Keywords

• Acetophenone,2-bromo-4'-(methylsulfonyl)- (6CI)
• Imrecoxib Impurity
• 2-Bromo-4'-(Methylsulfonyl)acetophenone

Quick Details

• ProName: 2-Bromo-1-[4-(methylsulfonyl)phenyl]-1...
• CasNo: 50413-24-6
• Molecular Formula: C9H9BrO3S
• Appearance: white or almost white crystalline powd...
• Application: Pharmaceutical research
• DeliveryTime: prompt delivery
• PackAge: food packages,foil bags
• Port: shenzhen/hongkong
• ProductionCapacity: 500 Gram/Year
• Purity: 95%+
• Storage: cool and dry
• Transportation: DHL,FedEx,UPS,EMS,TNT;
• LimitNum: 10 Milligram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

We supply over 20000 types of spot impurity reference materials, with sufficient supply and same day delivery to meet customers' urgent needs for replenishment at any time. The company has its own research and development center and laboratory, and the team members have over ten years of experience in developing drug impurity reference standards. Our website www.molcoo.com covers over 98% of cutting-edge generic drug projects, with complete structural formulas that greatly save customers time in impurity structure analysis and inference. All products undergo strict quality control testing and provide relevant information such as COA, H-NMR, C-NMR, MS/GC-MS, HPLC/GC purity, QNMR quantification, TGA thermogravimetric analysis, IR infrared, UV ultraviolet, two-dimensional (COSY, NOESY, HMBC, HMQC), etc. These structural confirmation spectra ensure quality and reliability. Our products have a wide range of categories, fast delivery time, good quality, and low prices, which can quickly solve various customer needs such as replenishment and consistency evaluation.

Details

Imrecoxib Impurity Reference Standard

Product Name: Imrecoxib Impurity Reference Standard

Product Details:

Imrecoxib impurity reference standards are high-purity reference materials used in drug development, quality control, and pharmaceutical analysis. These impurity reference standards assist researchers and quality control experts in accurately identifying and quantifying various impurities that may be present in imrecoxib drugs, thereby ensuring their safety and effectiveness.

Main Components:

They contain various specific impurities of imrecoxib, which are extracted from imrecoxib active pharmaceutical ingredients (APIs) or related formulations through precise separation and purification techniques.

Product Characteristics:

1. High Purity: The impurity reference standards undergo rigorous purification processes to ensure their purity meets analytical requirements.
2. Stability: Under appropriate storage conditions, the impurity reference standards remain stable and are resistant to degradation or deterioration.
3. Accuracy: The impurity reference standards aid in accurately identifying and quantifying impurities in imrecoxib drugs, improving the accuracy and reliability of analysis.

Applications:

1. Drug Development: Used to identify and quantify potential impurities during the synthesis and formulation development of imrecoxib drugs, ensuring drug quality.
2. Quality Control: Monitored and controlled the impurity content during the production of imrecoxib pharmaceuticals, ensuring compliance with quality standards.
3. Pharmaceutical Analysis: Served as reference materials for calibrating instruments and analytical methods during drug testing and inspection processes.

Storage Conditions:

Store according to the instructions on the packaging, typically in a dry, light-protected, and cool place, to ensure the stability and long-term availability of the impurity reference standards.