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N22851

Sigma-Aldrich

1-Nitropropane

≥98.5%

Synonym(s):

1-Nitropropane

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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

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Related Categories

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

WGK

WGK 1

Flash Point(F)

95.0 °F

Flash Point(C)

35 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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
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 S Fiala et al.
Carcinogenesis, 8(12), 1947-1949 (1987-12-01)
1-Nitropropane (1-NP), 2-nitropropane (2-NP), 1-azoxypropane (1-AP) and 2-azoxypropane (2-AP), were assayed for carcinogenicity by gavage in male Sprague-Dawley rats. 2-NP was given at 1 mmol/kg three times per week for 16 weeks. 1-NP (1 mmol/kg), 1-AP (0.1 mmol/kg), 2-AP (0.1
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
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
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