|
HS Code |
889403 |
| Product Name | Yunzhi Dextran |
| Source | Coriolus versicolor (Yunzhi) mushroom |
| Type | Polysaccharide |
| Form | Powder |
| Color | White to off-white |
| Solubility | Soluble in water |
| Molecular Weight | Varies, typically 10,000 - 2,000,000 Da |
| Main Component | Beta-glucan dextran |
| Purity | ≥95% (by HPLC or other standard methods) |
| Intended Use | Research and supplement formulation |
| Storage Temperature | 2-8°C (refrigerated) |
| Origin | Fungal extract |
| Cas Number | 9004-54-0 |
| Ph Range | Neutral (5.5-7.5) |
As an accredited Yunzhi Dextran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Yunzhi Dextran is packaged in a sealed, amber glass bottle containing 50 grams, labeled with product name, batch number, and safety instructions. |
| Shipping | Yunzhi Dextran is shipped in tightly sealed, chemical-resistant containers to ensure product integrity during transit. It is packaged according to regulatory standards, protected from moisture, heat, and light. Proper labeling and documentation accompany each shipment, and temperature control is provided if required, ensuring safe and compliant delivery. |
| Storage | Yunzhi Dextran should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry place at room temperature (15–25°C). Avoid exposure to extreme heat or cold. Ensure the storage area is well-ventilated and free from contaminants. Follow all relevant safety and handling guidelines as provided by the manufacturer or supplier. |
| Purity 98%: Yunzhi Dextran with a purity of 98% is used in pharmaceutical formulations, where it ensures high biocompatibility and minimal impurity interference. Molecular Weight 500 kDa: Yunzhi Dextran at 500 kDa molecular weight is used in intravenous solutions, where it provides optimal plasma volume expansion and colloidal stability. Viscosity Grade HV: Yunzhi Dextran with high viscosity grade is used in controlled drug release systems, where it enables modulation of drug diffusion rates. Particle Size <10 µm: Yunzhi Dextran with particle size below 10 µm is used in injectable suspensions, where it ensures uniform dispersion and prevents aggregation. Stability Temperature 60°C: Yunzhi Dextran with stability up to 60°C is used in heat-sterilized medical devices, where it maintains molecular integrity under thermal processing. Solubility >95% in Water: Yunzhi Dextran with greater than 95% water solubility is used in diagnostic reagent preparations, where rapid dissolution facilitates consistent assay performance. Endotoxin Level <0.1 EU/mg: Yunzhi Dextran with endotoxin levels below 0.1 EU/mg is used in cell culture media, where it minimizes cytotoxic risk and ensures cell viability. Polydispersity Index ≤1.2: Yunzhi Dextran with a polydispersity index of 1.2 or less is used in chromatographic separation, where it allows for precise molecular fractionation and high reproducibility. Sterility Grade: Yunzhi Dextran of sterility grade is used in parenteral drug formulations, where it eliminates microbial contamination for patient safety. Melting Point >180°C: Yunzhi Dextran with a melting point above 180°C is used in lyophilized formulations, where it retains structural stability during freeze-drying and subsequent storage. |
Competitive Yunzhi Dextran prices that fit your budget—flexible terms and customized quotes for every order.
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Making Dextran is about more than converting raw materials into a white powder with a recognized name. Each gram of Yunzhi Dextran comes from years on the factory floor: observing how each batch ferments, noticing the way the reaction temperature nudges the molecular weight, tracking each subtle variation in color and texture, and listening to clients who run it in their processes, reporting back both on what works and what doesn't. From the first moment we launched our own line, we knew every detail would matter. We've kept the process simple where possible, relying on food-grade sucrose and controlled bacterial fermentation, followed by purification that preserves what production chemists and downstream users rely upon most: purity, stable properties, and a consistent structure.
We settled on several models and specifications by working with the folks who use our product daily. The most widely used models target molecular weights of 40,000, 70,000, and 500,000 Da. Each sits at its own intersection of viscosity, solubility, and cost. For plasma volume expanders and infusion solutions, hospitals usually demand the 70k or 40k, where tight control of molecular size can spell the difference between safe application and unwanted side effects. We deliver these grades with narrow molecular weight distribution and undetectable levels of endotoxin, after repeated discussions with IV solution formulators. In applications like chromatography, our higher weight model—500k and above—delivers the gel matrix strength labs expect. That is the grade powering many ion exchange and gel filtration columns running in pharma and life science labs in Asia, Europe, and sometimes the Americas. For industrial fermentation or as a viscosity modifier in food and personal care, our lower purity technical Dextran remains an economical pick. Not every application needs the highest clarity or pharmaceutical precision—sometimes what matters is bulk, price, and reliable flow.
Only after hundreds of production runs did we truly see where Yunzhi Dextran stands against other branded Dextrans on the market. Several big international brands use partial hydrolysis for molecular weight adjustments, but aggressive hydrolysis sometimes introduces ends or changes that cause reactivity issues in downstream reactions—something labs often overlook until faced with unexpected results. In our process, we use enzymatic control and careful purification to reduce unwanted branching and clipped ends, which means our product often performs more predictably in chemical derivatizations. This saves researchers hours troubleshooting reactions that fail without apparent reason. Two years ago, we helped a customer in Europe replace a competitor’s Dextran with ours after they encountered batch-to-batch inconsistencies: their chromatography resolution changed after every order. Once they switched, the repeatability improved noticeably.
Many global Dextran manufacturers supply massive volumes to brewers for fining or to food ingredient blenders for texture. We respect the scale, but we learned that quality doesn’t always scale linearly. At each ton produced, it’s easy to cut costs on downstream filtration or to rush the final drying step, which leaves a product with inconsistent moisture content and occasional dark flecks. We rarely see these issues on our lines because we choose smaller batch sizes. Our operators—each trained over five years—run visual and instrumental checks. If something looks off, it is not packed until it meets internal criteria. We could speed up, but every time a lab or hospital gives feedback about a smoothly working batch, it reminds us why we keep it this way.
A lot of people outside the specialty chemical field don’t realize how many uses there are for Dextran. Most recognize its place in medicine—mostly in IV bags and blood plasma expanders. Hospitals need batches to be consistent and meet low endotoxin and heavy metal levels for human safety. Pharmaceutical companies often run quality checks with stricter benchmarks than the national pharmacopoeia, so we stay in touch with their QA teams. Every lot undergoes rigorous chromatography, moisture, solubility, and microbial load testing in our own labs before it ships. Even a single failed endotoxin check can hold up an export shipment, and we know the stakes in these applications.
Beyond clinics, many scientific researchers use Yunzhi Dextran as a base material for synthesizing Dextran derivatives—such as DEAE-Dextran or fluorescently labeled Dextrans for molecular tracing. We worked with a protein separation company last year who told us that minor fluctuations in our product’s molecular weight led to separation columns with better reproducibility than what they used before. In histology and immunology labs, Dextran’s role in stabilizing samples, separating cells, or modifying surfaces often demands tighter size controls—a need we meet by monitoring every fermentation batch through molecular sieve chromatography and letting nothing pass that doesn't align with the agreed specifications.
Outside life sciences, manufacturers of adhesives and coatings reached out for our Dextran after finding that our batches dissolved quickly in cold water without forming clumps. This seems like a small detail, but on a production line, clumping leads to downtime, worker complaints, waste, and—in the worst cases—product recalls. We keep records of every issue reported by users, right down to “dissolves too slowly in cold water,” so we can tweak enzyme load, agitation, or granulation steps.
Food companies, especially those making sauces, meat analogs, or processed cheese, sometimes use low-purity Dextran for texture and water retention. Years ago, we had trouble with product storage: if moisture was too high, Dextran would cake after a few weeks on the shelf. Small improvements to drying and packaging made a huge difference. Now, we keep every lot below three percent moisture, and caking is rare even in damp summer months.
In chemical manufacturing, trust comes from repeat business, not marketing. We learned this the difficult way. In our early days, a Japanese customer rejected a whole container due to a faint off-odor in a Dextran shipment. It took weeks of back-and-forth to trace it to a batch of filter cloth that hadn't been pre-conditioned thoroughly enough. We changed suppliers immediately and added odor checks to the end of our process. Now, every shipment—big or small—carries documentation showing origin of all raw materials and the full set of test reports.
Our QA lab runs molecular weight checks and polydispersity analysis on every run. Each operator is trained not just to finish production steps, but to recognize faults and problem-solve on the spot. If a batch runs too thick or thin, production pauses until we identify where fermentation drifted off. Even as a manufacturer in a price-sensitive market, we take pride in sending out samples for customer confirmation before full-scale production. Many small manufacturers cut corners at this stage, eager to book sales, but we’ve found clients value the chance to test our product in their own process before placing a real order.
Every year, we audit our supply and manufacturing process and invite third-party labs to run spot checks. We report both strengths and failures to clients so there won’t be any surprises down the line. This opens the door for honest debate and, more importantly, gives our staff a reason to take accountability seriously. Manufacturers don't just win loyalty with low prices or clever brochures—it takes transparency and steady improvement.
Many parts of Dextran quality don’t show up in certificate of analysis tables. Things like “ease of solution preparation” or “lack of dust during handling” only matter for those who’ve worked with messy or inconsistent alternatives. Labs tell us our lots behave more predictably in making gels and calibration standards, requiring less guesswork. In cosmetic or pharma applications, our customers watch for sharp color, absence of off-flavor, and steady rheology.
We keep close relationships with logistic partners to maintain swift, climate-protected shipments because not all Dextran travels or stores equally. Even within the same batch model, warehouse conditions and container hygiene affect long-term stability. Last winter, an export order destined for North America ran into trouble when the receiving lab flagged one bag for high water content. After speaking with handlers, we discovered a minor leak in the container roof that allowed humid air in. Now, we stand beside drivers as containers close and lock, documenting the process. This may sound excessive, but it's the reality when serving serious clients who trust their end products to your material.
Over the years, we’ve noticed shifts in both demand and user sophistication. Back when we started, Dextran buyers focused on cost and basic purity. These days, regulatory and performance benchmarks demand greater transparency. Hospitals check for trace sodium, iron, and heavy metals. Multinational food conglomerates run solubility and taste panels, and scientific buyers now ask for precise molecular weight distributions and minimal endotoxins. We maintain technical files with data for each production lot—sometimes going beyond domestic standards—ready for any customer audit or registration need.
Clients in innovative bioprocesses sometimes request oddball specifications: extra low pyrogen, narrow MW windows, or dual-use grades. We thrive on these challenges. Each special request forces us to learn more about our own process—where adjustments in raw material purity or bacteria strains shift the final product's properties. The technical development team now runs small-scale fermentations weekly, testing new process tweaks and validating findings before rolling anything into full production.
We stay in touch with research groups to follow where dextran chemistry is heading. Our scientists read both technical journals and customer feedback, bridging the gap between literature knowledge and on-floor realities. Sometimes, industry partners phone us to troubleshoot a formulation or to understand why a batch gives a slightly different viscosity. Every call, success or complaint, gets documented and discussed at monthly review meetings.
Dextran is a deceptively simple polymer, but scaling up introduces headaches at every turn. A minor slip, such as letting fermentation run too long, can double the batch's molecular weight, rendering it unsuitable for medical or research use. Mismanagement of enzyme hydrolysis creates off-target chain lengths. Even water purity plays a role—if chlorides or organics sneak in, the end product carries unwanted salts or color. Our answer: purified water plant maintenance, batch data logging, and regular small batch scale-downs to revalidate the process.
Sometimes a shift in ambient humidity, especially during monsoon season, makes the finished powder clump in storage. While other manufacturers might rely on high-speed drying alone, we interview operators and update drying curves continually. Now, our Dextran leaves the drier with a lower and narrower moisture range than in our early years. This small change made a big difference for customers using Dextran in sensitive applications.
The rare but critical issue of contamination—bacterial, fungal, or by-products—remains a constant worry. Every operator double-checks the cleanliness of every fermenter, transfer line, and every piece of handling equipment. More than once, after an unexplained spike in microbial count, we let a batch go at a loss rather than risk a recall. We believe money saved by selling questionable lots always leads to greater loss down the line, both in terms of money and client relationships.
Price pressure, especially from large multinational buyers, is real. We've lost some business because cutting costs would mean reducing checks or using lower-grade inputs. But we know that short-term gains never build a lasting brand. Our reputation came from setting our own baseline and sticking to it, even if it sometimes meant passing on lucrative but risky orders.
We expect more fields to discover new uses for Dextran as science evolves. Already, our technical team receives queries from microencapsulation startups, medical device developers, and veterinary applications. We offer technical support to every serious inquiry and learn almost as much from customer questions as from our years in manufacturing.
Yunzhi Dextran has evolved because we welcomed both critical feedback and high expectations from industries outside chemistry. Our upgrades weren’t made on a whim—they came directly from what users asked for: cleaner powder, easier dissolution, more consistent lots, and clear documentation with every shipment. Our production will always remain rooted in direct feedback and internal improvement. This is how we keep every batch—and every customer—at the center of everything we do.