Description

13-o-Deacetyltaxumairol Z is a specialized taxane diterpenoid derivative, a compound of significant interest in advanced pharmaceutical research and development. Its unique structural features make it a valuable intermediate and reference standard for the synthesis and study of novel bioactive molecules. This high-purity compound is primarily utilized by research institutions, pharmaceutical R&D departments, and fine chemical manufacturers focused on oncology and other therapeutic areas.

Application

• Pharmaceutical Intermediate: Serves as a key synthetic precursor in the research and development of novel taxane-based chemotherapeutic agents.
• Reference Standard: Used as a high-purity analytical standard in quality control laboratories for method development, validation, and compound identification.
• Biochemical Research: Employed in academic and industrial research to study structure-activity relationships (SAR), metabolic pathways, and biological mechanisms of taxane derivatives.
• Process Chemistry: Acts as a building block in the semi-synthesis of complex natural product analogs for screening and optimization.
• Active Pharmaceutical Ingredient (API) Development: Investigated for its potential direct application or as a derivative in the formulation of new drug candidates.

Basic Information

Product Name	13-o-Deacetyltaxumairol Z
CAS No.	220935-39-7
Molecular Formula	C29H36O9
Molecular Weight	528.59 g/mol
Synonyms	13-Deacetyltaxumairol Z; Taxumairol Z 13-O-deacetate; (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12-(Acetyloxy)-6,12b-dihydroxy-4,11-dimethoxy-4a,8,13,13-tetramethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benz[1,2-b]oxet-9-yl (2Z)-2-methylbut-2-enoate
EINECS	Contact for details

Quality Control

Our 13-o-Deacetyltaxumairol Z is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles as determined by advanced analytical techniques including HPLC, NMR, and MS. We are committed to meeting the stringent requirements of the pharmaceutical and research industries.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. For long-term storage, consider storing under inert atmosphere at -20°C to maximize stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 95.0%
Related Substances (HPLC)	Total impurities ≤ 5.0%
Residual Solvents (GC)	Complies with ICH guidelines
Water Content (KF)	≤ 1.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.