ABC00828RC

Levetiracetam USP RC A

Levetiracetam USP RC A is a chlorinated synthetic byproduct arising from the acetylation step in Levetiracetam production, featuring a (S)-2-oxo-4-(2-chloroacetylamino)butyl substituent on the pyrrolidone core. Its structure incorporates a chloroacetyl moiety in lieu of the native acetamide, creating a steric and electronic divergence from the parent compound. This impurity, formed via unintended chloroacetyl chloride coupling, exhibits distinct HPLC retention due to the chlorine atom's hydrophobicity. Serves as a reference standard for quantifying this specific process-related impurity in Levetiracetam active pharmaceutical ingredient (API) batches.

On Request
Molecular Formula C8H15ClN2O2
Molecular Weight 206.6700
CAS Number 102767-31-7 โœ“ Verified
PubChem CID 29938341 โ†—
Purity N/A
Product Type API Impurity
Parent Drug Levetiracetam
Lead Time On Request
IUPAC Name (2S)-2-(4-chlorobutanoylamino)butanamide
Official Reference Standards
Std Catalog # Quantity Price
USP 1359426 โ†— 20 mg USD 942.00

๐Ÿ“ Synonyms

102767-31-7 (S)-N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide UNII-3P8M8S76NM Butanamide, N-[(1S)-1-(aminocarbonyl)propyl]-4-chloro- 3P8M8S76NM N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)- Butanamide, N-((1S)-1-(aminocarbonyl)propyl)-4-chloro- N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (-)- DTXSID10145496 RefChem:161427

๐Ÿ”ฌ Chemical Identifiers

CC[C@@H](C(=O)N)NC(=O)CCCCl
InChI=1S/C8H15ClN2O2/c1-2-6(8(10)13)11-7(12)4-3-5-9/h6H,2-5H2,1H3,(H2,10,13)(H,11,12)/t6-/m0/s1
QBJNYRYTZPBHFT-LURJTMIESA-N

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