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Phorbol 12-Myristate 13-Acetate

    • Product Name Phorbol 12-Myristate 13-Acetate
    • Alias PMA
    • Einecs 245-401-6
    • 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
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    Specifications

    HS Code

    550885

    Product Name Phorbol 12-Myristate 13-Acetate
    Synonyms PMA, TPA, 12-O-Tetradecanoylphorbol-13-acetate
    Cas Number 16561-29-8
    Molecular Formula C36H56O8
    Molecular Weight 616.83 g/mol
    Appearance White to off-white powder
    Solubility Soluble in DMSO, ethanol, methanol
    Storage Temperature -20°C
    Purity Typically >98% (HPLC)
    Usage PKC activator, biological research
    Melting Point 141-143°C
    Canonical Smiles CCC(C)C(=O)OC1C(C2CCC3(C(C2C1C(=O)O)CCC4(C3CC=C4)C)C)OC(=O)CC

    As an accredited Phorbol 12-Myristate 13-Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear glass vial containing 1 mg Phorbol 12-Myristate 13-Acetate, sealed, labeled with chemical details, hazard symbols, and lot number.
    Shipping Phorbol 12-Myristate 13-Acetate is shipped as a hazardous material, typically on dry ice or with cold packs to maintain stability. Packaging complies with international safety regulations, featuring leak-proof, tightly sealed containers. Appropriate transport documentation, including safety data sheets, is included to ensure safe handling during transit, storage, and delivery.
    Storage Phorbol 12-Myristate 13-Acetate (PMA) should be stored desiccated and protected from light at -20°C in a tightly sealed container. PMA is sensitive to air, light, and moisture, with exposure potentially leading to degradation. Solutions, typically prepared in DMSO, should also be frozen at -20°C, aliquoted to avoid repetitive freeze-thaw cycles, and used under low-light conditions.
    Application of Phorbol 12-Myristate 13-Acetate

    Applications of Phorbol 12-Myristate 13-Acetate in Industrial Manufacturing

    As a specialized manufacturer of Phorbol 12-Myristate 13-Acetate (PMA), we are committed to ensuring that our material consistently supports precise, validated industrial applications. Below we present well-established downstream sectors where PMA is routinely deployed, providing sector-specific compliance norms, formulation principles, production integration, and representative end products.

    1. Cell-Based Assay Reagent Production for In Vitro Diagnostics

    Major diagnostics manufacturers use our material as a phorbol ester reagent for PKC pathway activation within cell-based immunological assay kits. The material undergoes rigorous purification and is batch-tested to meet analytical reference standards demanded by clinical and research sectors. Producers calibrate application rates based on target cell responsiveness and required activation thresholds, incorporating our material during master mix preparation or reagent kit blending phases. This targeted use ensures consistency in T-cell activation studies and immune pathway assay kits supplied for hospital and lab use.

    Industry compliance standards

    • IVD CE certification (Regulation (EU) 2017/746)
    • ISO 13485 Quality Management Systems
    • Good Manufacturing Practice (GMP) for Diagnostic Reagents
    • CLSI guidelines for analytical reagent performance

    Typical usage ratio

    • 1–100 nM per assay well, varying by cell type and assay endpoint sensitivity; individual adjustment according to cell line and target response

    Downstream process integration

    • Incorporation during in vitro diagnostic reagent kit assembly; dissolved in DMSO or ethanol and dosed during liquid reagent formulation; QC analysis for lot-specific activity prior to fill-finish step

    Final product types

    • Cell stimulation control solutions
    • Signaling pathway activation kits
    • Leukocyte function test kits for hospitals and research organizations
    • Quality control standards for immunological diagnostic devices

    2. Biomedical Research-Grade Stimulant Supply

    Global research supply companies use our PMA as a validated stimulant for signal transduction pathway studies, especially in immunology and neurobiology academic labs. Material is supplied under high-purity documentation and stability specifications, ensuring compatibility with strict institutional reagent sourcing and handling protocols. Laboratories dose the stimulant in precise concentrations, adapting to the cell system’s transfection parameters within workflow steps spanning cell treatment, signaling readouts, and downstream transcriptomic analyses.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation
    • OECD Good Laboratory Practice (GLP) Principles
    • Material Transfer Agreement (MTA) documentation (where applicable)
    • REACH registration (for EU research market)

    Typical usage ratio

    • 1–50 nM in culture medium; actual working concentration depends on cell population and experimental timeline

    Downstream process integration

    • Addition to cell plates shortly before induction of PKC activation; integrated during primary culture protocols or combined with ionomycin/calcium stimulants for coordinated response

    Final product types

    • Specialized research kits for cell signaling
    • Ready-to-use academic reagent vials for laboratory research
    • Stimulant control lots for standardized cell-based assays
    • Reference samples for cellular pathway investigation

    3. Pharmaceutical Preclinical Testing Services

    Contract research organizations use our material as a positive control agent in preclinical immunotoxicology and cell activation studies. Application occurs in regulatory-compliant lab settings, with lots traceable to GLP-certified batches. Formulators dilute or dissolve the ester to target concentrations and introduce it during cellular functional testing or toxicology assay setups. This procedure ensures that pharmaceutical clients receive reproducible, statistically validated controls for registration and submission studies.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • FDA 21 CFR Part 58 (GLP for Nonclinical Laboratory Studies)
    • ICH S6 Preclinical Safety Evaluation Requirements
    • SOCMA ChemStewards for responsible chemical management

    Typical usage ratio

    • 5–20 nM in the cell assay phase, set according to validated protocol or sponsor request

    Downstream process integration

    • Delivered directly to CRL/ CRO as a lot-certified control sample; formulated into dosing solutions used in in vitro immunotoxicity, lymphocyte activation, or cytotoxicity screening panels

    Final product types

    • CRO-supplied control panels for immune function assessment
    • Internal reference standards for cell-based screening reports
    • Custom-formulated testing reagent sets for clinical submission
    • Positive control solutions for contract evaluation reports

    4. Standardized Quality Control Reagent Formulation

    Producers of specialty cell biology and immunoassay kits utilize our raw material when formulating their standardized quality controls. Product purity, stability data, and homogeneity allowed manufacturers to maintain consistent batch reproducibility across international laboratory markets. The raw material enters the QC process during the creation of comparative standards, typically as a component of positive control vials that validate assay performance and instrument calibration.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ISO 15189 Requirements for Medical Laboratories
    • WHO Good Practices for National Pharmaceutical Control Laboratories
    • Pharmacopeia monographs for reference controls (where relevant)

    Typical usage ratio

    • 5–25 nM per ready-to-use control solution; determined by manufacturer’s validation to match instrument sensitivity

    Downstream process integration

    • Blended into positive assay control solutions at the control standard preparation stage; aliquoted for global kit shipments after confirming batch-to-batch consistency

    Final product types

    • Immunoassay kit positive controls
    • Flow cytometry reagent standards
    • Immunodiagnostic instrument calibration reagents
    • Comparative reference vials for research and hospital settings
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    Certification & Compliance
    More Introduction

    Phorbol 12-Myristate 13-Acetate: A Manufacturer’s Perspective

    Our Journey with Phorbol 12-Myristate 13-Acetate

    Producing each batch of Phorbol 12-Myristate 13-Acetate (PMA) draws on decades of technical knowledge and hands-on work at the reactor and purification bench. Over the years, we have worked with a wide range of biologically active molecules, but PMA demands special attention during every stage — from raw material sourcing to the final crystallization. Chemists recognize the structural complexity this compound brings. It’s more than just another reagent. Each molecule reflects the careful balance required between chemical stability and biological activity, a balance we protect throughout the production chain.

    For those outside the laboratory, PMA might simply be a functional chemical. Our experience tells a different story. The synthesis requires control over temperature, strict exclusion of water, and refined chromatographic techniques. End-users often focus on how PMA activates protein kinase C and triggers cellular responses in research settings. We look at every possible impurity that can creep in at each isolation step, because even minor contaminants risk skewing experimental data downstream.

    Technical Insights: Manufacturing Realities for High-Purity PMA

    No manufacturer takes short cuts if they understand the pain points researchers experience with unreliable reagents. We have refined our process since the earliest days, applying rigorous standards that go beyond the minimum industry requirements. Purity levels exceeding 99% are common for PMA, but reaching this target consistently calls for experience and hardware that can handle delicate separations. Our team analyzes each batch with HPLC, confirming that what we ship today performs to the same standard a year from now.

    Moisture and heat destroy PMA during storage. Our quality team calibrates every drying oven and checks each vial for residual solvents before final closure. Glassware, not plastic, preserves stability. Freezers rather than ambient shelves guarantee the compound arrives ready for immediate use — no time lost waiting for thawing or re-checking concentration.

    Customers sometimes ask why batches from one manufacturer differ from another’s. Our response: variations typically trace back to raw material quality, subtle differences in the reaction step, or sloppy finishing work. We control each step in-house, guaranteeing a consistent standard from gram-scale tubes up through large-volume orders. Researchers notice how our product dissolves, how it looks, and—even more—how control groups in bioassays react. Any deviation moves straight to our troubleshooting workflow.

    Specifying What Matters: Batch-to-Batch Performance, Not Just a CAS Number

    Phorbol 12-Myristate 13-Acetate answers to a single CAS number, but not every lot on the global market acts the same. The difference between a tightly controlled house preparation and a loose, poorly characterized product from elsewhere shows up in the details. Our batches adhere to molecular weight specifications, and our analytical team checks for the telltale signature on NMR every time. Consistency in melting point and crystalline habit matters, both for handling and for downstream research reproducibility.

    Researchers rely on the biological potency of PMA as a protein kinase C activator, but experience has taught us that trace oxidation products can dramatically change cell culture results. We track low-level impurities using UV and mass spectrometry, ensuring nothing slips through. This becomes especially important for pharmaceutical teams who run large screening projects where batch-to-batch variation destroys data integrity.

    Usage and Application: Perspective Beyond the Lab Bench

    PMA has earned a starring role as a tool in signal transduction research, tumor promotion models, and cell differentiation assays. Our manufacturing team sees it from a different angle: as a material that must hold up not just at the point of purchase but across long-term storage and repeated freeze-thaw cycles. Our clients often describe sudden drops in biological activity with untrusted suppliers. Every time that happens, their conclusions become questionable. Stability testing, both at ambient and long-term low temperatures, guides the final fill and ship protocols.

    Most of our top clients use PMA dissolved in DMSO or ethanol. They mention years of frustration with material that turns yellow or becomes insoluble from less discriminating sources. We designed our purification and drying sequences to meet these practical needs. The microcrystalline product stays bright and handles easily with standard pipettes, ideal for fast-paced lab environments. Because we maintain exacting purity, researchers avoid interference with secondary signals or artifacts, which can ruin months of cell-based work.

    As a manufacturer, we consider feedback directly from the end-users. Immunology teams tell us about their expectation that PKC activators perform in a highly reproducible fashion across multiple assays. We listen to cancer biology departments who need confidence that their differentiation studies do not shift with each lot number. Our commitment to process transparency — from raw material checks through finished product fill — comes from these conversations. Customers cite fewer troubleshooting incidents once they switch to our material, which means we have found ways to minimize costly downtime for their teams.

    Specific Differences Compared to Other Compounds: Molecular Precision Counts

    Compared to other phorbol esters, such as Phorbol 12,13-dibutyrate (PDBu), our PMA stands out for its higher biological activity in most mammalian systems. The cell-penetrating properties of PMA, rooted in the long-chain myristate ester at the 12-position, provide robust and immediate PKC activation. By contrast, short-chain derivatives show lower potency and more rapid breakdown in cellular contexts. Our technical chemists have evaluated these differences side-by-side. In our hands, only high-purity PMA achieves complete response at nanomolar concentrations, a requirement in experiments measuring cytokine release, cell proliferation, or differentiation.

    Among PKC activators, PMA shows a different handling profile than plant-derived crude extracts or semi-synthetic analogs. Our experience with these alternatives has confirmed that crude forms often hide non-specific activators, leading to noisy background in high-throughput screens. We have learned that a fully characterized, single-ingredient reagent eliminates ambiguities. This matters when downstream applications move toward more clinically relevant systems requiring robust interpretation of small signals.

    Practical Know-How: Safe Handling and Ongoing Support

    We approach every kilogram of PMA as a biologically active, hazardous material. Early in our company’s development, we learned the risks associated with even small spills. Direct skin contact carries the risk of irritation and biological activity at the exposure site. Our teams receive real-world safety training—routine isn’t enough when accidental exposure could affect lab staff. Each customer order includes a safety reminder, distilled from our operational practice. Most importantly, we maintain our SDS and safety literature in real time, so researchers never guess whether they’re working with a current document.

    On the technical support side, our specialized chemists understand the quirks and troubleshooting questions that come with live research. Years spent synthesizing, purifying, and batch-testing this complex molecule give us tools to answer queries on dissolution, storage, or low-yield situations. Instead of generic, one-size-fits-all scripts, we troubleshoot directly based on how a particular batch was manufactured. Customers share back their experimental results, which loops into our process improvements.

    Warehouse to Lab: Addressing Storage and Logistics Challenges

    Phorbol 12-Myristate 13-Acetate arrives at our docks as a high-purity crystalline solid, but its shelf life depends on how it moves through the supply chain. We learned early that exposure to moisture and temperature swings shortens product life and reduces analytical purity. Every shipment stays cold from our freezer to your bench, shipped in validated cold packs or dry ice as temperature requires. Each order’s lot number ties back to our in-house logbooks, which chart production details as well as storage events.

    Smaller, research-sized vials dominate the academic market, but larger-scale pharmaceutical or industrial projects receive custom packaging. Sometimes material gets aliquoted into single-use sizes to eliminate repeated freeze-thaw cycles. Dry ice, specialized insulation, and rigid secondary packaging come standard to avoid transport shock. Based on direct client conversations, we keep no product in long-term storage warehouses — everything ships made-to-order, matching the latest batch test results. This eliminates guesswork around expiration timelines.

    Continuous Process Improvement: Learning Through Feedback

    Being a manufacturer involves more than just scaling up recipes from academic protocols. Our team watches the latest research from cell biology, immunology, and oncology to anticipate new requirements for PMA applications. We periodically run pilot-scale syntheses to confirm our assumptions and stress-test our purification system. Client feed-back loops directly into our process review board. A journal article reporting an interference effect prompts our chemistry staff to pull samples, check batch files, and update process documentation.

    Pharmaceutical industry clients often perform extensive side-by-side comparisons of PMA from various suppliers. We partner with these teams before scale-up, sharing our analytical results and fielding direct questions about synthetic steps. The result: a more robust product that fits seamlessly into even the most sensitive bioassays. Immediate access to technical records makes these collaborations straightforward—we never rely on generic product description sheets or outdated test data.

    Why Purity, Transparency, and Experience Matter

    Decades of bench work have shown us that every percent of purity counts. Even a trace of oxidized byproducts or leftover starting materials could derail a multi-week screening campaign. Our team brings together analytical chemistry and practical troubleshooting to keep impurity profiles as low as current technology allows. Open communication with customers ensures no surprises, whether they are running a single western blot or setting up hundreds of parallel ELISA plates.

    Phorbol 12-Myristate 13-Acetate owes its high profile in the research world to its unwavering biological activity. We take pride in each batch that leaves our facility, knowing that consistency, purity, and open documentation set us apart from generic, low-grade alternatives. As a manufacturer, not a distributor or trader, we provide the full chain of custody from starting material through to your bench. Each researcher’s success validates the extra effort behind our process. For us, product quality is built on the foundation of scientific responsibility—delivering more than a chemical, but a trusted research tool grounded in hard-won experience.