Search Results for " Salbutamol "
Salbutamol EP Impurity L Hydrochloride
| SZ目录编号: | SZ-S003013 |
| CAS 号 | NA |
| 分子式 | C13H20ClNO3 : HCl |
| 分子量 | 273.8 : 36.5 |
| 投资状态 | In Stock |
| Rel. CAS No | 898542-81-9 (free base) |
化学名称: 4-[(1RS)-2-(tert-butylamino)-1-hydroxyethyl]-2-chloro-6-(hydroxymethyl)phenol hydrochloride (as per EP) ; 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-chloro-6-(hydroxymethyl)phenol hydrochloride (as per USP)
异名: Chloroalbuterol (USP) ; Salbutamol BP Impurity L
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: OC(C1=CC(CO)=C(O)C(Cl)=C1)CNC(C)(C)C.Cl
Salbutamol EP Impurity L Hydrochloride is chemically 4-[(1RS)-2-(tert-butylamino)-1-hydroxyethyl]-2-chloro-6-(hydroxymethyl)phenol hydrochloride (as per EP) ; 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-chloro-6-(hydroxymethyl)phenol hydrochloride (as per USP). It is also known as Chloroalbuterol (USP) ; Salbutamol BP Impurity L. Salbutamol EP Impurity L Hydrochloride is supplied with detailed characterization data compliant with regulatory guideline. Salbutamol EP Impurity L Hydrochloride can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Salbutamol .
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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