Tetracaine

• Product NameTetracaine
  CAS No.94-24-6
  Purity99%
  Min Quantity1Kilograms
  Price500~600
• View Contact Detail

• 
  Molecular Structure

Detailed Description

Product Name: Tetracaine

Product Name Tetracaine
Synonym Anetain, Amethocaine, Pontocaine,Ametop,Dicaine
CAS 94-24-6
MF C15H24N2O2
MW 264.36
EINECS 202-316-6
Assay 99%
Quality Standards Enterprise Standard/Pharma Grade
Appearance White powder
Package 25kg/Drum

Place of Origin China
Brand Name SMQ
Certification ISO9001, ISO14000, KOSHER
MOQ 1kg
Ref. Price USD 400/kg
Packaging Details 25kg/Drum, 1kg/bag
Delivery Time 1-2 days
Payment Terms T/T, Western union, Money gram
Supply Ability 5000 T/Month

2.Quick View:
Tetracaine (INN, 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.
It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.
3.Description:
(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) adrenaline, and 4 or 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.
(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.
• 
• Tetracaine