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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

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

Towards a Second Generation of Ionic Liquid Matrices (ILMs) for MALDI-MS of Peptides, Proteins, and Carbohydrates

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,...


More Articles


Related Compounds

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