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CAS

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24426-20-8

N,N,N',N''-tetraethyldiethylenetriamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24426-20-8 Structure

  • Basic information

    1. Product Name: N,N,N',N''-tetraethyldiethylenetriamine
    2. Synonyms: N,N,N',N''-tetraethyldiethylenetriamine
    3. CAS NO:24426-20-8
    4. Molecular Formula:
    5. Molecular Weight: 215.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24426-20-8.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: N,N,N',N''-tetraethyldiethylenetriamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N,N',N''-tetraethyldiethylenetriamine(24426-20-8)
    11. EPA Substance Registry System: N,N,N',N''-tetraethyldiethylenetriamine(24426-20-8)

  • 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: 24426-20-8(Hazardous Substances Data)

24426-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24426-20-8 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 24426-20:
(7*2)+(6*4)+(5*4)+(4*2)+(3*6)+(2*2)+(1*0)=88
88 % 10 = 8
So 24426-20-8 is a valid CAS Registry Number.

24426-20-8Downstream Products

24426-20-8Relevant 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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