Basic information Safety Supplier Related

1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE

Basic information Safety Supplier Related

1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Basic information

Product Name:
1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE
Synonyms:
  • I-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE
  • 1-(ALPHA,ALPHA,ALPHA-TRIFLUORO-O-TOLYL)-IMIDAZOLE
  • 1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE
  • 1-[2-(TRIFLUOROMETHYL)PHENYL]-1H-IMIDAZOLE
  • TRIM
  • 1-[2-(Trifluoromethyl)phenyl]-1H-imidazole 98%
  • 1-[2-(Trifluoromethyl)phenyl]-1H-imidazole98%
  • 1-(2-Trifluoromethylphenyl)imidazole, 98+%
CAS:
25371-96-4
MF:
C10H7F3N2
MW:
212.17
EINECS:
636-734-9
Product Categories:
  • Imidazol&Benzimidazole
Mol File:
25371-96-4.mol
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1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Chemical Properties

Melting point:
43 °C
Boiling point:
75°C 0,02mm
Density 
1.3253 (estimate)
Flash point:
75°C/0.025mm
storage temp. 
2-8°C
solubility 
Soluble in DMSO (up to 10 mg/ml) or in Ethanol (up to 20 mg/ml).
form 
White solid.
pka
4.96±0.10(Predicted)
color 
White
Sensitive 
Light Sensitive
BRN 
3955637
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
CAS DataBase Reference
25371-96-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
IRRITANT, LIGHT SENSITIVE
HS Code 
29339900

MSDS

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1-(2-TRIFLUOROMETHYLPHENYL)IMIDAZOLE Usage And Synthesis

Description

TRIM (25371-96-4) is a potent inhibitor of neuronal and inducible nitric oxide synthases, (IC50?= 28.2 and 27.0 μM respectively). Inhibits endothelial NOS with lower potency (IC50 = 1057.5 μM).1?TRIM displays antinociceptive activity?in vivo.2

Uses

TRIM is a potent inhibitor of neuronal nitric oxide synthase in vitro, in animal models.

Definition

ChEBI: 1-[2-(trifluoromethyl)phenyl]imidazole is a member of imidazoles.

Biological Activity

A potent inhibitor of neuronal and inducible NO synthases, with much lower affinity for the endothelial isoform (displays IC 50 values of 28.2, 27.0 and 1057.5 μ M respectively). Antinociceptive in vivo .

Biochem/physiol Actions

Potent nitric oxide synthase inhibitor. Because of the putative involvement of nitric oxide in depression and stress syndromes, TRIM was studied for its antidepressant effects, and found to reduce manifestations of stress in an animal model as well as fluoxetine.

References

1) Handy?et al. (1995), The antinociceptive effect of 1-(2-trifluoromethylphenyl)imidazole (TRIM), a potent inhibitor of neuronal nitric oxide synthase in vitro, in the mouse; Br. J. Pharmacol.,?116?2349 2) Handy?et al. (1996),?Inhibition of nitric oxide synthase by 1-(2-trifluoromethylphenyl) imidazole (TRIM) in vitro: antinociceptive and cardiovascular effects; Br. J. Pharmacol.,?119?423

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