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133280

Sigma-Aldrich

Butylisocyanid

97%

Synonym(e):

1-Butylisonitrile, 1-Isocyanobutane, Butyl isonitrile, n-Butyl isocyanide, n-Butyl isonitrile

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About This Item

Lineare Formel:
CH3(CH2)3NC
CAS-Nummer:
2769-64-4
Molekulargewicht:
83.13
EG-Nummer:
220-458-7
MDL-Nummer:
MFCD00000008
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848097
NACRES:
NA.22

Qualitätsniveau

100

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.396 (lit.)

Dichte

0.795 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine
isonitrile

Lagertemp.

2-8°C

SMILES String

CCCC[N+]#[C-]

InChI

1S/C5H9N/c1-3-4-5-6-2/h3-5H2,1H3

InChIKey

FSBLVBBRXSCOKU-UHFFFAOYSA-N

Verwandte Kategorien

Anwendung

Butyl isocyanide was used to study the crystal structure of carbon monoxide dehydrogenases-II isolated from Carboxydothermus hydrogenoformans. It was used to probe the mechanism of NO activation of the hemoprotein soluble guanylate cyclase. .

Biochem./physiol. Wirkung

Butyl isocyanide forms complex with ferric and ferrous iron of the heme in cytochrome P450.

Sonstige Hinweise

May form haziness and/or precipitate with no loss in purity.

Zubehör

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

FlameExclamation mark
GHS02,GHS07

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Oral - Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

69.8 °F - closed cup

Flammpunkt (°C)

21 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCQ1187
MKCM5462
MKCK9782
MKCH9404
MKCB1325V

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T H Tahirov et al.
Nature structural biology, 3(5), 459-464 (1996-05-01)
We have determined the structure of n-butylisocyanide-bound Rhodobacter capsulatus cytochrome c'. This is the first example of a ligand-bound structure of a class IIa cytochrome c. Compared with the structure of native cytochrome c', there are significant conformational changes of
D S Lee et al.
Biochemistry, 40(9), 2669-2677 (2001-03-22)
Alkyl-isocyanides are able to bind to both ferric and ferrous iron of the heme in cytochrome P450, and the resulting complexes exhibit characteristic optical absorption spectra. While the ferric complex gives a single Soret band at 430 nm, the ferrous
D Barrick et al.
Biochemistry, 40(13), 3780-3795 (2001-04-13)
The linkage between the proximal histidines and the proximal polypeptide in normal adult human hemoglobin (Hb A) has been proposed to play a major role in transmitting allosteric effects between oxygen binding sites [Perutz, M. F. (1970) Nature 228, 726-734].
C Mouro et al.
European journal of biochemistry, 267(1), 216-221 (1999-12-22)
An 1H-NMR study of ferric cytochrome P450cam in different paramagnetic states was performed. Assignment of three heme methyl resonances of the isocyanide adduct of cytochrome P450 in the ferric low-spin state was recently performed using electron exchange in the presence
Y Imai et al.
Biochimica et biophysica acta, 1337(1), 66-74 (1997-01-04)
Heme-external ligand interactions of P-450nor were examined spectrophotometrically and compared with those of other P-450s. Most nitrogenous ligands induced type II spectral changes on binding to ferric P-450nor, as did other P-450s. In contrast with other P-450s, 2-methylpyridine and 1-butanol
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