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HS Code |
113078 |
| Chemicalname | D-Mannitol |
| Casnumber | 69-65-8 |
| Molecularformula | C6H14O6 |
| Molarmass | 182.17 g/mol |
| Appearance | White crystalline powder |
| Meltingpoint | 165-170°C |
| Solubilityinwater | 21.6 g/100 mL (25°C) |
| Taste | Sweet |
| Odor | Odorless |
| Ph | 5.0–7.0 (5% solution) |
| Synonyms | Manna sugar, Mannite |
| Density | 1.52 g/cm³ |
| Einecsnumber | 200-711-8 |
As an accredited D-Mannitol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | D-Mannitol is packaged in a sealed, white plastic bottle containing 500 grams, labeled with product details, hazards, and safety instructions. |
| Shipping | D-Mannitol is typically shipped in sealed, moisture-resistant containers such as fiber drums, plastic pails, or high-density polyethylene bags to ensure product integrity. Packaging is clearly labeled according to regulatory standards. The chemical should be stored and transported in cool, dry conditions, away from incompatible substances and sources of ignition. |
| Storage | D-Mannitol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and incompatible substances such as strong oxidizers. Store away from direct sunlight and sources of ignition. Ensure the storage area is clearly labeled and complies with safety regulations for chemicals to prevent contamination and environmental exposure. |
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Purity 99%: D-Mannitol purity 99% is used in pharmaceutical tablet formulations, where it ensures consistent dosage uniformity and low impurity content. Particle Size 100 μm: D-Mannitol particle size 100 μm is used in oral suspensions, where it offers rapid dissolution and enhanced mouthfeel. Melting Point 166°C: D-Mannitol melting point 166°C is used in confectionery manufacturing, where it provides thermal stability during processing. Molecular Weight 182.17 g/mol: D-Mannitol molecular weight 182.17 g/mol is used in intravenous infusion solutions, where it guarantees accurate osmotic activity for clinical efficacy. Stability Temperature 40°C: D-Mannitol stability temperature 40°C is used in lyophilized pharmaceutical products, where it maintains structural integrity during storage. Low Hygroscopicity: D-Mannitol low hygroscopicity is used in food coatings, where it prevents moisture absorption and product clumping. Bulk Density 0.5 g/cm³: D-Mannitol bulk density 0.5 g/cm³ is used in powder blends, where it allows for efficient mixing and optimized flow properties. Reducing Sugar Content <0.1%: D-Mannitol reducing sugar content <0.1% is used in diagnostic reagent preparations, where it minimizes side reactions and ensures assay accuracy. Non-GMO grade: D-Mannitol non-GMO grade is used in health supplements, where it ensures absence of genetically modified organisms for regulatory compliance. USP grade: D-Mannitol USP grade is used in injectable formulations, where it meets pharmacopeial standards for patient safety. |
Competitive D-Mannitol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
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Tel: +8615365186327
Email: sales3@ascent-chem.com
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D-Mannitol has shaped the story of our factory over the past decade, evolving from a specialized sweetener into a staple ingredient for sectors as different as pharmaceuticals, food processing, and technical manufacturing. Watching the needs of our customers change over time shapes how we approach quality and production standards. We have seen first-hand that ingredient consistency is not just a talking point— it’s a demand that can only be met by controlling every stage of the process.
Our facility selects corn starch or saccharose sources with a trained eye, ensuring batches of raw material meet criteria surpassed by the local and national standards. Raw materials tell the story – they decide the trace minerals, water quality needs, and flow of the batch. If crops change, we adapt our pre-processing filtration. This is why our D-Mannitol (Model: DM99P) routinely exceeds purity levels above 99% and holds up under demanding laboratory scrutiny.
Working hands-on in production means continuous feedback. Over the years, pharmaceutical buyers told us stories of clogged tablet presses and caking problems from inconsistent mannitol. We responded by improving particle size controls. Our signature DM99P grade comes in medium-fine powder, with a moisture content below 0.2%, and a bulk density that resists settling or bridging. We rely on system audits, not guesswork, using laser particle sizers and moisture analyzers. Heavy metals are checked twice per lot, and our microbial limits track well inside pharmacopeial guidelines.
We engineer our process to cut out the need for unnecessary additives or blending aids. The product moves directly from purification to drying and final sieving. This tight control leads to a consistent product, helping customers avoid issues with downstream processing. Every manufacturer knows that unexpected downtime costs both money and reputation. We want to enable repeatable, efficient processes for everyone who relies on our mannitol.
Our direct relationships with end users shape the profile of our mannitol. Pharmaceuticals drive the highest volume, with most of our output pressed into solid dosage forms. Tablet makers want a diluent that handles pressure, flows correctly, and holds up in blends with active ingredients. Our mannitol does not degrade under compression. It keeps a smooth, clean taste, and resists hygroscopicity. Many in the medicated lozenge industry pointed to flavor persistence– we built purity and neutral taste to meet this expectation. Our DM99P works as both binder and sweetener. High compatibility means you can change actives or adjust dosages without reformulating your excipients.
In the food industry, confectioners reach for our mannitol to address sugar replacement needs. It offers sweetness at about half that of sucrose, so blends allow for calorie control without metallic aftertastes. Chewing gum manufacturers have clued us in on flow and anti-caking performance— we dialed in granular grades with tight moisture controls, so gum recipes don’t get sticky in humid climates. Many oral hygiene product brands look for a bright, lasting cooling effect. This is not just marketing— cooling intensity changes with particle size, so we lock in physical properties batch after batch.
Specialty technical users— battery electrolyte labs or anti-caking coatings for fertilizers— value stability over sweetness. They demand clear records for trace contaminants and want detailed impurity data. Our process yields a narrow impurity profile, hitting the needs for sensitive technical conversions. The product’s inertness and solubility save users costly reformulation.
Competitors often ask us whether it is worth the investment to insist on mannitol over other polyols, such as sorbitol or xylitol. The answer lies in performance. Mannitol does not promote tooth decay and barely registers on the glycemic index. This makes it critical for diabetic foods and oral hygiene products. Our experiences working with diabetic-focused foods taught us that even a small impurity or inconsistency in the crystalline form of an excipient can change flavor and metabolic effects. We put energy into stability, making DM99P resistant to moisture pick-up, so the shelf life stretches beyond that of typical sorbitol and xylitol blends.
Sorbitol absorbs water and can lead to caking in tablets or food mixes—a common customer complaint. Mannitol’s low hygroscopic nature keeps your powders dry longer, and extends storage times. As manufacturers, we watch how mannitol handles under high-speed tableting and how it disperses in mixers— performance is not just a laboratory story. Sorbitol sometimes carries a bitter aftertaste, while mannitol maintains a cleaner profile even in higher concentrations. It doesn’t just meet a technical specification; it actually improves the user experience for both end product manufacturers and consumers.
Over the years, we ran side-by-side tests of granulation efficiency using our own D-Mannitol and typical xylitol powders. We observed less sticking and smoother blends when using DM99P. These evaluations told us that our production controls matter on the factory floor, not just in certificates of analysis. Shifting an entire line over to mannitol can pay off in fewer rejected batches and a cleaner working environment.
From the earliest days, quality assurance sat inside production, not as an outside check. Our QC laboratory runs directly in line with every batch, with chemists overseeing tests for density, flow rate, and clarity. We don’t just run the minimum required by pharmacopeias; we push for undetectable levels of byproducts and monitor for any new contaminants based on trends in raw materials.
Customers invite us to their plants and ask for insights on how to solve tableting or blending issues that show up months after a formula change. Our team brings decades of hands-on experience to these collaborations. Many problems get solved by tracing the particle size or refining drying conditions. Sometimes an issue comes down to a difference in climate or equipment. We draw from our own production challenges— humidity control, filtration upgrades, and process troubleshooting— to make practical recommendations.
We hold ourselves to high standards, not from outside pressure, but because consistency saves everyone time. In food applications, even slight moisture variations affect bulk storage and packing lines. We take extra steps in packaging—not just using moisture-barrier bags, but purging with inert gases and adding moisture indicators for quality assurance you can check in real time. These decisions grow out of problems we’ve experienced first-hand, not as a marketing strategy.
As regulatory environments shift, so do testing regimens and documentation needs. Pharmaceutical and food authorities around the world have raised the bar on impurity profiles, solvent residues, and trace element controls. Our operation tracks and incorporates changes from the latest editions of international pharmacopeias and food grade agencies. We don’t wait for problems to appear at the customer end. Our production and QC teams conduct ongoing training so every shift stays current on what matters to each industry.
Requests for allergen-free, kosher, and halal grades have grown steadily. These certifications are more than paperwork—they call for strict process segregation and supplier screening. Our site rejected shared equipment with potential allergen cross-contact and devised workflows for traceability. We saw firsthand how a minor slip in documentation can hold up an export, or worse, trigger a recall. By treating every step–from raw input to shipping–as a quality checkpoint, we build trust with buyers who depend on our diligence.
The sustainability movement also shifts market expectations. Buyers want to know where materials come from and how waste is managed. Years ago, our waste stream management focused only on regulatory compliance. Today, we recover heat and recycle process water, which helped cut energy costs beyond what we forecast, and gave our staff buy-in to the broader purpose of our work. Customers have questioned our carbon footprint and traceability. We show them real data— not boasts. Our reclamation processes reduce water intake by more than 50% compared to older mannitol lines. We share these facts because shared challenges spark mutual improvement.
New users sometimes run into processing surprises with mannitol. For tablet makers, mixing with high-fat actives can clump the blend before compression. We advise customers on the right order of ingredient blending and the use of gentle agitation. In liquid suspensions, mannitol’s relatively low solubility means it can settle if agitation is not maintained. Over-concentration produces a hard pack at the bottom of tanks. These are practical problems, not theoretical ones.
Food technologists aiming to replace sugar sometimes overestimate mannitol’s impact on sweetness. Mannitol delivers about half the sweetness of sucrose, so it blends best with other polyols or high-intensity sweeteners. We’ve helped brands tailor their recipes to hit sweetness and texture targets. Trying to cut calories by direct sugar replacement leads to less than satisfying product profiles. Thoughtful blending or staged addition of mannitol into recipes preserves the clean flavor but reaches calorie targets.
Another challenge arises in large-scale handling. Open-air transfer of fine mannitol powder can lead to dust, with losses and operator discomfort. Some customers benefited by switching to our coarser, granular grade for the first stage, blending it with powders just prior to blending or compounding. We supply transfer recommendations and even help retrofit receiving silos to cut dust escape. We don’t stop at supply— we collaborate on day-to-day practicality.
Difficulties in packaging— particularly in tropical or humid locations— have also come up. Mannitol’s low hygroscopic nature is still not absolute; prolonged exposure to moist air eventually leads to caking. Sealed drums with internal liners, desiccant packets, and controlled warehouse environments protect the powder during long transit or storage. We adapt our supply chain to customer realities, not just what we expect at our own plant.
The relationship between manufacturer and user goes far beyond samples and specification sheets. We see common themes among successful product launches— deep technical exchange between our team and the customer’s R&D or process engineers, early sharing of lot-to-lot changes, and feedback on unexpected failures or successes.
Our best improvements started with a direct phone call from a customer, not with a market research report. One client, a confectioner, described a recurring granulation issue that only emerged during long overseas shipments. By bringing technical staff together, we identified vibration during shipping as the culprit and adjusted the packing protocol. The result was fewer product clumps and smoother customer manufacturing runs. We welcome site visits and process audits; our doors stay open so customers can see the process behind every drum or pallet.
We take pride in tracking and controlling process parameters in-house instead of relying on contract toll manufacturing. This approach ensures every lot reflects the documented process, and customers have a transparent window into what arrives at their loading dock. Shared troubleshooting and collaborative product evaluations build trust and solve problems quickly, often before official change notifications become necessary. Our commitment shows in repeat business, not sales pitches.
The story of our mannitol line tracks with advances in process control and automation. Our plant reinvests in updated crystallizers, driers, and real-time monitoring systems. These upgrades came after years of listening to customer pain points around lot variation, unpredictable powder behavior, and downtime in downstream systems. Our capital projects always begin with root-cause analysis of any recurring problem reported by a user.
Upgrades in filtration technology— such as switching to crossflow ultrafiltration— cut impurities sharply and improved whiteness in the final product. Our finishing step now runs under lower temperatures, preserving the crystalline structure and lowering the breakdown risk during tablet pressing. Temperature and pressure precision translate directly to batch reliability. People ask us why we work at this level of detail. The answer is clear: reliable production performance lowers cost for everyone along the supply chain.
We also invest in training for our team. Years spent in the same facility give staff a sixth sense for deviations others might miss. Sight, touch, and even sound play a part in daily operations. A sticking valve, a shift in the pitch of a mixer, unexpected dust at a certain step— these clues help us spot and solve problems before they grow. Staff turnover remains low because skilled employees find meaning in perfecting a process that ends up in life-saving medicines or trusted foods.
Our experience with D-Mannitol points to a clear fact: a manufacturer’s daily choices shape not just product quality, but customer relationships and end-user trust. Every day we learn— from unexpected trends in raw material quality, from feedback on process runs, from new technical standards, and from the creative ways our customers use this product.
We see D-Mannitol as a partnership point with our customers. Through open communication, careful process management, and shared problem-solving, we continue to deliver a product that meets the real demands of today’s market. If you build your business on a stable supply and want a hands-on partner—not just a name on a label—our doors are open. Our D-Mannitol is a result of thousands of hours of work, mistakes, improvements, and shared goals with the industry’s best. This isn’t just another polyol; it’s the backbone of dependable manufacturing.