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Ropinirole hydrochloride

Ropinirole hydrochloride Structure
CAS No.
91374-20-8
Chemical Name:
Ropinirole hydrochloride
Synonyms
ROPINIROLE HCL;REQUIP;4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone Hydrochloride;Requi;SKF-101468A;Ropinirole HCl API;Ropinirole Hcl ,99%;Ropinirole hydrochlo;Ropinib hydrochloride;Ropinero hydrochloride
CBNumber:
CB5420618
Molecular Formula:
C16H25ClN2O
Molecular Weight:
296.84
MOL File:
91374-20-8.mol
Modify Date:
2024/3/22 17:12:53

Ropinirole hydrochloride Properties

Melting point 241-243°C
storage temp. 2-8°C
solubility H2O: >10mg/mL
form powder
color light yellow
InChI InChI=1S/C16H24N2O.ClH/c1-3-9-18(10-4-2)11-8-13-6-5-7-15-14(13)12-16(19)17-15;/h5-7H,3-4,8-12H2,1-2H3,(H,17,19);1H
InChIKey XDXHAEQXIBQUEZ-UHFFFAOYSA-N
SMILES C12CC(=O)NC=1C=CC=C2CCN(CCC)CCC.Cl
CAS DataBase Reference 91374-20-8(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H400
Precautionary statements  P273-P301+P312+P330
Hazard Codes  Xn,N,Xi
Risk Statements  22-50/53-36/38
Safety Statements  36-60-61-37/39-26
RIDADR  UN 3077 9/PG 3
WGK Germany  3
RTECS  NM3288250
HS Code  2933790002
NFPA 704
0
2 0

Ropinirole hydrochloride price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) R2530 Ropinirole hydrochloride powder, ≥98% (HPLC) 91374-20-8 25MG ₹8973.93 2022-06-14 Buy
Sigma-Aldrich(India) R2530 Ropinirole hydrochloride powder, ≥98% (HPLC) 91374-20-8 100MG ₹40539.63 2022-06-14 Buy
Sigma-Aldrich(India) PHR1633 Ropinirole Hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material 91374-20-8 200MG ₹19896.35 2022-06-14 Buy
Product number Packaging Price Buy
R2530 25MG ₹8973.93 Buy
R2530 100MG ₹40539.63 Buy
PHR1633 200MG ₹19896.35 Buy

Ropinirole hydrochloride Chemical Properties,Uses,Production

Description

ReQuip was launched in the UK as a monotherapy or in combination with low-dose levodopa for the treatment of early-stage idiopathic Parkinson's disease. An eight step (24% overall yield) synthesis from isochroman provides access to ropinirole. It is a non-ergot postsynaptic dopamine D2 agonist with activity in the extrapyramidal system. It has weak or no significant activity at α2-adrenergic, 5-HT2 receptors and is inactive at 5-HT1, benzodiazepine, GABA, α1 and β adrenoreceptors. Thus it has essentially no CNS side effects, fewer dyskinesias and on-off fluctuations. In animals, it was able to reverse all motor deficits induced by MPTP. Tolerance is not developed and ropinirole has similar postsynaptic potency to apomorphine but with significantly less stereotyped behavior.

Chemical Properties

Off-White Solid

Uses

An antiparkinsonian agent. A selective dopamine D2-receptor agonist

General Description

Ropinirole hydrochloride,4-(2-(dipropylamino)ethyl)indolin-2-one hydrochloride(Requip), is a white to pale greenish yellow powder that isvery soluble in water. Ropinirole is rapidly absorbed afteroral administration with maximal plasma concentrationsgenerally reached after about 1.5 hours, and the eliminationhalf-life appears to be approximately 3 hours. Ropinirole isalso rapidly and extensively distributed from the vascularcompartment and shows low plasma protein binding that isindependent of its plasma concentration. This drug iscleared by metabolism in the liver, with only 10% being excretedunchanged. The main metabolite of ropinirole is theN-despropyl metabolite. The glucuronide of this metaboliteand the carboxylic acid metabolite, 4-carboxymethylindolin-2-one, account only for 10% of the administered dose.None of the metabolites is pharmacologically active, and theexcretion of ropinirole-derived products is mainly via theurine. The main CYP450 isozyme involved in the metabolismof ropinirole is CYP1A2. Inhibitors or inducers ofthis enzyme have been shown to alter the clearance ofropinirole.Ropinirole is believed to act as an agonist atpostsynaptic D2 receptors. Ropinirole is indicated for thetreatment of the signs and symptoms of idiopathic PD andmoderate to severe primary RLS.

Biological Activity

Selective D 2 -like receptor agonist (D 3 > D 2 > D 4 ). Causes biphasic spontaneous locomotor activity and contralateral circling in 6-OHDA-lesioned mice. Displays antiParkinsonian activity.

Ropinirole hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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Ropinirole hydrochloride Spectrum

Ropinirol hydrochloride 4-[2-(Dipropylamino)ethyl]-1,3-dihydro-2H-indol-2-one Hydrochloride Requi 1,3-dihydro-4-(2-(dipropylamino)ethyl)-2h-indol-2-onemonohydrochloride 1,3-dihydro-4-(2-(dipropylamino)ethyl)-2h-indol-2-onmonohydrochloride 4-(2-(dipropylamino)ethyl)-2-indolinonemonohydrochloride SKF-101468A ROPINIROLE HYDROCHLORIDE SKF 101468 hydrochloride, 4-[2-(Dipropylamino)ethyl]-1,3-dihydro-2H-indol-2-one hydrochloride 4-[2-(Dipropylamino)ethyl]-2-indolinone·hydrochloride 4-[2-(Dipropylamino)ethyl]indoline-2-one·hydrochloride Ropinirole Hcl ,99% SKF 101468 hydrochloride 4-(2-dipropylaminoethyl)-1,3-dihydroindol-2-one hydrochloride Ropinirole hydrochlo Ropinirole HCl API 2H-Indol-2-one, 4-[2-(dipropylaMino)ethyl]-1,3-dihydro-, hydrochloride (1:1) 4-(2-(DipropylaMino)ethyl)indolin-2-one hydrochloride Ropinirole (as hydrochloride) Ropinirole hydrochloride###Ropinirole 4(2DIPROPYLAMINOETHYL)1,3DHINDOLE2ONEHCL Ropinirole for peak identification 1 CRS Ropinirole hydrochloride CRS Ropinirole for peak identification 2 CRS Ropinirole for peak identification 1 Ropinirole for peak identification 2 Ropinirole hydrochloride USP/EP/BP Ropinirole HydrochlorideQ: What is Ropinirole Hydrochloride Q: What is the CAS Number of Ropinirole Hydrochloride Q: What is the storage condition of Ropinirole Hydrochloride Q: What are the applications of Ropinirole Hydrochloride TIANFU-CHEM Ropinirole hydrochloride Ropinirole Hydrochloride (1605205) 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone Hydrochloride REQUIP ROPINIROLE HCL Ropinero hydrochloride Ropinib hydrochloride 91374-20-8 1374-20-8 91347-20-8 C16H24N2OHCl Ropinirole Medicine intermediate Inhibitors Amine Heterocycles Intermediates & Fine Chemicals Pharmaceuticals