Description

9-Deoxy-16,16-Dimethyl-Tetranor-9-Methyleneprostaglandin E2 is a synthetic prostaglandin analog, a key intermediate in the development of advanced pharmaceutical compounds. This high-purity intermediate is valued for its role in creating potent and selective therapeutic agents targeting specific biological pathways. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of novel drugs, particularly in the fields of ophthalmology, dermatology, and metabolic regulation.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel prostaglandin-based drugs.
• Ophthalmic Research: Used in the development of next-generation treatments for glaucoma and ocular hypertension.
• Dermatological Formulations: Serves as a key precursor for compounds under investigation for hair growth stimulation and skin condition treatments.
• Metabolic Disorder Studies: Employed in research programs focused on developing therapies for metabolic and endocrine disorders.
• Chemical Synthesis: Used in organic synthesis for creating complex, biologically active molecules in laboratory settings.
• Reference Standard: Acts as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.

Basic Information

Product Name	9-Deoxy-16,16-Dimethyl-Tetranor-9-Methyleneprostaglandin E2
CAS No.	123283-87-4
Molecular Formula	C₂₂H₃₄O₄
Molecular Weight	362.51 g/mol
Synonyms	9-Deoxy-16,16-dimethyl-9-methylene-PGE2; 9-Deoxy-16,16-dimethyl-9-methyleneprostaglandin E2; 16,16-Dimethyl-9-deoxy-9-methyleneprostaglandin E2; 9-Methylene-16,16-dimethyl-9-deoxy-PGE2; Latanoprost Related Compound C; Latanoprost Impurity C; Travoprost Impurity; Bimatoprost Intermediate
EINECS	Contact for details

Quality Control

Our 9-Deoxy-16,16-Dimethyl-Tetranor-9-Methyleneprostaglandin E2 is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical quality attributes. Our production adheres to cGMP guidelines where applicable, ensuring the material meets the stringent requirements for pharmaceutical research and development.

Storage

Preserve in a tightly closed container, protected from light. Store at -20°C or below under an inert atmosphere (e.g., argon or nitrogen) to prevent oxidation. For long-term storage, keep the material desiccated to maintain stability. Allow the sealed container to reach room temperature before opening to minimize moisture condensation.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Maximum Impurity	≤ 0.5%
Residual Solvents (GC)	Meets ICH Q3C guidelines
Water Content (KF)	≤ 0.5%

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