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ChemicalBook--->CAS DataBase List--->4433-36-7

4433-36-7

4433-36-7 Structure

4433-36-7 Structure
IdentificationBack Directory
[Name]

3,4,5,6-TETRAHYDROPSEUDOIONONE
[CAS]

4433-36-7
[Synonyms]

FEMA 3059
TETRAMERAN
citronellylacetone
Tetrahydro-pseudo-ionone
6,10-dimethyl-9-undecen-2-on
6,10-Dimethylundec-9-en-2-on
3,4,5,6-TETRAHYDROPSEDOIONONE
6,10-DIMETHYL-9-UNDECEN-2-ONE
6,10-dimethylundec-9-en-2-one
3,4,5,6-TETRAHYDROPSEUDOIONONE
9-Undecen-2-one, 6,10-dimethyl-
[EINECS(EC#)]

224-634-4
[Molecular Formula]

C13H24O
[MDL Number]

MFCD00661065
[MOL File]

4433-36-7.mol
[Molecular Weight]

196.33
Chemical PropertiesBack Directory
[Boiling point ]

130-132 °C(Press: 11 Torr)
[density ]

0.838±0.06 g/cm3(Predicted)
[vapor pressure ]

0.6Pa at 20℃
[FEMA ]

3059 | 3,4,5,6-TETRAHYDROPSEUDOIONONE
[solubility ]

Practically insoluble in water, soluble in alcohol and oils.
[form ]

oily liquid
[color ]

Pale straw-colored or almost colorless
[Specific Gravity]

0.87
[Odor]

at 100.00 %. sweet floral balsam rose woody
[Odor Type]

floral
[JECFA Number]

1121
[LogP]

4.6 at 35℃
Hazard InformationBack Directory
[Chemical Properties]

Tetrahydro-pseudo-ionone has a sweet, floral, balsamic odor with a rose to woody quality. It has a sweet, fruity flavor, somewhat apple- and peach-like.
[Uses]

6,10-Dimethylundec-9-en-2-one finds some use in Rose compositions, where its peculiar oily softness lends very pleasant and natural notes, and also supPorts mildly green notes in the composition. It blends furthermore excellently with Vetiver and Labdanum, musks and Lavender products, and it can justly be classified as a very versatile perfume chemical. It is used in small amounts in berry flavors, fruit complexes, etc. at the rate of 1 to 15 ppm in the functional consumer products.
[Definition]

ChEBI: 6,10-Dimethylundec-9-en-2-one is a monoterpenoid.
[Preparation]

By hydrogenation of pseudo-ionone with colloidal palladium; this reaction leads to a product with considerable mixture; also from linalool plus acetic anhydride and sodium ethoxide, followed by hydrogenation; another method starts with geraniol via the acid chloride.
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