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Salbutamol EP Impurity D
Synchemia is a leading supplier of pharmaceutical-grade Salbutamol impurities, offering high-quality reference impurity standards for research and analytical purposes. Salbutamol EP Impurity D is one of the specified related substances listed in the European Pharmacopoeia (EP) monograph for Salbutamol, and must be controlled in both the active pharmaceutical ingredient (API) and finished product. mpurity D is structurally similar to salbutamol and generally not considered highly toxic at low levels. However, if levels exceed the ICH identification threshold (typically 0.1% for drugs dosed at ≥2 g/day), it must be: Identified Toxicologically qualified
Salbutamol EP Impurity D | CAS NO: 156339-88-7, also known as Salbutamol BP Impurity D ; Levalbuterol USP RC D ; Salbutamol Aldehyde Impurity is chemically expressed as 5-[(1RS)-2-(tert-butylamino)-1-hydroxyethyl]-2-hydroxybenzaldehyde(as per EP). Salbutamol EP Impurity D is supplied with comprehensive characterization data, in full compliance with applicable regulatory guidelines. Synchemia is a leading supplier and exporter of Salbutamol EP Impurity D. All Synchemia products are strictly intended for analytical testing purposes only and not for human use.
| Product name | Salbutamol EP Impurity D |
| SRC CAT No | SRC-S19145 |
| CAS No | 156339-88-7 |
| Mol.F. | C13H19NO3 |
| Mol.Wt. | 237.3 g/mol |
| Related CAS No. | 2624100-96-3 (Sulfate salt) |
| Inv Status | In Stock |
