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Shaanxi Kaishi Biotechnology Co., Ltd
$9
1-199 Others
$8
200-499 Others
$7
≥500 Others
Product Description
Nettle Extract 10:1 is a concentrated botanical ingredient derived from nettle, commonly identified as Urtica dioica. Produced at a nominal 10:1 herb-to-extract ratio, it is used in herbal supplement formulations, botanical blends, and Wellness Products. This extract is suitable for B2B buyers seeking a versatile nettle ingredient for capsules, tablets, and powdered formulations.
Nettle extract is obtained from nettle plant material through extraction and concentration processes. The 10:1 ratio indicates that approximately ten parts of starting botanical material are used to produce one part of extract by weight under the stated manufacturing convention. It describes the extraction ratio rather than a guaranteed concentration of any individual active compound.
Nettle contains naturally occurring constituents such as polyphenols, flavonoids, and other plant compounds. Its chemical profile can vary with the plant species, plant part, growing conditions, extraction solvent, and processing method. For procurement and formulation, the botanical identity, plant part, extract ratio, carrier content, and analytical specifications should be evaluated together.
| Item | Specification |
|---|---|
| Product Name | Nettle Extract 10:1 |
| Botanical Name | Urtica dioica L. or another declared Urtica species, depending on the raw material |
| Plant Family | Urticaceae |
| Plant Part | Leaf, aerial parts, or root, depending on the selected specification |
| Extract Ratio | 10:1 nominal herb-to-extract ratio |
| Product Category | Botanical extract / herbal extract |
| Appearance | Typically fine yellowish-brown to brown powder; color varies with plant part and processing |
| Odor and Taste | Characteristic herbal odor and taste |
| Identification | Botanical identity verification using appropriate macroscopic, microscopic, chromatographic, or other validated methods |
| Marker Compounds | Not inherently standardized by the 10:1 ratio; selected markers may be specified separately when required |
| Assay Method | HPLC or other validated analytical method appropriate to the specified marker; identification methods selected according to the product specification |
| Extract Ratio Verification | Manufacturing records and raw-material-to-extract yield documentation; the ratio alone does not establish active-compound content |
| Solvent System | Water or another suitable extraction solvent, depending on the manufacturing process |
| Carrier Content | May be carrier-free or contain a processing carrier, depending on the grade |
| Particle Size | Customizable to the intended blending, encapsulation, or tablet-manufacturing process |
| Moisture | Controlled according to the applicable product specification and stability requirements |
| Heavy Metals | Tested against the applicable product specification and target-market requirements |
| Microbiological Quality | Controlled according to the applicable botanical ingredient specification |
| Residual Solvents | Evaluated according to the extraction process and applicable requirements |
| CAS Number | Not applicable as a single defined chemical compound; nettle extract is a multicomponent botanical preparation |
| Molecular Formula | Not applicable; the extract contains multiple naturally occurring constituents |
| Molecular Weight | Not applicable; the extract does not have one defined molecular weight |
| Common Assay Grades | 10:1 extract ratio; marker-standardized grades can be specified separately when supported by analytical data |
| Storage | Store tightly sealed in a cool, dry place, protected from direct sunlight, moisture, and strong odors |
| Shelf Life | Typically 24 months under recommended storage conditions, subject to the product's assigned shelf life and supporting stability data |
| Packaging | Common options include 1 kg and 5 kg aluminum foil bags and 25 kg fiber drums with suitable inner liners; custom packaging is available |
| Application | Herbal supplements, botanical blends, capsules, tablets, and powdered formulations |
Nettle extract can be incorporated into botanical supplement formulations as a concentrated nettle ingredient. Product developers can evaluate it for capsules, tablets, and powder blends, considering the intended serving size, sensory profile, extract characteristics, and applicable market requirements.
The extract can be combined with other botanical ingredients in multi-herb formulations. Compatibility should be assessed for taste, color, moisture sensitivity, processing behavior, and the analytical requirements of the finished product.
For powder blends and tablets, the extract's flowability, bulk density, particle-size distribution, moisture level, and carrier content can affect blending uniformity and manufacturing performance. Formulation trials are recommended before full-scale production.
Nettle extract may be used as a raw material for private-label herbal products. Final product positioning, ingredient declarations, serving directions, and any structure/function claims should be reviewed for the target market before commercial release.
For nettle extract, the most important purchasing distinction is the difference between an extraction ratio and a standardized active-compound assay. A 10:1 ratio describes the nominal relationship between starting herb material and extract; it does not mean that the extract contains 10% active compounds or that every batch has the same chemical profile.
Nettle leaf and nettle root are not interchangeable raw materials. Their constituent profiles and common formulation uses differ. The purchase specification should name the botanical species and plant part rather than relying on the generic term “nettle extract.” Match the declared plant part to the intended product concept and the evidence supporting its proposed use.
If the product brief requires a particular marker concentration, request a separately defined assay specification and a suitable analytical method. HPLC may be appropriate for selected compounds, but the marker and method must fit the actual extract. Do not treat a 10:1 ratio as proof of a specific flavonoid, polyphenol, or other active-compound percentage.
Carrier ingredients can influence the extract's apparent composition, bulk density, flowability, and suitability for a label claim. Confirm whether the grade is carrier-free or contains a processing aid, and review the extraction solvent and residual-solvent controls where relevant. These details help determine whether two products labeled 10:1 are genuinely comparable for formulation and procurement.
Common packaging configurations include 1 kg and 5 kg aluminum foil bags for sampling, pilot production, and smaller manufacturing runs, as well as 25 kg fiber drums with suitable inner liners for bulk supply. Actual packaging selection depends on order volume, shipping conditions, moisture protection, and handling requirements. Custom packaging can be arranged for suitable commercial quantities.
Nettle extract can be considered for custom botanical blends and finished supplement development. OEM and private-label projects may include raw-material specification selection, ingredient blending, dosage-form development, packaging selection, and label customization. Capsule, tablet, or powder formats should be selected according to formulation feasibility, target-market regulations, and the requirements of the finished product.
Before production, confirm the botanical species, plant part, extraction ratio, carrier status, analytical requirements, target market, and finished-product format. This information helps establish an appropriate purchasing specification and reduces the risk of substituting non-equivalent botanical materials.
Quality evaluation for nettle extract should reflect the botanical nature of the ingredient and its intended use. Relevant controls may include:
Incoming inspection should compare the COA with the agreed specification rather than relying on the product name or extract ratio alone. Technical documents and third-party testing can be used to support procurement and quality review, subject to the actual documentation available for the selected grade.
Keep nettle extract in a tightly closed, moisture-resistant container in a cool, dry environment away from direct sunlight and strong odors. Minimize exposure to humid air during dispensing and repackaging. Use clean, dry handling equipment and follow the storage conditions and retest or expiry information stated in the applicable batch documentation.
No. The 10:1 designation normally describes the nominal herb-to-extract ratio, not a 10% active-compound assay. Active constituents vary with species, plant part, extraction conditions, and processing. If a formulation requires a defined marker concentration, specify the marker and request analytical documentation for that grade.
No. Leaf and root extracts are derived from different plant parts and can have different constituent profiles and formulation purposes. The botanical species and plant part should be explicitly stated in the purchase specification and supporting documentation to help prevent raw-material substitution or inaccurate ingredient declarations.
Buyers commonly request a Certificate of Analysis (COA), Technical Data Sheet (TDS), and Safety Data Sheet (SDS). The COA should be reviewed for identity, relevant assay results, and applicable quality parameters. Additional botanical traceability, solvent, microbiological, or heavy-metals documentation may be appropriate depending on the product and target market.
Start with the intended dosage form and the required botanical identity. For capsules, review flowability, moisture, and carrier content; for tablets, assess compression behavior and excipient compatibility. If the label or formulation requires a marker assay, define its acceptance range and analytical method separately from the 10:1 ratio.
Nettle Extract 10:1 is a versatile botanical ingredient for herbal supplement development, botanical blends, and powdered dosage forms. Reliable sourcing depends on confirming the plant part, botanical identity, extract ratio, carrier content, and applicable analytical controls rather than assuming the ratio defines active-compound strength.
Contact us today to request samples, a COA, technical documents, and a wholesale quotation for nettle extract 10:1.
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