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N-Hydroxy Ropinirole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

954117-22-7

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954117-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 954117-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,1,1 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 954117-22:
(8*9)+(7*5)+(6*4)+(5*1)+(4*1)+(3*7)+(2*2)+(1*2)=167
167 % 10 = 7
So 954117-22-7 is a valid CAS Registry Number.

954117-22-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(dipropylamino)ethyl]-1-hydroxy-3H-indol-2-one

1.2 Other means of identification

Product number -
Other names 4-[2-(Dipropylamino)ethyl]-1,3-dihydro-1-hydroxy-2H-indol-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:954117-22-7 SDS

954117-22-7Upstream product

954117-22-7Downstream Products

954117-22-7Relevant articles and documents

Development and validation of Ropinirole hydrochloride and its related compounds by UPLC in API and pharmaceutical dosage forms

Krishnaiah,Murthy, M. Vishnu,Reddy, A. Raghupathi,Kumar, Ramesh,Mukkanti

experimental part, p. 348 - 355 (2011/04/22)

A novel stability-indicating gradient reverse phase ultra performance liquid chromatographic (RP-UPLC) method was developed for the determination of purity of Ropinirole in presence of its impurities and forced degradation products. The method was developed using Waters Aquity BEH 100 mm, 2.1 mm, 1.7 μm C-8 column with mobile phase containing a gradient mixture of solvent A and B. The eluted compounds were monitored at 250 nm. The run time was within 4.5 min which Ropinirole and its four impurities were well separated. Ropinirole was subjected to the stress conditions of oxidative, acid, base, hydrolytic, thermal and photolytic degradation. Ropinirole was found to degrade significantly in oxidative and base stress conditions and stable in acid, water, hydrolytic and photolytic degradation conditions. The degradation products were well resolved from main peak and its impurities, thus proved the stability indicating power of the method. The developed method was validated as per International Conference on Harmonization (ICH) guidelines with respect to specificity, linearity, limit of detection, limit of quantification, accuracy, precision and robustness. This method was also suitable for the assay determination of Ropinirole in pharmaceutical dosage forms and dissolution studies.

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