Description

Lanosta-7,24-Dien-21-Oic Acid, 3-Hydroxy-, (3α,13α,14β,17α,20S)- is a high-purity, functionalized lanostane-type triterpenoid derivative of significant interest in advanced organic synthesis and pharmaceutical research. This compound serves as a critical chiral building block and a key intermediate for the development of novel bioactive molecules, including potential therapeutic agents and reference standards. It is primarily utilized by research institutions, pharmaceutical R&D departments, and fine chemical manufacturers focused on steroid chemistry, natural product synthesis, and drug discovery programs.

Application

• Pharmaceutical Intermediate: Serves as a key chiral synthon in the multi-step synthesis of complex steroid-like molecules and potential drug candidates.
• Biochemical Research: Used as a reference standard or a precursor in metabolic pathway studies and enzyme inhibition assays related to triterpenoid biosynthesis.
• Natural Product Synthesis: Acts as a crucial intermediate for the semi-synthesis or total synthesis of complex natural products belonging to the lanostane family.
• Fine Chemical Production: Employed in the manufacture of specialized, high-value chemicals for academic and industrial research applications.
• Material Science Research: Investigated as a potential precursor for novel organic materials with specific chiral or structural properties.

Basic Information

Product Name	Lanosta-7,24-Dien-21-Oic Acid, 3-Hydroxy-, (3α,13α,14β,17α,20S)-
CAS No.	82509-40-8
Molecular Formula	C30H46O3
Molecular Weight	454.70 g/mol
Synonyms	(20S)-3α,13α,14β,17α-Tetrahydroxylanosta-7,24-dien-21-oic Acid; 3α,13α,14β,17α-Tetrahydroxy-20S-lanosta-7,24-dien-21-oic Acid; 3-Hydroxylanosta-7,24-dien-21-oic Acid; Lanosta-7,24-diene-21-oic Acid, 3-hydroxy-, (3α,13α,14β,17α,20S)-; Lanostadienoic Acid Derivative; Triterpenoid Acid Intermediate
EINECS	Contact for details

Quality Control

Our Lanosta-7,24-Dien-21-Oic Acid, 3-Hydroxy-, (3α,13α,14β,17α,20S)- is manufactured under strict quality control protocols to ensure batch-to-batch consistency and high purity suitable for research and synthesis. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP principles for pharmaceutical intermediates, and specifications can be tailored to meet specific project requirements, including custom purity grades or analytical method validation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); ensure the container is sealed tightly after each use to prevent degradation due to moisture absorption. For long-term storage, consider using desiccants or storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 95.0%
Loss on Drying	≤ 2.0%
Specific Rotation	Contact for details
Heavy Metals	< 20 ppm
Residual Solvents	Complies with ICH guidelines

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