133868-46-9

Basic information

• Product Name: VALNEMULIN HYDROCHLORIDE
• Synonyms: VALNEMULIN HYDROCHLORIDE;econor;VALNEMULIN HCL;Etodoiac;Acetic acid,[[2-[[(2R)-2-aMino-3-Methyl-1-oxobutyl]aMino]-1,1-diMethylethyl]thio]-,(3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyldecahydro-5-hydroxy-4,6,9,10-tetraMethyl-1-oxo-3a,9-propano-3aH-cyclopentacycloocten-8-ylester, Monohydrochloride (9CI);ValneMulin hyd;Acetic acid, 2-[[2-[[(2R)-2-amino-3-methyl-1-oxobutyl]amino]-1,1-dimethylethyl]thio]-, (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyldecahydro-5-hydroxy-4,6,9,10-tetramethyl-1-oxo-3a,9-propano-3aH-cyclopentacycloocten-8-yl ester, hydrochloride (1:1);Valnemulin hydrochloride Solution, 100ppm
• CAS NO: 133868-46-9
• Molecular Formula: C31H53ClN2O5S
• Molecular Weight: 601.28
• EINECS: 1308068-626-2
• Product Categories: API;Inhibitors
• Mol File: 133868-46-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 672.7 °C at 760 mmHg
• Flash Point: 360.6 °C
• Appearance: /
• Storage Temp.: 0-6°C
• Solubility: DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
• Merck: 14,9911
• CAS DataBase Reference: VALNEMULIN HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: VALNEMULIN HYDROCHLORIDE(133868-46-9)
• EPA Substance Registry System: VALNEMULIN HYDROCHLORIDE(133868-46-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 133868-46-9(Hazardous Substances Data)

Usage

Chemical Properties

White to Off-White Solid

Uses

Different sources of media describe the Uses of 133868-46-9 differently. You can refer to the following data:
1. Hydrochloride salt Valnemulin, semisynthetic antibiotic; derivative of pleuromutilin. Antibacterial.
2. Valnemulin hydrochloride is the salt prepared from valnemulin taking advantage of the basic amino group which protonates and readily forms the salt in hydrochloric acid solutions. The hydrochloride is the preferred formulation for pharmaceutical applications. Valnemulin is a broad spectrum antibiotic used to control gastrointestinal infections in animals, and shows no cross resistance to other antibiotic classes. Like all the pleuromutilins, valnemulin inhibits protein synthesis by binding to domain V of 23S RNA.
3. Valnemulin Hydrochloride is a semisynthetic antibiotic; derivative of pleuromutilin. Antibacterial.