V9889

Valacyclovir hydrochloride hydrate

≥98% (HPLC), solid

• Sinónimos: 2-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)ethyl ester monohydrochloride, L-Valine, Valtrex
• Fórmula empírica (notación de Hill): C₁₃H₂₀N₆O₄ · HCl · xH₂O
• Número de CAS: 124832-27-5
• Peso molecular: 360.80 (anhydrous basis)
• UNSPSC Code: 12352200
• PubChem Substance ID: 329830241
• NACRES: NA.32

Propiedades

• Quality Level: 100
• assay: ≥98% (HPLC)
• form: solid
• storage condition: desiccated
• color: white
• solubility: H₂O: >20 mg/mL
• antibiotic activity spectrum: viruses
• mode of action: DNA synthesis | interferes
• storage temp.: room temp
• SMILES string: O.Cl.CC(C)[C@H](N)C(=O)OCCOCn1cnc2C(=O)NC(N)=Nc12
• InChI: 1S/C13H20N6O4.ClH.H2O/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20;;/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20);1H;1H2/t8-;;/m0../s1
• InChI key: KNOVZDRKHSHEQN-JZGIKJSDSA-N

Descripción

Biochem/physiol Actions

Valacyclovir hydrochloride hydrate is potent inhibitor of viral DNA polymerase. It is a prodrug of acyclovir that is useful in viral, AIDS, and immune system regulation research.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302
• pcodes: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves