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226637

Sigma-Aldrich

Butylnitrit

95%

Synonym(e):

n-Butyl nitrite

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About This Item

Lineare Formel:
CH3(CH2)3ONO
CAS-Nummer:
544-16-1
Molekulargewicht:
103.12
Beilstein:
1701036
EG-Nummer:
208-862-1
MDL-Nummer:
MFCD00002058
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24853580
NACRES:
NA.22

Dampfdruck

760 mmHg ( 78 °C)

Qualitätsniveau

100

Assay

95%

Form

liquid

Brechungsindex

n20/D 1.376 (lit.)

bp

78 °C (lit.)

Löslichkeit

alcohol: miscible(lit.)
diethyl ether: miscible(lit.)

Dichte

0.882 g/mL at 25 °C (lit.)

Lagertemp.

2-8°C

SMILES String

CCCCON=O

InChI

1S/C4H9NO2/c1-2-3-4-7-5-6/h2-4H2,1H3

InChIKey

JQJPBYFTQAANLE-UHFFFAOYSA-N

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Allgemeine Beschreibung

The photodissociation dynamics of butyl nitrite was studied using time-resolved Fourier transform infrared (TR-FTIR) emission spectroscopy. The effects of butyl nitrite on methyl cobalamin and 5-methyl tetrahydrofolate were studied.

Piktogramme

FlameSkull and crossbones
GHS02,GHS06

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

8.6 °F - closed cup

Flammpunkt (°C)

-13 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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Min Ji et al.
The Journal of chemical physics, 130(17), 174314-174314 (2009-05-12)
We report on the photodissociation dynamics study of n-butyl nitrite and isoamyl nitrite by means of time-resolved Fourier transform infrared (TR-FTIR) emission spectroscopy. The obtained TR-FTIR emission spectra of the nascent NO fragments produced in the 355 nm laser photolysis
Tsuyoshi Taniguchi et al.
Chemical communications (Cambridge, England), 49(22), 2198-2200 (2013-02-12)
A method for direct functionalization of three positions including an unactivated C-H bond of aliphatic alkenes using tert-butyl nitrite and molecular oxygen to give γ-lactols has been developed. The present reaction proceeds through a sequence of radical processes involving oxynitration
J D Osterloh et al.
Journal of pharmaceutical sciences, 74(7), 780-782 (1985-07-01)
The uptake of butyl nitrite by rats (500 g, one rat/chamber) was determined over a 5-min exposure period. About 44% of the starting amount (771-3855 ppm) of n-butyl nitrite was consumed in 5 min. Three rats per exposure concentration were
G R Newell et al.
The American journal of medicine, 78(5), 811-816 (1985-05-01)
Early reports of the acquired immune deficiency syndrome (AIDS) in homosexual men suggested that the cause might be related to homosexual life-style practices, including use of recreational drugs. Inhalation of volatile nitrites is a possible contributing factor in AIDS because
G R Newell et al.
Pharmacotherapy, 4(5), 284-291 (1984-09-01)
Volatile nitrite in the form of amyl nitrite was used for 100 years for the treatment of angina pectoris. In spite of recognized toxicity, its use in this form was considered safe. During the 1960s prescriptions were not required for
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