Schmerzlinderndes Lokalanästhetikum Tetracain-Pulver als Analgetikum
Schnelle Details
| Produktname |
Tetracain |
| Alias |
Amethocain; Pontocaine; Dicaine; Laudocaine |
| CAS-Registrierungsnummer |
94-24-6 |
| Einecs-Nr |
202-316-6 |
| Molekularformel |
C15H24N2O2 |
| Molekulargewicht |
264.36 |
| Reinheit |
99% |
| White Powder Muscle Building Steroide Epiandrosteron |
White Powder Muscle Building Steroide Epiandrosteron |
| Aussehen |
white crytalline powder |
Beschreibung:
Tetracain, also known as amethocaine, is a local anesthetic used to numb the eyes, Nase, or throat. Tetracaine may also be used before starting an intravenous to decrease pain from the procedure. Typically it is applied as a liquid to the area. Onset of effects when used in the eyes is within 30 seconds and last for less than 15 Protokoll.
Tetracain wurde patentiert 1930 und kam 1990 in die medizinische Anwendung 1941. Es steht auf der Liste der unentbehrlichen Arzneimittel der Weltgesundheitsorganisation, Die effektivsten und sichersten Medikamente, die in einem Gesundheitssystem benötigt werden. Die Großhandelskosten in den Entwicklungsländern betragen ca 1.34 zu 1.63 USD pro 10 ml-Flasche. In the United Kingdom the eye drops cost the NHS about 0.49 pounds per dose.
Tetracaine Application
(1).In der biomedizinischen Forschung, tetracaine is used to alter the function of the calcium release pathway (Lannottine receptor), which controls the release of calcium from intracellular stores. Dicaine is an allosteric blocker for channel function. In geringen Konzentrationen, tetracaine causes initial inhibition of spontaneous calcium release events, whereas at high concentrations, tetracaine is completely released.
(2).Dinkaine is T in Tac, 5 zu 12% Tetracain, 5M (countless), half (0.5 ‰) oder 0.05% (1 In 2000), 4% oder 10% of the salt used for ENT surgery Acid salts, and emergency departments that require rapid surface numbness, especially when children are injured in the eyes, ears or other sensitive parts.
(3).Tetracain wird aus 4-Butylaminobenzoesäure synthetisiert. The esterification reaction is carried out by acid catalysis to form ethyl ester. The base-catalyzed transesterification is achieved by boiling ethyl 4-butylaminobenzoic acid with an excess of 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.
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