Photo credits: ScenTree SAS

Jasmonal H®

Floral > Light Flowers > White Flowers > Anisic > Green Fruits

Hexyl Cinnamaldehyde ; Hexyl Cinnamaldehyde ; 2-(phenylmethylidene)octanal ; 2-benzylidene octanal ; Hexyl cinnamal ; Hexyl cinnamic aldehyde ; 2-hexyl-3-phenyl-2-propenal ; Alpha-N-hexyl-beta-phenyl acrolein ; 2-(phenylmethylidene)octanal

Photo credits: ScenTree SAS

Ingredient Name	Learn more	Naturality	MOQ	Purity
ALPHA HEXYL CINNAMIC ALDEHYDE JAHRSPO-1	Discover	-	10 grs	97 - 100
Jasmonal H - 30 Gr	Discover	-	30grs	-
Hexyl Cinnamic Aldehyde	Discover	Synthetic Aroma Chemicals	-	-

ALPHA HEXYL CINNAMIC ALDEHYDE

JAHRSPO-1

Jasmonal H - 30 Gr

Hexyl Cinnamic Aldehyde

General Presentation

CAS N° :
101-86-0
EINECS number :
202-983-3
FEMA number :
2569
FLAVIS number :
5,041

JECFA number :
686
Volatility :
Heart
Price Range :
€

Physico-chemical properties

Appearance :
Colorless liquid
Density :
0,955
Refractive Index @20°C :
1,548 - 1,552
Optical rotation :
Donnée indisponible.
Vapor pressure :
0,00051 mmHg @25°C
Flash Point :
151°C (303,8°F)

Molecular formula :
C₁₅H₂₀O
Molecular Weight :
216,32 g/mol
Log P :
5,3
Fusion Point :
18°C (64,4°F)
Boiling Point :
311°C (591,8°F)
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Uses in perfumery :

Jasmonal H® is used in notes of jasmine and lily of the valley, for a waxy facet, close to narcissus, and for trail. Formerly used to replace Hedione®.

Year of discovery :

1930

Natural availability :

Jasmonal H® is found in trace amounts in Roman Chamomile EO and rice. However, it is the synthetic Jasmonal H® that is most often used in perfumery.

Isomerism :

Jasmonal H® has two possible diastereoisomers. However, it is the mixture of the two isomers that is used in perfumery.

Synthesis precursor :

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

Synthesis route :

As for Jasmonal A®, the synthesis of Jasmonal H® is made by condensation of benzaldehyde with Octanal (Aldehyde C-8), using an excess of benzaldehyde and gradually adding the Aldehyde C-8 in the reaction medium in order to avoid its self-condensation.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell.
Jamsonal A colors through time.

Other comments :

Jasmonal A® is more powerful, rising and soapy, but less watery than Jasmonal H®.
Jasmonal H® is one of the 26 allergens in perfumery.

Labelling

Allergens :

This ingredient does not contain any allergen.

Signal word :

Warning

Hazard pictograms :

Precautionary statements :

HAZARD	PRECAUTION
H317 May cause an allergic skin reaction. H400 Very toxic to aquatic life. H411 Toxic to aquatic life with long lasting effects.

IFRA

IFRA 51^th :

This ingredient is restricted by the 51th amendment

Restriction type :
RESTRICTION
Cause of restriction :
DERMAL SENSITIZATION
Amendment :
49

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
1,8 %	0,53 %	11 %	9,9 %	2,5 % 2,5 % 2,5 % 2,5 %		5,8 %
Cat.5 A B C D			Cat.6
2,5 % 2,5 % 2,5 % 2,5 %			5,8 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
20 % 20 %		1 %	19 %	69 % 69 %	38 % 38 %	No Restriction
Cat.10 A B	Cat.11 A B	Cat.12
69 % 69 %	38 % 38 %	No Restriction

Disclaimer :

ScenTree is solely responsible for the information provided here.

To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library

Jasmonal H®

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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 :