Clarithromycin EP impurity G

Product Name Clarithromycin EP impurity G
Alternate Names Clarithromycin Impurities, Impurities of Clarithromycin
CAT No. CS-O-11828
CAS No. 127182-44-9
Category Impurities
Stock IN-Stock
Mol. Wt. 776.99 g/mol
Mol. For. C₃₉H₇₂N₂O₁₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Clarithromycin
Purity 98.11
Therapeutic Anti-Cancer / Oncology
Smileys C[C@@](OC)(C[C@H](/C([C@@H]1C)=N\OC)C)[C@@H]([C@H]([C@]([C@H](C(O[C@H](CC)[C@@](C)(O)[C@@H]1O)=O)C)([H])O[C@@](O[C@@H](C)[C@@H]2O)([H])C[C@@]2(C)OC)C)O[C@@](O[C@H](C)C[C@@H]3N(C)C)([H])[C@@H]3O
Canonical Smiles CCC1C(C(C(C(=NOC)C(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)OC)C)C)O)(C)O
InchIKey BZXVFUGKJGEBBE-HQQTWTRQSA-N
Inchl InChI=1S/C39H72N2O13/c1-16-27-39(10,46)32(43)22(4)29(40-49-15)20(2)18-38(9,48-14)34(54-36-30(42)26(41(11)12)17-21(3)50-36)23(5)31(24(6)35(45)52-27)53-28-19-37(8,47-13)33(44)25(7)51-28/h20-28,30-34,36,42-44,46H,16-19H2,1-15H3/b40-29+/t20-,21-,22+,23+,24-,25+,26+,27-,28+,30-,31+,32-,33+,34-,36+,37-,38-,39-/m1/s1
IUPAC (3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-12,13-dihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-7-methoxy-10-methoxyimino-3,5,7,9,11,13-hexamethyl-oxacyclotetradecan-2-one
Controlled No
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Clarithromycin EP impurity G, also known as 14-hydroxy-6-O-methylerythromycin A, is a chemical compound that is commonly used as a reference standard in the pharmaceutical industry. It is an impurity that is found in Clarithromycin, which is a macrolide antibiotic that is used to treat a wide range of bacterial infections. Clarithromycin EP impurity G is used to identify and quantify the impurity in Clarithromycin drugs during quality control testing. It is important to monitor the levels of impurities in pharmaceuticals because they can affect the safety and efficacy of the drug. The chemical formula of Clarithromycin EP impurity G is C40H68N2O14, and it has a molecular weight of 812.98 g/mol. It is a white to off-white powder that is soluble in water and has a melting point of 173-175°C. Clarithromycin EP impurity G is synthesized by the methylation of 14-hydroxyerythromycin A using diazomethane. It is a semi-synthetic compound that is structurally related to erythromycin A. In conclusion, Clarithromycin EP impurity G is an important reference standard that is used to ensure the quality and safety of Clarithromycin drugs. Its usage and chemical information are critical for the pharmaceutical industry to produce safe and effective drugs for patients.

Related Compounds

Clarithromycin EP impurity D | Clarithromycin-N-methyl-13C-D3 | Clarithromycin EP impurity O | Clarithromycin 2’-O-Acetate | Clarithromycin_EDO | Clarithromycin EP impurity N | Clarithromycin_MEDO | Clarithromycin EP impurity F | Clarithromycin EP impurity A | Clarithromycin 9-Oxime | Clarithromycin EP impurity H | Clarithromycin_EO | Clarithromycin EP impurity I | Clarithromycin EP impurity K | Clarithromycin EP impurity C | N-Nitroso-N-Desmethyl-Clarithromycin | Clarithromycin EP impurity L | Clarithromycin EP impurity B | Clarithromycin EP impurity P | Clarithromycin EP impurity J | Clarithromycin EP impurity E | Clarithromycin EP impurity M | Clarithromycin Impurity 4 | Clarithromycin Corresponding impurity of erythromycin E |

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