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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 | 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. |
Applications of Phenylthiohydantoin-Threonine in Industrial ManufacturingPhenylthiohydantoin-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 SequencingProtein 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
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2. Peptide Mapping and Bioanalytical ServicesCDMOs 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
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3. Pharmaceutical Amino Acid Derivative SynthesisSpecialty 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
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4. Diagnostic Kit and Reference Material ProductionDiagnostic 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
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5. Proteomic Research and Custom Reagent ProductionAcademic 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
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Competitive Phenylthiohydantoin-Threonine prices that fit your budget—flexible terms and customized quotes for every order.
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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.
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.
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.
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.
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.
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.
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.
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.