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3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate

    • Product Name 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate
    • Alias H-Phe-OBzl Tos
    • 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

    341182

    Product Name 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate
    Molecular Formula C23H23NO4S
    Molecular Weight 409.50 g/mol
    Appearance White to off-white solid
    Purity Typically >98%
    Cas Number 86684-68-4
    Solubility Soluble in organic solvents such as methanol and dichloromethane
    Melting Point Around 110-115°C
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms Benzyl (S)-3-phenylalaninate p-toluenesulfonate
    Functional Class Protected amino acid derivative
    Usage Used in peptide synthesis
    Optical Activity [α]D +23° (c=1, MeOH)
    Hazard Class Irritant
    Hs Code 29224985

    As an accredited 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 10 grams of 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate, tightly sealed with a tamper-evident cap.
    Shipping **Shipping Description:** 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate is shipped in tightly sealed containers to prevent moisture and contamination. It is handled as a non-hazardous, stable solid, shipped at ambient temperature. Appropriate labeling and documentation are provided, complying with chemical transport regulations. Store and transport in cool, dry conditions away from incompatible substances.
    Storage **Storage for 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate:** Store in a cool, dry, and well-ventilated area, tightly sealed in an inert atmosphere such as under nitrogen or argon. Protect from moisture, light, and sources of ignition. Keep away from incompatible substances like strong oxidizers. Store at 2–8°C (refrigerated) for optimal stability. Clearly label the container and handle with standard laboratory precautions.
    Application of 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate

    Applications of 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate in Industrial Manufacturing

    3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate is an essential intermediate for peptide synthesis, pharmaceutical APIs, chiral chemical production, and specialty material manufacture. As a dedicated manufacturer, we deliver this compound to a select range of experienced industrial partners who utilize its unique chemical structure and reliability for high-value end uses. Below, we outline the specific downstream fields and advanced applications, referencing actual industry practices.

    1. Custom Peptide Synthesis in Pharmaceutical API Manufacturing

    This material serves as a protected phenylalanine derivative in solid-phase peptide synthesis (SPPS) and solution-phase routes, especially for manufacturing bioactive peptides and polypeptide APIs required under strict cGMP guidelines. Its benzyl ester group allows precise deprotection, improving fragment condensation yields. Process engineers select this derivative when regulatory filing demands a validated amino acid building block with controlled impurity profiles. The downstream integration involves automated synthesizers or batch reactors, where optimization of deprotection and coupling sequences is performed according to the final peptide’s critical quality attributes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) monographs for amino acids and peptide APIs
    • Japanese Pharmacopoeia (JP) monographs for peptide APIs

    Typical usage ratio

    • 1.05–1.2 molar equivalents relative to other amino acid monomers per peptide step; adjusted as per API-scale and optimization for regioselectivity and minimization of racemization.

    Downstream process integration

    • Enters at the chain-elongation stage during peptide assembly on solid supports or in solution-phase for stepwise elongation; benzyl deprotection performed post-assembly to yield free acid terminus.

    Final product types

    • Oligopeptide and polypeptide APIs (e.g., hormone analogs, diagnostic peptides)
    • Peptidomimetics for pharmaceutical development
    • Research-grade synthetic peptides for preclinical trials
    • Enzyme substrate analogs for advanced pharmaceutical R&D

    2. Chiral Intermediate in Active Pharmaceutical Ingredient (API) Synthesis

    Our compound acts as a key chiral intermediate in the multi-step synthesis of APIs requiring precise stereochemistry, notably non-peptide drugs containing phenylalanine fragments. This application involves nucleophilic substitution and ester exchange reactions where the protected amino acid promotes high enantiopurity and aids in purification steps. QA departments validate incoming lots for chiral purity, with the compound’s tosylate counterion enhancing crystallinity and stability before downstream transformations.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • US FDA guidance for chiral drug substance controls
    • EU GMP Annex 13 for intermediate handling
    • USP General Chapters <1007> “Good Manufacturing Practices for Bulk Pharmaceutical Excipients”

    Typical usage ratio

    • 0.95–1.1 molar equivalents in relation to subsequent reagents; quantity tuned to minimize excess unreacted intermediate and maximize throughput based on process yield studies.

    Downstream process integration

    • Charged during intermediate or late-stage API assembly; follows with catalytic hydrogenolysis for benzyl group removal or tosyl exchange, prior to further derivatization or cyclization steps.

    Final product types

    • Chiral beta-phenylalanine-based antihypertensive APIs
    • Intermediates for central nervous system pharmaceuticals
    • Precursor for amino acid-derived small molecule drugs
    • Chemical building blocks for custom high-value API syntheses

    3. Protected Amino Acid in Diagnostic Reagent Production

    The protected phenylalanine ester finds use in diagnostic reagent manufacturing, particularly for assembling peptide substrates used in enzyme assays and immunodiagnostics. Analytical control teams require reliable protection of functional groups to enable sequential assembly and labeling, without premature hydrolysis. Our controlled crystallization method ensures consistent bulk density and particle size, optimizing the material’s solubility and performance during automated cartridge or plate loading.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices Quality Management Systems
    • US FDA 21 CFR Part 820 for In Vitro Diagnostic Devices
    • CE Mark IVD Directive 98/79/EC
    • ISO 14971 Risk Management for Medical Devices

    Typical usage ratio

    • 0.8–1.3 molar equivalents per amino acid addition, variant based on substrate sequence length and downstream derivatization efficiency.

    Downstream process integration

    • Added during manual or automated fragment coupling; deprotection and final labeling steps occur after full sequence assembly for batch or continuous diagnostic kit filling.

    Final product types

    • Chromogenic and fluorogenic peptide substrates
    • Enzyme-linked immunosorbent assay (ELISA) reagents
    • Synthetic calibrators and standards for clinical diagnostics
    • Affinity tags for protein purification columns

    4. Specialty Chemical Intermediate for High-Purity Functional Materials

    This protected amino acid derivative functions in the synthesis of monomers and specialty intermediates used in high-performance materials, especially for electronics and optoelectronics industries. It provides well-defined chirality and a protected amine group, allowing further functionalization by Suzuki-Miyaura or Buchwald-Hartwig coupling reactions. Material engineers employ this intermediate for multi-step syntheses where purity and protection compatibility prevent byproduct formation and ensure traceability in final material certification.

    Industry compliance standards

    • REACH (EC 1907/2006) registration for raw materials
    • RoHS Directive 2011/65/EU for electronics materials
    • ISO 9001:2015 for chemical material manufacture
    • JIS K 5600 chemical testing in functional material applications

    Typical usage ratio

    • 1.0 molar equivalent per coupling partner; scaled according to target batch size and desired molecular weight for downstream conversion.

    Downstream process integration

    • Incorporated at the primary functionalization stage, then subjected to palladium-catalyzed couplings or amide bond formation; final deprotection occurs prior to isolation of polymerizable or device-ready compounds.

    Final product types

    • Stereospecific monomers for conducting polymers
    • Functionalized intermediates for organic electronic components
    • Optoelectronic material precursors
    • Chiral selectors for analytical and separation columns

    5. Research-Grade Material for Academic and Industrial R&D Synthesis

    This compound is widely employed in synthesis research laboratories, including pharmaceutical R&D and advanced chemical engineering institutes, where customization of side-chain and backbone is necessary for mechanistic studies or for designing new candidate molecules. Researchers benefit from the benzyl- and tosyl-protected format for iterative protection-deprotection strategies, especially in exploratory SAR (structure-activity relationship) projects or total synthesis pathways. Our analytical support ensures batch homogeneity and trace conformer analysis for publication or patent submission requirements.

    Industry compliance standards

    • GLP (Good Laboratory Practice, OECD Principles)
    • Institutional chemical safety (COSHH, OSHA laboratory standards)
    • ISO/IEC 17025:2017 for research laboratory competence
    • Controlled handling regulations (GHS/CLP) for amino acid derivatives

    Typical usage ratio

    • Flexible, typically 0.98–1.25 equivalents per synthetic step, according to experimental purpose and route optimization.

    Downstream process integration

    • Added in manual or automated multi-step synthesis, with benzyl/tosyl protection tailored for specific stepwise or convergent assembly; deprotected via catalytic or acidic conditions for product isolation.

    Final product types

    • Library compounds for SAR/HTS screening
    • Experimental peptide and polypeptide analogs
    • Structural reference materials for NMR/X-ray studies
    • Synthetic intermediates for grant-based research projects
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    Certification & Compliance
    More Introduction

    Getting Acquainted with 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate

    Stepping into the world of complex amino acid derivatives, 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate stands out for practical reasons that go beyond simple numbers on a page. Over the years working at our chemical plant, this compound has evolved from an obscure specialty item into a recurring request from peptide chemists and research professionals who value reliability. Its place in synthesis labs rests on a set of properties that might sound routine, but which, in our experience, call for attentive and exacting production methods. Not every variation of phenylalanine ester can fill its shoes.

    Model and Appearance—What You See, Why It Matters

    This substance appears as a white to off-white solid, sometimes leaning toward crystalline, depending on batch conditions and storage. We’ve spent a good amount of time on our purification systems to achieve appearances that reveal quality before anyone even picks up an NMR tube. For those who grow suspicious of yellowing or clumped material, rest assured that what leaves our finishing unit aligns with the expected specifications seasoned peptide chemists have come to expect.

    With a molecular weight in the neighborhood established and a known, reproducible melting point, each batch tells us its story during the QC run. The ester group is protected by a benzyl moiety, and the 4-toluenesulphonate (tosylate) salt confers enhanced solubility and stability. For bench chemists, these details translate into workable material—a compound that dissolves cleanly in commonly used organic solvents and resists hydrolysis during handling. Not every phenylalanine derivative on the market can state the same, especially as you increase order quantities for pilot or production scale.

    How Usage Has Shaped Our Focus

    Our experience has been that 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate finds its primary application as an intermediate in peptide synthesis. The benzyl ester function protects the carboxyl group during stepwise assembly of oligopeptides, letting the reactive side chain of phenylalanine remain selective and controllable. Customers rely on the high yield and reproducibility that come when starting with clean, well-characterized material. Their own, sometimes multi-month, synthetic campaigns hinge on purity and traceability—something that can only come by tightly managing process variables in our reactor systems.

    Not all research labs have the same standards or workflows. Some prefer alternative protecting groups or different counterions. What sets this tosylate salt apart is the relatively straightforward deprotection and removal steps at the conclusion of their synthesis cycles. Several reports, and our own customer feedback, point out its ease of work-up compared with variants such as hydrochloride or free base forms. Where processes require minimal aqueous extractions, the tosylate proves particularly popular, reducing troublesome salt removal or product loss.

    Why Labs Keep Coming Back to This Variant

    Consistency matters. Over a decade of batches, few things have been more important to repeat customers than reproducible performance—crystals that dissolve at the right rate, with minimal insoluble residues, and that keep the synthetic pathway rolling. The alternative, sometimes encountered with lower-purity material, involves frustrating night shifts and costly re-runs. Our site audit protocols, insistence on high-grade solvents, and system for in-process monitoring came about through feedback from researchers left flat-footed after bad experiences elsewhere.

    We have noticed, too, that peptide coupling using this benzyl ester salt leads to higher conversion rates under milder conditions. Some older literature points to side-product formation and lower yields when using the free acid under harsher coupling agents. The benzyl group survives aggressive activation, keeping side reactions at bay. In our own process, repeated assays and spectral analyses—HPLC, mass spec, and carbon/proton NMR—confirm the product’s purity and the absence of common byproducts.

    Setting This Product Apart From Similar Items

    Researchers sometimes compare this product to other phenylalanine derivatives such as the methyl ester, tert-butyl ester, or salts using nitrate or perchlorate counterions. Each has its own set of trade-offs, no doubt. The benzyl ester strikes a sensible balance between ease of deprotection and robust protection throughout the synthesis. Methyl and tert-butyl esters, despite their utility, often require more forceful conditions for removal or, in some hands, lead to product instability if crude solvents or unoptimized reagents enter the mix. Our product, owing to the steric and electronic nature of the benzyl group, holds up better in extended, multi-step work.

    Using the toluenesulfonate salt instead of a hydrochloride has earned positive reviews for improved solubility in polar aprotic solvents such as DMF and DMSO. A significant number of our customers running scale-up reactions have documented reduced precipitation incidents—a well-known headache with less soluble salts. On occasion, researchers request alternative forms and, by running head-to-head process trials, repeatedly come back to the tosylate for both convenience and lower cost to purify at the end stage.

    There is another practical detail: this variant often ships more readily owing to its physical stability. Our plant, located within reach of large logistics corridors, has seen how heat, humidity, and even minor transit delays can challenge less robust analogues. Whereas the free acid or hydrochloride versions sometimes arrive as cakes or sticky oils, the tosylate holds form, keeps dust and residues to a minimum, and stores well for extended periods under typical laboratory conditions.

    Specification and Quality – Lessons From the Factory Floor

    Instead of stringing together technical bullet points, our approach starts with the pressing question: how much can you trust what comes in the drum or bottle? We produce each batch under GMP-inspired conditions, but not every chemist on our team accepts paperwork as gospel. The reality is, experienced hands can often tell before any GC trace whether a batch meets the mark: flow, texture, aroma, and how the first aliquot dissolves under stirring. While specs such as purity by HPLC (>98%), residual solvents, and elemental analyses shape documentation, our process chemists back this up with spot testing throughout the drying and packaging phases. The feedback loop stretches back to the reaction tank—any deviation from the established crystallization routine or purification profile triggers an in-depth review. It isn’t only about hitting a number; it involves relentless attention to those details that affect your next step, not simply our next transaction.

    Addressing Common Issues—Not Every Batch Is Born Equal

    Some buyers approach these intermediates with stories of failed couplings, odd impurities, or irreproducibility from one delivery to the next. We’ve fielded countless calls, emails, and sometimes exasperated visits from researchers stuck mid-campaign, who turn to us for help pinning down what went wrong. Often, the root cause turns up as simple process drift in upstream synthesis or cutting corners on purification—issues we sorted out in our own plant after some tough lessons. Our operators have learned that rushed crystallization leads to occlusion of mother liquor, lower product purity, and—all too often—costly reruns for clients. Our standard requires careful, gradual temperature drops and extended filtration, timed for each batch’s subtle differences. Strict control of moisture is another important factor; a few mismanaged hours with the drying equipment can introduce variable hydration, changing the apparent weight and influencing subsequent reactions downstream.

    Trace byproducts, particularly unresolved esters or sulfonate salts, have no place in the final product. Scientists who scrutinize all incoming raw materials can spot the difference when the batch follows an in-house approach, where we monitor UV cutoff and track minor impurity peaks during every scale-up. If the customer reports a hiccup, our technical support not only reviews the internal QC but, if necessary, guides customers through troubleshooting, helping tighten up their own handling protocols.

    Building for Scale – Knowledge From Repetition

    Scaling production of complex amino acid derivatives presents a world of challenges. Our facility grew out of small-lot synthesis, but market demand for this compound forced us to rethink everything, from reactor volume to how we package and ship. Walk the shop floor and you’ll see steel reactors now outfitted with automated feed systems. Solvents circulate with recycling loops, and every stage is rigorously logged, ensuring traceability for every kilogram produced. The outcome: no unexplained batch-to-batch variation, tighter control over crystallization, and a shortened feedback cycle if an issue does appear down the line.

    Frequent collaboration with end-users, particularly those running peptide production at pilot scale, has helped us fine-tune process variables. Attention to filtration speed, agitation rates, and washing protocols has minimized inclusions and improved purity beyond initial specification. When one group reported carryover of byproducts impacting their column chromatography, we set aside time on our pilot line to adjust temperature ramps and investigate solvent polarity impacts during each stage. The result was a tweak in our purification sequence—higher yields for everyone involved and a batch history that now guides our process for every order.

    Understanding Global Needs

    The global appetite for advanced peptide building blocks shows no sign of slowing. Regulatory and safety standards mean that suppliers must document every step, but genuine reliability comes down to deeper process knowledge. Our technical team attends annual industry meetings, not simply to network, but to gather user feedback and anticipate changes in synthetic protocols. In reviewing demand patterns, we’ve found wide adoption of the 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate in both academic and industrial research. Its robust profile suits everything from small-scale screening to multi-gram batch production for pharmaceutical intermediates.

    Regional differences shape some of the requests we get—from preferences for kosher or halal certification to queries about second- or third-party analytical guarantees. Our QA and documentation keep pace, always grounded in hands-on familiarity with what it takes to keep synthesis lines moving without delay. We have sidestepped price wars with distributors by emphasizing that our compound’s real value lies in every process step being under our own roof, overseen by chemists who have handled every form and byproduct. We work with a full in-house analytics suite: mass spectrometry, multiple chromatography stations, and FTIR analyses—tools that confirm each batch matches its certificate in substance and spirit.

    Supply Reliability—A Product of Planning and Experience

    Nearly two decades of experience managing chemical supply chains showed us that bottlenecks seldom originate in big disasters, but rather through overlooked details: solvent shortages, unplanned maintenance, staffing gaps, and documentation drift. We took these lessons to heart; now, inventory control, preventive maintenance, and robust vendor ties ensure the plant never gets caught flat-footed by an unexpected bump in demand. Around the clock, our production team monitors output, checks supply logistics, and keeps close tabs on cargo handling partners to reduce transit times and handling risks.

    Packaging choices make a difference. Through hard-won trial and error, we landed on moisture-resistant, inert-liner packaging. This approach shields contents from temperature swings and light exposure while keeping labels easy to read. Our warehouse operates under regulated temperature and humidity, and our tracking protocols link every container to production details, so chemists know exactly what went into— and came out of— each batch run.

    Feedback Loops: How Customer Input Drives Improvements

    The best process refinements have grown straight from customer partnerships. We’ve fielded troubleshooting calls at midnight, worked through weekends to chase down outlying HPLC traces, and swapped real-time results with labs halfway across the globe. This hands-on problem solving forged a feedback system stronger than any audit or industry checklist.

    Customer feedback pointed us toward optimizing filtration steps after some reported minor solid residues post-dissolution. Our process team made adjustments, launched small-scale pilot runs, and followed up with each involved client for validation. More than once, new end-use applications—unexpected by our R&D planners—have emerged, from bespoke hormone mimics to designer peptide projects. Each time, we retool our systems, batch by batch, to keep up with demand and exceed expectation.

    Environmental and Safety Considerations in Manufacturing

    Safety and sustainability in chemical manufacturing extend beyond catchphrases to daily, practical routines. In handling benzyl-protected amino acid derivatives and sulfonate salts, our plant enforces robust PPE policies, localized venting, and solvent reclamation. Not only does this keep personnel safe, but it trims costs and minimizes emissions entering local waste streams. Every operator works under the assumption that personal vigilance and double-checking each transfer outweigh any shortcut.

    Effluent and solid waste are monitored with real-time analytics, triggering flagged interventions well before compliance limits approach. Our newer initiatives center around reducing chlorinated waste streams, opting where possible for greener solvents and minimizing sulfones and sulfonates in process waste. Sustainability reports, once a compliance concern, now serve as learning tools for incremental gains in both process yield and staff safety. Over time, this manifests in both cleaner product and a better workplace—outcomes our partners, large and small, now expect from us.

    Progress Never Pauses—Adapting to Change

    Chemical manufacturing, particularly for specialty compounds such as 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate, does not reward complacency. Techniques evolve, user needs shift, equipment demands upgrading, and regulatory scrutiny intensifies. Our team invests not just in equipment, but also in training, cross-functional teams, and new analytical methods. Routine review cycles have spotted opportunities to fine-tune not only the synthesis, but marketing, packaging, and order fulfillment.

    Recent upgrades included a semi-automated packaging line, which reduced manual errors and freed staff for high-skill tasks, leading to steadier throughput and more dependable lead times. By inviting chemists from outside the plant for on-site walkthroughs, we encountered unexpected questions that spurred yet more process improvements, instilling a culture where anyone can challenge the status quo—if it makes the material better or easier to use.

    The Human Element—Craft, Skill, and Judgment

    For us, high-quality 3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate is as much a measure of expertise as it is of process parameters. Crafting this compound at scale, repeatedly, has taken both science and judgment. Newcomers often marvel at automated reactor controls, but it is the longstanding staff—those who remember the plant’s earliest years—who spot subtle viscosity shifts, odd scents, or off-color tinctures that precede analytical evidence. Their calls have preempted more issues than any checklist or monitor could alone.

    Among the greatest strengths our company brings is the human habit of asking, “What if…?” and “Could this step be cleaner, faster, or safer?” Every meaningful process gain began as a conversation on the floor or in the break room. When customers reach out with new applications or unforeseen problems, we answer not just as suppliers, but as partners who know firsthand what is at stake: weeks (sometimes months) of careful research, investment, and focus.

    An Enduring Choice for Synthetic Professionals

    3-Phenyl-L-Alanine Benzyl Ester 4-Toluenesulphonate represents more than a chemical. For us as manufacturers, and for our partners in the field, it stands for predictability that comes from hands-on attention, an eye for detail, and a willingness to evolve with every batch, every request, and every challenge met along the way. That makes it a mainstay on the shelves of labs pushing the boundaries of peptide science.