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N22851

Sigma-Aldrich

1-Nitropropane

≥98.5%

Sinónimos:

1-Nitropropane

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About This Item

Fórmula lineal:
CH3CH2CH2NO2
Número de CAS:
108-03-2
Peso molecular:
89.09
Beilstein/REAXYS Number:
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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Nitromethane ACS reagent, ≥95%

Sigma-Aldrich

360554

Nitromethane

2-Nitroethanol 97%

Sigma-Aldrich

146633

2-Nitroethanol

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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