Pharmaceutical Levetiracetam Raw Material Levetiracetam Powder Levetiracetam

• Powder: Yes
• Customized: Customized
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Adult
• State: Powder
• Purity: >99%
• Model NO.: D-sung Levetiracetam
• Product Name: Levetiracetam
• Name: Levetiracetam Powder
• Appearance: White Powder
• Color: White
• Grade: Pharmaceutical Grade
• Assay: HPLC 99%
• Application: Pharmaceutical
• Specific: COA
• Test Method: HPLC
• Shelf Life: 2 Years
• CAS No.: 102767-28-2
• Mf: C8h14n2o2
• MW: 170.20896
• Melting Point: 118-119 C
• Density: 1.168
• Transport Package: Negotiable
• Specification: 99%
• Trademark: D-sung
• Origin: Shaanxi Xi′an
• Production Capacity: 1000kg/Month

Product Description

Pharmaceutical Levetiracetam Raw Material Levetiracetam Powder Levetiracetam

Product Description

Product Details

Products	Levetiracetame
Synonyms	(S)-2-(2-Oxopyrrolidin-1-yl)butanamide
CAS	102767-28-2
Molecular Formula	C8H14N2O2
Molecular Weight	170.21
Shelf Life	2 Years When Properly Stored

Levetiracetam, alias levanteracetam, levitestat, levetiracetam, is a white crystalline powder chemical. Chemical name (S) -α-ethyl-2-oxo-1-pyrrolidine acetamide, molecular formula C8H14N2O2, molecular weight of 170.20900. Levetiracetam as antiepileptic drugs, clinically mainly for adults and children over the age of 4 epilepsy partial seizures plus treatment.

Application&Function

Levetiracetam, marketed under the trade names Keppra among others, is a medication used to treat epilepsy. It is used for partial onset, myoclonic, or tonic-clonic seizures. It is the S-enantiomer of etiracetam. Levetiracetam is available by mouth in two forms: immediate release and extended release.[3] It is also available by injection. An immediate release tablet has been available as a generic in the United States since November 2008, and in the UK since 2011. The United States patent for the extended release tablet will expire on September 17, 2028. It was initially patented by UCB Pharma.

Specification