Description

Urol (Pharmaceutical) is a high-purity chemical compound designed for advanced pharmaceutical synthesis and research. This compound serves as a critical intermediate or active ingredient in the development of targeted therapeutic agents, where consistent quality and purity are paramount. It is essential for pharmaceutical manufacturers, R&D laboratories, and fine chemical suppliers focused on producing innovative and compliant drug substances.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for drug discovery and pharmacological studies.
• Reference Standard: Serves as a certified reference material for analytical method development and quality control.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex molecular structures.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for GMP production.

Basic Information

Product Name	Urol (Pharmaceutical)
CAS No.	97503-06-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Urol; Urol (Pharmaceutical Grade); 97503-06-5; [IUPAC Name - Contact for details]; [Common Chemical Name - Contact for details]; [Potential Trade Name 1]; [Potential Trade Name 2]
EINECS	Contact for details

Quality Control

Our Urol (Pharmaceutical) is manufactured under a quality management system and undergoes rigorous analytical testing to ensure it meets stringent specifications for pharmaceutical use. We provide comprehensive Certificates of Analysis (COA) with each batch, detailing purity, identity, and impurity profiles. The product is suitable for applications requiring high standards of quality and traceability.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 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.