Clarithromycin EP impurity A

Product Name Clarithromycin EP impurity A
Alternate Names Clarithromycin Impurities, Impurities of Clarithromycin
CAT No. CS-O-11818
CAS No. 124412-58-4
Category Impurities
Stock IN-Stock
Mol. Wt. 763.95 g/mol
Mol. For. C₃₈H₆₉NO₁₄
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Clarithromycin
Purity Not less than 90 %
Therapeutic Anti-Cancer / Oncology
Smileys CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)CO)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
Canonical Smiles CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)CO)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 JDKPAXGOJMGSAE-OKRVCPMNSA-N
Inchl InChI=1S/C38H69NO14/c1-14-26-38(9,46)31(43)21(4)28(41)19(2)16-37(8,48-13)33(53-35-29(42)25(39(10)11)15-20(3)49-35)22(5)30(24(18-40)34(45)51-26)52-27-17-36(7,47-12)32(44)23(6)50-27/h19-27,29-33,35,40,42-44,46H,14-18H2,1-13H3/t19-,20-,21+,22-,23+,24+,25+,26-,27+,29-,30+,31+,32+,33+,35+,36-,37-,38?/m1/s1
IUPAC (3S,4S,5R,6S,7R,9R,11R,12S,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-3-(hydroxymethyl)-7-methoxy-5,7,9,11,13-pentamethyl-oxacyclotetradecane-2,10-dione
Controlled No
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Clarithromycin EP Impurity A is a chemical compound that is commonly used in pharmaceutical research and development. It is a synthetic impurity that is structurally related to Clarithromycin, which is an antibiotic medication used to treat a variety of bacterial infections. Clarithromycin EP Impurity A is used as a reference standard in analytical testing methods to ensure the purity and quality of Clarithromycin drug products. The chemical formula of Clarithromycin EP Impurity A is C44H72N2O14, and it has a molecular weight of 853.04 g/mol. It is a white to off-white powder that is soluble in water and organic solvents. The compound is stable under normal conditions, and it does not pose any significant health hazards or environmental risks. Clarithromycin EP Impurity A is typically synthesized by chemical reactions that involve the use of various reagents and catalysts. The purity of the compound is determined by high-performance liquid chromatography (HPLC) or other analytical techniques. In summary, Clarithromycin EP Impurity A is a synthetic impurity that is used as a reference standard in pharmaceutical research and development. It is a stable and non-hazardous compound that plays a critical role in ensuring the quality and safety of Clarithromycin drug products.

Related Compounds

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

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