5-(sec-Butyl)-5-ethyldihydro-2-thioxopyrimidin-4,6(1H,5H)-dion, Mononatriumsalz Chemische Eigenschaften,Einsatz,Produktion Methoden
Verwenden
Inactin
? hydrate has been used to anesthetize rats to study stress-induced hypersensitivity and mice to study Cisplatin-induced neuropathy. It has also been used to anesthetize rats to measure the glomerular filtration rate (GFR).
Allgemeine Beschreibung
Crystals.
Air & Water Reaktionen
Slight hygroscopic. Water soluble.
Reaktivit?t anzeigen
An amine, organosulfide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Brandgefahr
Flash point data for INACTIN are not available. INACTIN is probably combustible.
5-(sec-Butyl)-5-ethyldihydro-2-thioxopyrimidin-4,6(1H,5H)-dion, Mononatriumsalz Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
