EP0056500A2 - Ester der 2,2,-Dimethyl-Propionsäure, ihre Verwendung als Riechstoffe und eine sie enthaltende Zusammensetzung - Google Patents
Ester der 2,2,-Dimethyl-Propionsäure, ihre Verwendung als Riechstoffe und eine sie enthaltende Zusammensetzung Download PDFInfo
- Publication number
- EP0056500A2 EP0056500A2 EP81201262A EP81201262A EP0056500A2 EP 0056500 A2 EP0056500 A2 EP 0056500A2 EP 81201262 A EP81201262 A EP 81201262A EP 81201262 A EP81201262 A EP 81201262A EP 0056500 A2 EP0056500 A2 EP 0056500A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- formula
- pivalate
- perfuming
- compounds
- dimethyl
- 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.)
- Withdrawn
Links
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
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
Definitions
- the invention relates to the field of perfumes.
- it relates to a series of esters of 2,2-dimethyl-propionic acid useful as perfume ingredients.
- Said esters can be represented by the formula in which the symbol R represents a hydrogen atom or a methyl group and Z represents a bivalent radical of formula
- a more specific subject of the invention is the use of said compounds of formula (I) as perfuming ingredients, in particular their use in the pure state or as a mixture with one or more ingredients perfuming a solvent or a support.
- esters see for example S. Arctander, Perfume and Flavor Chemicals, Montclair N.J. 1969, Sections nos. 294, 310, 338, 345, 346, 991 and following 7. Whether they are derived from aliphatic or aromatic acids or alcohols, they are almost all cited in the specialized literature. Very surprisingly, however, nowhere is there any mention of the higher esters of 2,2-dimethylpropionic acid (pivalic acid), more particularly of the esters of araliphatic alcohols and, consequently, of the interest that such compounds could have for the perfume industry.
- the compounds (I) can therefore be advantageously used as perfuming ingredients, in fine perfumery as well as during the perfuming of products such as soaps, detergents, cleaning products or cosmetic products for example. They can be used, among other things, for the preparation of very diverse perfume compositions, such as fruity, floral, rose, lily of the valley or jasmine compositions, for example, even woody, chypre or fern, to which they contribute to give more richness and roundness. .
- the compounds (I) can be used both in the pure state and in mixture with one or more of the perfuming ingredients usual in the art, a solvent or a support .
- compositions for perfumes for example, interesting olfactory effects can be obtained by the use of said compounds (I) at a rate of about 1 to 20, sometimes 30% relative to the weight of said composition, or even 50% or more when preparing bases or hearts for perfumes. Amounts less than 1% may also be used, especially when perfuming products such as soaps or detergents for example.
- the compounds of the invention have the advantage of being perfectly stable in the various environments of use. Their inertia with regard to the effect exerted by acidic, oxidizing or reducing agents, for example, is such that their use can be extended to the scent of very diverse articles such as soaps, hair sprays, talcs or detergents. In addition, their stability with regard to light is also excellent, hence their good storage life. Finally, the compounds of formula (1) have proved to be biologically harmless under the conditions of use envisaged.
- a basic perfuming composition was prepared as indicated below:
- the base thus prepared has a generic flowery odor within which there is a characteristic "thrush" note.
- This perfuming composition is perfectly suited for perfuming shampoos or hair lotions.
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)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH271/81 | 1981-01-16 | ||
CH27181 | 1981-01-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0056500A2 true EP0056500A2 (de) | 1982-07-28 |
EP0056500A3 EP0056500A3 (de) | 1982-11-17 |
Family
ID=4183199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81201262A Withdrawn EP0056500A3 (de) | 1981-01-16 | 1981-11-12 | Ester der 2,2,-Dimethyl-Propionsäure, ihre Verwendung als Riechstoffe und eine sie enthaltende Zusammensetzung |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0056500A3 (de) |
JP (1) | JPS57139039A (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4524021A (en) * | 1983-05-05 | 1985-06-18 | International Flavors & Fragrances Inc. | Perfumery uses of esters of phenyl alkanols |
WO2005110967A1 (de) * | 2004-05-12 | 2005-11-24 | Symrise Gmbh & Co. Kg | 3-methylbenzylisobutyrat |
WO2010140076A1 (en) * | 2009-06-04 | 2010-12-09 | Firmenich Sa | Phenol ester as perfuming ingredient |
US8363787B2 (en) | 2009-03-25 | 2013-01-29 | General Electric Company | Interface for liquid metal bearing and method of making same |
-
1981
- 1981-11-12 EP EP81201262A patent/EP0056500A3/de not_active Withdrawn
-
1982
- 1982-01-14 JP JP350482A patent/JPS57139039A/ja active Pending
Non-Patent Citations (4)
Title |
---|
CHEMICAL ABSTRACTS, vol 66, 1967, page 5294, no. 55873e, Columbus Ohio (USA); Kang-Jen Liu et al.: 'Microstructure of poly(I-alpha-methyl benzyl methacrylate in solution' & Am.Chem.Soc., Div. Polymer Chem., Preprints 6(2), 904-909, 1965 * |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, vol. 74, pages 4968-4969 'New compounds' * |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 73, 15th mars 1951, pages 901-903, E.H. Man et al.: 'The claisen acylation of methyl ketones with branched chain aliphatic esters' * |
S.ARCTANDER: "Perfume and flavor chemicals", 1969, Montclair, N.J.(USA); * |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4524021A (en) * | 1983-05-05 | 1985-06-18 | International Flavors & Fragrances Inc. | Perfumery uses of esters of phenyl alkanols |
WO2005110967A1 (de) * | 2004-05-12 | 2005-11-24 | Symrise Gmbh & Co. Kg | 3-methylbenzylisobutyrat |
US7494967B2 (en) | 2004-05-12 | 2009-02-24 | Symrise Gmbh & Co. Kg | 3-methylbenzyl-isobutyrate |
EP2065360A2 (de) | 2004-05-12 | 2009-06-03 | Symrise GmbH & Co. KG | 3-Methylbenzylisobutyrat |
US7638479B2 (en) | 2004-05-12 | 2009-12-29 | Symrise Gmbh & Co. Kg | 3-methylbenzyl-isobutyrate |
EP2065360A3 (de) * | 2004-05-12 | 2012-02-29 | Symrise AG | 3-Methylbenzylisobutyrat |
US8363787B2 (en) | 2009-03-25 | 2013-01-29 | General Electric Company | Interface for liquid metal bearing and method of making same |
WO2010140076A1 (en) * | 2009-06-04 | 2010-12-09 | Firmenich Sa | Phenol ester as perfuming ingredient |
CN102458349A (zh) * | 2009-06-04 | 2012-05-16 | 弗门尼舍有限公司 | 作为加香成分的苯酚酯 |
CN102458349B (zh) * | 2009-06-04 | 2013-09-25 | 弗门尼舍有限公司 | 作为加香成分的苯酚酯 |
US8648032B2 (en) | 2009-06-04 | 2014-02-11 | Firmenich Sa | Phenol ester as perfuming ingredient |
Also Published As
Publication number | Publication date |
---|---|
JPS57139039A (en) | 1982-08-27 |
EP0056500A3 (de) | 1982-11-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Designated state(s): CH DE FR GB IT NL |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Designated state(s): CH DE FR GB IT NL |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 19831023 |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: KASTNER, DIETRICH Inventor name: SUNDT, ERLING Inventor name: CHAPPAZ, ROGER |