EP1102832A2 - Riechstoff-zusammensetzungen - Google Patents
Riechstoff-zusammensetzungenInfo
- Publication number
- EP1102832A2 EP1102832A2 EP99924838A EP99924838A EP1102832A2 EP 1102832 A2 EP1102832 A2 EP 1102832A2 EP 99924838 A EP99924838 A EP 99924838A EP 99924838 A EP99924838 A EP 99924838A EP 1102832 A2 EP1102832 A2 EP 1102832A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- methylcyclohex
- butanal
- enyl
- aldehyde
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 title abstract description 4
- FFFSOJPRLLQQAA-UHFFFAOYSA-N 3-(4-methylcyclohex-3-en-1-yl)-2-methylidenebutanal Chemical compound O=CC(=C)C(C)C1CCC(C)=CC1 FFFSOJPRLLQQAA-UHFFFAOYSA-N 0.000 claims abstract description 19
- VJYFMQREUJXCQV-UHFFFAOYSA-N Limonene aldehyde Chemical compound O=CCC(C)C1CCC(C)=CC1 VJYFMQREUJXCQV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims description 41
- 239000003205 fragrance Substances 0.000 claims description 28
- 150000001299 aldehydes Chemical class 0.000 claims description 5
- 239000002537 cosmetic Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 2
- 230000001476 alcoholic effect Effects 0.000 claims 1
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 7
- 239000002304 perfume Substances 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 229940087305 limonene Drugs 0.000 description 3
- 235000001510 limonene Nutrition 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 238000007037 hydroformylation reaction Methods 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 244000263375 Vanilla tahitensis Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
Definitions
- the invention relates to special fragrance compositions which contain 90-70% by weight of 2-methylene-3- (4-methylcyclohex-3-enyl) butanal and 10-30% by weight of limonaldehyde.
- Limonene whose rational IUPAC name is l-methyl-4-isopropenyl-cyclohex-l-ene, is a well-known natural product.
- the structural formula of limonene (3) is shown below:
- 2-methylene-3- (4-methylcyclohex-3-enyl) butanal (1) can be used as a fragrance according to the information given in DE 29 21 619 C3. However, nothing is disclosed in DE 29 21 619 C3 about the properties of special mixtures of (1) with other olfactory compounds.
- fragrance industry has a constant need for new fragrances with interesting fragrance notes to complement the range of naturally available fragrances and to make the necessary adjustments to changing fashionable flavors as well to meet the ever increasing need for odor improvers for everyday products such as cosmetics and cleaning agents.
- fragrance compositions which contain 90-70% by weight of 2-methylene-3- (4-methylcyclohex-3-enyl) butanal (1) and 10-30% by weight of limonene aldehyde (2) , are characterized by perfume notes of extremely interesting perfume with fine shades.
- the odor profiles of these fragrance compositions according to the invention are qualitatively different, original and novel compared to the individual components (1) and (2).
- the invention relates to fragrance compositions which contain 90-70% by weight of 2-methylene-3- (4-methylcyclohex-3-enyl) butanal (1) and 10-30% by weight of limonene aldehyde (2).
- the fragrance compositions according to the invention contain, in addition to the compulsory components (1) and (2) mentioned, a maximum of 5% by weight of further olfactory components.
- Another object of the invention is the use of aldehyde mixtures as fragrances, the aldehyde mixtures being mixtures which contain 90-70% by weight of 2-methylene-3- (4-methylcyclohex-3-enyl) butanal and 10-30 wt.% Limonenaldehyd contain
- the odor profile of the fragrance compositions according to the invention is original and novel.
- perfume compositions they enhance harmony and charisma as well as adhesion, whereby the dosage is adjusted to the desired fragrance, taking into account the other components of the composition.
- the fragrance compositions according to the invention are particularly suitable for modifying and enhancing known compositions. Their ability to contribute to the refinement of compositions should be particularly emphasized.
- fragrance compositions according to the invention round off and harmonize the olfactory notes of a wide range of known compositions, but without dominating in an unpleasant manner.
- the usable proportions of the fragrance compositions according to the invention in fragrance compositions range from 0.001 to 70% by weight, in each case based on the overall composition.
- the fragrance compositions according to the invention and compositions of this type can be used both for perfuming cosmetic preparations such as lotions, creams, shampoos, soaps, ointments, powders, aerosols, toothpastes, mouthwashes, deodorants and in exquisite perfumery.
- perfuming technical products as well as detergents and cleaning agents, Fabric softener, fabric treatment agent or tobacco.
- the compositions are metered into them in an olfactory effective amount, in particular in a concentration in the range from 0.05 to 2% by weight, based on the entire product.
- these values are not intended to represent any limit values, since the experienced perfumer can also achieve effects with lower concentrations or build new types of complexes with even higher doses.
- a mixture was obtained by mixing 80% by weight of 2-methylene-3- (4-methylcyclohex-3-enyl) butanal (1) and 20% by weight of limonene aldehyde (2) - both statements refer to the entire composition fragrance composition according to the invention produced.
- compositions K-1, K-2 and K-3 listed in Table 1 below were produced.
- the basis of comparison is K-1 (a Muguet composition), according to the invention is K-2, the composition K-3 is used for further comparison.
- Table 1 the details in the columns headed K-1 to K-3 mean parts by weight.
- the components specified in column 1 the following applies to the manufacturers: * Henkel KGaA a) PFW (Perfume Flavors Worldwide) b) Givaudan c) Charabot d) Hüls AG e) Firmenich f) International Flavor and Fragrances
- composition K-2 Compared to Kl, composition K-2 has a significantly fresher green smell of agrumen, which gives the aldehydic floral base and the harmoniously integrated wood base a beautiful appearance and good diffusivity.
- composition K-3 also has a fresh, well-radiating note of agrumen, but the harmony from the balsamic fund is severely impaired and disturbed by an isolated vanilla note.
- Table 1 Table 1:
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19820657A DE19820657A1 (de) | 1998-05-08 | 1998-05-08 | Riechstoff-Zusammensetzungen |
| DE19820657 | 1998-05-08 | ||
| PCT/EP1999/002902 WO1999058629A2 (de) | 1998-05-08 | 1999-04-29 | Riechstoff-zusammensetzungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1102832A2 true EP1102832A2 (de) | 2001-05-30 |
| EP1102832B1 EP1102832B1 (de) | 2004-12-22 |
Family
ID=7867124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99924838A Expired - Lifetime EP1102832B1 (de) | 1998-05-08 | 1999-04-29 | Riechstoff-zusammensetzungen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6451758B1 (de) |
| EP (1) | EP1102832B1 (de) |
| JP (1) | JP2002514681A (de) |
| DE (2) | DE19820657A1 (de) |
| ES (1) | ES2233052T3 (de) |
| IL (1) | IL139484A0 (de) |
| WO (1) | WO1999058629A2 (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE275186T1 (de) * | 1999-05-19 | 2004-09-15 | Firmenich & Cie | Anwendung von substituierten acetaldehyden mit einem cyclischen substituent als riechstoffbestandteile |
| DE10026004A1 (de) * | 2000-05-25 | 2001-11-29 | Cognis Deutschland Gmbh | 3,3-Dimethylcyclohexan-Derivate |
| DE10206771A1 (de) * | 2002-02-19 | 2003-08-28 | Cognis Deutschland Gmbh | Verwendung von Hexenal-Derivaten als Riechstoffe |
| DE102005061073B4 (de) * | 2005-12-21 | 2020-10-22 | Symrise Ag | Parfümkomposition mit 3-(4-Methyl-cyclohex-3-enyl)-butyraldehyd und 1,8-p-Menthadien |
| GB0622037D0 (en) * | 2006-11-04 | 2006-12-13 | Quest Int Serv Bv | Novel fragrance compounds |
| ATE461267T1 (de) * | 2007-01-02 | 2010-04-15 | Symrise Gmbh & Co Kg | Mischungen mit 3-(4-methyl-cyclohex-3-enyl)- butyraldehyd und 2,6-dimethyl-7-octen-2-ol |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2849642A1 (de) * | 1978-11-16 | 1980-06-04 | Henkel Kgaa | Neue aldehyde und deren verwendung als riechstoffe |
| DE2921619C3 (de) | 1979-05-28 | 1982-05-19 | Ruhrchemie Ag, 4200 Oberhausen | 2-Methylen-3-(4-methylcyclohex-3-enyl)-butanal und 2-Methylen-3-(4-methylcyclohexyl)-butanal und Verfahren zu ihrer Herstellung |
| DE3360037D1 (en) * | 1982-04-15 | 1985-02-07 | Firmenich & Cie | 1(7)p-menthene-9-al and its use as a perfuming and flavouring agent |
| US5068363A (en) | 1990-09-27 | 1991-11-26 | International Flavors & Fragrances Inc. | Cyclohexenylmethloxabicyclooctanes, processes for preparing same, intermediates used in said processes and organoleptic uses of said cyclohexenylmethloxabicyclooctanes and intermediates therefor |
-
1998
- 1998-05-08 DE DE19820657A patent/DE19820657A1/de not_active Withdrawn
-
1999
- 1999-04-29 US US09/674,941 patent/US6451758B1/en not_active Expired - Lifetime
- 1999-04-29 ES ES99924838T patent/ES2233052T3/es not_active Expired - Lifetime
- 1999-04-29 WO PCT/EP1999/002902 patent/WO1999058629A2/de not_active Ceased
- 1999-04-29 IL IL13948499A patent/IL139484A0/xx unknown
- 1999-04-29 EP EP99924838A patent/EP1102832B1/de not_active Expired - Lifetime
- 1999-04-29 JP JP2000548423A patent/JP2002514681A/ja active Pending
- 1999-04-29 DE DE59911336T patent/DE59911336D1/de not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9958629A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| DE19820657A1 (de) | 1999-11-11 |
| ES2233052T3 (es) | 2005-06-01 |
| IL139484A0 (en) | 2001-11-25 |
| JP2002514681A (ja) | 2002-05-21 |
| WO1999058629A2 (de) | 1999-11-18 |
| US6451758B1 (en) | 2002-09-17 |
| DE59911336D1 (de) | 2005-01-27 |
| WO1999058629A3 (de) | 2001-03-29 |
| EP1102832B1 (de) | 2004-12-22 |
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