Description

Dibromo Impurity CAS NO 1352492-08-0 is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for ensuring the quality, safety, and regulatory compliance of pharmaceutical products and advanced materials. It is primarily utilized by researchers and quality control professionals in the pharmaceutical, agrochemical, and fine chemical industries for method development, validation, and impurity profiling.

Application

• Pharmaceutical Impurity Reference Standard: Used for the identification, quantification, and control of process-related impurities and degradation products in Active Pharmaceutical Ingredients (APIs).
• Analytical Method Development & Validation: Serves as a critical component in developing and validating HPLC, GC, and LC-MS methods for purity analysis.
• Quality Control & Assurance: Employed as a system suitability standard and for routine batch testing in QC laboratories to ensure product specifications are met.
• Regulatory Compliance & Documentation: Essential for preparing regulatory submission documents (e.g., for FDA, EMA) that require detailed impurity characterization.
• Research & Development: Used in synthetic chemistry R&D to study reaction pathways, by-products, and to optimize purification processes.
• Stability Studies: Acts as a marker compound in forced degradation and long-term stability studies to monitor product integrity.

Basic Information

Product Name	Dibromo Impurity
CAS No.	1352492-08-0
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	1,2-Dibromo Impurity; Dibromo Related Compound; Dibromo Analog; Dibromo Derivative; CAS 1352492-08-0; Dibromo Process Impurity; Dibromo By-product; Dibromo Reference Standard
EINECS	Contact for details

Quality Control

Our Dibromo Impurity is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including chromatographic purity assays and spectroscopic identification, to ensure it meets the high standards required for reference materials. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and trace impurity profiles is provided with every shipment to support your quality and regulatory needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5% Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines

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