|
HS Code |
549924 |
| Generic Name | Mannitol |
| Chemical Formula | C6H14O6 |
| Molecular Weight | 182.17 g/mol |
| Appearance | White crystalline powder |
| Solubility In Water | Very soluble |
| Pharmacologic Class | Osmotic diuretic |
| Route Of Administration | Intravenous |
| Storage Temperature | 15-30°C |
| Cas Number | 69-65-8 |
| Indications | Reduction of intracranial pressure, treatment of cerebral edema, promotion of urinary excretion of toxins |
As an accredited Mannitol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A white, plastic 500g bottle labeled "Mannitol, USP" with hazard symbols, batch number, and manufacturer's details clearly displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Mannitol: Typically loaded with 15-18 metric tons, packaged in 25 kg bags on pallets, moisture-protected. |
| Shipping | Mannitol is typically shipped in solid form, packaged in sealed, moisture-resistant containers such as fiber drums or plastic-lined bags to protect it from humidity. It is not classified as hazardous for transport. Proper labeling and documentation are required, and storage should be in a cool, dry place away from incompatible substances. |
| Storage | Mannitol should be stored in a tightly closed container at room temperature (15–30°C), protected from moisture, heat, and direct sunlight. Keep it in a dry, well-ventilated area away from incompatible substances. Avoid exposure to strong acids or oxidizing agents. Ensure the storage area is labeled and compliant with safety regulations to prevent contamination or accidental use. |
| Shelf Life | Mannitol typically has a shelf life of 3-5 years when stored in tightly closed containers at cool, dry conditions, away from moisture. |
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Purity 99.5%: Mannitol with purity 99.5% is used in pharmaceutical tablet formulations, where it ensures high compressibility and uniform drug delivery. Melting Point 166-170°C: Mannitol with a melting point of 166-170°C is used in lyophilized injection preparations, where it stabilizes active pharmaceutical ingredients during freeze-drying. Particle Size 50 μm: Mannitol with a particle size of 50 μm is used in oral powder blends, where it provides excellent flowability and homogeneity. Low Hygroscopicity: Mannitol with low hygroscopicity is used in chewable vitamin tablets, where it prevents moisture-induced degradation and extends shelf life. Molecular Weight 182.17 g/mol: Mannitol with a molecular weight of 182.17 g/mol is used in diagnostic test strips, where it provides consistent osmotic balance and precise analytical results. Stability up to 120°C: Mannitol with stability up to 120°C is used in food coating applications, where it maintains integrity and prevents surface crystallization during processing. Granule Form: Mannitol in granule form is used in direct compression tablet manufacturing, where it enables rapid tablet formation and reduces processing time. |
Competitive Mannitol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
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Tel: +8615371019725
Email: sales7@bouling-chem.com
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For decades, our plant has focused on the production of polyol-based excipients, with Mannitol standing out for both its versatility and our consistent demand from the pharmaceutical and food sectors. Unlike other excipients, Mannitol (chemical formula C6H14O6) offers a stability and sweetness profile that appeals to formulators facing specific processing and consumer requirements. Each batch emerging from our facility upholds strict molecular specifications, which is vital—impurities or minute inconsistencies can undermine product safety or performance in sensitive formulations.
Our Mannitol line covers a spectrum of grades, with crystalline and powder forms leading the way. The size and moisture profile come as a direct result of tightly managed crystallization and drying stages. We conduct ongoing monitoring not only for purity, but for consistency in particle distribution, as this directly impacts both the texture in food use and compressibility for tablet manufacturing. Our process aims for a typical moisture content not exceeding 0.5%, safeguarding hygroscopic stability—a feature highly regarded in humid regions or where shelf life is a major concern.
We supply Mannitol to some of the largest tablet pressing facilities and confectionery manufacturers in the region. Pharmaceutical technicians trust our product for both direct compression and wet granulation, citing our reliable flow properties and low reactivity. In tablets, especially, sub-par flow can stall production or result in weight variation, a headache any operator has experienced at least once. Consistent flow and compressibility, achieved through years of adjusting our recrystallization and milling, help reduce downtime and reject rates, issues that weigh heavily on the bottom line.
Food manufacturers count on the gentle sweetening provided by Mannitol, especially for sugar-free and reduced-calorie products. Compared to common sweeteners like sorbitol, Mannitol provides a cooling sensation and lower caloric contribution. In chewing gum centers or dusting powders, end users frequently mention the smooth, cool feel of our Mannitol, which emerges naturally from the structure of the polyol itself, not an added effect. Years ago, one of our long-term partners, a global sugar-free gum brand, switched entirely to our fine-particle model when seeking a dusting agent that wouldn’t clump under ambient warehouse conditions—a small adjustment in our post-crystallization sieving delivered that result.
Our customers frequently compare Mannitol with sorbitol, lactose, and even xylitol. Mannitol possesses a unique advantage—notably its low reactivity and resistance to Maillard browning in direct-compression tablets or coatings. In contrast, lactose can brown or degrade under heat or long storage, and sorbitol, though widely used, attracts more moisture leading to caking and reduced shelf life. Formulators with delicate actives—especially those sensitive to water or heat—prefer Mannitol precisely for this reason.
For injectable pharmaceuticals, our Mannitol passes stringent requirements for endotoxins and residual solvents, supporting its role as an osmotic diuretic or as an excipient in lyophilized vials. Production lines for parenteral-grade Mannitol face more demanding controls; our site operates with dedicated equipment and fully segregated lots, recognizing that a single deviation could compromise entire clinical batches or put patients at risk. Pharmacy chains and IV solution fillers rely on these specifications not just for safety but for ensuring each patient receives the intended dose and experience.
Our formulations and models reflect decades of dialogue with production teams and R&D labs. Customers call us not just asking about mesh size or purity, but describing actual problems—granulation sticking, column clogging, powder bridging, or taste acceptance in chewables. We translate this feedback directly into our process control improvements, ingredient testing regimes, and the introduction of new models. One example comes from tableting operations running at high speed; we learned years ago that a narrowly distributed medium particle size prevents both fines build-up and caplet chipping, which otherwise wastes hours on cleaning and blockage removal. In those lines, our calibrated powder specification now performs steadily across thousands of shifts.
In recent years, we faced increased scrutiny from regulatory bodies and end users about trace contaminants—nitrosamines, residual solvents from upstream hydrogenation, or rare allergens. We answered by enhancing our purification and monitoring regimes beyond base compliance levels, and by implementing PCR testing when sourcing non-GMO feedstock. As producers, we have learned from experience that transparency and traceability are not just compliance boxes; they reduce the frequency of recalls and instill real confidence across the supply chain.
Tableting grades of our Mannitol reflect the core needs articulated by formulation scientists and production engineers. Direct compression often favors a particle size between 100 to 300 microns for uniform die fill, a range that we tune using precision screeners. Smoother surfaces and narrow size spread guard against weight variation—no small matter at high throughput. Hardness and friability targets depend directly on compaction pressure and particle shape. We maintain a feedback loop with tablet press operators and routinely tweak our drying and milling parameters, so operators can run with fewer “press stops” due to sticking or capping.
Disintegration and dissolution rates also display strong dependence on our production choices. A subtle change in crystalline form can shift a dispersible tablet’s mouthfeel or delay the onset of relief in orodispersible products. Our customers in both OTC and prescription markets rely on us to maintain consistency because small shifts can trigger major reformulation work. Inter-lot consistency means production managers run smoother operations, spending less time recalibrating or adjusting blends.
Mannitol’s taste profile offers something that customers and consumers alike remember. In food and oral care products, it stands out from other polyols not just because it sweetens, but for the cooling effect as it dissolves. This arises from the product’s negative heat of solution—a property rooted in the chemistry, not just processing. Our plant’s drying and milling approach, refined year over year, safeguards this sensory feature. Confectioners and oral health companies have pivoted to our Mannitol, prioritizing that clean, refreshing finish over the heavier, sometimes syrupy taste of sorbitol or the harsher sweetness of aspartame.
Taste masking is another front where Mannitol excels. In chewable pharmaceuticals or supplements, actives can leave a bitter or metallic trail—an unpalatable experience that can damage both compliance and reputation. Mannitol’s neutral background, combined with lack of reactivity, allows formulators to mask unwelcome flavors more easily. Our direct work with flavor houses and formulators has kept us keenly aware of the real-world advantages here. When working with pediatric lines or geriatric tablets, taste truly makes the difference between acceptance and failure.
Navigating the regulatory environment surrounding pharmaceutical and food excipients means adapting—standards evolve, and expectations rise. We have invested in validated cleaning protocols, documented allergen controls, and digital traceability from raw material intake through finished lot shipment. Quality departments visit our processing rooms regularly; unannounced audits are now a fact of life. By keeping process logs tight and extended certificate of analysis details available within hours, we demonstrate not just compliance but proactive attentiveness, which partners in regulated sectors demand at every purchasing cycle.
Supply chain disruptions and logistics challenges over recent years have underscored why direct manufacturer relationships matter. By holding buffer stocks of key grades and keeping multiple production lines flexible, we cut down on both delay risk and price spikes passed down the chain. Customers who had previously relied on trading intermediaries noted a marked difference during bottleneck periods—direct supplier relations helped bridge inventory gaps and avoided formulation shutdowns. Experience has shown us that real transparency in inventory and lead time planning helps prevent costly line stoppages.
Over time, requests for customized grades have increased. Tablet and chewable vitamin lines may specify a higher hardness or a surface-smooth powder; rapid-dissolving oral care products might seek extra-fine particle Mannitol to speed up disintegration. Our R&D teams run pilot-scale batches alongside partner customers, adjusting crystallization rates and sifting to match specific endpoints. This technical freedom sets us apart—large-scale chemical manufacturing often resists change, but our model places iterative cooperation at the core. Industry relationships built over years ensure project transitions move beyond theory and into actual process adjustments.
We also address requests for non-GMO feedstocks, halal or kosher certification, and reduced environmental footprint. Sourcing managers in the nutraceutical and wellness industries push for these features not just from ethical or label claims but from growing consumer pressure for transparency. We’ve invested in segregated process trains, supplier audits, and dedicated documentation workflows. These commitments have reaped dividends in both customer loyalty and smoother international clearance.
Formulators testing out new excipient blends raise one recurring issue—shelf stability. Bulk caking, unexpected moisture uptake, loss of flow, or degradation all cut into product performance. Our production sweeps for low moisture and regular evaluation for particle compaction mitigate many standard storage dangers. We review field returns data quarterly with partners; over the past five years, customer claims for clumping or degraded performance have trended downward, the result of improvements in both process management and post-production testing.
Packaging also counts—years of shipping taught us that seemingly minor tweaks in bag liners, moisture barriers, and lot labeling reduce downstream loss. Our operations and shipping supervisors interface regularly with major customers’ warehousing teams, discussing how real-world handling conditions affect usability. These relationships, born out of years of direct, hands-on experience, have led to simple but powerful process changes—double-sealing for longer-haul logistics or pallet anti-tipping configurations, all designed in response to actual incidents, not just theoretical best case.
Production and R&D teams frequently compare excipients based on cost, process stability, taste profile, and downstream versatility. Mannitol stands tall among sugar alcohols due to several factors. Its lower hygroscopicity compared to sorbitol means fewer headaches from clumping or dosing errors. In direct-compression tablet lines, it outperforms many sugars and even xylitol from the standpoint of punch cleanability and reduced sticking. Lactose, long regarded as a staple, runs into both allergen and browning risks, particularly in high-temperature or moisture-variable operations. Overhead by managing lot failures or spoilage can easily eclipse any upfront cost differential.
Sweetness difference may seem minor but matters greatly for patient or consumer acceptance. Our customers report consistent feedback that Mannitol’s clean, mild profile lets actives and flavors stand forward, rather than overwhelm with excess sweetness. For clients who specialize in pediatric or geriatric populations, this moderation is more appealing than high-intensity or lingering sweeteners, which can hinder repeat compliance.
Chemicals manufacturing increasingly asks for continuous improvement, particularly in environmental stewardship. Our site has invested in both water recapture and waste heat recovery from dryers to cut our energy and resource use. Customers and industrial peers visiting our facility reference these upgrades as real differentiators. On the global front, more customers ask about carbon footprint, logistics emissions, and sourcing transparency. As manufacturers, we see this as an ongoing dialogue—continuous upgrades in production and resource management, not just a certification to be filed away.
In parallel, technical teams are investigating new uses for Mannitol, from 3D-printed pharmaceuticals to advanced nutraceutical blends. We share insights and failures from these trials routinely with our network, seeing every new use case as a chance to refine both our production and our communications. Demand for rapid-dissolving and high-stability formats continues to rise, reshaping our own product development roadmap. Each trend points toward greater need for reliability not just batch-to-batch, but year-over-year—a challenge that keeps us honest and accountable.
Industrial lines and bench-top R&D demand different approaches. We often field simultaneous requests for kilogram samples and multi-tonne contracts, and real innovation arises when these groups talk to one another. Scale-up introduces hurdles—shear effects, residence times, and scale-dependence in drying don’t map neatly from lab to plant. Our engineering staff, many of whom have worked in both process and development roles, guide these transitions, heading off bottlenecks and providing real data as projects move closer to commercialization.
On the technical side, our R&D group invests in both physical property mapping and sensorial trials, not just chemical analysis. Tablets, gums, and powders travel from factory floors to boardrooms for hands-on evaluation with actual end users. We adjust practices—like sifter settings or crystallization rate—to align with trends and real customer experiences, not just published specifications. Mistakes do happen, and feedback, when honest, improves us more than any sales meeting or audit. Failures documented, process adapted, outcome improved—the heart of robust manufacturing.
Our most successful long-term relationships grow from honest communication, rapid decision making, and trust. Customers—whether developing a breakthrough medication or revamping a classic food favorite—want more than a commodity supplier. Pulling together across production, R&D, and logistics teams, we provide not just consistent product but informed problem solving. This manifests in practical advice, line-side troubleshooting, and pinpoint adjustments that make the difference between smooth launch and stalled project.
Supply agreements built on years of honest back-and-forth weather market fluctuations, regulatory changes, and unexpected events. From the plant floor to the customer’s blending tanks, shared goals and fast information flow anchor these partnerships. As a manufacturer, our job does not end when a truck leaves our loading docks. Real partnership means supporting far beyond order fulfillment.
Continuous improvement frames everything we do with Mannitol. From raw material validation through packing and post-market support, every team member has seen how even small process shifts ripple through to customers. Plant upgrades, team retraining, and daily quality reviews keep our lines ready for both routine volume and next-generation requests. By approaching each run with both the eyes of an operator and the perspective of our clients, we avoid complacency and keep adapting as new needs surface across the industries we support.
End-use applications evolve, regulatory landscapes shift, and consumer demands grow more nuanced. We remain committed to being more than a bulk supplier, answering with direct experience, technical acumen, and a focus on both safety and satisfaction. Every batch shipped carries the weight of our collective expertise and the trust our customers place in us—a responsibility that shapes our approach, every step from feedstock to finished product.