Cistanche Tubulosa Extract

Cistanche Tubulosa Extract

Product name: Cistanche tubulosa extract
Appearance: Brown yellow powder
Active ingredients: Total glycosides, Echinacoside, Acteoside
Test method: UV, HPLC
Sample: 10-20g for free
Certificate: ISO, KOSHER, HACCP, FDA
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Description
Technical Parameters

What is Cistanche Tubulosa Extract?

 

Cistanche Tubulosa Extract is a botanical extract of Cistanche tubulosa, an extract made of the stem of a desert shrub that has found application in functional formulations in the nutraceutical industry, dietary supplement industry, and health food manufacturing industry. To people buying it, it is usually provided as uniform powder with managed qualities on the look, purity, residues of solvents, moisture, and content of active-markers like total phenylethanoid glycosides (usually comprising of echinacoside and acteoside as quality measures). It is appreciated due to its stable supply of raw materials and performance of the extract in every batch, and its ability to fit most product formats such as tablets, capsules, functional beverages, and blended powders. It is chosen by manufacturers due to its composition profile and the ability to make formulations rather than because of consumer-focused health communications. The glycosides and polysaccharides present in it naturally provide a functional and plant-based ingredient that can be implemented in the formula designed to target either general vitality-oriented or botanical-oriented product lines. Due to its low aroma, good solubility properties based on the extraction process, and stable flow properties when well granulated, it is a popular ingredient for formulators who require consistency in its performance during blending, granulation, or encapsulation.

 

Cistanche-Tubulosa-Extract

 

COA

 

Test Item Specification Method Result
Appearance Fine light brown to yellowish powder Visual Inspection Light brown powder
Odor & Taste Characteristic mild herbaceous Sensory Conforms
Extract Type Water / Hydroethanolic extract Supplier Specification Conforms
Active Marker: Echinacoside ≥8% HPLC 8.20%
Active Marker: Acteoside ≥2% HPLC 2.30%
Loss on Drying ≤5% AOAC 925.10 3.20%
Ash Content (Total) ≤8% AOAC 923.03 6.50%
Particle Size 100% through 80 mesh Laser Diffraction / Sieve Analysis Conforms
pH (1% solution) 4.5–6.0 pH Meter 5.2
Lead (Pb) ≤2.0 mg/kg ICP-MS 1.2 mg/kg
Arsenic (As) ≤1.0 mg/kg ICP-MS 0.6 mg/kg
Cadmium (Cd) ≤1.0 mg/kg ICP-MS 0.4 mg/kg
Mercury (Hg) ≤0.1 mg/kg ICP-MS 0.05 mg/kg
Total Plate Count ≤1000 CFU/g USP <2021> / AOAC 450 CFU/g
Yeast & Mold ≤100 CFU/g USP <2021> / AOAC 35 CFU/g
E. coli Negative USP <2021> / AOAC Not Detected
Salmonella Negative USP <2021> / AOAC Not Detected

 

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Features

 

Cistanche Extract can be described as a unique blend of phenylethanoid glycosides, polysaccharides, as well as low-aroma plant constituents, which provide it with a stable physical and chemical profile, which is suitable for complex formulations. The extract is usually a fine, brown-yellow to brown powder that is highly dispersible in water-based systems and medium soluble based on the ratio of extract and the solvent employed. Its marker compounds, echinacoside and acteoside, have predictable chromatographic behaviour, giving the formulators an opportunity to observe batch consistency based on HPLC or UV procedures. The extract exhibits a relatively low level of hygroscopicity in comparison with most botanical powders and facilitates the blending process and minimises caking problems in very moist conditions. Since it is thermally stable, it can also be spray-dried, granulated, or compressed into tablets without requiring special processing temperatures, thus it is compatible with standard manufacturing equipment. Also, its light taste and low smell contribute to not covering difficulties in multi-herb or beverage usage. A combination of these attributes gives formulators access to a dependable, vegetable ingredient that can be easily incorporated into capsules, tablets, functional powders, and beverage premixes and will assist them in achieving strong consistency and predictability.

 

How to Store Properly?

 

1. Store in a Cool, Dry Environment

Store the product in a temperature-regulated warehouse, not in the presence of heat and direct sunlight. Constant ambient conditions are used to maintain the physical integrity and keep the moisture away.

2. Maintain Low Humidity Levels

Though the extract has a rather low hygroscopicity, it is recommended to store it in a dry place with a regulated humidity level to prevent the formation of clumps and the alteration of the flow characteristics.

3. Avoid Frequent Exposure to Air

Do not open the sealed packaging before it is necessary, and seal any half-used material as soon as possible. Reducing air exposure would conserve the stability of the marker compounds and eliminate the possibility of contamination.

4. Use Clean, Dedicated Storage Containers After Opening

When the product must be shipped after breaking the original seal, it is necessary to use containers of food or pharmaceutical quality that resist the emission of moisture, dust, and unpleasant smells.

5. Keep Away from Strong Odours and Volatile Materials

Keep the extract, fragrant ingredients, essential oils, solvents, and other volatile compounds apart in order to avoid cross-absorbing the odors.

6. Follow FIFO Inventory Rotation

Institute a first-in, first-out system in order to avoid using the old batches late, hence helping in being able to maintain the same performance in production.

7. Prevent Mechanical Pressure

Heavy items should not be stacked on top of the packaged Cistanche Deserticola Extract because too much weight will compress the powder and compromise the handling of the powder in downstream processing.

 

Cistanche-Tubulosa-Extract-usage

 

Recommended Usage

 

In the case of manufacturers, it is possible to implement Cistanche Powder Bulk under different dosage versions concentrating on its flow properties, particle size distribution, and its interaction with both dry and liquid bases. In capsule and tablet applications, the extract is usually mixed with excipients, which allow it to be dispersed uniformly, with its intermediate bulk density and stable powder characteristics allowing it to be readily integrated during any stage of the pre-mixing, granulation, or direct compression; to ensure that the fill weight is always the same and the powder is not segregated, formulators may vary the proportion of binders or flow agents. In liquid preparations, e.g., botanical shots, functional beverages, it is preferable that the extract should be dispersed under some form of controlled agitation and that the solubility and stability of the suspension can be considered dependent on the extraction technique adopted; appropriate emulsifiers or stabilisers can be used to attain a monolithic appearance and to stop sedimentation. Within any form, gradual addition during blending is used to ensure even dispersion, whereas controlled processing temperature is used to maintain the physical integrity of the extract and consistency of the marker profile during the entire processing.

 

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