Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

N22851

Sigma-Aldrich

1-Nitropropane

≥98.5%

Synonym(s):

1-Nitropropane

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

About This Item

Linear Formula:
CH3CH2CH2NO2
CAS Number:
108-03-2
Molecular Weight:
89.09
Beilstein:
506236
EC Number:
203-544-9
MDL number:
MFCD00007407
UNSPSC Code:
12352100
PubChem Substance ID:
24897565
NACRES:
NA.22

vapor density

3.1 (vs air)

Quality Level

100

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
GHS02,GHS06

Signal Word

Danger

Hazard Statements

H226,H302 + H312,H331

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

Slide 1 of 2

1 of 2

Nitromethane ACS reagent, ≥95%

Sigma-Aldrich

360554

Nitromethane

2-Nitroethanol 97%

Sigma-Aldrich

146633

2-Nitroethanol

E Roscher et al.
Mutagenesis, 5(4), 375-380 (1990-07-01)
The metabolic pathways leading to genotoxicity of nitropropanes in mammalian cells were investigated by measuring the effects of 2-nitropropane (2-NP) and 1-nitropropane (1-NP) on various cell lines characterized for their expression of cytochrome P450-dependent mono-oxygenases. Cells used were the rat
Anna Fryszkowska et al.
The FEBS journal, 279(22), 4160-4171 (2012-09-18)
Enzymes are natural catalysts, controlling reactions with typically high stereospecificity and enantiospecificity in substrate selection and/or product formation. This makes them useful in the synthesis of industrially relevant compounds, particularly where highly enantiopure products are required. The flavoprotein pentaerythritol tetranitrate
U Andrae et al.
Carcinogenesis, 9(5), 811-815 (1988-05-01)
The genotoxicity of 2-nitropropane (2-NP) and 1-nitropropane (1-NP) was investigated by measuring the induction of DNA repair synthesis in rat liver cells in vitro and in vivo. 2-NP strongly induced DNA repair synthesis in both cases. When applied in vivo
U Kliesch et al.
Mutation research, 192(3), 181-184 (1987-11-01)
Micronucleus tests were carried out in bone marrow of mice treated with 1-nitropropane, 2-nitropropane and cisplatin. For 1-nitropropane and 2-nitropropane the results were negative. With cisplatin a dose-dependent increase in the number of polychromatic erythrocytes with micronuclei was observed. The
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
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