Description

Evodiamine is a prominent indoloquinazoline alkaloid naturally isolated from the fruit of *Evodia rutaecarpa*. This bioactive compound is valued for its significant role in pharmacological research and development. It serves as a critical reference standard and active ingredient for researchers and manufacturers in the pharmaceutical, nutraceutical, and life science sectors.

Application

• Pharmaceutical Reference Standard: Used for the identification, assay, and quality control of related herbal extracts and finished products in pharmacopoeial testing.
• Dietary Supplement Formulation: Incorporated as a key bioactive component in nutraceutical products targeting metabolic and wellness applications.
• Biomedical Research: Serves as a crucial tool compound in preclinical studies investigating mechanisms related to inflammation, pain, and metabolic pathways.
• Natural Product Isolation & Standardization: Essential for standardizing extracts of *Evodia rutaecarpa* to ensure consistent potency and efficacy.
• Cosmeceutical Ingredients: Explored for potential use in topical formulations due to its bioactive properties.

Basic Information

Product Name	Evodiamine
CAS No.	518-17-2
Molecular Formula	C19H17N3O
Molecular Weight	303.36 g/mol
Synonyms	8,13,13b,14-Tetrahydro-14-methylindolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(7H)-one; Evodiamin; Rutecarpine isomer; Evodia alkaloid
EINECS	Contact for details

Quality Control

Our Evodiamine is produced and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for research and development. Certificates of Analysis (COA) detailing all specifications are available upon request.

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 low-humidity environment to maintain stability.

Specification

Item	Specification
Appearance	White to light yellow 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	≤ 10 ppm

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