Description

Shatavarin Iv CAS NO 84633-34-1 is a high-purity, standardized steroidal saponin compound isolated from the roots of *Asparagus racemosus* (Shatavari). This bioactive phytochemical is valued for its role as a key analytical reference standard and active pharmaceutical ingredient (API) in the development of nutraceutical and pharmaceutical formulations. It is primarily sought by manufacturers and research institutions in the pharmaceutical, nutraceutical, and cosmeceutical industries for product development and quality control.

Application

• Pharmaceutical Reference Standard: Used as a primary standard in HPLC and LC-MS methods for the identification and quantification of Shatavarin IV in raw materials and finished products.
• Nutraceutical Formulations: Incorporated into dietary supplements and herbal extracts targeting women's health, adaptogenic, and galactagogue effects.
• Research & Development: Serves as a critical compound in preclinical and clinical studies investigating the pharmacological properties of *Asparagus racemosus*.
• Cosmeceutical Products: Utilized in advanced skincare formulations for its potential antioxidant and skin-conditioning properties.
• Quality Control (QC) & Assurance: Essential for in-house QC laboratories to verify the potency and authenticity of Shatavari extracts.
• API Synthesis: Acts as a starting material or intermediate for the semi-synthesis of novel steroidal derivatives.

Basic Information

Product Name	Shatavarin IV
CAS No.	84633-34-1
Molecular Formula	C44H70O17
Molecular Weight	855.0 g/mol
Synonyms	Shatavarin IV; Shatavarin-4; (25R)-3β-[(O-β-D-Glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→4)]-β-D-glucopyranosyl)oxy]-26-[(β-D-glucopyranosyl)oxy]-22-hydroxyfurost-5-en; Asparagoside A; Racemoside A
EINECS	Contact for details

Quality Control

Our Shatavarin IV is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for assay and purity, to ensure it meets stringent specifications for use as a reference standard and API. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment. We support compliance with GMP, ICH Q7, and relevant pharmacopeial guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at 2-8°C. This product is hygroscopic (moisture-sensitive) and should be handled in a low-humidity environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Residual Solvents	Conforms to ICH Q3C

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