Carene

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Carene
Carene
Names
IUPAC name
3,7,7-trimethylbicyclo[4.1.0]hept-3-ene
Identifiers
13466-78-9 YesY
ChEMBL ChEMBL506854 N
ChemSpider 10660720 YesY
Jmol 3D model Interactive image
KEGG C11382
PubChem 26049
UNII H2M15SNR6N
  • InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6-8H,4-5H2,1-3H3 YesY
    Key: KALFVDDBBPRATR-UHFFFAOYSA-N YesY
  • InChI=1/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6-8H,4-5H2,1-3H3
    Key: KALFVDDBBPRATR-UHFFFAOYAY
  • CC2(C)C\1CCC(C)/C=C/12
Properties
C10H16
Molar mass 136.24 g/mol
Density 0.867 g/cm3
Boiling point 168 to 169 °C (334 to 336 °F; 441 to 442 K) at 705 mmHg
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Carene, or delta-3-carene, is a bicyclic monoterpene which occurs naturally as a constituent of turpentine,[1] with a content as high as 42% depending on the source. Carene has a sweet and pungent odor. It is not soluble in water, but miscible with fats and oils.

Health

In higher concentrations, delta-3-carene can be a skin irritant or central nervous system depressant.

Aromas

Aromas attributed to carene include sweet, pine, cedar, woodsy, and pungent.

Natural sources

Natural sources of carene include turpentine (pine extract), rosemary, and cedar.

References

  1. Haz-Map Agents