3'-(N,N-Didemethyl)Azithromycin

Product Name 3'-(N,N-Didemethyl)Azithromycin
Alternate Names Azithromycin Impurities, Impurities of Azithromycin
CAT No. CS-O-07321
CAS No. 612069-27-9
Category Impurities
Stock IN-Stock
Mol. Wt. 720.93 g/mol
Mol. For. C₃₆H₆₈N₂O₁₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Azithromycin
Purity 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)C[C@@H]3N)([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(CC(O3)C)N)O)(C)O)C)C)C)O)(C)O
InchIKey PCDDIDGPAIGEHC-GGNUPITBSA-N
Inchl InChI=1S/C36H68N2O12/c1-13-25-36(10,44)29(40)22(6)38(11)17-18(2)15-34(8,43)31(50-33-27(39)24(37)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/h18-31,33,39-41,43-44H,13-17,37H2,1-12H3/t18-,19-,20+,21-,22-,23+,24+,25-,26+,27-,28+,29-,30+,31-,33+,34-,35-,36-/m1/s1
IUPAC (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-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-1-oxa-6-azacyclopentadecan-15-one
Controlled No
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Azithromycin EP Impurity E is a chemical compound that is commonly used as a reference standard for the analysis and identification of impurities in Azithromycin. Azithromycin is a broad-spectrum antibiotic that is used to treat a variety of bacterial infections, including respiratory tract infections, skin infections, and sexually transmitted infections. As with all pharmaceutical products, it is important to ensure that the Azithromycin used is of high quality and purity in order to maximize its effectiveness and minimize the risk of negative side effects. Azithromycin EP Impurity E is a synthetic compound that is produced through a series of chemical reactions. It is characterized by its chemical structure, which includes a nitrogen-containing heterocyclic ring and a five-membered lactone ring. This compound is typically used in the laboratory as a reference standard for the analysis of Azithromycin, as it is a known impurity that can be present in the drug product. The presence of impurities in pharmaceuticals can affect the purity, potency, and safety of the drug, which is why it is important to use reference standards like Azithromycin EP Impurity E to ensure the quality of the product.

Related Compounds

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

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