p-Menthane

p-Menthane
File:Menthane, p-trans.svg	File:Menthane, p-cis.svg
Names
	IUPAC name 1-isopropyl-4-methylcyclohexane
Identifiers
CAS Number	99-82-1 check;
3D model (JSmol)	Interactive image;
ChemSpider	7179;
ECHA InfoCard	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
EC Number	202-790-4;
E number	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
PubChem CID	7459;
UNII	CGW5GN8TXU check;
CompTox Dashboard (EPA)	{{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).;
	InChI InChI=1S/C10H20/c1-8(2)10-6-4-9(3)5-7-10/h8-10H,4-7H2,1-3H3 Key: CFJYNSNXFXLKNS-UHFFFAOYSA-N;
	SMILES CC1CCC(CC1)C(C)C;
Properties
Chemical formula	C10H20
Molar mass	140.270 g·mol−1
Appearance	Colorless liquid
Density	0.8086 g/cm3
Boiling point	168 °C (334 °F; 441 K)
Solubility in organic solvents	Soluble
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

p-Menthane is a hydrocarbon with the formula (CH₃)₂CHC₆H₁₀CH₃. It is the product of the hydrogenation or hydrogenolysis of various terpenoids, including p-cymene, terpinolenes, phellandrene, and limonene. It is a colorless liquid with a fragrant fennel-like odor. It occurs naturally, especially in exudates of Eucalyptus fruits. The compound is generally encountered as a mixture of the cis and trans isomers, which have very similar properties

References

p-Menthane

References

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