Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

226637

Sigma-Aldrich

Butyl nitrite

95%

Synonym(s):

n-Butyl nitrite

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3(CH2)3ONO
CAS Number:
544-16-1
Molecular Weight:
103.12
Beilstein:
1701036
EC Number:
208-862-1
MDL number:
MFCD00002058
UNSPSC Code:
12352100
PubChem Substance ID:
24853580
NACRES:
NA.22

vapor pressure

760 mmHg ( 78 °C)

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.)

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

FlameSkull and crossbones
GHS02,GHS06

Signal Word

Danger

Hazard Statements

H225,H301,H330

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

8.6 °F - closed cup

Flash Point(C)

-13 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Abu Khaled et al.
Biochemical and biophysical research communications, 135(1), 201-207 (1986-02-26)
The effects of butyl nitrite, a frequently used recreational drug, on methyl cobalamin and 5-methyl tetrahydrofolate were investigated by using 1H and 31P NMR spectroscopies. While no effect could be observed in organic solvents, strong interactions of butyl nitrite with
L D Fechter et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 12(1), 56-61 (1989-01-01)
Butyl nitrite is the predominant and presumed active ingredient in a variety of commercial preparations sold as "room odorizers." These compounds have significant abuse potential, giving the user the sensation of a "rush", which may be related to their intense
D P McFadden et al.
Journal of applied toxicology : JAT, 5(3), 134-139 (1985-06-01)
Mice were exposed by inhalation to n-butyl, iso-butyl sec-butyl or tert-butyl nitrite in a dynamic airflow chamber 7 h per day for 60 days at concentrations that caused less than 20% fatalities. Under these conditions, body-weight gain was depressed over
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service