Description

Caudatin CAS NO 38395-02-7 is a bioactive steroidal compound belonging to the class of C21 steroids, known for its specific structural configuration and potential biological activities. This high-purity reference standard is critical for research and development in the pharmaceutical and life sciences sectors, where precise chemical identity and consistency are paramount. It is primarily utilized by researchers and quality control laboratories in pharmaceutical development, natural product chemistry, and as a standard for analytical method development and validation.

Application

• Pharmaceutical Reference Standard: Serves as a high-purity certified reference material (CRM) for the identification, assay, and impurity profiling of related pharmaceutical compounds and natural extracts.
• Biochemical Research: Used as a key intermediate or standard in studies investigating the biological activity, metabolism, or structure-activity relationships (SAR) of steroidal compounds.
• Natural Product Analysis: Employed as an analytical standard for the quantification and qualification of Caudatin in complex plant matrices and herbal medicinal products.
• Quality Control (QC) & Quality Assurance (QA): Essential for calibrating analytical instruments (e.g., HPLC, LC-MS) and validating testing methods to ensure product consistency and regulatory compliance in manufacturing.
• Academic Research: Utilized in university and institutional labs for chemical synthesis projects, pharmacological screening, and phytochemical studies.

Basic Information

Product Name	Caudatin
CAS No.	38395-02-7
Molecular Formula	C28H38O7
Molecular Weight	486.60 g/mol
Synonyms	Caudatin; 12-O-Acetyl-16-O-(2-methylbutyryl)tetrahydroxypregn-4-ene-3,20-dione; 3β,12β,14β,16β-Tetrahydroxy-12-acetoxy-16-(2-methylbutyryloxy)pregn-4-ene-3,20-dione; Pregn-4-ene-3,20-dione, 3,12,14,16-tetrahydroxy-, 12-acetate 16-(2-methylbutanoate), (3β,12β,14β,16β)-; NSC 169915
EINECS	Contact for details

Quality Control

Our Caudatin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity assessment and spectroscopic methods (NMR, MS) for structural confirmation, to ensure it meets the high standards required for research and development. Certificates of Analysis (COA) with detailed chromatographic data and batch-specific results are provided to guarantee traceability and reliability for your critical applications.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. The product is light-sensitive and should be handled accordingly to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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