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Tedizolid Phosphate Impurity CAS NO 1239662-49-7


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CAS No.:1239662-49-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Tedizolid Phosphate Impurity CAS NO 1239662-49-7 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 active pharmaceutical ingredient (API) Tedizolid Phosphate. It is primarily required by pharmaceutical manufacturers, analytical laboratories, and research institutions for method development, validation, and impurity profiling in accordance with ICH guidelines.

Application

  • Pharmaceutical Impurity Profiling and Identification as a specified impurity in Tedizolid Phosphate API.
  • Analytical Method Development and Validation for HPLC, UPLC, and LC-MS techniques.
  • Quality Control and Assurance (QC/QA) in pharmaceutical manufacturing to monitor and control impurity levels.
  • Stability Studies to track the formation of degradation products under various stress conditions.
  • Regulatory Compliance and Documentation for submissions to agencies like the FDA and EMA.
  • Research and Development (R&D) of Tedizolid Phosphate and related oxazolidinone antibiotics.
  • Calibration Standard for quantitative analysis in pharmaceutical testing laboratories.

Basic Information

Product Name Tedizolid Phosphate Impurity
CAS No. 1239662-49-7
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Tedizolid Phosphate Related Compound; Tedizolid Impurity; (R)-3-(4-(2-(2-Methyltetrazol-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one Phosphate; Oxazolidinone impurity; TR-700 FA Impurity; Sivextro Impurity
EINECS Contact for details

Quality Control

Our Tedizolid Phosphate Impurity is manufactured under strict quality systems. Each batch undergoes rigorous analytical testing, including HPLC purity analysis and spectroscopic identification (IR, NMR, MS), to ensure it meets the high standards required for pharmaceutical reference materials. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profile is provided with every shipment to support your regulatory and quality needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 95.0%
Related Substances (HPLC) Individual unspecified impurity: ≤ 1.0% Total impurities: ≤ 5.0%
Residual Solvents (GC) Complies with ICH Q3C
Water Content (KF) ≤ 5.0% w/w

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

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