Description

Ulipristal is a selective progesterone receptor modulator (SPRM) with significant therapeutic applications. This compound matters for its targeted mechanism of action, offering a high degree of biological specificity and efficacy. It is primarily needed by pharmaceutical manufacturers and research institutions engaged in developing treatments for gynecological conditions and emergency contraception.

Application

• Active Pharmaceutical Ingredient (API): Core component in the manufacture of prescription medications for emergency contraception (e.g., ella®).
• Gynecological Therapeutics: Used in the development and production of treatments for uterine fibroids (leiomyomas) and related conditions.
• Hormone Receptor Research: A critical reference standard and tool compound in preclinical studies investigating progesterone receptor pathways.
• Pharmaceutical Development: Serves as a key intermediate or final API in formulation R&D for novel drug delivery systems.
• Clinical Trial Materials: Supplied as a high-purity compound for use in regulated clinical research and trials.
• Reference Standard: Utilized in analytical laboratories for method development, validation, and quality control testing of pharmaceutical products.

Basic Information

Product Name	Ulipristal
CAS No.	159811-51-5
Molecular Formula	C29H35NO4
Molecular Weight	461.59 g/mol
Synonyms	Ulipristal Acetate; CDB-2914; VA-2914; 17α-Acetoxy-11β-[4-(N,N-dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione; PGL4001; 11β-[4-(Dimethylamino)phenyl]-17α-hydroxy-19-norpregna-4,9-diene-3,20-dione 17-acetate
EINECS	Contact for details

Quality Control

Our Ulipristal is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for assay and related substances, to ensure compliance with pharmaceutical-grade standards. Comprehensive Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are available upon request to support your regulatory and quality assurance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation.

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%
Related Substances (HPLC)	Total impurities ≤2.0%
Single Unknown Impurity	≤0.5%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%

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