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2-Methyl-L-Phenylalanine Monohydrate

    • Product Name 2-Methyl-L-Phenylalanine Monohydrate
    • Alias 2-Me-L-Phe·H2O
    • Einecs 253-981-8
    • 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

    796901

    Product Name 2-Methyl-L-Phenylalanine Monohydrate
    Chemical Formula C10H13NO2·H2O
    Molecular Weight 199.23 g/mol
    Cas Number 121855-03-6
    Appearance White to off-white crystalline powder
    Purity ≥98%
    Solubility Soluble in water
    Optical Rotation [α]20/D +15° to +25° (c=1, H2O)
    Storage Temperature 2-8°C
    Synonyms L-α-Amino-2-methylbenzenepropanoic acid monohydrate
    Stability Stable under recommended storage conditions
    Chirality L-isomer

    As an accredited 2-Methyl-L-Phenylalanine Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tamper-evident cap, 25 grams, labeled with product name, CAS number, purity, storage instructions, and hazard symbols.
    Shipping 2-Methyl-L-Phenylalanine Monohydrate is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. It should be transported at ambient temperature, away from direct sunlight and incompatible substances. Proper labeling in accordance with chemical regulations ensures safe handling and compliance during shipping and delivery.
    Storage 2-Methyl-L-Phenylalanine Monohydrate should be stored tightly sealed in a cool, dry, well-ventilated area, away from moisture, heat, and direct sunlight. Keep it at 2–8°C (refrigerator temperature) and protect it from incompatible substances. Always use appropriate personal protective equipment when handling. Ensure container is properly labeled and store according to relevant chemical safety regulations.
    Application of 2-Methyl-L-Phenylalanine Monohydrate

    Applications of 2-Methyl-L-Phenylalanine Monohydrate in Industrial Manufacturing

    2-Methyl-L-Phenylalanine Monohydrate enables specialized molecular design and peptide synthesis for pharmaceutical, biotech, and fine chemical sectors. Our facility supports high-purity production to meet industry-specific downstream requirements. See below for practical application fields and integration details.

    1. Peptide Active Pharmaceutical Ingredient (API) Synthesis

    Peptide drug manufacturers utilize 2-Methyl-L-Phenylalanine Monohydrate as a chiral building block when designing targeted peptide APIs, notably in metabolic disorder and oncology drug development. Our material supports solution-phase and solid-phase peptide synthesis, entering the sequence where unnatural analogues are required for improved in vivo performance. Stringent quality control during raw material release aligns with FDA, EMA, and ICH Q7 standards. Customers determine incorporation ratios per target peptide length and activity profile, commonly between 1% and 6% molar substitution. Integration occurs during the stepwise amino acid coupling phase, followed by chromatographic purification and lyophilization. Resulting APIs include single-entity peptide actives, combination drugs, and next-generation biopharmaceuticals approved for clinical use.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • USP General Chapter <1045> Biotechnology-Derived Articles

    Typical usage ratio

    • 1%–6% of the total peptide sequence (molar basis), adjustable per design protocol and biological target.

    Downstream process integration

    • Incorporated during stepwise peptide elongation in SPPS/Fmoc or Boc protocols by direct coupling to resin or solution-phase intermediate.

    Final product types

    • Metabolic peptide APIs (e.g., GLP-1 analogs)
    • Cancer therapeutic peptides
    • Investigational peptide drug substances
    • Modified peptide intermediates for further API development

    2. Synthetic Enzyme Substrate & Inhibitor Research

    Biotech R&D teams employ our product for the synthesis of modified substrates and inhibitors used in enzyme activity assays and structure-activity relationship (SAR) studies. This application provides researchers with enhanced selectivity, site-specific labeling, or resistance to proteolytic degradation. Dosing levels typically range from 0.01 mmol to 0.5 mmol per substrate batch, determined by substrate library scale or inhibitor potency optimization. The material enters the initial condensation or amidation step in custom organic synthesis or combinatorial chemistry pipelines. End products include non-clinical probe molecules, lead optimization tools, and functionalized intermediates for further derivatization.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management System
    • Relevant institutional review board (IRB) protocols for assay validation

    Typical usage ratio

    • 0.01 mmol–0.5 mmol per substrate or inhibitor batch, precisely adjusted for reaction scale and research protocol.

    Downstream process integration

    • Dissolved as initial monomer in custom synthesis for modified peptide or amino acid-derived inhibitor preparation; utilized in high-throughput screening (HTS) and SAR workflows.

    Final product types

    • Modified enzyme substrates
    • Bespoke protease inhibitors
    • Peptidomimetic research molecules
    • Fluorescently labeled assay components

    3. Chiral Ligand and Catalyst Precursor Manufacturing

    Specialty chemicals producers select this material when designing chiral ligands and organocatalysts for asymmetric synthesis pathways. Its sterically demanding side chain enables fine control in transition metal-catalyzed reactions such as hydrogenation or cross-coupling in agrochemical and fine chemicals production. Manufacturers standardly incorporate this amino acid derivative at 5%–30% molar ratio with respect to the metal precursor or other ligand units. The product integrates at the ligand assembly or derivatization stage, directly impacting enantioselectivity during downstream catalytic runs. Finished products include chiral phosphine ligands, peptide-based catalysts, and immobilized catalyst supports for industrial synthesis lines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH Registration (where applicable in EU markets)
    • Responsible Care® Program Commitments

    Typical usage ratio

    • 5%–30% molar ratio against ligand or catalyst precursor base, determined during catalyst formulation optimization studies.

    Downstream process integration

    • Reacted with phosphine or amine reagents during the ligand construction phase; introduced in batch or semi-continuous chiral catalyst production units.

    Final product types

    • Chiral phosphine and phosphoramidite ligands
    • Peptidic organocatalysts
    • Solid-supported asymmetric catalysts
    • Chiral intermediates for fine chemical production

    4. Diagnostic Reagent Synthesis for Clinical Testing Kits

    Producers of in vitro diagnostic (IVD) kit components rely on this non-proteinogenic amino acid to modify peptide antigens and calibrators, raising assay specificity or introducing measurable tags. Quality-certified production lines adopt GMP principles to ensure batch traceability and low endotoxin content, meeting requirements for CE-IVD and FDA 21 CFR 820 standards. Recommended usage spans from 0.2% to 4% of total diagnostic peptide or protein content, defined during standardized formulation trials and performance validation. Downstream, the ingredient enters through site-specific chemical modification or direct solid-phase incorporation, resulting in reproducible, high-purity peptide antigen stocks. This enables production of immunoassay controls, quantitative calibration peptides, and antibody screening kits distributed to clinical labs.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management Systems
    • US FDA 21 CFR 820 Quality System Regulation
    • European Union IVDR (Regulation (EU) 2017/746)
    • CE IVD Marking Requirements

    Typical usage ratio

    • 0.2%–4% w/w of total diagnostic peptide/protein mass, validated per assay format and detection limit.

    Downstream process integration

    • Introduced during chemical modification or chain elongation for peptide antigen or calibrator synthesis, followed by purification ahead of kit assembly.

    Final product types

    • Peptide immunoassay standards
    • Quantitative diagnostic calibrators
    • Labeled peptide antigens for ELISA kits
    • Clinical antibody screening panels

    5. Nutritional Supplement Research and Specialty Feed Applications

    Animal nutrition companies and advanced supplement developers occasionally trial 2-Methyl-L-Phenylalanine Monohydrate for its role in experimental feed efficiency and metabolic effect studies, especially in high-value aquaculture or laboratory animal formulations. Material quality aligns with FAMI-QS and ISO feed safety requirements. Dosage levels generally range from 0.01% to 0.3% of total amino acid fraction, based on tolerance, species requirements, and intended metabolic outcomes. Application occurs during amino acid premix blending, prior to granulation, extrusion, or pelleting in feed manufacturing lines. The end formulations support research on improved protein utilization, customized amino acid fortification blends, and pilot-scale specialty feeds for scientific use or niche animal care markets.

    Industry compliance standards

    • FAMI-QS Code of Practice for Specialty Feed Ingredients
    • ISO 22000:2018 Food Safety Management Systems
    • EU Regulation (EC) No 1831/2003 on additives for animal nutrition
    • US FDA Center for Veterinary Medicine (CVM) Compliance Policy Guides

    Typical usage ratio

    • 0.01%–0.3% of the total amino acid mix per feed batch, selected via nutritional trial protocols and safety assessments.

    Downstream process integration

    • Blended with main amino acid premix; subjected to thermal and pressure processing during feed manufacture; QC for homogeneity and stability in pilot feeding trials.

    Final product types

    • Experimental feed premixes for research trials
    • Specialty amino acid blends for aquaculture
    • Laboratory rodent and zebrafish diets
    • Custom animal nutrition prototypes for metabolic studies

    6. Fine Chemical and Advanced Material Intermediate Synthesis

    Advanced materials laboratories and fine chemical companies utilize 2-Methyl-L-Phenylalanine Monohydrate to provide chirality and functional group diversity in the preparation of pharmaceutical intermediates, liquid crystal compounds, and optoelectronic materials. Each customer aligns procurement and usage with ISO 9001 or specific pharma supplier qualification systems, focusing on impurity profile and optical purity. Process engineers introduce the raw material at the targeted synthetic step, including amidation, esterification, and cross-coupling in organic synthesis workflows. Typical input levels span 1%–25% of the reagent list, determined by molecular design and downstream purification demands. Outputs expand to specialty fine chemicals, chiral intermediates for further synthesis, and niche performance materials in R&D settings.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Customer-specific supplier qualification protocols
    • REACH/CLP Registration (where required in EU)

    Typical usage ratio

    • 1%–25% of the total reactant input per synthesis batch, variable by molecular blueprint and downstream yield optimization.

    Downstream process integration

    • Employed as primary or secondary chiral reagent during multistep organic synthesis, typically before key resolution or protection/deprotection stages.

    Final product types

    • Chiral synthons for active intermediates
    • Custom building blocks for material chemistry
    • Liquid crystal and optoelectronic compound precursors
    • Advanced R&D fine chemicals for specialty applications
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    Certification & Compliance
    More Introduction

    2-Methyl-L-Phenylalanine Monohydrate: A Chemist’s Perspective

    Looking Closer at 2-Methyl-L-Phenylalanine Monohydrate

    In our years of hands-on synthesis and production, we have seen many specialty amino acid derivatives enter the market, each offering its own benefits for modern research and industry applications. 2-Methyl-L-Phenylalanine Monohydrate stands out among them. Its subtle structural difference—a methyl group attached to the phenylalanine backbone—translates to distinct behavior in both chemical and biological contexts. This monohydrate form, carrying a single water of crystallization, offers good handling, storage stability, and reliable results batch after batch.

    Model and Specifications Shaped by Direct Production Experience

    Over time, we’ve refined our process parameters to produce 2-Methyl-L-Phenylalanine Monohydrate with tight control over every aspect, from starting materials to packaging. The crystalline powder displays high purity, with HPLC analysis typically showing values above 99%, while water content hovers right around the monohydrate mark, ensuring reproducibility when weighing or dissolving. Our spectroscopic checks, including NMR and IR, confirm correct methylation and stereochemistry, keeping unwanted isomers and by-products out of the picture.

    Texture and color offer cues for hands and eyes. The product arrives as a white to off-white, fine crystalline material—never clumpy or yellowed, reflecting both clean synthesis and meticulous drying. Odor and taste, if present, point to trace impurities, so our batches remain virtually odorless, an overlooked but often telling sign of true chemical quality.

    Why End Users Value This Amino Acid Derivative

    2-Methyl-L-Phenylalanine Monohydrate attracts attention in modern peptide synthesis, pharmaceutical research, and structure-function studies in bioengineering. Our collaboration with academic teams and industrial R&D has shown this compound’s unique impact on peptide backbone rigidity and hydrophobicity. Compared with standard L-Phenylalanine, adding that one methyl group to the aromatic ring influences the way peptides fold, bind, and perform in various assays.

    Medicinal chemists use 2-Methyl-L-Phenylalanine Monohydrate for SAR (Structure-Activity Relationship) studies, exploring how minor modifications in side chain architecture shift binding affinities or pharmacokinetic properties. Peptide chemists appreciate the predictable coupling behavior—protected or unprotected, acid or base conditions, this material reacts consistently, reducing surprises in solid-phase or solution-phase synthesis. Its water of crystallization ensures predictable mass during formulation, reducing errors in molarity and stoichiometry—a benefit former users of the anhydrous version will recognize all too well.

    In protein engineering and design, researchers employ this amino acid to build sequence libraries, optimizing for robustness or enzyme selectivity. That methyl group, though small, acts as a probe into how slight non-natural modifications can resist enzymatic degradation or slightly adjust hydrophobic packing in protein cores. For years, biopharmaceutical projects have relied on this chemical as a marker, a modulator, and a test of nature’s limits.

    Comparing Directly to Standard L-Phenylalanine and Similar Derivatives

    Years of synthesis work have taught us never to underestimate the impact of a methyl group’s placement. Standard L-Phenylalanine offers broader biological compatibility, but users aiming for improved metabolic stability, subtly altered aromatic stacking, or site-specific labeling reach for its 2-methyl analog. The side chain bulk changes peptide clearance in vivo, and small shifts in hydrophobicity can make or break an assay’s selectivity.

    With our monohydrate form, solubility in water or common biological buffers sits in a familiar range, similar to L-Phenylalanine, making it accessible for cell culture, enzyme studies, and formulation work. Lab techs working day by day with amino acid analogs know that dustiness or unexpected hygroscopicity complicates weighing and solution prep—here, the monohydrate structure keeps the product free-flowing and manageable, even in humid environments. In contrast, the anhydrous version demands careful desiccation and often cakes on the scoop.

    Moving beyond application, cost and purity also play roles. L-Phenylalanine remains the cheaper and more easily sourced bulk amino acid, but the specialized synthesis route for the 2-methyl analog, with its extra steps and careful chromatographic separation, justifies the price for the performance and reliability it brings. Purity and batch reproducibility top the concerns for pharmaceutical researchers, and as direct manufacturers, our protocols minimize batch-to-batch drift, outperforming off-brand or import resellers where trace contamination or incorrect isomer ratios frequently appear.

    Technical Handling and Quality Under Practical Lab Conditions

    The demands of synthetic chemistry often expose the shortcomings of marginal raw materials. Our years of bench work remind us that a chemical is only useful if it behaves predictably every time. 2-Methyl-L-Phenylalanine Monohydrate resists caking under most storage conditions and dissolves into clear, particle-free solutions without mysterious residue. Solubility checks, run monthly as part of our QC, consistently reach published values in both neutral and mildly acidic media. Peptide coupling reactions with standard activation protocols proceed without the stubborn by-product formation that sometimes plagues less pure sources or anhydrous grades stored under poor humidity control.

    Storage presents few difficulties. Packed in robust, moisture-resistant containers, the product tolerates typical room temperature lab storage while maintaining crystal integrity. Many users note that return visits to the bottle—weeks or months later—yield material that scoops as freshly as the day it was opened, avoiding the frustrating clumping that results from poorly controlled crystallization or low-level hydrolysis.

    For critical research and scaled project work, the availability of consistent lot documentation—certified by our in-house analytical chemists—adds comfort. Each batch travels with full analytical documentation, cross-checked against historic benchmarks in our archive, rather than ad hoc sampling or vague generalities. This ensures that grant-funded research, regulatory submissions, or industrial optimization proceed without reactivity surprises or delayed timelines caused by out-of-spec raw materials.

    Feedback from Real Users and Practical Results

    We welcome open feedback from our academic collaborators, contract research organizations, and pharmaceutical labs. Direct users confirm that the clean handling and reliable titration data simplify day-to-day work. For those building peptides by hand, lengthy dissolution times or inconsistent crystallinity quickly slow progress. Our customers report streamlined workflow during both manual and automated synthesis, with rare need for troubleshooting compared to bulk imports or secondary-market material.

    One peptide chemist relayed how switching to our 2-Methyl-L-Phenylalanine Monohydrate reduced ambiguous peaks on HPLC traces, clarifying both product and intermediate purity. In pharmaceutical research, teams value the reproducibility our product brings to PK/PD assay development—where even minor setbacks in intermediary purity can waste weeks, if not months, of project time. Sales and purchasing teams often note reduced back-and-forth with their internal users, once analysts see the expected spectra match reference standards every time.

    Demand also comes from the protein engineering world. Structural biologists find that the compound’s predictable properties make it ideal for co-crystallization with enzymes, exploring how the methyl group restricts side chain motions or nudges aromatic stacking. One university group used it as part of a substrate library for probing enzyme specificity, with results that directly guided the next generation of catalyst designs. None of this success happens by accident; care starts in the production suite and carries through to your benchtop.

    Challenges in Manufacturing and How We Tackle Them

    Producing 2-Methyl-L-Phenylalanine Monohydrate brings technical hurdles not shared by more common amino acids. Methylation must occur selectively on the aromatic ring, not on vulnerable side chains or the amine group. Years ago, inconsistent reactivity and by-product profiles hampered yield and purity. Through repeated process trials, we optimized catalytic and stoichiometric conditions—balancing methylating agent selection, temperature, and solvent choice for both safety and end product integrity.

    Crystallization, crucial for a monohydrate form, challenges even seasoned operators. Initial crystallization attempts sometimes produced heterogeneous hydrates or residual solvent inclusion. These errors only show themselves on re-dissolving or through careful Karl Fischer water titration. Our team established rigorous drying and rehydration steps, which deliver reliably single-hydrate form, untainted by mixed-batch artefacts. This nuanced understanding only comes from direct, ongoing engagement with both production chemistry and real-world user needs.

    Waste minimization and environmental burden also weigh upon each batch. We have transitioned from legacy methylating agents toward options with lower environmental and personnel health impacts. In-process capture and recycling, batch-to-batch water monitoring, and process control analytics brought both waste volume and off-gas exposure well below sector norms.

    Continuous Improvement and Role in Research Progress

    We’ve witnessed enormous growth in the use of non-standard amino acids, driven by drug discovery and synthetic biology’s expanding ambitions. Where 2-Methyl-L-Phenylalanine Monohydrate once served niche projects, it has now become a staple in diverse molecular design campaigns—ranging from GPCR ligand studies to next-generation peptide therapeutics.

    Process improvements don’t rest. Each year our analytical and synthetic teams review global feedback, new published synthetic routes, and changing regulatory standards, updating our production as needed. Discontinuities in product performance never go unnoticed, as repeat customers and their results form our best early warning system. Rigorous, hands-on oversight and real-time process upgrades maintain our edge, ensuring standards meet not just current, but emerging, expectations.

    Requests for alternative salt forms, different hydrate content, or custom packaging sometimes arise. We address these through our flexible batch production capabilities, learned through a mix of market demand and the direct experience of scaling up from pilot to commercial runs. For clients handling unique research pipelines, this customization keeps their innovation on track without requiring broad compromise in formulation.

    Supporting Advanced Chemical and Biological Discovery

    Our team keeps close ties with those who rely on 2-Methyl-L-Phenylalanine Monohydrate to push scientific boundaries. In collaborations, the stories that matter often happen at the benchtop: a PhD student troubleshooting cyclization yield, a lead scientist working late to optimize a peptide library, a formulator evaluating shelf-life for early-stage therapeutics. Each batch, clean and consistent, keeps those moments focused on science rather than battling raw material problems.

    From the careful sourcing of chiral starting materials, through multi-step synthesis, right down to lot traceability and on-time shipping, we know every variable matters. Peptide-based medical advances, enzyme engineering campaigns, and fundamental protein folding studies depend on the reliability inherent to every bottle we provide. Our team has seen rushed and inconsistent source material slow entire programs—not because of any mistake at the discovery stage, but due to something as simple as an unstable hydrate form or imprecise methyl placement.

    Each technical advance, whether in reaction methodology, purification, or analytics, finds its way into our production suite once proven. Annual audits and bench reviews ensure our process evolves without abandoning proven strengths. For us, the story of 2-Methyl-L-Phenylalanine Monohydrate is not just about a chemical structure or purity spec, but about unbroken trust across the laboratory community, built from firsthand work and ongoing relationships.

    Looking Ahead: The Path Forward

    Chemical manufacturing shapes more than just supply chains. In offering 2-Methyl-L-Phenylalanine Monohydrate, we recognize our responsibility to both the scientific and broader industrial world. Future developments in personalized medicine, programmable biomaterials, or next-generation diagnostics will demand even tighter control, both in material specification and in data support.

    We will keep investing in both people and equipment to raise analytical standards, automate batch tracking, and widen options for customized variants. Partnerships—grounded in technical transparency and proven product performance—form the backbone of this approach. We know that whether you’re running a discovery screen or building scale-up protocols, material confidence allows ideas and breakthroughs to flourish without internal bottlenecks.

    Behind every vial of 2-Methyl-L-Phenylalanine Monohydrate stands years of practical manufacturing, iterative process adjustment, and direct feedback from the field. As research grows more ambitious, specialized reagents like ours will continue to underpin work at the interface of chemistry and biology, pushing the boundary of what’s possible one reaction, one protein, and one discovery at a time.