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1-(1-Pyrrolidinyl)-2-propanamine, also known as NMP, N-Methyl-2-pyrrolidone, or 1-Methyl-2-pyrrolidone, is an organic solvent and a highly versatile chemical compound. It is characterized by its excellent solvency properties, high boiling point, low volatility, and the ability to dissolve a wide range of substances, making it a valuable component in various industrial applications.

50998-03-3

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50998-03-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(1-Pyrrolidinyl)-2-propanamine is used as a solvent for the production of pharmaceuticals, facilitating the dissolution and processing of various compounds in the manufacturing process.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1-Pyrrolidinyl)-2-propanamine serves as a solvent for the production of agrochemicals, aiding in the formulation and application of these products.
Used in Electronics Industry:
1-(1-Pyrrolidinyl)-2-propanamine is utilized as a solvent in the electronics industry for the manufacturing of electronic components and devices, enhancing the production process through its solvency properties.
Used in Coatings and Inks:
As a solvent for coatings and inks, 1-(1-Pyrrolidinyl)-2-propanamine helps in the application and drying process, providing a smooth and even finish.
Used in Cleaning Agents:
1-(1-Pyrrolidinyl)-2-propanamine is used in cleaning agents for its ability to dissolve a wide range of substances, making it effective in removing dirt and contaminants.
Used in Petrochemical Industry:
In the petrochemical industry, 1-(1-Pyrrolidinyl)-2-propanamine is employed as a solvent in the manufacturing process, contributing to the production of various petrochemical products.
It is important to handle 1-(1-Pyrrolidinyl)-2-propanamine with care, as it may be harmful if ingested, inhaled, or in direct contact with skin. Proper safety measures should be taken during its use and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 50998-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,9 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50998-03:
(7*5)+(6*0)+(5*9)+(4*9)+(3*8)+(2*0)+(1*3)=143
143 % 10 = 3
So 50998-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2/c1-7(8)6-9-4-2-3-5-9/h7H,2-6,8H2,1H3

50998-03-3 Well-known Company Product Price

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  • Aldrich

  • (CBR01743)  1-(1-Pyrrolidinyl)-2-propanamine  AldrichCPR

  • 50998-03-3

  • CBR01743-1G

  • 4,512.69CNY

  • Detail

50998-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-2-pyrrolidin-1-yl-ethylamine

1.2 Other means of identification

Product number -
Other names 1-(1-Pyrrolidinyl)-2-propanamine

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:50998-03-3 SDS

50998-03-3Downstream Products

50998-03-3Relevant academic research and scientific papers

Method of treating chloroquine-resistant malaria with aminoquinoline derivatives

-

, (2008/06/13)

Novel aminoquinoline derivatives of the general formula STR1 are described. Also described are methods for the treatment of malaria pathogens, particularly chloroquine-resistance malaria pathogens with compounds of formula I or the pharmaceutically acceptable salts and hydrolyzable esters thereof.

DIRECT NUCLEOPHILIC SUBSTITUTION IN 2-HALOALKYLAMINES: NEW ROUTE TO SUBSTITUTED ETHYLENEDIAMINES

Chechik, V. O.,Bobylev, V. A.

, p. 1501 - 1502 (2007/10/03)

Nucleophilic substitution in 2-haloalkylamines in weakly polar media was found to proceed partially without intermediate formation of aziridines.This makes it possible to obtain pure substituted ethylenediamines.

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