Chemistry:Tetraethylmethane

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Tetraethylmethane
Skeletal formula of tetraethylmethane
Ball and stick model of tetraethylmethane
Spacefill model of tetraethylmethane
Names
Preferred IUPAC name
3,3-Diethylpentane[1]
Identifiers
3D model (JSmol)
ChemSpider
UNII
Properties
C9H20
Molar mass 128.259 g·mol−1
Appearance Colourless liquid
Odor Odourless
Density 724 mg mL−1
Melting point −34 to −30 °C; −29 to −22 °F; 239 to 243 K
Boiling point 145.8 to 146.6 °C; 294.3 to 295.8 °F; 418.9 to 419.7 K
1.5 nmol Pa−1 kg−1
Thermochemistry
278.2 J K−1 mol−1
333.4 J K−1 mol−1
−6.1261–−6.1229 MJ mol−1
Hazards
NFPA 704 (fire diamond)
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineHealth code 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
3
0
0
Related compounds
Related alkanes
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Tetraethylmethane is a branched alkane with 9 carbon atoms. It is a highly flammable and volatile liquid at room temperature. It is one of the isomers of nonane.

References

  1. "Tetraethylmethane - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=14020&loc=ec_rcs. Retrieved 11 March 2012. 

See

External links

  • Alder, Roger W.; Allen, Paul R.; Hnyk, Drahomír; Rankin, David W. H.; Robertson, Heather E.; Smart, Bruce A.; Gillespie, Ronald J.; Bytheway, Ian (1999). "Molecular Structure of 3,3-Diethylpentane (Tetraethylmethane) in the Gas Phase as Determined by Electron Diffraction and ab Initio Calculations". The Journal of Organic Chemistry 64 (12): 4226–4232. doi:10.1021/jo981779m.