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Loperamide hydrochloride

Loperamide hydrochloride Suppliers list
Company Name: Henan DaKen Chemical CO.,LTD.
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Products Intro: Product Name:Loperamide hydrochloride
CAS:34552-83-5
Purity:99.00% Package:100g,500g,1KG,10KG,100KG
Company Name: Shanghai Bojing Chemical Co.,Ltd.
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Products Intro: Product Name:Loperamide hydrochloride
CAS:34552-83-5
Purity:99% Package:1kg;25kg;200kg Cardboard barrels Remarks:crystalline
Company Name: Henan Tianfu Chemical Co.,Ltd.
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Purity:99% Package:500G;1KG;5KG;25KG
Company Name: Hebei Chisure Biotechnology Co.LTD
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Products Intro: Product Name:Loperamide HCl
CAS:34552-83-5
Purity:99 Package:1KG;100USD
Company Name: Shanghai Zheyan Biotech Co., Ltd.
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Products Intro: Product Name:Loperamide Hydrochloride
CAS:34552-83-5
Purity:98% Package:5g/25g/100g

Lastest Price from Loperamide hydrochloride manufacturers

  • Loperamide hydrochloride
  • US $10.00 / Kg/Drum
  • 2021-04-03
  • CAS:34552-83-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 5000tons per month
  • Loperamide hydrochloride
  • US $0.00 / Kg/Bag
  • 2021-03-09
  • CAS:34552-83-5
  • Min. Order: 1Kg/Bag
  • Purity: Above 99%
  • Supply Ability: 5000kg/month
Loperamide hydrochloride Basic information
Product Name:Loperamide hydrochloride
Synonyms:4-(4-(p-chlorophenyl)-4-hydroxy-1-piperidyl)-n,n-dimethyl-2,2-diphenylbutyra;4-(p-chlorophenyl)-4-hydroxy-n,n-dimethyl-alpha,alpha-diphenyl-1-piperidine;blox;butyramidehcl;dissenten;fortasec;imodium;imosec
CAS:34552-83-5
MF:C29H34Cl2N2O2
MW:513.5
EINECS:252-082-4
Product Categories:IMODIUM;Other APIs;ACTIVE PHARMACEUTICAL INGREDIENTS;Intermediates & Fine Chemicals;Pharmaceuticals;Isotope Labeled Compounds;Opioid receptor and opioid-like receptor;Amines;Heterocycles
Mol File:34552-83-5.mol
Loperamide hydrochloride Structure
Loperamide hydrochloride Chemical Properties
Melting point 223-225°C
density 1.1905 (rough estimate)
refractive index 1.6100 (estimate)
storage temp. Store at RT
solubility Slightly soluble in water, freely soluble in ethanol (96 per cent) and in methanol.
pka8.66(at 25℃)
form neat
Merck 14,5571
CAS DataBase Reference34552-83-5(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
HS Code 29333990
ToxicityLD50 in mice (mg/kg): 75 s.c.; 28 i.p.; 105 orally; in rats (mg/kg): 185 orally (Niemegeers)
MSDS Information
ProviderLanguage
SigmaAldrich English
Loperamide hydrochloride Usage And Synthesis
Chemical PropertiesWhite Solid
OriginatorImodium,Janssen,UK,1975
UsesLabeled Loperamide, which is used as an antidiarrheal
UsesCa channel blocker
UsesLoperamide hydrochloride is a Ca2+ channel protein inhibitor and MOR activator.
IndicationsLoperamide hydrochloride (Imodium) structurally resembles both haloperidol and meperidine. In equal doses, loperamide protects against diarrhea longer than does diphenoxylate. It reduces the daily fecal volume and decreases intestinal fluid and electrolyte loss. Loperamide produces rapid and sustained inhibition of the peristaltic reflex through depression of longitudinal and circular muscle activity.The drug also possesses antisecretory activity, presumably through an effect on intestinal opioid receptors.
DefinitionChEBI: A hydrochloride obtained by combining loperamide with one equivalent of hydrochloric acid. Used for treatment of diarrhoea resulting from gastroenteritis or inflammatory bowel disease.
Manufacturing Process23.6 parts of 2-oxo-3,3-diphenyl-tetrahydrofuranare melted at 100°C in an oil-bath and gaseous hydrogen bromide is introduced into it during 3 hours. The reaction mixture is cooled and triturated in benzene. The product is filtered off, washed with petroleum ether and dried in an exsiccator, yielding 4-bromo-2,2-diphenylbutyric acid; MP 127.5%.
To a stirred suspension of 16 parts of 4-bromo-2,2-diphenylbutyric acid in 150 parts of chloroform are added dropwise 16 parts of thionyl chloride and the whole is stirred and refluxed for 2 hours. The reaction mixture is evaporated,yielding 4-bromo-2,2-diphenyl-butyrylchloride as a residue.
60 parts of 4-bromo-2,2-diphenylbutyrylchloride are dissolved in 400 parts of toluene and gaseous dimethylamine is introduced slowly into the solution while cooling (temperature is kept at about 0°C). The introduction is ceased when dimethylamine escapes from the cooler, and stirring is continued for 2 hours at ordinary temperature. The precipitated product is filtered off and dissolved in a minimum quantity of water. The product is extracted with chloroform. The extract is dried and evaporated. The residue solidifies on triturating in 4-methyl-2-pentanone. The solid is filtered off and dried, yielding dimethyl -(tetrahydro-3,3-diphenyl-2-furylidene)ammonium bromide; MP 169° to 171.5°C.
A mixture of 6.33 parts of 4-(p-chlorophenyl)-4-piperidinol, 8 parts of sodium carbonate, 0.2 part of potassium iodide and 240 parts of 4-methyl-2- pentanone is distilled azeotropically. Then there are added 12.12 parts of dimethyl-(tetrahydro-3,3-diphenyl-2-furylidene)ammonium bromide (from the preceding step) and the whole is stirred and refluxed for about 15 hours. The reaction mixture is filtered hot and the filtrate is evaporated.
The oily residue is dissolved in 2-propanol and to this solution is added an excess of 2-propanol previously saturated with gaseous hydrogen chloride. The whole is evaporated and the oily residue is warmed in diluted hydrochloric acid solution. Upon the addition of toluene, the salt is precipitated. It is filtered off, boiled in acetone, and filtered off again after cooling, yielding 4- (p-chlorophenyl)-4-hydroxy-N,N-dimethyl-α,α-diphenylpiperidine-1-butyramide hydrochloride; MP 222.1°C.
Brand nameImodium (Janssen); Imodium (McNeil).
Therapeutic FunctionAntidiarrheal
Biological ActivityHigh 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.
Mechanism of actionLoperamide also is a potent inhibitor of intestinal CYP3A4, increasing the intestinal absorption of other CYP3A4 substrates. The clinically significant drug interactions of loperamide with coadministered CYP3A4 and CYP2C8 substrates or inhibitors would be limited, however, because of its two metabolic pathways.
PharmacokineticsLoperamide is marketed as capsules (2 mg) and liquid (1 mg/5 mL) preparations. The recommended dose is 4 mg initially and an additional 2 mg following each diarrheal stool. The dose should not exceed 16 mg/day. It is too lipophilic to dissolve in water for an intravenous dosage form, a property that limits its abuse potential. The compound is highly lipophilic and undergoes slow dissolution, thus limiting the bioavailability of the agent to approximately 40% of the dose. Its low oral bioavailability also can be attributed to first-pass metabolism by both CYP2C8 and CYP3A4 to its primary N-demethyl metabolite. Peak plasma levels are reached in approximately 5 hours, with an elimination half-life of approximately 11 hours. Approximately 1% of the dose is excreted into the urine unchanged.
Clinical UseLoperamide is effective against a wide range of secretory stimuli and can be used in the control and symptomatic relief of acute diarrhea that is not secondary to bacterial infection.
Side effectsAdverse effects associated with its use include abdominal pain and distention, constipation, dry mouth, hypersensitivity, and nausea and vomiting.
Loperamide hydrochloride Preparation Products And Raw materials
Raw materialsThionyl chloride-->Dimethylamine-->Hydrochloric acid-->Hydrogen bromide-->4-(4-Chlorophenyl)piperidin-4-ol
Tag:Loperamide hydrochloride(34552-83-5) Related Product Information
tert-Butylchlorodiphenylsilane Dacthal Dimethyl sulfoxide ETHANE DMC Dimethyl sulfate Dimethyl phthalate Topotecan hydrochloride Xylene N,N-Dimethylformamide Dimethyl ether (S)-3-AMINO-1-PHENYL-PROPAN-1-OL BIS-(3-PHENYL-PROPYL)-AMINE N-ETHYL-4-HYDROXYPIPERIDINE 3-PHENYL-3-PENTANOL 1-methyl-4-phenylpiperidin-4-ol N,N,N',N'-TETRAMETHYL-1,4-BUTANEDIAMINE Loperamide hydrochloride