h
hexane
Chemical compound
Also known as CH3-[CH2]4-CH3 · hexyl hydride · normal-hexane · n-hexane
- Formula
- C₆H₁₄
1
- C₆H₁₄
- Mass
- 86.11 Da
1
- 86.11 Da
- Melting point
- -219°F
- , -95°C
1
- , -95.3°C
- Boiling point
- 156°F
- , 341.9 K
1
- , 68.7°C
- +1 more
- Density
- 0.66 g/cm³
- Solubility
- 0.002 gram per 100 gram of solvent
Overview
Chemistry
All data
134 statements · 63% with external sources · numbers in brackets are citations
- Canonical SMILES
- CCCCCC
1
- CCCCCC
- Speed of sound
- 1,083 m/s temperature: 20°C · state of matter: liquid
1
- 1,083 m/s temperature: 20°C · state of matter: liquid
- Immediately dangerous to life or health
- 3,883 milligram per cubic metre
- Vapor pressure
- 124 millimetre of mercury temperature: 68°F
- Lower flammable limit
- 1.1 volume percent
- Upper flammable limit
- 7.5 volume percent
- Ionization energy
- 10.18 eV
- 10.13 eV
- Time-weighted average exposure limit
- 180 milligram per cubic metre applies to jurisdiction: none · runtime: 10 h
- 1,800 milligram per cubic metre applies to jurisdiction: United States · runtime: 8 h
- Safety classification and labelling
- NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response nfpa health: 2 · nfpa fire: 3 · nfpa instability: 0
- Part of
- response to hexane subject has role: reactant
1
- response to hexane subject has role: reactant
- Found in taxon
- Aglaia odoratissima
- Olea europaea
2
Sources- 1.Stated in Analysis of volatiles from callus cultures of olive Olea europaea
- 2.Stated in Medicinal flowers. III. Marigold. (1): hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligoglycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalis
- Paeonia lactiflora
1
- Elaeis guineensis
1
- Perilla frutescens var. frutescens
- Laetiporus sulphureus var. miniatus
- Carica papaya
- Subject has role
- male reproductive toxicant(since 2017)
1
Sources- 1.Stated in California Proposition 65 list of chemicalsoehha.ca.gov/chemicals/n-hexaneRetrieved 2020-02-26
- male reproductive toxicant(since 2017)
On other databases
58 identifiers linking hexane across the web's reference databases
- Art & Architecture Thesaurus ID300111669
- CA PROP 65 IDn-hexane
- CAB ID18863
- CAMEO Chemicals ID851
- Cannabis Database ID000733
- CAS Registry Number110-54-3
- CCDC Number103189
- CDB Chemical ID3969569
- ChEBI ID29021
- ChEMBL IDCHEMBL15939
- ChemSpider ID7767
- CSD RefcodeHEXANE01
- DSSTOX compound identifierDTXCID001917
- DSSTox substance IDDTXSID0021917
- EC number203-777-6
- ECHA Substance Infocard ID100.003.435
- Encyclopædia Britannica Online IDscience/hexane
- Freebase ID/m/0qkf1
- Gmelin number1985
- Great Russian Encyclopedia portal IDgeksan-0ddc82
- HCIS ID2402
- HSDB ID91
- Human Metabolome Database IDHMDB0029600
- ICSC ID0279
- IEDB Epitope ID116866
- InChIInChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3
- InChIKeyVLKZOEOYAKHREP-UHFFFAOYSA-N
- J-GLOBAL ID200907049635895623
- JSTOR topic ID (archived)hexanes
- KBpedia IDHexane
- KEGG IDC11271
- KNApSAcK IDC00049006
- Lex IDhexan
- LIPID MAPS IDLMFA11000007
- MassBank accession IDMSBNK-Fac_Eng_Univ_Tokyo-JP002348
- Microsoft Academic ID (discontinued)2777077568
- Nikkaji IDJ1.977A
- NMRShiftDB structure ID10016353
- NSC number68472
- Online PWN Encyclopedia ID3910738
- OpenAlex IDC2777077568
- OSHA Occupational Chemical Database ID112
- PDB ligand IDHEX
- PDB structure ID2TIO
- PesticideInfo chemical IDPRI4369
- PSH ID5957
- PubChem CID8058
- Quora topic IDHexane
- Reaxys registry number1730733
- RTECS numberMN9275000
- SPLASHsplash10-052f-9000000000-d534432d96279fe04f73
- SureChEMBL ID399
- UM-BBD compound IDc0829
- UN number1208
- UniChem compound ID15236
- UNII2DDG612ED8
- WordNet 3.1 Synset ID14931273-n
- ZVG number510789