Clarithromycin EP impurity F

Product Name Clarithromycin EP impurity F
Alternate Names Clarithromycin Impurities, Impurities of Clarithromycin
CAT No. CS-T-57950
CAS No. 128940-83-0
Category Impurities
Stock IN-Stock
Mol. Wt. 761.98 g/mol
Mol. For. C₃₉H₇₁NO₁₃
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@@H]([C@@H]([C@H](C(O[C@@H]1CC)=O)C)O[C@@](O[C@@H](C)[C@@H]2O)([H])C[C@@]2(C)OC)[C@H]([C@@](C)(C[C@H](C([C@@H]([C@@H](O)[C@]1(C)OC)C)=O)C)OC)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)O)(C)OC
InchIKey ZABLXHVYLJLDOX-HIKKGGSBSA-N
Inchl InChI=1S/C39H71NO13/c1-16-27-39(10,48-15)32(43)22(4)29(41)20(2)18-38(9,47-14)34(53-36-30(42)26(40(11)12)17-21(3)49-36)23(5)31(24(6)35(45)51-27)52-28-19-37(8,46-13)33(44)25(7)50-28/h20-28,30-34,36,42-44H,16-19H2,1-15H3/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,11R,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-12-hydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-7,13-dimethoxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
Controlled No
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Clarithromycin EP impurity F, also known as 1'-N-Desmethyl Clarithromycin, is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for quality control purposes. It is a structural impurity of Clarithromycin, a macrolide antibiotic that is used to treat a wide range of bacterial infections. The presence of Clarithromycin EP impurity F in Clarithromycin samples can affect the purity and potency of the drug, and can also lead to adverse effects in patients. The chemical formula of Clarithromycin EP impurity F is C38H68N2O13, and its molecular weight is 760.95 g/mol. It is a white to off-white crystalline powder, and its melting point ranges from 168°C to 170°C. Clarithromycin EP impurity F is soluble in methanol, ethanol, and acetone, but is insoluble in water. In terms of its usage, Clarithromycin EP impurity F is primarily used as a reference standard in the quality control of Clarithromycin drugs. It is also used in the development and validation of analytical methods for the detection and quantification of Clarithromycin impurities. The presence of Clarithromycin EP impurity F in Clarithromycin samples can affect the purity and potency of the drug, and can also lead to adverse effects in patients. Therefore, it is important to accurately detect and quantify this impurity to ensure the safety and efficacy of Clarithromycin drugs.

Related Compounds

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

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