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1-nitropropane
Sign in to saveAlso known as nitropropane, 1-NP, 3-nitropropane
1-Nitropropane (1-NP) is a solvent. It is a colorless liquid, an isomer of 2-nitropropane (2-NP), and classified as a nitro compound.
In the Vinony graph
Within Vinony's link graph, 1-nitropropane is referenced by 9 other articles, and connects out to base, mass density and chemical formula.
It sits within the topics Chembox image size set, ECHA InfoCard ID from Wikidata and Nitroalkanes.
Its subject is documented across 8 Wikipedia language editions.
Chemical data
- Formula
- C3H7NO2
- Molecular weight
- 89.09 g/mol
- IUPAC name
- 1-nitropropane
- SMILES
- CCC[N+](=O)[O-]
- InChIKey
- JSZOAYXJRCEYSX-UHFFFAOYSA-N
- XLogP
- 0.9
- Polar surface area
- 45.8 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 89.048
Show 15 more facts
- canonical SMILES
- CCC[N+](=O)[O-]
- immediately dangerous to life or health
- 3640
- melting point
- -108.0
- boiling point
- 269
- chemical formula
- C₃H₇NO₂
- NIOSH Pocket Guide ID
- 0459
- density
- 1.00
- vapor pressure
- 8
- flash point
- 96
- solubility
- 1
- lower flammable limit
- 2.2
- ionization energy
- 10.81
- time-weighted average exposure limit
- 90
- Commons category
- 1-Nitropropane
- electric dipole moment
- 3.66
via Wikidata · CC0
~1 min read
Encyclopedic overview
5 sectionsContents
- Preparation
- Uses
- Safety
- Reactions
- References
1-Nitropropane (1-NP) is a solvent. It is a colorless liquid, an isomer of 2-nitropropane (2-NP), and classified as a nitro compound.
==Preparation== 1-nitropropane is produced industrially by the reaction of propane and nitric acid. This reaction forms four nitroalkanes: nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane. 1-nitropropane is also a byproduct of the process for making 2-nitropropane, which is done by vapour phase nitration of propane.
Excerpted from Wikipedia’s “1-nitropropane” article, available under the CC BY-SA 4.0 licence.
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