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226637

Butyl nitrite

Name: Butyl nitrite
Brand: ALDRICH

95%

Synonym(s):

n-Butyl nitrite

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About This Item

Linear Formula:

CH₃(CH₂)₃ONO

CAS Number:

544-16-1

Molecular Weight:

103.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24853580

EC Number:

208-862-1

Beilstein/REAXYS Number:

1701036

MDL number:

MFCD00002058

Assay:

95%

Form:

liquid

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Properties

vapor pressure

760 mmHg ( 78 °C)

Quality Level

100

assay

95%

form

liquid

refractive index

n20/D 1.376 (lit.)

bp

78 °C (lit.)

solubility

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

density

0.882 g/mL at 25 °C (lit.)

functional group

O-nitroso, nitroso

storage temp.

2-8°C

SMILES string

CCCCON=O

InChI

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

InChI key

JQJPBYFTQAANLE-UHFFFAOYSA-N

Description

General description

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.

pictograms

GHS02,GHS06

signalword

Danger

hcodes

H225,H301,H330

pcodes

P210 - P233 - P240 - P241 - P242 - P304 + P340 + P310

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

8.6 °F - closed cup

flash_point_c

-13 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Photolysis of n-butyl nitrite and isoamyl nitrite at 355 nm: a time-resolved Fourier transform infrared emission spectroscopy and ab initio study.

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

S-nitrosyl glutathione-mediated hepatocyte cytotoxicity.

B A Meloche et al.

Xenobiotica; the fate of foreign compounds in biological systems, 23(8), 863-871 (1993-08-01)

1. The addition of n-butyl nitrite (BN) to isolated rat hepatocytes caused rapid S-nitrosyl glutathione (GSNO) formation, then a concomitant decrease in protein thiols, followed by a marked ATP depletion. Cytotoxic concentrations of BN also caused lipid peroxidation after a

Volatile nitrites. Use and adverse effects related to the current epidemic of the acquired immune deficiency syndrome.

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

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Global Trade Item Number

SKU	GTIN
226637-100G	04061836825812
226637-25G	04061836825829