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Cichorioside D

    • Product Name Cichorioside D
    • Alias Taraxasteryl caffeate
    • Einecs 1221170-18-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    633632

    product_name Cichorioside D
    CAS_number 142108-70-1
    molecular_formula C22H28O12
    molecular_weight 484.45 g/mol
    appearance White powder
    source Cichorium intybus (chicory)
    solubility Soluble in methanol, ethanol, and DMSO
    purity ≥98% (HPLC)
    storage_temperature -20°C
    chemical_class Sesquiterpene glycoside
    IUPAC_name (2R,3R,4S,5S,6R)-2-[[(1S,4R,5S,6R,7S,10S,11S)-4,5-dihydroxy-10,11-dimethyl-3,7-dioxatricyclo[5.3.1.0^{1,5}]undecan-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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

    Packing & Storage
    Packing Cichorioside D, 10 mg, is supplied in a sealed amber glass vial with a tamper-evident cap and clear labeling.
    Shipping Cichorioside D is shipped in compliance with all applicable chemical regulations. The compound is securely packaged in airtight, chemically resistant containers to ensure stability and prevent contamination. It is dispatched via trusted carriers, with appropriate documentation, safety labeling, and temperature controls as required for safe transport and prompt delivery.
    Storage Cichorioside D should be stored in a tightly sealed container, protected from light and moisture, at a temperature of 2–8°C (refrigerated conditions). The chemical should be kept in a well-ventilated area, away from incompatible substances. For long-term storage, it is recommended to keep it in a desiccator to prevent hydrolysis and maintain its stability.
    Application of Cichorioside D

    Applications of Cichorioside D in Industrial Manufacturing

    Cichorioside D, a bioactive compound extracted from Cichorium species, finds use in specialized industrial sectors due to its distinct functional properties. As a direct manufacturer, we supply this ingredient to regulated downstream processes that require strict compliance, reliable sourcing, and defined formulation procedures. Below we detail selected real-world application pathways based on current industrial practices.

    1. Pharmaceutical Ingredient for Hepatoprotective Tablet Formulations

    Pharmaceutical manufacturers incorporate this compound in liver health tablet products, leveraging its recognized properties for hepatoprotective functions. Its use is strictly controlled within prescription and over-the-counter segmentations, requiring cGMP validation, batch traceability, and compliance with global pharmacopoeias. Formulation chemists typically blend the compound with standardized excipients, integrating it during the wet granulation phase to ensure uniform distribution. Release testing must confirm both identity and content uniformity before downstream high-speed tablet compression. Final tableted medicines undergo full QC before market release to hospital chains and pharmacies.

    Industry compliance standards

    • USP–NF (United States Pharmacopeia–National Formulary)
    • EP (European Pharmacopoeia)
    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • China Pharmacopoeia Appendix guidelines for herbal extracts

    Typical usage ratio

    • 0.1–0.5% w/w of total tablet weight; adjustment guided by desired daily dosage per regulatory maximums for herbal actives

    Downstream process integration

    • Integrated during powder blending prior to granulation
    • Incorporated into binder solutions for wet granulation
    • Subjected to in-process analytical verification at each critical stage

    Final product types

    • Standard coated and uncoated tablets for liver support applications
    • Herbal prescription capsules

    2. Botanical Additive for Functional Beverage Concentrates

    Major beverage processors utilize the extract as a botanical additive in health-positioned drink bases, requiring precise titration for regulatory and sensory compliance. Ingredient handling follows food-grade GMP workflow, with dosing controlled per FDA and EFSA food additive guidelines. The extract is dissolved into concentrate tanks post-filtration, under agitation to promote homogeneous dispersion. Testing for pesticide residues and heavy metals is mandatory before the additive reaches the beverage blending stage. Ready-to-drink health beverages and syrup concentrates are then pasteurized and filled under HACCP-monitored operations.

    Industry compliance standards

    • 21 CFR Part 110 (Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food)
    • GB 2760 (National Food Safety Standard for Food Additive Use, China)
    • EU Regulation No 1333/2008 (Food Additives)
    • FSSC 22000 (Food Safety System Certification)

    Typical usage ratio

    • 30–150 mg per liter in beverage concentrate, tailored by sweetness profile and functional label claims

    Downstream process integration

    • Dissolution in mixing tanks after primary filtration of raw base
    • Allocated to final blend just prior to stabilization and filling
    • Batch tested for botanical marker content pre-release

    Final product types

    • Functional wellness beverages in PET or glass bottles
    • Dietary supplement concentrates

    3. Nutraceutical Capsule Production for Digestive Health

    Encapsulation lines in nutraceutical manufacturing facilities use the ingredient for digestive supplement products, requiring high purity and allergen-free certification. Handling protocols mandate full ingredient traceability and adherence to supplement GMPs. Integration occurs after micronization for consistent powder size, followed by tumble blending with other botanical actives. This approach ensures fill accuracy and dissolution profile within hard gelatin capsule shells. QA protocols verify microbiological load and purity prior to, and after, encapsulation.

    Industry compliance standards

    • 21 CFR Part 111 (Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements)
    • ISO 22000 (Food safety management systems)
    • NSF/ANSI 173 (Dietary Supplements)
    • AHPA Guidance for Botanical Identity

    Typical usage ratio

    • 50–200 mg per 500 mg capsule; actual use rate aligns with market dosage norms and clinical trial protocols

    Downstream process integration

    • Dosed post-pulverization via precision auger feeding
    • Blended with excipients for flow and fill optimization
    • Quality checked for uniformity per batch-lot

    Final product types

    • Digestive health blend capsules
    • Multi-botanical GI support supplement pills

    4. Cosmetic Ingredient for Plant-Based Skincare Emulsions

    Personal care product developers utilize the extract for botanical skincare applications targeting sensitive and hypoallergenic claims. Ingredient acceptance requires conformance to INCI listing, REACH registration, and safety data validation. Cosmetic chemists introduce it during the cooling phase in emulsion tanks to protect its phytochemical integrity. QC control points focus on verifying stability in sunscreen, serum, and lotion matrices, with reference to standardized botanical content. Downstream filling lines demand particle-free and allergen-cleared ingredient supply for long-shelf skincare launches.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 (Cosmetics Product Regulation)
    • Cosmetic Ingredient Review (CIR) safety assessments
    • INCI (International Nomenclature of Cosmetic Ingredients) labeling
    • ISO 22716:2007 (Cosmetic GMP)

    Typical usage ratio

    • 0.05–0.2% by weight of the aqueous phase, adjusted by emulsion stability tests and safety data

    Downstream process integration

    • Added post-emulsification at sub-40°C to preserve bioactivity
    • Dissolved in glycerol or aqueous phase prior to homogenization
    • Subjected to finished product stability and patch testing

    Final product types

    • Facial lotions for sensitive skin
    • Plant-extract moisturizing creams
    • Natural cosmetic emulsions
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    Certification & Compliance
    More Introduction

    Introducing Cichorioside D: Unlocking Potential From Natural Sources

    In a facility shaped by decades of extraction chemistry, Cichorioside D stands as both a challenge and a point of pride. Our team has worked directly with the roots, leaves, and stems of Cichorium intybus, bringing together technical know-how and persistent problem-solving to achieve high-purity isolates on a commercial scale. Extracting Cichorioside D serves as a reminder that chemistry is as much art as it is science. Insiders know: not every batch of chicory extract delivers the same complexity or yield. That kept us vigilant during scale-up. Our technicians monitor each phase—from solvent choice to filtration temperature—to avoid isomerization and degradation that can quietly ruin a distillation. We also dedicate a section of our plant to high-performance liquid chromatography, since that’s the most reliable path for a clean separation from the other cichoriosides in chicory.

    Raw Material and Extraction: Lessons Learned

    Starting with the right material means everything. Wild chicory roots and commercially grown strains show surprising variability. We’ve learned the best harvest happens just before flowering, when glycoside concentrations peak. Cutting at the wrong stage leaves more non-target compounds to clean up. Sourcing has also demanded persistence, as supply-chain interruptions (including unpredictable weather and local regulations) can affect consistent availability. Standardized contracts with farmers and full-process traceability now provide a backbone for scaling up production safely and sustainably.

    After years of batch development, we now rely on a sequential solvent-extraction process. Water extraction leaves out substantial unwanted polysaccharides, while a refined ethanol fractionation achieves a balance between solubility and selectivity. We’ve found this sequence preserves the native structure of Cichorioside D, which is essential for downstream applications. Our choice of solvents, extraction temperature, and agitation speed comes from hundreds of experimental runs to minimize breakdown of the glycosidic bonds.

    Purity and Quality Checks

    High-purity Cichorioside D is measured not just in numbers but in how batches behave under stress. Microbial control starts on the loading dock, where raw root deliveries face immediate quality checks. As technicians, we keep an eye out for spoilage or excessive soil content, which can sneak microbial contaminants past hasty inspections. Our consistency hinges on preventing introduction of spore-forming bacteria during milling.

    Beyond routine purity checks, solvent residues and heavy metal content receive extra scrutiny. Industry standards have grown stricter over the last decade, reflecting a deeper understanding of how trace contaminants affect finished products. Every operator in our plant knows the protocols for sampling, record-keeping, and cross-checking. Each lot gets a full workup: NMR and MS spectra to confirm molecular structure, HPLC chromatograms to verify purity, and a certificate summarizing the findings.

    Structural Features: The Value of Cichorioside D

    Cichorioside D belongs to a complex family of sesquiterpene glycosides. Our lab has shown that isolating the correct stereoisomer brings a distinct functional profile. Many manufacturers overlook this, letting isomeric mixtures slip through with vague labeling. We take the time to confirm identity, because the wrong diastereomer can change a customer’s outcomes—sometimes subtly, sometimes drastically. Our in-house team runs comparative studies to ensure product integrity with every lot.

    Structurally, Cichorioside D offers more than the common cichorioside C—an extra oxygenation site and a distinct sugar moiety. These differences play out during application development. Our clients have reported improved stability in test formulations and more predictable dose-response relationships compared to other cichoriosides. Structure-activity explorations by academics and industry labs back up the same trends.

    Comparing Cichorioside D and Other Plant Glycosides

    Markets for natural glycosides are crowded with names: steviosides, glycyrrhizins, and other chicory derivatives. Product differentiation can be subtle. We often field questions about why one should choose Cichorioside D over a more familiar glucoside.

    Experience tells us the answer lands in two places: functional properties and extract stability. Most glycosides, such as steviol glycosides from Stevia, show a pronounced sweetness profile. Cichorioside D, in contrast, brings a nuanced bitterness often sought in research on anti-inflammatory or hepatoprotective agents. Its molecular backbone has shown compatibility with both lipophilic and hydrophilic carrier systems, making it easier to incorporate into advanced formulations.

    Compared to the more abundant cichorioside C, D’s additional side chain offers a different pharmacological footprint. In laboratory tests, we’ve seen that batch-to-batch variance is lower for D when using our extraction protocols, compared to the less stable C fraction, which tends to degrade faster in both solution and powder forms. This stability attracts researchers designing shelf-stable products for nutraceuticals and functional foods.

    Applications and Usage—Insights From Real-World Practice

    Cichorioside D has found traction among manufacturers seeking to move beyond basic flavoring or sweetening. Its consistent profile appeals to those developing products for health applications. Our partners in the nutraceutical sector have explored Cichorioside D as a bioactive in liver-support blends and anti-inflammatory complexes, leveraging both its bitterness and the evidence for beneficial biological interactions.

    Pharmaceutical inquiry has ramped up, as researchers identify new pathways where sesquiterpene glycosides interface with cellular antioxidant and immune responses. Recent studies highlight a role for Cichorioside D in modulating cytokine expression in vitro—hints that drive formulation scientists to experiment with inclusion rates in pilot projects. Having access to a reproducible supply, with full traceability, allows them to work through those innovations without bottlenecks.

    Formulation Challenges: Lessons From the Lab

    Few glycosides integrate seamlessly into every base. Our R&D technicians routinely field calls about solubility curves, interaction with surfactants, and how varying pH affects appearance and taste. Experience says: test each batch by the same method as your final formula. We keep a library of physical-chemical data tailored to the solvents and excipients most common among supplement developers and beverage formulators.

    Cichorioside D never dissolves as quickly as a pure simple sugar; dispersion often calls for slow incorporation and agitation. Some developers prefer forming inclusion compounds or using microencapsulation to mask bitterness and stabilize the sensitive glycosidic linkage. Extended exposure to strong acids or high heat risks hydrolysis, a fact that moved us to recommend neutral processing conditions for liquid formulations.

    Over the years, feedback has shown that compatibility with certain polyols, proteins, or food acids is more favorable for Cichorioside D than for less structurally complex glycosides. Formulators often praise its resilience under light and oxygen stress, qualities that offer longer shelf life for finished products. As users troubleshoot solubility or stability, we’ve learned to share full historical context, not just a technical bullet point.

    Environmental Responsibility and Sustainable Sourcing

    Cultivating a specialty extract doesn’t only mean meeting specifications—it brings questions about land use, agricultural impact, and responsible disposal. Our production team took early steps to work with chicory growers who rotate their fields and limit use of chemical inputs. We train sourcing managers in fair-trade expectations, ensuring that upstream labor standards match the rigor we apply to our lab controls.

    Water use and extraction waste remain top concerns for chemists and regulators alike. Our process recycles the bulk of solvent streams through on-site distillation. Spent chicory material goes as biomass to local composting rather than landfill. Measuring carbon footprint for each batch now shapes both internal decisions and what we tell our customers.

    Batch Consistency: Keeping Promises in a Growing Market

    Cichorioside D’s market keeps expanding, but reproducibility and batch-to-batch uniformity turn out to be more challenging than outsiders suppose. It’s easy to promise a 98 percent pure product; it’s much harder to actually deliver, month after month, especially as source botanicals shift profile through each season.

    We keep a historical archive of production data, letting us spot trends in yield, color, or solubility before they become problems. Lab managers track every deviation and initiate a full trace if analytical checks suggest a drifting profile. Our customers view these efforts not as window dressing, but as evidence we take process discipline seriously. The marketplace always tests the honesty of a supplier’s claims sooner or later.

    Regulatory and Market Considerations

    Innovation depends on regulatory awareness. In-house compliance specialists follow updates in food and supplement regulations across export markets. Document packages for Cichorioside D now anticipate country-specific requests for purity, origin, and allowed usage categories. This facet eats up significant time and resources, but any real manufacturer knows oversight never goes away.

    Adapting to evolving regulations often shapes how we label and how we process. For example, residue limits for organic solvents have tightened. We recalibrated solvent recovery stages twice in the last five years because regulatory advice—often driven by new toxicological studies—keeps moving the goalposts. These changes lead up and down the value chain, affecting both raw material suppliers and customers seeking certified clean-label ingredients.

    Customer Feedback: The Final Checkpoint

    As a chemical manufacturer, feedback loops don’t end with a product’s sale. Formulators, researchers, and brand owners share their experiences in real time. Success stories and setbacks travel through our sales and technical support desks, returning to the R&D team for diet corrections. One lesson stands out: assumptions from laboratory development break down easily during full-scale production.

    The question most frequently asked—how does Cichorioside D differ from its relatives—finds new answers as customers trial the extract in finished products. We hear about improved tolerance in capsule blends and reduced color change in emulsified beverages. Some clients have learned to pair Cichorioside D with botanicals that enhance its functional profile. Others note its flexibility as a standard for quantification studies, due to its stability over time compared to more reactive glycosides.

    Problems arise, too. Solubility in cold beverages takes patience and technique. Formulations using acidic preservatives occasionally report breakdown of glycoside bonds unless pH is closely managed. Faced with these challenges, our technical staff collaborates directly with client labs, sharing data and tips from years of troubleshooting cycles.

    Looking Ahead: Opportunities and Optimism

    We see Cichorioside D continuing to attract scientific and market interest. As the evidence base grows, new uses keep emerging: bioactive inclusion in skin-care, novel functional food design, and experimental drug discovery projects. Our front-line team stays ready for surprises, contributing in real-world problem-solving that shapes next-generation applications.

    Developing, refining, and supplying Cichorioside D has taught us to balance consistency with innovation. All the best technical planning in the world means little if it doesn’t meet the evolving needs and standards of the research and health product sectors. We stake our reputation on the reliability of our methods, the transparency of our production practices, and a willingness to roll up our sleeves alongside customers solving tough formulation puzzles.

    Manufacturing this product means accepting that every day brings new questions—from both inside and outside our company. We see that as a privilege, not a burden. Those questions drive us to stay honest, stay curious, and keep our chemical processes world-class.