Description

Angiolam A CAS NO 99267-41-1 is a high-purity pharmaceutical intermediate and research chemical. This compound is critical for the synthesis and development of advanced therapeutic agents, particularly in the field of cardiovascular and metabolic disease research. It is essential for pharmaceutical manufacturers, biotechnology R&D laboratories, and academic research institutions focused on novel drug discovery and process development.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular medications.
• Biochemical Research: Used as a reference standard and reagent in metabolic pathway studies and enzyme inhibition assays.
• Drug Discovery & Development: Serves as a core scaffold for medicinal chemistry optimization and the creation of novel drug candidates.
• Process Chemistry: Employed in scale-up and optimization of manufacturing routes for target molecules in GMP environments.
• Academic Research: Utilized in university and institutional labs for pharmacological and pharmacokinetic studies.

Basic Information

Product Name	Angiolam A
CAS No.	99267-41-1
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Angiolam A; 99267-41-1; UNII-9FZ6L5175Y; 9FZ6L5175Y; SCHEMBL218422; DTXSID701330163; AKOS040759623; DB08299
EINECS	Contact for details

Quality Control

Our Angiolam A is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the stringent requirements for pharmaceutical R&D and manufacturing. Certificates of Analysis (COA) documenting full specifications are available for every lot upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep container tightly sealed when not in use to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 1.0%

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