Cefpodoxime Proxetil EP Impurity E

Product Name Cefpodoxime Proxetil EP Impurity E
Alternate Names Cefpodoxime Proxetil Impurities, Impurities of Cefpodoxime Proxetil
CAT No. CS-O-13514
CAS No. 217803-89-9
Category Impurities
Stock IN-Stock
Mol. Wt. 585.61 g/mol
Mol. For. C₂₂H₂₇N₅O₁₀S₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Cefpodoxime Proxetil
Purity 95%
Therapeutic Antibiotics
Smileys O=C(C(N1[C@@]2([H])[C@H](NC(/C(C3=CSC(N)=N3)=N\OC)=O)C1=O)=C(CS2)COC(C)=O)OC(C)OC(OC(C)C)=O
Canonical Smiles CC(C)OC(=O)OC(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)C(=NOC)C3=CSC(=N3)N)COC(=O)C
InchIKey JRBKWVHQXXREQH-KMMUMHRISA-N
Inchl InChI=1S/C22H27N5O10S2/c1-9(2)35-22(32)37-11(4)36-20(31)16-12(6-34-10(3)28)7-38-19-15(18(30)27(16)19)25-17(29)14(26-33-5)13-8-39-21(23)24-13/h8-9,11,15,19H,6-7H2,1-5H3,(H2,23,24)(H,25,29)/b26-14-/t11?,15-,19-/m1/s1
IUPAC 1-propan-2-yloxycarbonyloxyethyl (6R,7R)-3-(acetyloxymethyl)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
Controlled No
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Cefpodoxime Proxetil EP Impurity E is a chemical compound that is used in the pharmaceutical industry as a reference standard for testing and quality control purposes. It is a known impurity in Cefpodoxime Proxetil, which is a third-generation cephalosporin antibiotic used to treat a wide range of bacterial infections. The chemical formula of Cefpodoxime Proxetil EP Impurity E is C15H16N2O4S, and it has a molecular weight of 316.36 g/mol. It is a white to off-white crystalline powder that is soluble in methanol and slightly soluble in water. The purity of this impurity is usually determined by high-performance liquid chromatography (HPLC) and should be no more than 0.5%. Cefpodoxime Proxetil EP Impurity E is typically used as a reference standard in the development and validation of analytical methods for the detection and quantification of impurities in Cefpodoxime Proxetil. It is also used in the characterization of Cefpodoxime Proxetil formulations and in stability studies to assess the degradation products of the drug. In conclusion, Cefpodoxime Proxetil EP Impurity E is an important reference standard in the pharmaceutical industry that plays a critical role in ensuring the safety and efficacy of Cefpodoxime Proxetil products. Its chemical properties and usage make it an essential component in drug development and quality control.

Related Compounds

Cefpodoxime Proxetil | Cefpodoxime Proxetil EP Impurity J | Cefpodoxime Proxetil EP Impurity G | a,b-Cefpodoxime proxetil sulfooxide | Cefpodoxime Proxetil Impurity K | Cefpodoxime Proxetil EP Impurity B (Mixture of isomers) | Cefpodoxime Proxetil Dimer Impurity 2 (6R 7R 6'R 7'R -dimer) | Cefpodoxime Proxetil isopropoxycarbonyl analog | Cefpodoxime Proxetil EP Impurity A (Cefpodoxime Acid) | Cefpodoxime Proxetil Dimer Impurity 1 ( 6R,7R, 6'S,7'S-dimer) (EP imp-I) | Cefpodoxime Proxetil EP Impurity M | Cefpodoxime Proxetil EP Impurity D | Cefpodoxime Proxetil EP Impurity C | Cefpodoxime Proxetil 4,7-seco-Dimer | O-Desisopropyl-O-ethyl Cefpodoxime Proxetil | Cefpodoxime Proxetil sulfoxide | Cefpodoxime Proxetil EP Impurity F (E and Z Mixture) | Cefpodoxime Proxetil Isopropylcarbamate | Cefpodoxime Proxetil EP Impurity G (E and Z Mixture) | Cefpodoxime Proxetil EP Impurity F | Cefpodoxime proxetil Boc-L-alanine impurity (E and Z Mixture) | Cefpodoxime Proxetil Impurity 2 | N-Nitroso Cefpodoxime Proxetil |

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