Specialty Chemicals
  • N,N-Dimethylaminobutane

    • Product Name   :   

      N,N-Dimethylaminobutane

    • CAS No   :   

      927-62-8

    • Project State   :   

      Commercial

    General Description

    Good factory supply good N,N-Dimethylaminobutane 927-62-8

    • Molecular Formula:C6H15N
    • Molecular Weight:101.192
    • Appearance/Colour:colourless liquid 
    • Vapor Pressure:44.6mmHg at 25°C 
    • Melting Point:-60 °C 
    • Refractive Index:n20/D 1.398(lit.)  
    • Boiling Point:95.9 °C at 760 mmHg 
    • PKA:9.83±0.28(Predicted) 
    • Flash Point:25°F 
    • PSA:3.24000 
    • Density:0.75 g/cm3 
    • LogP:1.34810 

    N,N-Dimethylaminobutane(Cas 927-62-8) Usage

    Synthesis Reference(s)

    Journal of the American Chemical Society, 106, p. 7122, 1984 DOI: 10.1021/ja00335a042

    Air & Water Reactions

    Highly flammable. Partially soluble in water.

    Reactivity Profile

    N,N-DIMETHYL-N-BUTYLAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

    Hazard

    Moderately toxic by ingestion. Low toxic- ity by inhalation and skin contact. A moderate eye irritant.

    Flammability and Explosibility

    Nonflammable

    Definition

    ChEBI: A tertiary amine consisting of n-butane having a dimethylamino substituent at the 1-position.

    General Description

    A clear liquid with an ammonia-like odor. Flash point 20°F. Boiling point 201°F. Density 0.72 g / cm3. Ingestion may irritate or burn the mouth, throat, esophagus and stomach. May cause nausea, vomiting and diarrhea. Inhalation of vapors may irritate the respiratory system and cause pulmonary edema. Contact with the skin may cause burns. Eye contact may cause corrosion to the eyes and contact with the vapor may temporarily blur vision. Vapors heavier than air and may travel considerable distance to a source of ignition and flash back.

    InChI:InChI=1/C6H15N/c1-4-5-6-7(2)3/h4-6H2,1-3H3/p+1

    927-62-8 Relevant articles

    Palladium-Assisted Amination of Olefins. A Mechanistic Study

    Hegedus, Louis S.,Akermark, Bjorn,Zetterberg, Krister,Olsson, Lars F.

    , p. 7122 - 7126 (1984)

    The mechanism of the palladium-assisted ...

    Intermittent synthesis method N and N -dimethyl n-butylamine

    -

    Paragraph 0031-0034, (2021/09/26)

    The invention relates to N. The inventio...

    Zirconium-hydride-catalyzed site-selective hydroboration of amides for the synthesis of amines: Mechanism, scope, and application

    Han, Bo,Jiao, Haijun,Wu, Lipeng,Zhang, Jiong

    , p. 2059 - 2067 (2021/09/02)

    Developing mild and efficient catalytic ...

    The selective reductive amination of aliphatic aldehydes and cycloaliphatic ketones with tetragonal zirconium dioxide as the heterogeneous catalyst

    Bai, Peng,Li, Jiacong,Tong, Xinli,Wang, Shun,Zhang, Haigang,Zhang, Ming

    , (2020/07/17)

    A selective reductive amination of aliph...

    Ionic liquid/H2O-mediated synthesis of mesoporous organic polymers and their application in methylation of amines

    Yu, Xiaoxiao,Yang, Zhenzhen,Zhang, Hongye,Yu, Bo,Zhao, Yanfei,Liiu, Zhenghui,Ji, Guipeng,Liu, Zhimin

    supporting information, p. 5962 - 5965 (2017/07/10)

    Mesoporous Tr?ger's base-functionalized ...

    927-62-8 Process route

    methanol
    67-56-1

    methanol

    N-butylamine
    109-73-9,85404-21-3

    N-butylamine

    phosphonic acid diethyl ester
    762-04-9

    phosphonic acid diethyl ester

    N-n-butyl-N-methylamine
    110-68-9

    N-n-butyl-N-methylamine

    O-ethyl methylphosphonic acid
    1610-33-9

    O-ethyl methylphosphonic acid

    N,N-dimethylbutylamine
    927-62-8

    N,N-dimethylbutylamine

    N,N,N-trimethylbutylamine ion
    7685-30-5

    N,N,N-trimethylbutylamine ion

    phosphonic acid monomethyl ester
    13590-71-1

    phosphonic acid monomethyl ester

    Ethylphosphorige Saeure
    15845-66-6

    Ethylphosphorige Saeure

    Conditions
    Conditions Yield
    at 25 ℃; Rate constant; Mechanism; other amines and dialkyl phosphites;
    butyltrimethylammonium bis(trifluoromethylsulfonyl)azanide
    258273-75-5

    butyltrimethylammonium bis(trifluoromethylsulfonyl)azanide

    (Z)-2-Butene
    590-18-1

    (Z)-2-Butene

    methane
    34557-54-5,27936-85-2

    methane

    trans-2-Butene
    624-64-6

    trans-2-Butene

    trifluoromethan
    75-46-7

    trifluoromethan

    N,N-dimethylbutylamine
    927-62-8

    N,N-dimethylbutylamine

    N-ethyl-N-methylbutan-1-amine
    66225-40-9

    N-ethyl-N-methylbutan-1-amine

    2-methylprop-1-en-1-amine
    63742-07-4

    2-methylprop-1-en-1-amine

    ammonia
    7664-41-7

    ammonia

    hydrogen
    1333-74-0

    hydrogen

    N-butylamine
    109-73-9,85404-21-3

    N-butylamine

    isobutene
    115-11-7,15220-85-6

    isobutene

    trimethylamine
    75-50-3

    trimethylamine

    n-butane
    106-97-8,9003-29-6,9021-92-5

    n-butane

    Conditions
    Conditions Yield
    In acetonitrile; for 8h; Electrochemical reaction;

    927-62-8 Upstream products

    • 50-00-0
      50-00-0

      formaldehyd

    • 3858-78-4
      3858-78-4

      n-butylamine hydrochloride

    • 7685-30-5
      7685-30-5

      N,N,N-trimethylbutylamine ion

    • 760-79-2
      760-79-2

      N,N-dimethylbutyramide

    927-62-8 Downstream products

    • 50-00-0
      50-00-0

      formaldehyd

    • 110-68-9
      110-68-9

      N-n-butyl-N-methylamine

    • 123-72-8
      123-72-8

      butyraldehyde

    • 124-40-3
      124-40-3

      dimethyl amine

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