share

Delafloxacin Impurity 6 CAS NO 2097714-11-7


Unit Price:

CAS No.:2097714-11-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Delafloxacin Impurity 6 CAS NO 2097714-11-7 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 the antibiotic Delafloxacin during its development and manufacturing. It is primarily required by pharmaceutical R&D laboratories, quality control (QC) departments, and contract research organizations (CROs) for method validation, impurity profiling, and stability studies.

Application

  • Pharmaceutical Impurity Profiling and Identification in Delafloxacin API and finished drug products.
  • Analytical Method Development and Validation (HPLC, LC-MS) for accurate quantification of related substances.
  • Quality Control and Release Testing to meet ICH Q3A/B guidelines and regulatory submission requirements.
  • Stability Studies to monitor impurity formation under various stress conditions.
  • Reference Standard for Pharmacopeial Testing to ensure compliance with USP/EP monographs.
  • Research and Development of Delafloxacin synthesis pathways and degradation studies.

Basic Information

Product Name Delafloxacin Impurity 6
CAS No. 2097714-11-7
Molecular Formula C18H12ClF3N4O4
Molecular Weight 440.76 g/mol
Synonyms 1-(6-Amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid; Delafloxacin Related Compound 6; ABT-492 Impurity 6; RX-3341 Impurity 6; WO-3034 Impurity 6; (1R,2S)-1-(6-Amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid
EINECS Contact for details

Quality Control

Our Delafloxacin Impurity 6 is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC purity determination, identity confirmation (IR, MS), and residual solvent analysis, to ensure compliance with high-grade reference standard specifications. A comprehensive Certificate of Analysis (COA) with batch-specific data is provided to support your regulatory and research needs.

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 should be handled in a dry environment to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white solid
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference
Purity (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Water Content (KF) ≤ 1.0% w/w
Residual Solvents (GC) Complies with ICH Q3C

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.