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Phenylthiohydantoin-Threonine

    • Product Name Phenylthiohydantoin-Threonine
    • Alias PTH-Thr
    • Einecs 252-220-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    339537

    Chemical Name Phenylthiohydantoin-Threonine
    Abbreviation PTH-Threonine
    Molecular Formula C12H13N3O3S
    Appearance White to off-white solid
    Solubility Soluble in methanol, ethanol, and dimethyl sulfoxide
    Cas Number 10116-98-6
    Melting Point 177-179°C
    Storage Temperature 2-8°C
    Application Used in Edman degradation for protein sequencing
    Purity Typically ≥ 98%
    Synonyms PTH-Thr, N-Phenylthiohydantoin-Threonine
    Iupac Name 3-Phenyl-2-thioxoimidazolidin-4-one-5-(2-hydroxypropanoic acid)
    Hazard Statements Handle with care; may cause irritation
    Smiles CC(C(=O)N1C(=O)NC(=S)C1)c2ccccc2O

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

    Packing & Storage
    Packing Phenylthiohydantoin-Threonine, 100 mg, supplied in an amber glass vial with tamper-evident seal, labeled with product details and safety warnings.
    Shipping Phenylthiohydantoin-Threonine is shipped in tightly sealed containers under cool, dry conditions to ensure stability and prevent degradation. The package is clearly labeled as a research chemical and handled according to standard safety protocols. Shipping complies with all relevant local and international regulations for non-hazardous laboratory chemicals.
    Storage Phenylthiohydantoin-Threonine should be stored in a cool, dry, and well-ventilated area away from light and moisture. Keep the container tightly closed and store at temperatures between 2–8°C (refrigerated conditions) to maintain stability. Avoid exposure to incompatible substances and handle under a chemical fume hood if possible. Properly label the storage container to prevent accidental misuse.
    Application of Phenylthiohydantoin-Threonine

    Applications of Phenylthiohydantoin-Threonine in Industrial Manufacturing

    Phenylthiohydantoin-Threonine plays a critical role in sectors utilizing advanced peptide sequencing, biochemical synthesis, and analytical processes. As the direct manufacturer, we supply this raw material to clients demanding precise molecular building blocks and strict conformance to international standards across multiple specialized industries.

    1. Automated Edman Degradation for Protein Sequencing

    Protein sequencing laboratories globally rely on phenylthiohydantoin derivatives as essential intermediates in the Edman degradation process. Our material enters directly as the threonine-specific reagent in automated amino acid sequencing platforms. Here, reagent purity and consistency critically impact cycle yield and signal clarity. Clients integrate it within microfluidic or batch reaction steps, following controlled dosing protocols set by standardized sequencing workflows. Only batches meeting strict analytical purity and phase compatibility can support high-throughput, compliant protein analytics in pharmaceutical R&D and biotechnological QC.

    Industry compliance standards

    • ISO 13485:2016 (for instrumentation and analytical reagent manufacture)
    • US Pharmacopeia General Chapter <1047> (Protein Sequencing and Identification)
    • FDA 21 CFR Part 211 (applicable to diagnostic reagent components)

    Typical usage ratio

    • 15–50 µmol per sequencing cycle, precisely adjusted based on sample load and protocol sensitivity requirements

    Downstream process integration

    • Dosed after the coupling step to react with exposed N-terminal threonine residues
    • Removed by organic phase extraction between degradation cycles
    • Monitored via HPLC to verify identity and remove incomplete derivatives before further sequencing steps

    Final product types

    • Protein sequence data for biopharmaceutical patents
    • Analytical reference peptides
    • Validated diagnostic test kits
    • Research-grade sequencing service reports

    2. Peptide Mapping and Bioanalytical Services

    CDMOs and bioanalytical service providers incorporate our material during peptide mapping, especially for threonine recognition and fragmentation studies. Accurate mapping supports biosimilar comparability and post-translational modification detection. Laboratories use the compound in tandem with mass spectrometry and electrophoresis platforms, closely controlling purity grades to meet GxP data integrity requirements. Operators rely on batch-to-batch uniformity and comprehensive traceability, as regulated by industry and client audit protocols.

    Industry compliance standards

    • ICH Q6B (Specifications: Test Procedures and Acceptance Criteria for Biotechnological/Biological Products)
    • OECD GLP principles (Good Laboratory Practice)
    • EN ISO/IEC 17025 (Testing and Calibration Laboratories Accreditation)

    Typical usage ratio

    • 5–30 µmol per peptide mapping run; adjusted according to the complexity and length of peptide chains under investigation

    Downstream process integration

    • Introduced post-digestion during threonine-specific fragmentation analysis
    • Used in calibration sets to identify baseline threonine signals
    • Purified using preparative chromatography before MS analysis

    Final product types

    • Peptide identification reports for regulatory submissions
    • Biosimilarity assessment documentation
    • Batch-release testing data for biopharmaceuticals
    • Structural certificates for therapeutic proteins

    3. Pharmaceutical Amino Acid Derivative Synthesis

    Specialty API manufacturers use this compound for stereospecific protection and identification of threonine during multi-step peptide or small molecule synthesis. Our manufacturing provides custom synthesis lots with defined enantiomeric purity and solvent-soluble forms, supporting batch records and full traceability. Clients use the deliverable as a protected intermediate, with integration protocols tailored to GMP API environments. Compliance documentation accompanies all shipments to facilitate site audits and regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • Ph. Eur. 2.2.46 (Chromatographic Purity of Peptides)
    • US FDA DMF (Drug Master File) reference for regulated APIs

    Typical usage ratio

    • 0.1–2% w/w vs. total substrate mass in protected threonine intermediate synthesis steps; adjusted to achieve required protection degree and final API purity

    Downstream process integration

    • Incorporated during N-terminal protection or side-chain derivatization steps
    • Cleaved before final deprotection to yield free peptide or amino acid
    • Assessed with chiral HPLC to verify enantiomeric excess prior to transfer to the next stage

    Final product types

    • Threonine-protected peptide intermediates
    • Chiral building blocks for pharmaceuticals
    • Synthetic peptides for vaccine and API active core segments
    • Small-molecule leads involving threonine residues

    4. Diagnostic Kit and Reference Material Production

    Diagnostic kit manufacturers source this compound for use in reference panels and calibration standards, particularly for protein and peptide sequencing quality control. We supply carefully validated lots with defined impurity profiles and Certificates of Analysis matched to reference methods. Production sites apply rigid acceptance criteria, tracking identity and lot performance to ensure assay consistency and compliance during kit assembly and shipment for global clinical diagnostics markets.

    Industry compliance standards

    • IVDR EU 2017/746 (In Vitro Diagnostic Medical Devices Regulation)
    • ISO 15189:2022 (Medical Laboratories – Requirements for Quality and Competence)
    • CLSI C62-A (Mass Spectrometry in the Clinical Laboratory)

    Typical usage ratio

    • 0.5–5 µmol per diagnostic kit calibration batch; varies according to kit throughput and regional calibration frequency

    Downstream process integration

    • Dosed as part of peptide calibration reference mix
    • Quality controlled through lot-to-lot comparative analytics
    • Integrated into liquid or lyophilized reference material for end-user reconstitution

    Final product types

    • Protein sequencing calibration kits
    • Clinical laboratory control panels
    • Reference reagents for diagnostic assay validation
    • Peptide quantitation standards for hospital laboratories

    5. Proteomic Research and Custom Reagent Production

    Academic and industrial proteomics centers utilize our material to synthesize custom reagents and standards for advanced protein structure studies. Batch-specific documentation supports grant-funded research and commercial method validation. Researchers integrate the derivative during sequence-specific labeling of threonine in peptides, under strict storage and transport controls. Collaborations require real-time technical support for order customization, ensuring research reproducibility and publication-valid experimental workflows.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for lab reagent production)
    • GLP-compliant traceability protocols for custom synthesis projects
    • Funding agency data transparency and reagent audit guidelines

    Typical usage ratio

    • Custom–determined; research groups use 1–20 µmol per experiment, adapted for peptide concentration and labeling method

    Downstream process integration

    • Dosed during sequence-specific peptide labeling steps
    • Purified using HPLC or gel-filtration, monitored with MS or NMR
    • Packaged in single-use or multi-use vials depending on experiment scale

    Final product types

    • Published proteomic workflows
    • Custom reference peptides for mass spectrometry
    • Labeled threonine peptide standards
    • Analytical research materials for scientific communication
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    Certification & Compliance
    More Introduction

    Introducing Phenylthiohydantoin-Threonine: Experience from the Manufacturer’s Perspective

    A Closer Look at Phenylthiohydantoin-Threonine

    In the chemical industry, quality control defines every batch we make and each innovation we shape. Phenylthiohydantoin-Threonine, known among professionals as PTH-Threonine, continues to hold a meaningful place in the daily routines of sequencing laboratories and peptide chemistry departments. Those of us who manufacture this compound move beyond surface-level purity figures. We see it as both a necessary tool and a mark of a production process you can trust.

    Moisture, temperature, and trace contaminants can easily compromise a product in this category. Achieving clear, crystalline PTH-Threonine that delivers both seat-of-the-pants reliability and repeatable results doesn’t happen by accident. Our control of input L-Threonine, our handling of phenyl isothiocyanate, and our patience throughout crystallization all contribute to the final character of the product. The team in the plant knows from experience the value of slow, careful filtration when we observe that extra speck settling at the bottom of a vessel.

    Each batch we ship is the outcome of hundreds of checks that don’t always appear on paper. Chemists lean over glassware, checking clarity and color, talking through the process as a team. More than one newer technician has learned the hard way that jumping ahead saves no time if the residue needs to be removed and repurified. The final crystals come packed, not fluffed, thanks to steady cooling and patterned agitation. Watching an experienced process lead direct evaporative steps underscores that hands-on attention never grows outdated.

    Model and Specifications—What We Manufacture

    For laboratories and peptide sequencing operations, knowing what you’re getting each time you open a bottle really matters. PTH-Threonine, as we make it, shares a standard molecular formula—C11H12N2O3S. White to off-white crystalline powder describes what you see, yet behind this appearance lies structural certainty. High-performance liquid chromatography (HPLC) typically shows a single main peak. Any reputable chemical manufacturer aims for a minimum purity of 98 percent, but it’s the absence of byproducts from raw material carry-over that sets apart what we deliver.

    Years of customer feedback and our own troubleshooting forced us to adopt stricter approaches to both yield and purity. For a residue as notoriously troublesome as residual phenyl isothiocyanate, we learned that hot solvent washes—while effective for smaller lots—do not scale with the same neatness for larger production. Through dozens of cycles, we optimized replacement solvent flow rates and drying times until we saw both better yields and lower analytical background in repeated sequencing reactions.

    Grain size stays consistent because filtration means nothing if the finished product compacts or forms dust during transfer. Operators wear out gloves and lose track of time adjusting filter settings on our Buchner funnels or switching up the vacuum strength on drying ovens. You’ll see the difference in the physical texture of a well-made batch of PTH-Threonine—free-flowing, easy to weigh, and less prone to cake than products that only exist on paper as a line in a catalog.

    Usage—Why Laboratories Ask for PTH-Threonine

    We see our PTH-Threonine leave the loading dock bound for research institutes, clinical sequencing facilities, and specialty contract labs. They use it within the Edman degradation cycle, transforming N-terminal threonine residues into a stable, isolable derivative. For research chemists mapping protein structure, success hinges on each cycle yielding a reliable, readable phenylthiohydantoin adduct. Inconsistent quality or unexpected contaminants can hide key signal peaks or, worse, introduce ghost peaks and interfere with sequence determination.

    Many labs still trust in the classic Edman method, even as newer, automated sequencing equipment gains ground. The reason: reliability and recognized chemistry. Automated analyzers depend on reagents they can trust, with predictable elution points in chromatograms and no background artifacts. When a systematic error in amino acid assignment appears, it often leads analysts back to the basic reagents—the quality of PTH-Threonine matters every bit as much as the operator’s skill.

    Outside the familiar peptide sequencing field, some synthetic laboratories adopt PTH-Threonine as an analytical standard or as a calibration tool. Its established properties, strong retention time on HPLC, and accessible structure carry value whenever accuracy takes priority. On several occasions, technical service teams called us about issues that turned out to stem from switching between grades or manufacturers, especially when the consistency of peak area or retention time suddenly changed. The product from our own facility rarely figures in such calls, which we treat as proof of the importance of stubbornly consistent manufacturing.

    How PTH-Threonine Differs from Other Related Products

    Peptide and protein chemists deal with the full alphabet of amino acid derivatives, each with its quirks. PTH-Threonine isn’t interchangeable with PTH derivatives of alanine, glycine, or serine. Threonine’s extra hydroxyl group and side chain complicate both the Edman process and subsequent HPLC analysis. Even minor impurities—such as unreacted L-Threonine or incomplete cyclization byproducts—disrupt the delicate chromatography balance researchers rely on for sequence reading.

    Among PTH derivatives, threonine often receives extra scrutiny because of its role as a branch point in biological sequences. Its hydrophilicity and tendency to form hydrogen bonds translate into more complex chromatographic behavior. We see more requests for retention time data and reference spectra for PTH-Threonine than for simpler analogues. Years ago, we noticed that commercial suppliers often didn’t keep up with requests for such technical data. As the actual manufacturer, we document each batch and keep traceable spectra on file. Focusing on in-house production allows us to provide reference standards immediately if a lab calls with questions about an unexpected result.

    Compared to bulk amino acids or even protected amino acid derivatives, the PTH forms demand tighter environmental controls. The instability of the thiohydantoin ring in certain conditions means we keep storage cool and dry, not just for inventory but throughout production transfers. Because we create rather than source this product, we control transport and handling so there’s little risk of breakdown. Chemists at other operations tell us the difference whether a derivative arrives freshly packed or has spent extra time exposed to high humidity.

    Challenges We Address in Manufacturing PTH-Threonine

    Every facility faces different operational bottlenecks. For PTH-Threonine, avoiding cross-contamination ranks at the top. We run dedicated equipment for PTH derivatives to eliminate carry-over from other amino acids—especially those that present risks of side-chain exchange. Everyone on the manufacturing floor recognizes the importance of shutting down a line to clean, even for what looks like a quick product change.

    Some batches challenge us with erratic crystallization. Variations in source material, minor power dips in drying ovens, even seasonal humidity spikes—all impact the outcome. A well-drilled team notices differences by sight and smell before any analytical report flags a problem. Once, a run of product showed slightly altered melting behavior. Fast interpretation at the plant level avoided three days of product waste. Such experiences train everyone to pay close attention and keep up both formal and informal lines of communication.

    Another challenge arrives with increasing customer sophistication. Research groups ask for more documentation, tighter impurity profiles, and verification not just of structure but origin of raw materials. We welcome that. Certifications change fast, and regulation always evolves. Stable, vertically integrated manufacturing lets us answer those requests with our own data rather than third-party assurances. If the market pushes for greener chemistry or non-petroleum solvents, we experiment and adapt in our own labs before rolling out changes. This flexibility distinguishes direct manufacturing from simply filling drums and relabeling.

    Why Consistency Matters—A Manufacturer’s Reflection

    Every operator and chemist in our company speaks to consistency from lived experience. A single off-spec drum can set off a month of troubleshooting in a downstream laboratory. We’ve heard from academic groups who noticed a drift in HPLC retention for PTH-Threonine that traced back to a bad run from a less careful supplier. Fast support and willingness to swap in a confirmed, stable batch turned new labs into regular clients. Every time you cut corners on solvent control, rush a filtration step, or skip a purity check because of demands for higher volume, problems show up two steps downstream.

    Patience, repetition, and the ability to pause and rerun a check deliver real value for demanding users. By overseeing the whole process—ordering and prequalifying L-Threonine, running the cyclization with fresh reagents, protecting the crystallizing mixture from light and moisture, and documenting each batch—we almost always catch issues before a product leaves the plant. Discussions about cost per gram rarely capture the value of this kind of consistency, but once a research group depends on your output, they remember which supplier solved or skipped problems in the first place.

    Potential Solutions and Real-World Adjustments

    Making PTH-Threonine isn’t a static business. Power costs for drying change, regulations update, and customer requirements evolve. We adjust our own repair schedules and batch sizes to match, rolling out improvements as new information lands. When smaller peptide labs asked for 10-gram lots split across multiple vials, we acquired small-batch filling lines rather than repacking large containers by hand. Reducing batch contamination risks took investment in cleanroom upgrades, which also meant revising training for every technician. Instead of resting on old procedures, we use feedback loops—direct reports from users in the field, not just spreadsheets from purchasing agents.

    As newer peptide synthesis and sequencing platforms demand tighter controls and different solvent compatibilities, we adjust protocols as needed. Several times, our analytical team flagged minute traces of legacy reagents in finished product, leading to a full process review. We upgraded glassware and replaced reactor linings to eliminate memory effects, even though the capital outlay was non-trivial. Shortcuts save little in a business where residue profiles reach into parts-per-million territory, especially for laboratories running highly sensitive HPLC approaches.

    Improvement doesn’t always mean automation or throwing money at the latest machine. Practical know-how—recognizing when a freshly crystalized batch seems too tacky, noting small changes in color or residue, listening to the experience of veteran staff—improves outcomes more than fancy software. There remains no substitute for time on the production floor and the readiness to repeat a step if it isn’t quite right. That steady attention bleeds into every shipment we send, and you can’t measure it in paperwork.

    Trust Through Direct Manufacturing: Closing Thoughts from the Floor

    Lab managers and research scientists don’t just want chemicals that fit a technical sheet—they need to trust the quality built into every bottle. That trust comes easier from hands that made the batch, not just moved the container from a factory half a world away. Direct answers to detailed technical questions matter more as research expands and regulatory oversight tightens.

    From the shop floor to the R&D office, manufacturing PTH-Threonine means listening to feedback, anticipating issues, and refusing to settle for inconsistent lots. Every change—big or small—passes through the filter of hands-on experience. For our team, Phenylthiohydantoin-Threonine stands as a test of craft, discipline, and care in chemical manufacturing. That’s the story behind every fresh batch and each reliable shipment.