N-octylimidazole

Suppliers

Names

[ CAS No. ]:
21252-69-7

[ Name ]:
N-octylimidazole

[Synonym ]:
N-1-octylimidazole
1H-Imidazole,1-octyl
1-octyl-1H-imidazole
1-octyl-imidazole
N-Octyl imidazole
3-octylimidazole

Chemical & Physical Properties

[ Density]:
0.92 g/cm3

[ Boiling Point ]:
302.4ºC at 760 mmHg

[ Molecular Formula ]:
C11H20N2

[ Molecular Weight ]:
180.29000

[ Flash Point ]:
136.7ºC

[ Exact Mass ]:
180.16300

[ PSA ]:
17.82000

[ LogP ]:
3.24360

[ Vapour Pressure ]:
0.00178mmHg at 25°C

[ Index of Refraction ]:
1.499

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933290090

Synthetic Route

Precursor & DownStream

Precursor

  • Imidazole
  • 1-Bromooctane
  • 1-Iodooctane
  • Octylamine
  • 1-Chlorooctane

DownStream

  • 1-Methyl-3-Octylimidazolium Trifluoromet
  • 1-methyl-3-octyl-imidazolium tetrafluoroborate
  • 1-(anthracen-9-ylmethyl)-3-octyl-1,2-dihydroimidazol-1-ium,chloride

Customs

[ HS Code ]: 2933290090

[ Summary ]:
2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Metabolic activation of 2-methylfuran by rat microsomal systems.

Toxicol. Appl. Pharmacol. 78(3) , 370-6, (1985)

2-Methylfuran (2-MF), a constituent of cigarette smoke and coffee, causes necrosis of liver, lungs, and kidneys in rodents. 2-MF is metabolically activated by mixed-function oxidases to acetylacrolein...

Disulfiram metabolism as a requirement for the inhibition of rat liver mitochondrial low Km aldehyde dehydrogenase.

Biochem. Pharmacol. 42(7) , 1361-6, (1991)

In humans and animals, disulfiram produces a disulfiram-ethanol reaction after an ethanol challenge, the basis of which is the inhibition of liver aldehyde dehydrogenase (ALDH). Disulfiram and the met...

K. Imagawa et al.

Chem. Lett. , 527, (1994)


More Articles


Related Compounds

  • tert-butyl N-[3-amino-2-(5-chloro-2-fluorophenyl)-2-methylpropyl]carbamate
  • 4-{4-[(Tert-butoxy)carbonyl]morpholin-3-yl}oxane-4-carboxylic acid
  • 4,4-Difluoro-1-(5-nitrofuran-2-yl)cyclohexane-1-carboxylic acid
  • tert-butyl N-[2-amino-2-(6-chloro-1-methyl-1H-indol-3-yl)ethyl]carbamate
  • 2-(4-{[(Tert-butoxy)carbonyl]amino}-2-hydroxyphenyl)-2,2-difluoroacetic acid
  • Tert-butyl 2-(5-chloropyridin-2-yl)piperazine-1-carboxylate
  • Methyl 5-[2-(aminooxy)propan-2-yl]furan-2-carboxylate
  • Tert-butyl 3-(4-fluoropyridin-2-yl)piperazine-1-carboxylate
  • Tert-butyl 3-(2-methoxyquinolin-3-yl)piperazine-1-carboxylate
  • Methyl 3-(aminomethyl)heptanoate
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