Search Results for " Budesonide "
Budesonide EP Impurity I
| N° de SZ CAT: | SZ-B022010 |
| Número CAS | 113930-13-5 |
| Mol.F. | C25H34O7 |
| Peso Molecular | 446.5 |
| Status de Fatura | In Stock |
Nome Químico: 11β,17,21-Trihydroxy-3,20-dioxopregna-1,4-dien-16α-yl butanoate (as per EP)
Sinônimo: 16α-Butyloxy Prednisolone ; 16α-Hydroxyprednisolone 16-butyrate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: CCCC(O[C@]1([H])C[C@@]2([H])[C@]3([H])CCC4=CC(C=C[C@]4(C)[C@@]3([H])[C@@H](O)C[C@]2(C)[C@@]1(O)C(CO)=O)=O)=O
Budesonide EP Impurity I is chemically 11β,17,21-Trihydroxy-3,20-dioxopregna-1,4-dien-16α-yl butanoate (as per EP). It is also known as 16α-Butyloxy Prednisolone ; 16α-Hydroxyprednisolone 16-butyrate. Budesonide EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Budesonide EP Impurity I 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 Budesonide.
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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