Search Results for " Levothyroxine "
Levothyroxine EP Impurity A
| SZ目录编号: | SZ-L022002 |
| CAS 号 | 55-06-1 |
| 分子式 | C15H11I3NO4 : Na |
| 分子量 | 650.0 : 23.0 |
| 投资状态 | In Stock |
| Rel. CAS No | 6893-02-3 (free base) |
化学名称: Sodium (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid (as per EP) ; Sodium (O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-) L-Tyrosine) (as per USP)
异名: Liothyronine Sodium (USP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC2=CC=C(O)C(I)=C2.[Na+]
Levothyroxine EP Impurity A is chemically Sodium (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid (as per EP) ; Sodium (O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-) L-Tyrosine) (as per USP). It is also known as Liothyronine Sodium (USP). Levothyroxine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Levothyroxine EP Impurity A 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 Levothyroxine.
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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