Uracil

Product Overview

Uracil, identified by CAS number 66-22-8, is a fundamental pyrimidine nucleobase that plays a critical role in the synthesis of various pharmaceutical compounds and nucleoside analogs. As a key building block in organic chemistry, it serves as a precursor for the development of antiviral agents, anticancer medications, and other therapeutic intermediates. Our manufacturing facility produces Uracil using advanced synthesis routes to ensure consistent industrial purity and reliability for large-scale production needs.

We understand the stringent requirements of the pharmaceutical industry. Therefore, our Uracil is manufactured under strict quality management systems, ensuring that every batch meets or exceeds international standards for chemical intermediates. Whether you are developing new drug formulations or scaling up existing production lines, our product provides the foundational quality necessary for successful synthesis outcomes.

Technical Specifications

Physical and Chemical Properties

Understanding the physical characteristics of Uracil is vital for process optimization. Our product exhibits a density of approximately 1.321 g/cm3 and possesses a high melting point exceeding 300 degrees Celsius, indicating thermal stability suitable for various reaction conditions. The flash point is recorded at 220.2 degrees Celsius, and the refractive index is measured at 1.501. These properties make it a robust material for handling in standard industrial laboratory and manufacturing environments.

Industrial Applications

Uracil is primarily utilized as a pharmaceutical intermediate. Its most significant application lies in the synthesis of guanosine and other nucleoside derivatives. These derivatives are essential components in the production of antiviral drugs and chemotherapy agents. Additionally, Uracil serves as a valuable research chemical in biochemical studies involving RNA metabolism and genetic expression. Our clients leverage our high-purity material to ensure efficient reaction yields and minimal impurity profiles in their final active pharmaceutical ingredients.

Quality Assurance and Packaging

Quality is the cornerstone of our operation. Each production batch undergoes rigorous testing via High-Performance Liquid Chromatography (HPLC) to verify purity levels. We provide a comprehensive Certificate of Analysis (COA) with every shipment, detailing all critical quality attributes. Our standard packaging consists of 25 kg drums, designed to protect the product from moisture and contamination during transit. However, we offer flexible packaging solutions tailored to specific customer requirements to facilitate seamless integration into your supply chain.

Storage and Handling

To maintain the integrity of Uracil, it should be stored in a cool, ventilated area away from direct sunlight and sources of ignition. The packaging must remain sealed when not in use to prevent absorption of moisture. Proper handling procedures should be followed in accordance with standard laboratory safety protocols. By adhering to these storage guidelines, customers can ensure the long-term stability and performance of the material in their manufacturing processes.