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Shaanxi Kaishi Biotechnology Co., Ltd
$50
1-199 Kilogram
$40
200-499 Kilogram
$35
≥500 Kilogram
Product Description
Docetaxel 99% API is a high-purity pharmaceutical active ingredient belonging to the taxane class of compounds. It is supplied as a quality-controlled raw material for pharmaceutical formulation and research applications, with identity, purity, analytical testing, and documentation requirements designed for regulated pharmaceutical manufacturing environments.
Docetaxel is a semi-synthetic taxane derivative structurally related to paclitaxel. It is manufactured as an active pharmaceutical ingredient (API) and evaluated according to pharmaceutical quality standards, including assay, identity confirmation, impurity profile, and stability-related parameters.
Unlike Nutritional Ingredients, Docetaxel API requires pharmaceutical-grade quality control and is intended for qualified pharmaceutical manufacturers and authorized research or development applications. Finished dosage forms, regulatory status, and market authorization requirements depend on the applicable country regulations.
| Item | Specification |
|---|---|
| Product Name | Docetaxel API |
| API Category | Pharmaceutical Active Ingredient |
| Compound Class | Taxane derivative |
| CAS Number | 114977-28-5 |
| Molecular Formula | C43H53NO14 |
| Molecular Weight | 807.88 g/mol |
| Appearance | White to off-white crystalline powder |
| Assay | Typically ≥99% by validated pharmaceutical analytical method |
| Identification Method | HPLC and other validated pharmaceutical identification methods |
| Purity Testing | Assay, related substances, residual solvents, water content, and other applicable pharmaceutical quality parameters |
| Storage | Store in a tightly sealed container under recommended pharmaceutical storage conditions, protected from excessive heat, moisture, and light |
| Packaging | Pharmaceutical-grade sealed packaging according to material protection and customer requirements |
| Documentation | COA, specification sheet, and technical documentation available according to supply requirements |
| Supply Type | Bulk API supply for qualified pharmaceutical applications |
For pharmaceutical procurement, Docetaxel quality evaluation focuses on more than assay percentage alone. Buyers typically review identity, assay, impurity profile, residual solvent control, analytical methodology, documentation completeness, and batch consistency.
| Quality Parameter | Purpose | Procurement Consideration |
|---|---|---|
| Assay | Confirms active ingredient content | Evaluate according to validated analytical methods |
| Related Substances | Controls impurity profile | Important for pharmaceutical quality assessment |
| Residual Solvents | Verifies process-related solvent control | Review against applicable pharmaceutical standards |
| Identity Testing | Confirms compound identity | Supports raw material qualification |
| Documentation | Supports quality review | Includes technical and batch-related records |
Docetaxel is a pharmaceutical active ingredient used in regulated medicine development and manufacturing. Any finished dosage formulation, labeling, handling requirements, and clinical use information must follow applicable pharmaceutical regulations and authorized product documentation.
Docetaxel API sourcing requires controlled quality systems, analytical verification, and appropriate technical documentation. Pharmaceutical manufacturers typically evaluate suppliers based on material consistency, testing capability, documentation support, and compliance with applicable quality requirements.
High-purity Docetaxel API provides pharmaceutical developers with a clearly defined active ingredient specification for regulated manufacturing processes. Reliable sourcing depends on verified assay results, impurity control, analytical consistency, and complete technical documentation.
Professional API supply programs focus on quality assurance, documentation transparency, stable production capability, and support for qualified pharmaceutical customers.
Docetaxel API should be packaged using suitable pharmaceutical-grade containers designed to protect material integrity during storage and transportation. Storage conditions should follow the applicable product specification and technical documentation.
Docetaxel 99% API indicates that the active pharmaceutical ingredient meets a high assay specification according to the applicable analytical method. Pharmaceutical buyers should also evaluate impurity profile, identification results, documentation, and batch consistency.
Typical pharmaceutical procurement reviews include certificate of analysis, product specification, analytical testing information, and technical documentation required for material qualification according to the buyer’s quality system.
No. API is the active ingredient used by qualified pharmaceutical manufacturers in the development or production of finished dosage forms. Finished products require separate formulation, manufacturing, regulatory review, and authorization processes.
Docetaxel 99% API is a pharmaceutical-grade active ingredient requiring strict quality evaluation, analytical verification, and controlled handling. Selecting reliable API specifications and documentation supports pharmaceutical development and regulated manufacturing requirements.
Contact us today to request samples, a COA, technical documents, and a wholesale quotation for Docetaxel API.
Packaging & Delivery
| Selling Units: | Kilogram |
|---|
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