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Piperazine, 1-ethyl-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 49860-76-6 Structure
  • Basic information

    1. Product Name: Piperazine, 1-ethyl-4-methyl-
    2. Synonyms:
    3. CAS NO:49860-76-6
    4. Molecular Formula: C7H16N2
    5. Molecular Weight: 128.217
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 49860-76-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Piperazine, 1-ethyl-4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperazine, 1-ethyl-4-methyl-(49860-76-6)
    11. EPA Substance Registry System: Piperazine, 1-ethyl-4-methyl-(49860-76-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 49860-76-6(Hazardous Substances Data)

49860-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49860-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,6 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49860-76:
(7*4)+(6*9)+(5*8)+(4*6)+(3*0)+(2*7)+(1*6)=166
166 % 10 = 6
So 49860-76-6 is a valid CAS Registry Number.

49860-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-4-methylpiperazine

1.2 Other means of identification

Product number -
Other names 1-Methyl-4-ethylhexahydropyrazin

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:49860-76-6 SDS

49860-76-6Downstream Products

49860-76-6Relevant articles and documents

Method for selectively preparing N-monomethylamine compound

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Paragraph 0027; 0034-0035, (2017/08/29)

The invention discloses a method for selectively preparing an N-monomethylamine compound. The method takes an amine compound, formaldehyde and H2 as reaction raw materials; the raw materials react in a reaction medium in the presence of a compound catalyst at 30 DEG C-180 DEG C for 2h-48h, so as to obtain the N-monomethylamine compound; and the compound catalyst is composed of oxides of at least two of the following metal or oxides of least one of the following metal and at least one metal simple substance: aluminum, copper, nickel, cobalt and iron. According to the method for preparing the N-monomethylamine compound, the conversion ratio and the selectivity of N-monomethylamine are relatively high; the H2 is used as a reducing agent and is clean, cheap and environment-friendly; the catalyst utilized by the method is cheap, simple to prepare and high in catalysis efficiency; and the method has mild preparation and reaction conditions and the catalyst has no corrosiveness, is easy to separate and can be repeatedly used.

PROCESS FOR PRODUCING N-METHYL OR N,N-DIMETYL AMINES

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Paragraph 0059, (2015/02/18)

A process for producing N-methyl or N,N-dimethyl amines, which comprises using amine compound, nitro-containing compound or nitrile compound as a starting material, carbon dioxide as a methylating agent and hydrogen gas as a reducing agent, and allowing them to react in a sealed reactor for 6 to 48 h in a reaction medium at a reaction temperature of 80 to 180 ° C. in the presence of a composite catalyst, so as to provide N-methyl or N,N-dimethyl amines. The process of the present invention is simple and under relative mild reaction conditions. By means of the process of the invention, the target products can be prepared at low cost with a high yield. The catalysts used have a high catalytic activity and can be separated from the reaction system simply and reused. Furthermore, the whole process of the present invention is environmental-friendly and facilitates the cycling use of carbon dioxide.

N-Methylation of amine and nitro compounds with CO2/H2 catalyzed by Pd/CuZrOx under mild reaction conditions

Cui, Xinjiang,Zhang, Yan,Deng, Youquan,Shi, Feng

supporting information, p. 13521 - 13524 (2015/01/09)

An active Pd/ZrCuOx catalyst was prepared for the reductive amination of CO2. The N-methylation of amines and nitro compounds with CO2/H2 can be realized with up to 97% yield under relatively mild reaction condi

Methylation of amines, nitrobenzenes and aromatic nitriles with carbon dioxide and molecular hydrogen

Cui, Xinjiang,Dai, Xingchao,Zhang, Yan,Deng, Youquan,Shi, Feng

, p. 649 - 655 (2014/01/17)

CO2/H2 was successfully employed in alkylation reactions by performing CO2 reduction and amine N-methylation in one-pot. In the presence of a simple CuAlOx catalyst, N-methyl or N,N-dimethyl amines with different structures can be selectively synthesized with up to 96% yields by applying amine, nitrobenzene and nitrile as starting materials.

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