File:Structure_of_n-Pentan.svg · Wikimedia Commons · See Wikimedia Commons
n-pentane
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Pentane is an organic compound with the formula C5H12—that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane (dimethylpropane). Cyclopentane is not an isomer of pentane because it has only 10 hydrogen atoms where pentane has 12.
N-pentane is a simple organic compound made of five carbon atoms and twelve hydrogen atoms (C5H12), belonging to a group of molecules called alkanes. It's one of three possible structural arrangements of these atoms, though "pentane" in scientific naming specifically refers to the n-pentane form.
AI-generated from the Wikipedia summary — may contain errors.
Chemical data
- Formula
- C5H12
- Molecular weight
- 72.15 g/mol
- IUPAC name
- pentane
- SMILES
- CCCCC
- InChIKey
- OFBQJSOFQDEBGM-UHFFFAOYSA-N
- XLogP
- 3.4
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Research
2,904 papers- n-Pentane. CAS# 109-66-0.ReviewJournal of toxicology and environmental health. Part A · 1999Galvin JB, Marashi FDOI: 10.1080/009841099157412
- Crystal structure of N,N,N',N'-tetra-methyl-ethane-di-amine.Acta crystallographica. Section E, Crystallographic communications · 2022Schrimpf T, Otte F, Strohmann CDOI: 10.1107/S2056989021012457
- Study on the Adsorption Law of n-Pentane in Silica Slit Nanopores.ACS omega · 2024Yu C, Xu Q, Meng F et al.DOI: 10.1021/acsomega.4c06105
- Adsorption and separation of n/iso-pentane on zeolites: A GCMC study.Journal of molecular graphics & modelling · 2018Fu H, Qin H, Wang Y et al.DOI: 10.1016/j.jmgm.2017.12.003
- A comparative study on the neurotoxicity of n-pentane, n-hexane, and n-heptane in the rat.British journal of industrial medicine · 1980Takeuchi Y, Ono Y, Hisanaga N et al.DOI: 10.1136/oem.37.3.241
- Two-Body Metastable Dissociation of n-Pentane and n-Hexane Triplet Dications in Intense Femtosecond-Laser Fields.The journal of physical chemistry. A · 2021Hoshina K, Shirota T, Tsuge MDOI: 10.1021/acs.jpca.1c06567
- Bis[1,2-bis-(4-tert-butyl-phen-yl)ethyl-ene-1,2-di-thiol-ato(1-)]nickel(II) pentane 0.25-solvate.Acta crystallographica. Section E, Crystallographic communications · 2023Das Gupta T, Applebaum J, Broussard W et al.DOI: 10.1107/S205698902300097X
- Synthesis of Carborane-Backbone Metallacycles for Highly Selective Capture of n-Pentane.Journal of the American Chemical Society · 2022Guo ST, Cui PF, Liu XR et al.DOI: 10.1021/jacs.2c10201
via PubMed
Wikidata facts
- Mass
- 72.094
Show 18 more facts
- boiling point
- 309.2
- ionization energy
- 10.35
- canonical SMILES
- CCCCC
- chemical formula
- C₅H₁₂
- vapor pressure
- 420
- Commons category
- Pentane
- NIOSH Pocket Guide ID
- 0486
- density
- 0.63
- time-weighted average exposure limit
- 2950
- speed of sound
- 1008
- immediately dangerous to life or health
- 4425
- melting point
- -129.7
- flash point
- -57
- solubility
- 0.04
- lower flammable limit
- 1.5
- upper flammable limit
- 7.8
- ceiling exposure limit
- 1800
- molar enthalpy of vaporization
- 26.43
Sources (9)
via Wikidata · CC0
~6 min read
Article
9 sectionsContents
- History
- Isomers
- Industrial uses
- Laboratory use
- Physical properties
- Reactions
- Production and occurrence
- References
- External links
Pentane is an organic compound with the formula C5H12—that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane (dimethylpropane). Cyclopentane is not an isomer of pentane because it has only 10 hydrogen atoms where pentane has 12.
Pentanes are components of some fuels and are employed as specialty solvents in the laboratory. Their properties are very similar to those of butanes and hexanes.
Gallery (25)
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