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naturally, it can also be found in cannabis distillates. Greater concentrations of carene in a distillate give it an earthier taste and smell. 3-Carene is also present in
827:
395:
878:
Mediavilla, Vito, Simon
Steinemann, Essential oil of Cannabis sativa L. strains. Journal of the International Hemp Association, 1997, 4(2):80-82.
566:
844:
944:
360:
727:, with a content as high as 42% depending on the source. Carene has a sweet and pungent odor, best described as a combination of
734:
A colorless liquid, it is not soluble in water, but miscible with fats and oils. It is chiral, occurring naturally both as the
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Except where otherwise noted, data are given for materials in their
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27:"Carene" redirects here. For the town of ancient Mysia, see
369:
InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6-8H,4-5H2,1-3H3
379:
InChI=1/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6-8H,4-5H2,1-3H3
684:
468:170–172 °C (338–342 °F; 443–445 K)
281:
91:
828:Ullmann's Encyclopedia of Industrial Chemistry
8:
820:
818:
811:Institute for Occupational Safety and Health
731:needles, musky earth, and damp woodlands.
344:
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33:
868:(12th ed.). 1996. p. 300. 1885.
769:industry and as a chemical intermediate.
301:
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723:rings. It occurs as a constituent of
372:Key: KALFVDDBBPRATR-UHFFFAOYSA-N
167:
147:
7:
825:M. Eggersdorfer (2005). "Terpenes".
780:, giving the fruit a characteristic
382:Key: KALFVDDBBPRATR-UHFFFAOYAY
272:
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25:
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506:
501:
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430:
59:3,7,7-Trimethylbicyclohept-3-ene
40:
772:Because carene can be found in
670:(at 25 °C , 100 kPa).
758:induces rearrangement, giving
424:
1:
738:and enantio-enriched forms.
966:
26:
889:"What is Delta 3 Carene?"
807:GESTIS Substance Database
765:. Carene is used in the
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945:Sweet-smelling chemicals
837:10.1002/14356007.a26_205
784:-like flavor and aroma.
561:Precautionary statements
831:. Weinheim: Wiley-VCH.
750:gives 3,4-caranediol.
403:CC2(C)C\1CCC(C)/C=C/12
715:consisting of fused
55:Preferred IUPAC name
448: g·mol
129:Beilstein Reference
36:
935:Bicyclic compounds
893:ionizationlabs.com
742:Reactions and uses
697:Infobox references
458:0.86 g/cm (20 °C)
34:
895:. Ionization Labs
705:Chemical compound
703:
702:
531:Hazard statements
325:CompTox Dashboard
117:Interactive image
16:(Redirected from
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748:peracetic acid
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711:is a bicyclic
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619:P303+P361+P353
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29:Carene (Mysia)
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950:Wood extracts
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940:Cyclopropanes
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19:
930:Monoterpenes
925:Cyclohexenes
897:. Retrieved
892:
883:
874:
863:
826:
771:
760:
756:ferric oxide
745:
733:
721:cyclopropane
708:
707:
522:
479:
169:ChEMBL506854
76:Identifiers
66:Other names
865:Merck Index
717:cyclohexene
713:monoterpene
517:Signal word
412:Properties
207:100.033.367
914:Categories
788:References
725:turpentine
491:Pictograms
441:Molar mass
303:H2M15SNR6N
180:ChemSpider
104:3D model (
93:13466-78-9
83:CAS Number
752:Pyrolysis
651:P403+P235
647:P370+P378
635:P333+P313
631:P332+P313
615:P302+P352
611:P301+P310
482:labelling
314:UN number
228:236-719-3
220:EC Number
70:Car-3-ene
35:3-Carene
899:6 August
774:cannabis
736:racemate
709:3-Carene
473:Hazards
189:10660720
134:1902767
68:Δ-Carene
18:3-carene
920:Flavors
809:of the
805:in the
803:Record
767:perfume
763:-cymene
690:what is
688: (
454:Density
446:136.238
270:PubChem
243:663435
149:CHEBI:7
843:
685:verify
682:
523:Danger
396:SMILES
258:C11382
160:ChEMBL
49:Names
778:mango
754:over
361:InChI
318:2319
283:26049
140:ChEBI
106:JSmol
901:2020
841:ISBN
782:pine
719:and
659:P501
655:P405
643:P363
639:P362
627:P331
623:P321
607:P280
603:P273
599:P272
595:P264
591:P261
587:P243
583:P242
579:P241
575:P240
571:P233
567:P210
553:H412
549:H317
545:H315
541:H304
537:H226
294:UNII
249:KEGG
833:doi
729:fir
480:GHS
330:EPA
273:CID
916::
891:.
855:^
839:.
817:^
795:^
657:,
653:,
649:,
645:,
641:,
637:,
633:,
629:,
625:,
621:,
617:,
613:,
609:,
605:,
601:,
597:,
593:,
589:,
585:,
581:,
577:,
573:,
569:,
551:,
547:,
543:,
539:,
484::
434:16
428:10
903:.
849:.
835::
761:p
680:N
431:H
425:C
332:)
328:(
108:)
31:.
20:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
