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Home > products > Chemical Intermediates > Itopride Hydrochloride CAS 122892-31-3

Itopride Hydrochloride CAS 122892-31-3

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 122892-31-3

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Highlight:
CAS NO::
122892-31-3
Appearance::
White Or Pale Brownish Crystal
Molecular Formula::
C20H27ClN2O4
Molecular Weight::
394.89200
EINECS NO::
602-905-1
MDL NO::
MFCD00881710
CAS NO::
122892-31-3
Appearance::
White Or Pale Brownish Crystal
Molecular Formula::
C20H27ClN2O4
Molecular Weight::
394.89200
EINECS NO::
602-905-1
MDL NO::
MFCD00881710
Itopride Hydrochloride CAS 122892-31-3

Product Description:

Product Name: Itopride hydrochloride CAS NO: 122892-31-3

 

 

Synonyms:

N-[4-[2-(Dimethylamino)ethoxy]benzyl]-3,4-dimetho-xybenzamide Hydrochloride;

N-(p-(2-(Dimethylamino)ethoxy)benzyl)veratramide Hydrochloride;

Benzamide, N-[[4-[2-(dimethylamino)ethoxy]phenyl]methyl]-3,4-dimetho-xy-, hydrochloride (1:1);

 

 

Chemical & Physical Properties:

Appearance: white or pale brownish crystal

Assay :≥99.0%

Boiling Point: 510.1℃ at 760 mmHg

Melting Point: 194-1950℃

Flash Point: 262.3℃

Vapor Pressure: 1.6E-10mmHg at 25℃

 

 

Safety Information:

HS Code: 2924299090

Caution Statement: P273; P501

Symbol: GHS09

Hazard Declaration: H410

Signal Word: Warning

 

 

Dopamine D2-receptor antagonist with anticholinesterase activity. Gastroprokinetic. Itopride hydrochloride is an AChE inhibitor (acetylcholinesterase) and D2DR inhibitor.Target: AChEItopride is a gastroprokinetic benzamide derivative. The IC50 of itopride with AChE (2.04 +/- 0.27 microM) was, however, 100-fold less than that with BuChE, whereas in the case of neostigmine with AChE (11.3 +/- 3.4 nM), it was 10-fold less. The inhibitory effect of itopride on cholinesterase (ChE) activity in guinea pig gastrointestine was much weaker than that on pure AChE. the IC50s of itopride against ChE activities were found to be about 0.5 microM. The IC50 of itopride for electric eel and guinea pig gastrointestinal AChE inhibition was 200 times and 50 times as large as that of neostigmine, respectively [1].

 

 

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