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HS Code |
157722 |
| Product Name | Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt |
| Chemical Formula | C9H7O6P · 3C6H15N |
| Molecular Weight | 585.70 g/mol |
| Cas Number | 82692-90-6 |
| Appearance | White to off-white powder |
| Solubility | Soluble in water |
| Storage Temperature | 2-8°C |
| Purity | ≥98% |
| Synonyms | PEP Tris(cyclohexylammonium) salt |
| Application | Biochemical research, enzyme assays |
| Sensitivity | Hygroscopic |
| Ph Range Of Solution | 6.0-8.0 (20 mM in H2O) |
| Inchi Key | LYISMLKUSSKKMP-LALPHMFDSA-N |
| Ec Number | 616-694-2 |
As an accredited Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle with secure screw cap, labeled "Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt, 1 gram," featuring hazard and storage instructions. |
| Shipping | Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt is shipped in a tightly sealed container, protected from moisture, light, and heat. It is packaged according to chemical safety regulations to ensure stability and prevent contamination or degradation during transit. Handle as a non-hazardous laboratory reagent unless otherwise specified by your supplier. |
| Storage | Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt should be stored in a tightly closed container at 2–8°C (refrigerated). Protect it from moisture, light, and excessive heat. Store in a dry, well-ventilated area, away from incompatible substances. Follow standard laboratory safety procedures and consult the Safety Data Sheet (SDS) for detailed handling and storage guidelines. |
Applications of Phosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt in Industrial ManufacturingPhosphoenolpyruvic Acid Tris(Cyclohexylammonium) Salt serves specialized biochemical and biotechnological industries requiring high purity reagents for enzymatic and metabolic research, diagnostic reagent production, and select pharmaceutical manufacturing workflows. As a raw material supplier with direct synthesis capabilities, we ensure traceability and processability that meet advanced requirements across well-established use cases. 1. Clinical Biochemistry Reagent FormulationEnzyme-coupled diagnostic kits for blood chemistry analyzers frequently rely on phosphoenolpyruvic acid salts as a critical substrate in multi-enzyme determination assays, especially for creatine kinase (CK) and pyruvate kinase (PK) activity testing. The material undergoes dissolution and precise dosing into buffered reagent premixes, supporting consistent colorimetric response in automated wet biochemistry platforms. Control of purity, moisture, and ionic profile is essential to maintain batch-to-batch reactivity, and formula adjustment depends on specific device parameters. Industry compliance standards
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2. Biochemical Research Reagent PreparationBiotechnology laboratories and reagent companies depend on phosphoenolpyruvic acid salts as a phosphate group donor in ATP regeneration systems for in vitro enzyme kinetics analysis and metabolic pathway research. Direct integration occurs during buffer system setup for spectrophotometric or fluorometric enzyme assays, requiring careful pH and ionic strength control to preserve enzyme-substrate specificity during experimental runs. Industry compliance standards
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3. Pharmaceutical API Synthesis Quality ControlsIn select pharmaceutical synthesis routes, phosphoenolpyruvic acid salt acts as a reference compound or functional intermediate in ATP-dependent reaction monitoring and metabolic studies during process development. Quality control laboratories use the compound for calibration and method validation in HPLC and enzymatic purity assays, ensuring compliance with regulatory documentation and process reproducibility. Industry compliance standards
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4. Diagnostic Enzyme Production (Industrial-Scale Fermentation)Producers of recombinant enzymes for diagnostic and biochemical reagent markets use phosphoenolpyruvic acid salts as a vital substrate feed in fermentation and downstream enzyme quality assessment. During process scaling, the salt enables enzyme screening and activity testing under GMP-compliant conditions, optimizing downstream purification efficiency and product lot qualification. Industry compliance standards
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5. Medical Device Calibration SolutionsMedical device manufacturers supplying clinical spectrophotometric analyzers routinely prepare calibration and linearity solutions based on phosphoenolpyruvic acid salt for use in device performance verification. Inclusion into these solutions assures stable reactivity and precise enzyme-substrate interactions, critical for quality assurance in controlled healthcare settings and during device servicing. Industry compliance standards
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As producers with decades in the field of fine chemical synthesis, we encounter questions about phosphoenolpyruvic acid tris(cyclohexylammonium) salt nearly every week. There’s good reason for this. Researchers and production managers want durable, high-purity biochemical intermediates they do not need to second-guess. In practical research and diagnostic tool development, this compound often proves indispensable. It’s not simply another lab chemical—its role turns critical, especially in enzymology and metabolic pathway analysis.
Throughout our experience, reliability and cost-effectiveness have shaped every batch. We have learned that reliable sourcing matters just as much as laboratory efficacy. Phosphoenolpyruvic acid tris(cyclohexylammonium) salt—often called PEP-CHX, to keep things brief—supports some of the most sensitive processes in today’s biochemistry and clinical industries.
Many users ask about specification and why there even needs to be such scrutiny surrounding a “simple” compound. We produce PEP-CHX with a model based on laboratory-validated reference standards. What sets our product apart lies not in a claim on paper, but in actual measured purities and consistent salt ratios. Each production sequence undergoes meticulous testing, including NMR, elemental analysis, and HPLC confirmation, minimizing batch-to-batch deviations and the risk of unknown impurity spikes.
In our facilities, trace moisture and by-product ions are tightly controlled—an overlooked but real concern in the market. A single percent more water or trace inorganic contamination can disrupt kinetic studies, throw off calibration in diagnostic assays, or affect shelf stability. We have improved our drying and crystallization steps, leading to an end product with high solubility in water and reliable stability under common laboratory storage conditions.
PEP-CHX to us means more than reaching a stated limit test. Chemists, technicians, and those validating research tools need predictable solubility and pH behavior. Cyclohexylammonium, as a counterion, offers increased stability versus some alkali salts, especially if you store product open bench for hours or need extended storage. Years ago, contamination and lot drift from careless handling created real headaches. Now, with modern air-handling, packaging, and monitoring, consistent material properties no longer feel out of reach.
Our product typically presents as a white to off-white crystalline powder. Each shipment matches a phosphoenolpyruvate content confirmed by NMR and titration, with cyclohexylammonium counterions kept at an exact 3:1 ratio—a small technical detail but one that influences reactivity and solubility in buffered solutions. Published assay values fall above 98% pure for the dominant species, in line with major enzyme assay suppliers and international standards.
Our typical lot size ranges from gram-scale pilot runs for small biochemistry groups to hundreds of kilograms destined for industrial enzyme manufacturers. As a practical consideration, we never bring PEP-CHX to market without redundant confirmation of melting point, moisture content analysis (by Karl Fischer, not simple desiccator exposure), and HPLC verification for degradation products. This approach adds cost, but it means fewer downstream failures for our customers and fewer emergency production halts on our own line.
Inside research labs, PEP-CHX has multiple roles. Years ago, the compound gained traction as a substrate in glycolysis pathway investigations and has since secured its place as a standard reactant for pyruvate kinase and other related enzyme assays. This central role in ATP-generating reactions means any researcher studying metabolism likely keeps a supply on hand. You’ll also see demand rise each time a new diagnostic kit enters the market—our customers know kit manufacturers can’t compromise on substrate reliability.
In clinical chemistry, precise PEP-CHX batches allow developers to design multilayer test strips and instrumental reagents where kinetic accuracy matters. Signal drift or artifact bands usually trace back to poor-quality reagents. Diagnostic instrument manufacturers often knock on our door once they realize that their prior supplier’s quality couldn’t support year-after-year calibration or stability needs.
We also hear from synthetic biology companies. They rely on our PEP-CHX for their engineered pathway work, guiding developments in cell-free ATP regeneration, novel enzyme screening, and even in-vitro production pipelines. We tailor production according to whether lots go toward immediate analytical use, R&D tool-building, or bulk industrial fermentation. Across applications, every user gets a product with the same core characteristics.
Our reactors aren’t run by remote commands. Chemists and line workers with years on the job oversee every critical stage. From phosphorylation through selective salt exchange and drying, we’ve seen the pitfalls that arise from shortcuts—especially with cyclohexylammonium counterion incorporation. Extended purification, regular glassware checks, and environmental monitoring prevent contamination or side reactions. It’s this groundwork of skilled experience that keeps recalls rare and confidence high.
We collect feedback directly from end users after every major lot, updating purification and monitoring steps as issues or new research hit the field. Sometimes, changing user demands force a tweak in crystallization timing or solvent gradient. We welcome this engagement, because our own line workers see first-hand how these changes impact yield and cost, and researchers gain from material that behaves as their protocols expect.
PEP appears in multiple salt forms. Cyclohexylammonium salts come with unique solubility and handling characteristics. Sodium and potassium salts dissolve more quickly in some buffers, but tend to show lower stability, especially if exposed to repeated freeze-thaw cycles or air. During our trials, we noticed that cyclohexylammonium salts stand up better to repeated manipulations and extended storage on bench tops, reducing the number of failed assays in high-throughput applications.
We manufactured sodium and potassium salts for years before shifting significant resources to cyclohexylammonium forms. The feedback that drove this shift didn’t come only from papers and journals; technicians and QC teams saw i t themselves in stored reference lots. For applications needing batch-to-batch reproducibility, such as clinical assay development or synthetic enzymatic processes, cyclohexylammonium shows less unpredictable drift and fewer false positives or negatives in endpoint readings. We think this difference comes from the steric and hydration environment provided by cyclohexylammonium, a feature that seems uninteresting until you deal with the fallout of variable enzyme kinetics or shelf-life failings.
As the direct manufacturer, we track these differences—not just from commercially available reference materials, but from our own stored inventory and real customer performance logs. With each request for customization, whether changing hydration levels or even small tweaks in particle size, we collect and review outcome data. It’s not about one salt being “better” universally—users pick according to stability, cost, and the tolerance of their specific method or instrument.
Producing PEP-CHX goes beyond mixing and crystallizing. One persistent challenge involves preventing trace contaminants from entering the production stream. Ambient air alone can introduce moisture or dust at levels that ruin sensitive enzyme assays down the line. In our history, we’ve found even tiny process modifications lead to outsize changes in purity. For that reason, we regularly tweak protocols after observing annual weather cycle effects or following customer feedback. Upgrading our air-handling and extending drying times raised purity above standard industry benchmarks and we saw fewer complaints of false high readings in user calibrations.
Another hard-learned lesson involves packaging and transport. This compound stays stable in-house, but rough handling or bad packaging leads to caking, strange odor development, or even color changes. By switching to vapor-proof and puncture-resistant multilayer bags, sealed under inert gas, we dramatically reduced customer complaints and helped maintain reactivity throughout long international transport. We actively track every batch shipped through multiple climate zones, and test random samples on arrival, just to make sure our partner labs receive exactly what they expect.
Over time, buyers have shifted preference toward direct supply chains. This isn’t marketing spin. Feedback loops between our production floors and end users create real technical improvements. While distributors serve a purpose, our experience shows that close communication between developer and manufacturer results in smoother troubleshooting and faster response to new regulatory, analytical, or purity needs.
Direct relationships also bring improved information flow. Instead of fielding support tickets that dead-end in bureaucracy, our technical leads meet directly with teams troubleshooting new, complex assay builds or field-diagnosing unexpected results. In many cases, we’ve been able to suggest protocol shifts or provide alternate lot blends based on detailed production histories most third parties could only guess at.
Consistency matters the most during regulatory submissions or high-value application validation—for example, when a biomedical device company stakes years of work on a single enzyme-substrate batch behaving exactly as intended. We keep back samples of every lot, meaning any questions that arise months later—regarding purity, stability, or even just packaging questions—can be answered from direct, on-hand historical material, not vague records or third-party logbooks.
Phosphoenolpyruvic acid tris(cyclohexylammonium) salt, as an advanced biochemical intermediate, demands ongoing investment from manufacturers. Raw material sourcing for the core phosphate backbone takes flexibility—global markets shift and new synthetic approaches sometimes become practical or necessary. We have reduced reliance on single-source feedstocks through multi-country alliances and rigorous pre-shipment verification. Shortages no longer send us scrambling or force substitute materials.
We confront environmental and safety requirements not with checklists, but by routinely integrating audit findings and regulatory updates directly into our facility protocols. Waste minimization, chemical recycling, and even alternate solvent trials have grown from side projects to core upgrades. Raw data from our eco-monitoring shapes reactor vent filtering or new solvent reclamation schedules. Even minor changes in handling sequence or staff training directly cut waste output or improve energy efficiency.
Customers increasingly want supply chain documentation, proof of sustainable sourcing, and reduced environmental liabilities. As a direct manufacturer, we openly invite customer or regulator audits and provide verified supply chain traceability from raw phosphate import to final shipping. Laboratory scientists, procurement officers, and even regulatory bodies now expect this, and our practices directly reflect years-long relationships built on transparent operation. There’s no quick fix for green chemistry, but we treat each season as another chance to improve, educate our staff, and avoid shortcuts that undercut the next customer’s results.
customers in biochemistry, medical devices, and industrial research benefit from more than just a product. Buying direct builds mutual understanding, drives technical improvements, and keeps everyone honest about what’s possible. Ultimately, our approach involves open dialogue, honest feedback collection, and ongoing process adjustment. Each batch shipped stands for everything we’ve learned, and everything we plan to keep improving.
By keeping our expertise close and our quality controls precise, we help chemists, technicians, and research organizations stay focused where they should—on developing and proving out new science, not tracking down why their substrates or intermediates failed. Every gram of phosphoenolpyruvic acid tris(cyclohexylammonium) salt shipped carries the weight of our manufacturing heritage, upgraded by each new challenge and every customer collaboration. Buyers who value consistency, traceability, and genuine technical partnership tend to stay with direct manufacturers for a simple reason—they can see, measure, and rely on the difference.