Acetylcysteine EP impurity D
95%
- Product Code: 105706
Alias:
Dacisteine; (R)-2-Acetamido-3-(acetylthio)propionic acid
CAS:
18725-37-6
| Molecular Weight: | 205.23 g./mol | Molecular Formula: | C₇H₁₁NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00152052 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Acetylcysteine EP impurity D is primarily used in the pharmaceutical industry as a reference standard for quality control and analytical purposes. It plays a critical role in ensuring the purity and consistency of acetylcysteine, a medication widely used for its mucolytic and antioxidant properties. By identifying and quantifying this impurity during the manufacturing process, pharmaceutical companies can maintain compliance with regulatory standards and ensure the safety and efficacy of acetylcysteine-based products. Additionally, it aids in research and development efforts to optimize production processes and minimize the presence of impurities in final drug formulations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $141.76 |
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| 1.000 | 10-20 days | $323.22 |
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Acetylcysteine EP impurity D
Acetylcysteine EP impurity D is primarily used in the pharmaceutical industry as a reference standard for quality control and analytical purposes. It plays a critical role in ensuring the purity and consistency of acetylcysteine, a medication widely used for its mucolytic and antioxidant properties. By identifying and quantifying this impurity during the manufacturing process, pharmaceutical companies can maintain compliance with regulatory standards and ensure the safety and efficacy of acetylcysteine-based products. Additionally, it aids in research and development efforts to optimize production processes and minimize the presence of impurities in final drug formulations.
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