Ethyl 2-methylbenzoate as a fragrance

Ethyl 2-methylbenzoate addresses the challenges in the perfume industry by enhancing positive fragrance aspects, improving stability and solubility, and ensuring biodegradability and safety, making it an effective fragrance agent.

JP2025517570AActive Publication Date: 2025-06-05SYMRISE GMBH & CO KG
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Patent Information

Application Number
JP2024570883
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Filing Date
2022-05-31
Publication Date
2025-06-05
Estimated Expiration
2042-05-31

AI Technical Summary

Technical Problem

The perfume industry faces challenges in creating new fragrances that meet specific market needs, as existing fragrances often have undesirable odor aspects, poor solubility, stability issues, and require high dosages. Additionally, there is a demand for fragrances with high biodegradability and safety for human and environmental use.

Method used

The use of ethyl 2-methylbenzoate as a fragrance agent, which enhances positive fragrance aspects, improves stability and solubility, reduces dosage requirements, and provides excellent biodegradability and safety.

Benefits of technology

Ethyl 2-methylbenzoate effectively enhances the positive and beneficial fragrance aspects of other perfumes, while reducing undesirable odors, improving stability and solubility, and meeting the demands for biodegradability and safety.

✦ Generated by Eureka AI based on patent content.

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Patent Text Reader

Abstract

The present invention proposes the use of ethyl 2-methylbenzoate as a fragrance.
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Description

[Technical field]

[0001] The present invention relates to the use of ethyl 2-methylbenzoate as a fragrance. Furthermore, the present invention relates to fragrance compositions, their uses and methods for imparting, modifying and / or enhancing specific fragrance notes. [Background technology]

[0002] In the perfume industry, new fragrance creations are constantly sought. However, the creation of new fragrances and fragrance compositions entails many challenges. For example, in order to satisfy a specific need of the market and to offer a product that matches the specific profile required by the customer, it is necessary to select a small number of specific compositions of fragrances from the almost infinite number of possible structures known from the prior art. The right fragrance may show very beneficial performances, but when combined with other fragrances, it may develop unpleasant and therefore unfavourable odour aspects, making it difficult or even impossible to use for certain purposes.

[0003] A second important challenge concerns the need to provide a fragrance composition that not only meets a specific odor profile, but also has so-called secondary beneficial properties. Indeed, many fragrance compositions known on the market not only have significant drawbacks in use, such as poor solubility and poor stability on storage, but also fail in subjective tasks, such as richness, charisma, etc. Furthermore, many of the known fragrance compositions require high dosages to obtain the desired odor result. Another demand for today's fragrances is high biodegradability and dermatological and toxicological safety. Therefore, there is a particular demand to provide fragrances that, even in small amounts, have a significant effect on other fragrances, changing a rather unpleasant odor impression into a positive one and / or enhancing a pleasant odor impression. Summary of the Invention [Problem to be solved by the invention]

[0004] The problem underlying the present invention was therefore to provide novel fragrances capable of enhancing the positive and beneficial fragrance aspects of other fragrances, and / or (at the same time) reducing, suppressing and / or masking the undesirable and unpleasant fragrance aspects.In particular, said novel fragrances should also be characterized by improving the stability, solubility and overall performance of other fragrances, and reducing the dosage required.Finally, said fragrance composition itself should have excellent biodegradability and be harmless to humans and the environment. [Means for solving the problem]

[0005] This problem is solved by using ethyl 2-methylbenzoate as the flavoring agent.

[0006] The ethyl 2-methylbenzoate used according to the invention may exist in any stereoisomeric form or as a mixture of any stereoisomers.

[0007] All that has been said herein for ethyl 2-methylbenzoate, and in particular the advantages described herein, also apply to mixtures of stereoisomers of ethyl 2-methylbenzoate used or employed in accordance with the present invention.

[0008] Ethyl 2-methylbenzoate has olfactory properties that are highly unique and clearly different from and superior to those of known odorants. The suitability of ethyl 2-methylbenzoate as a fragrance agent was previously unknown. It is therefore particularly surprising to discover a fragrance agent with valuable, interesting and complex olfactory properties in an already well-studied field.

[0009] Ethyl 2-methylbenzoate has the following structural formula: [ka] and preferably has the following characteristics: Cas number: 87-24-1.

[0010] As mentioned above, its suitability as a fragrance is unclear. Similarly, no exact odor description is available, but according to the inventors, ethyl 2-methylbenzoate has a strong, medicinal, fresh odor, second only to methyl salicylate.

[0011] As a result, the inventors have made the surprising discovery that ethyl 2-methylbenzoate is suitable as a fragrance and that, in small amounts, it can provide special effects in combination with other fragrances, particularly fragrances having aromatic and spicy notes.

[0012] In a preferred embodiment according to the present invention, ethyl 2-methylbenzoate is used in the perfume composition to obtain at least one of the following perfume notes: strong note, clean note, floral note, natural note, voluminous note, fruity note, fresh note, spicy note, persistent note, complex note, fine note, green note, low sweaty note, low animal note, low mushroom note and / or low terpene note. Further preferred is the use of ethyl 2-methylbenzoate to impart, modify and / or enhance aromatic perfume notes and / or spicy perfume notes. Preferably, ethyl 2-methylbenzoate is used to enhance aromatic perfume notes and / or spicy perfume notes. However, this is particularly surprising in light of the above odor description, since ethyl 2-methylbenzoate does not impart a significant odor of its own, and even enhances warm odor notes and / or spicy odor notes. In a preferred embodiment according to the invention, ethyl 2-methylbenzoate enhances the aromatic and / or spicy notes of other perfumes.

[0013] Particularly surprising is the fact that the ethyl 2-methylbenzoate used according to the invention can impart a very complex and varied overall sensory impression, which can usually only be achieved by a mixture of several components (such as a mixture of essential oils or spices).

[0014] In addition to the primary, i.e. olfactory, properties, ethyl 2-methylbenzoate also possesses secondary properties, in particular high substantivity compared to fragrances with similar olfactory properties, high stability in certain media and preparations, high extensibility and also biodegradability.

[0015] In connection with the preferred use for imparting, modifying and / or enhancing perfume notes, ethyl 2-methylbenzoate is also recognized to perform excellent functions as a so-called booster.Preferably, ethyl 2-methylbenzoate is used as a booster of the warm notes, spicy notes and / or aromatic notes of other perfumes.In other words, by using ethyl 2-methylbenzoate together with other perfumes, their warm odor notes, spicy odor notes and / or aromatic odor notes are enhanced.

[0016] In addition, the ethyl 2-methylbenzoate used according to the present invention can increase the intensity of the perfume mixture (perfume composition) and round out the overall smell of said mixture.Therefore, the compounds described herein can be used to impart more strength, cleanliness, florality, naturalness, volume, fruitiness, freshness, spiciness, warmth, persistence, complexity, fineness, greenness, less sweatiness, less animal odor, less mushroom odor and / or less terpene odor to the perfume composition, and in particular, the compounds can be used to impart more aromaticity, spiciness and / or warmth to the perfume composition.

[0017] Furthermore, ethyl 2-methylbenzoate is suitable as an agent for increasing the substantivity and / or staying power of perfume compositions.

[0018] Ethyl 2-methylbenzoate can be used in a variety of products; it can be used as a single fragrance, but it can also be particularly advantageously combined with other fragrances in different ratios to form fragrance mixtures, which can lead to the creation of new and original perfume compositions. Thus, one aspect of the present invention relates to fragrance mixtures comprising ethyl 2-methylbenzoate and optionally further components, such as solvents.

[0019] The fragrance composition according to the present invention comprises or consists of ethyl 2-methylbenzoate and at least one further fragrance. Preferably, the fragrance composition according to the present invention comprises or consists of ethyl 2-methylbenzoate and two or more further fragrances. More preferably, the fragrance composition according to the present invention comprises or consists of ethyl 2-methylbenzoate and three or more further fragrances. Most preferably, the fragrance composition according to the present invention comprises or consists of ethyl 2-methylbenzoate and four or more further fragrances.

[0020] The ethyl 2-methylbenzoate according to the invention is usually used in an organoleptically effective amount, ie in a total amount which exerts an organoleptic effect.

[0021] Preferably, the weight ratio of ethyl 2-methylbenzoate to the total amount of further flavourings is in the range of from 1:10 to 1:100, preferably from 1:25 to 1:50.

[0022] In this context, it is preferred that the total amount of ethyl 2-methylbenzoate is in the range from 0.0001 to 99.9% by weight, preferably from 0.001 to 99.5% by weight, particularly preferably from 0.01 to 99% by weight, 0.01 to 90% by weight, 0.01 to 50% by weight, 0.01 to 20% by weight, particularly preferably from 0.01 to 1.5% by weight and in particular from 0.01 to 1.0% by weight, in each case based on the total weight of the composition.

[0023] In a preferred embodiment according to the invention, ethyl 2-methylbenzoate is present in said fragrance composition in an organoleptically effective amount sufficient to modify an existing fragrance to make said fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, more green, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance aromatic and / or spicy fragrance notes.Thus, in a preferred embodiment according to the invention, ethyl 2-methylbenzoate is preferably combined with at least one aromatic and / or spicy fragrance in the fragrance composition.

[0024] Examples of fragrances which can be advantageously combined with ethyl 2-methylbenzoate in the context of the present invention can be found, for example, in S. Arctander, Perfume and Flavor Materials, Vol. I and II, Montclair, NJ 1969, self-published, or K. Bauer ei a / ., Common Fragrance and Flavor Materials, 4th Edition, Wiley-VCH, Weinheim 2001.

[0025] Specific examples include: extracts from natural sources such as essential oils, concretes, absolutes, resins, resinoids, balsams, tinctures, etc. Further specific examples are as follows: Ambergris tincture;Amyris oil;Angelica seed oil;Angelica root oil;Anise oil;Valerian oil;Basil oil;Tree moss absolute;Bay oil;Artemisia oil;Benzoecin;Bergamot oil;Beeswax absolute;Birch tar oil;Bitter almond oil;Savory oil;Bucco leaf oil;Cabreuva oil;Cade oil;Calmus oil;Camphor oil;Cananga oil;Cardamom oil;Cascarilla oil;Cassia oil;Cassius absolute;Castrea absolute;Cedar leaf oil;Schi Dahwood oil;Cistus oil;Citronella oil;Citron oil;Copaiba balsam;Copaiba balsam oil;Coriander oil;Costus root oil;Cumin oil;Cypress oil;Davana oil;Dill herb oil;Dill seed oil;Eau de broth absolute;Oak moss absolute;Elemi oil;Tarragon oil;Eucalyptus citriodora oil;Eucalyptus oil;Fennel oil;Spruce needle oil;Galbanum oil;Galbanum resin;Geranium oil;Grapefruit peel oil;Guaiacwood oil;Gurjun balsam;Gurjun balsam oil; Helichrysum absolute;Helichrysum oil;Ginger oil;Iris root absolute;Iris root oil;Jasmine absolute;Calamus oil;Blue chamomile oil;Roman chamomile oil;Carrot seed oil;Cascarilla oil;Pine needle oil;Spearmint oil;Caraway oil;Labdanum oil;Labdanum absolute;Labdanum resin;Lavandin absolute;Lavandin oil;Lavender absolute;Lavender oil;Lemongrass oil;Lavegio Ile;lime oil distilled;lime oil pressed;linaloe oil;litre cubeba oil;bay leaf oil;mace oil;marjoram oil;mandarin oil;massoir bark oil;mimosa absolute;musk grain oil;musk tincture;muscat sage oil;nutmeg oil;myrrh absolute;myrrh oil;myrtle oil;clove leaf oil;clove flower oil;neroli oil;olibanum absolute;olibanum oil;oponax oil;orange flower absolute;orange oil;origanum oil;palmarosa oil;patchouli oil;perilla oil;Balsam of Peru oil;Parsley leaf oil;Parsley seed oil;Petitgrain oil;Peppermint oil;Pepper oil;Allspice oil;Pine oil;Pauly oil;Rose absolute;Rosewood oil;Rose oil;Rosemary oil;Sage oil Dalmatian;Sage oil Spanish;Sandalwood oil;Celery seed oil;Spicy lavender oil;Star anise oil;Styrax oil;Tagetes oil;Fir needle oil;Tea tree oil;Turpentine oil;Thyme oil;Tolu balsam;Tonka absolute;Tuberose absolute;Vanilla extract;Violet leaf absolute;Verbena oil;Vetiver oil;Juniper berry oil;Wine yeast oil;Wormwood oil;Wintergreen oil;Ylang oil;Hyssop oil;Civet absolute;Cinnamon leaf oil;Cinnamon bark oil and fractions thereof or components isolated therefrom;

[0026] Individual odorants from the hydrocarbon group, such as 3-carene; α-pinene; β-pinene; α-terpinene; γ-terpinene; p-cymene; bisabolene; camphene; caryophyllene; cedrene; farnesene; limonene; longifolene; myrcene; ocimene; valencene; (E,Z)-1,3,5-undecatriene; styrene; diphenylmethane; Individual odorants from the group of aliphatic alcohols, such as hexanol; octanol; 3-octanol; 2,6-dimethylheptanol; 2-methyl-2-heptanol; 2-methyl-2-octanol; (E)-2-hexenol; 1-octen-3-ol; a mixture of 3,4,5,6,6-pentamethyl-3 / 4-hepten-2-ol and 3,5,6,6-tetramethyl-4-methyleneheptan-2-ol; (E,Z)-2,6-nonadienol; 3,7-dimethyl-7-methoxyoctan-2-ol; 9-decenol; 10-undecenol; 4-methyl-3-decen-5-ol; Individual odorants from the group of aliphatic aldehydes and their acetals, such as hexanal; heptanal; octanal; nonanal; decanal; undecanal; dodecanal; 2-methyloctanal; 2-methylnonanal; (E)-2-hexenal; (Z)-4-heptenal; 2,6-dimethyl-5-heptenal; 10-undecenal; (E)-4-decenal; 2-dodecenal; 2,6,10-trimethyl-9-undecenal; 2,6,10-trimethyl-5,9-undecadienal; heptanal diethyl acetal; 1,1-dimethoxy-2,2,5-trimethyl-4-hexene; citronellyloxyacetaldehyde; 1-(1-methoxy-propoxy)-(E / Z)-3-hexene; Individual odorants from the group of aliphatic ketones and their oximes, such as 2-heptanone; 2-octanone; 3-octanone; 2-nonanone; 5-methyl-3-heptanone; 5-methyl-3-heptanone oxime; 2,4,4,7-tetramethyl-6-octen-3-one; 6-methyl-5-hepten-2-one; Individual odorants from the group of aliphatic sulfur-containing compounds, such as 3-methylthiohexanol; 3-methylthiohexyl acetate; 3-mercaptohexanol; 3-mercaptohexyl acetate; 3-mercaptohexyl butyrate; 3-acetylthiohexyl acetate; 1-menthen-8-thiol; Individual odorants from the group of aliphatic nitriles, such as 2-nonenoic acid nitrile; 2-undecenoic acid nitrile; 2-tridecenoic acid nitrile; 3,12-tridecadienoic acid nitrile; 3,7-dimethyl-2,6-octadecenoic acid nitrile; 3,7-dimethyl-6-octenoic acid nitrile; Individual odorants from the group of esters of aliphatic carboxylic acids, such as (E)- and (Z)-3-hexenyl formate; ethyl acetoacetate; isoamyl acetate; 3,5,5-trimethylhexyl acetate; 3-methyl-2-butenyl acetate; (E)-2-hexenyl acetate; (E)- and (Z)-3-hexenyl acetate; octyl acetate; 3-octyl acetate; 1-octen-3-yl acetate; ethyl butyrate; butyl butyrate; isoamyl butyrate; hexyl butyrate; ( (E)- and (Z)-3-Hexenyl isobutyrate;Hexyl crotonate;Ethyl isovalerate;Ethyl 2-methylpentanoate;Ethyl hexanoate;Allyl hexanoate;Ethyl heptanoate;Allyl heptanoate;Ethyl octanoate;Ethyl (E,Z)-2,4-decadienoate;Methyl 2-octynate;Methyl 2-nonynate;Allyl 2-isoamyloxyacetate;Methyl 1,3,7-dimethyl-2,6-octadien-eoate;4-Methyl-2-pentylcrotonate; Individual odorants from the group of acyclic terpene alcohols, e.g. geraniol; nerol; lavadulol; nerolidol; farnesol; tetrahydrolinalool; tetrahydrogeraniol; 2,2-dimethyl-3-(3-methylphenyl)propan-1-ol; 2,6-dimethyl-7-octen-2-ol; 2,6-dimethyloctan-2-ol; 2-methyl-6-methylene-7-octen-2-ol; 2,6-dimethyl-5,7-octadien-2-ol; 2,6-dimethyl-3,5-octadien-2-ol; 3,7-Dimethyl-4,6-octadien-3-ol; 3,7-Dimethyloct-6-en-1-ol; (2E)-3,7-Dimethylocta-2,6-dien-1-ol; 3,7-Dimethyl-1,5,7-octatrien-3-ol; 2,6-Dimethyl-2,5J-octatrien-1-ol; and their formates, acetates, propionates, isobutyrates, butyrates, isovalerates, pentanoates, hexanoates, crotonates, tiglates and 3-methyl-2-butenoates; Individual odorants from the group of acyclic terpene aldehydes and ketones, such as citronellal; 7-methoxy-3,7-dimethyloctanal; 2,6,10-trimethyl-9-undecenal; geranylacetone; geranial, dimethyl acetal and diethyl acetal of neral, Individual odorants from the group of cyclic terpene alcohols, such as menthol; isopulegol; α-terpineol; terpinenol-4; menthan-8-ol; menthan-1-ol; menthan-7-ol; borneol; isoborneol; linalool oxide; nopol; cedrol; ambrinol; vetiverol; guaiol; and their formates, acetates, propionates, isobutyrates, butyrates, isovalerates, pentanoates, hexanoates, crotonates, tiglates, 3-methyl-2-butenoates; Individual odorants from the group of cyclic terpene aldehydes and ketones, such as menthone; isomenthone; 8-mercaptomenthan-3-one; carvone; camphor; fenchone; α-ionone; β-ionone; α-n-methylionone; β-n-methylionone; α-isomethylionone; β-isomethyl-ionone; α-irone; β-damascenone; 1-(2,4,4-trimethyl-2-cyclohexen-1-yl)-2-buten-1-one; 1,3,4,6,7,8a-Hexahydro-1,1,5,5-tetramethyl-2H-2,4a-methano-naphthalen-8(5H)-one;2-Methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal;Nootkatone;Dihydronootkatone;4,6,8-Megastigmatrien-3-one;α-Sinensal;β-Sinensal;Acetylated cedarwood oil (methyl cedryl ketone); Individual odorants from the group of cyclic alcohols, such as 4-tert-butylcyclohexanol; 3,3,5-trimethylcyclohexanol; 3-isocamphylcyclohexanol; 2,6,9-trimethyl-Z2,Z5,E9-cyclododecatrien-1-ol; 2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol; 4-cyclohexylbutan-2-ol; Individual odorants from the group of cycloaliphatic alcohols, such as α,3,3-trimethylcyclohexylmethanol; 1-(4-isopropylcyclohexyl)ethanol; 2-methyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)butanol; 2-methyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)-2-buten-1-ol; 3-methyl-5-(2,2,3-trimethyl-3- 1-(2,2,6-trimethylcyclohexyl)pentan-3-ol;1-(2,2,6-trimethylcyclohexyl)hexan-3-ol;3-Methyl-5-(2,2,3-trimethyl-3-cyclopent-1-yl)-4-penten-2-ol;3,3-Dimethyl-5-(2,2,3-trimethyl-3-cyclopent-1-yl)-4-penten-2-ol;1-(2,2,6-trimethylcyclohexyl)pentan-3-ol;1-(2,2,6-trimethylcyclohexyl)hexan-3-ol; Individual odorants from the group of cyclic and cycloaliphatic ethers, such as cineol; cedryl methyl ether; cyclododecyl methyl ether; 1,1-dimethoxycyclododecane; (ethoxymethoxy)cyclododecane; α-cedrene epoxide; 3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan; 3a-ethyl-6,6,9a-trimethyldodecahydronaphtho[2,1-b]furan; 1,5,9-trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene; rose oxide; 2-(2,4-dimethyl-3-cyclohexen-1-yl)-5-methyl-5-(1-methylpropyl)-1,3-dioxane; Individual odorants from the group of cyclic and macrocyclic ketones, e.g. 4-tert-butylcyclohexanone; 2,2,5-trimethyl-5-pentylcyclopentanone; 2-heptylcyclopentanone; 2-pentylcyclopentanone; 2-hydroxy-3-methyl-2-cyclopenten-1-one; 3-methyl-cis-2-penten-1-yl-2-cyclopenten-1-one; 3-methyl-2-pentyl-2-cyclopenten-1-one; 3-methyl-4-cyclo Pentadecenone;3-Methyl-5-cyclopentadecenone;3-Methylcyclopentadecanone;4-(1-ethoxyvinyl)-3,3,5,5-tetramethylcyclohexanone;4-tert-pentylcyclohexanone;5-Cyclohexadecen-1-one;6,7-Dihydro-1,1,2,3,3-pentamethyl-4(5H)-indanone;8-Cyclohexadecen-1-one;9-Cycloheptadecen-1-one;Cyclopentadecanone;Cyclohexadecanone; Individual odorants from the group of cycloaliphatic aldehydes, such as 2-methyl-4-(2,2,6-trimethyl-cyclohexen-1-yl)-2-butenal; 4-(4-hydroxy-4-methylpentyl)-3-cyclohexenecarbaldehyde; 4-(4-methyl-3-penten-1-yl)-3-cyclohexenecarbaldehyde; Individual odorants from the group of cycloaliphatic ketones, such as 1-(3,3-dimethylcyclohexyl)-4-penten-1-one; 2,2-dimethyl-1-(2,4-dimethyl-3-cyclohexen-1-yl)-1-propanone; 1-(5,5-dimethyl-1-cyclohexen-1-yl)-4-penten-1-one; 2,3,8,8-tetramethyl-1,2,3,4,5,6,7,8-octahydro-2-naphthalenyl methyl ketone; methyl 2,6,10-trimethyl-2,5,9-cyclododecatrienyl ketone; tert-butyl-(2,4-dimethyl-3-cyclohexen-1-yl) ketone; Individual odorants from the group of esters of cyclic alcohols, such as 2-tert-butylcyclohexyl acetate; 4-tert-butylcyclohexyl acetate; 2-tert-pentylcyclohexyl acetate; 4-tert-pentylcyclohexyl acetate; 3,3,5-trimethylcyclohexyl acetate; Decahydro-2-naphthyl acetate; 2-cyclopentylcyclopentyl crotonate; 3-pentyltetrahydro-2H-pyran-4-yl acetate; Decahydro 2,5,5,8a-tetramethyl-2-naphthyl acetate;4,7-methano-3a,4,5,6,7,7a-hexahydro-5,resp.6-indenyl acetate;4,7-methano-3a,4,5,6,7,7a-hexahydro-5,resp.6-indenyl propionate;4,7-methano-3a,4,5,6,7,7a-hexahydro-5,resp.6-indenyl isobutyrate;4,7-methanooctahydro-5,resp.6-indenyl acetate; Individual odorants from the group of esters of cycloaliphatic alcohols, for example 1-cyclohexylethyl crotonate; Individual odorants from the group of esters of cycloaliphatic carboxylic acids, such as allyl 3-cyclohexylpropionate; allyl cyclohexyloxyacetate; cis- and trans-methyldihydrojasmonate; cis- and trans-methyljasmonate; methyl 2-hexyl-3-oxocyclopentanecarboxylate; ethyl 2-ethyl-6,6-dimethyl-2-cyclohexenecarboxylate; ethyl 2,3,6,6-tetramethyl-2-cyclohexenecarboxylate; ethyl 2-methyl-1,3-dioxolane-2-acetate; Individual odorants from the group of aromatic aliphatic alcohols, for example: benzyl alcohol; 2-phenylethanol; 1-phenylethyl alcohol; 3-phenylpropanol; 2-phenylpropanol; 2-phenoxyethanol; 2,2-dimethyl-3-phenylpropanol; 2,2-dimethyl-3-(3-methylphenyl)propanol; 1,1-dimethyl-2-phenylethyl alcohol; 1,1-dimethyl-3-phenylpropanol; 1-ethyl-1-methyl-3-phenylpropanol; 2-methyl-5-phenylpentanol; 3-methyl-5-phenylpentanol; 3-phenyl-2-propen-1-ol; 4-methoxybenzyl alcohol; 1-(4-isopropylphenyl)ethanol; Individual odorants from the group of esters of araliphatic alcohols and aliphatic carboxylic acids, such as benzyl acetate; benzyl propionate; benzyl isobutyrate; benzyl isovalerate; 2-phenylethyl acetate; 2-phenylethyl propionate; 2-phenylethyl isobutyrate; 2-phenylethyl isovalerate; 1-phenylethyl acetate; α-trichloromethylbenzyl acetate; α,α-dimethylphenylethyl acetate; α,α-dimethylphenylethyl butyrate; cinnamyl acetate; 2-phenoxyethyl isobutyrate; 4-methoxybenzyl acetate; Individual odorants from the group of araliphatic ethers, such as 2-phenylethyl methyl ether; 2-phenylethyl isoamyl ether; 2-phenylethyl 1-ethoxyethyl ether; phenylacetaldehyde dimethyl acetal; phenylacetaldehyde diethyl acetal; hydratropaldehyde dimethyl acetal; phenylacetaldehyde glycerol acetal; 2,4,6-trimethyl-4-phenyl-1,3-dioxane; 4,4a,5,9b-tetrahydroindeno[1,2-d]-m-dioxine; 4,4a,5,9b-tetrahydro-2,4-dimethylindeno[1,2-d]-m-dioxine; and individual odorants from the group of araliphatic aldehydes, such as benzaldehyde; phenylacetaldehyde; 3-phenylpropanal; hydratropaldehyde 4-Methylbenzaldehyde;4-Methylphenylacetaldehyde;3-(4-ethylphenyl)-2,2-dimethylpropanal;2-Methyl-3-(4-isopropylphenyl)propanal;2-Methyl-3-(4-isobutylphenyl)propanal;3-(4-tert-butyl-phenyl)propanal;Cinnamaldehyde;α-Butylcinnamaldehyde;α-Hexylcinnamaldehyde;3-Methyl-5-phenylpentanal;4-Methoxybenzaldehyde;4-Hydroxy-3-methoxybenzaldehyde;4-Hydroxy-3-ethoxybenzaldehyde;3,4-Methylenedioxybenzaldehyde;3,4-Dimethoxybenzaldehyde;2-Methyl-3-(4-methoxyphenyl)propanal;2-Methyl-3-(4-methylenedioxyphenyl)propanal; Individual odorants from the group of aromatic and araliphatic ketones, e.g. acetophenone; 4-methylacetophenone; 4-methoxyacetophenone; 4-tert-butyl-2,6-dimethylacetophenone; 4-phenyl-2-butanone; 4-(4-hydroxyphenyl)-2-butanone; 1-(2-naphthalenyl)ethanone; 2-benzofuranylethanone; (3-methyl-2-benzofuranyl)ethanone Benzophenone;1,1,2,3,6-Hexamethyl-5-indanyl methyl ketone;6-tert-Butyl-1,1-dimethyl-4-indanyl methyl ketone;1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-5-indenyl]ethanone;5',6',7',8'-Tetrahydro-3',5',6',8',8'-hexamethyl-2-aceto-naphthone; Individual odorants from the group of aromatic and araliphatic carboxylic acids and their esters, for example: benzoic acid;phenylacetic acid;methyl benzoate;ethyl benzoate;hexyl benzoate;benzyl benzoate;methyl phenylacetate;ethyl phenylacetate;geranyl phenylacetate;phenylethyl phenylacetate;methyl cinnamate;ethyl cinnamate;benzyl cinnamate;phenylethyl cinnamate;cinnamyl cinnamate;allyl phenoxyacetate;methyl salicylate;hexyl salicylate;cyclohexyl salicylate;cis-3-hexenyl salicylate;benzyl salicylate;ethyl phenyl salicylate;methyl 2,4-dihydroxy-3,6-dimethylbenzoate;ethyl 3-phenylglycidate;ethyl 3-methyl-3-phenylglycidate; Individual odorants from the group of heterocyclic compounds, such as 2,5-dimethyl-4-hydroxy-2H-furan-3-one; 2-ethyl-4-hydroxy-5-methyl-2H-furan-3-one; 3-hydroxy-2-methyl-4H-pyran-4-one; 2-ethyl-3-hydroxy-4H-pyran-4-one; Individual odorants from the lactone group, such as 1,4-octanolide; 3-methyl-1,4-octanolide; 1,4-nonanolide; 1,4-decanolide; 8-decen-1,4-olide; 1,4-undecanolide; 1,4-dodecanolide; 1,5-decanolide; 1,5-dodecanolide; 4-methyl-1,4-decanolide; 1,15-pentadecanolide; 1,16-Hexadecanolide;9-Hexadecen-1,16-olide;10-Oxa-1,16-hexadecanolide;11-Oxa-1,16-hexadecanolide;12-Oxa-1,16-hexadecanolide;Ethylene-1,12-dodecanedioate;Ethylene-1,13-tridecanedioate;2,3-Dihydrocoumarin;Octahydrocoumarin.

[0027] In a further preferred embodiment of the invention, ethyl 2-methylbenzoate is combined with other fragrances, preferably having one or more, particularly preferably two, three, four, five or more, aromatic and / or spicy odor notes.

[0028] Correspondingly, the present invention also relates to perfume compositions comprising one, two, three, four, five or more other perfumes delivering spicy and / or aromatic odour notes.

[0029] The ethyl 2-methylbenzoate used according to the invention advantageously achieves (at least in part) an odor enhancement of spicy and / or aromatic notes.

[0030] In a preferred embodiment according to the invention, the at least one further fragrance is selected from the group consisting of (1R,2S,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2S,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1R,2R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, [2-( 2-Methylbutan-2-yl)cyclohexyl]acetate, terpinen-4-ol, isobornyl acetate, 6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptanpin-2(10)-ene, (1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene ((-)-α-pinene), 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, anethole, cinnamaldehyde, methyl-4(or 1)-isopropyl-1(or 4)-methylbicyclo[ 2.2.2]oct-5-ene-2-carboxylate, (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene, isoeugenyl methyl ether, 4-allyl-2-methoxyphenol, 2-butyl-4,4,6-trimethyl-1,3-dioxane, cumic aldehyde, 2,3,3-trimethylindan-1-one, pinanol, dihydromyrcenol, terpinyl acetate, 3-methyl-5-phenylpent-2-enenitrile, acetic acid Selected from the group consisting of geranyl, benzaldehyde, ionone alpha, benzyl salicylate, phenylethyl alcohol, 3,7-dimethyloct-6-en-1-ol, methyl dihydrojasmonate, (5E)-3-methylcyclopentadec-5-en-1-one, (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan, 3-ethoxy-4-hydroxybenzaldehyde, and 4-hydroxy-3-methoxybenzaldehyde.

[0031] Preferably, ethyl 2-methylbenzoate is combined with one or more, particularly preferably two, three, four, five or more of these preferred other fragrances.

[0032] Perfume oil compositions (=perfume mixtures) containing 4-cyclohexyl-2-butanol are advantageously used in perfumery in liquid form, either undiluted or diluted with a solvent, suitable solvents being, for example, ethanol, isopropanol, diethylene glycol monoethyl ether, glycerin, propylene glycol, 1,2-butylene glycol, dipropylene glycol, diethyl phthalate, triethyl citrate, isopropyl myristic acid, etc.

[0033] Furthermore, the perfume composition according to the present invention can be adsorbed on a carrier that ensures both the fine distribution of perfume in the product and the controlled release during use.Such carriers can be porous inorganic materials, such as light sulfates, silica gel, zeolites, plaster, clay, clay granules, aerated concrete, or organic materials, such as wood, cellulosic materials, sugar, dextrin (e.g. maltodextrin) or plastics, such as PVC, polyvinyl acetate or polyurethane.The combination obtained from the composition according to the present invention and a carrier material is also understood as the perfume composition according to the present invention.

[0034] The perfume compositions according to the invention can also be microencapsulated, spray-dried as inclusion complexes or as extrudates and added in this form, for example, to the product to be perfumed.

[0035] If necessary, the properties of the composition thus modified can be further optimized with a view to a more targeted release of the perfume by so-called "coating" with a suitable material, for which purpose waxy plastics such as polyvinyl alcohol are preferably used, so that the product thus obtained is an article according to the invention.

[0036] A further aspect of the present invention relates to the use of a fragrance composition to modify an existing fragrance in said fragrance composition to make said existing fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, more green, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance the aromatic and / or spicy fragrance notes of said existing fragrance. Thus, in a preferred embodiment according to the present invention, ethyl 2-methylbenzoate is preferably used together with at least one aromatic and / or spicy fragrance in a fragrance composition to enhance the spicy and / or aromatic notes of said at least one aromatic and / or spicy fragrance.

[0037] Preferably, the existing fragrance is selected from the fragrances listed above. More preferably, the existing fragrance is selected from the following: (1R,2S,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2S,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1R,2R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, [2-(2-methylbutan-2-yl) Cyclohexyl]acetate, terpinen-4-ol, isobornyl acetate, 6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-2(10)-ene, (1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene ((-)-α-pinene), 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, anethole, cinnamaldehyde, methyl-4(or 1)-isopropyl-1(or 4)-methylbicyclo[2.2.2]octane -5-ene-2-carboxylate, (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene, isoeugenyl methyl ether, 4-allyl-2-methoxyphenol, 2-butyl-4,4,6-trimethyl-1,3-dioxane, cumic aldehyde, 2,3,3-trimethylindan-1-one, pinanol, dihydromyrcenol, terpinyl acetate, 3-methyl-5-phenylpent-2-enenitrile, geranyl acetate , benzaldehyde, ionone alpha, benzyl salicylate, phenylethyl alcohol, 3,7-dimethyloct-6-en-1-ol, methyl dihydrojasmonate, (5E)-3-methylcyclopentadec-5-en-1-one, (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan, 3-ethoxy-4-hydroxybenzaldehyde, 4-hydroxy-3-methoxybenzaldehyde.

[0038] The further preferred embodiments listed above also apply to the use of said fragrance composition.

[0039] The perfume compositions according to the invention can be advantageously used for the manufacture of perfumed articles according to the invention in concentrated form, in solution or in the modified forms described above. Specific examples of such articles include B. perfume extracts, eau de parfums, eau de toilettes, aftershaves, eau de colognes, preshave products, splash colognes and fragrant refreshing towels, as well as acidic, alkaline and neutral cleaning agents, such as floor cleaners, window cleaners, dishwashing detergents, bathroom and sanitary cleaners, abrasive emulsions, solid and liquid toilet cleaners, powder and foam carpet cleaners, fabric fresheners, ironing aids, liquid detergents, detergent powders, fragrance imparting agents, laundry pretreatment agents, such as bleaches, soaking agents, stain removers, fabric softeners, laundry soaps, laundry tablets, as well as disinfecting fresheners in liquid, gel-like or solid carrier-applied form, aerosol sprays, waxes and polishes, such as furniture polishes, floor waxes, shoe creams, as well as personal care products, such as bar and liquid soaps, shower gels, shampoos, shaving soaps, shaving foams, bath oils, oil-in-water, water-in-oil and water-in-oil-in-water. cosmetic emulsions of the type such as skin creams and lotions, face creams and lotions, sun protection creams and lotions, after-sun creams and lotions, hand creams and lotions, foot creams and lotions, depilatory creams and lotions, after-shave creams and lotions, sun tanning creams and lotions, hair care products such as hair sprays, hair gels, hair setting lotions, hair conditioners, permanent hair dyes, semi-permanent hair dyes, hair shaping agents such as cold wave agents, hair straighteners, hair lotions, hair creams, hair lotions, deodorants and antiperspirants such as underarm sprays, roll-ons, deodorant sticks, deodorant creams, decorative cosmetics such as eye shadows, nail polishes, lipsticks, mascaras, as well as products such as candles, lamp oils, incense, insecticides, repellents, fuels, etc.

[0040] Of course, the fragrance composition according to the invention can also be included in cosmetic and household compositions.

[0041] Another aspect of the present invention is a method for modifying an existing fragrance to make it stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, more green, less sweaty, less animalic, less mushroomy and / or less terpenic and / or to enhance spicy and / or aromatic fragrance notes, comprising the steps of: (a) providing ethyl 2-methylbenzoate; (b) providing at least one additional flavoring; (c) adding said ethyl 2-methylbenzoate to said at least one further fragrance in a sensory effective amount sufficient to modify said at least one further fragrance to make said fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance spicy and / or aromatic fragrance notes. The present invention relates to a method comprising or consisting of the steps of:

[0042] Preferably, said at least one further fragrance and said existing fragrance are the same compound(s).Thus, in a preferred embodiment according to the present invention, said ethyl 2-methylbenzoate is added to said at least one further fragrance in an organoleptically effective amount sufficient to modify said at least one further fragrance to make said fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, more long-lasting, more complex, more delicate, more green, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance spicy and / or aromatic fragrance notes.

[0043] Preferably, the weight ratio of ethyl 2-methylbenzoate to the total amount of said further flavouring is in the range of 1:10 to 1:100, preferably in the range of 1:25 to 1:50.

[0044] In this context, it is preferred that the total amount of ethyl 2-methylbenzoate is in the range from 0.0001 to 99.9% by weight, preferably from 0.001 to 99.5% by weight, particularly preferably from 0.01 to 99% by weight, 0.01 to 90% by weight, 0.01 to 50% by weight, 0.01 to 20% by weight, particularly preferably from 0.01 to 1.5% by weight and in particular from 0.01 to 1.0% by weight, in each case based on the total weight of the composition.

[0045] Preferably, ethyl 2-methylbenzoate is combined with one or more, particularly preferably two, three, four, five or more, other fragrances having spicy and / or aromatic odor notes.

[0046] The ethyl 2-methylbenzoate used according to the invention advantageously (at least in part) achieves an odour enhancement of spicy and / or aromatic perfume notes.

[0047] In a preferred embodiment according to the invention, said at least one further fragrance is selected from the group consisting of: (1R,2S,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2S,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1R,2R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, [2- (2-Methylbutan-2-yl)cyclohexyl]acetate, terpinen-4-ol, isobornyl acetate, 6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-2(10)-ene, (1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene ((-)-α-pinene), 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, anethole, cinnamaldehyde, methyl-4(or 1)-isopropyl-1(or 4)-methylbicyclo [2.2.2]Oct-5-ene-2-carboxylate, (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene, isoeugenyl methyl ether, 4-allyl-2-methoxyphenol, 2-butyl-4,4,6-trimethyl-1,3-dioxane, cumic aldehyde, 2,3,3-trimethylindan-1-one, pinanol, dihydromyrcenol, terpinyl acetate, 3-methyl-5-phenylpent-2-enenitrile, acetic acid The compound is selected from the group consisting of geranyl acid, benzaldehyde, ionone alpha, benzyl salicylate, phenylethyl alcohol, 3,7-dimethyloct-6-en-1-ol, methyl dihydrojasmonate, (5E)-3-methylcyclopentadec-5-en-1-one, (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan, 3-ethoxy-4-hydroxybenzaldehyde, and 4-hydroxy-3-methoxybenzaldehyde.

[0048] Preferably, ethyl 2-methylbenzoate is combined with one or more, particularly preferably two, three, four, five or more of these preferred other fragrances.

[0049] The further preferred embodiments listed above also apply to the method of the present invention.

[0050] A further aspect of the invention relates to a perfumed product comprising ethyl 2-methylbenzoate and two or more other perfumes, and optionally other ingredients, the mixture of which comprises: (a) modifying the olfactory profile of said two or more other fragrance ingredients to make said olfactory profile stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or (b) an amount that enhances the spicy and / or aromatic notes of the olfactory characteristics of said two or more other flavorings; It is characterized by containing ethyl 2-methylbenzoate.

[0051] In a preferred embodiment, the perfumed product is selected from cosmetics, hygiene products and / or household products. The further preferred embodiments listed above also apply to the perfumed products of the present invention.

[0052] Preferably, said perfumed article is selected from the group consisting of detergents and cleaning agents, hygiene or care products, preferably body care and hair care, cosmetics and household products, preferably perfume extracts, eau de parfum, eau de toilette, aftershave lotions, eau de cologne, preshave products, splash cologne, perfumed refreshing tissues, acidic, alkaline or neutral cleaning agents, fabric fresheners, ironing aids, liquid detergents, washing powders, laundry pre-treatments, fabric softeners, cleaning tablets, disinfectants, surface disinfectants, air fresheners, aerosol sprays, waxes and polishes, personal care products, hand creams and lotions, foot creams and lotions, depilatory creams and lotions, aftershave creams and lotions, suntan creams and lotions, hair care products, hair care products, decorative cosmetics products, candles, lamp oils, incense, insecticides, repellents and fuels. Most preferably, said perfumed product is selected from alcohol perfumes, personal hygiene products, cleaning or care products for household use.

[0053] Furthermore, it is preferred for the perfumed product according to the present invention that the ethyl 2-methylbenzoate is contained in an organoleptically effective amount sufficient to give the consumer one or more olfactory characteristics selected from the group consisting of stronger odor notes, cleaner odor notes, more floral odor notes, more natural odor notes, more voluminous odor notes, more fruity odor notes, more fresh odor notes, more persistent odor notes, more complex odor notes, more delicate odor notes, more green odor notes, less sweaty odor notes, less animal odor notes, less mushroom odor notes and / or less terpene odor notes and / or enhanced spicy odor notes and / or aromatic odor notes.It is also preferred that the total amount of 4-ethyl 2-methylbenzoate is within the range of 0.00001 to 10% by weight, preferably 0.0001 to 5% by weight, particularly preferably 0.001 to 2% by weight, more preferably 0.005 to 1% by weight, based on the total weight of the perfumed product.

[0054] The above-mentioned additives, auxiliaries and / or active substances are preferably not odoriferous substances. They can be, for example, preservatives, antibacterial agents, chelating agents, detergents, emulsifiers, oils and fats, etc., and in principle, all substances used as additives, auxiliaries and / or active ingredients in cosmetic products, in particular fragrance compositions, and household compositions.

[0055] Below, the invention is further characterized on the basis of examples. EXAMPLES

[0056] Example 1: Synthesis of ethyl 2-methylbenzoate

[0057] Ethyl 2-methylbenzoate according to formula I can be prepared according to known methods described in the art.

[0058] [ka] Odor of ethyl 2-methylbenzoate: A strong, medicinal, fresh odor, second only to methyl salicylate.

[0059] Example 2: Description of the Pleasant Perfume Odor after Addition of Ethyl 2-Methylbenzoate to Perfumes with Spicy and / or Aromatic Odor Notes

[0060] [Table 1] TIFF2025517570000004.tif249160 TIFF2025517570000005.tif69169

[0061] Example 3: Spicy and / or aromatic perfume oils

[0062] [Table 2] According to the expert panel, the addition of ethyl 2-methylbenzoate enhances the warm spice of the fragrance composition. In particular, the nutmeg and clove notes are enhanced by this effect. The pumpkin part of the fragrance blends well with the accentuated spice mix. The perfume oil was evaluated at 3% in a candle formulation.

[0063] [Table 3] According to the Expert Panel, the addition of ethyl 2-methylbenzoate covers the citronella character of this note, making it more spicy and sharp, like ginger. The clove note is enhanced by ethyl 2-methylbenzoate, which gives the ginger note a warm undertone. The perfume oil was evaluated at 1.2% in soap formulations.

[0064] [Table 4] TIFF2025517570000009.tif12169 According to the expert panel, the addition of Ethyl 2-Methylbenzoate gives a boosting effect to the body of the aromatic Rosemary, which is elevated by the top note of Eucalyptus. Ethyl 2-Methylbenzoate makes the fragrance more intense and lively and balances the scent profile. The perfume oil was evaluated at 0.5% in liquid soap.

[0065] [Table 5] According to the expert panel, the addition of ethyl 2-methylbenzoate enhanced the odour notes of this delicate fragrance due to its booster function. Furthermore, ethyl 2-methylbenzoate made the fragrance more aromatic. In combination with ethyl 2-methylbenzoate, the fragrance had a livelier, spicy, peppery body. The perfume oil was evaluated at an alcohol content of 0.10%.

Claims

1. Use of ethyl 2-methylbenzoate as a fragrance.

2. Use of ethyl 2-methylbenzoate in a fragrance composition to obtain at least one of the following fragrance notes: strong note, clean note, floral note, natural note, voluminous note, fruity note, fresh note, spicy note, persistent note, complex note, delicate note, green note, note with less sweaty smell, note with less animal smell, note with less mushroom smell and / or note with less terpene smell.

3. 3. Use according to claims 1 and / or 2 for imparting, modifying and / or enhancing aromatic odour notes and / or spicy odour notes.

4. 3. Use according to claims 1 and / or 2 for enhancing aromatic and / or spicy odour notes.

5. A fragrance composition comprising or consisting of ethyl 2-methylbenzoate and at least one further fragrance.

6. 6. The fragrance composition according to claim 5, wherein a weight ratio of ethyl 2-methylbenzoate to the total amount of other fragrances is within the range of 1:10 to 1:

100.

7. 7. The fragrance composition according to claim 5, wherein the amount of ethyl 2-methylbenzoate is in the range of 0.01 to 50% by weight, based on the total weight of the fragrance composition.

8. 7. The fragrance composition according to claim 5, wherein the amount of ethyl 2-methylbenzoate is in the range of 0.01 to 1.5% by weight, based on the total weight of the fragrance composition.

9. 9. The fragrance composition according to claim 5, wherein ethyl 2-methylbenzoate is present in the fragrance composition in an organoleptically effective amount sufficient to modify an existing fragrance to make it stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance aromatic and / or spicy fragrance notes.

10. The at least one further fragrance may be selected from the group consisting of (1R,2S,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1S,2S,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, (1R,2R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-ol, [2-(2-methylbutan-2-yl)cyclohexyl] Acetate, terpinen-4-ol, isobornyl acetate, 6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-2(10)-ene, (1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene ((-)-α-pinene), 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, anethole, cinnamaldehyde, methyl-4(or 1)-isopropyl-1(or 4)-methylbicyclo[2.2.2]oct-5-ene-2-carboxyle ester, (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene, isoeugenyl methyl ether, 4-allyl-2-methoxyphenol, 2-butyl-4,4,6-trimethyl-1,3-dioxane, cuminic aldehyde, 2,3,3-trimethylindan-1-one, pinanol, dihydromyrcenol, terpinyl acetate, 3-methyl-5-phenylpent-2-enenitrile, geranyl acetate, benzaldehyde, ionone α, salicyl 10. The fragrance composition according to claim 5, wherein the aromatic carboxylic acid ester is selected from the group consisting of benzyl acetate, phenylethyl alcohol, 3,7-dimethyloct-6-en-1-ol, methyl dihydrojasmonate, (5E)-3-methylcyclopentadec-5-en-1-one, (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan, 3-ethoxy-4-hydroxybenzaldehyde, and 4-hydroxy-3-methoxybenzaldehyde.

11. Use of a fragrance composition according to any one of claims 5 to 10 to modify an existing fragrance in said fragrance composition to make said existing fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic and / or to enhance the aromatic and / or spicy fragrance notes of said existing fragrance.

12. 1. A method for modifying an existing fragrance to make it stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic and / or enhance aromatic and / or spicy fragrance notes, comprising the steps of: (a) providing ethyl 2-methylbenzoate; (b) providing at least one additional flavoring; (c) adding said ethyl 2-methylbenzoate to said at least one further fragrance in a sensory effective amount sufficient to modify said at least one further fragrance to make said fragrance stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, greener, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or to enhance aromatic and / or spicy fragrance notes.

20. A method comprising or consisting of the steps of:

13. A perfumed product comprising ethyl 2-methylbenzoate and two or more other perfumes, and optionally other ingredients, the mixture of which comprises: (a) modifying the olfactory profile of said two or more other fragrances to make said olfactory profile stronger, cleaner, more floral, more natural, more voluminous, more fruity, more fresh, longer-lasting, more complex, more delicate, more green, less sweaty, less animalic, less mushroomy and / or less terpenic, and / or (b) an amount that enhances the aromatic and / or spicy notes of the olfactory profile of said two or more other flavorings; A perfumed product comprising ethyl 2-methylbenzoate.

14. 13. The perfumed product of claim 12, wherein the product is selected from cosmetics, hygiene products and / or household products.

15. 13. The perfumed product of claim 12, wherein the product is selected from an alcohol-based perfume, a personal hygiene product, or a cleaning or care product for household use.

Citation Information

Patent Citations

  • Agrochemical emulsion

    JP1998130104A

  • Method for producing sea algae flavor

    JP2005143465A

  • Method for producing flavor of crustacean

    JP2005160402A

  • Cleaning composition with improved dispensability and suspendability

    JP2016526057A

  • Use of methyl benzoic acid ester in perfume compositions

    US20050170998A1