Pharmaceutical Raw Powder Tetracaine Hydrochloride Powder CAS No. 136-47-0

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Xi'an Frazer Biotech Co., Ltd.

VIP   Audited Supplier 6 years
Profile Certified by SGS/BV
  • Shaanxi, China
  • Jacky (Mr.)  
    Manager
FLZ-S0801tetracaine
Yes
Customized
GMP, HSE, ISO 9001, USP, BP
Elderly, Children, Adult
White Crystalline Powder
>99%
White Cyrstalline Powder
136-47-0
2 Years
HPLC
Store Cool Dry Place
Natural
Strictly Quality Control
7-10days
264.36300
C15h24n2o2
Xi'an Frazer Biotech Co., Ltd.
Foil Bag
99%
China
Product Description

Pharmaceutical Raw Powder Tetracaine Hydrochloride Powder CAS NO. 136-47-0

Specification

Test ItemsSpecificationTest Results
Appearancewhite crystalline powderconfirm
IdentificationABC in Passconfirm
SolubilityVery soluble in water, soluble in Alcohol; insoluble in Ether and Benzeneconfirm
USP Reference standardsUSP Tetracaine Hydrochloride RS,USP Endotoxin RS.confirm
Melting point145~150 degree146.0~147.5 degree
Chromatographic purityIn Passconfirm
Related substanceNot more than the reference solution 0.05%confirm
Heavy metals≤10ppmconfirm
PH4.5-6.55.8
Residue on ignition≤0.10%0.05%
Loss on Drying≤ 0.5%0.19%
Assay98.0 -101.0%100.1%


What is Tetracaine ?

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 

Function and Application of Tetracaine 

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.
 
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.


 
 
 


 

 
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