|
HS Code |
158374 |
| Product Name | Ursolic Acid Sodium |
| Chemical Formula | C30H47NaO3 |
| Molecular Weight | 478.68 g/mol |
| Appearance | White to off-white powder |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Cas Number | 6199-67-3 |
| Storage Conditions | Store in a cool, dry place |
| Melting Point | 285-288°C |
| Ph Value | Neutral to slightly alkaline in solution |
| Stability | Stable under recommended storage conditions |
| Odour | Odourless |
| Synonym | Ursolate sodium |
| Usage | Pharmaceutical and cosmetic applications |
| Source | Derived from natural plant sources |
As an accredited Ursolic Acid Sodium factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ursolic Acid Sodium is packaged in a sealed, opaque 100g HDPE bottle, clearly labeled with product name, batch number, and handling instructions. |
| Shipping | Ursolic Acid Sodium is securely packaged in airtight, moisture-resistant containers to maintain stability during transit. It is shipped as a non-hazardous chemical under standard chemical shipping regulations. Protective labeling and documentation accompany the shipment, ensuring safe handling and compliance with international transport guidelines for laboratory and industrial use. |
| Storage | Ursolic Acid Sodium should be stored in a tightly sealed container, away from moisture and direct sunlight. It is best kept in a cool, dry, and well-ventilated area, ideally at room temperature (20–25°C). Protect from sources of heat and incompatible substances. Proper storage ensures product stability and maintains its chemical integrity for laboratory or industrial use. |
| Purity 98%: Ursolic Acid Sodium with purity 98% is used in pharmaceutical formulations, where it ensures high bioactive content for enhanced therapeutic efficacy. Particle Size D90 <10 μm: Ursolic Acid Sodium with particle size D90 <10 μm is used in topical dermatological creams, where it promotes rapid and uniform skin absorption. Solubility >50 mg/mL (water): Ursolic Acid Sodium with solubility greater than 50 mg/mL (water) is used in injectable solutions, where it provides optimal dosing flexibility and bioavailability. Stability Temperature up to 80°C: Ursolic Acid Sodium with stability temperature up to 80°C is used in heat-processed nutraceutical blends, where it maintains structural integrity during production. Molecular Weight 490.7 g/mol: Ursolic Acid Sodium with molecular weight 490.7 g/mol is used in analytical reference standards, where it allows precise quantification and reproducibility in assays. Assay ≥99% (HPLC): Ursolic Acid Sodium with assay ≥99% (HPLC) is used in clinical research studies, where it guarantees accuracy and reliability for pharmacological investigations. pH Stability Range 3-8: Ursolic Acid Sodium with pH stability range 3-8 is used in liquid dietary supplements, where it ensures chemical stability across various formulations. Melting Point 217-220°C: Ursolic Acid Sodium with melting point 217-220°C is used in solid dispersion systems, where it supports consistent melting behavior during processing. Bulk Density 0.5 g/cm³: Ursolic Acid Sodium with bulk density 0.5 g/cm³ is used in tablet manufacturing, where it enhances powder flow and compaction properties. Residual Solvent <0.5%: Ursolic Acid Sodium with residual solvent less than 0.5% is used in food-grade applications, where it meets regulatory safety standards for consumer health. |
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From deep within our reactors to the moment each drum leaves the filling line, Ursulic Acid Sodium passes through hands that know the ins and outs of plant chemistry. Over the years, this compound has moved far past niche discussions, finding its way into mainstream applications across pharmaceuticals, cosmetics, and research-driven nutrition. We’ve worked through its quirks and production challenges not from behind an office desk, but from up close, tracking every batch as it wears the actual fingerprints of our team.
Ursulic acid forms naturally in herbs like rosemary and apple peels, best known for its shiny, waxy presence. Industry mainly knows it for anti-inflammatory and antioxidant uses, a big reason research groups keep it in focus. In the pure compound, its low water solubility sets up the main hurdle: how to get ursonic properties into a workable ingredient? Ursolic Acid Sodium opens new options. By modifying ursolic acid with sodium, we move from a stubborn, sticky powder into a fine, off-white granular material that blends well in water-based formulations.
We start with natural triterpene sources, but a long chain of extraction ensures consistency. Steam stripping, solvent extraction, and precise crystallization anchor the process. The real magic happens during sodium salt formation. We monitor temperature and pH with care, because a sliver outside optimum leads to impurity build-up or inefficient conversion.
Each stage links back to the source. Whether we use rosemary leaves or apple peels, plant age and season affect the initial content. Over the past decade, we’ve documented these seasonal swings and built adjustment steps into our batch records. The change to sodium, a process chemists call saponification, changes not only solubility but also handling. Before this tweak, ursolic acid would cling to glass, layer awkwardly, and sometimes even resist full mixing in granulators. That means more plant downtime and more filter changes.
As a sodium salt, our final product, coded internally as 'UA-Na 98', runs at a minimum of 98% content by HPLC, with moisture below 2% and sodium content confirmed by ICP-OES. We run additional impurity profiling since some customers develop sensitive formulations. Removing traces of solvents and keeping heavy metals low builds trust batch after batch. Stability samples run on real warehouse shelves—nobody wants a white powder that browns or cakes up after a month in a hot truck.
Ask an R&D manager to swap between these forms and you’ll hear about more than purity metrics. In practice, standard ursolic acid works for oil-based creams and slow-dissolving tablets, places where water solubility matters less. The sodium salt, on the other hand, works better for liquid systems—injectables, water-based gels, microemulsions, or beadlet pre-mixes. Some cosmetic groups insist on sodium salt for clear serums where any cloudiness ruins the final effect.
From a processing angle, this translates into easier weighing, less static stickiness, and cleaner tank washes. No more scraping the last ten grams from mixing blades. In nutraceuticals, the ability to dissolve directly in water means more flexibility for drinks, syrups, or oral thin films. If the final dose needs transparent liquids, only the sodium form works—there’s no shortcut using the base compound.
Solubility in water rises from less than 0.01%—practically unusable for many purposes—to well over 5% in the sodium salt. Analytical chemists appreciate this, since HPLC sample prep no longer involves harsh solvents or sonication steps. This cuts down on running costs and waste container volumes, a detail few outsiders appreciate until they stand by the waste disposal tank.
Ensuring consistent content and purity doesn’t just tick regulatory boxes. We’ve pulled dozens of historical COAs to learn that even a 1% moisture spike changes compressibility and shelf-life. For markets in northern climates, water pickup can mean caked product by spring. Our plant leans on walk-in dehumidifiers, closed conveyors, and a double-layer bag policy in every drum, because several years ago we saw a shipment rejected for visible clumping. Every problem like that becomes a new SOP written in real language the plant team reads every day.
Our HPLC assays don’t just run at end product. In-line NIR monitoring now checks reaction end points for the sodiumization step, trimming sampling delays. This change shrank out-of-spec reactions within the first three months of use. Some clients ask for an extra run using LC-MS, and we oblige with a split sample held for six months—a kind of insurance that survives audit days.
Trace sodium and potential organic impurities follow the sample to archive. Not all impurity questions come from regulators; sometimes, our long-term clients want stability reports with real data points beyond the sixty-day norm. Even small changes like a 0.1% drop in active matter get flagged and explained in each batch certificate, because once a formulation drifts, nobody wants to hunt for root cause after the launch.
Any chemical manufacturer with years behind the monitor and mixer comes to respect local and international guidelines—not because of the threat of fines, but because a near-miss or minor incident leaves a lasting mark on a team. Ursolic Acid Sodium comes from natural origins, but sodium compounds bring their own handling quirks. We train everyone—forklift operator to QC chemist—not just in the basic PPE but in handling small-scale spills and avoiding accidental inhalation of fine powders. In the past, we shifted from open drums to sealed containers with one-way valves, lowering dust by 70% as measured in air monitors.
Disposal of process filtrates also gets its share of attention. Neutralization steps target both residual solvents and pH balance before anything reaches a wastewater tank. Neither regulators nor our neighbors take shortcuts lightly. A few years ago, increasing water solubility of the sodium form meant clarifying every single effluent pathway, so engineering and safety teams built new holding tanks and in-line sensors to chart every liter that leaves the sodiumization bay. Nothing gets signed off until it matches both the letter and spirit of local permits.
On logistics, water solubility again makes a difference. Any spill—on the loading dock or in transit—needs different clean-up protocols compared to clinging, greasy plant extracts. The sodium salt wipes up and neutralizes with less risk of staining or residue, and packaging teams have found this lowers turnaround time between campaigns.
Even end users see some of this attention: our batch labels carry the full solvent list and dry-down date for transparency. We’ve seen more requests for particulate- and allergen-free certifications, not only for food but also for topical products. Our plant now directs packaging air toward a constant HEPA zone, reserving the oldest production suite for batch quarantines if routine air tests catch any outside readings.
Over the past ten years, we’ve observed our sodium form branch from research-grade vials to production drums. Pharmaceutical companies outline how the sodium version dissolves in aqueous solutions for accurate dosing in trials. Formulation scientists highlight how it opens new shelf-stable possibilities in injectables compared to the raw form. In dermal applications, cosmetic chemists tell us they can combine it straight into gels and serums with no need for a secondary solubilizer. This cuts three steps, lowers batch cycle times, and simplifies cleaning validations—labor hours drop by a visible margin.
The dietary supplement world pulls from both sides. Traditional capsules and tablets use base ursolic acid for slow-release needs, but liquid suspensions and quick-dissolve products only succeed with the sodium modification. Marketing teams aim for label claims about origin and solubility; our documentation adds weight to these with actual assay results.
Some agricultural formulators use ursolic acid sodium in experiments for plant health, but this part of the market remains small and mostly in pilot phase. Nutraceutical manufacturers usually ask detailed questions: How does it flow? Can you run it through a standard auger filler or is bridge formation a risk? What's the dusting profile? We’ve gathered enough user data to confirm that UA-Na 98 outperforms traditional ursolic acid on both flow and static control, especially in high-speed lines. In our own plant, line workers swapped heavy sweepers for handheld vacuums—emphasizing the ease of daily handling.
From mid-size biotech companies comes an interesting point: easier dissolution in buffers means more productive analytical runs. One QC project manager told us every gram saved on sample waste pays back after a single production run. That kind of payback stays top of mind for every manufacturing manager watching the bottom line.
Every year, we receive requests from university labs and start-ups seeking a tweak: different grades, smaller lots, adjusted moisture content, or new analytical documentation. Our batch records go deep—down to raw lot origin and line operator signoffs—so we can grant one-off requests if the application warrants. Working with sodiumized ursolic acid means collaborating directly on formulation; it’s not always a drop-in replacement for natural ursolic acid. Sometimes a customer needs advice about pH compatibility, or about the effect of buffer salts.
We keep technical teams available not only for after-sale troubleshooting but for honest feedback—if an application in complex matrices won't benefit from the sodium form, we’ll state that up front. Years in production teach us that fewer surprises at launch save time, reputation, and material waste both for us and the downstream user.
Peer-reviewed papers drive much of our custom requests. When a prominent group publishes on ursolic acid sodium for metabolic health, suppliers know that inquiries will spike—not always from purchase-ready buyers, but from those charting early trial runs. We document every process tweak and caveat, keeping confidentiality for proprietary recipes but sharing practical insights on batch performance, color stability, and even shipping temperature impacts.
For users running stability assessments or small-scale GMP manufacturing, our plant sends matching control samples for every custom lot. This close cycle of feedback often yields better future lots for all customers—supplier and formulator learn together.
The sodium salt’s improved water attraction means that warehouse conditions matter more than with the neutral form. We keep all shipments in double polyethylene liners within tight-sealed fiber drums, stamped with desiccant charge dates. While it sounds like a detail from logistics, the choice of bag and drum got refined after multiple back-and-forth shipments—cases where other packaging led to stack lean, sieve breakages, and rejected pallets.
We understand that for countries with wider humidity swings, small leaks in packaging quickly lower final value, as apparent from feedback when we trialed thinner liners. Now, all drums pass a vacuum drop test before palletization. In summer transport, trailer temperatures often top critical storage recommendations. We track this with temperature loggers—an initiative sparked after a customer reported off-color product due to a four-day dock hold in peak heat. That data allowed us to redesign our delivery timetables and work with shippers who can guarantee climate-stable lanes.
None of these solutions came from textbooks; each patch-up, improvement, and new policy tracks back to real-world problems. Facility staff lead review of every rejected load—if a batch gets turned back by a customer, they walk through every step until a root-cause correction emerges. Drums showing stress or damage become case studies in packaging meetings; nothing changes more process behavior than the image of lost material from a single mishandled pallet.
Over the last few years, customer discussions have moved steadily toward green chemistry and renewable resources. We source botanical raw material directly from growers with documented regrowth cycles. Our extraction partners now build in traceability from field to drum, reporting pesticide use, harvest times, and drying cycles.
On site, solvent recycling has improved behind quiet investments in new distillation columns. Glycerin and light hydrocarbons recover at over 95% efficiency, compared to 60% a decade ago. This improvement shows itself both in disposal certifications and lowered raw material purchases—cost and waste lines drop together. Every year, local audits inspect compliance as much with a spirit of improvement as with a threat of penalty. When a process can’t meet the latest environmental rule, the change happens by consensus with regulators, not by shortcut.
We’ve seen interest rise for documentation about supply chain and residual solvent profiles—an issue that rarely figured in sales conversations ten years back. Now it forms part of every lot’s supporting paperwork, available through digital COA platforms that matter to our larger buyers.
Over the past decade, ingredient focus has moved from single-purpose compounds toward multi-functional ingredients. The sodium form of ursolic acid fits this trend on both technical and marketing fronts. Buyers look for active roles in both food and skin health fields, supported by rising consumer interest in botanically sourced actives.
In our operation, we notice each uptick in technical inquiries as new research appears. As studies link ursolic acid sodium to metabolic and cardiovascular pathways, we prepare technical summaries and lot documentation weeks ahead of market waves. A large share of interest also comes from pilot-scale manufacturers, not just giants in healthcare or food.
For the pharma sector, growing demand for water-soluble actives with plant-based origins keeps focus on sodium salts. Some clients face regulatory questions about ingredient origins and modifications. Our role becomes part-educator, part-supplier, translating plant chemistry into practical, scalable value.
Compared with other triterpenoid sodium salts—like oleanolic acid sodium—our product finds wider interest for use in cosmetic and wellness applications, partly due to its traditional roots in folk medicine.
With changes in global transportation and digital traceability, we track every drum not just for logistics, but for tamper-evidence, shipment timing, and last-mile stability. Increasing transparency means every lot leaves with not just a printed label, but a digital record accessible by the customer and their auditors.
We don’t just ship product and step away; each feedback—positive or negative—creates a loop for us to refine batches, improve process controls, or clarify labeling. The shift toward clean-label and eco-friendly sourcing isn’t a slogan, but a series of investments, policy changes, and supply chain improvements made real over time. We see these changes not just as obstacles, but as opportunities: to tighten batch records, engage more closely with procurement partners, and anticipate where ursolic acid sodium fits in future industry cycles.
Some trends, like stricter microbiological standards or zero-solvent residue requirements, force us to rethink both primary extraction and post-processing. Others, like on-demand custom lots for virtual drug screening or seasonal ingredient demand surges, require short-turn adaptation at the plant level.
Through decades of production, our focus remains the same: get the batch right, match real customer use, and learn each nuance in storage, handling, or formulation. Each drum of ursolic acid sodium leaving our facility has made that journey through many hands and real process adjustments—factory, lab, and customer floor—all working toward a finished product that isn’t just another ingredient, but the outcome of experience, history, and close conversation with every partner down the line.