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24426-21-9

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24426-21-9 Usage

General Description

1,2-Ethanediamine, N1-[2-(diethylamino)ethyl]-N1,N2,N2-triethyl- is a chemical compound with the molecular formula C10H28N4. It is a tertiary amine that is commonly used as a corrosion inhibitor, surfactant, and polymerization agent in various industrial processes. This chemical is also utilized in the synthesis of pharmaceuticals and has been researched for its potential application in drug delivery systems. It is important to handle this compound with caution, as it can cause irritation to the skin, eyes, and respiratory system, and should only be used and handled by trained professionals in a controlled laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 24426-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,2 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24426-21:
(7*2)+(6*4)+(5*4)+(4*2)+(3*6)+(2*2)+(1*1)=89
89 % 10 = 9
So 24426-21-9 is a valid CAS Registry Number.

24426-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[2-(diethylamino)ethyl]-N,N,N'-triethylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N,N,N',N",N"-pentaethyldiethylenetriamine

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:24426-21-9 SDS

24426-21-9Downstream Products

24426-21-9Relevant articles and documents

ALKYLATION OF ACYCLIC AND CYCLIC DIAMINES AND POLYAMINES

Zagudullin, R. N.,Baimetov, Z. M.

, p. 889 - 894 (2007/10/02)

Alkylation of diamines and polyamines by allyl and methallyl chlorides or by chloropropenes has been used to obtain polyalkylpolyamines that had not been described previously.The alkylation of the polyamines by allyl and methallyl chlorides proceeds more energetically in comparison with the alkylation by ethyl chloride or chloropropenes.The alkylation of either cyclic and acyclic polyamines begins with the primary amino group.With increasing length of the chain and the alkyl radical at the nitrogen of the alkylated polyamines, their capability for reacting with the evolved hydrogen chloride drops off, and this leads to a decrease in yield of the desired products owing to the loss of activity of the original or partly alkylated polyamines.

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