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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)

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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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’.

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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
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
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)
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