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24229-53-6

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24229-53-6 Usage

General Description

N2-(2-aminoethyl)-N1,N1-dimethylethylenediamine, also known as AE- DMEDA, is a chemical compound with the molecular formula C6H16N4. It is a versatile, water-soluble, and stable compound commonly used as a chelating agent, particularly in metal ion extraction and purification processes. It is also used as a catalyst in various chemical reactions, including polymerization and cross-linking processes. AE- DMEDA is known for its ability to form stable complexes with a wide range of metal ions, making it valuable in industrial and laboratory applications. Additionally, it is used in pharmaceutical and agricultural products, and in the synthesis of organic compounds. Overall, this chemical plays a crucial role in various industries and scientific fields due to its unique properties and versatile applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24229-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24229-53:
(7*2)+(6*4)+(5*2)+(4*2)+(3*9)+(2*5)+(1*3)=96
96 % 10 = 6
So 24229-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H17N3/c1-9(2)6-5-8-4-3-7/h8H,3-7H2,1-2H3

24229-53-6SDS

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 N'-[2-(dimethylamino)ethyl]ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names Diethylenetriamine,1,1-dimethyl

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:24229-53-6 SDS

24229-53-6Relevant articles and documents

Dehydrogenative Coupling of Ethanol and Ester Hydrogenation Catalyzed by Pincer-Type YNP Complexes

Gusev, Dmitry G.

, p. 6967 - 6981 (2016/10/14)

The "Y" donor group (Y = -OMe, -SEt, -PPh2, -NH2, -NMe2, -Py, pyrrolidinyl, quinolyl) of the pincer-type ruthenium complexes RuHCl(CO)[κ3-YNP] has a dramatic influence on the catalytic activity in the dehydrogenative homocoupling and cross-coupling of ethanol and ester hydrogenation reactions. The observations are connected with the mechanisms of the catalytic reactions, and this paper provides evidence for ester C-O bond formation/cleavage assisted by the bifunctional catalysts in an outer-sphere fashion, reminiscent of the Tishchenko chemistry.

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