Basic information Safety Supplier Related

4-(TERT-BUTYL)-2,6-DIMETHYLANILINE

Basic information Safety Supplier Related

4-(TERT-BUTYL)-2,6-DIMETHYLANILINE Basic information

Product Name:
4-(TERT-BUTYL)-2,6-DIMETHYLANILINE
Synonyms:
  • 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE
  • 2-Amino-5-(tert-butyl)-m-xylene, 4-(tert-Butyl)-2,6-xylidine
  • 4-(tert-Butyl)-2,6-dimethylaniline 98%
  • Benzenamine, 4-(1,1-dimethylethyl)-2,6-dimethyl-
  • 2,6-Dimethyl- 4-tert-butyl-aniline
CAS:
42014-60-8
MF:
C12H19N
MW:
177.29
Product Categories:
  • Amines
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
Mol File:
42014-60-8.mol
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4-(TERT-BUTYL)-2,6-DIMETHYLANILINE Chemical Properties

Melting point:
29-29.5 °C
Boiling point:
96 °C
Density 
0.9321 g/cm3(Temp: 25 °C)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
4.63±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
42014-60-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22-36/37/38-36
Safety Statements 
26-36/37/39
RIDADR 
2810
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
HS Code 
2921420090
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4-(TERT-BUTYL)-2,6-DIMETHYLANILINE Usage And Synthesis

Synthesis

6279-89-6

42014-60-8

5-(tert-butyl)-1,3-dimethyl-2-nitrobenzene (15 g, 0.072 mol) was mixed with stannous chloride (41 g, 0.216 mol) in 300 mL of ethanol and the reaction was heated at reflux for 24 hours. Upon completion of the reaction, the reaction mixture was cooled to room temperature and neutralized by slowly adding aqueous potassium hydroxide solution under stirring. Subsequently, the reaction mixture was extracted with ethyl acetate to separate the organic phase. The organic phase was purified by column chromatography to give 7 g of 4-tert-butyl-2,6-dimethyl-aniline ([Intermediate 8-b]) in 58% yield.

References

[1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987, p. 1 - 8
[2] Chemistry Letters, 1983, p. 1373 - 1374
[3] Journal of Chemical Research - Part S, 2000, # 6, p. 290 - 291
[4] Patent: KR2015/124677, 2015, A. Location in patent: Paragraph 0291; 0296-0299
[5] Organometallics, 2010, vol. 29, # 24, p. 6723 - 6731

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