • Einecs 84122-46-7
    • 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
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    Specifications

    HS Code

    988755

    Product Name Boc-4-Methyl-D-Phenylalanine
    Cas Number 112883-18-0
    Molecular Formula C15H21NO4
    Molecular Weight 279.33 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Synonyms Boc-D-(4-Me)-Phe-OH
    Solubility Slightly soluble in water, soluble in organic solvents like DMSO and methanol
    Storage Temperature 2-8°C (refrigerated)
    Melting Point 102-107°C
    Protection Group tert-Butoxycarbonyl (Boc)
    Optical Activity D-isomer
    Chemical Category Unnatural amino acid, Protected amino acid

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 10 grams of Boc-4-Methyl-D-Phenylalanine, labeled with product details and safety information.
    Shipping Boc-4-Methyl-D-Phenylalanine is shipped in a tightly sealed container to prevent moisture and contamination. It is packed with appropriate labeling and shipped at ambient temperature unless specified otherwise. Chemical handling regulations are followed, and documentation such as the Safety Data Sheet (SDS) is included for safe transportation and compliance with shipping standards.
    Storage Boc-4-Methyl-D-Phenylalanine should be stored in a cool, dry, well-ventilated area away from direct sunlight and moisture. Keep the container tightly closed and in a chemical storage cabinet at 2–8°C (refrigerator temperature). Protect from incompatible materials, such as strong acids and oxidizers. Proper labeling and secure handling are recommended to maintain stability and prevent contamination.
    Application of Boc-4-Methyl-D-Phenylalanine

    Applications of Boc-4-Methyl-D-Phenylalanine in Industrial Manufacturing

    As a manufacturer specializing in protected amino acids, we supply Boc-4-Methyl-D-Phenylalanine for advanced synthesis across high-value downstream sectors. The following industrial scenarios highlight specific applications where this material plays a critical role, with attention to regulatory adherence, proven formulation practices, and finished product integration.

    1. Peptide Therapeutics Manufacturing

    Pharmaceutical companies use this compound during the solid-phase peptide synthesis of complex drug candidates where chiral purity and steric control influence pharmacology. Its protected structure allows precise incorporation at constrained positions in long chain polypeptides, supporting research and pilot-scale production of new peptide-based drugs targeting oncology, endocrinology, and rare diseases.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211, US FDA)
    • European Pharmacopoeia (Ph. Eur.) monographs for synthetic peptides
    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP General Chapter <1047> Peptide Standards

    Typical usage ratio

    • 0.5–2.5 molar equivalents per coupling step, adjusted per peptide sequence and length
    • Higher loading (up to 5 eq.) for sterically hindered couplings or iterative fragment assembly

    Downstream process integration

    • Direct input at the protected amino acid coupling stage in solid-phase peptide synthesis (SPPS) or solution-phase assembly
    • Participates prior to Boc deprotection and resin cleavage during post-synthesis processing

    Final product types

    • Investigational peptide active pharmaceutical ingredients (APIs)
    • Custom research peptides for preclinical and early clinical studies
    • Lead candidates in therapeutic peptide pipelines
    • Reference standards for analytical and release testing

    2. Enzyme Substrate Analogs for In Vitro Assay Development

    Specialty reagent producers integrate Boc-4-Methyl-D-Phenylalanine into protected peptides for testing enzyme specificity in preclinical workflows. Its methylated side-chain structure allows differentiation between natural and modified substrate utilization, serving both assay development and screening of protease inhibitors for biochemical research tools.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (applied to reagent manufacturing)
    • OECD Principles of Good Laboratory Practice (GLP, ENV/MC/CHEM(98)17)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU Regulation 1907/2006)
    • NIH guidelines for chemical reagent sourcing in funded projects

    Typical usage ratio

    • 1 molar equivalent per coupling position within synthetic substrate peptides
    • Optimization from 0.8 to 1.2 eq. based on peptide complexity and assay sensitivity requirements

    Downstream process integration

    • Introduced during the solid-phase synthesis of oligopeptides designed as enzyme substrates or analogs
    • Participation precedes derivatization or reporter group conjugation for fluorescent or colorimetric readouts

    Final product types

    • Peptide substrates for fluorometric or colorimetric enzyme assays
    • Inhibitor screening kits for drug discovery
    • Tools for biochemical pathway elucidation
    • Multiplex assay panels for research and diagnostics

    3. Custom Building Blocks for Peptidomimetic Development

    Biotech firms developing novel peptidomimetics employ Boc-4-Methyl-D-Phenylalanine as a non-natural amino acid scaffold to increase proteolytic stability or alter conformational properties in small molecule therapeutics and chemical biology probes. The introduced methyl substituent targets improved pharmacokinetics or bioactivity profiles for downstream products in lead optimization campaigns.

    Industry compliance standards

    • ISO 13485:2016 for medical device and in vitro diagnostic manufacturing (when used in diagnostic reagent development)
    • USP-NF standards for research-grade chemicals
    • REACH (EU) and TSCA (US) chemical substance regulations for research chemicals
    • GMP laboratory protocols for non-clinical research substances

    Typical usage ratio

    • 0.5–2 equivalents per custom monomer insertion step in library synthesis workflows
    • Modulated between 0.5 to 3 eq., matching the degree of backbone modification required by the intended structure-activity relationship study

    Downstream process integration

    • Used in the manual or automated synthesis of peptidomimetic oligomers, entering during iterative coupling steps
    • Common in fragment-based assembly for lead candidate production prior to purification and analytical characterization

    Final product types

    • Peptidomimetic drug leads for medicinal chemistry projects
    • Stabilized peptide mimics for in vitro cellular assays
    • Bioactive probes for receptor or ion channel studies
    • Diagnostic ligands with enhanced stability

    4. Stereospecific Intermediate for Chiral Fine Chemical Synthesis

    Chiral intermediate suppliers and fine chemical producers employ Boc-4-Methyl-D-Phenylalanine in multi-step synthesis, taking advantage of its defined stereochemistry to set absolute configuration within high-value end molecules such as specialty agrochemicals and advanced pharmaceutical intermediates. The methyl-substituted aromatic system tailors the properties of next-step products, supporting proprietary API precursor development.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing process control
    • GMP guidelines for chemical intermediates (as per PIC/S recommendations)
    • Hazardous Substance Management (REACH, EU Regulation 1907/2006)
    • Chemical Substance Control Law (CSCL, under Japanese law for chiral intermediates)

    Typical usage ratio

    • 1 equivalent at the key intermediate stage, typically 0.8–1 eq. depending on availability and downstream reactivity requirements
    • May increase to 2 eq. to drive completion of selective coupling or condensation reactions

    Downstream process integration

    • Fed in at controlled temperature and pH into the condensation or amidation step
    • Often followed by selective deprotection and further functional group conversion

    Final product types

    • Enantiomerically pure advanced intermediates for APIs
    • Chiral building blocks for specialty chemical synthesis
    • Modified amino acid derivatives for further fine chemical processes
    • Single-isomer agrochemical precursors

    5. Analytical Grade Reference Standards for Peptide QC

    Contract testing organizations and peptide manufacturers require high-purity, well-characterized Boc-4-Methyl-D-Phenylalanine as a reference material to verify chiral integrity and quantitative response in analytical systems. The use of this compound as a standard improves traceability during HPLC, LC-MS, and capillary electrophoresis method validation for industrial peptide QC.

    Industry compliance standards

    • ISO/IEC 17025:2017 for calibration and testing laboratories
    • USP Reference Standard certification requirements
    • FDA 21 CFR Part 11 (electronic records for QC traceability)
    • ICH Q2(R1) Validation of Analytical Procedures

    Typical usage ratio

    • Standard addition levels range from 0.01 to 0.1% w/w relative to test sample volume for calibration curves
    • Calibration point concentrations selected per method linear range, typically 1–10 μg/mL

    Downstream process integration

    • Prepared as a calibration or control standard in analytical sample queues
    • Used in method validation for peptide quantification, purity profiling, or enantiomer resolution

    Final product types

    • Peptide analytical reference standards
    • Certified control samples for pharmaceutical release testing
    • Calibration standards for HPLC and LC-MS in peptide QC labs
    • Chiral purity assay benchmarks
    Free Quote

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    Certification & Compliance
    More Introduction

    Boc-4-Methyl-D-Phenylalanine: A Closer Look from the Manufacturer’s Side

    Our Experience with Boc-4-Methyl-D-Phenylalanine Production

    Producing Boc-4-Methyl-D-Phenylalanine starts long before raw materials meet in a reactor. At our facility, we design every step around reproducibility and high standards, using real-time feedback and batch-by-batch analysis to steer each stage. It is easier to promise purity on paper than to achieve it consistently on the plant floor. Over the years, we have refined our routes to limit byproducts and improve yields, responding both to market feedback and our own continuous quality improvement.

    Boc-4-Methyl-D-Phenylalanine, known for the N-tert-butoxycarbonyl (Boc) protection on the amino group, fits a niche in peptide synthesis where strict selectivity and chirality matter. It is not just another amino acid derivative. Once the reaction begins, minor differences in temperature, solvent purity, or mixing efficiency visibly affect outcome. Technicians monitor these variables closely, using sampling and in-house analytical tools. Finished product moves only after confirming that it matches the expected optical rotation and NMR profile. Over time, the protocols adapt based on customer feedback and the lessons drawn from any unexpected blip.

    The Structure and Its Relevance for Synthetic Design

    The backbone of this molecule, with a methyl group at the para position of the phenyl ring on the D-isomer of phenylalanine, often drives choices in peptide synthesis projects that avoid standard L-analogues. The D-configuration resists enzymatic degradation better, eastablishing importance in design of bioactive peptides or peptidomimetics where stability is key. Boc protection remains essential where acid-labile groups need safeguarding during synthesis. Years ago, working with an unprotected version, we often saw side reactions complicate purification. Returning clients pushed us to maintain rigorous standards with moisture and air sensitivity, as even slight hydrolysis shifts product purity.

    Physical Characteristics: More Than Meets the Eye

    Specification sheets can list melting points and appearance, but actual batches often tell their own story. Boc-4-Methyl-D-Phenylalanine leaves our plant as a white to off-white crystalline powder. We keep particle size in a defined range—fine enough to dissolve smoothly for solid-phase synthesis, coarse enough to avoid dusting losses and concerns in weighing. We maintain residual solvent limits below industry standards, avoiding sticky particles or uneven crystallization. The odorless nature signals to us that the protection steps and washes performed as intended. If a batch emerges with unusual lump formation or faint discoloration, we halt packing and check for microimpurities, never sending uncertain material downstream.

    Key Differences: D- vs L- Phenylalanine Analogues

    Some customers, unfamiliar with the impact of chirality, ask if Boc-4-Methyl-D-Phenylalanine can substitute for the more common L-form or unmodified D-phenylalanine. From a manufacturing lens, preparing the D-isomer ramps up both the synthetic complexity and cost. Enantiomeric purity sits above 99%, supported by chiral HPLC traces and periodic retention time mapping against reference materials. Each impurity, even below one percent, signals potential issues in target peptide function or downstream coupling. Projects using peptides for diagnostics, pharmaceuticals, or enzyme studies depend on these rigorous controls. Over years, we learned to never skip a test based on past successes—sometimes a tiny shift in supplier for a raw material gives rise to a new minor impurity.

    We once had a client approach us after inconsistencies from traders. They traced issues to misidentified enantiomers and erratic protection group stabilities. Our own testing, retracing their route, showed how even small manufacturing deviations cause batches of Boc-4-Methyl-D-Phenylalanine to behave differently in SPPS or fragment condensation. By controlling each variable ourselves, we demonstrate value not through claims but with actual usable outcomes in complex projects.

    Usage in Peptide Chemistry

    Boc-4-Methyl-D-Phenylalanine plays a focused role in synthetic peptide chemistry, especially in research and preclinical drug spaces. As part of short and medium chain peptides, it brings steric effects and a hydrophobic edge that researchers tweak for resistance or target binding. Lab protocols draw on this amino acid to fine-tune receptor selectivity or block undesired enzymatic cleavage. Some creative chemists build cyclic peptides with Boc-4-Methyl-D-Phenylalanine units as a way to introduce rigidity without sacrificing solubility. The methyl group, sitting at the para position, modifies electronic and steric environments enough to affect biological activity, as documented in peer-reviewed studies.

    Talking use cases, we see demand both from medical research programs designing enzyme-resistant analogues and from industrial sectors iterating on peptide-based catalysts. Many times, our clients provide detailed feedback—solubility measurements, coupling efficiencies, or aberrant side-products—and expect us to help interpret outcomes or suggest potential adjustments in synthesis. Direct calls between researcher and factory technician encourage a problem-solving relationship that traders or resellers cannot match.

    Manufacturing Controls and Challenges

    Boc-4-Methyl-D-Phenylalanine synthesis typically requires precise temperature and pH management during Boc-protection, followed by purification steps that remove byproducts and preserve the fragile D-configuration. In early days, we struggled with scale-up, as container geometry or stirring regimes led to incomplete protection or local overheating. Our team regularly revises SOPs on reactor loading and discharge, using trace-level analytics to call out batch deviations. Caking, static buildup, and trace metal contamination once plagued some early runs; now we precondition vessels and validate process water before every shift.

    Handling D-isomers tests the commitment to separation science, since unwanted racemization can ruin batches and cost time. Our facility uses calibrated columns, regularly challenged with standards, while technicians understand the difference between sharp, chiral purity and simple TLC cleanliness. Over the years, investments in real-time NMR feedback, robust drying systems, and controlled atmosphere storage cut waste and guarantee the right material reaches customers in proper condition—not degraded, not contaminated, just as we promised on the COA.

    Product Quality: Verification beyond Paperwork

    From our end, real assurance does not end with a COA or standard certificate. Each batch leaves the facility only after a panel reviews HPLC, NMR, MS, and moisture results. Unusual results—such as an unexpected minor peak or unexplained moisture—receive a full process audit before approval. Our own experience shows that over-reliance on supplier documentation, without verifying with in-house methods, only invites problems later in peptide assembly or scale-up.

    We regularly invite customers for facility audits and open our documentation. Every reagent’s lot number can be traced to its use in a specific batch. Regulatory expectations demand rigorous documentation, but it's the hands-on training—every technician, chemist, and quality control analyst handling material repeatedly—that builds confidence in consistent outcomes.

    Comparisons with Other Protected Amino Acids

    Some clients weigh Boc-4-Methyl-D-Phenylalanine against Fmoc- or Cbz-protected versions or even unsubstituted phenylalanine analogues. Operational requirements drive these choices. Boc-protected forms support acid-catalyzed deprotection better, making them the go-to in older solid-phase strategies and cases where base-sensitive groups exist elsewhere in the peptide chain. Fmoc groups, favored in automated synthesis, respond best to base-driven release, yet introduce their own risks of side-reactions under strong base. Differences play out in performance more than paperwork, and application-specific needs take precedence.

    One thing stands clear—Boc-4-Methyl-D-Phenylalanine shines where combinations of hydrophobic and stability traits create separation in both biological and synthetic space. Peptides that rely on modified phenylalanine residues often show measurable pharmacokinetic advantages. Some R&D projects that shifted between Cbz or Fmoc protections later found that Boc derivatives reduced purification headaches, thanks in part to cleaner separation of side-products.

    Environmental and Safety Considerations in Manufacturing

    Production demands close attention to environmental safety. All solvents used in synthesis undergo recovery and purification prior to waste treatment. Each piece of process equipment faces cleaning validation to prevent cross-contamination—constantly monitored by visible tagging and daily log checks. Waste streams, solvent emissions, and residual amine vapors require active carbon trapping and caustic scrubbing, documented in our monthly emission audits.

    Factory safety also means technician training—each step, from powder handling to final QC, includes full personal protective equipment and documented procedures. Technicians report near-misses directly to plant management, using these reports to improve engineering controls or workflow design for future runs. Years of daily experience built a culture where pride in product goes hand in hand with pride in a safe workplace.

    Customer Collaboration and Technical Support

    Direct feedback from researchers often shapes our priorities and guides process improvements. When issues arise with solubility or coupling, our technical support team partners closely with development chemists to review conditions and suggest alternatives. Recently, a customer’s inconsistent yields with Boc-4-Methyl-D-Phenylalanine prompted a factory review. Adjusting the addition sequence and drying protocol not only resolved the immediate problem but enhanced overall process robustness in subsequent runs.

    Some partners request milligram-scale trial batches or targeted modifications. Supporting these requests means challenging our own procedures, running pilot batches, and committing resources that a simple trading company would never entertain. Years of this practice taught us that a close supplier-developer partnership speeds innovation more reliably than generic advice ever could.

    The Importance of Ingredient Transparency

    Demand for full traceability has increased over the last decade. Researchers wanting Boc-4-Methyl-D-Phenylalanine frequently ask about not only batch testing but also the origins of supplied reagents, the sterility controls used, and whether we support green chemistry initiatives. From our end, providing batch-level documentation and purity test data helps remove doubt and instill confidence.

    Ingredient transparency plays an essential role beyond regulatory compliance. A minor impurity, overlooked in bulk commodity material, can destroy performance in drug development or diagnostics. Open data, transparent documentation, and responsive feedback cycles demonstrate that our material meets more than just internal company benchmarks or written industry standards.

    Market Trends and Future Directions

    Demand for unique amino acid derivatives continues to evolve. Boc-4-Methyl-D-Phenylalanine currently occupies a specialized space, yet interest rises yearly as peptide therapeutics and custom screening libraries proliferate. Manufacturer experience highlights that responsiveness—ability to scale small or large, tailor drying protocols, and act on analytical feedback—sets long-term suppliers apart from short-term merchants or third-party sources.

    We see global research pushing for new peptide drugs and diagnostic agents, many of which require modified amino acids with specific physicochemical properties. Boc-4-Methyl-D-Phenylalanine plays a role here by granting researchers the flexibility to tune molecules for resistance against enzymatic cleavage or enhanced receptor selectivity. The science fueling this demand is unforgiving of inconsistency.

    Concluding Insights from the Factory Floor

    Experience, not just certifications, sustains our reputation with Boc-4-Methyl-D-Phenylalanine. Each kilogram reflects iterations on process design, hands-on training, and open dialogue with chemists and engineers. We constantly adapt—testing purification methods, tightening quality checks, and soliciting user feedback—advancing not only compliance but practical problem-solving. Routine monitoring, meaningful data-sharing, and factory transparency bolster reliability and support customer outcomes in complex biotechnology projects.

    Manufacturing Boc-4-Methyl-D-Phenylalanine asks for more than routine. From process startup to packaging, hands and minds at every level commit to detail—tracking trends, responding to requests, and maintaining safety as non-negotiable. Our growth depends on real trust built batch by batch, not abstract claims or standard templates.

    Technical details help, but working out solutions stems from a close understanding of both factory realities and research needs. Boc-4-Methyl-D-Phenylalanine, a specialty product developed in-house, draws on this blend of experience, technical rigor, and open communication. Every batch, tested and shipped, signifies not only chemical purity but decades of accumulated knowledge, lessons learned, and shared success with the research and development community.