|
HS Code |
643526 |
| Product Name | Dibutyryl Cyclic Adenosine Phosphate |
| Abbreviation | dbcAMP |
| Cas Number | 36931-31-6 |
| Molecular Formula | C18H24N5O8P |
| Molecular Weight | 485.38 g/mol |
| Appearance | White to off-white powder |
| Solubility | Soluble in water |
| Storage Temperature | -20°C (desiccated) |
| Purity | Typically >98% |
| Usage | Cell-permeable analog of cAMP |
| Synonyms | N6,2'-O-Dibutyryladenosine-3',5'-cyclic monophosphate |
| Stability | Stable under recommended storage conditions |
| Hs Code | 29349990 |
| Melting Point | 136-139°C |
| Ph 1 Solution | 6.5-8.0 |
As an accredited Dibutyryl Cyclic Adenosine Phosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dibutyryl Cyclic Adenosine Phosphate is packaged in a 1g amber glass vial, tightly sealed and labeled with handling precautions. |
| Shipping | Dibutyryl Cyclic Adenosine Phosphate is shipped in tightly sealed containers, protected from light and moisture. The chemical should be transported at controlled room temperature, following all safety and regulatory guidelines. Proper labeling and documentation are provided to ensure safe handling and compliance during domestic or international shipping. |
| Storage | Dibutyryl Cyclic Adenosine Phosphate should be stored at -20°C in a tightly sealed container, protected from light and moisture. Avoid repeated freeze-thaw cycles; aliquot if necessary. Keep the compound in a dry, inert atmosphere to maintain stability and prevent decomposition. Follow all safety guidelines and consult the manufacturer's instructions for specific storage requirements. |
| Purity 98%: Dibutyryl Cyclic Adenosine Phosphate with 98% purity is used in cellular signaling pathway research, where enhanced signal specificity and reproducibility are achieved. Molecular Weight 491.38 g/mol: Dibutyryl Cyclic Adenosine Phosphate with a molecular weight of 491.38 g/mol is applied in neuronal differentiation studies, where consistent intracellular cAMP delivery promotes uniform differentiation. Stability temperature 4°C: Dibutyryl Cyclic Adenosine Phosphate stable at 4°C is utilized in cold storage protocols, where prolonged compound integrity supports extended experimental timelines. Aqueous Solubility ≥10 mg/mL: Dibutyryl Cyclic Adenosine Phosphate with aqueous solubility ≥10 mg/mL is implemented in in vitro pharmacological assays, where optimal solubility ensures homogeneous dosing and reliable data. Melting Point 120-124°C: Dibutyryl Cyclic Adenosine Phosphate with a melting point of 120-124°C is incorporated into thermal processing pipelines, where controlled melting prevents degradation during sample preparation. Endotoxin Level <0.1 EU/mg: Dibutyryl Cyclic Adenosine Phosphate with endotoxin level below 0.1 EU/mg is suitable for primary cell culture applications, where minimized endotoxin reduces cytotoxicity and supports cell viability. Sterility Tested: Dibutyryl Cyclic Adenosine Phosphate sterility tested is used in tissue engineering experimentation, where sterile conditions eliminate contamination risk and maintain experimental consistency. Optical Purity >99%: Dibutyryl Cyclic Adenosine Phosphate with optical purity greater than 99% is chosen for enantioselective biochemical studies, where high stereochemical purity ensures accurate biological response. Particle Size <10 μm: Dibutyryl Cyclic Adenosine Phosphate with particle size less than 10 μm is employed in sustained-release formulation development, where fine particle distribution enhances controlled release characteristics. pH Stability 6.5-7.5: Dibutyryl Cyclic Adenosine Phosphate with pH stability between 6.5-7.5 is selected for physiological buffer systems, where stable pH prevents compound hydrolysis and ensures repeatable outcomes. |
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As a dedicated manufacturer specializing in nucleotides, we've seen Dibutyryl Cyclic Adenosine Phosphate (dbcAMP) play a central role in various biochemical and pharmaceutical applications for decades. The full chemical designation, Dibutyryl cAMP, sets it apart thanks to its unique modification: butyryl groups added to the cAMP backbone. This feature transforms the compound into a cell-permeable analog of endogenous cyclic AMP. Researchers do not need to depend solely on native cAMP, which can struggle with cellular uptake. With dbcAMP, intracellular cAMP signaling can be studied more directly and efficiently, giving laboratories a reliable tool for targeted investigations.
Our dbcAMP, supplied as a white to off-white crystalline powder, comes with a proven high purity level. Typical lots reach over 98% purity by HPLC. Through our synthesis, we avoid common byproducts that complicate downstream processes. Each batch undergoes rigorous verification to confirm it offers consistent solubility and reactivity, ideal for both academic and industrial labs. In solid form, dbcAMP resists moisture better than more sensitive analogs, simplifying storage and handling during routine work. For research, we provide detailed spectroscopic and chromatographic documentation with every delivery.
Many customers are familiar with the classic cyclic AMP for activating protein kinase A or modulating intracellular pathways. Classic cAMP, though, cannot cross the plasma membrane efficiently, making direct supplementation of intact cells challenging. Dibutyryl cAMP’s lipophilic butyryl modifications overcome this barrier, allowing the compound to diffuse readily across cell membranes. This characteristic allows researchers to experiment with intracellular pathways directly, rather than manipulating cells through indirect stimulation or permeabilization.
Compared to other analogs like 8-bromo-cAMP, dbcAMP boasts better membrane permeability and hydrolytic stability. We’ve compared side-by-side responses in various primary cell lines; dbcAMP consistently delivers prompt and strong physiological effects. This improves data reliability and eliminates the need for additional solvents or surfactants to assure bioavailability. For those working with sensitive or primary cultures, this translates to greater cell survival and response predictability across replicates.
Labs exploring gene expression, cell differentiation, or signal transduction benefit from the predictable activity of dbcAMP. Muscle, nerve, and endocrine tissue models all show robust and reproducible responses to dbcAMP, particularly in in vitro differentiation protocols. For example, dbcAMP has remained a staple in protocols converting embryonic stem cells into neurons. In our experience supplying major academic centers, labs can streamline protocols knowing this analog reduces batch-to-batch performance variability.
In metabolic research, imported dbcAMP enters cells and rapidly elevates intracellular cAMP levels. This triggers downstream kinases and promotes the phosphorylation events that underpin many metabolic and hormonal signaling cascades. Reliable and robust elevations save valuable time in early-phase screening or mechanistic studies. After collaborating with pharmaceutical development teams optimizing hormone analogs, we’ve seen dbcAMP make dose-response studies far more consistent.
Older protocols, which relied on less permeable analogs, often resulted in patchy or misleading results. With the butyryl modification, experiments investigating PKA-mediated responses or phosphodiesterase activity yield clearer answers. Usage also extends to immunology studies, where dbcAMP helps probe immune cell activation and cytokine release.
Neuronal cell culture protocols incorporate dbcAMP to force maturation and guide axonal outgrowth. In our own in-house cytology experiments, primary neurons exposed to dbcAMP differentiate sharply, with defined neurites and advanced electrophysiological properties. Several publications from groups we supply have shown that protocols substituting standard cAMP with dbcAMP yield faster and more synchronous neuron differentiation. It makes protocol optimization and scale-up more predictable—critical in high-throughput screening and regenerative medicine research.
dbcAMP’s cell permeability and slow metabolic breakdown have also made it a standard tool to maintain dopaminergic neuron health in Parkinson’s disease models. We’ve helped teams shift from alternate cyclic nucleotides that failed to deliver sufficient, sustained activation of intracellular cAMP pathways. Supplies of high-purity dbcAMP prevent cross-contamination with other nucleotide analogs, removing additional variables in sensitive neuronal assays.
Cardiomyocyte researchers employ dbcAMP to activate heart cells through protein kinase A pathways. This application demands high-purity reagent, as inconsistencies quickly appear as variations in cell contractility and stress response. Variability also threatens data reliability for pharmacological studies focused on beta-adrenergic modulation. We ensure each lot undergoes uniform quality control using both electrical and structural cell-based assays before reaching our customers.
In muscle tissue studies, dbcAMP supports differentiation of myoblasts into myotubes. Working with groups studying muscular dystrophies, we’ve seen research projects advance rapidly thanks to the repeatable effects of dbcAMP on muscle fiber formation, fusion, and contractile function. Material derived from our controlled synthesis allows for tracing downstream effects with minimal off-target pathway stimulation—ideal for both classical and state-of-the-art muscle models.
Our experience shows that ease of handling translates directly into better data. Since dbcAMP resists ambient moisture, users report longer storage lives and consistent concentration in solution even after repeated weighing and dispensing. Standard cAMP and some less-stable analogs often clump or degrade unless stored under strict inert conditions. With dbcAMP, many institutions run work for weeks from a single batch, avoiding variation and maintaining precise dose-response profiles.
Customers have struggled with some analogs hydrolyzing during extended tissue culture protocols, leading to erratic cellular responses and wasted material. Our production approach tightly controls moisture and temperature exposure during packing, keeping dbcAMP potent right up to the day it’s used. This stability means more reliable experimental controls and less recalibration between runs.
Precision matters in kinase activation assays and phosphorylation pathway studies. dbcAMP yields instantly soluble solutions in common assay buffers without precipitating or requiring ultrasonic dispersion. This solubility helps avoid uneven distribution in multi-well plate assays or microfluidic applications. In our pilot studies, protein kinases given precisely measured dbcAMP respond linearly over concentration ranges relevant to research and commercial pharma investigations.
We advise against using generic nucleotide solutions or outdated analogs for cAMP pathway work where rigor and repeatability guide publication or regulatory submission. Over the years, we’ve fielded requests for troubleshooting failed kinase assays or inconsistent gene reporter responses. In a high percentage of these cases, swapping out the analog for our high-purity dbcAMP yielded a sharp uptick in performance and clarity of results.
Regenerative medicine platforms require precise control over intracellular signaling. dbcAMP’s membrane permeability makes it a go-to for guiding stem cell fate in engineered tissues. Numerous customers confirmed that using our dbcAMP in three-dimensional spheroid cultures led to more uniform differentiation and greater yield of desired cell types. For tissue engineering groups building neuron-rich scaffolds, dbcAMP enables efficient conversion and maturation across cell populations, cutting protocol optimization time significantly.
Groups we support also report fewer problems related to inconsistent compound delivery into cell aggregates or hydrogels, a significant bottleneck for high-throughput drug screening and preclinical research. Our stringent batch testing and documentation give customers confidence when scaling up from microplates to liter-scale bioreactors.
Endogenous adenosine monophosphate hardly enters intact cells and is subject to rapid degradation by phosphodiesterases. In contrast, the butyryl chains on dbcAMP delay metabolic breakdown, permitting sustained effect with less frequent supplementation. Other analogs, such as 8-bromo-cAMP, provide moderate improvement in cell permeability, but produce variable results because of different rates of hydrolysis or issues related to membrane transporters. Over the years, we’ve confirmed that only dbcAMP allows sensitive cell types, including adult stem cells, to show constant and measurable cAMP-linked signaling without introducing toxicity or interfering with other metabolic pathways.
Our production lines offer dbcAMP in a range of standard pack sizes appropriate for both small-scale R&D and larger industrial projects. We’ve responded to requests for bulk supply on short timelines, and maintain adequate capacity to accommodate expanding pharma pipelines and biotech innovation cycles. Our facility enables lot-to-lot consistency, so teams running multi-year studies never face project delays or need to recalibrate their protocols due to shifting raw material profiles.
We work alongside our customers to tailor delivery schedules based on project milestones, supporting uninterrupted research activity. This familiarity with researchers’ daily challenges goes well beyond what traders or general chemical wholesalers can offer, and our technical team stands ready to consult on protocol tweaks that may get the most from our batches.
Ensuring batch conformity with industry standards and relevant pharmacopeias ranks high on our list. We audit every stage of production and document certificate of analysis parameters, retaining archival samples for third-party validation in major studies. This keeps our dbcAMP accessible for both regulated preclinical programs and standard non-regulatory research. We devote resources to preserving chemical identity, avoiding mixing or mislabeling that can sabotage sensitive biological work.
We continuously monitor incoming raw materials and maintain tight process controls with validated in-process analytical checkpoints. Our facility’s in-house quality labs run full-spectrum characterization before we approve any lot for shipment. Transparent documentation gives customers assurance during audits, regulatory submission, or publication in top-tier journals.
Labs may run into repeated assay hiccups because of reagent inconsistency, especially among lesser-known brands or distributors lacking direct control over synthesis. We’ve seen groups spend months trouble-shooting only to discover subtle impurities in analogs provided by middlemen. By producing dbcAMP ourselves and following up batch tracking, we guarantee direct traceability from starting material to finished vial.
Some researchers have transitioned from purchasing off-the-shelf analogs to sourcing dbcAMP from established industrial manufacturers. After making the switch, many groups see a dramatic improvement in reproducibility and a decrease in experiment-to-experiment variation. Our technical support team works with researchers to adjust protocols with clear, specific recommendations—not canned advice or vague troubleshooting tips. This hands-on supply chain stance anchors our relationships with both academic and commercial innovation partners.
Pharmaceutical partners using our dbcAMP in high-throughput screens or secondary validation workflows count on documentation at every production step. We provide full data on purity, spectral analysis, and batch composition, supporting regulatory and patent submissions worldwide. Whether a customer is screening kinase inhibitors or investigating second messenger signaling, the reliability and availability of our dbcAMP helps projects advance from bench to clinical candidate selection without sudden delays due to reagent quality questions.
As researchers intensify their focus on programmable cell therapies and pathway-directed treatments, consistent cAMP modulation remains a pivotal requirement. We work with companies requiring specialized packaging or sterile solutions for integration with automated robotic platforms, ensuring product characteristics suit modern discovery labs and GMP-standard pilot lines.
Production of purified nucleotide analogs brings with it substantial responsibilities. We design our synthesis process to minimize byproduct generation and avoid halogenated solvents, in response to both regulatory requirements and environmental stewardship. Waste treatment complies with local and international standards. Periodic reviews of solvent recovery and effluent streams help us sustain benchmark yields while keeping our environmental footprint low.
We train all manufacturing staff in proper reagent management, equipping them to avoid both cross-contamination and unsafe exposure during production and packaging. This ensures both worker safety and higher confidence in batch-to-batch purity, a major point of difference compared to resellers lacking direct control over their products’ journey to the consumer.
Scientist feedback shapes our ongoing product development. Over time, we’ve honed our diagnostic and technical support services based on common lab pain points and shifting research priorities. Changes in assay conditions or the push for higher throughput often drive us to test new packaging methods or recommend alternative storage options to minimize risk of hydrolysis or adsorptive losses.
We take pride in keeping channels open between our process chemists and those driving research at the bench. This dialogue gives us a deeper understanding of what users need from their reagents. People working under tight timelines or pursuing projects where exploratory data carries high stakes turn to direct manufacturers because we can change quickly, rooted in continual awareness of evolving industry demands.
Every batch of Dibutyryl Cyclic Adenosine Phosphate that leaves our facility carries with it decades of hard-won manufacturing knowledge, a deep understanding of laboratory applications, and an active commitment to quality. Our process does not just produce material meeting analytical standards; it supplies a tool that supports discovery, enables repeatable experiments, and underpins advances in cell signaling, regenerative medicine, and pharmacology. Created through a well-controlled, transparent process, our dbcAMP continues to play a vital supporting role as researchers pursue new approaches to health and disease at the cellular and molecular level.