Citric Acid DC

    • Product Name: Citric Acid DC
    • Chemical Name (IUPAC): 2-hydroxypropane-1,2,3-tricarboxylic acid
    • CAS No.: 77-92-9
    • Chemical Formula: C6H8O7
    • Form/Physical State: White or almost white, granular powder
    • Factroy Site: Aeschengraben 27, Floor 22-23, 4051 Basel, Switzerland
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Jungbunzlauer
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    Specifications

    HS Code

    768724

    Product Name Citric Acid DC
    Chemical Formula C6H8O7
    Appearance White, crystalline powder
    Odor Odorless
    Solubility In Water Very soluble
    Molecular Weight 192.12 g/mol
    Ph Value Approximately 2.2 (1% solution)
    Melting Point 153 °C
    Loss On Drying <1.0%
    Bulk Density 0.70 - 0.90 g/cm³
    Main Application Direct compression tableting
    Assay ≥99.5% (on dry basis)
    Storage Conditions Keep in a cool, dry place
    Cas Number 77-92-9
    Einecs Number 201-069-1

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

    Packing & Storage
    Packing Citric Acid DC is packaged in a 25 kg white, food-grade fiber drum with a tamper-evident seal and clear labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for Citric Acid DC: 25kg bags, 20 metric tons per container, securely palletized to prevent damage during transit.
    Shipping **Citric Acid DC** is typically shipped in sealed, moisture-proof bags or fiber drums to maintain quality and prevent contamination. Packaging usually ranges from 25 kg bags to larger bulk containers. Shipments are handled in compliance with safety regulations, and storage in a cool, dry place is recommended to preserve product integrity.
    Storage Citric Acid DC should be stored in a cool, dry, well-ventilated area, away from moisture, heat, and direct sunlight. Keep the container tightly closed and away from incompatible substances such as strong acids and bases. Store in its original packaging or in containers made from materials resistant to corrosion. Ensure storage areas are clean to prevent contamination.
    Shelf Life Citric Acid DC typically has a shelf life of two years when stored in a cool, dry place in sealed packaging.
    Application of Citric Acid DC

    Purity 99.5%: Citric Acid DC Purity 99.5% is used in pharmaceutical tablet formulation, where it ensures consistent excipient quality and safe ingestion.

    Particle size 100 mesh: Citric Acid DC Particle size 100 mesh is used in direct compression processes, where it improves tablet uniformity and compressibility.

    Moisture content <0.5%: Citric Acid DC Moisture content <0.5% is used in nutraceutical powder blends, where it prevents clumping and preserves blend stability.

    Flowability index >95: Citric Acid DC Flowability index >95 is used in automated tableting operations, where it enhances manufacturing throughput and reduces production downtimes.

    Bulk density 0.8 g/cm³: Citric Acid DC Bulk density 0.8 g/cm³ is used in effervescent granule production, where it optimizes dissolution speed and product homogeneity.

    Stability temperature up to 40°C: Citric Acid DC Stability temperature up to 40°C is used in storage and distribution of finished dosage forms, where it maintains ingredient integrity under elevated temperatures.

    Loss on drying ≤0.4%: Citric Acid DC Loss on drying ≤0.4% is used in oral solid dosage forms, where it supports regulatory compliance and minimizes shelf-life degradation.

    Non-GMO: Citric Acid DC Non-GMO is used in dietary supplement manufacturing, where it meets clean label requirements and supports consumer safety.

    Heavy metals <5 ppm: Citric Acid DC Heavy metals <5 ppm is used in food acidulation systems, where it ensures compliance with international food safety standards.

    Assay ≥99.5%: Citric Acid DC Assay ≥99.5% is used in beverage powder formulations, where it delivers reliable taste profile and maximizes product consistency.

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    Certification & Compliance
    More Introduction

    Introducing Citric Acid DC: Focused on Tableting Performance

    Understanding What Sets Citric Acid DC Apart

    In the world of food, pharmaceutical, and nutraceutical manufacturing, ease of processing can be a bigger challenge than the chemistry itself. Years ago, our team spent countless hours breaking down the tablet defects that plagued so many production lines: capping, chipping, weight inconsistencies, and poor dissolution. Most issues pointed back to the raw ingredients, especially acids. Standard citric acid—usually available as a fine crystalline powder or granulated—just doesn’t perform optimally in direct compression. Granular material tends to dust up, segregate, or resist consolidation under pressure. That’s where years of hands-on work in our blending rooms led us to develop our direct compressible model: Citric Acid DC.

    This specialized grade is not simply citric acid pressed into a different shape. The team examined flow properties at each step—from initial ingredient handling through to the final punch in the tablet press. Every batch relies on neutral, food-safe binders selected not for marketing buzzwords but for how they actually perform on the line. We worked with tableting operators, checking flow rates, blend consistency, and compaction characteristics. The result is a product that flows smoothly, compacts readily, and produces reliably strong, clean tablets across a range of standard machines.

    Specifications Developed One Problem at a Time

    Early in development, we noticed how hydroscopic powders would throw off water activity inside our blending lines. The core specification here is moisture content: our Citric Acid DC targets a low and consistent range, as tighter water control reduces sticking or clumping in tableting hoppers and feeders. Particle size matters just as much. We tune our mesh spec to avoid segregation while still offering enough compressibility. No customer ever asked for a number on a data sheet; they asked for performance at the press, so that drove our mesh and density targets.

    Compressibility and flow are tested lab-batch by lab-batch. That means We don’t just take supplier data at face value; we simulate actual compaction setups using the same presses as our customers—single punch, rotary, or lab-scale pilot plants. If you’re familiar with standard granular citric acid, you’ll find our DC grade needs far less pre-blending: no need to rely on extra glidants or super-disintegrants just to get basic tablet formation with no sticking. Bulk density falls in a range optimized for direct press work, avoiding the low densities that make tablets fragile or the high densities that lead to lamination.

    Intended Uses Backed by Hands-On Experience

    Many producers started asking us to explain where Citric Acid DC fits best. In practice, it shines wherever direct compression saves time, labor, and cost. Chewable tablets, effervescent formats, nutraceuticals, and vitamin blends have all benefitted in actual production runs. Watching how our DC blends hold up in high-speed presses, we’ve seen a dramatic drop in blend rejection rates compared to when operators run classic powder grades. It’s specifically constructed to minimize dusting, which not only helps with air quality but reduces material loss and keeps equipment cleaner.

    Long before “clean label” became industry standard, we sat with regulatory colleagues hammering out which excipients pass muster for food and pharmaceutical use. Our binders and flow agents meet global compendia (USP, EP, JP). No foreign or allergenic additives. We source binders with consistent performance, meeting both stringent purity requirements and the practical demands of high-throughput manufacturing.

    Direct Compression: Real Benefits from Manufacturing Perspective

    Direct compression isn’t just a trend; it’s a real strategy for cutting process times, reducing cycle count, and limiting points of failure in blended formulae. Traditional wet-granulation routes for acid-containing tablets require extra drying steps, specialized granulation binders, and frequent cleaning to avoid batch contamination. We’ve seen with our own eyes that switching to Citric Acid DC clears away a good portion of those headaches. No more grappling with sticky, inconsistent wet mass—just blend and press. The result? Fewer cleaning cycles, higher OEE numbers, and lower batch rejection rates. Our data from several mid-sized nutraceutical customers shows a drop in tablet friability and a rise in overall tablet output after the switch to our DC grade.

    Scale-up surprises often cause the most frustration. In pilot runs, laboratory powders sometimes behave perfectly, but once you jump to a 200- or 300-kilo lot, uneven blends and flow issues can wreak havoc. Our facility moved to Citric Acid DC for its own internal test runs long before releasing it commercially, and we documented the difference right away. Before, employees spent three or four hours cleaning rotary dies; now, the reduction in sticking has dropped that to under an hour per batch. Manufacturing uptime matters—every hour saved can mean one or two extra full batches a week.

    What Goes Into Each Batch Matters Just as Much

    As a chemical manufacturer, raw material control defines everything we do. We won’t source subgrade acids or cut corners on batch release. Weekly raw material sampling by our lab technicians is standard. Each lot goes through physical and chemical analysis: identity validation, purity, moisture, and flow rates. We screen for heavy metals and potential cross-contaminants, especially for pharmaceutical and food-grade applications where purity stands at the front line. Our internal lab technicians test finished lots for functionality; each pass includes compressibility and hardness. No shipment leaves our site until we’ve stress-tested it ourselves with tablet presses, compiled full COAs, and double-checked conformity to customer requirements.

    We recognize that not every plant uses the same compaction parameters or excipient blends, so we maintain tight process controls from the moment citric acid arrives at our site. Automated sifting, humidity controls in the blending suite, and closed transfer systems preserve quality at each stage. No two batches are exactly alike, but our tight QC ensures operators see confidence-inspiring performance from the first drum to the last.

    Key Differences from Conventional Citric Acid Products

    Teams who work the lines quickly notice the difference between standard granular or powder citric acid and Citric Acid DC. Standard grades are made for bulk handling, liquids, or foods—not compressing into robust tablets. Conventional citric acid isn’t designed to carry itself through the punishment of a tablet press or ice cream line where automated feeders can bridge or clog. Even after vigorous sieving, regular acid forms can dust or segregate under vibration, which introduces dose variability in an otherwise tightly regulated process.

    Citric Acid DC contains binders—selected and tested for compatibility, clean taste, and regulatory compliance—making it suitable for finished formats requiring immediate and sustained integrity. Formulators no longer need to reach for an assortment of additives to correct sticking or poor compaction. Our experience shows direct tests of blend flow, compressibility, and stability set this product apart. Uniform granulation comes from not just the raw acid quality, but from how each excipient interacts under pressure and impacts finished tablet friability, hardness, and dissolution rates.

    Incidentally, for producers that have switched away from traditional granulated acid or even spray-dried citric acid, feedback centers on reduction in dust generation during high-speed blending and transfer steps. Lower airborne particulate helps with both operator safety and batch yield, and machinery longevity benefits from less powder accumulation inside hoppers and compression dies.

    Supporting Industry Needs: Feedback and Continuous Improvement

    Staying close to customers means gathering feedback not just from purchase managers, but also production supervisors, maintenance techs, and quality control teams. Over the last decade, process engineers visiting our site brought up segregration—where powders “demix” in transfer lines—as a major cause of batch inconsistency. Citric Acid DC’s particle characteristics counter this, with few fines and more flow-friendly structure. We optimized the blend so operators achieve consistent press fill every time, not just under ideal conditions.

    For effervescent applications, we learned early through several clients that high-purity DC citric acid guarantees more reliable reactivity and easier granule wetting. This reduces foaming variability, speeding up both scale-up and day-to-day production. As a result, our Citric Acid DC now appears in everything from sports effervescents to kids’ vitamin chews, and formulators consistently report lower rejected batch rates.

    Troubleshooting support does not end at dispatch. We often work hands-on with customers during tablet scale-up, reviewing compaction data or adjusting binder content for unusually humid conditions or blends with high-dose actives. We try to solve problems before they ever leave the mixing floor, leveraging our own learning in both large-scale production and small-scale pilot work to make sure nobody on the line loses time to a compressibility or flow issue.

    No Compromises on Product Integrity or Regulatory Compliance

    Plant and QA managers remain keenly focused on regulatory compliance. We source only food grade and pharma grade excipients, and rigorously screen every lot for additive declaration conformity. At every level—raw acid to binder selection—our focus centers on traceability and transparent declarations. We maintain documentation ready for audit, from allergen-free statements to full batch trace records.

    In our early days, we saw the pain that comes if even a single barrel of questionable acid makes it to the compounding area. Now, our release process means direct testing of finished lots and not just certifications on paper. Customers solve compliance headaches with documentation that stands up to scrutiny, regardless of whether product is destined for a chewable vitamin, a sports supplement, or a pharmaceutical line.

    Practical Considerations—Warehouse to Line

    Citric Acid DC arrives packaged to defend against humidity and environmental swings. Our operators experienced fewer caked bags, even in warm and damp warehouse conditions. Palletized drums protect against transit damage, so nothing leaks or breaks open mid-delivery. In day-to-day use, line teams appreciate how each batch pours quickly, blends reliably with a broad range of tableting actives and carriers, and limits the need for long cycle blend times.

    Consider cleaning routines: with Citric Acid DC, the product barely cakes or bridges inside hoppers and gravity feed systems. We traced a 35 percent reduction in manual equipment cleaning cycles after regular implementation in a customer’s effervescent contract facility. Lower cleaning times turn into more shifts devoted to real production, not maintenance.

    Solving Real-World Production Challenges

    One of the consistent complaints from medium and large-scale press operators concerns high dust loads. Over time, using conventional citric acid often meant routine cartridge replacement in dust extraction systems and frequent shutdowns to vacuum out partitioned blending rooms. Since the majority of our DC runs, dusting cut almost by half, and we measured a significant dip in total airborne particulate during weekly air monitoring. Less dust not only improves working conditions but directly affects batch accuracy—every particle that escapes into the air means a little less active in the mix.

    Compaction consistency defines success in any tableting line. Throughout years of hands-on work here and at customer sites, we found that poor-quality acids—ones with variable water content or inconsistent particle size—cause ‘soft spots’ or lamination in tablets. With Citric Acid DC’s targeted specification, blends stay cohesive, resulting in tablets that can take transport, packaging, and consumer handling without loss of integrity. High-moisture, poorly blended acids increase the risk of sticking—fastest route to tablet jams and broken product. We built out our moisture management facilities after the fifth time a customer needed us to reprocess a “slow-flowing, sticky” batch of imported acid that ruined the day’s output.

    Ongoing Research and Reliable Supply

    Our research group continues pilot studies with new binders to further improve compaction profile while minimizing total excipient addition. Some of the best ideas for new blends arise from conversations with production users—every year we review new feedback and test at both lab and pilot plant scale. For certain customers, we customize particle size or adjust the level of binder to meet atypical press or product requirements.

    Supply reliability matters in a globalized world where ingredient disruptions can bring a facility to a halt. We keep safety stocks of raw citric acid and excipients on site, minimizing the need for last-minute substitution or batch blending. Finished goods storage uses humidity-controlled environments to preserve flow and compaction properties until delivery.

    A Manufacturer’s Perspective on Trust and Support

    Building a direct compressible line took years of process trials, failed batches, and hands-on troubleshooting. Every quality or production supervisor knows the pain of a failed batch traced back to an inconsistent ingredient. That experience pushes us to improve every cycle, and we test, mix, and validate in-house before asking anyone else to trust a single kilo in their formula. We welcome visits from customers because transparency in manufacturing wins more trust than any marketing sheet or generic statement. Sharing what we’ve learned—both setbacks and solutions—adds value for the entire tableting and formulation community.

    Citric Acid DC doesn’t just fill a data sheet; it meets production realities. Each new batch builds on years of client feedback, third-party validation, and hard data collected from real lines. We’ve tried nearly every form of acid across dozens of applications, and Citric Acid DC stands out as the most production-friendly, operator-tested, and batch-reliable solution on the market for anyone needing a direct compressible format. This commitment to hands-on troubleshooting, honest communication, and high standards remains at the core of how our team approaches both new developments and daily manufacturing.