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HS Code |
849273 |
| Chemical Name | Crystalline Mannitol |
| Molecular Formula | C6H14O6 |
| Molar Mass | 182.17 g/mol |
| Appearance | White, crystalline powder |
| Solubility In Water | 16-22 g/100 mL at 25°C |
| Melting Point | 165-170°C |
| Taste | Sweet, non-hygroscopic |
| Odor | Odorless |
| Ph Of 5 Percent Solution | 5.5 - 7.0 |
| Cas Number | 69-65-8 |
| Stability | Stable under normal conditions |
| Synonyms | D-Mannitol, Mannite |
| Storage Conditions | Store in a cool, dry place |
| Grade | Pharmaceutical/Food grade |
| Density | 1.52 g/cm³ |
As an accredited Crystalline Mannitol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Crystalline Mannitol is packaged in a 25 kg high-density polyethylene (HDPE) bag, inner polyethylene liner, ensuring purity and moisture protection. |
| Container Loading (20′ FCL) | 20′ FCL: Crystalline Mannitol is packed in 25 kg bags, 16~18 metric tons per 20-foot container, food/pharma grade. |
| Shipping | Crystalline Mannitol should be shipped in tightly sealed containers to protect it from moisture and contamination. Store and transport at room temperature, away from incompatible substances and strong oxidizers. Follow all relevant regulations for non-hazardous chemicals. Ensure clear labeling and include the material safety data sheet (MSDS) with the shipment for reference. |
| Storage | Crystalline Mannitol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances. Protect it from excessive heat, direct sunlight, and strong oxidizing agents. Ensure containers are clearly labeled, and avoid sources of contamination. Follow all relevant safety and regulatory guidelines to maintain its quality and stability. |
| Shelf Life | Crystalline Mannitol typically has a shelf life of 2–3 years when stored in a cool, dry place in tightly sealed containers. |
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Purity 99%: Crystalline Mannitol with Purity 99% is used in pharmaceutical tablet formulations, where it ensures high tablet hardness and uniformity. Particle Size 50 microns: Crystalline Mannitol with Particle Size 50 microns is used in oral solid dosage forms, where it provides excellent compressibility and smooth mouthfeel. Melting Point 166°C: Crystalline Mannitol with Melting Point 166°C is used in confectionery manufacturing, where it guarantees thermal stability during processing. Moisture Content <0.5%: Crystalline Mannitol with Moisture Content <0.5% is used in nutritional supplements, where it minimizes clumping and enhances storage stability. Bulk Density 0.48 g/cm³: Crystalline Mannitol with Bulk Density 0.48 g/cm³ is used in dry powder inhalation products, where it improves powder flow and aerosolization efficiency. Microbial Limit <100 cfu/g: Crystalline Mannitol with Microbial Limit <100 cfu/g is used in injectable solutions, where it ensures low microbial contamination risk and enhances patient safety. pH 5.5–7.5 (5% solution): Crystalline Mannitol with pH 5.5–7.5 (5% solution) is used in intravenous infusions, where it maintains physiological compatibility and minimizes irritation. BSE/TSE Free Grade: Crystalline Mannitol of BSE/TSE Free Grade is used in parenteral preparations, where it complies with stringent safety regulations and supports global distribution. |
Competitive Crystalline Mannitol prices that fit your budget—flexible terms and customized quotes for every order.
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In our years manufacturing crystalline mannitol, few products attract as many curious questions from both new and established partners. Most know mannitol as a common name, but the crystalline grade sets itself apart with unique characteristics. On our production floor, attention turns not only to purity and reliable supply, but also the physical attributes such as particle size, flow characteristics, and bulk density. Often, customers arrive with expectations shaped by powders, granules, or blends found in the larger market, but our crystalline mannitol answers to specifications set by the direct needs of pharmaceutical, food, and industrial applications.
As producers, our focus lands on raw material traceability, stringent process control, and precision filtration to achieve a >99% pure end product. Each batch emerges from monitored crystallization processes and multistage purification, approaches honed over decades rather than improvised to suit trend shifts. Crystalline mannitol's appeal, in our experience, comes from its dependable physical stability—white, odorless, fine crystals that dissolve cleanly in water and display minimal hygroscopic tendencies. This gives it practical advantages for manufacturers needing bulking, sweetening, or tablet-forming agents that resist stickiness and lump formation in storage.
Our partners in the pharmaceutical industry frequently turn to crystalline mannitol thanks to its non-cariogenic nature, low reactivity, and high tolerability. Acting as a direct compression excipient in tablets, its robust crystal structure supports easy tableting, consistent hardness, and predictable disintegration. Contrasted with spray-dried variants, direct compression crystalline mannitol often demonstrates a denser structure. Energies poured into monitoring moisture and ensuring fine control during the crystallization phase translate into higher robustness on the customer side. As manufacturers, witnessing reduced sticking, less dust, and smooth process flows in our customers’ factories builds confidence in both product and supplier. Our own technical staff routinely trouble-shoot compaction or flow-related questions, offering fact-based insights on adjusting press speeds or binder ratios thanks to years refining our own lines for these performance markers.
Crystalline mannitol becomes a backbone ingredient in sugar-free confections, baked goods, and chewing gums. Several clients appreciate its lower caloric value and lack of aftertaste, supporting formulations that call for sugar reduction without compromise in taste or texture. From a manufacturer's view, the ability to keep moisture absorption low means longer product shelf-life. We see clients return for the sensory attributes—crystalline mannitol provides a cool, clean mouthfeel, and the fine crystals don't alter texture in sensitive candy or gum formulations. Differences from more amorphous sugars, such as sorbitol or xylitol, show up in mouth cooling, lower glycemic impact, and a more neutral backdrop for flavor systems. Much effort inside our plant centers on meeting pure food-grade standards: absence of foreign matter, tight microbial control, and no cross-contamination with allergens. Bulk shipments direct from us routinely pass third-party tests, confirming that strict in-house controls benefit finished goods further down the supply chain.
Having produced both crystalline mannitol and similar alcohols, we notice distinctions beyond sweetness or caloric values. Mannitol’s lower solubility in water, compared to sorbitol or maltitol, leads to a reduced tendency to attract water. In manufacturing, this pays dividends: powders and tablets resist clumping, wrappers remain free from sticky residues, and process machinery needs less aggressive cleaning. Some competitors may rely on external anti-caking agents, but our tightly crystalline model of mannitol often delivers stability on its own.
Beyond dryness, crystalline mannitol shines with a slow, clean dissolution—especially valuable for time-release oral medications or lozenge-style candies. Unlike amorphous or semi-crystalline alternatives, stability over long storage periods stays high, reducing risk for expensive recalls or urgent re-batching. Our control over batch-to-batch uniformity is rooted in experience. Updated gravimetric feeders, automated crystallizers, and in-line monitoring all serve to guarantee physical and chemical specs. This helps clients avoid variability that could throw production lines out of tolerance or disrupt quality checks.
Our crystalline mannitol comes in several grades, including fine crystals and coarser granulations. Particle sizing remains a core feature. Years of customer feedback shaped current offerings, from sub-100 micron powder suited for precision tableting, to mid-range 200–300 micron crystals favored in food coatings, up to larger granules enabling slow, controlled dissolution in specialty products. Each grade targets a specific outcome, not just a box to tick on a datasheet. By refining downstream sieving and blending, we align output to concrete process feedback—examples include avoiding blinding of screens in tablet lines or ensuring even dispersion in chewing gum kneaders.
Our laboratory analytics operate to both international and local standards. Alongside typical chemical identity and purity checks, we measure moisture content, clarity in solution, heavy metals, and microbial contamination. These tests, drawn from years of audit feedback, underpin a simple commitment: crystalline mannitol from our lines does not compromise on food or drug safety. Our records support this with every shipment.
Much confusion in the marketplace stems from equating crystalline and spray-dried mannitol. The latter, while still mannitol by chemical structure, displays significantly different handling aspects—lower bulk density, higher surface area, and more tendency to attract moisture rapidly. On the manufacturing floor, using the wrong grade can clog feeders, impair blending, or even over-lubricate tablet surfaces. Our technical team maintains direct dialogue with client process engineers, often running parallel samples to benchmark performance and eliminate expensive trial-and-error. Advice often circles back to practical details: hopper design, humidity control, feeder speed, and finished product shelf goals.
Crystalline mannitol’s relatively solid crystal matrix offers higher compressibility for direct compression, making it a favorite for high-speed tablet presses or continuous mixing lines. Its stability appeals to formulators managing sensitive actives or flavors. The physical presence—distinctly free-flowing, non-dusting, and bright—signals both quality and ease for downstream blending. Decades observing the effects of stray moisture or uncontrolled particle sizes inform continuous investment into both raw materials and operator training—the result can be seen in the reliability experienced by our pharmaceutical and food partners.
Shipments do not leave our gates without full traceability to individual production lots. We log source materials, process parameters, and quality control data on a digital backbone, supporting both routine orders and urgent audits. Global food and drug regulations, particularly concerning contamination risk, drive us to invest in dedicated clean zones, frequent changeovers, and constant staff training. While crystalline mannitol is not especially hazardous, continuous focus on cross-contamination risk pays off during third-party inspections or sudden recall investigations. Our plant runs certified environmental management controls, reducing waste by recycling wash water, using energy-efficient crystallization, and regularly tuning solvent recovery units. These investments may not show on a product label, but they build resilience and compliance into every kilogram shipped.
Several partners ask about residual solvents or by-products. Our process chemistry keeps entirely to food-safe reagents, and our multi-stage purification extracts unreacted substrates. Analytical records stretching back years confirm this, and we provide historical trend reports on request. With a combination of automation and operator skill, batch-to-batch consistency remains high—clients rarely find themselves juggling adjustments to specification based on supply fluctuations.
Crystalline mannitol’s physical stability in storage has concrete paybacks for bulk handlers and warehouse teams. Sacks and containers stored even in moderately humid conditions retain free-flowing texture, limiting bridging or rat-holing that slow peel-off or bag emptying. We advise partners on simple methods such as sealed liners and climate-controlled storage to maximize shelf time. Direct shipments absorb less warehouse labor—no need to resort products or break up clumps before feeding into automated processes.
On occasion, we see concerns about packaging interaction or shelf stability, particularly in queasy transport or variable climate conditions. Our standard sacks, lined cartons, and intermediate bulk containers pass rigorous drop and compression tests, with alternatives for specific temperature or moisture extremes available. So far, documented incidents of off-odor, discoloration, or visible changes in appearance remain rare—thanks to control at both process and packing stages.
Several of our long-standing pharmaceutical clients pursued new direct compression technology using crystalline mannitol as their base. High compaction tolerance and reliable humidity resistance let these partners reduce the use of binders and anti-caking agents, lowering cost and, sometimes, side effects for end users. We worked side-by-side with formulators, running test lots, adjusting granule size, and fine-tuning moisture levels drawn from real-world line start-ups. The results—tablets with high mechanical strength, rapid and predictable dissolution, and taste-masking capabilities—emphasize direct benefits coming straight from careful manufacturing practice.
On the food side, confectioners seeking sugar-free or reduced-calorie options discovered our crystalline mannitol brings more than simple sweetness. It imparts texture, heat absorption, and flavor clarity missing from more amorphous sugars. These technical benefits reveal themselves most plainly after several seasons of storage tests, flavor evaluations, and consumer trials.
Downstream attempts to replace crystalline mannitol with alternatives—such as spray-dried or amorphous powders—reveal challenges not always visible on spec sheets. Ease of handling, susceptibility to moisture, and process compatibility often surface as make-or-break criteria. Our team’s willingness to share process insights, not just bulk orders, helps customers realize these differences early, reducing changeover costs or troubleshooting down the line.
While the core chemistry of mannitol remains unchanged, sustainability pressures guide us toward greener sources and smarter processes. We audit suppliers for renewable feedstock use, minimize waste through careful water management, and take part in industry groups focused on lowering the carbon footprint in sugar alcohol production. These steps flow from a long-held commitment to environmental stewardship—a mindset reinforced each time regulatory demands shift or buyers request documentation for their own eco-labels.
Critically, the global rise in health-conscious foods and pharmaceuticals elevates the need for trustworthy crystalline mannitol supply. Supply shocks, adulteration incidents, or inconsistent batches can erode hard-won confidence faster than any marketing can repair. Our willingness to speak plainly about capacity, flexibility, and raw material security assures clients of uninterrupted supply—even as global logistics or trade politics shift unpredictably.
Among emerging directions, continuous process improvement sets the pace. New sensors, faster analytics, and data-sharing platforms allow us to predict deviations, reduce waste, and cut lead times for both regular and custom grades. Customer collaborations—particularly long-term development partnerships—help us fine-tune output by collecting feedback on mixing, compaction, and dissolution long beyond the point of purchase. These efforts ground our production in real-world needs, not just in-house theory.
In practice, the demands of crystalline mannitol production reach beyond just chemistry. Investments go into operator training, dust capture, and sanitation systems. Regular audit cycles—both from internal quality and external partners—teach us to respond to shifts in customer requirements. When equipment downtime threatens supply, our long-run maintenance plans, backed by redundant storage and component supply, have repeatedly minimized disruption.
Factory upgrades pay off when screeners, dryers, and conveyors work together seamlessly. Every time we rework a process, product quality comes under the microscope: visible particles, odors, or flowability problems drive us back to root cause analysis, not shortcut fixes. Direct customer complaints about caking or color shifts receive immediate action and investigation. Only by closing this feedback loop can improvement become permanent.
Years spent as the actual source of crystalline mannitol shape a practical perspective. Unlike resellers or aggregators, solutions come straight from production knowledge—if a tablet capping issue arises, if unexpected flow stalling occurs mid-batch, we know which production tweak to apply. Experiences shared in technical troubleshooting, formulation support, and bulk logistics all spring from accountability for the entire production cycle. It also means adaptation is faster: changes to particle sizing, packaging options, or even custom batch runs get answered without delay or obfuscation.
Buyers aiming for transparency receive thorough, real-time insight into everything from raw material origins to shipment timing. Our involvement in audits, regulatory reviews, and customer site visits brings a reality check to paperwork claims—questions get met with honest answers and supporting data, not vague platitudes. This foundation, constructed over years of repeat experience, reinforces trust and gains business that values direct, solution-oriented relationships.
Growing demand for high-quality, reliable excipients and food ingredients matches our ongoing investments in people, process, and infrastructure. We keep pace with pharmaceutical advances, regulatory shifts, and dietary trends by developing new grades, introducing more stringent controls, and upgrading plant technology. As ingredient transparency becomes a market differentiator, our clear documentation and open technical support stands out from those who simply move boxes from one warehouse to another.
Dedicated teams, both in manufacturing and quality control, shape the evolution of our crystalline mannitol to meet tomorrow’s demands. Lessons drawn from ongoing collaborations guide improvements as much as changes in equipment or market expectations. The result is more than a specification sheet—it is a relationship between those who make an ingredient and those who rely on it for safety, performance, and innovation.
For anyone seeking to understand the practical role of crystalline mannitol—in pharmaceuticals, foods, or allied industries—insights gained on the production floor bring answers that serve far beyond simple compliance or technical data. With each batch, each shipment, the accumulated experience of manufacturing turns ingredient into advantage, one well-made crystal at a time.