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HS Code |
949377 |
| Chemical Name | 1,1-Dimethyl-4-Phenylpiperazinium Iodide |
| Cas Number | 54-92-2 |
| Molecular Formula | C12H19IN2 |
| Molecular Weight | 334.20 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 196-198°C |
| Solubility | Soluble in water |
| Synonyms | DMPP Iodide; DMPP |
| Storage Temperature | 2-8°C (refrigerated) |
| Usage | Nicotinic acetylcholine receptor agonist |
| Pubchem Cid | 60946 |
As an accredited 1,1-Dimethyl-4-Phenylpiperazinium Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, tamper-evident HDPE bottle containing 5 grams of 1,1-Dimethyl-4-Phenylpiperazinium Iodide; labeled with CAS number and hazard warnings. |
| Shipping | 1,1-Dimethyl-4-Phenylpiperazinium Iodide is shipped in tightly sealed containers, protected from light and moisture. It is packed according to chemical safety regulations and labeled appropriately. During transit, temperature and handling precautions are observed to prevent degradation, ensuring safe and compliant delivery to laboratories or research facilities. |
| Storage | 1,1-Dimethyl-4-Phenylpiperazinium Iodide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at room temperature (15-25°C). Avoid exposure to heat, incompatible substances, and strong oxidizers. Ensure proper labeling and store away from food and drink to prevent accidental ingestion or contamination. |
Applications of 1,1-Dimethyl-4-Phenylpiperazinium Iodide in Industrial ManufacturingOur factory delivers high-purity 1,1-Dimethyl-4-Phenylpiperazinium Iodide (DMPP Iodide) to support complex downstream operations requiring controlled analytical, chemical, or pharmaceutical synthesis. Below, we introduce the primary industrial sectors utilizing this specialty compound, with practical details reflecting global regulatory frameworks and established factory-scale practices. 1. Pharmaceutical Research and Active Pharmaceutical Ingredient (API) DevelopmentPharmaceutical manufacturers source DMPP Iodide as a cholinergic agonist standard in early-stage pharmacological screening, analytical reference, and as a building block in the synthesis of novel central nervous system (CNS) agents. R&D teams use the material primarily in dose-response binding studies, bioactivity assays, and for producing intermediates where selective muscarinic or nicotinic receptor agonism is under investigation. Industry compliance standards
Typical usage ratio
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2. Neuroscience Tool Compound ProductionIndustry-grade DMPP Iodide supports the manufacture of tool compounds for academic and industrial neuroscience laboratories. It serves as a benchmarking agent in receptor functional assays, for signal transduction testing, and in tissue-based neurophysiology studies including patch clamp protocols and synaptic transmission analysis. Industry compliance standards
Typical usage ratio
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3. Reference Standard Supply for Analytical LaboratoriesChemical analysis companies require DMPP Iodide as a certified analytical reference standard in the development and calibration of HPLC, LC-MS, and GC/MS quantification methods, specifically for the routine detection of trace cholinergic agents or novel synthetic analogues. Strict batch-to-batch reproducibility and certificate of analysis (CoA) documentation is critical in these settings. Industry compliance standards
Typical usage ratio
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4. Contract Manufacturing for Custom Fine Chemical SynthesisSpecialty fine chemical entities order DMPP Iodide as an advanced starting material or quaternary ammonium salt source for custom API intermediates or specialty ligands. These processes often involve N-alkylation, N-oxide formation, or further substitution to generate advanced structures for medicinal chemistry programs or for catalyst precursor evaluation. Industry compliance standards
Typical usage ratio
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The chemical world rarely stands still, and we have seen firsthand in our plant just how rapidly new applications and demands arrive for specialty compounds like 1,1-Dimethyl-4-Phenylpiperazinium Iodide, known in laboratories as DMPP Iodide. Our team has spent years scaling its production, troubleshooting equipment, and fielding questions from industry researchers who depend on batch-to-batch consistency and purity. The technical and laboratory fields have kept this compound in steady demand, especially for neuropharmacological and receptor assay work.
DMPP Iodide’s formula brings together a piperazinium ring, substituted with two methyl groups, and a phenyl group at the four position, neutralized as the iodide salt. Years ago in our synthesis development, controlling the substitution pattern and salt formation presented hurdles. Iodide handling requires vigilance; moisture and light regulation are not optional if the final compound is to stay white and avoid decomposition. Over the years, storage containers, packaging lines, and working environments improved, so our yields kept rising and fewer end users reported issues with discoloration or off-odors.
In our experience supplying universities, biotech firms, and pharmacology research teams, DMPP Iodide regularly appears in studies on nicotinic acetylcholine receptors. The compound acts as a potent agonist at these receptor subtypes and has become a gold standard when researchers probe cholinergic signaling. The industry’s continuing focus on neurodegenerative diseases and neurotransmitter pathways means DMPP Iodide often features in projects aiming to unravel basic brain chemistry or screen for new drug candidates.
On the manufacturing floor, keeping purity high is not a suggestion—DMPP Iodide with even slight byproduct traces leads to ambiguous data in receptor studies. Over time, we adopted additional purification steps and validated new analytical methods beyond ordinary melting point or TLC checks. High-performance liquid chromatography (HPLC) allows our QA lab to catch contaminants that earlier generations missed. Customers started to notice. Conversations moved away from “I need another shipment” toward “I see clear data signals—can you supply enough for a full trial series?” That has been one of our biggest points of pride.
In the early days, we found out the hard way that meeting published reference standards—like a nominal ≥98% purity—will not always satisfy meticulous researchers. Rather than chasing tight margins with only cost in mind, we developed protocols to deliver DMPP Iodide routinely at ≥99% purity. Even at this threshold, analytical feedback from research labs highlighted the need to control moisture content. Because iodide is hygroscopic, labs occasionally reported weight variations or solubility shifts if samples absorbed trace water during shipment. By shifting bottle-capping systems and adopting advanced desiccant use, we reduced these complaints.
Specification also includes polymorphic control and particle size. Our shift toward micronized powder allowed better solution preparation, minimizing clumping and undissolved residues in buffer solutions. The switch was not seamless—it meant redefining powder-handling steps to cut down on static and dust loss. Still, the feedback from neurochemistry groups made it worthwhile. Every gram leaves our facility with a certificate that includes batch HPLC traces, residual solvent reports, and water analysis by Karl Fischer titration.
Our conversations with academic and industry end-users repeatedly highlight two major uses for DMPP Iodide: as a tool in pharmacological profiling of nicotinic acetylcholine receptors, and as a reference agonist during signal transduction experiments. Historically, most labs introduced synthetic agonists and assessed ion channel opening or downstream enzymatic pathways. DMPP Iodide’s robust, predictable action ensures reliable experimental calibration.
We have partnered with contract research organizations running central nervous system (CNS) models who rely on DMPP Iodide to validate hit compounds in screening cascades. Often, researchers will ask for supporting documentation verifying our analytical data and proof that individual batches match previously purchased ones. Consistency here is not marketing fluff but a result of carefully archived process data. Our technicians measure each reaction in-process, tracking pH curves, mixing speeds, and temperature ramps, then correlating these parameters to the final product properties. This data pool helps us tweak reaction conditions the next time a subtle batch deviation surfaces.
We regularly engage with labs comparing DMPP Iodide from various sources. A common theme: uncertainty about compound integrity hampers progress. Overseas material with inconsistent water load or subpar purity often leads to convoluted data curves. Over the years, the market became filled with repackaged chemical product—resold at a markup, sometimes even mixed with anti-caking agents or stabilizers unlisted on paperwork. We don’t cut or blend. Our DMPP Iodide leaves our reactors, enters a monitored drying process, and heads straight for sealed containers that get labeled by batch origin.
Making DMPP Iodide from scratch rather than sourcing intermediates offers a better grip on raw material origins. We source starting amines and haloalkanes from trusted process partners who can provide traceability. Several times, a new shipment of phenylpiperazine failed our impurity screen, setting us back almost a week. Refusing to compromise batch quality sometimes means production delays, especially with raw material crunches, but long-term credibility with the research community justifies slower deliveries over inferior output.
Anyone regularly sourcing pharmacological agonists knows the contrast between DMPP Iodide and related tool compounds. Take 1,1-dimethyl-4-phenylpiperazinium chloride, for instance. Although similar structurally, the chloride salt offers different solubility and hygroscopicity. Many labs find iodide easier to handle under ambient conditions, with less risk of rapid moisture uptake during bench weighing. The heavier iodide ion also influences receptor-binding assays, which has implications for comparability across studies—something we learned in discussions with pharmacology faculty standardizing protocols after switching from chloride to iodide forms.
DMPP sulfate faces some logistical barriers—greater deliquescence and a lower molecular weight per equivalent of active cation mean that error margins rise during manual weighing. Our in-house trials with these alternatives showed higher batch rejection rates, mostly from inconsistent drying and purity drops. For work demanding precise stoichiometry or solution stability across multiple experiment runs, our research partners lean toward DMPP Iodide after trying other salts.
Early on, we understood that simple bench analytics would not build long-term loyalty. Modern applications for DMPP Iodide often require researchers to defend data rigor in published work, which means audited trace reports and comprehensive documentation. Our approach relies not just on in-process checks but stringent release criteria: certificate of analysis with every shipment, stability data, and, if requested, impurity profiling below 0.1%. Delivering detailed batch documentation eats up lab time, but this is a shared language for many of our partners—especially those operating in regulated research or pharmaceutical development.
Unexpected issues rarely stay hidden for long—a spike in residual solvent or the appearance of a new impurity peak triggers a process audit. Weekly in-house recalibrations of our chromatographs and moisture balances ensure that the analytical side keeps pace with process improvements. As a result, documented customer complaints are vanishingly rare, and repeat business has become our strongest marketing.
DMPP Iodide presents the same risks typical of quaternary ammonium compounds, but the iodide counterion adds another layer of care. Factory protocols require staff to wear gloves and handle the material away from open air and moisture sources. Early on, overlooking this led to caking in stored drums and occasional batch downgrades. We redesigned our cleanrooms and now restrict DMPP Iodide processing to dehumidified zones. This attention to environmental detail has a ripple effect: customers report fewer handling issues and more reproducible assay results.
From our vantage point, end-users in research settings benefit from careful aliquoting and storage in tightly sealed desiccators. Our technical bulletins—drafted from direct production experience, not template legalese—encourage dissolution in dry solvents and warn about exposing bulk material to open lab air. These seemingly minor practical tips create tangible improvements in the longevity and utility of each shipment.
Interest in DMPP Iodide grew sharply in the past decade as high-throughput screening and disease model studies burgeoned. Demand cycles can spike unpredictably, putting stress on raw material pipelines. Because we manage all key synthesis steps in-house, our exposure to external volatility stays relatively low, but we have learned to maintain expanded stockpiles of both feedstock and packaging materials.
Our shift to just-in-time manufacturing for hospital and university buyers helped, but bulk requests from industry sometimes arrive with short notice. We have built modular reactor systems specifically sized for mid-scale batches, balancing flexibility with contamination risk. This means we can keep production moving during unexpected supply chain hiccups, but we do face pressure from the ongoing rise in global specialty chemical prices.
We also watch regulatory changes closely, especially as import and export restrictions change for some piperazine derivatives and iodide compounds. By keeping our compliance paperwork and analytical data prepared ahead of schedule, we dodge hold-ups at customs that have reportedly stalled competitors’ packages for weeks.
Manufacturing DMPP Iodide, like any organic iodide, produces process waste streams—aqueous washings, spent solvents, and iodine-containing residues. Over the years, we invested in a solvent reclaiming scheme and neutralization tanks to shrink our footprint. Our in-plant waste separation keeps iodine out of general streams and enables periodic regeneration for re-use. Not all industry players take this route, but we see long-term value—not only for environmental compliance but for cost containment as iodine can be costly to source or dispose of.
Reducing solvent emissions by upgrading to enclosed handling and recycling setups made a measurable difference to air quality zones inside and outside our facility. Feedback loops between the environmental management team and process engineers mean ongoing improvement—each new campaign brings opportunities to fine-tune recovery rates and shrink landfill loads.
Our journey with DMPP Iodide has taught us that supporting researchers extends beyond shipping bottles with a certificate of analysis. Projects change, protocols advance, and analytical details matter more as labs pursue publication or regulatory approval. We field questions on compound solubility, batch archival, and even specific reaction performance under alternate pH buffering systems. Many times, collaborating scientists share unpublished data or troubleshooting anecdotes, which feeds back into our quality and support workflows.
Workshops and technical bulletins based on our manufacturing insights have equipped end-users to maximize product shelf-life, troubleshoot solubility quirks, and prepare reproducible solutions from bulk material. Direct conversations with lab managers and principal investigators offer insights that drive our next process improvement. These conversations keep us honest and focused—not just selling chemicals, but actively supporting scientific advance.
Changing regulatory climates continually impact specialty chemicals. Iodide salts like DMPP face close scrutiny under international guidelines, especially as their use spreads in research labs in North America, Europe, and Asia. Registration and safety data filing claims more internal time and resources than in years past, but this helps build mutual trust across the industry. More frequently, academic labs inquire about REACH status, impurity profile disclosure, and validation for animal research, making robust record-keeping and transparency routine rather than exception.
An interesting change over the last several years has been the focus shift toward multidisciplinary research. DMPP Iodide, once planted firmly within neuropharmacology, now appears in projects exploring molecular recognition, biomimetic systems, and even some bioelectronic applications. As new uses come to light, we stand ready to adapt production and quality monitoring strategies, ensuring that each unique application can build on solid and predictable starting material.
The essence of reliable chemical supply lies within daily diligence—attention to raw material quality, vigilant in-process monitoring, unflagging batch documentation, and an honest willingness to admit and fix problems. DMPP Iodide production taught us that expectations are always rising, and success follows the pace of process improvement as much as demand. No single lot moves without sign-off from technical operators and quality leads, and raw honesty about yield or process deviation pays off in returns—better trust and stronger, longer-standing partnerships.
Our advice to both industry partners and research groups is the same: always seek clarity about your compound’s origins, analytical data, and batch reproducibility. Only through sustained engagement between manufacturer and end-user can new scientific ventures proceed with confidence, and only by sharing the technical story do we push toward higher standards each production cycle. DMPP Iodide stands as just one example of what close collaboration between practical chemistry and applied science can accomplish.