Products

Ascorbic Acid DC Granule 90

    • Product Name: Ascorbic Acid DC Granule 90
    • Chemical Name (IUPAC): (5R)-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxyfuran-2(5H)-one
    • CAS No.: 50-81-7
    • Chemical Formula: C6H8O6
    • Form/Physical State: Granule
    • Factroy Site: No. 1, Qiyuan Avenue, Wangyuan Industrial Park, Yongning County, Ningxia
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Ningxia Qiyuan Pharmaceutical Co., Ltd
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    Specifications

    HS Code

    570410

    Product Name Ascorbic Acid DC Granule 90
    Chemical Name Ascorbic Acid
    Appearance White to off-white granular powder
    Vitamin Content Approximately 90% Ascorbic Acid
    Solubility Freely soluble in water
    Granule Size Typically 12-60 mesh
    Application Used in direct compression tablet manufacturing
    Cas Number 50-81-7
    Stability Stable under recommended storage conditions
    Storage Conditions Store in a cool, dry place, protected from light
    Bulk Density 0.60 - 1.00 g/ml
    Country Of Origin Varies by manufacturer
    Packaging Usually packed in 25 kg fiber drums

    As an accredited Ascorbic Acid DC Granule 90 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ascorbic Acid DC Granule 90 is packaged in a 25 kg fiber drum lined with double polyethylene bags to ensure freshness and protection.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Ascorbic Acid DC Granule 90, packed in 20kg/carton, total 10 MT (500 cartons) per container.
    Shipping **Shipping Description:** Ascorbic Acid DC Granule 90 is packaged in sealed, moisture-resistant containers or fiber drums, typically lined with food-grade polyethylene bags. The product is shipped in compliance with relevant safety regulations, protected from light, heat, and humidity to preserve quality. Handle with care to avoid damage and contamination during transport.
    Storage Ascorbic Acid DC Granule 90 should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of heat. Keep the container tightly closed and protected from contamination. Store at temperatures below 25°C to preserve stability and prevent degradation. Avoid storage alongside incompatible materials, such as oxidizing agents, to ensure product quality and safety.
    Shelf Life Ascorbic Acid DC Granule 90 typically has a shelf life of 24 months when stored in a cool, dry, and sealed condition.
    Application of Ascorbic Acid DC Granule 90

    Purity 90%: Ascorbic Acid DC Granule 90 with 90% purity is used in direct compression tablet formulations, where it ensures high vitamin C content and consistent dosage.

    Particle Size 100-200 μm: Ascorbic Acid DC Granule 90 with particle size 100-200 μm is used in chewable vitamin tablets, where it provides excellent mouthfeel and uniform blending.

    Moisture Content <2%: Ascorbic Acid DC Granule 90 with moisture content below 2% is used in high-speed tablet manufacturing, where it minimizes caking and enhances product stability.

    Flowability: Ascorbic Acid DC Granule 90 with superior flowability is used in automated filling lines, where it reduces production downtime and increases throughput consistency.

    Stability Temperature up to 40°C: Ascorbic Acid DC Granule 90 stable up to 40°C is used in tropical climate packaging, where it maintains its potency during storage and transportation.

    Disintegration Time <10 min: Ascorbic Acid DC Granule 90 with rapid disintegration time under 10 minutes is used in effervescent tablets, where it ensures quick nutrient release and optimal bioavailability.

    Bulk Density 0.60 g/cm³: Ascorbic Acid DC Granule 90 with a bulk density of 0.60 g/cm³ is used in compact tablet design, where it supports precise dosing and space-efficient packaging.

    Compressibility Index <15%: Ascorbic Acid DC Granule 90 with a compressibility index below 15% is used in high-speed rotary presses, where it leads to smooth tablet production and minimal weight variation.

    Loss on Drying <0.5%: Ascorbic Acid DC Granule 90 with loss on drying less than 0.5% is used in pharmaceutical applications, where it guarantees long shelf-life and prevents degradation.

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    Certification & Compliance
    More Introduction

    Ascorbic Acid DC Granule 90: Shaped by Reliability and Precision Manufacturing

    For decades, ascorbic acid—commonly known as Vitamin C—has proven itself as a foundation for health, nutrition, and food technology. From our position in chemical manufacturing, trends in direct compression technology have given our Ascorbic Acid DC Granule 90 a place in the hands of both formulators and production specialists who value consistency, ease of handling, and a well-calibrated performance profile. Each granule results from the hard work of process engineers and technicians refining granulation, drying, and particle size control so processors have something dependable to work with—never powdery, never caking, even in large-scale batch environments.

    Purpose and Development Process

    Ascorbic Acid DC Granule 90 entered our portfolio after extensive customer requests for improved performance in tablet and supplement production. Our powder-grade ascorbic acid serves well for many traditional processes, but compromise creeps in when machinery demands exact flow rates and non-dusty feeds. Producers face machine jams, inconsistent tablet weights, and rework. These problems cost both time and material. Direct compression brings clear advantages, and our granules answer this by maintaining compressibility and steadily releasing the active ingredient—free of binders that may muddle label declarations.

    We reformulated specifically for direct compressibility. Through careful adjustment of moisture content, granule size distribution, and carrier selection, finished DC Granule 90 strikes a balance between strong mechanical binding in tableting and speedy dissolution. Granulation happens under strict hygienic design, with sieves and blending systems that respect particle integrity. Customers notice the difference at the press: batches move faster, waste drops, and finished tablets display sharp breaks with minimal friability. Engineers working on the tablet line report fewer stoppages and more predictable output values.

    How It Differs from Standard Ascorbic Acid Powder

    The story in our factory stretches beyond differences picked up on a product data sheet. Several times a year, food supplement companies visit to discuss scale-up headaches. Standard ascorbic acid powder behaves unpredictably in high-speed settings. Particles cake into augers and hoppers. Dust clouds lead to sanitation headaches, component loss, and occupational health complaints. Agglomeration attempts in-house usually lack process controls and fall short in stability testing.

    Our engineering staff address “flowability”—a telling metric in manufacturing—through particle size measurement and angle of repose testing. DC Granule 90 clears these hurdles where ungranulated materials cannot. Each lot receives hands-on assessment and mechanical flow testing using rotary feeders and tablet presses that mirror real-life industry conditions, not just laboratory setups. This is why, compared to a standard USP ascorbic acid powder, DC Granule 90 passes straight into the mixer or compression line, sidestepping the extra step of pre-processing or wet granulation.

    Practical Application in Nutritional Supplements

    Customers building chewable tablets, effervescent tablets, and high-dose vitamin cores rely on predictable blend behavior. Pharmaceutical grade, solvent-free, and manufactured in an FSSC 22000-certified facility, our DC Granule 90 responds directly to calls for clean label support. Production technicians report blending times that drop by as much as 40%, and mixing uniformity that reflects in tighter assay results.

    One site manager for a mid-sized vitamin line described a transition from ascorbic acid powder to DC Granule 90: dust levels in the air dropped below detection thresholds, routine line cleaning became less frequent, and batch yields improved measurable by several kilograms per shift. Since powder has a habit of stratifying in blenders and settling in V-mixers, tablets produced with powder often show weight and potency differences from start to finish of a batch. DC Granule 90 resists this “segregation” thanks to its optimized granule dimension and narrow size range.

    Effervescent tablets take benefit from the low moisture and non-hygroscopic nature of our granules. Some effervescent recipes incorporate sweeteners and bicarbonates fragile to moisture pick-up; granules with controlled water content protect stability, extend shelf life, and keep the dissolution experience sharp. Flavor masking improves, bitterness readjusts, and consumers receive a finished product free of grittiness—the direct result of years calibrating our granulation system.

    Food Fortification and Process Challenges

    In the fortification of cereals, beverages, and dairy replacement drinks, food engineers use our DC Granule 90 for its dust-free handling and stable dispersion. In extrusion, rotary mixers, or ribbon blenders, a consistently sized granule simplifies dosing and scatter. Large-scale beverage powder filling lines—especially those deploying automated augers—show less product build-up and practically no bridging. Our production supervisors find that most end users gain efficiency, loss through “product on the floor” drops, and batches reach labeled content with less risk of overage or underage. Process control tickets reflect fewer deviations, which is what quality departments and auditors need to see.

    Cereal manufacturers push for rigorous fortification levels and tight GMP controls. Direct compression granules withstand thermal stress better than powder in puffed cereal lines, keeping vitamin content on target through the process. Uniform coating on each cereal piece means improved nutritional declaration and fewer customer complaints about hot spots or invisible dosing. Dairy alternative brands use the granule for high-acid applications, where flow characteristic and resistance to caking overcome sticky messes and line downtime.

    Granule Structure and Manufacturing Oversight

    As a manufacturer, we tune particle size and distribution carefully. Each batch passes through calibrated screens, laser diffraction testing, and angle-of-repose analysis. Customers mustn’t fight blockages in capsule fillers or rotary presses. Practically speaking, our batches run within 90% (w/w) ascorbic acid content, using a food-grade excipient matrix that does not introduce major allergens or animal derivatives. Our lab does not just report potency; it monitors carrier integrity, possible degrading trends over time, and non-visible process residues. X-ray fluorescence and rapid moisture analyzers guide every release.

    We draw on decades of granulation science: too hard, and granules fail to break down and dissolve; too soft, and they revert to a dusty powder under pneumatic transfer. The final product descends as a free-flowing, robust granule, neither clumping in summer humidity nor scattering at the first mix.

    Supporting Consumer Health and Regulatory Confidence

    As ingredient trends shift toward clean label and transparency, our customers seek reliable, traceable supply chains and a finished ingredient that can be labeled honestly. Our DC Granule 90 represents a commitment to single-site manufacturing, documented traceability, and full audit support. Nutrition brands worried about consumer trust look for suppliers that audit the process—not just for heavy metals or microbial content, but also adulterants and cross-contaminants. Finished granules arrive with lot-based documentation detailing not just certificate of analysis but also allergen declarations, processing aids usage, and full trace mineral analysis where required.

    In regulatory inspections, auditors often focus on granule consistency and process repeatability. Our operations team runs batch records past experienced QA managers and third-party inspectors. If a lot falls outside the published specifications for flow, particle size, or ascorbic acid content, it doesn’t leave the site. This commitment reflects industry best practice and a deep respect for consumer safety. It’s not just about compliance—product reputation and public health ride on these controls.

    Meeting Market and Customer Needs

    Over the last decade, trends like vegan supplements, sugar-free health tablets, and compact effervescent drink tabs have pushed manufacturers to adapt. Our development chemists partner closely with both startups and established brands in North America, Europe, and Asia. They bring feedback from warehouses, filling rooms, and mixing halls straight back into our process rooms. If a granule batch sticks or segregates in their plant, our production staff adjust drying rates, sifter mesh sizes, or screening duration. This iterative loop keeps granule quality improving year over year.

    From experience, we know many customers choose DC granules specifically to replace manual pre-mixing and add safety to their plant environments. Notebook logs show a marked drop in reported slip hazards and airborne dust alarms after switching from powder to granule. Each year, plant managers send us incident logs highlighting a double-digit reduction in cleanup events and operator complaints once they make the switch. Over time, this becomes more than an ingredient difference—it influences site culture, worker safety, and overall throughput.

    Difference versus Agglomerated and Coated Vitamins

    Not every granulated ascorbic acid product on the market offers identical results. Some grades focus primarily on agglomeration or use heavy binders to create coarse granules that resemble sugar pearls. We’ve benchmarked DC Granule 90 against these coated and agglomerated types, and our trials show a better balance between compaction and dissolution rate. Binders can hinder solubility and cause off-flavors in chewables and fizzy drinks. DC Granule 90 harnesses a low-excipient matrix, keeping label declarations straightforward and ingredient count low.

    Our QC analysts regularly run side-by-side tests of DC Granule 90 against imported, non-direct compression grades, including coated types aimed at stability. Finished tablets from these alternatives tend to dissolve slower and sometimes display inconsistent vitamin C release kinetics in dissolution tests. Production managers working with effervescents or multivitamins come back to DC Granule 90 for faster blend times, cleaner taste, and a record of successful audits from both domestic and global regulators.

    Integration With Automated Equipment

    Modern tablet and sachet lines don’t forgive inconsistent ingredients. From high-speed slant feeders to precision sachet fillers with vision inspection, plant machinery finds every flaw in powder handling. Equipment calibration in our own pilot plant found standard powder introducing variability into feeder mechanisms during continuous runs. DC Granule 90, shaped through regular particle profile checks, moves smoothly through screw feeders, bowl blenders, and vibratory weighers. Factory logs show a clear reduction in downtime attributed to bridging, arching, or slow refill rates once DC Granule 90 entered production workflows.

    Field engineers relay the same data: filling lines switch from frequent monitoring and adjustment with powder to mostly hands-off with DC granule. This allows operators to focus on other value-added tasks—line safety, documentation, or early identification of upstream problems.

    Shelf Life Assurance and Packaging

    Granules with unstable water content can trigger rapid spoilage or loss of activity. Our production follows tightly controlled drying steps with atmospheric monitoring and rapid loss-on-drying analyzers. Every package ships in low-permeability, food-grade bags, tested for permeability against oxygen and water vapor. We add nitrogen flushing and vacuum sealing as needed for sensitive destination climates or longer logistics chains. Stability studies support long shelf life under room temperature and warehouse conditions, protecting downstream production schedules from last-minute ingredient changes.

    Production runs match customer forecasts so ingredient remains as fresh as possible. Warehouse staff take pride in seeing low returns and minimal loss claims—each shipment reflects cumulative improvements in plant discipline.

    Adapting to Clean Label and Sustainability Demands

    Clean label demands challenge manufacturers to simplify additives and present fully traceable sources. DC Granule 90 moves through our facility under batch-specific tracking, and every auxiliary ingredient—carrier, flow aid, or processing material—receives annual certification to food grade or higher standards. Users seeking plant-based or animal-free inputs can access our annual traceability documentation, showing non-GMO, non-animal, and gluten-free status backed by third-party audits and internal GC-MS screening. Our production lines avoid common allergens and cross-contact materials to reduce risk for customers targeting regulated EU, North American, and Asia-Pacific markets.

    On the environmental side, engineering managers monitor energy usage per batch, water discharge, and emissions metrics. Our process improvements focus on minimizing granulation wash water and recycling process air through specialized filters. Each season, operational upgrades and process audits shave points off our energy and material use per kilogram produced. This, in the long run, insulates both us and our customers from volatile raw material prices and environmental scrutiny.

    Reactive Process Improvement and Future Direction

    Every feedback call or incident trace leads back to production. We run ongoing training and process simulations using feedback from high-throughput manufacturing partners. If a customer flags clumping, delayed discharge, or flavor interaction, our team dives to root cause. Adjustments may follow—shifting excipient ratios, optimizing the drying curve, or updating carrier selection to avoid cross-reactivity with flavors or actives. In rare cases, site-based trials run at customer premises, closing the loop between bench, pilot, and full-scale production.

    Looking ahead, pressures on both ingredient transparency and automated processing lines continue to grow. We invest not only in expanded pilot plant facilities but also in digital process tracking, so each lot of DC Granule 90 tells a story from its raw material entry all the way through to the shipping dock. AI-driven particle imagery and near-line moisture sensors feed real-time corrections, and operators take pride in running some of the tightest tolerance margins in the market.

    Summary Insights from the Manufacturing Floor

    DC Granule 90 has a story that stretches far beyond specification sheets and catalog descriptions. Its gains stem from relentless process refinement, a close listen to customer experience, and technical advances inscribed in every shipment. Every bag reflects lab technicians, process engineers, QA staff, and supply planners whose discipline bridges the gap between chemical science and practical outcomes. From our view as a direct manufacturer, a good granule saves more than labor; it keeps promise to customers and, ultimately, delivers measurable value in every bottle, blister, or mix it touches.