tert-Butylamine


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  • tert-Butylamine
  • 75-64-9
  • C4H11N
  • 73.138
  • colourless liquid
Inquiry

Factory supply good quality tert-Butylamine 75-64-9 with stock

  • Molecular Formula:C4H11N
  • Molecular Weight:73.138
  • Appearance/Colour:colourless liquid 
  • Vapor Pressure:5.7 psi ( 20 °C) 
  • Melting Point:-67 °C 
  • Refractive Index:n20/D 1.377(lit.)  
  • Boiling Point:44.399 °C at 760 mmHg 
  • PKA:10.68(at 25℃) 
  • Flash Point:-9 °C 
  • PSA:26.02000 
  • Density:0.744 g/cm3 
  • LogP:1.44390 

tert-Butylamine(Cas 75-64-9) Usage

Chemical Description

Tert-butylamine, 2,6-diisopropylaniline, 2,4,6-trimethylaniline, 2,4,6-tri-tert-butylaniline, and isopropylamine are amines used as solvents.

Production Methods

tert-Butylamine is manufactured by reacting isobutylamine with sulfuric acid followed by cyanide to tert-butylformamide. Hydrolysis yields t-butylamine. It is used as a solvent and in organic syntheses.

Air & Water Reactions

Highly flammable. May be sensitive to air . Soluble in water.

Reactivity Profile

tert-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 is generated in combination with strong reducing agents, such as hydrides. Undergoes highly exothermic reaction with 2,2-dibromo-1,3-dimethylcyclopropanoic acid [J. Chem. Soc., 1, 1979, 2324].

Health Hazard

Inhalation causes irritation of nose, mouth, and lungs. Ingestion causes irritation of mouth and stomach. Contact with liquid causes severe irritation of eyes and moderate irritation of skin.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: Liquid will attack some plastics; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Flush with water; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Poison by ingestion. Moderately toxic to humans by inhalation. A corrosive liquid. See also n-BUTYLAMINE and AMINES. Very dangerous fire hazard when exposed to heat or flame. Very exothermic reaction with 2,2-dibromo-l,3 dimethylcyclopropanoic acid. To fight fire, use alcohol foam. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Dry it with KOH or LiAlH4, and/or distil it from CaH2 or BaO. [Beilstein 4 IV 657.]

Definition

ChEBI: Tert-butylamine is a primary aliphatic amine that is ethylamine substituted by two methyl groups at position 1. It is a conjugate base of a tert-butylammonium.

General Description

Tert-butylamine appears as a clear colorless liquid with an ammonia-like odor. Flash point 70°F. Less dense (at 6.2 lb / gal) than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion.

InChI:InChI=1/C4H11N/c1-4(2,3)5/h5H2,1-3H3/p+1

75-64-9 Relevant articles

Competitive Condensation and Proton-Transfer Processes in the Reaction of t-C4H9+ Ions with Ammonia in Gaseous Systems at Atmospheric Pressure

Attina, Marina,Cacace, Fulvio,Giacomello, Pierluigi,Speranza, Maurizio

, p. 6896 - 6898 (1980)

-

Factors Controlling Amination of 2-Methylpropene over Proton-exchanged Zeolite Catalysts

Mizuno, Noritaka,Tabata, Masahiro,Uematsu, Takeshi,Iwamoto, Masakuzu

, p. 3513 - 3514 (1993)

The number and strength of Broensted aci...

Reactions of bromoacetylene with primary amine on a butterfly-type tetrairon core to give isonitrile and methyne through oxidation and deprotonation

Okazaki, Masaaki,Tsuchimoto, Takahiro,Nakazawa, Yuki,Takano, Masato,Ozawa, Fumiyuki

, p. 3487 - 3489 (2011)

Reaction of [(η5-C5H4Me) 4Fe4(HCCH)(HCC-...

A shaped binderless ZSM-11 zeolite catalyst for direct amination of isobutene to tert-butylamine

Zhang, Wanshuo,Gao, Shangyao,Xie, Sujuan,Liu, Hui,Zhu, Xiangxue,Shang, Yongchen,Liu, Shenglin,Xu, Longya,Zhang, Ye

, p. 168 - 175 (2017)

A shaped binderless and two binder-conta...

Amination of 2-Methylpropene over Proton-Exchanged ZSM-5 Zeolite Catalysts

Mizuno, Noritaka,Tabata, Masahiro,Uematsu, Takeshi,Iwamoto, Masakazu

, p. 249 - 256 (1994)

The reaction between 2-methylpropene and...

Reaction of tert-butylimine of phenylpropiolic aldehyde with substituted imidazole-2-thiones

Karpov,Belyaev,Orlova,Davidovich,Garabadzhiu

, p. 766 - 767 (2015)

-

Pd nanoparticles prepared by grafting of Pd complexes on phenol-functionalized carbon supports for liquid phase catalytic applications

Hermans, Sophie,Diverchy, Chantal,Dubois, Vincent,Devillers, Michel

, p. 263 - 271 (2014)

An activated carbon was functionalized b...

Organic promoter-driven fast synthesis of zeolite beta and its acceleration mechanism

Zhao, Dongpu,Chu, Weifeng,Wang, Yanan,Zhu, Xiangxue,Li, Xiujie,Xie, Sujuan,An, Jie,Xin, Wenjie,Liu, Shenglin,Xu, Longya

, p. 24614 - 24624 (2018)

Zeolite beta, an important catalytic mat...

C?H Bond Activation by an Imido Cobalt(III) and the Resulting Amido Cobalt(II) Complex

Kraus, Florian,Pietzonka, Clemens,Reckziegel, Alexander,Werncke, C. Gunnar

, p. 8527 - 8531 (2020)

The 3d-metal mediated nitrene transfer i...

PROCESS FOR PREPARATION OF TERT-BUTYLAMINE AND PROPIONIC ACID SALTS FROM N-TERTIARY BUTYL ACRYLAMIDE

-

Page/Page column 16-17, (2021/11/13)

Disclosed is a process (100) for convers...

A Lewis Base Nucleofugality Parameter, NFB, and Its Application in an Analysis of MIDA-Boronate Hydrolysis Kinetics

García-Domínguez, Andrés,Gonzalez, Jorge A.,Leach, Andrew G.,Lloyd-Jones, Guy C.,Nichol, Gary S.,Taylor, Nicholas P.

supporting information, (2022/01/04)

The kinetics of quinuclidine displacemen...

Diverse Oxidative C(sp2)-N Bond Cleavages of Aromatic Fused Imidazoles for Synthesis of α-Ketoamides and N-(pyridin-2-yl)arylamides

Xu, Fangzhou,Wang, Yanyan,Xun, Xiwei,Huang, Yun,Jin, Zhichao,Song, Baoan,Wu, Jian

, p. 8411 - 8422 (2019/05/17)

An efficient and chemoselective C(sp2)-N...

75-64-9 Process route

niobium pentachloride
10026-12-7

niobium pentachloride

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

tert-butylamine

Conditions
Conditions Yield
79%
ethyl N-tert-butylcarbamate
1611-50-3

ethyl N-tert-butylcarbamate

ammonia
7664-41-7

ammonia

1,1-dimethylethylurea
1118-12-3

1,1-dimethylethylurea

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

tert-butylamine

urea
57-13-6

urea

urethane
51-79-6

urethane

Conditions
Conditions Yield
at 180 ℃;

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