Skip to Content
Merck
All Photos(2)

Key Documents

N22851

Sigma-Aldrich

1-Nitropropane

≥98.5%

Synonym(s):

1-Nitropropane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2CH2NO2
CAS Number:
Molecular Weight:
89.09
Beilstein:
506236
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.1 (vs air)

vapor pressure

7.5 mmHg ( 20 °C)

Assay

≥98.5%

form

liquid

autoignition temp.

788 °F

IVD

for in vitro diagnostic use

refractive index

n20/D 1.401 (lit.)

bp

131-132 °C (lit.)

density

0.998 g/mL at 25 °C (lit.)

SMILES string

CCC[N+]([O-])=O

InChI

1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3

InChI key

JSZOAYXJRCEYSX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °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

Customers Also Viewed

J Ong et al.
European journal of pharmacology, 264(1), 49-54 (1994-10-13)
In the guinea-pig isolated ileum, both baclofen (5-100 microM) and gamma-aminobutyric acid (GABA; 5-100 microM) induced a bicuculline-insensitive depression of cholinergic twitch contractions which was reversibly and competitively antagonised by 3-amino-1-nitropropane (50-250 microM). 3-Amino-1-nitropropane (pA2 = 5.0 +/- 0.1) was
M L Cunningham et al.
Toxicology and applied pharmacology, 110(3), 505-513 (1991-09-15)
2-Nitropropane (2-NP) is mutagenic in a number of short-term mutagenicity assays in vitro and in vivo, and is a potent hepatocarcinogen in rats. A structural isomer, 1-nitropropane (1-NP), is mutagenic in V79 cells and can induce unscheduled DNA synthesis in
I Linhart et al.
Chemico-biological interactions, 80(2), 187-201 (1991-01-01)
Unlike primary nitroalkanes, such as 1-nitropropane, the secondary nitroalkane 2-nitropropane is geno- and hepatotoxic. Nitroalkanes exist in equilibrium with alkane nitronates. In order to investigate the relationship between nitroalkane toxicity and generation and stability of nitronates, propane 1- or 2-nitronate
Inhalation exposure of rats to vapors of 1-nitropropane at 100 ppm.
T B Griffin et al.
Ecotoxicology and environmental safety, 6(3), 268-282 (1982-06-01)
E George et al.
Carcinogenesis, 10(12), 2329-2334 (1989-12-01)
2-Nitropropane (2-NP) is a rat liver carcinogen, whilst the 1-isomer is non-carcinogenic in rodents. Although DNA repair tests in the rat liver discriminated clearly between the carcinogenic and the non-carcinogenic isomer, uniformly negative results have been published for the mouse

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