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Names | |||
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Preferred IUPAC name
2-Methylpropan-2-amine
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Other names
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Identifiers | |||
3D model (Jmol)
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605267 | |||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.000.808 | ||
EC Number | 200-888-1 | ||
1867 | |||
MeSH | tert-butylamine | ||
PubChem CID
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RTECS number | EO3330000 | ||
UN number | 3286 | ||
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Properties | |||
C4H11N | |||
Molar mass | 73.14 g·mol−1 | ||
Appearance | Colorless liquid | ||
Odor | fishy, ammoniacal | ||
Density | 0.696 g/mL | ||
Melting point | −67.50 °C; −89.50 °F; 205.65 K | ||
Boiling point | 43 to 47 °C; 109 to 116 °F; 316 to 320 K | ||
Miscible | |||
log P | 0.802 | ||
Vapor pressure | 39.29 kPa (at 20 °C) | ||
Refractive index (nD)
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1.377 | ||
Thermochemistry | |||
191.71 J K−1 mol−1 | |||
Std molar
entropy (S |
233.63 J K−1 mol−1 | ||
Std enthalpy of
formation (ΔfH |
−151.1–−150.1 kJ mol−1 | ||
Std enthalpy of
combustion (ΔcH |
−2.9959–−2.9951 MJ mol−1 | ||
Hazards | |||
Safety data sheet | rose-hulman.edu | ||
GHS pictograms | |||
GHS signal word | DANGER | ||
H225, H302, H314, H331 | |||
P210, P261, P280, P305+351+338, P310 | |||
EU classification (DSD)
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F C | ||
R-phrases | R11, R20/22, R35 | ||
S-phrases | S16, S26, S36/37/39, S45 | ||
NFPA 704 | |||
Flash point | −38 °C (−36 °F; 235 K) | ||
380 °C (716 °F; 653 K) | |||
Explosive limits | 1.7–9.8% | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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464 mg kg−1(oral, rat) | ||
Related compounds | |||
Related alkanamines
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Related compounds
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2-Methyl-2-nitrosopropane | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|||
Infobox references | |||
tert-Butylamine is an organic chemical compound with the formula (CH3)3CNH2. It is a colorless liquid with a typical amine-like odor. tert-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and isobutylamine.
tert-Butylamine is produced commercially by the Ritter reaction of isobutene with hydrogen cyanide under acidic conditions to give the formamide:
In the laboratory, it can be prepared by the hydrogenolysis of 2,2-dimethylethylenimine, or via tert-butylphthalimide.
tert-Butylamine is used as an intermediate in the preparation of the sulfenamides such as N-tert-butyl-2-benzothiazylsulfenamide and N-tert-butyl-2-benzothiazylsulfenimide. As rubber accelerators, these compounds modify the rate of vulcanization or rubber. A variety of pesticides are derived from this amine, including terbacil, terbutryn, and terbumeton.
In pharmacology under the name erbumine, tert-butylamine has been used as a counterion in drug substances such as perindopril erbumine.