Levetiracetam

Levetiracetam

Nome del prodotto Levetiracetam
Numero CAS 102767-28-2
Formula molecolare C8H14N2O2
Peso molecolare 170.21 g/mol
Aspetto Polvere cristallina di colore da bianco a bianco sporco
Analisi (HPLC) 98.0% – 102.0% (on dried basis)
Perdita per essiccazione ≤ 0,51 TP3T
Residuo di combustione ≤ 0,11 TP3T
Metalli pesanti ≤ 20 ppm
Solubilità Sparingly soluble in water, soluble in methanol and ethanol
Confezione 25 kg fiber drum with double polyethylene liner

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Levetiracetam Structure

Sinonimi: (S)-2-(2-Oxopyrrolidin-1-yl)butanamide, α-Ethyl-2-oxo-1-pyrrolidineacetamide, Keppra, Etiracetam, UCB L059, Levitiracetam

Levetiracetam has become a go-to API for formulators targeting epilepsy and beyond. Its unique binding to synaptic vesicle protein 2A (SV2A) sets it apart from traditional sodium-channel blockers, driving demand in both human and veterinary neurology. As patents expire, generic entries are surging, and procurement teams are actively qualifying new suppliers to secure consistent, high-purity material. The compound also shows promise in neuropathic pain and mood disorders, widening its commercial footprint.

This second-generation antiepileptic is a chiral pyrrolidine derivative, synthesized through a multi-step route that demands tight stereochemical control. The (S)-enantiomer is the active form, and regulatory agencies enforce strict limits on the (R)-impurity. Manufacturers must navigate complex crystallization and purification to meet pharmacopeial standards, making supplier selection a critical decision for both quality and cost.

LyvBio supplies Levetiracetam with assay 98.0–102.0% (HPLC) and full documentation, including elemental impurities and residual solvents. Our material is manufactured under cGMP and is available in commercial quantities. Whether you are developing a generic oral solid or exploring new delivery systems, our team supports your technical and regulatory needs with responsive service and reliable supply.

Product Overview & Composition

Levetiracetam is a white to off-white crystalline powder, freely soluble in methanol and ethanol, and sparingly soluble in water. It is chemically stable under normal storage conditions, with a molecular weight of 170.21 g/mol. The API is typically milled to a consistent particle size distribution to ensure blend uniformity in tablet and capsule formulations.

Our Levetiracetam is produced via a proprietary synthesis that minimizes chiral impurities and controls particle size. Each batch is tested for assay, related substances, residual solvents, and heavy metals to meet EP, USP, and ICH Q3A/B requirements. The material is non-hygroscopic and compatible with common excipients.

Key Applications

  • Epilepsy treatment: As monotherapy or adjunctive therapy for partial-onset, myoclonic, and primary generalized tonic-clonic seizures in adults and children.
  • Veterinary medicine: Used off-label for seizure control in dogs and cats, often where phenobarbital is ineffective or poorly tolerated.
  • Neuropathic pain: Investigated as an adjunct in diabetic neuropathy and postherpetic neuralgia, though not FDA-approved for these indications.
  • Mood disorders: Studied for bipolar disorder and anxiety, with some evidence of mood stabilization.
  • Research: Employed as a reference standard in analytical method development and as a tool compound in SV2A binding studies.

Quality & Standards

Parametro Specifiche
Analisi (HPLC) 98.0% – 102.0%
Perdita per essiccazione ≤ 0,51 TP3T
Metalli pesanti ≤ 20 ppm
Residuo di combustione ≤ 0,11 TP3T
Limiti microbiologici Conta aerobica totale ≤ 1000 UFC/g; lieviti e muffe ≤ 100 UFC/g; assenza di E. coli

Packaging & Supply

  • Confezionamento: 25 kg fiber drum with double polyethylene liner, or as per customer request.
  • MOQ: 25 kg.
  • Tempi di consegna: 3-5 business days (stock items)
  • Documentazione: COA, MSDS, TDS e documentazione normativa disponibili su richiesta

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