Keywords

• 1-Phenol-4-sulfonamide,2-nitro- (6CI)
• Venetoclax Impurity 61
• 4-Hydroxy-3-nitrobenzenesulfonamide

Quick Details

• ProName: Venetoclax Impurity 61
• CasNo: 24855-58-1
• Molecular Formula: C6H6N2O5S
• Appearance: White to off white powder
• Application: for drug impurity for drug standards,f...
• DeliveryTime: 1-2 weeks
• PackAge: 10mg/25mg/50mg/100mg/1000mg/5000mg
• Port: Shenzhen/hongkong
• ProductionCapacity: 5000 Milligram/Day
• Purity: 95%+ or 98%+
• Storage: -20℃
• LimitNum: 25 Milligram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

• Advantages: This impurity reference standard features high purity and excellent stability. Through strict quality inspection and control processes, it can provide a reliable reference standard for drug research and development, quality control, and other aspects, ensuring the accuracy and consistency of experimental data.

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Our products are mainly drug impurity reference products, drug standards, analytical chemistry, standard substances, organic chemical synthesis, chemical custom synthesis. For impurity localization, quantification, and quality control in drug development processes. Our laboratory area is more than 5000 square meters, we have more than 20 analytical instruments such as HPLC and MS/LC-MS/GC-MS, we also have TGA, IR and other testing instruments. We have the most advanced SFC preparation separation equipment. We can provide a full range of impurity reference/standard products required for drug development. Most of the impurities are synthesized through the process, there are also many items of impurities can not be obtained by synthetic means, need to be obtained through raw materials, intermediates, crude products or side reactions contained in the trace target compounds, Hubei Moke has a professional impurity preparation and separation technology team, equipped with professional SFC preparation and separation equipment. It can carry out efficient and accurate separation of impurities for complex projects, and solve the problem of impurity preparation for customers.

1. We integrate R&D, production and sales. A 5,000-square-meter high-standard bio-intelligent manufacturing base can ensure high quality and fast delivery of products. The professional sales team ensures that you don't need to worry about pre-sales and after-sales.

2. We focus on pharmaceutical standards, pharmaceutical intermediates, pharmaceutical impurity controls, peptide customization, our own laboratory, and undertake customized synthesis projects.

3. We offer products from gram grade to g grade, in addition, some product specifications and packaging can be customized.

4. We have been deeply engaged in the pharmaceutical field for ten years and have rich experience. At present, customers are all over the world, and have been highly recognized and trusted by customers.

5. We can provide a variety of safe ways to transport goods for you to choose.

Details

Venetoclax Impurity 24855-58-1

• Product Number: V028061

   

• English Name: Venetoclax Impurity 61

• English Alias: 4-hydroxy-3-nitrobenzenesulfonamide

• CAS Number: 24855-58-1

• Molecular Formula: C6H6N2O5S

• Molecular Weight: 218.19

• Advantages: This impurity reference standard features high purity and excellent stability. Through strict quality inspection and control processes, it can provide a reliable reference standard for drug research and development, quality control, and other aspects, ensuring the accuracy and consistency of experimental data.

• Applications: It is mainly applied to the fields of impurity research, quality analysis, and control of Venetoclax drugs. In the drug research and development process, it can be used to determine the content of impurities in drugs and evaluate the safety and effectiveness of drugs. In the quality control of pharmaceutical production, it can effectively detect the presence of this impurity in products, ensuring that the quality of drugs meets the standards.

• Background Description: With the continuous improvement of the pharmaceutical industry's requirements for drug quality and safety, the research on drug impurities has become increasingly important. As an important drug, the research on the impurities of Venetoclax is of great significance for ensuring drug quality, efficacy, and patient medication safety. The study of Venetoclax Impurity 61, as one of these impurities, is a crucial part of the drug quality control system.

• Research Status: Currently, research on Venetoclax Impurity 61 is ongoing. Researchers are committed to developing more accurate and efficient detection methods to improve the ability to identify and quantify this impurity. At the same time, studies on its generation mechanism during drug synthesis and its impact on drug performance are also gradually advancing, aiming to provide more comprehensive theoretical support and technical guidance for drug research, development, and production.