| HS Code | 333288 |
| Chemicalname | 1,2-Dimyristoyl-sn-glycero-3-phosphocholine |
| Abbreviation | DMPC |
| Molecularformula | C36H72NO8P |
| Molecularweight | 677.93 g/mol |
| Casnumber | 18194-24-6 |
| Synonyms | Dimyristoylphosphatidylcholine |
| Appearance | White powder or solid |
| Meltingpoint | 23-24°C |
| Solubility | Soluble in chloroform and methanol |
| Storagetemperature | -20°C |
| Application | Membrane studies, liposome preparation |
| Purity | Typically >99% |
| Lipidcategory | Phosphatidylcholine (PC) |
| Chirality | sn-Glycero backbone |
| Iupacname | 2-(dimyristoylphosphoryl)oxy-3-(trimethylammonio)propyl ester |
As an accredited 1,2-Dimyristoyl-sn-glycero-3-phosphocholine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass vial containing 100 mg of 1,2-Dimyristoyl-sn-glycero-3-phosphocholine, clearly labeled with product details and safety warnings. |
| Shipping | 1,2-Dimyristoyl-sn-glycero-3-phosphocholine is typically shipped at a temperature of -20°C to ensure stability and prevent degradation. The product is securely packaged in sealed containers, with insulated packaging and dry ice or ice packs, following standard chemical safety and transport regulations for sensitive, non-hazardous biological reagents. |
| Storage | 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) should be stored as a dry powder at –20°C, protected from light and moisture. When dissolved, use appropriate solvents and store aliquots under inert gas, such as nitrogen or argon, at –20°C to prevent oxidation and hydrolysis. Always keep the container tightly closed and return unused powder immediately to cold storage. |
1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) finds specialized use across biotechnology, pharmaceutical manufacturing, and analytical research. As an experienced industrial manufacturer, we deliver DMPC that meets precise standards for downstream processes. The material supports complex applications in lipid-based formulations, diagnostic research, and advanced drug delivery development. Below are key application scenarios with detailed technical insight.
DMPC serves as a primary phospholipid in the assembly of liposomal vesicles for controlled drug delivery systems. Process engineers combine DMPC with cholesterol and PEGylated lipids to achieve tailored encapsulation efficiency for both small molecule and biopharmaceutical actives. Formulators emphasize stoichiometric balance and phase transition characteristics to produce liposomes with stable bilayer morphology and specified release profiles. Knowledge of DMPC's thermotropic properties directly impacts particle size, lamellarity, and cargo retention during downstream production.
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Specialized research facilities depend on DMPC to reconstitute membrane proteins into lipid bilayers that mimic cellular environments for NMR and X-ray crystallography studies. DMPC's short acyl chains allow for formation of small, well-defined bicelles or vesicles that support native folding and function of integral membrane proteins. Carefully controlled lipid to protein ratios and buffer conditions enable high fidelity in biophysical assessments and high-resolution structure determination.
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Analytical laboratories use DMPC to formulate unilamellar or multilamellar vesicles as reference standards in DSC, ITC, and permeability experiments. Controlled vesicle size and lamellarity provide reproducible thermal transition benchmarks and membrane permeability profiles. The precise transition temperature of DMPC vesicles, along with their well-defined bilayer structure, supports accurate calibration for thermal and transport studies in pharmaceutical research and material science.
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Specialty vaccine manufacturers incorporate DMPC as a functional lipid in nanoparticle adjuvant systems to modulate immune response and antigen uptake. DMPC participates in structuring uniform, biocompatible lipid nanoparticles in combination with synthetic phospholipids and immunostimulatory moieties. Optimized processing ensures particle stabilization and storage stability, while attention to lipid purity and analysis underpins batch reproducibility for clinical and commercial vaccines.
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Cosmetics manufacturers utilize DMPC as a skin-mimetic lipid in encapsulated delivery systems for active ingredient stabilization and controlled release. Formulators deploy DMPC within multi-lamellar vesicles, liposomes, or niosomal structures to protect sensitive actives from oxidation and enhance dermal penetration. The selection of DMPC's specific phase transition improves shelf-life and product aesthetics, aligning with strict regulatory and purity requirements in the personal care sector.
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Competitive 1,2-Dimyristoyl-sn-glycero-3-phosphocholine prices that fit your budget—flexible terms and customized quotes for every order.
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Producing 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) in our facility is a blend of refined skill and dedication to the standards researchers rely on for consistent results. This phospholipid has anchored itself as a staple in both academic labs and commercial biotech space because of its repeatable behavior and compatibility in lipid model systems. Most of the requests we receive come from groups who recognize phosphatidylcholines as fundamental building blocks, but demand the purity, traceability, and physical properties that only originate from strong process control.
There is no room for compromise in certain lines of research, especially as the industry pushes further into structural biology, membrane protein studies, and liposomal drug formulation. Our batches of DMPC are upgraded specifically for sensitive analytical applications: high-pressure liquid chromatography, nuclear magnetic resonance, dynamic light scattering, and electron microscopy. For each production run, our teams track moisture content, polymorphic purity, acyl chain homogeneity, and ensure low peroxide values.
Small changes in raw material quality can change lipid hydration and lamellar phase transitions. Direct experience has shown that even subtle impurities in the sn-glycero backbone or uneven chain lengths will wreck the delicate balance needed for reliable vesicle formation or protein insertion. Every batch is subject to thin-layer chromatography and phosphorus quantification before shipping -- habits that prevent costly project delays for the research teams using it.
The 14-carbon myristoyl chains of DMPC play a practical role beyond just fulfilling the textbook lipid bilayer recipe. Research focused on bilayer dynamics often chooses DMPC because its thermal transition temperature (Tm) – just under room temperature – fits experimental protocols that need rapid-switching between gel and liquid crystalline phases. We know development teams who calibrate calorimetry instruments precisely on DMPC because its phase behavior is so reproducible batch to batch.
Other lipids like DPPC (16:0) or DSPC (18:0) shift Tm higher, which complicates measurements and limits compatibility with temperature-sensitive molecules. In contrast, natural source lecithins and egg-PC products include a mixed bag of acyl chains, and that inconsistency often distorts results where sharp phase behavior or predictable vesicle leakage is core to the experiment. Fixed chain length from fully synthetic DMPC guarantees control over membrane thickness, surface charge, and hydration forces — all elements that underpin trustworthy kinetic or permeability data.
Pharmaceutical scientists asked us for DMPC with well-defined physical and chemical properties so they could standardize liposomal formulations. Pure DMPC vesicles offer a near-ideal starting surface for adding cholesterol, PEG-lipids, or targeting moieties. In encapsulation work, we have seen clear shifts in solute leakage, bilayer permeability, and colloidal stability based on how stringently the DMPC is purified. High-quality DMPC gives sharper size distributions after extrusion and lowers batch-to-batch variability that can otherwise force repeat reformulation.
In clinical and preclinical development, formulators must hit tight reproducibility targets. They convert powdered DMPC into lamellar vesicles or multilamellar liposomes on demand. Without uniform fatty acid chains or precise head group stereochemistry, the results drift. In our own history, clients flagged inexplicable jumps in drug release rates only to trace it back to inconsistent feedstocks from resellers using distillation blends or animal extracts. Our in-house process gives customers a material with both certificate traceability and the documented reproducibility essential for regulatory filings.
Some think all phosphatidylcholines can swap places due to their shared backbone or head group, but our experience producing DMPC proves otherwise. Where DMPC shines is in the narrow gap between its physical chemistry and the reproducibility of the data produced with it. Chain length, synthetic versus natural source, and the identity of stereoisomers matter. In some peer-reviewed studies, side-by-side comparisons show DMPC producing sharper transitions in differential scanning calorimetry than mixed-chain lecithins.
Fatty acid chain composition impacts membrane packing, permeability, and protein reconstitution success rates. The single-molecule purity that comes from a synthetic route — as opposed to semi-synthetic egg or soy lecithins — translates into cleaner, more interpretable NMR spectra, sharper melting transitions, and more predictable surfactant properties in self-assembly. Over years of manufacturing, we've refined protocols so each kilo of DMPC leaves the line with consistent hydration capacity and vesicle-forming reliability, because minor chain-length contamination (even one carbon out of place) can throw major experiments into disarray.
On paper, many phosphatidylcholines look similar due to structural motifs. In practical laboratory and scale-up settings, these differences emerge quickly. For example, cell-free membrane protein studies tend to favor DMPC to reconstitute functional proteins, because its transition temperature lets users test function at various physiologically relevant states. Using DPPC, the system runs hotter, risking protein denaturation or conformational artifacts.
We’ve fielded calls from researchers switching from natural PC extracts to DMPC, noticing tighter control over vesicle leakiness, liposome drug retention, and protein-lipid binding reproducibility. Synthetic lipids deliver unmatched control, while animal-sourced alternatives can shift composition from batch to batch, sometimes introducing cholesterol or polyunsaturated chains at unpredictable levels. That throws off calorimetry, vesicle fusion, or encapsulation efficiency and leads to wasted effort trying to pin down variables that DMPC sidesteps.
Downstream users working in areas like pulmonary surfactants or artificial cell systems lean heavily on DMPC’s clean phase transitions and clear interpretation in biophysical measurements. In our plant, purity upgrades target this core customer base. For those blending custom lipid mixtures or optimizing drug carrier liposomes, having a guaranteed baseline from DMPC lowers troubleshooting, supports automation, and speeds up regulatory documentation.
DMPC synthesis exposes technical limits in both chemistry and processing scale. Glycerol backbone derivatization, chain attachment, and head group introduction all invite non-ideal products if not managed under tightly watched temperature and reagent controls. During earlier manufacturing days, we observed acyl migration and unwanted byproducts when reaction times or purification parameters shifted, even slightly.
Top-quality DMPC relies on full chain-of-custody for all precursors, including verification of fatty acid length and purity before the esterification step. Our quality teams use mass spectrometry and high-resolution NMR for every synthesized lot. This verifies retention of stereochemistry and screens for contaminants such as partial acyl chains, oxidized products, or head-group methylation byproducts. Production yields rise, and waste falls, by mapping small details – not just the global picture.
Water activity and storage conditions have direct consequences. DMPC powders are hygroscopic, easily absorbing ambient moisture that can promote hydrolysis or affect vesicle formulation. By controlling environmental humidity throughout packing and storage, the material keeps its powdered state, so users consistently hydrate and form vesicles without surprises in turbidity or viscosity.
Maintaining batch-to-batch uniformity only comes from experience and investment in in-line analytical tools. Our operators monitor every crystallization and filtration step: colorimetric phosphorus assays, visual clarity, powder flow tests. These tangible, real-world adaptations reflect lessons learned after years of fielding customer queries or supporting troubleshooting during sensitive experiments.
Academic biochemistry and biophysics labs use DMPC in fundamental research. Whether studying protein-lipid interactions, the molecular basis of membrane permeability, or the mechanisms of vesicle fusion and fission, scientists need single-variable controls — synthetic DMPC supplies this. Having worked alongside academic partners, we see frustrations disappear and analysis timelines speed up as soon as the material removes batch-based variables.
Synthetic routes guarantee chain length and headgroup stereochemistry, offering confidence in calorimetric measurements, dual polarization interferometry, and spectrophotometric kinetics. That makes comparison across different labs feasible, and allows meta-analyses of published data. Our own support team is in constant contact for troubleshooting how DMPC performs in different biochemical setups — from solubilizing hydrophobic small molecules, to supporting membrane protein folding, to forming nanodiscs with membrane scaffold proteins.
Collaborations with industrial R&D groups often expand beyond making the base molecule. In some projects, chemists look for DMPC derivatives: fluorescently labeled, biotinylated, or stabilized against oxidation for high-throughput screens. The high-quality baseline we maintain means these modifications start from a clean substrate, simplifying route planning and minimizing purification overhead. For rapid-scaling biotechs, the ability to order in both gram and kilogram quantities — with identical specifications — has become a core part of their pipeline planning.
Modern manufacturing doesn’t just focus on process yield or material cost. DMPC and other phospholipids fall under scrutiny as regulatory agencies and customers expect safe handling, full composition disclosure, and tight environmental controls. Our plant went zero-waste-to-landfill more than two years ago, driven by both regulatory policy and market preference.
Raw material traceability and allergen controls are simple on paper, but the actual challenge comes in segregating lines and preventing cross-contamination in facilities also producing other phospholipids. Mastering this complexity keeps batch approvals on time and eliminates downstream issues for clients tagging drugs for regulatory filings. Being able to provide full analytical dossiers for every lot supports both preclinical and GMP customers, while our open audit policy lets users verify every point in the supply chain.
Packaging and logistics also play a role — as material moves from synthesis, through QC, into the warehouse, and then onward to climate-controlled shipment. The DMPC leaving the dock is protected against temperature swings, light exposure, and moisture contact, so that it generates the same results on a customer’s bench as it did during our final QC.
As more clients work in pharmaceuticals or therapeutic development, we’ve invested further in documentation, chain-of-custody inventory, and sustainability metrics, all reported straight to purchasing and regulatory groups. Sustainable DMPC sourcing and verifiable green chemistry approaches continue driving our investment roadmap, making sure the product stays reliable and future-proofed against both new market demands and evolving policy frameworks.
Year after year, scientists bring us puzzles that only show up with deeply characterized, high-purity DMPC. One research team investigating fusion proteins needed DMPC with ultra-low oxidation for subtle fluorescence quenching experiments. Close coordination between process chemists, QC, and the customer’s technical leads led us to engineer additional oxygen-removal steps and perform periodic peroxide checks beyond standard protocol. That resulted in more reliable, background-free measurements on their end.
We’ve also collaborated with groups needing non-traditional packaging or rapid-deployment shipments as field conditions changed, reflecting the difference between large-scale commodity chemical production and a real partnership with the scientific community. These experiences feed back into our regular operations, so even standard customers benefit from a supply chain that’s tuned for both innovation and predictability.
Producing DMPC goes beyond mixing chemical components. Every progressive improvement in purity, batch consistency, and process flexibility traces back to problems solved for researchers, R&D teams, and manufacturers in drug development and diagnostics. Technical staff train to recognize batch-to-batch subtleties, troubleshoot surface activity anomalies, and adapt new purification techniques based on feedback from the exact users relying on the material for their discoveries.
As synthetic techniques and automation improve, the gap between bespoke manufactured DMPC and natural product alternatives continues to widen. Labs looking to minimize background variables and accelerate product development now choose synthetic DMPC not only for its traceable composition but as a foundation for building more complex lipid mixtures or functionalized vesicles.
Our journey producing DMPC has taught us the critical value of transparency, technical partnership, and relentless process refinement. This ensures every vial or drum of DMPC supports the full spectrum of cutting-edge scientific work — from single-molecule membrane studies up to scalable, regulated pharmaceutical formulations. From the factory floor to the research bench, the practical value of well-manufactured DMPC shows up in every reproducible experiment, every successful formulation, and every innovation in lipid science.