Description

Seco-Neokadsuranic Acid A is a specialized triterpenoid compound derived from the *Kadsura* plant genus, known for its unique seco-lanostane skeleton. This high-purity reference standard is critical for pharmaceutical research and development, particularly in the study of bioactive natural products. It serves as an essential analytical standard for quality control in the production of herbal extracts and as a key intermediate in the synthesis of novel therapeutic agents targeting inflammation and metabolic disorders.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the identification and quantification of Seco-Neokadsuranic Acid A in raw botanical materials and finished herbal products.
• Bioactivity Research: Serves as a pure compound for in-vitro and in-vivo studies investigating anti-inflammatory, hepatoprotective, and anti-cancer properties.
• Natural Product Synthesis: Acts as a key chiral intermediate or precursor in the semi-synthesis of more complex natural product derivatives for drug discovery programs.
• Analytical Method Development: Essential for developing and validating HPLC, LC-MS, and TLC methods in quality control laboratories for herbal medicine manufacturers.
• Academic Research: Used in universities and research institutes for phytochemical studies, structural elucidation, and metabolic pathway analysis.

Basic Information

Product Name	Seco-Neokadsuranic Acid A
CAS No.	124817-74-9
Molecular Formula	C30H46O5
Molecular Weight	486.7 g/mol
Synonyms	3,4-Seco-9βH-lanosta-4(28),7,24-triene-3,26-dioic acid, 21,23-epoxy-7-oxo-; Neokadsuranic acid A seco derivative; Kadsuranic acid A seco- form; (4aS,6aR,6bS,8aR,12aS,14bR)-10-(Carboxymethyl)-4a,6a,6b,9,9,12a-hexamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14b-octadecahydropicene-2-carboxylic acid
EINECS	Contact for details

Quality Control

Our Seco-Neokadsuranic Acid A is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis. We provide a detailed Certificate of Analysis (COA) with each shipment, ensuring traceability and compliance with research-grade standards. Custom purification to meet specific pharmacopoeial or client specifications is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store at 2-8°C in a dry, cool environment. For long-term storage, consider storing under an inert atmosphere at -20°C. The compound is light-sensitive (store away from light) and should be handled in a manner to minimize exposure to air and moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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