3-deoxyazithromycin

Chemical Name 3-deoxyazithromycin
Alternate Names Azithromycin Impurities, Impurities of Azithromycin
CAT No. CS-O-07320
CAS Registry# 307974-61-4
Category Impurities
Stock IN-Stock
Mol. Wt. 732.99 g/mol
Mol. For. C₃₈H₇₂N₂O₁₁
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Azithromycin
Purity 95%
Therapeutic Antibiotics
Smileys 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(C)C)O)(C)O)C)C)C)O)C
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(C)C)O)(C)O)C)C)C)O)C
InchIKey JBYIGHZCRVMHAK-VINPOOLWSA-N
Inchl InChI=1S/C38H72N2O11/c1-15-28-22(4)30(41)25(7)40(13)19-20(2)17-37(9,45)34(51-36-31(42)27(39(11)12)16-21(3)47-36)23(5)32(24(6)35(44)49-28)50-29-18-38(10,46-14)33(43)26(8)48-29/h20-34,36,41-43,45H,15-19H2,1-14H3/t20-,21-,22+,23+,24-,25-,26+,27+,28-,29+,30+,31-,32+,33+,34-,36+,37-,38-/m1/s1
IUPAC (2R,3R,4S,5R,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-4,10-dihydroxy-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 B is a chemical compound used as a reference standard and impurity marker in the quality control of Azithromycin, an antibiotic medication used for the treatment of various bacterial infections. Azithromycin EP Impurity B is also known as desmethyl-azithromycin, which is a derivative of Azithromycin. This compound is synthesized and purified for use in the laboratory setting as an analytical standard. Azithromycin EP Impurity B is a white to off-white powder or crystal that has a molecular weight of 417.95 g/mol. The compound has a melting point of 128-131°C and is soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO). The chemical structure of Azithromycin EP Impurity B is similar to that of Azithromycin, with the exception of the presence of a hydroxyl group instead of a methyl group at the C-3 position of the lactone ring. This structural difference is significant, as it affects the biological activity and pharmacokinetics of the compound. In conclusion, Azithromycin EP Impurity B is a valuable analytical tool in the quality control of Azithromycin, providing a reference standard and impurity marker for the identification and quantification of this antibiotic medication. Its chemical properties and structure play an important role in the understanding and evaluation of the pharmacological activity and safety of Azithromycin.

Related Compounds

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

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