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ETHYL-DI-N-PROPYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20634-92-8 Structure
  • Basic information

    1. Product Name: ETHYL-DI-N-PROPYLAMINE
    2. Synonyms: ETHYL-DI-N-PROPYLAMINE;N,N-DipropylethylaMine;N,N-Dipropylethylamine;1-Propanamine, N-ethyl-N-propyl-
    3. CAS NO:20634-92-8
    4. Molecular Formula: C8H19N
    5. Molecular Weight: 129.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20634-92-8.mol
  • Chemical Properties

    1. Melting Point: -76.53°C (estimate)
    2. Boiling Point: 132°C(lit.)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.8070
    6. Refractive Index: 1.4100-1.4140
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ETHYL-DI-N-PROPYLAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ETHYL-DI-N-PROPYLAMINE(20634-92-8)
    11. EPA Substance Registry System: ETHYL-DI-N-PROPYLAMINE(20634-92-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. RIDADR: 2733
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 3/8
    8. PackingGroup: III
    9. Hazardous Substances Data: 20634-92-8(Hazardous Substances Data)

20634-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20634-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20634-92:
(7*2)+(6*0)+(5*6)+(4*3)+(3*4)+(2*9)+(1*2)=88
88 % 10 = 8
So 20634-92-8 is a valid CAS Registry Number.

20634-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-propylpropan-1-amine

1.2 Other means of identification

Product number -
Other names ethyl-dipropyl-amine

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:20634-92-8 SDS

20634-92-8Relevant articles and documents

Homogeneous Catalytic Activation of C-N Bonds. Alkyl Exchange between Tertiary amines.

Shvo, Youval,Laine, Richard M.

, p. 753 - 754 (1980)

We have found that several transition metal cluster compounds act as homogeneous catalyst precursors in alkyl exchange reactions of tertiary amines; treatment of mixtures of Et3N and Pr3N with either Ru3(CO)12, Os3(CO)12, or Ir4(CO)12 and water leads to very efficient alkyl exchange.

Transalkylation Reaction. Homogeneous Catalytic Formation of C-N Bonds

Wilson, Robert B.,Laine, Richard M.

, p. 361 - 369 (2007/10/02)

We have performed kinetic and mechanistic studies on homogeneous ruthenium-catalyzed transalkylation of tertiary amines.From these studies we have derived a kinetic expression for transalkylation catalysis based on initial reaction rates.We find that transalkylation proceeds most efficiently in alcoholic solvents (e.g., MeOH or EtOH), under a slight pressure of CO, with a mixed-metal, iron-ruthenium catalyst.The mechanism appears to be in one which a metal cluster of at least two and most probably three atoms binds the amine through insertion into an α C-H bond to give a metallazacyclopropane or metal-iminium complex.Nucleophilic attack by free amine on the complex, or an immediate derivative, follows, and subsequent rearrangement of the intermediate formed gives transalkylation products.The catalyst system has been tested as a synthetic tool for the oligomerization and cyclization of tertiary diamines.These preliminary studies have been quite succesful.Thus, N,N,N',N'-tetramethylethylenediamine can be transformed into Me3N and N,N'-dimethylpiperazine with good conversion and high selectivity.N,N,N',N'-Tetraethylethylenediamine can be transformed into Et3N and the linear, perethyl, ethylenediamine dimer, trimer, tetramer, and pentamer with excellent conversion.

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