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HS Code |
815949 |
| Product Name | 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) |
| Common Name | BAPTA-AM |
| Cas Number | 126150-97-8 |
| Molecular Formula | C38H48N2O16 |
| Molecular Weight | 784.79 g/mol |
| Appearance | Off-white solid |
| Solubility | Soluble in DMSO, ethanol, and DMF |
| Storage Temperature | -20°C (desiccated, protected from light) |
| Purity | Typically ≥98% |
| Usage | Cell-permeable calcium chelator |
| Melting Point | Requires experimental determination |
| Synonyms | BAPTA tetraacetoxymethyl ester |
| Inchi Key | DRISDZKJAKYHJO-UHFFFAOYSA-N |
As an accredited 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) (BAPTA-AM) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | BAPTA-AM, 50 mg: Supplied in an amber glass vial with a screw cap, labeled with chemical name, quantity, and safety information. |
| Shipping | BAPTA-AM is shipped at room temperature, typically in a tightly sealed vial to protect it from moisture and light. For long-term storage, refrigeration at 2–8°C is recommended upon receipt. The product is classified as non-hazardous, but appropriate handling and protective equipment should be used during transit and upon opening. |
| Storage | 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) (BAPTA-AM) should be stored at –20°C, protected from light and moisture. The compound is sensitive to hydrolysis and should be kept in a tightly sealed container under inert gas if possible. Minimize exposure to air and use desiccants to prevent degradation. Store as a dry, solid form for best stability. |
Applications of 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) (BAPTA-AM) in Industrial ManufacturingAs the direct manufacturer of BAPTA-AM, we support advanced sectors with high-purity calcium chelators optimized for specialized industrial workflows. Our extensive production and technical experience ensure consistency for diverse downstream industrial partners that require tight quality control and formulation flexibility. 1. Biotech Cell-Based Assay Reagent ProductionMajor producers of ready-to-use reagents for intracellular calcium detection rely on BAPTA-AM as a membrane-permeable Ca2+ chelating agent. It enters downstream synthesis during the formulation of live cell assay kits, where stability, cell permeability, and controlled hydrolysis are critical. Producers comply with stringent reagent and diagnostic quality certifications while determining concentrations based on assay throughput, tissue type, and plate format. Industry compliance standards
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2. Neuroscience and Cardiovascular Research Tools ManufacturingSuppliers of research materials for brain and cardiac studies use BAPTA-AM for generating buffers and perfusates with controlled intracellular calcium conditions. Downstream customers demand precise purity and documented performance for products entering laboratory and translational workflows targeting calcium signaling. Additive ratios are selected based on specific animal or human tissue models to balance chelation strength and cell membrane penetration. Industry compliance standards
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3. High-Precision Live Cell Imaging Media ProductionManufacturers of advanced cell imaging media depend on BAPTA-AM to limit cytoplasmic calcium transients during time-lapse and confocal microscopy. Industrial partners enhance media formulations with this chelator at controlled dosages to enable high-resolution recording of intracellular events in mammalian and other vertebrate cells, ensuring media meets performance benchmarks and regulatory purity specifications for live-cell imaging workflows. Industry compliance standards
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4. Custom Calcium Flux Assay Plate ManufacturingProducers of pre-plated, ready-to-use calcium flux assay systems incorporate BAPTA-AM to deliver defined Ca2+ sequestration directly in multiwell assay plates. The chelator is precisely dispensed in micro-volumes during dispensing or lyophilization for homogeneity and reproducibility across large QC batches. Standards mandate control of possible cross-contamination, accurate label claims, and batch consistency in finished plates for clinical research or screening. Industry compliance standards
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5. Pharma-Grade Excipient for Intracellular Chelation in Cell Therapy ManufacturingCell therapy contract manufacturers integrate BAPTA-AM to achieve precise chelation of intracellular Ca2+ loads during transfection, electroporation, or storage of engineered cell lines. This application calls for full adherence to current GMP, traceable excipient documentation, and batch-specific verification of cell compatibility, requiring precision dosing to prevent undesired ion depletion or toxicity within cell therapy product workflows. Industry compliance standards
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BAPTA-AM, formally known as 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester), continues to redefine what researchers can achieve in cell biology, neuroscience, and calciomics. Serving laboratories and industrial partners directly from our manufacturing base, we have witnessed how BAPTA-AM transforms calcium measurement, manipulation, and imaging, driving discoveries across disciplines. We manufacture this compound for consistent quality and stringent purity controls, knowing that users demand reliability at every turn.
BAPTA-AM's molecular structure embodies a balance between its chelating core and the four acetoxymethyl ester groups. These ester moieties mask the carboxylic acid groups, producing a lipophilic neutral complex. Manufactured with a focus on batch reproducibility, users receive crystals or powder, free from contaminants that can impact kinetics or introduce interference during experiments. Our process targets minimal residual solvent, eliminating potential disruptions in sensitive cellular assays.
The acetoxymethyl esters hold central importance. Many researchers struggle with delivering ionic chelators across cell membranes, often resorting to mechanical or electroporation techniques that disturb cell health. By masking negative charges, BAPTA-AM crosses membranes passively, entering live cells efficiently. Intracellular esterases then cleave the AM groups, unmasking the active BAPTA chelator precisely where calcium capture is required. This feature sets it apart from salts like BAPTA or EDTA that linger in extracellular spaces or require invasive techniques for delivery.
The past decade has seen an explosion in the use of BAPTA-AM for studying calcium-dependent signaling. As the main manufacturer, we have collaborated with academic and industrial researchers who track rapid, transient changes in calcium within neurons, myocytes, and immune cells. With a fast association rate for Ca2+ (kon ~1.5x108 M-1s-1) and high affinity (Kd ~ 170 nM for Ca2+), BAPTA-AM provides the temporal and spatial fidelity necessary for capturing sharp signaling events.
Unlike indicators such as Fura-2 or Fluo-4, which have secondary spectral applications, BAPTA-AM’s primary value is its selective chelation. The molecule binds Ca2+ with minimal impact on Mg2+ concentrations, which is critical when monitoring or modulating calcium flux in environments where magnesium is abundant. We routinely see its use in experiments aimed at distinguishing between calcium-driven and magnesium-driven mechanisms, especially in neurobiology assays sensitive to magnesium artifacts.
BAPTA-AM finds its place in a range of applications. In neurobiology, labs rely on it to modulate action potential-induced calcium influx, investigating excitotoxicity or plasticity phenomena in cultured neurons or acute slices. Cardiac researchers adopt it for studies of arrhythmogenic events by clamping intracellular calcium in myocytes. In immunology, BAPTA-AM assists teams exploring Ca2+-dependent degranulation or cytokine release from T cells and mast cells. The compound’s quick internalization and rapid hydrolysis open new doors for experiments that require simultaneous modulation of intracellular calcium across entire cell populations.
A key point often raised is BAPTA-AM's compatibility with fluorescence microscopy and flow cytometry. Unlike some analogues, it does not interfere with standard excitation or emission channels. This quality allows users to combine calcium modulation with real-time imaging, sometimes even in parallel with genetically encoded calcium indicators. In manufacturing, matching spectral purity and minimizing colored impurities ensures that imaging and reading results stay clear and reproducible.
In our direct collaborations, we see advanced imaging labs pairing BAPTA-AM with electrophysiology, optical trapping, or optogenetics. These integrative approaches demand rigorous control over both the timing and location of calcium modulation. The cell-permeable design lets researchers target specific regions, time points, and cell types, avoiding artifacts that may arise from more broadly acting or less selective agents.
Manufacturing quality underpins every difference that matters in real experiments. BAPTA-AM differs markedly from its parent acid, BAPTA, in terms of usability. Its AM esters create a neutral molecule that crosses lipid bilayers without cytotoxic carriers or physical disruption. In contrast, BAPTA acid itself stays ionized and fails to cross intact membranes under physiological conditions. This leads to practical limits in studies involving living cells or animal tissues.
Many labs consider using EDTA-AM or EGTA-AM for calcium chelation, hoping to replicate results. Unlike BAPTA-AM, these alternatives display weaker calcium affinity, slower kinetics, and, for EDTA, significant zinc binding. Our experience shows that BAPTA-AM’s rapid binding and highly selective Ca2+ affinity eliminate these confounders, providing more actionable data from each trial. An added benefit is the compound's faster intracellular activation, which means effects can be observed almost immediately in time-lapse imaging or high-throughput screening setups.
We constantly evaluate reports of performance differences. Consistent feedback points to BAPTA-AM’s unique combination of rapid entry, precise activation, and low cytotoxicity across a variety of primary cell lines and organotypic cultures. Our batches are manufactured with special focus on controlling hydrolysis rates. By supplying BAPTA-AM with uniform AM protection, users avoid batch-to-batch variability that has led to failed experiments when sourcing from less experienced suppliers.
Laboratory outcomes depend heavily on initial reagent quality. We manufacture BAPTA-AM to over 98% purity. Each lot undergoes HPLC and NMR quality control—not just a formality, but as a guard against degradation products that can skew sensitive fluorescence or electrophysiological readouts. The compound comes vacuum-sealed, stored under argon, and shipped cold, all actions proven to prolong shelf life. Our knowledge of BAPTA-AM’s oxygen and hydrolysis sensitivity shapes every step from crystallization to dispatch.
Users typically dissolve BAPTA-AM in anhydrous DMSO or DMF, preparing aliquots under dry, inert conditions. We recommend minimal exposure to light and humidity during both storage and use, as ester hydrolysis can begin within hours on the bench. Practical experience confirms these storage precautions extend active shelf life beyond six months in most settings, enabling researchers to plan studies without risk of last-minute reorders due to spoilage.
By producing BAPTA-AM in-house from bulk starting materials, we maintain full control over precursor quality, reaction intermediates, and final crystallization. Quality feedback loops run from our operators’ daily records to long-term stability studies. This approach ensures researchers receive product that behaves the same way every time, from quick, consistent hydrolysis inside cells to a lack of colored degradation products under high magnification. We have supported teams working on everything from patch clamp assays in single neurons to high-throughput screens in immune cell populations.
The manufacturing environment itself reflects our commitment. Each production run takes place in positive-pressure suites, with microbially filtered air and strict exclusion of transition metals, which can compromise chelation chemistry or introduce fluorescent impurities. Operators wear full cleanroom attire, minimizing risks of particulate contamination or errant hydrolysis. Traditional glassware sometimes leaches metal ions—so we switched to high-density plastics for all product contact points, tailoring our process for the chelator’s unique requirements.
In our interactions with customers, we hear recurring concerns about the stability and activity of loaded BAPTA-AM, especially during long imaging sessions or experiments that require cells to remain healthy for hours. To address this, we test each new manufacturing batch in model cell cultures, confirming not only the purity but the biological activity and absence of undesired side products. These in-house assays inform adjustments to our esterification protocols, keeping hydrolysis rates and activation times within narrow, reliable bounds.
Some research projects push BAPTA-AM to the edge: very high ambient calcium, rare cellular phenotypes, or combined use with radical scavengers and unusual buffers. Our development teams work with these labs directly. In calcium-rich environments, we help adjust concentration protocols so that the chelation does not deplete available calcium beyond physiological levels. For rare or sensitive cell types, we provide guidance on loading concentrations and co-solvent use, minimizing cytotoxicity or off-target effects. These efforts feed back into ongoing research, improving the next productions.
BAPTA-AM does not pose the same environmental persistence risks found in some traditional chelators, which can accumulate and interfere with aquatic life. Our process eliminates organic and metal-based impurities at source, achieving a cleaner waste stream and reducing the risk to operators and end users. Waste solutions receive on-site neutralization and capture, in line with growing expectations for sustainable chemical manufacturing. Staff training covers all handling and disposal aspects, with monitoring in place for airborne esters or solvents—a bar often overlooked by resellers or second-tier manufacturers.
Handling BAPTA-AM safely in the lab requires respect for its reactive ester groups. We provide end-user guidance, drawn from real spill and exposure scenarios in our own facility. Rapid cleanup teams rely on activated charcoal and proper PPE, with immediate area ventilation. The lessons learned feed into both safety instructions and improved packaging for final product dispatch. Our policy is not just compliance, but genuine prevention and transparent risk-sharing with users.
Scientists push boundaries daily, and as a manufacturer, watching their breakthroughs motivates constant adaptation. Sometimes, a lab will request BAPTA-AM with a unique particle size or solubility profile for microinjection or novel dispensing devices. We work directly with them, modifying crystallization or grinding steps, so the reagent fits the exact delivery method. This degree of custom support rarely comes from distributors. Other research groups need extremely rapid turnaround, especially those racing deadlines for grant-funded projects. Our manufacturing team prioritizes these cases, leveraging internal stocks and reserve capacity to ensure timelines are met.
In an era of increasingly multiplexed and automated workflows, new applications for BAPTA-AM arise. Robotics platforms capable of screening hundreds of cell cultures demand not just high purity but also minimal lot-to-lot drift. Our direct feedback from automation engineers informs modifications to drying and packaging protocols, creating a product that flows cleanly through automated systems without clumping or static. Labs operating at this scale benefit from our approach: every batch ships with both chemical and user experience improvements.
Every year brings new findings about intracellular calcium and its role in disease mechanisms, development, and therapy. Our ongoing research ties into this wave. By continually refining BAPTA-AM’s synthesis, we create solutions that keep pace with these demands. Teams working in gene therapy, for example, require BAPTA-AM that dissolves fully in custom non-aqueous buffers, to introduce directly into viral delivery systems. Stem cell researchers have pressed for modifications in purity protocol, so their cells retain pluripotency after chelation. We feed these requests back into manufacturing, tightening quality controls and exploring new protective groups for even faster in-cell activation.
Collaborative testing with leading institutes ensures every batch holds up under both routine and frontier conditions. Experiments in microfluidics or organ-on-a-chip platforms test BAPTA-AM in ways not imagined just a few years ago. We see intracellular imaging performance, stability, and compatibility emerge as competitive differentiators—areas where small improvements in manufacturing lead to large leaps for the scientific community.
Working as the manufacturer, we maintain long-term supply agreements with organizations both large and small. By shipping directly, we ditch unnecessary transit, repeated repackaging, and the risk of contamination or mix-ups that creep in with intermediary distribution. Customers come back for the unfiltered support—detailed troubleshooting, application notes based on our own test runs, and the flexibility to refine orders mid-project. In this way, every vial of BAPTA-AM delivers not just a chemical, but a piece of a working relationship rooted in honesty and ongoing improvement.
With every batch leaving our facility, our hope is for BAPTA-AM to serve not just as a research tool, but as an enabler of discovery, reliability, and creative experimentation. Manufacturing is not just about chemical synthesis, but about listening and responding to the real problems scientists face every day. That’s the spirit that defines not only our product standards, but the entire story of BAPTA-AM’s place in modern science.