Clarithromycin EP impurity I

Product Name Clarithromycin EP impurity I
Alternate Names Clarithromycin Impurities, Impurities of Clarithromycin
CAT No. CS-T-51698
CAS No. 118058-74-5
Category Impurities
Stock IN-Stock
Mol. Wt. 589.76 g/mol
Mol. For. C₃₀H₅₅NO₁₀
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Clarithromycin
Purity 95%
Therapeutic Anti-Cancer / Oncology
Smileys C[C@@](OC)(C[C@H](C([C@@H]1C)=O)C)[C@@H]([C@H]([C@@H]([C@H](C(O[C@H](CC)[C@@](C)(O)[C@@H]1O)=O)C)O)C)O[C@@](O[C@H](C)C[C@@H]2N(C)C)([H])[C@@H]2O
Canonical Smiles CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)O)C)OC2C(C(CC(O2)C)N(C)C)O)(C)OC)C)C)O)(C)O
InchIKey QTLYNHBYTKOXTE-LOOUJMBSSA-N
Inchl InChI=1S/C30H55NO10/c1-12-21-30(8,37)25(35)17(4)22(32)15(2)14-29(7,38-11)26(18(5)23(33)19(6)27(36)40-21)41-28-24(34)20(31(9)10)13-16(3)39-28/h15-21,23-26,28,33-35,37H,12-14H2,1-11H3/t15-,16?,17+,18+,19-,20?,21-,23+,24?,25-,26-,28?,29-,30-/m1/s1
IUPAC (3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-4,12,13-trihydroxy-7-methoxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
Controlled No
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Clarithromycin EP Impurity I is a chemical substance that is used in the pharmaceutical industry as a reference standard and quality control agent for the analysis of Clarithromycin, a commonly prescribed antibiotic drug. The impurity is a byproduct of the manufacturing process of Clarithromycin and is present in small quantities in the final product. The chemical name for Clarithromycin EP Impurity I is 6-O-Methylerythromycin A. It is a macrolide antibiotic that belongs to the group of erythromycin derivatives. The molecular formula of the impurity is C38H68N2O13, and its molecular weight is 760.95 g/mol. The impurity is a white to off-white powder that is soluble in water and methanol. The usage of Clarithromycin EP Impurity I is essential in the evaluation of the quality and purity of Clarithromycin. The impurity is used as a reference standard for the identification and quantification of impurities in Clarithromycin samples. It is also used to validate the analytical methods used for the analysis of Clarithromycin. In conclusion, Clarithromycin EP Impurity I is an essential chemical substance used in the pharmaceutical industry for the analysis and quality control of Clarithromycin. Its chemical properties and usage make it an essential reference standard for the identification and quantification of impurities in Clarithromycin samples.

Related Compounds

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

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