1006062-28-7

Basic information

• Product Name: Losartan Impurity D
• Synonyms: O-Trityl Losartan;5-[4'-[[2-Butyl-4-chloro-5-[(triphenylMethoxy)Methyl]-1H-iMidazol-1-yl]Methyl][1,1'-biphenyl]-2-yl]-;Losartan EP IMpurity I;Losartan Trityl Ether (IMpurity I);5-(4'-((2-butyl-4-chloro-5-((trityloxy)methyl)-1H-imidazol-1-yl)methyl)-[1,1'-biphenyl]-2-yl)-1H-tetrazole;5-[4'-[[2-Butyl-4-chloro-5-[(triphenylmethoxy)methyl]-1H-imidazol-1-yl]methyl][1,1'-biphenyl]-2-yl]-2H-tetrazole;Losartan Impurity D;Losartan Trityl Ether
• CAS NO: 1006062-28-7
• Molecular Formula: C22H23ClN6O
• Molecular Weight: 422.91062
• Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Heterocycles;Impurities
• Mol File: 1006062-28-7.mol

Chemical Properties

• Melting Point: 136-139?C
• Boiling Point: 814.599 °C at 760 mmHg
• Flash Point: 446.453 °C
• Appearance: /
• Density: 1.218 g/cm³
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), DMSO, Methanol (Slightly, Heated, Sonicated)
• CAS DataBase Reference: Losartan Impurity D(CAS DataBase Reference)
• NIST Chemistry Reference: Losartan Impurity D(1006062-28-7)
• EPA Substance Registry System: Losartan Impurity D(1006062-28-7)

Safety Data

• Hazardous Substances Data: 1006062-28-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Losartan Impurity D is used as a reference material for the development and validation of analytical methods in the pharmaceutical industry. It helps in the identification, quantification, and quality control of Losartan in drug products.
Used in Research and Development:
Losartan Impurity D serves as a valuable compound for researchers to study the chemical properties, stability, and potential interactions of Losartan in various experimental settings. This contributes to a better understanding of the drug's behavior and its potential effects on human health.
Used in Quality Control:
Losartan Impurity D is utilized in the quality control process of Losartan drug products to ensure that the purity and potency of the active pharmaceutical ingredient meet the required standards. It aids in the detection and quantification of impurities, which is crucial for maintaining the safety and efficacy of the medication.