Description

2'-Deoxy-2'-Ethylcytidine is a modified nucleoside analog of significant interest in advanced pharmaceutical research and development. This compound serves as a critical building block and intermediate in the synthesis of novel antiviral and anticancer therapeutics. It is primarily utilized by research institutions, pharmaceutical companies, and CDMOs engaged in the development of nucleoside-based drugs, including prodrugs and targeted therapies. The high-purity material is essential for ensuring the efficacy and safety profiles of the final active pharmaceutical ingredients.

Application

• Pharmaceutical Intermediate: A key synthetic precursor in the production of novel antiviral and anticancer nucleoside analogs.
• Antiviral Drug Research: Used in the R&D of therapeutics targeting viruses such as hepatitis and herpes, where modified nucleosides inhibit viral replication.
• Oncology Research: Investigated as a building block for antimetabolite drugs designed to disrupt cancer cell DNA synthesis.
• Prodrug Development: Employed in the design and synthesis of prodrugs to enhance bioavailability and targeted delivery of active agents.
• Biochemical Research: Serves as a substrate or inhibitor in enzymatic studies to understand nucleoside metabolism and related pathways.
• Reference Standard: Used as a high-purity analytical standard for quality control and method development in pharmaceutical manufacturing.

Basic Information

Product Name	2'-Deoxy-2'-Ethylcytidine
CAS No.	119410-83-2
Molecular Formula	C11H17N3O4
Molecular Weight	255.27 g/mol
Synonyms	2'-Deoxy-2'-ethylcytidine; 1-(2-Deoxy-2-ethyl-β-D-ribofuranosyl)cytosine; 2'-Ethyl-2'-deoxycytidine; 2'-Ethylcytidine; 2'-C-Ethylcytidine; Cytidine, 2'-deoxy-2'-ethyl-; 2'-Deoxy-2'-ethylcytidine (C2'-ethylcytidine)
EINECS	Contact for details

Quality Control

Our 2'-Deoxy-2'-Ethylcytidine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and stringent controls for residual solvents and impurities to meet research and pharmaceutical-grade standards. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment to ensure full traceability and compliance with your project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Heavy Metals	< 10 ppm

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