Azithromycin EP Impurity Q

Product Name Azithromycin EP Impurity Q
Alternate Names Azithromycin Impurities, Impurities of Azithromycin
CAT No. CS-O-34800
CAS No. 2095879-65-3
Category Impurities
Stock IN-Stock
Mol. Wt. 918.1 g/mol
Mol. For. C44H75N3O15S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Azithromycin
Canonical Smiles CCC1C(C(C(N(CC(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)NS(=O)(=O)C4=CC=C(C=C4)NC(=O)C)O)(C)O)C)C)C)O)(C)O
InchIKey DBZCHNDJNSRJPU-RBQZDAPESA-N
Inchl InChI=1S/C44H75N3O15S/c1-14-33-44(11,54)37(50)27(6)47(12)22-23(2)20-42(9,53)39(25(4)36(26(5)40(52)60-33)61-34-21-43(10,57-13)38(51)28(7)59-34)62-41-35(49)32(19-24(3)58-41)46-63(55,56)31-17-15-30(16-18-31)45-29(8)48/h15-18,23-28,32-39,41,46,49-51,53-54H,14,19-22H2,1-13H3,(H,45,48)/t23-,24-,25+,26-,27-,28+,32+,33-,34+,35-,36+,37-,38+,39-,41+,42-,43-,44-/m1/s1
IUPAC N-[4-[[(2S,3R,4S,6R)-2-[[(2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-2-ethyl-3,4,10-trihydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,6,8,10,12,14-heptamethyl-15-oxo-1-oxa-6-azacyclopentadec-11-yl]oxy]-3-hydroxy-6-methyloxan-4-yl]sulfamoyl]phenyl]acetamide
Controlled No
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Azithromycin EP Impurity Q is a chemical compound that is widely used in the pharmaceutical industry as a reference standard for the determination of purity and quality of Azithromycin, a commonly prescribed antibiotic medication. This impurity is a degradation product of Azithromycin, and its presence in the medication can indicate potential issues with the manufacturing process or storage conditions. Azithromycin EP Impurity Q is chemically known as (9E,12R,13S,14R,15R,17R,18R,19R,20S,21S,22E,24Z)-13-[(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)oxy]-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14,19-octamethyl-6,7,8,14,19,20,21,22-octahydro-17H-oxepino[2,3-b]pyridine-17,21-dicarboxylic acid. Its molecular formula is C44H76N2O18 and its molecular weight is 924.1 g/mol. Azithromycin EP Impurity Q is typically used as a reference standard in analytical testing methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). It is also used in the development and validation of analytical methods for the detection and quantification of Azithromycin and its related impurities. In summary, Azithromycin EP Impurity Q is an important chemical compound in the pharmaceutical industry that plays a crucial role in ensuring the quality and purity of Azithromycin-based medications.

Related Compounds

N,N-Didesmethyl N,N-dinitroso Azithromycin | Azithromycin 13C2 | Azithromycin EP Impurity C | Desosaminylazithromycin | N-nitroso azithromycin EP impurity M | Descladinose 6-N-Desmethyl Azithromycin | Azithromycin EP impurity I | Azithromycin EP Impurity L | Azithromycin impurity P | Azithromycin EP Impurity F | Azaerythromycin A | Azithromycin EP Impurity O | Azithromycin EP impurity P | N-Desmethyl Azithromycin B | N-Nitroso Desmethyl Azithromycin | N-Desmethyl 13(4-C,4-O-methylene)-pyranosyl Azithromycin | Azithromycin Impurity R | Azithromycin EP Impurity K | Azithromycin EP Impurity G |

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