Description

Norgestrel Acetate is a synthetic progestin steroid, a key pharmaceutical intermediate and active pharmaceutical ingredient (API). Its primary commercial value lies in its role in the synthesis of potent hormonal agents used in various therapeutic applications. This compound is essential for manufacturers in the pharmaceutical and life sciences industries developing contraceptive and hormone replacement therapies.

Application

• Pharmaceutical Intermediate: A critical building block in the multi-step synthesis of advanced progestogen APIs.
• Active Pharmaceutical Ingredient (API): Used in the formulation of hormonal contraceptives, including certain oral pills and implants.
• Hormone Replacement Therapy (HRT): A component in medications designed to manage menopausal symptoms and related conditions.
• Research & Development: Serves as a reference standard and starting material in steroid chemistry research within academic and industrial laboratories.
• Veterinary Pharmaceuticals: Employed in the development of hormonal treatments for animal health.

Basic Information

Product Name	Norgestrel Acetate
CAS No.	18290-31-8
Molecular Formula	C23H30O3
Molecular Weight	354.49 g/mol
Synonyms	13-Ethyl-17-hydroxy-18,19-dinor-17α-pregn-4-en-20-yn-3-one acetate; 17α-Ethynyl-17β-hydroxy-18-methyl-4-estren-3-one acetate; 18-Methylnorethindrone acetate; d-Norgestrel acetate; Levonorgestrel acetate (Note: often refers to the active enantiomer); (17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-en-20-yn-3-one acetate; 17α-Ethynyl-17β-hydroxy-18-methylestr-4-en-3-one acetate
EINECS	Contact for details

Quality Control

Our Norgestrel Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets exacting standards suitable for pharmaceutical use. Certificates of Analysis (COA) are provided with every shipment, detailing all critical parameters.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from heat and incompatible materials.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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