Description

Ergonovine Tartrate is a high-purity pharmaceutical-grade salt of the ergot alkaloid ergonovine. This compound is critical for its potent uterotonic activity, making it a key active pharmaceutical ingredient (API) in specialized obstetric and gynecological formulations. It is essential for manufacturers in the pharmaceutical industry requiring a reliable and consistent supply of this potent therapeutic agent for the production of injectable solutions and other dosage forms.

Application

• Primary Active Pharmaceutical Ingredient (API) in uterotonic medications for postpartum hemorrhage management.
• Key component in diagnostic and research reagents for studying smooth muscle contraction and vascular tone.
• Raw material for the synthesis of more complex ergot alkaloid derivatives in pharmaceutical research.
• Reference standard in analytical chemistry and quality control laboratories for HPLC and other assay methods.
• Used in preclinical and clinical research studies investigating uterine physiology and related therapeutic pathways.

Basic Information

Item	Details
Product Name	Ergonovine Tartrate
CAS No.	75088-32-3
Molecular Formula	C23H31N3O10
Molecular Weight	509.51 g/mol
Synonyms	Ergonovine Hydrogen Tartrate; D-Lysergic Acid Propanolamide Tartrate; Ergometrine Tartrate; 9,10-Didehydro-N-(2-hydroxy-1-methylethyl)-6-methylergoline-8β-carboxamide (2R,3R)-2,3-dihydroxybutanedioate; Basergin; Ergotrate; Cornocentin; Panergot; Secacornin
EINECS	Contact for details

Quality Control

Our Ergonovine Tartrate is manufactured under strict quality systems to meet the rigorous standards required for pharmaceutical actives. Each batch is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling via advanced techniques like HPLC. A Certificate of Analysis (COA) documenting compliance with agreed specifications 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 material is hygroscopic (moisture-sensitive) and light-sensitive; containers must be kept tightly sealed in a dry environment away from direct light exposure to maintain stability and potency.

Specification

Item	Specification
Appearance	White or almost white, crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water (KF)	≤ 5.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%

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