3'-De(Dimethylamino)-3'-Oxoazithromycin

Product Name 3'-De(Dimethylamino)-3'-Oxoazithromycin
Alternate Names Azithromycin Impurities, Impurities of Azithromycin
CAT No. CS-O-07328
CAS No. 612069-25-7
Category Impurities
Stock IN-Stock
Mol. Wt. 719.90 g/mol
Mol. For. C₃₆H₆₅NO₁₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Azithromycin
Purity "Not less than 95% "
Therapeutic Antibiotics
Smileys C[C@@H]([C@@H]([C@H](C(O[C@@H]([C@@](C)(O)[C@@H]1O)CC)=O)C)O[C@@](O[C@@H](C)[C@@H]2O)([H])C[C@@]2(C)OC)[C@H]([C@](O)(C[C@H](CN([C@@H]1C)C)C)C)O[C@@](O[C@H](C)CC3=O)([H])[C@@H]3O
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(=O)CC(O3)C)O)(C)O)C)C)C)O)(C)O
InchIKey AMNAVVMCWWSBHN-AWHKAWBESA-N
Inchl InChI=1S/C36H65NO13/c1-13-25-36(10,44)29(40)22(6)37(11)17-18(2)15-34(8,43)31(50-33-27(39)24(38)14-19(3)46-33)20(4)28(21(5)32(42)48-25)49-26-16-35(9,45-12)30(41)23(7)47-26/h18-23,25-31,33,39-41,43-44H,13-17H2,1-12H3/t18-,19-,20+,21-,22-,23+,25-,26+,27-,28+,29-,30+,31-,33+,34-,35-,36-/m1/s1
IUPAC (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-11-[(2S,3S,6R)-3-hydroxy-6-methyl-4-oxooxan-2-yl]oxy-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-azacyclopentadecan-15-one
Controlled No
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Azithromycin EP Impurity N is a chemical substance that is commonly used in the pharmaceutical industry as a reference standard for the quality control of Azithromycin, an antibiotic medication that is used to treat a wide range of bacterial infections. This impurity is a byproduct of the synthesis of Azithromycin and is usually present in very small amounts in the final drug substance. Chemically, Azithromycin EP Impurity N has the molecular formula C38H71NO13 and a molecular weight of 761.98 g/mol. It is a white to off-white powder that is soluble in water, methanol, and ethanol. The impurity is stable under normal conditions of storage and handling. The usage of Azithromycin EP Impurity N is critical in ensuring the quality and safety of Azithromycin drug products. It is used as a reference standard to verify the identity, purity, and content of Azithromycin in drug formulations during quality control testing. This impurity is also used as a standard for the development and validation of analytical methods for the quantification of Azithromycin in drug products. Overall, Azithromycin EP Impurity N is an important chemical substance in the pharmaceutical industry that plays a crucial role in ensuring the quality and efficacy of Azithromycin drug products.

Related Compounds

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

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