N-tert-Butylisopropylamine

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Names

[ CAS No. ]:
7515-80-2

[ Name ]:
N-tert-Butylisopropylamine

[Synonym ]:
MFCD00061615
EINECS 231-370-3
2-methyl-N-propan-2-ylpropan-2-amine

Chemical & Physical Properties

[ Density]:
0.727 g/mL at 25ºC(lit.)

[ Boiling Point ]:
98ºC(lit.)

[ Melting Point ]:
-38°C (estimate)

[ Molecular Formula ]:
C7H17N

[ Molecular Weight ]:
115.21700

[ Flash Point ]:
26 °F

[ Exact Mass ]:
115.13600

[ PSA ]:
12.03000

[ LogP ]:
2.17380

[ Index of Refraction ]:
n20/D 1.398(lit.)

[ Water Solubility ]:
It has optimal solubility in water.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02, GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H226-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C

[ Risk Phrases ]:
10-34

[ Safety Phrases ]:
26-36/37/39-45

[ RIDADR ]:
UN 2733 3/PG 2

[ WGK Germany ]:
3

[ RTECS ]:
LZ6651000

[ Packaging Group ]:
II

[ HS Code ]:
2921199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • tert-Butylamine
  • 2-Bromopropane
  • Methanol
  • 1-tert-butyl-1-isopropyl-3-phenylurea
  • 1,3-di-tert-butyl-1-isopropylurea
  • diisopropyl sulfate
  • N-2,6-Dimethylphenyl-N'-t-Bu,N'-isopropylharnstoff
  • Acetone
  • Isopropyl 4-methylbenzenesulfonate
  • p-Xylene

DownStream

  • Benzene,1-methyl-4-[(4-methylphenyl)methyl]-
  • lithium N-tert-butylisopropylamide
  • p-Xylene
  • potassium tert-butyl(isopropyl)amide
  • n-isopropyl-n-methyl-tert-butylamine

Customs

[ HS Code ]: 2921199090

[ Summary ]:
2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Enamines from terminal epoxides and hindered lithium amides.

J. Am. Chem. Soc. 126(22) , 6870-1, (2004)

A new reactivity mode of lithium amides with epoxides leads to hindered enamines. The reaction of some of these enamines with unactivated primary and secondary alkyl halides is described, which expand...


More Articles

Related Compounds

  • N-(tert-Butoxycarbonyl)-3-(2-furyl)-L-alanine
  • N-tert-butyl-4-[(3,4-dimethyl-N-methylsulfonylanilino)methyl]benzamide
  • N-tert-butyl-2-methyl-5-phenyl-2,3-dihydropyridin-6-amine
  • N-tert-butyl-4,6-bis(tert-butylamino)-1,3,5-triazine-2-sulphenamide
  • N-tert-Butyloxycarbonyl Glutathione Dimethyl Diester Disulfide Dimer
  • N-tert-butylprop-2-enamide,N-propan-2-ylprop-2-enamide
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 2-{1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperidin-4-yl}-1,8-naphthyridine
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 2,5-Dioxopyrrolidin-1-yl 3-bromo-5-(trifluoromethoxy)benzoate
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • Poly[oxy(dimethylsilylene)], I+/--(5-hexen-1-yldimethylsilyl)-I-[(5-hexen-1-yldimethylsilyl)oxy]-