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Merck

209864

4-tert-Butylaniline

99%

Synonym(s):

4-(1,1-Dimethylethyl)aniline, 4-(1,1-Dimethylethyl)benzenamine, 4-Amino-tert-butylbenzene, 4-t-Butylphenylamine, 4-tert-Butylbenzenamine, 4-tert-Butylphenylamine, p-(tert-Butyl)phenylamine, p-tert-Butylaniline

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About This Item

Linear Formula:
(CH3)3CC6H4NH2
CAS Number:
769-92-6
Molecular Weight:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24852597
EC Number:
212-215-9
Beilstein/REAXYS Number:
2205786
MDL number:
MFCD00007899
Assay:
99%
Form:
liquid

Key Documents

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InChI key

WRDWWAVNELMWAM-UHFFFAOYSA-N

InChI

1S/C10H15N/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,11H2,1-3H3

SMILES string

CC(C)(C)c1ccc(N)cc1

assay

99%

form

liquid

refractive index

n20/D 1.538 (lit.)

bp

90-93 °C/3 mmHg (lit.)

mp

15-16 °C (lit.)

density

0.937 g/mL at 25 °C (lit.)

Quality Level

100

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Application

4-tert-Butylaniline was used in the synthesis of:
  • 4-tert-Butyl-4′,4″-dinitrotriphenylamine, new triphenylamine-containing diamine monomer
  • 2-oxopyrimido[4,5-d]pyrimidin-5(6H)-one

General description

Schiff base formation reaction between 4-tert-butylaniline and 4-tert-butylbenzaldehyde in ethanol has been carried out using the matrix-assisted laser desorption ionization-chip system.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBF5396V
STBB7541V
S35756V
STBB7541
05712HH

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Novel aromatic polyamides and polyimides functionalized with 4-tert-butyltriphenylamine groups.
Hsiao S-H, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(15), 4579-4592 (2006)
Christopher G Thomson et al.
Bioorganic & medicinal chemistry letters, 21(14), 4281-4283 (2011-06-15)
A novel and robust synthesis of the fragment, 2-amino-5-tert-butylpyridine, has been described, which has been shown to have improved physicochemical properties over 4-tert-butylaniline, when considering drug-like properties. The synthesis also yields fragments containing more highly oxidised precursors to the tert-butyl
Self-complementary hydrogen bonding heterocycles designed for the enforced self-assembly into supramolecular macrocycles.
Marsh A, et al.
Chemical Communications (Cambridge, England), 13, 1527-1528 (1996)
Monica Brivio et al.
Lab on a chip, 5(4), 378-381 (2005-03-26)
The integration of a monitoring port along the microfluidic path of a MALDI-chip integrated device is described. Optimization of the microreactor design allows longer reaction and measuring times. The Schiff base reaction between 4-tert-butylaniline (1) and 4-tert-butylbenzaldehyde (2) in ethanol
Ji Han Kim et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(38), 9060-9070 (2019-04-16)
Organic light-emitting diodes are currently under research to achieve high efficiency and long life by using thermally activated delayed fluorescence (TADF) materials. In particular, many studies have focused on ensuring high efficiency in fluorescent devices by introducing TADF materials. Herein

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