Specialty Chemicals
  • N,N'-DI-TERT-BUTYLETHYLENEDIAMINE

    • Product Name   :   

      N,N'-DI-TERT-BUTYLETHYLENEDIAMINE

    • CAS No   :   

      4062-60-6

    • Project State   :   

      Commercial

    General Description

    N,N'-DI-TERT-BUTYLETHYLENEDIAMINE 4062-60-6 with purity >99% Low price in stock

    • Molecular Formula:C10H24N2
    • Molecular Weight:172.314
    • Appearance/Colour:COLORLESS TO YELLOW LIQUID 
    • Melting Point:53.35°C 
    • Refractive Index:n20/D 1.43(lit.)  
    • Boiling Point:208.7 °C at 760 mmHg 
    • PKA:10.49±0.38(Predicted) 
    • Flash Point:76.7 °C 
    • PSA:24.06000 
    • Density:0.815 g/cm3 
    • LogP:2.54440 

    4062-60-6 Relevant articles

    Design, Isolation, and Spectroscopic Analysis of a Tetravalent Terbium Complex

    Rice, Natalie T.,Popov, Ivan A.,Russo, Dominic R.,Bacsa, John,Batista, Enrique R.,Yang, Ping,Telser, Joshua,La Pierre, Henry S.

    , p. 13222 - 13233 (2019)

    Synthetic strategies to yield molecular ...

    Synthesis and reactivity of the stable silylene N,N′-di-tert-butyl-1,3-diaza-2-sila-2-ylidene

    Haaf,Schmedake,Paradise,West

    , p. 1526 - 1533 (2000)

    The synthesis and several reactions of t...

    Method for synthesizing N, N-di-di-tert-butyl ethylenediamine

    -

    Paragraph 0016-0023, (2021/10/11)

    The invention belongs to medicine. The i...

    Near quantitative synthesis of urea macrocycles enabled by bulky N-substituent

    Yang, Yingfeng,Ying, Hanze,Li, Zhixia,Wang, Jiang,Chen, Yingying,Luo, Binbin,Gray, Danielle L.,Ferguson, Andrew,Chen, Qian,Z, Y.,Cheng, Jianjun

    , (2021/03/16)

    Macrocycles are unique molecular structu...

    Effect of ligand substituents in olefin polymerisation by half-sandwich titanium complexes containing monoanionic iminoimidazolidide ligands-MAO catalyst systems

    Nomura, Kotohiro,Fukuda, Hiroya,Katao, Shohei,Fujiki, Michiya,Kim, Hyun Joon,Kim, Dong-Hyun,Zhang, Shu

    scheme or table, p. 7842 - 7849 (2011/09/20)

    Various half-sandwich titanium complexes...

    4062-60-6 Process route

    1,4-di-tert-butyl-1,4-diazabutadiene
    28227-42-1,30834-74-3

    1,4-di-tert-butyl-1,4-diazabutadiene

    N,N'-di-tert-butylethylenediamine
    4062-60-6

    N,N'-di-tert-butylethylenediamine

    Conditions
    Conditions Yield
    With lithium aluminium tetrahydride; at 0 - 20 ℃;
    89%
    With sodium tetrahydroborate; In methanol; at 0 - 25 ℃; Inert atmosphere;
    With hydrogen; nickel; In toluene; at 60 ℃; under 22502.3 Torr; Temperature; Reagent/catalyst; Autoclave;
    ethylene dibromide
    106-93-4

    ethylene dibromide

    <i>tert</i>-butylamine
    75-64-9

    tert-butylamine

    N,N'-di-tert-butylethylenediamine
    4062-60-6

    N,N'-di-tert-butylethylenediamine

    Conditions
    Conditions Yield
    In hexane; water; for 72h; Heating;
    72%
    In water; 1.) 0 deg C to ambient temperature (slowly), 2.) reflux, overnight;
    70%
    ethylene dibromide; tert-butylamine; With sodium hydroxide; In water; at 0 ℃; for 1h;
    In water; at 25 ℃; for 72h;
    56%
    With water;

    4062-60-6 Upstream products

    • 106-93-4
      106-93-4

      ethylene dibromide

    • 75-64-9
      75-64-9

      tert-butylamine

    • 107-06-2
      107-06-2

      1,2-dichloro-ethane

    • 30834-74-3
      30834-74-3

      N-((E,2E)-2-{[(E)-1,1-dimethylethyl]imino}ethylidene)-2-methyl-2-propanamine

    4062-60-6 Downstream products

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      854929-38-7

      1,3-di-tert-butyl-1,3,2-diazaphospholidine-2-oxide

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      67104-96-5

      2-benzenesulfonyl-5-tert-butyl-[1,2,5]thiadiazolidine 1,1-dioxide

    • 99727-73-8
      99727-73-8

      [Pt(NHC(C6H5)N(C4H9)CH2CH2NH(C4H9))Cl2(NC(C6H5))]

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