ChemicalBook--->CAS DataBase List--->3720-16-9

3720-16-9

3720-16-9 Structure

3720-16-9 Structure
IdentificationBack Directory
[Name]

Celery ketone
[CAS]

3720-16-9
[Synonyms]

FEMA 3357
FEMA 3577
Livescone
CELERY KETONE
Celery ketone USP/EP/BP
3-Methyl-5-propylcyclohex-2-enon
3-methyl-5-propylcyclohex-2-enone
3-methyl-5-propyl-2-cyclohexen-1-on
3-methyl-5-propyl-2-Cyclohexen-1-one
3-Methyl-5-propylcyclohex-2-en-1-one
2-Cyclohexen-1-one, 3-methyl-5-propyl-
3-METHYL-5-PROPYLCYCLOHEX-2-EN-1-ONE(CELERYKETONE)
[EINECS(EC#)]

223-069-0
[Molecular Formula]

C10H16O
[MDL Number]

MFCD00482082
[MOL File]

3720-16-9.mol
[Molecular Weight]

152.23
Chemical PropertiesBack Directory
[Boiling point ]

110-113 °C(Press: 9 Torr)
[density ]

0.904±0.06 g/cm3(Predicted)
[vapor pressure ]

4.5-7.6Pa at 20-25℃
[FEMA ]

3577 | 3-METHYL-5-PROPYL-2-CYCLOHEXEN-1-ONE
[Odor]

at 10.00 % in dipropylene glycol. fresh celery green cumin
[Odor Type]

herbal
[JECFA Number]

1113
[Major Application]

flavors and fragrances
[Cosmetics Ingredients Functions]

PERFUMING
[LogP]

2.5 at pH7
[Surface tension]

53.2mN/m at 1g/L and 21℃
[EPA Substance Registry System]

2-Cyclohexen-1-one, 3-methyl-5-propyl- (3720-16-9)
Safety DataBack Directory
[WGK Germany ]

WGK 2
[TSCA ]

TSCA listed
[HS Code ]

2914290090
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Aquatic Chronic 3
Hazard InformationBack Directory
[Description]

3-Methyl-5-propyl-2-cyclohexen-l-one has a warm, spicy, woody odor with a similar flavor at low levels. May be prepared by condensation of butyric aldehyde with ethyl acetoacetate in the presence of diethylamine and subsequent saponification with a 10% KOH solution; or by condensation in the presence of piperidine in ethanol solution.
[Chemical Properties]

3-Methyl-5-propyl-2-cyclohexen-1-one has a warm, spicy, woody odor
[Definition]

ChEBI: 3-Methyl-5-propyl-2-cyclohexen-1-one is a member of cyclohexenones.
[Preparation]

By condensation of butyric aldehyde with ethyl acetoacetate in the presence of diethylamine and subsequent saponification with a 10% KOH solution, or by condensation in the presence of piperdine in ethanol solution
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