Ribavirin EP Impurity G (Free Base)
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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

39030-43-8Ribavirin EP Impurity G (Free Base)

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Catalogue No.:VE0025223
CAS No.:39030-43-8
Mol. Formula:C8H12N4O5
Mol. Weight:244.20 g/mol

Additional information on CAS 39030-43-8

Parent drug

Ribavirin

IUPAC Name

1-β-D-Ribofuranosyl-1H-1,2,4-triazole-5-carboxamide

Pharmacopoeial Synonyms

Ribavirin N-Isomer

Other Synonyms

2-[(2R, 3R, 4S, 5R)-3, 4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1, 2, 4-triazole-3-carboxamide

Smiles

OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C(C(N)=O)=NC=N2)O1

InChI

InChI=1S/C8H12N4O5/c9-6(16)7-10-2-11-12(7)8-5(15)4(14)3(1-13)17-8/h2-5, 8, 13-15H, 1H2, (H2, 9, 16)/t3-, 4-, 5-, 8-/m1/s1

Description

Ribavirin EP Impurity G (Free Base) | CAS 39030-43-8 | also known as Ribavirin N-Isomer or 2-[(2R | 3R | 4S | 5R)-3 | 4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1 | 2 | 4-triazole-3-carboxamide | is a configurational isomeric impurity encountered during ribavirin manufacture. It is routinely characterized in impurity profiles by orthogonal analytical methods such as reversed phase HPLC with UV detection and LC-MS for accurate mass confirmation. The impurity exhibits moderate polarity and aqueous solubility typical of ribose-containing nucleosides and may arise from N-ribosylation isomerization under acidic or thermal stress. Detailed retention behavior | MS fragmentation data and qualified limits inform control strategies | specification setting and stability assessments during process development.

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