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Local Anesthetic (Raw Powder)

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Health Care White Crystalline Effictive Tetracaine Pharmaceutical Raw Materials

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Local Anesthetic (Raw Powder)
Certification: ISO9001, USP, BP, GMP, SGS
Model Number: Tetracaine base raw powder CAS 94-24-6
Minimum Order Quantity: 10g
Delivery Time: Within 24 hours after receive your payment
Payment Terms: T/T, Western Union, MoneyGram, Bitcoin
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Health Care White Crystalline Effictive Tetracaine Pharmaceutical Raw Materials

Abstract

Name Tetracaine
Chemical name 2-(Dimethylamino)ethyl 4-(butylamino)benzoate; 2-
(Dimethylamino)ethyl p-(butylamino)benzoate;
Synonym 4-(butylamino)-benzoicaci2-(dimethylamino) ethylester
; Amethocaine; Anetain
CAS No 94-24-6
Molecular Formula C15H24N2O2
Molecular weight 264.36
Purity 99%
Appearance White crystalline powder
Certification USP/ISO9001
Standard Enterprise Standard

 

Description

Tetracaine was patented in 1930 and came into medical use in 1941.
It is on the World Health Organization’s List of Essential Medicines, the most effective and safe medicines needed in a health system. The wholesale cost in the developing world is about 1.34 to 1.63 USD per 10 ml bottle.

 

 

Application

 

1. 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.
2. Tetracaine is the T in Tac, a mixture of 5 to 12 per cent tetracaine, 5M(per myriad), a half per mille (0.5‰), or .05 per cent (1 part in 2000) , and 4 or 10 per cent 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.
3. Tetracaine 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.

 

 

 

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