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Phenylthiohydantoin-DL-Alanine

    • Product Name Phenylthiohydantoin-DL-Alanine
    • Alias PTH-DL-Ala
    • Einecs 252-700-8
    • 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
    VTB
    Specifications

    HS Code

    247777

    Name Phenylthiohydantoin-DL-Alanine
    Synonyms PTH-DL-Alanine
    Chemical Formula C10H10N2O2S
    Molecular Weight 222.27 g/mol
    Cas Number 7398-91-0
    Appearance Off-white to beige crystalline powder
    Solubility Soluble in methanol and ethanol
    Melting Point 176-178 °C
    Storage Temperature 2-8 °C
    Purity Typically ≥ 98%
    Application Used in amino acid sequencing (Edman degradation)
    Smiles CC(C(=O)N1C(=O)NC2=CC=CC=C12)S

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

    Packing & Storage
    Packing A sealed amber glass bottle labeled "Phenylthiohydantoin-DL-Alanine, 1 gram," with hazard symbols and storage instructions included.
    Shipping Phenylthiohydantoin-DL-Alanine is shipped in tightly sealed containers to protect it from moisture and contamination. It is handled with care, following relevant chemical safety regulations. The package includes clear labeling and safety documentation. Temperature and storage conditions are controlled during transit to ensure chemical stability and integrity upon arrival.
    Storage Phenylthiohydantoin-DL-Alanine should be stored in a tightly sealed container, protected from light and moisture, at a temperature of 2–8°C (refrigerated conditions). Ensure it is kept in a cool, dry, and well-ventilated area away from incompatible substances. To maintain stability and prevent degradation, avoid prolonged exposure to air and elevated temperatures. Use appropriate lab safety protocols when handling.
    Application of Phenylthiohydantoin-DL-Alanine

    Applications of Phenylthiohydantoin-DL-Alanine in Industrial Manufacturing

    Phenylthiohydantoin-DL-Alanine serves as a core intermediate in peptide chemistry and sequencing workflows. Its well-controlled manufacture enables reliable downstream performance in life science production, biochemical research, and select high-value chemical synthesis verticals. The following scenarios detail real industrial applications, relevant compliance requirements, usage ratios, process integration methods, and commercial product endpoints.

    1. Automated Amino Acid Sequencing Reagents

    Our material functions as an essential derivative in Edman degradation for automated N-terminal sequencing of peptides and proteins. Analytical-grade quality and precise compositional control ensure compatibility with sequencers used by core laboratories and contract research organizations. Integration focuses on minimizing background signals and achieving quantifiable release of the corresponding thiohydantoin derivative for detection steps. Manufacturers require full traceability and strict contiguity in lots to maintain reproducibility across sequencing runs, with batch QC tailored to chromatography and mass spectrometry performance endpoints.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory reagent control
    • GLP (Good Laboratory Practice) for use in regulated test environments
    • FDA 21 CFR Part 820 for analytical supply components
    • ICH Q7 for GMP manufacturing of pharmaceutical intermediates (when used in peptide APIs)

    Typical usage ratio

    • Applied at 0.5–1.5 equivalents per amino acid site; adjust based on peptide length and sequencing throughput requirements
    • Optimization based on detection sensitivity and waste minimization in high-throughput workflows

    Downstream process integration

    • Engaged in in-cycle derivatization post-peptidyl coupling
    • Mixed in automated reagent cartridges for direct sequencer injection
    • Pre-tested for compatibility with both high and low throughput sequencing platforms
    • Batched under low-moisture conditions to maintain reactivity

    Final product types

    • Commercial N-terminal sequencing reagent kits
    • Core reagent packs for automated sequencers (e.g., protein/peptide sequencing machines)
    • Custom research sequencing workstations
    • Quality control test kits for biopharmaceutical industry release

    2. Peptide Reference Standards Manufacturing

    Peptide manufacturers use our material in the development of reference standards for food safety, environmental testing, and pharmaceutical impurity profiling. Its purity and certificate of analysis facilitate regulatory acceptance where traceability and reference accuracy are essential. Production strictly monitors batch contamination and cross-reactivity, supporting downstream purification and certification workflows prior to global distribution. Manufacturing scale and comprehensive documentation align with traceable supply chain needs of major analytical laboratories and regulatory bodies.

    Industry compliance standards

    • USP <1225> on validation of compendial procedures
    • ISO 17034 for reference material producers
    • Ph. Eur. and JP pharmaceutical monographs for impurity standards
    • ISO/IEC 17043 for proficiency testing sample providers

    Typical usage ratio

    • 15–35 mg per 10 g of synthesized peptide, adjusted by sensitivity of target analyte and detection limit requirements
    • Ratio confirmed during lot release by synthesis yield and standard calibration

    Downstream process integration

    • Integrated post-solid phase peptide synthesis for modified reference peptide labeling
    • Utilized during reference mixing and final lyophilization stages
    • Handled in controlled areas to minimize environmental cross-contamination
    • Applied in documentation protocols for regulatory audit traceability

    Final product types

    • Certified peptide reference standards
    • Pharmaceutical impurity marker panels
    • Food allergen detection assay kits
    • Environmental monitoring peptide controls

    3. Custom Peptide Synthesis for Research & Diagnostics

    This material is a cornerstone additive in academic, preclinical, and diagnostic peptide synthesis, especially where modified amino acid residues or derivatives are needed for functional studies. When used in custom synthesis services, the compound ensures high sequence fidelity and enables structural validation for peptides featuring N-terminal modifications. Synthesis chemists adjust stoichiometry and sequence assembly strategy to maximize coupling efficiency, guided by customer or protocol-specific reactivity data. The focus remains on consistent in-process control and readiness for downstream purification.

    Industry compliance standards

    • ISO 9001 for chemical synthesis batch records
    • REACH registration for European supply
    • OECD GLP for non-clinical diagnostic use

    Typical usage ratio

    • 0.8–1.2 equivalents per coupling event, based on peptide chain length and target sequence complexity
    • Fine-tuned based on resin loading, amino acid reactivity, and solvent/media optimization

    Downstream process integration

    • Introduced post-resin swelling as derivatization reagent
    • Blended with coupling additives (e.g., HBTU, HATU) for capped or modified sequences
    • Employed during acetylation or specific N-terminal blocking steps
    • Assessed via in-process HPLC for purity prior to cleavage and purification

    Final product types

    • Custom peptide API candidates for preclinical evaluation
    • Diagnostic peptide controls for immunoassays
    • Functionalized research peptides for molecular interaction studies
    • Peptide labeling substrates for proteomics

    4. Biopharmaceutical Analytical Controls

    Contract manufacturing organizations and biotech firms employ this substance in QA/QC workflows for verifying the identity and purity of peptide drug substances. Its derivatization capability supports mass spectrometry and chromatographic identification of amino acid sequences and post-translational modifications. Analytical teams require lot consistency, with careful specification of contaminant levels that might affect signal-to-noise ratio during analysis. The upstream traceability directly impacts method validation and release testing, particularly in regulated GMP environments.

    Industry compliance standards

    • ICH Q6B for biological product characterization
    • Ph. Eur. 2.2.56 for peptide mapping by LC-MS
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation
    • USP <1058> for analytical instrument qualification

    Typical usage ratio

    • 6–12 mg per sample, adjusted for analytical batch size and quantification sensitivity
    • Modified per analytical platform requirements (LC-MS/MS, UPLC, etc.)

    Downstream process integration

    • Added during pre-analysis derivatization step
    • Directly used as standard in protein sequence validation assays
    • Prepared alongside analytical reference matrices for calibration
    • Supplied under controlled temperature to prevent hydrolysis

    Final product types

    • Batch-release analytical control kits
    • Protein identity verification reagents
    • GMP peptide reference controls
    • Analytical system performance standard panels
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    Certification & Compliance
    More Introduction

    Phenylthiohydantoin-DL-Alanine: Putting Experience into Practice

    The Result of Improving Sanger Sequencing Efficiency

    In the fine chemical world, some compounds earn their keep through reliability and repeat performance. Phenylthiohydantoin-DL-Alanine (PTH-DL-Ala) fits squarely in this category. For companies like ours that specialize in amino acid derivatives, the journey from raw materials to a reagent-grade product isn’t just a string of steps. Every stage—from sourcing amino acids to establishing crystallization conditions—depends on hands-on technical expertise. We learned early that shortcuts don’t lead to reliable phenylthiohydantoin products, especially for researchers running Edman degradation or exploring peptide sequencing workflows.

    Model and Specifications: Where Discipline Meets Observation

    We supply PTH-DL-Alanine as a solid crystalline powder. The model is not just a catalog entry for us—it is the result of years spent refining each batch’s purity profile and stability. Purity, for us, goes well past numbers on a certificate of analysis; it shows up as crisp peaks in HPLC traces and as consistent reactions during downstream analysis. Our material is odorless, shows a white to slight off-white appearance, and keeps its structure even in humid climates. From time to time, clients will point out slight color shifts, and we treat those observations as sources of learning, fine-tuning drying and packaging. Over the years, tightening control over granulometry and using inert atmosphere packaging has given us a consistent product, time after time.

    The Path from Alanine to PTH-Alanine

    The backbone of PTH-DL-Alanine is alanine, a non-polar amino acid encountered at the intersection of biochemistry and industrial synthesis. Phenylthiohydantoin, as a derivative, formed the cornerstone of the Edman degradation method. By bonding phenylisothiocyanate to the N-terminal, and then cyclizing to form the thiohydantoin ring, the process captures each residue for subsequent identification. After years working with process teams, we saw firsthand that even small slip-ups—temperature swings, moisture incursion, variable pH—make the difference between a clean cyclic product and a sticky, unreliable material.

    Some projects required large-scale output, others called for microgram batches destined for academic groups exploring rare protein structures. Our process never varies in its attention to contamination control. Copper, iron, and chloride traces matter deeply in this field, as even parts-per-million contamination can throw off sequencing runs. So, for each run of PTH-DL-Ala, we draw from high-grade solvents, invest in frequent line cleaning, and run batch-specific impurity assessments.

    Usage Driven by Trust—Not Hype

    PTH-DL-Alanine always ends up where it’s supposed to: analytical chemistry benches, peptide sequencing robots, and protein identification labs. Our customers care most about what happens after the compound leaves our hands. If the residue assignment goes awry, entire research hypotheses get thrown into question. In a crowded market, we have seen short-lived attempts to cut costs at the expense of accuracy. These don’t last. Instead, reliable sequencing reagents build trust. Scientists and lab managers tend to remember both their best and worst suppliers, and feedback loops travel quickly in this specialized niche.

    Phenylthiohydantoin-DL-Alanine lends itself to amino acid sequence analysis thanks to the stability of the thiohydantoin ring. During Edman degradation, after modification and cleavage, the individual PTH-amino acid is analyzed using either chromatography or mass spectrometry. Minor impurities, or the presence of a single incorrect isomer, distort peak interpretation. Several customers have reported to us—often unsolicited—how a switch to our material solved recurring issues in routine analysis. From our own tests, we see lower background interference compared to generic manufacturers.

    Real Differentiation: Not All Phenylthiohydantoin Products Are Alike

    Many manufacturers list PTH-amino acids as if they were interchangeable. That premise doesn’t hold up in laboratory settings. Some years ago, we investigated several commercial samples of PTH-DL-Alanine. We discovered significant batch-to-batch variability. Melting points shifted by several degrees, IR and NMR spectra included unidentified peaks, and sample homogeneity left much to be desired. This reinforced something we had already learned through experience: consistent process control makes the difference between a passable reagent and a premier one.

    Our PTH-DL-Alanine stands apart not because of a trademarked logo, but due to robust batch records, traceable raw materials, and practical stability data. We store each batch for long-term stability reference and maintain a reserve for post-sale analytical checks so researchers can compare results if questions arise months later. Specifications aren’t defined by marketing teams—they are defined by what repeatedly works under real laboratory conditions. The DL-form (containing both D and L enantiomers) responds differently from the pure L-form in chiral separation and in enzyme-digestion workflows, and our team counsels clients about the distinct applications each variant supports.

    Process Insights: What Experience Has Taught Us

    Making PTH-DL-Alanine looks straightforward on paper. In reality, it demands carefully staged pyrophosphate reactions, steady temperature ramps, and immediate drying when the product crystallizes. We employ seasoned operators—some with more than 15 years on this production line—who know how to read the texture of a semi-dry cake or spot early signs of incomplete cyclization. Several years back, we revamped our solvent recovery system after finding trace residues in what should have been ultra-pure output. Ever since, we track not only solvents used but also storage conditions, drum history, and line flush cycles.

    Sometimes, researchers ask how our product compares to standard reference materials. We regularly participate in external proficiency programs where the same batch gets sent for double-blind analysis. Our results line up closely with gold standards, even under stress testing that simulates extended storage and high humidity.

    Process deviations do happen. During one unusually hot summer, a spike in rejected batches traced back to equipment drift in a cooling jacket. Our reaction team documented everything and initiated a continuous electronic monitoring system, cutting out any future ambiguity about internal temperature mismatches. In chemical manufacturing, recognition of small problems before they turn into major issues separates long-term suppliers from those who chase quick sales.

    Serving a Global Network: Moving Beyond Transactional Supply

    Laboratory research knows no borders. Our batches find their way to Europe, North America, and Asia almost daily, and each market asks different questions about documentation, sustainability, and traceability. To address these, we developed full batch-traceable logs, including solvent origins and batch-specific impurity scans. Researchers sometimes visit our facility to run pilot-scale reactions or to cross-check our product against in-house materials. We encourage these exchanges, and often pick up tips that push us toward even better operational discipline.

    Our technical support team comes from the same production floor. When customers call, they are not routed through a distant office. Instead, they reach people who have actually weighed, tested, and shipped PTH-DL-Alanine themselves. Over time, this builds partnerships rooted in shared goals rather than one-off transactions. In recent years, we’ve worked with several universities and pharmaceutical pioneers, sharing test results and comparing performance data to push the edge of what our reagents can do.

    Reducing Residual Contaminants: The Small Details Matter

    One often-overlooked point with phenylthiohydantoin derivatives concerns their residual contaminants. During cyclization, side reactions can introduce sulfides or unreacted isothiocyanate. Our QA group runs regular batch checks for both, using sensitive colorimetric and HPLC methods. For customers with advanced analytical instruments, we supply extended data showing trace byproduct levels. In challenging sequencing campaigns, minor background peaks either clarify or confuse residue identification, so small investments in cleanup and control during manufacturing contribute to success in the field.

    Some peer companies use bulk-grade phenylisothiocyanate for cyclization. We found early on that this leads to recurring impurities, so we stick to reagent-grade material, despite higher costs. For customers running preparative-scale projects, we can share actual chromatograms to support their risk assessment and method development.

    Product Packaging Informed by Real-World Handling

    We use tightly sealed HDPE bottles for packaging, each stamped with batch and lot numbers for traceability. For shipments headed to humid climates, we prepare moisture-absorbing secondary packaging and advise clients to open containers in dry boxes. This stems from freight experience—years ago, a batch suffered clumping and color shift due to warehouse delays in a tropical port. We learned from that, instituting pre-shipping climate checks and on-request, double-bagging for sensitive orders.

    Standard package sizes suit both small-lab users and pilot-scale customers. We often receive special requests for odd-sized aliquots, and our filling line accommodates those runs with minimal delay. Our staff documents and photographs each shipment before sealing, supplying these records to QC managers upon request.

    Supporting Documentation Builds Confidence

    Each shipment leaves accompanied by a full spectral profile package, impurity data, and a certificate of analysis. Our QA staff prepares each file based on actual batch results, not generic templates. Customers can request supporting chromatograms, drying curves, or NMR printouts. Particularly in regulated laboratories, this level of documentation accelerates both in-house validation and compliance checks.

    Both experienced and new customers often ask for guidance on storing and handling PTH-DL-Alanine. We keep storage advice practical—clear, out of direct sunlight, stable room temperature, and moisture-free. If a laboratory faces repeated humidity spikes or long-term storage questions, we share our own accelerated aging data, letting technical staff plan for backup or reorder intervals.

    Responding to Market Changes: Price, Access, and Partnerships

    Over the last years, laboratory procurement teams have grown more price-conscious. As raw material costs rise, transparency about sourcing and batch sizes has become a bigger part of our day-to-day work. Sometimes, we field questions about switching from reagent-grade to lower-purity alternatives for cost savings. We explain that sequence readouts depend on reactivity and clarity, and that a clean chromatogram is worth the extra cost. Most labs return to higher-grade materials after trials with lower-cost alternatives expose limitations.

    We extend flexible volume discounts for universities and research groups running high-throughput sequencing. Side collaborations have led to improvements on both sides. By agreeing to blinded product evaluations and sharing detailed feedback, we have tuned our purification steps and fine-tuned reagent drying.

    Shipping regulations can change quickly. We stay up to date on the newest transit guidelines for chemical reagents, investing in compliance so that customers receive materials quickly and without avoidable customs holdups.

    Partnership through Troubleshooting

    Manufacturing isn’t just about delivering a compound. Long-term clients expect us to stand by product performance. Some months ago, a sequencing lab reported unexpected background contamination. Our team reviewed possible causes and compared their chromatograms with our own QC records, tracking the source to residual solvents in sample prep, not our product. Tackling these questions in detail strengthens trust and improves outcomes for everyone involved.

    At times, we collect feedback on residue identification, retention time drift, or isomer separation. Research groups working on novel proteins occasionally request specialized derivatives for atypical runs. We either develop custom batches or connect labs with peers who have run similar experiments, building community and advancing methods together.

    Technical troubleshooting is as much a part of our work as synthesis. We maintain open lines, so if a client’s equipment fails to read a standard, or a routine run stalls, we work through the details together. That collaborative mindset drives both reliability and innovation in the compound’s use.

    Environmental Awareness in a Changing World

    Every chemical manufacturer faces rising expectations for sustainability. In response, we invested in solvent recycling, reduced water usage, and established better waste segregation protocols. Our process now includes quarterly environmental audits and targeted reductions in resource consumption per kilogram of product. Environmental responsibility doesn’t end at site boundaries. Through partnerships, we’ve shifted much of our shipping to recycled packing materials and leaner box sizes, balancing regulatory compliance with reduced transit waste.

    Trade groups and clients often request environmental impact statements, and we’re honest about our progress. No process stands still, but through small, repeated changes our team has reduced our ecological footprint without sacrificing product reliability or purity.

    Lessons Learned and Looking Ahead

    Our experience with Phenylthiohydantoin-DL-Alanine runs deep, reinforced by every batch produced, every QC pass or fail, and every call from a lab team half a world away. The compound’s value is measured not just in purity or price, but in the trust that develops between researcher and supplier. We’ve found that attention to detail—a properly dried sample, a careful impurity scan, a follow-up phone call—matters as much as raw technical skill.

    In a field where reputation is built on every chromatogram and every experimental run, we continue refining the process. This means listening to scientists, being honest about process challenges, and making small changes for better outcomes. Phenylthiohydantoin-DL-Alanine sums up what matters about manufacturing for scientific research: reliability, responsiveness, and a willingness to improve through experience.