Clarithromycin EP impurity N

Product Name Clarithromycin EP impurity N
Alternate Names Clarithromycin Impurities, Impurities of Clarithromycin
CAT No. CS-O-11830
CAS No. 144604-03-5
Category Impurities
Stock IN-Stock
Mol. Wt. 729.94 g/mol
Mol. For. C38H67NO12
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Clarithromycin
Purity Not less than 95%
Therapeutic Anti-Cancer / Oncology
Smileys C[C@@](OC)(C[C@H](C(/C(C)=C/[C@](C)(O)[C@@H](CC)O1)=O)C)[C@@H]([C@H]([C@@H]([C@H](C1=O)C)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(=O)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)(C)O
InchIKey XBRPMQCVVSGOJB-LUHVZOSXSA-N
Inchl InChI=1S/C38H67NO12/c1-15-27-36(8,44)17-20(2)29(40)21(3)18-38(10,46-14)33(51-35-30(41)26(39(11)12)16-22(4)47-35)23(5)31(24(6)34(43)49-27)50-28-19-37(9,45-13)32(42)25(7)48-28/h17,21-28,30-33,35,41-42,44H,15-16,18-19H2,1-14H3/b20-17+/t21-,22-,23+,24-,25+,26+,27-,28+,30-,31+,32+,33-,35+,36+,37-,38-/m1/s1
IUPAC (3R,4S,5S,6R,7R,9R,11E,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-13-hydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-7-methoxy-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradec-11-ene-2,10-dione
Controlled No
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Clarithromycin EP impurity N is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Clarithromycin, which is a semi-synthetic macrolide antibiotic used to treat various bacterial infections. It is also known as 6-O-Methylerythromycin A and has a molecular formula of C41H68N2O14. Clarithromycin EP impurity N is a white to off-white crystalline powder that is sparingly soluble in water but soluble in most organic solvents. It is a derivative of erythromycin and differs from Clarithromycin by the presence of a methyl group attached to the 6-position of the erythronolide ring. The usage of Clarithromycin EP impurity N is mainly in the development and validation of analytical methods for the quantification of impurities in Clarithromycin. It is also used for the characterization of Clarithromycin and its related substances in quality control during the manufacturing process. Chemically, Clarithromycin EP impurity N is classified as a macrolide antibiotic and its structure contains a large lactone ring with several functional groups attached. Its purity is typically measured using high-performance liquid chromatography (HPLC) and is required to be above 98% for use as a reference standard. Overall, Clarithromycin EP impurity N is an important reference standard that plays a vital role in ensuring the quality and safety of Clarithromycin-based medications.

Related Compounds

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

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