factory lower price 34552-83-5

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100 Kilogram	Negotiable

100 Kilogram

Negotiable

Min.Order :100 Kilogram
Purity: 99%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

Loperamide hydrochloride 34552-83-5 C29H34Cl2N2O2

Quick Details

Appearance:powder
Application:34552-83-5
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

Superiority:

Loperamide hydrochloride Basic information

Product Name:	Loperamide hydrochloride
Synonyms:	LABOTEST-BB LT00134703;LOSERAMIN;LOPERAMIDE HCL;LOPERAMIDE HYDROCHLORIDE;4-(4-CHLOROPHENYL)-4-HYDROXY-N,N-DIMETHYL-ALPHA,ALPHA-DIPHENYL-1-PIPERIDINBUTYRAMIDE HYDROCHLORIDE;4-(4-CHLOROPHENYL)-4-HYDROXY-N,N-DIMETHYL-ALPHA,ALPHA-DIPHENYL-1-PIPERIDINEBUTANAMIDE HYDROCHLORIDE;4-(4-chlorophenyl)-4-hydroxy-n,n-dimethyl-alpha,alpha-diphenylpiperidine-1-butyramide monohydrochloride;4-[P-CHLOROPHENYL]-4-HYDROXY-N,N-DIMETHYL-ALPHA,ALPHA-DIPHENYL-1-PIPERIDINEBUTYRAMIDE HYDROCHLORIDE
CAS:	34552-83-5
MF:	C29H34Cl2N2O2
MW:	513.5
EINECS:	252-082-4
Product Categories:	ACTIVE PHARMACEUTICAL INGREDIENTS;Intermediates & Fine Chemicals;Pharmaceuticals;Isotope Labeled Compounds;Opioid receptor and opioid-like receptor;Amines;Heterocycles;IMODIUM;Other APIs
Mol File:	34552-83-5.mol

Loperamide hydrochloride Chemical Properties

mp	223-225°C
storage temp.	Store at RT
Merck	5571
CAS DataBase Reference	34552-83-5(CAS DataBase Reference)

Safety Information

Hazard Codes	T
Risk Statements	25
Safety Statements	45
RIDADR	UN 2811 6.1/PG 3
WGK Germany	3
RTECS	TM4960000
HazardClass	6.1(b)
PackingGroup	III

MSDS Information

Provider	Language
SigmaAldrich	English

Loperamide hydrochloride Usage And Synthesis

Chemical Properties	White Solid
Usage	Labeled Loperamide, which is used as an antidiarrheal
Usage	Ca channel blocker
Biological Activity	High affinity μ -opioid receptor agonist with peripheral selectivity (K i values are 2, 48 and 1156 nM for μ -, δ - and κ -opioid receptors respectively). Antidiarrhoeal and antihyperalgesic agent. Also a Ca 2+ channel blocker; at low micromolar concentrations it blocks broad spectrum neuronal HVA Ca 2+ channels and at higher concentrations it reduces Ca 2+ flux through NMDA receptor operated channels.

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