Isoborneol

Isoborneol
Names
	IUPAC name (1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol, (1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-ol
Identifiers
CAS Number	+: 16725-71-6 d; -: 10334-13-1; rac: 124-76-5;
3D model (JSmol)	+: Interactive image; -: Interactive image; rac: Interactive image;
ChEBI	+: CHEBI:191949;
ChEMBL	+: ChEMBL4294644; -: ChEMBL3560760;
ChemSpider	+: 16739225; -: 4882019;
PubChem CID	+: 6973640; -: 6321405;
UNII	+: 8GDX32M6KF; -: 20U67Z994U; rac: L88RA8N5EG;
UN number	1312
	InChI +: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m0/s1 Key: DTGKSKDOIYIVQL-OYNCUSHFSA-N; -: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1 Key: DTGKSKDOIYIVQL-MRTMQBJTSA-N;
	SMILES +: C[C@]12CC[C@H](C1(C)C)C[C@@H]2O; -: C[C@@]12CC[C@@H](C1(C)C)C[C@H]2O; rac: CC1(C2CCC1(C(C2)O)C)C;
Properties
Chemical formula	C10H18O
Molar mass	154.253 g·mol−1
Appearance	white or colorless solid
Melting point	212–214 °C (414–417 °F; 485–487 K) + or -; 210–215 °C for rac
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H228
Precautionary statements	P210, P240, P241, P280, P370+P378
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Isoborneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an exo position. The endo diastereomer is called borneol. Being chiral, isoborneol exists as enantiomers.