Tetracaine

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Tetracaine
Posting date : Nov 24, 2014
Membership
Free Member Scince Oct 14, 2014
FOB Price
USD 400/kg
Min. Order Quantity
1kg
Supply Abillity
5000 T/Month
Port
Shenzhen
Payment Terms
T/T, Western union, Money gram
Package
25kg/Drum, 1kg/bag
Keyword :
Category
Contact
April
Selling Leads Detail
Company Info
 
Quick Detail
Place of Origin
China [CN]
Brand Name
SMQ
Model Number
C15H24N2O2
HS-CODE
-
Package & Delivery Lead Time
Package
25kg/Drum, 1kg/bag
Delivery Lead Time
Within 3 Work Days
Detailed Description
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

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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.

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