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3,5-Bis(trifluoromethyl)benzylamine

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3,5-Bis(trifluoromethyl)benzylamine Basic information

Product Name:
3,5-Bis(trifluoromethyl)benzylamine
Synonyms:
  • RARECHEM AL BW 0137
  • TIMTEC-BB SBB000829
  • 3,5-DI(TRIFLUOROMETHYL)BENZYLAMINE
  • [3,5-BIS(TRIFLUOROMETHYL)PHENYL]METHANAMINE
  • 3,5-BIS(TRIFLUOROMETHYL)BENZYLAMINE
  • 3,5-BIS(TRIFLUOROMETHYL)BENZYLAMINE, TEC H., 80%
  • 3,5-Bis(TrifluroMethyl)BenzylAmine
  • MBT-BYM
CAS:
85068-29-7
MF:
C9H7F6N
MW:
243.15
EINECS:
285-290-9
Product Categories:
  • Amines
  • C9 to C10
  • Nitrogen Compounds
  • Amine
Mol File:
85068-29-7.mol
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3,5-Bis(trifluoromethyl)benzylamine Chemical Properties

Melting point:
50-55 °C(lit.)
Boiling point:
82-84 °C (15 mmHg)
Density 
1.3653 (estimate)
Flash point:
173 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
soluble in Methanol
form 
Crystalline Mass, Powder, Crystals and/or Chunks
pka
8.32±0.10(Predicted)
color 
White to beige
Sensitive 
Air Sensitive
BRN 
7209267
CAS DataBase Reference
85068-29-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34-21/22
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3259 8/PG 2
WGK Germany 
3
10-34
Hazard Note 
Corrosive
HazardClass 
8
PackingGroup 
III
HS Code 
29214990

MSDS

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3,5-Bis(trifluoromethyl)benzylamine Usage And Synthesis

Chemical Properties

Colorless to light yellow liqui

Uses

3,5-bis(Trifluoromethyl)benzylamine is used in preparation of nitrile by catalytic oxidation of amines.

Synthesis

401-95-6

85068-29-7

The general procedure for the synthesis of 3,5-bis(trifluoromethyl)benzenemethanamine from 3,5-bis(trifluoromethyl)benzaldehyde was as follows: to a 300 mL autoclave was added 145.3 g (0.60 mol) of 3,5-bis(trifluoromethyl)benzenemethanaldehyde and 60 mL of cooled ethanol solution containing 10.3 g (0.60 mol) of liquid ammonia, followed by the addition of 2 g of nickel ruanide. The mixture was heated to 40 °C and the reaction was stirred under hydrogen pressure (9 MPa) for 1 hour. The temperature was then raised to 70 °C and the reaction was continued for 30 min. Upon completion of the reaction, the reaction product solution was drained and filtered to remove the catalyst. Analysis of the reaction solution by gas chromatography confirmed the formation of 128.9 g (0.53 mol) of 3,5-bis(trifluoromethyl)benzylamine in 89% yield and 93% selectivity. 124.0 g (0.51 mol) of 3,5-bis(trifluoromethyl)benzylamine was isolated by vacuum distillation in 85% yield, and the purity determined by gas chromatography was ≥99%.The results of ICP analysis of the total elements showed that Li, Na, K, Mg, Ca, Sr, Ba, Sc, Y, Ti, Zr, V, Nb, Cr, Mo, W, Mn, Fe, Ru, Co were not detected; Rh, Ni, Pd, Pt, Cu, Ag, Au, Zn, Cd, Al, In, Si, Sn, Pb, P, Sb, and S were detected, and the contents of group 1 and group 2 elements were ≤1 ppm.

References

[1] Patent: EP1500641, 2005, A1. Location in patent: Page 12

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