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2(RS)-4-Methyl-1-(3-Methylpyridin-2-yl)-2-phenylpiperazine is a chemical compound with the molecular formula C18H20N2. It is an impurity found in Mirtazapine (M365000), which is a medication primarily used to treat major depressive disorder.

191546-94-8

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191546-94-8 Usage

Uses

Used in Pharmaceutical Industry:
2(RS)-4-Methyl-1-(3-Methylpyridin-2-yl)-2-phenylpiperazine is used as an impurity in the production of Mirtazapine (M365000) for the treatment of major depressive disorder. As an impurity, it is essential to monitor and control its presence in the final product to ensure the safety and efficacy of the medication.

Check Digit Verification of cas no

The CAS Registry Mumber 191546-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,4 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191546-94:
(8*1)+(7*9)+(6*1)+(5*5)+(4*4)+(3*6)+(2*9)+(1*4)=158
158 % 10 = 8
So 191546-94-8 is a valid CAS Registry Number.

191546-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1-(3-methylpyridin-2-yl)-2-phenylpiperazine

1.2 Other means of identification

Product number -
Other names -

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:191546-94-8 SDS

191546-94-8Downstream Products

191546-94-8Relevant academic research and scientific papers

Method for preparing mirtazapine impurity K

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Paragraph 0040-0042, (2020/05/12)

The invention discloses a method for preparing a mirtazapine impurity K. The method comprises the steps of adopting 2-chloro-3 methyl-5-nitropyridine as a starting raw material to carry out aromatic nucleophilic substitution reaction with 1-methyl-3-phenylpiperazine at high temperature under a catalyst condition, thus synthesizing 4-methyl-1-(3-methyl-5-nitropyridine-2-yl)-2-phenylpiperazine; carrying out reduction reaction to synthesize 5-methyl-6-(4-methyl-2-phenylpiperazine-1-yl)-pyridine-3-amino; carrying out diazo-reaction on the 5-methyl-6-(4-methyl-2-phenylpiperazine-1-yl)-pyridine-3-amino and a sodium nitrite water solution in a hydrochloric acid solution, reducing at low temperature through a hypophosphorous acid water solution, and synthesizing to obtain the high-purity mirtazapine impurity K. According to the scheme of the invention, an impurity comparison product can be quickly, simply, conveniently and efficiently obtained, and the method makes a contribution to strictly controlling the quality of mirtazapine through adopting an external standard method (i.e., an impurity comparison product method).

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