Photo credits: ScenTree SAS

Frambinone®

Fruity > Berries > Musky > Dry Woods

Raspberry Ketone® ; 4-(4-hydroxyphenyl)butan-2-one ; 4-(3-oxobutyl)phenol ; Para-hydrobenzyl acetone ; 1-para-hydroxyphenyl-3-butanone ; 4-(4-hydroxyphenyl)-2-butanone ; 1-(4- hydroxyphenyl)-3-butanone ; Para-hydroxyphenylbutanone ; N112 ; N 112 ; Oxanone ; Oxyphenylon ; Rasketone ; Raspberry keytone ; Rastone ; Rheosmin

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	MOQ	Purity
	Frambinone - 30 Gr	-	Visit website	-		-	-
	RASPBERRY KETONE	RASK-1	Visit website	-		10 grs	99.5 - 100

Frambinone - 30 Gr

Certifications :

RASPBERRY KETONE

ID : RASK-1

Chine

Certifications :

General Presentation

CAS N° :
5471-51-2
EINECS number :
226-806-4
FEMA number :
2588
FLAVIS number :
07.055

JECFA number :
728
Volatility :
Heart/Base
Price Range :
€€

Physico-chemical properties

Appearance :
White solid
Density :
N/A
Refractive Index @20°C :
Donnée indisponible.
Optical rotation :
Donnée indisponible.
Vapor pressure :
0,0010 mmHg @20°C
Flash Point :
94°C (201,2°F)

Molecular formula :
C₁₀H₁₂O₂
Molecular Weight :
164.20 g/mol
Log P :
0,94
Fusion Point :
83°C (181,4°F)
Boiling Point :
292°C (557,6°F)
Detection Threshold :
0,1 ppm (0,00001%)

Chemistry & Uses

Uses in perfumery :

Frambinone® brings a fruity evocation in all types of accords. Used in raspberry reconstitutions and other red fruit notes.

Year of discovery :

1918

Natural availability :

Frambinone® is present in several fruits and is extractable in its natural state, but only synthetic Frambinone® is used in perfumery.

Isomerism :

The meta and ortho positional isomers of Frambinone® are not used in perfumery. Styrallyl acetate, Eugenol and Benzyl Propionate are some of the constitutional isomers of Frambinone® that are used in perfumery. Their smell is however very different, as it is fruity-rhubarb, spicy or floral-white flowers.

Synthesis precursor :

Frambinone® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Frambinone® is synthesized in two steps. The first is a condensation between 4-hydroxybenzaldehyde and acetone, to obtain 4-hydroxybenzalacetone. A catalytic and selective hydrogenation of the double bond formed allows to obtain the final product, Frambinone®.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Data not available.

Labelling

Allergens :

This ingredient does not contain any allergen.

IFRA

IFRA 51^th :

This ingredient is restricted by the 51th amendment

Restriction type :

RESTRICTION

Cause of restriction :

DEPIGMENTATION

Amendment :

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
0,68 %	1 %	0,27 %	1 %	1 % 0,14 % 0,27 % 0,045 %		0,82 %
Cat.5 A B C D			Cat.6
1 % 0,14 % 0,27 % 0,045 %			0,82 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
0,41 % 0,41 %		0,045 %	1 %	1 % 1 %	0,045 % 0,045 %	78 %
Cat.10 A B	Cat.11 A B	Cat.12
1 % 1 %	0,045 % 0,045 %	78 %

Contributions from other sources
4-(4-Hydroxyphenyl)butan-2-one has been found in natural extracts but only at trace levels.

Frambinone®

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General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico-chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :