What is Taraxacum Officinale Dandelion Extract?
Taraxacum Officinale Dandelion Extract is a standardized botanical crude material derived from selected parts of Taraxacum officinale created in response to application in the industrial sector of the nutraceutical, food, and botanical formulation industry, whereby consistency, traceability, and formulation compatibility are essential. It is usually produced by a controlled extraction process - aqueous or ethanol-based extraction process - followed by purification, concentration, and drying technologies to produce a stable powder ingredient with a definite ratio of extract or a definite marker compound. The extract is appreciated due to its reproducible chemical profile that typically comprises a range of phenolic compounds, flavonoid complexes, and naturally occurring carbohydrate fractions that can enable the formulators to deal with an input material that is predictable and well characterized. Its physicochemical characteristics, such as moderate bulk density, controlled moisture content, and good dispersibility, enable it to be readily incorporated in different formulation systems without necessarily having to change the process a lot. Moreover, suppliers usually provide the opportunity to vary specifications, i.e., customized extract strength, mesh size, carrier system to suit various manufacturing needs, be it direct blending, premix development, or contract production.

COA
| Item | Specification | Result | Method |
| Assay (Extract Ratio) | 10:1 | Conforms | TLC |
| Appearance | Brown to dark light fine powder | Conforms | Visual |
| Odor | Characteristic | Conforms | Organoleptic |
| Taste | Characteristic | Conforms | Organoleptic |
| Particle Size | 95% Pass 80 Mesh | Conforms | USP <786> |
| Loss on Drying | ≤5.0% | 0.03 | USP <731> |
| Ash Content | ≤5.0% | 0.02 | USP <281> |
| Bulk Density | 0.40–0.60 g/ml | 0.52 g/ml | USP Method |
| Heavy Metals | ≤10 ppm | Conforms | ICP-MS |
| Lead (Pb) | ≤2.0 ppm | 0.48 ppm | ICP-MS |
| Arsenic (As) | ≤1.0 ppm | 0.21 ppm | ICP-MS |
| Cadmium (Cd) | ≤1.0 ppm | 0.09 ppm | ICP-MS |
| Mercury (Hg) | ≤0.1 ppm | 0.02 ppm | ICP-MS |
| Total Plate Count | ≤10,000 CFU/g | 1,200 CFU/g | AOAC |
| Yeast & Mold | ≤1,000 CFU/g | 85 CFU/g | AOAC |
| E. coli | Negative | Negative | AOAC |
| Salmonella | Negative | Negative | AOAC |
| Staphylococcus aureus | Negative | Negative | AOAC |
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Main Ingredients
Taraxacum Officinale Extract includes a complex formulation of naturally occurring phytochemicals that determine its industrial worth and versatility in formulation, with phenolic acids and flavonoids being the most prevalent types of bioactive compounds. Chlorogenic acid, caffeic acid, luteolin, and its glycosides are commonly found in huge quantities and smaller quantities of sesquiterpene lactones, sterols, and polysaccharide fractions such as inulin-type fructans. Phenolic acids and flavonoids are among them, and in general, they are regarded as the most important markers to use as the basis of standardization, as they are abundant, stable, and constant across the production batches, and therefore, they are the primary points of quality control and specification. It is these compounds that give the extract its typical physicochemical behavior, such as water solubility, middle polarity, and the ability to be compatible with a variety of formulation matrices, which facilitates its use in manufacturing in the form of tablets, capsules, premixes, and liquid systems. The composition is adaptable to the extraction and concentration processes to fulfill the requirements of a particular client, which gives flexibility to the contract manufacturers and brand proprietors who require reproducible and supply-stable botanical ingredients to use in a variety of industrial uses.
Process
1. Raw Material Selection and Cleaning
The root and/or aerial parts of dandelion are of high quality, which is obtained in controlled cultivation or confirmed wild collection. Raw materials undergo a process of cleaning to eliminate soil, debris, and foreign substances.
2. Size Reduction
The purified plant material is broken or milled mechanically to create more surface area and, therefore, allows easier extraction of target phytochemicals.
3. Extraction
The extraction of the milled material is done using aqueous or hydroalcoholic conditions of controlled temperature and pH. This process is the selective solubilisation of significant phenolic acids, flavonoids, and other water-soluble components.
4. Filtration and Clarification
The extract solution is filtered to eliminate all the plant fibers and particulate matter, and a clear liquid that can be further concentrated is obtained.
5. Concentration
To reduce the amount of solvent and preserve the integrity of sensitive compounds, the filtered extract is concentrated under reduced pressure with the help of vacuum evaporators.
6. Drying
The concentrated extract is then turned into a stable powder either through a spray drying process or a freeze-drying process. Optimization of the parameters of the process is done to maintain solubility, flowability, and chemical consistency.
7. Standardization and Quality Control
The dried extract is standardized to desired concentrations of primary marker compounds (e.g., phenolic acids or flavonoids) and passes through stringent quality control regarding moisture, particle size, solvents remaining, and microbial boundaries.
8. Packaging
The completed Dandelion Extract is packed in moisture-free, non-airtight containers with labels to trace the batches. This guarantees stability in the long run and distribution bulkiness.

Suitable For
End products that include Dandelion Extract Powder will target the mass market consumers who use the product in their daily lives as part of their dietary supplements, herbal formulations, and fortified food products. Its flexibility allows it to be used in both general adult populations whose values are focused on health-friendly and natural ingredients, and groups of people interested in wellness-friendly lifestyle products without specifying the target health conditions. The brand owners and contract manufacturers can develop consumer products that capitalize on the markets that favor clean-label, plant-based, and multifunctional ingredients because the extract has a neutral sensory profile and can be used with a variety of dosage forms, including capsules, tablets, powders, and liquid concentrates, which facilitates mass distribution and broad product positioning.
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