Description

Peruvoside is a potent cardiac glycoside derived from natural sources, known for its specific biological activity. This high-purity compound is critical for pharmaceutical research and development, particularly in the study of cardiac function and therapeutic agents. It serves as a valuable reference standard and active pharmaceutical ingredient (API) intermediate for researchers and manufacturers in the life sciences sector.

Application

• Pharmaceutical Reference Standard: Used for quality control, method validation, and calibration in analytical laboratories.
• Cardiac Drug Research: A key intermediate in the research and development of novel therapeutic agents targeting heart conditions.
• Biochemical Studies: Employed in pharmacological and toxicological studies to investigate mechanisms of action and dose-response relationships.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a critical building block or precursor in the synthesis of complex pharmaceutical compounds.

Basic Information

Product Name	Peruvoside
CAS No.	1182-87-2
Molecular Formula	C30H46O8
Molecular Weight	534.69 g/mol
Synonyms	Peruvoside; 3β-[(O-2,6-Dideoxy-β-D-ribo-hexopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-14-hydroxy-19-oxo-5β-card-20(22)-enolide; NSC 169015; Thevetin B; Cerberoside
EINECS	214-644-4

Quality Control

Our Peruvoside is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the stringent requirements for research and pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (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.