Search Results for " Doxorubicin "
Doxorubicin EP Impurity C
| SZ目录编号: | SZ-D051008 |
| CAS 号 | NA |
| 分子式 | C27H28BrNO10 : 2(H2O) : HBr |
| 分子量 | 606.4 : 2(18.0) : 80.9 |
| 投资状态 | Custom Synthesis |
| Rel. CAS No | 65026-79-1 (free base) ; 60873-68-9 (HBr salt) ; 29742-67-4 (HCl salt) |
化学名称: (8S,10S)-10[(3-Amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-8-(bromoacetyl)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione dihydrate hydrobromide
异名: Doxorubicin BP Impurity C
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: OC1=C(C[C@](C(CBr)=O)(O)C[C@@H]2O[C@@](O[C@@H](C)[C@H]3O)([H])C[C@@H]3N)C2=C(O)C(C4=O)=C1C(C5=CC=CC(OC)=C45)=O.[2H2O].Br
Doxorubicin EP Impurity C is chemically (8S,10S)-10[(3-Amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-8-(bromoacetyl)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione dihydrate hydrobromide. It is also known as Doxorubicin BP Impurity C. Doxorubicin EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Doxorubicin EP Impurity C 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 Doxorubicin.
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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