Photo credits: ScenTree SAS

Methyleugenol

Spicy > Cool Spices > Mossy > Earthy

1,2-dimethoxy-4-prop-2-enylbenzene ; 4-allyl veratrole ; 4-allyl-1,2-dimethoxybenzene ; 4-allyl-1,2-dimethoxybenzol ; 4-allylveratrole ; 1,2-dimethoxy-4-(2-propen-1-yl)benzene ; 1,2- dimethoxy-4-allyl benzene ; Eugenol methyl ether ; Veratrole methyl ether ; 1,2-dimethoxy-4-prop-2-enylbenzene

Photo credits: ScenTree SAS

Ingredient Name	ID	Comments	Naturality	MOQ	Purity
Méthyl Eugenol - 30gr	-	Visit website	-	-	-
Methyl Eugenol	CL-801	Visit website	Natural	400 Kgs	100
METHYL EUGENOL	MEG-1	Visit website	-	10 grs	98

Méthyl Eugenol - 30gr

Certifications :

Methyl Eugenol

ID : CL-801

Indonesia

Certifications : Certifications : Kasher Certifications : Halal Certifications : UEBT

METHYL EUGENOL

ID : MEG-1

Inde

Certifications :

General Presentation

CAS N° :
93-15-2
EINECS number :
202-223-0
FEMA number :
2475
FLAVIS number :
Donnée indisponible.

JECFA number :
1790
Volatility :
Heart
Price Range :
€€

Physico-chemical properties

Appearance :
Colorless liquid
Density :
1,035
Refractive Index @20°C :
1,532 – 1,536
Optical rotation :
Donnée indisponible.
Vapor pressure :
< 0,075 mmHg @20°C
Flash Point :
117°C (242,6°F)

Molecular formula :
C₁₁H₁₄O₂
Molecular Weight :
178,23 g/mol
Log P :
2,4
Fusion Point :
-4°C (24,8°F)
Boiling Point :
248°C (478,4°F)
Detection Threshold :
68 ppb à 8,5 ppm (0,00085%)

Chemistry & Uses

Uses in perfumery :

Methyl Eugenol is used in rosy floral notes, carnation, lilac, jasmine, hyacinth and other heady flowers. Useful in a chocolate or coffee note.

Year of discovery :

Data not available.

Natural availability :

Methyl Eugenol is present in the Bay St-Thomas EO, Tuberose Absolute and Angelica Root EO among others, Methyl Eugenol can be extracted from these plants in its natural state.

Isomerism :

Methyl Isoeugenol is a position isomer of Methyl Eugenol. Their smell is different : Methyl Isoeugenol is more floral, reminiscent of Tuberose Absolute, while Methyl Eugenol is more spicy. Both are keeping an earthy and wet facet, more noticeable for Methyl Eugenol. Canthoxal® is an isomer of Methyl Eugenol. Its smell is however radically different, as it is marine and aldehydic.

Synthesis precursor :

Methyl Eugenol is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Methyl Eugenol is obtained synthetically from Eugenol by a methylation reaction. This etherification reaction is made by a Williamson synthesis, which consists in forming a sodium alkoxide in the presence of pure sodium in the reaction medium, and then reacting the obtained eugenolate with methyl chloride.

Stability :

Becomes red under the effect of light. This raw material is not convenient in every functional base : can't be used in a candle or shower gel base.

Other comments :

Methyl Eugenol is one of the 26 allergens in perfumery.
It has a less floral smell than Methyl Isoeugenol.

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 :

DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

Amendment :

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
0,00042 %	0,0015 %	0,00042 %	0,011 %	0,0015 % 0,00021 % 0,00042 % 0,000069 %		0,0010 %
Cat.5 A B C D			Cat.6
0,0015 % 0,00021 % 0,00042 % 0,000069 %			0,0010 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
0,00042 % 0,00042 %		0,000069 %	0,0017 %	0,00062 % 0,0021 %	0,000069 % 0,000069 %	0,066 %
Cat.10 A B	Cat.11 A B	Cat.12
0,00062 % 0,0021 %	0,000069 % 0,000069 %	0,066 %

Annexe I :

Some regulated synthetic ingredients are found in nature and in certain proportions in natural ingredients. This presence in nature has to be taken into account when calculating limits of use recommended by the IFRA. In case you do not know these concentrations, you can use the ones estimated by the IFRA. Here they are :

List of regulated compounds contained in this ingredient
Ingredient Name	Botanical Name	CAS N°	Estimated Concentration
Basil oil, chemotype estragole	Ocimum basilicum L.	8015-73-4	0,39
Basil oil, chemotype linalool	Ocimum basilicum L.	8015-73-4	0,2
Basil oleoresin, chemotype estragole	Ocimum basilicum L.	8015-73-4	0,2
Bay leaf, West Indian, oil	Pimenta racemosa (Mill.) J.W. Moore	8006-78-8	2
Calamus oil	Acorus calamus L.	8015-79-0	0,3
Cananga oil	Cananga odorata (Lam.) Hook. f. & Thomson (forma macrophylla Steenis)	68606-83-7	0,2
Cinnamon leaf oil	Cinnamomum zeylanicum Blume	8015-91-6	0,01
Michelia alba flower oil	Michelia x alba DC. (champaca x montana)		2,06
Michelia alba leaf oil	Michelia x alba DC. (champaca x montana)		0,33
Champaca absolute	Michelia champaca L.	8006-76-6	0,01
Labdanum oil	Cistus ladaniferus L.	8016-26-0	0,05
Citronella oil, Java type	Cymbopogon winterianus Jowitt	8000-29-1	0,1
Clove bud oil	Syzygium aromaticum L.	8000-34-8	0,1
Clove bud oil terpenes	Syzygium aromaticum (L.) Merr. & L.M.Perry	8000-34-8	0,1
Clove leaf oil	Syzygium aromaticum L.	8000-34-8	0,1
Clove stem oil	Syzygium aromaticum L.	8000-34-8	0,06
Elemi oil	Canarium luzonicum (Blume) A. Gray	8023-89-0	0,4
Elemi resinoid	Canarium luzonicum (Blume) A. Gray	8023-89-0	0,09
Tarragon oil	Artemisia dracunculus L.	8016-88-4	0,3
Hyssop oil	Hyssopus officinalis L.	8006-83-5	0,2
Laurel leaf oil	Laurus nobilis L	8007-48-5	3,22
Lemongrass oil, East Indian	Cymbopogon flexuosus (Nees ex Steudel) Will. Watson	8007-02-1	0,05
Mastic absolute	Pistacia lentiscus L.	68991-39-9	0,01
Mastic oil	Pistacia lentiscus L.	68991-39-9	0,02
Lovage root oil	Levisticum officinale Koch	8016-31-7	0,13
Mace oil	Myristica fragrans Houtt.	8007-12-3	1,2
Mace oleoresin	Myristica fragrans Houtt.	8007-12-3	0,6
Myrtle oil	Myrtus communis L.	8008-46-6	1
Nutmeg oil	Myristica fragrans Houtt.	8008-45-5	1,2
Nutmeg oleoresin	Myristica fragrans Houtt.	8008-45-5	0,6
Allspice oil	Pimenta dioica (L.) Merr.	8006-77-7	8,5
Allspice oleoresin	Pimenta officinalis Lindl.	8006-77-7	5,1
Pimenta leaf oil	Pimenta officinalis Lindl.	8006-77-7	6
Rose oil	Rosa x damascena Mill.	8007-01-0	2
Rose water stronger	Rosa x centifolia L.	8007-01-0	0,04
Rose absolute	Rosa x damascena Mill.	90106-38-0	0,43
Rose concrete	Rosa x damascena Mill.	90106-38-0	0,5
Savory winter oil	Satureja montana L.		0,13
Tea tree oil	Melaleuca alternifolia (Maiden & Betche) Cheel	68647-73-4	0,05
Thyme absolute	Thymus vulgaris L.	8007-46-3	0,01
Thyme oil, red	Thymus vulgaris L.	8007-46-3	0,01
Thyme oil, white	Thymus vulgaris L.	8007-46-3	0,03
Tuberose absolute	Poliantes tuberosa L.	8024-05-3	1,8
Tuberose concrete	Poliantes tuberosa L.	8024-05-3	1,07
Verbena absolute	Lippia citriodora (L.) Kunth	8024-12-2	0,1
Ylang ylang oil I	Cananga odorata (Lam.) Hook. f. &Thomson oil (forma genuine Steenis)	8006-81-3	0,04
Ylang ylang oil II	Cananga odorata (Lam.) Hook.f.&Thomson forma genuina	8006-81-3	0,03
Ylang ylang oil III	Cananga odorata (Lam.) Hook. f. &Thomson oil (forma genuine Steenis)	8006-81-3	0,04
Bucchu absolute, betulina	Agathosma betulina (P.J.Bergius) Pillans	84649-93-4	0,02
Bucchu oil, crenulata	Agathosma crenulata (L.) Pill.	92346-82-2	0,19
Hyacinth absolute	Hyacinthus orientalis L.	8023-94-7	1,5
Ocatea cymbarum oil	Ocotea cymbarum Kunth	68917-09-9	0,3
Sassafras bark oil	Sassafras albidum (Nutt.) Nees	8006-80-2	0,3
Snakeroot oil	Asarum canadense L.	8016-69-1	40

Methyleugenol

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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 :