n-isopropyl-n-methyl-tert-butylamine
Names
[ CAS No. ]:
85523-00-8
[ Name ]:
n-isopropyl-n-methyl-tert-butylamine
[Synonym ]:
N-isopropyl-N-methyl-butylamine
N-isopropyl-N-methyl-t-butylamine
tert-butyl-N-methyl-N-isopropylamine
N-tert.-Butyl-N-methyl-N-isopropylamin
Methyl-isopropyl-tert.-butyl-amin
tert-butylisopropylmethylamine
N-Isopropyl-N-methyl-tert-butylamine
Chemical & Physical Properties
[ Density]:
0.767 g/mL at 25ºC(lit.)
[ Boiling Point ]:
127ºC(lit.)
[ Melting Point ]:
-76.53°C (estimate)
[ Molecular Formula ]:
C8H19N
[ Molecular Weight ]:
129.24300
[ Flash Point ]:
49 °F
[ Exact Mass ]:
129.15200
[ PSA ]:
3.24000
[ LogP ]:
2.12510
[ Index of Refraction ]:
n20/D 1.419(lit.)
MSDS
Safety Information
[ Symbol ]:
GHS02, GHS07
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H225-H315-H319-H335
[ Precautionary Statements ]:
P210-P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
F,Xi
[ Risk Phrases ]:
11-36/37/38
[ Safety Phrases ]:
16-26-36
[ RIDADR ]:
UN 1993 3/PG 2
[ WGK Germany ]:
3
[ HS Code ]:
2921199090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
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
J. Am. Soc. Mass Spectrom. 20 , 1790-1800, (2009)
Second generation ionic liquid matrices are developed, examined, and tested. They have shown a wide mass detection range (<1000 Da to >270,000 Da) for proteins and peptides with greater S/N ratios tha...
Recent advances in the synthesis of ammonium-based rotaxanes.Molecules 15(5) , 3709-30, (2010)
The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rath...
Asymmetric synthesis of primary amines via the spiroborate-catalyzed borane reduction of oxime ethers.Org. Lett. 9(9) , 1793-5, (2007)
[reaction: see text] The enantioselective borane reduction of O-benzyloxime ethers to primary amines was studied under catalytic conditions using the spiroborate esters 5-10 derived from nonracemic 1,...