Strongest Topical Anesthetic Powder Tetracaine HCl

Strongest Topical Anesthetic Powder Tetracaine HCl

Description du produit

Alias : Chlorhydrate de tétracaïne ,2-Dimethylaminoethyl 4-n-butylaminobenzoate hydrochloride;
4-(Butylamino)benzoic acid 2-(dimethylamino)ethyl ester hydrochloride
N ° CAS : 136-47-0
EINECS : 205-248-5
MF : C15H25ClN2O2
MW : 300.82
Point de fusion : 149°C
Essai : 99%
Classe : Qualité pharmaceutique

Fabricant : china
Usage : Local anesthetic; Mainly used in mucosa anesthetic.
The function is stronger than Procaine and Lidocaine.

Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

What is Tetracaine Hydrochloride?

Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

Tetracaine is the T in Tac, a mixture of 5 à 12 per cent tetracaine, 5‱ (per myriad), a half per mille (0.5‰), ou .05 per cent (1 part in 2000) adrenaline, et 4 ou 10 per cent cocaine hydrochloride used in ear, nose & throat surgery and in the emergemcy department where numbing of the surface is needed rapidly, especially when children have been injured in the eye, ear, or other sensitive locations.

Tetracaine Hydrochloride Application :

Tétracaïne (AUBERGE, also known as amethocaine; trade name Pontocaine. Ametop and Dicaine) is a potent local anesthetic of the ester group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia.
In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.