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DIHYDROACTINIDIOLIDE

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DIHYDROACTINIDIOLIDE Basic information

Product Name:
DIHYDROACTINIDIOLIDE
Synonyms:
  • (2,6,6-trimethy1-2-hydroxycyclohexylidene)-acetic acid lactone
  • 4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one
  • 4,5,7,7a-Tetrahydro-4,4,7a-trimethyl-2(6H)benzofuranone
  • 4,4,7a-Trimethyl-2,4,5,6,7,7a-hexahydrobenzofuran-2-one
  • 4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one
  • Dihydroactinolide
  • 2,4,5,6,7,7a-Hexahydro-4,4,7a-trimethylbenzofuran-2-one
  • 2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic acid lactone
CAS:
15356-74-8
MF:
C11H16O2
MW:
180.24
EINECS:
239-390-4
Mol File:
15356-74-8.mol
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DIHYDROACTINIDIOLIDE Chemical Properties

Melting point:
42-43°
Boiling point:
296℃
Density 
1.05
FEMA 
4020 | (+/-)-(2,6,6-TRIMETHYL-2-HYDROXYCYCLOHEXYLIDENE)ACETIC ACID GAMMA-LACTONE
Flash point:
120℃
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
Off-White
Odor
at 100.00 %. ripe apricot fruity plum berry grape tropical fruit woody
Odor Type
fruity
JECFA Number
1164
LogP
2.26
EPA Substance Registry System
2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl- (15356-74-8)
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DIHYDROACTINIDIOLIDE Usage And Synthesis

Chemical Properties

(+/–)-(2,6,6-Trimethyl-2-hydroxycyclohexylidene) acetic acid gamma-lactone has a powerful musky or coumarin like odor. As this compound is formed from photooxidation of carotene-like structures, its taste is related to certain fruit types at their peak of ripeness.

Occurrence

Reportedly present in lemongrass and sweet grass oil.

Definition

ChEBI: Dihydroactinidiolide is a member of benzofurans.

Preparation

Prepared in a patented process by degradation of beta-carotene in the presence of nitrogen and air.

DIHYDROACTINIDIOLIDESupplier

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