| HS Code | 573516 |
| Product Name | Azelaic Acid, Encapsulated Azelaic Acid, Ultrafine Azelaic Acid |
| Cas Number | 123-99-9 |
| Appearance | White to off-white powder |
| Purity | ≥99% |
| Molecular Formula | C9H16O4 |
| Molecular Weight | 188.22 g/mol |
| Solubility | Slightly soluble in water, soluble in alcohols |
| Ph Range | 4.5 - 6.5 (10% aqueous suspension) |
| Particle Size | <10 microns (Ultrafine grade) |
| Storage Conditions | Store in a cool, dry place, tightly sealed |
| Usage | Topical skincare ingredient for acne and hyperpigmentation |
| Encapsulation Material | Lipid-based or polymer-based carrier |
| Stability | Stable under recommended storage conditions |
| Odor | Slight characteristic odor |
| Melting Point | 105-112°C |
As an accredited Azelaic Acid, Encapsulated Azelaic Acid, Ultrafine Azelaic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White opaque HDPE bottle, sealed with a secure screw cap, labeled for 100g content, featuring hazard and handling instructions. |
| Shipping | Azelaic Acid, Encapsulated Azelaic Acid, and Ultrafine Azelaic Acid are securely packed in airtight, chemical-resistant containers, protected against moisture, heat, and light. Shipping is handled by certified carriers, with all regulatory and safety documentation included, ensuring compliance with local and international transportation requirements for chemical substances. |
| Storage | Azelaic Acid, Encapsulated Azelaic Acid, and Ultrafine Azelaic Acid should be stored in tightly sealed containers, away from moisture and direct sunlight, at a cool temperature (15-25°C). Avoid exposure to heat and incompatible substances. Keep containers in a well-ventilated area, away from sources of ignition, and follow manufacturer-specific guidelines for stability and shelf life. |
Our production of Azelaic Acid and its specialized forms—Encapsulated Azelaic Acid and Ultrafine Azelaic Acid—is designed for precise integration into modern industrial workflows. By focusing on established downstream manufacturing sectors, we deliver material quality and consistency that meet stringent quality controls and regulatory benchmarks worldwide. Below are detailed industrial scenarios where these chemistries support process efficiency, compliance, and product value.
Dermocosmetic manufacturers incorporate ultrafine and encapsulated forms to maximize active loading in high-performance facial creams and serums targeting skin clarity, tone regulation, and acne. Encapsulation techniques enable ingredient stability and gradual release in the end product, while micronized variants ensure homogeneous dispersal at the lab-to-production scale. Compliance with globally harmonized cosmetic requirements calls for rigorous stability, purity, and release profile verification during both pilot and full-scale production. In manufacturing, azelaic acid enters during the emulsion or dispersion blending stage after all water- and oil-phase actives have been solubilized, supporting both O/W and W/O chassis for category-specific products.
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Industrial-scale pharmaceutical gel and cream production lines rely on azelaic acid grades conforming to pharmacopeial monographs for acne, rosacea, and pigmentation disorders. Downstream pharmaceutical processors require high purity and particle control to meet regulatory release consistency and therapeutic effectiveness. Encapsulated variants reduce irritation potential and extend shelf stability, critical for batch manufacturing at ambient or low-temperature mixing stages. Pharmacologically active concentrations demand precise solvent system selection and validated homogenization parameters to achieve optimal viscosity and extended release within hydrogel matrices.
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Personal care manufacturers deploy both ultrafine and encapsulated grades as targeted actives in odor-neutralizing deodorant and leave-on body formulations. These materials exhibit selective bacteriostatic activity against skin flora, helping reduce malodor generation without resorting to heavy metals or formaldehyde donors. Process engineers incorporate azelaic acid at the emulsification or fragrance addition stage, balancing loading levels for antimicrobial performance with in-use skin safety. Quality control departments test final products for stability and prolonged functional activity under real-use temperature and humidity exposures.
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Manufacturers in the polymer sector employ azelaic acid as a key dicarboxylic monomer in high-performance polyamide (nylon) and polyester polyol synthesis. Its use helps impart flexibility, improved cold resistance, and hydrolytic stability to engineering plastics and specialty hot-melt adhesives. In production workflows, azelaic acid combines with diamines or diols during controlled melt polycondensation reactions, where consistent molecular weight distribution and low residual color are critical. Downstream QC teams analyze residual monomer content and mechanical property targets to meet both internal and customer-specific performance specifications.
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Metalworking fluid producers utilize azelaic acid as a biodegradable base component in water-soluble lubricants and semi-synthetic cutting fluids. Its dicarboxylic structure contributes to enhanced corrosion inhibition for ferrous and non-ferrous alloys while offering stable emulsion formation. Typical blending operations introduce the acid at the neutralization or co-emulsification stage, often as salt derivatives, enabling compatibility with extreme-pressure additives. Process controls assess emulsion stability, pH maintenance, and anti-corrosion efficiency under simulated use conditions in machining and grinding systems.
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Producers of specialty plasticizers utilize azelaic acid as a starting material for dialkyl azelates and branched ester plasticizers designed for PVC and certain medical device polymers. The resulting esters impart low migration, enhanced flexibility, and improved low-temperature performance in both rigid and flexible vinyl formulations. Batch esterification and downstream purification dictates precise acid-to-alcohol feeding, real-time monitoring for conversion, and advanced vacuum technology for residual monomer removal. Product application specialists set concentration according to final PVC article properties and regulatory migration requirements.
Industry compliance standards
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Competitive Azelaic Acid, Encapsulated Azelaic Acid, Ultrafine Azelaic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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We have spent years working with azelaic acid—observing its physical nature, managing every step of purification, and understanding exactly how its particles behave in different processing methods. Our team stands on actual plant floors, so every batch carries that mark of real-world know-how. Azelaic acid stands out because it doesn’t just fill a slot on a formulation sheet; it solves problems—from persistent skin conditions in dermal applications to niche chemical syntheses in industrial labs. Formulated right, this straightforward dicarboxylic acid offers a clean, reliable backbone for creams, chemical reactions, and polymer blends.
We once focused solely on standard azelaic acid. Breaking the material into ultrafine grades involved deep research—repeated milling, particle classification, tight control of humidity and temperature. Our shift toward ultrafine azelaic acid wasn’t just scientific curiosity. In cosmetics and personal care, clumpy textures or gritty sensations signal product failure. Ultrafine grades flow better, blend seamlessly, and boost absorption in topical products. Encapsulation raised engineering challenges: selecting shell materials, setting release rates, confirming no unwanted reactions. Encapsulated azelaic acid now allows us to offer slow-release benefits, reduced irritation, and extended shelf life. These advances moved us past bulk raw materials and toward precision-engineered ingredients.
Our standard azelaic acid usually arrives in pure white crystalline powder. Years of repeated analysis have refined our confidence in delivering consistent assay values (range generally exceeding 99%). Through regular titration and chromatography, we confirm minimal residual solvents and trace metals. For the ultrafine version, strict sieving and advanced milling technologies produce particle sizes often less than 10 microns. We monitor distribution curves on every lot, not just a spot check—slight shifts alert us to calibration drift or process wear. For encapsulated azelaic acid, particle dimensions fall in the range suited for final formulation—often in the 20–50 micron window—balancing smooth feel with steady release time. Every model reflects years of precision, trial, and feedback from real formulation labs.
Handling azelaic acid on a production scale comes with surprises. Its hygroscopic nature demands sealed storage, especially in humid regions. Sometimes clients run into clumping; we know how milling conditions or tiny temperature drops in transit can set off caking. Ultra-fine powder—though prized for blending—brings increased dust and static. Our team switches up protective gear protocols to keep operations and people safe. Plant-scale encapsulation of azelaic acid uncovered another lesson: uniform coating depends on precise agitation rates and careful solvent evaporation, not just a standardized recipe. These aren’t textbook concerns, but hands-on truths that matter once tons—not grams—are in play.
Cosmetics formulators often share stories about the irritation risk with direct azelaic acid application. We’ve spent years testing and mapping correlations—particle size, shell thickness, pH stability—so every batch of encapsulated azelaic acid delivers consistent results. Encapsulation shields active molecules during storage, lands gently on the skin, and allows gradual, targeted release. Consumer tolerance improves, handling becomes less tricky, and users enjoy less risk of burning or redness. In addition, encapsulated forms withstand hot-fill and thermal cycling seen in automated creams production. This flexibility means less wastage, longer shelf life, and more predictable outcomes.
Formulators often debate whether to select standard or ultrafine azelaic acid. Our lab teams regularly run split-batch trials—testing standard crystalline powder versus ultrafine micronized samples in otherwise identical emulsions or gels. What emerges? Ultrafine grades disperse faster, integrate without visible grit, and show improved physical appearance in finished products. In pigment-sensitive applications, such as skin-lightening creams, ultrafine azelaic acid assures inertness and less streaking. The trade-off includes greater dust risk in processing and higher filtration requirements, but production teams adapt by adjusting ventilation and dust collection systems. Standard grades maintain their role where slow dissolution or bulk chemical synthesis are priorities—here, cost and simplicity remain strong arguments.
Encapsulated azelaic acid sets itself apart in stability tests and irritation mitigation. Guided by repeated customer feedback and in-house dermatological patch studies, we understand encapsulation reduces peak acid exposure on skin. Our pilot lines proved that encapsulated azelaic acid outperforms unmodified powder in heated filling and long-haul transport. Formulations maintain expected viscosity, actives haven’t shifted, finished goods return fewer complaints. As shelf life expectations stretch, companies count on encapsulation to keep actives potent across regions—dry, humid, or variable. Innovation in our plant focuses on new shell materials, aiming to further minimize allergen risk or offer “green” label claims. Encapsulation isn’t gimmickry; it reflects ongoing engineering and real market demand.
Azelaic acid has found loyal users in dermatology. Acne and rosacea products frequently call for it. From the plant floor, our teams know even minor impurities or particle agglomerates alter customer perception or trigger quality returns. Dermatology requires not just the correct molecule, but repeatable, predictable performance—consistency at each scaleup, each shipment. Encapsulated azelaic acid has changed possibilities for brands aiming to promise “gentle” or “gradual” results. Our ultrafine grades allow for transparent gels and smooth lotions that perform without feeling sandy or leaving residues. Companies developing new treatments trust manufacturing partners with deep lot-to-lot controls, so their claims meet clinical reality.
On our site, sustainability isn’t theoretical. The acid itself emerges from processes with a renewable content—vegetable oils supply the backbone for many runs. Years ago, we moved to closed-loop water and solvent recycling. Waste reduction became a talking point long before regulation caught up. For encapsulated azelaic acid, our chemists trimmed off-shell solvent use and sourced biodegradable or non-irritant encapsulation polymers. Hazard reduction drives plant upgrades, not just compliance. We also design production to minimize dust and ambient acid vapors, reducing risk for both employees and surrounding communities. Every improvement folds back into cleaner, safer, and more sustainable azelaic acid lines.
Propagating consistent quality over months and years means taming batch variability. Raw material specifications shift; climate and seasons alter processing outcomes—our team tracks yield and purity by hour and day, not just batch total. Unexpected shifts in ambient temperature or humidity can subtly alter acid crystallization or flow characteristics. Over time, our response includes revised handling, intermediate storage tweaks, and operator retraining. Analytical teams troubleshoot every lot—stray particles or off-target pH pull our focus. Working with encapsulated grades introduces challenges in releasing actives predictably at scale. Only ongoing analysis and feedback—direct from brand formulators, contract manufacturers, and clinical teams—keep us honest and on-guard for drift.
We engage with formulation teams early. Some focus on creams, others on serums, foams, or infrastructure chemicals. Each application draws out different qualities from azelaic acid: a gel needs particle fineness, while a mask can allow coarser grains. Discussion often moves beyond technical sheets—chemists share insights on preservative interactions, viscosity troubles, or blending quirks. We’ve tested scores of stabilizers, surfactants, and emulsifiers to eliminate separation or pH instability with both bulk and pre-encapsulated grades. Our role doesn’t end at shipping: we help adapt manufacture to match pilot scale “show” samples. Supporting brands in compliance, labeling, and claims verification gives us a unique view of market shifts and real customer success.
Data-driven manufacturing matters for azelaic acid. On our lines, each batch receives close scrutiny: melting point, assay, particle size range, free acid content, and water. Unpackaged powder is tested for tone, odor, and tactile feel. With ultrafine and encapsulated grades, flowability and dust propensity require adjusted in-line controls. Encapsulated lots require both mechanical property checks and release-time studies in real emulsions. We track customer feedback on each lot—smoothness in creams, plug-free pump performance, and no visible sediment in clear gels. These performance markers do not emerge from “routine” work; they reflect daily vigilance, adaptation, and pride in results.
Formulators tell us azelaic acid’s role often depends on the final product’s claims and user experience. A transparent serum prioritizes complete dissolution—ultrafine acid enables this. A leave-on night cream may use encapsulated forms to layer actives for long-term exposure. In anti-acne blends, azelaic acid partners with niacinamide or salicylic acid, but only if no cross-reactions appear in testing. Learning from final users—dermatologists and skincare brands—forces us to chase even lower impurity profiles. Brand return rates, texture complaints, or unexpected changes in finished product color all drive us back to revise production protocols. Feedback loops close only when both manufacturer and user commit to joint improvement.
We engage directly with evolving regulations. Past years have seen demand for lower heavy metals, trace solvents, and allergen declarations. Our internal audits reached beyond mandated targets, so our products meet and often exceed key standards: REACH, EU Cosmetic Regulation, and regional FDA equivalents. We control supply chain quality at input, not just output. For encapsulation, all shell materials receive toxicological review, supporting safety dossiers as brands approach global launches. Documentation isn’t paperwork; it shields our partners, proving that azelaic acid—from basic to encapsulated—arrives fully prepared for registration and consumer scrutiny.
Our motivation doesn’t rest on current product lines. Lab teams iterate on faster, more energy-efficient synthesis. Chemists develop lower-residue washing steps, exploring greener, single-use solvents. Recent partnerships with university research labs probe ways to further shrink particle size or enable intelligent encapsulation—linked to pH, temperature, or user-triggered release. Ongoing improvements target not just the primary molecule, but also the environmental and sensory impact of each grade. Rapid adoption of encapsulated azelaic acid signals how innovation flourishes at the intersection of manufacturing, research, and formulation.
Many firms offer azelaic acid, but few manufacture and oversee every stage—from incoming vegetable oil through to high-purity acid, ultrafine grades, and encapsulated innovations. This hands-on approach has fostered expertise in troubleshooting, adapting, and delivering feedback-driven product improvements. Recognizing the limits of technical sheets, our team provides in-person and remote troubleshooting services for clients at every manufacturing stage. By maintaining deep production oversight and control, we know each grade of our azelaic acid delivers not just on purity and performance, but also reliability and responsiveness in the face of formulation or regulatory change.
Demand continues to evolve. Brands seek green chemistry, gentler skin application, and demonstrable efficacy in actives. Bulk buyers watch price and supply chain stability; niche formulators press for precise delivery and minimal regulatory risk. We invest in backward integration—controlling upstream input volatility—and seek renewable feedstock options. Pilot plants run test batches on new encapsulation media, researching next-generation performance. As ingredient suppliers and true manufacturers, we help set—not just follow—the pace of change. Our azelaic acid portfolio is more than a set of specifications; it reflects lived experience, adaptive improvement, and real collaboration with users across industries.
Years of azelaic acid production have taught us that behind every specification stands a network of decisions, tests, and direct feedback from the field. Ultrafine azelaic acid and encapsulated grades represent more than new products; they reflect persistent engineering, quality demands, and the ongoing needs of cosmetic, dermatology, and specialty chemical industries. Reliability, adaptability, and openness to feedback drive us—connecting factory floor realities with end-user requirements. We remain committed to shaping the future of azelaic acid, supporting formulators in making safe, effective, and innovative products for the world.