71676-00-1 Usage
Uses
Used in Pharmaceutical Industry:
AMisulpride IMpurity D is used as a reference material for quality control and analytical purposes in the development and manufacturing of antipsychotic medications. It helps ensure the purity, potency, and safety of the final drug product by serving as a benchmark for comparison during testing and analysis.
Used in Research and Development:
AMisulpride IMpurity D is utilized as a research tool in the study of the metabolism and pharmacokinetics of Amisulpride. It aids scientists in understanding the metabolic pathways and the effects of the drug on the human body, ultimately contributing to the improvement of antipsychotic treatments and the development of new medications.
Used in Regulatory Compliance:
AMisulpride IMpurity D is employed as a regulatory reference standard in the pharmaceutical industry. It is used to ensure that the manufacturing processes and final products meet the required quality and safety standards set by regulatory authorities, such as the FDA and EMA. This helps maintain the integrity and reliability of the pharmaceutical products available to patients.
Check Digit Verification of cas no
The CAS Registry Mumber 71676-00-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,7 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71676-00:
(7*7)+(6*1)+(5*6)+(4*7)+(3*6)+(2*0)+(1*0)=131
131 % 10 = 1
So 71676-00-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H25N3O4S/c1-4-19-7-5-6-11(19)10-18-16(20)12-8-15(24(3,21)22)13(17)9-14(12)23-2/h8-9,11H,4-7,10,17H2,1-3H3,(H,18,20)
71676-00-1Relevant academic research and scientific papers
Preparation method for pharmacopoeia impurity of amisulpride
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, (2021/06/26)
The invention reports a preparation method for a pharmacopoeia impurity of amisulpride, and particularly relates to a preparation method for the pharmacopoeia impurity D of amisulpride. The method is simple and easy to operate, mild in condition, high in yield, low in energy consumption and pollution and suitable for laboratory-level standard substance preparation.
New derivatives of 4-amino-5-alkyl sulphonyl orthoanisamides, methods of preparing them and their application as psychotropic agents
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, (2008/06/13)
There are provided certain N-(1-lower alkyl-2-pyrrolidylmethyl)2-lower aly-4-amino-5-lower alkyl sulphonyl benzamides and derivatives thereof which provide surprising antiapomorphine and antiserotonin activity.
