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内容: HPLC、MASS/LC-MS、1H NMR、FT-IR、含量、構造解析レポート（SER）、および製品に応じた追加分析データ。

Minocycline EP Impurity G

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カタログ番号:	VE0017091
CAS番号:	N/A
分子式:	C25H33ClN4O7
分子量:	537.01 g/mol

見積もり依頼

RFQリストに追加

に関する追加情報 Minocycline EP Impurity G

親薬物

Minocycline

IUPAC名

(4S, 4aS, 5aR, 12aS)-4, 7, 9-Tris(dimethylamino)-3, 10, 12, 12a-tetrahydroxy-1, 11-dioxo-1, 4, 4a, 5, 5a, 6, 11, 12a-octahydrotetracene-2-carboxamide hydrochloride

薬局方同義語

N/A

Other Synonyms

9-Dimethylamino Minocycline Hydrochloride/ Minocycline 4,7,9-Tris-Dimethylamino Impurity Hydrochloride

SMILES

O=C(C1=C(O)[C@@H](N(C)C)[C@@](C[C@@]2([H])C(C(C3=C(O)C(N(C)C)=CC(N(C)C)=C3C2)=O)=C4O)([H])[C@@]4(O)C1=O)N.[H]Cl

Inchl

InChI=1S/C25H32N4O7.ClH/c1-27(2)13-9-14(28(3)4)19(30)16-11(13)7-10-8-12-18(29(5)6)21(32)17(24(26)35)23(34)25(12,36)22(33)15(10)20(16)31;/h9-10,12,18,30,32-33,36H,7-8H2,1-6H3,(H2,26,35);1H/t10-,12-,18-,25-;/m0./s1

説明

The compound Minocycline EP Impurity G is a highly characterized reference material that meets stringent regulatory standards, including those set by USP, EMA, JP, and BP. This product is essential for a variety of applications, such as analytical method development, method validation (AMV), and Quality Control (QC), particularly in the context of Minocycline production. It is suitable for use in both Abbreviated New Drug Applications (ANDA) and New Drug Applications (NDA). Additionally, the product comes with a detailed Structure Elucidation Report (SER), ensuring its precision and reliability for comprehensive analytical use.