N-butylisocyanide

Suppliers

Names

[ CAS No. ]:
2769-64-4

[ Name ]:
N-butylisocyanide

[Synonym ]:
EINECS 220-458-7
MFCD00000008
Butyl isocyanide
NBN
n-Butyl isocyanide
tert-butylisonitrile
n-butyl isonitrile

Chemical & Physical Properties

[ Density]:
0.795 g/mL at 25 °C(lit.)

[ Molecular Formula ]:
C5H9N

[ Molecular Weight ]:
83.13170

[ Flash Point ]:
69 °F

[ Exact Mass ]:
83.07350

[ LogP ]:
0.93650

[ Index of Refraction ]:
n20/D 1.396(lit.)

[ Storage condition ]:
0-6°C

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H302 + H312 + H332

[ Precautionary Statements ]:
P210-P280

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

[ Hazard Codes ]:
Xn: Harmful;F: Flammable;T: Toxic;

[ Risk Phrases ]:
R11

[ Safety Phrases ]:
S7-S16-S23-S36/37/39

[ RIDADR ]:
UN 1993 3/PG 2

[ WGK Germany ]:
3

[ HS Code ]:
2926909090

Synthetic Route

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

n-Butyl isocyanide oxidation at the [NiFe4S4OH(x)] cluster of CO dehydrogenase.

J. Biol. Inorg. Chem. 17(2) , 167-73, (2012)

Carbon monoxide dehydrogenases (CODHs) catalyze the reversible oxidation of carbon monoxide by reaction with water to yield carbon dioxide, two protons, and two electrons. Two principal types of CODHs...

Butyl isocyanide as a probe of the activation mechanism of soluble guanylate cyclase. Investigating the role of non-heme nitric oxide.

J. Biol. Chem. 282(49) , 35741-8, (2007)

Nitric oxide (NO) is a physiologically relevant activator of the hemoprotein soluble guanylate cyclase (sGC). In the presence of NO, sGC is activated several hundredfold above the basal level by a mec...

Kinetics of intramolecular charge transfer with N-phenylpyrrole in alkyl cyanides.

J. Phys. Chem. A 109(8) , 1497-509, (2005)

For the electron acceptor/donor molecule N-phenylpyrrole (PP), the fast intramolecular charge transfer (ICT) reaction accompanied by dual fluorescence from a locally excited (LE) and an ICT state is i...


More Articles


Related Compounds

  • tetrakis(tert-n-butylisocyanide)nickel(0)
  • N-tert-butyl-3-nitroaniline
  • N-octanoyl benzotriazole
  • N,N-Dimethylcarbamic acid m-isopropylphenyl ester
  • N-(diaminomethylidene)pyrrolidine-1-carboximidamide,hydrochloride
  • (-)-N-(1-Methylethyl)phosphoramidothioic acid O-methyl O-(2,4-dichlorophenyl) ester
  • 4-Chloro-6-cyclopropylthieno[2,3-d]pyrimidine
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-(3-Methoxy-1,2-oxazol-5-yl)propan-2-one
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1-(2-Furanylmethyl)-2-(nitromethylene)imidazolidine
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde