Basic information Safety Supplier Related

2,4-Dimethyldiphenylamine

Basic information Safety Supplier Related

2,4-Dimethyldiphenylamine Basic information

Product Name:
2,4-Dimethyldiphenylamine
Synonyms:
  • 2,4-DIMETHYLDIPHENYLAMINE
  • PHENYL(2,4-XYLYL)AMINE
  • N-PHENYL-2,4-XYLIDINE
  • N-Phenyl-2,4-xylidine Phenyl(2,4-xylyl)amine
  • 2,4-DiMethyl-N-phenylaniline
  • TRIS(4-BROMOPHENYL)2,4-DIMETHYL DIPHENYLAMINE
  • 2,4-DiMethyl-N-phenylbenzenaMine
  • N-(2,4-dimethylphenyl)aniline
CAS:
25078-04-0
MF:
C14H15N
MW:
197.28
EINECS:
677-190-2
Mol File:
25078-04-0.mol
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2,4-Dimethyldiphenylamine Chemical Properties

Melting point:
43°C
Boiling point:
170°C 3mm
Density 
1.049±0.06 g/cm3(Predicted)
Flash point:
0°C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
powder to lump
pka
1.11±0.40(Predicted)
color 
White to Yellow
InChI
InChI=1S/C14H15N/c1-11-8-9-14(12(2)10-11)15-13-6-4-3-5-7-13/h3-10,15H,1-2H3
InChIKey
BWYYRZBQXLCZJL-UHFFFAOYSA-N
SMILES
C1(NC2=CC=CC=C2)=CC=C(C)C=C1C
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Safety Information

Risk Statements 
20/21/22-36/37/38
Safety Statements 
22-26-36/37/39
HS Code 
2921.49.5000
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2,4-Dimethyldiphenylamine Usage And Synthesis

Chemical Properties

white crystalline.

Uses

2,4-Dimethyldiphenylamine is mainly used in organic synthesis and pharmaceutical intermediates.

Synthesis

108-90-7

95-68-1

25078-04-0

GENERAL STEPS: A solution of potassium tert-butoxide (KOtBu, 102.1 mg, 1.3 eq.) and complex 3a (10-50 mL, 0.01-0.05 mol, prepared from 4.6 mg of complex 3a dissolved in 1.0 mL of dichloromethane) was added to a Schlenk reaction tube under nitrogen atmosphere. The reaction tube was sealed and the solvent was removed under reduced pressure. Toluene (0.5 mL), 2,4-dimethylaniline (0.84 mmol) and chlorobenzene (0.70 mmol) were then added sequentially. The reaction mixture was stirred vigorously at the indicated temperature for 3 to 24 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography to afford the target product 2,4-dimethyldiphenylamine.

References

[1] Advanced Synthesis and Catalysis, 2008, vol. 350, # 5, p. 652 - 656
[2] Tetrahedron, 2017, vol. 73, # 52, p. 7308 - 7314

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