JPS6075426A - Alcohol for cosmetic - Google Patents
Alcohol for cosmeticInfo
- Publication number
- JPS6075426A JPS6075426A JP58182494A JP18249483A JPS6075426A JP S6075426 A JPS6075426 A JP S6075426A JP 58182494 A JP58182494 A JP 58182494A JP 18249483 A JP18249483 A JP 18249483A JP S6075426 A JPS6075426 A JP S6075426A
- Authority
- JP
- Japan
- Prior art keywords
- ethanol
- residue
- alcohol
- wine
- cosmetics
- 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.)
- Pending
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 110
- 239000002537 cosmetic Substances 0.000 title abstract description 16
- 235000014101 wine Nutrition 0.000 claims abstract description 23
- 238000000855 fermentation Methods 0.000 claims abstract description 14
- 230000004151 fermentation Effects 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims description 13
- 241000219095 Vitis Species 0.000 claims description 6
- 235000009754 Vitis X bourquina Nutrition 0.000 claims description 6
- 235000012333 Vitis X labruscana Nutrition 0.000 claims description 6
- 235000014787 Vitis vinifera Nutrition 0.000 claims description 6
- 240000000560 Citrus x paradisi Species 0.000 claims description 5
- 239000002304 perfume Substances 0.000 abstract description 11
- 239000000706 filtrate Substances 0.000 abstract description 8
- 241000219094 Vitaceae Species 0.000 abstract description 4
- 238000009835 boiling Methods 0.000 abstract description 4
- 235000021021 grapes Nutrition 0.000 abstract description 4
- 230000000873 masking effect Effects 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 238000000605 extraction Methods 0.000 abstract description 2
- 239000002085 irritant Substances 0.000 abstract 2
- 231100000021 irritant Toxicity 0.000 abstract 2
- 239000003205 fragrance Substances 0.000 description 11
- 239000002994 raw material Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000001953 sensory effect Effects 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241000220317 Rosa Species 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- -1 colognes Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- OCLXJTCGWSSVOE-UHFFFAOYSA-N ethanol etoh Chemical compound CCO.CCO OCLXJTCGWSSVOE-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 238000013094 purity test Methods 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 235000015961 tonic Nutrition 0.000 description 2
- 230000001256 tonic effect Effects 0.000 description 2
- 229960000716 tonics Drugs 0.000 description 2
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- 244000178870 Lavandula angustifolia Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241001593968 Vitis palmata Species 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 235000019990 fruit wine Nutrition 0.000 description 1
- 239000001760 fusel oil Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、香水、オーデコロンその他の香粧料の原料と
して用いられるアルコールに係り、特にエタノールの刺
激臭をマスキングした香粧材用アルコールに関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to alcohol used as a raw material for perfumes, colognes, and other cosmetics, and particularly to alcohol for cosmetics that masks the pungent odor of ethanol.
香水、オーデコロン、頭髪化粧料その他の香粧料の主成
分であるエタノールは、収斂、清浄、殺菌、可溶化、乾
燥促進、刺激の付与などの目的で広く用いられている。Ethanol, which is the main component of perfumes, colognes, hair cosmetics, and other fragrances, is widely used for purposes such as astringency, cleansing, sterilization, solubilization, acceleration of dryness, and stimulation.
このエタノールは、一般に糖蜜類、澱粉質、パルプ廃液
等を原料として発酵法により作られるため、生産地や原
料等の相違によりかなり異なった固有の匂いと、焼くよ
うな味を有するものが多い。This ethanol is generally produced by fermentation using molasses, starch, pulp waste liquid, etc. as raw materials, so it often has unique smells and burnt tastes that vary depending on the place of production and raw materials.
合成法によるエタノールも近年無臭に近いもの1−
が入手できるようになってきてはいるが、これにても未
だ品質的に充分とはいえない。In recent years, ethanol produced by synthetic methods has become nearly odorless and has become available, but even this is still not of sufficient quality.
そこで、果実酒を蒸溜したり、地中海沿岸で栽培される
ジャスミン、ローズ、ラベンダー等の花精油を採取した
残渣を利用してエタノールの刺激臭をマスキングした香
粧材用アルコールが香水、オーデコロン類の溶剤として
使用されている。Therefore, alcohol for perfumes and colognes is produced by masking the pungent odor of ethanol by using the residue obtained by distilling fruit wine or extracting essential oils from flowers such as jasmine, rose, and lavender grown on the Mediterranean coast. Used as a solvent.
しかし、上記香粧材用アルコールのマスキング原料は生
産量が限定されているため少量且つ高価なものとなって
いる。However, since the production amount of the masking raw material for alcohol for cosmetic materials is limited, it is produced in small quantities and is expensive.
この発明は上記事情に鑑み、エタノールの刺激臭を効果
的にマスキングすると共に調合香料とも好適に調和しう
る高品質且つ廉価な香粧材用アルコールを得ることを主
目的とするものである。In view of the above-mentioned circumstances, the main object of the present invention is to obtain a high quality and inexpensive alcohol for perfumery materials which can effectively mask the pungent odor of ethanol and can suitably harmonize with blended fragrances.
本発明者らは、上記目的達成のため長年に亘る鋭意研究
の結果、ブドウ酒製造過程等で得られるブドウ果実発酵
残渣のエタノール可溶成分が、エタノールの刺激臭をマ
スキングし、且つ調合香料とも優れた調和を保つことを
知り、この発明を完成するに至ったものである。As a result of many years of intensive research to achieve the above objective, the present inventors have discovered that the ethanol-soluble components of the grape fruit fermentation residue obtained during the grape wine manufacturing process can mask the pungent odor of ethanol and can also be used as a blended flavor. Knowing that excellent harmony can be maintained, this invention was completed.
2−
即ち、この発明では、上記目的達成のためエタノールと
、ブドウ酒製造過程等で得られるブドウ果実発酵残渣の
エタノール可溶成分とからなるという技術手段を採った
。2- That is, in this invention, in order to achieve the above-mentioned object, a technical means is adopted which consists of ethanol and an ethanol-soluble component of the grape fruit fermentation residue obtained in the grape wine manufacturing process.
これにより、ブドウ酒製造過程等で得られるブドウ果実
発酵残渣のエタノール可溶成分に含まれた発酵臭によっ
て、エタノールの刺激臭がマスキングされると共に調合
香料とも優れた調和を保つことができる。As a result, the irritating odor of ethanol is masked by the fermentation odor contained in the ethanol-soluble components of the grape fruit fermentation residue obtained in the wine manufacturing process, etc., and excellent harmony can be maintained with the blended fragrance.
ここで、本発明で用いられるブドウ酒製造過程等で得ら
れるブドウ果実発酵残渣(以下、「ワイン滓」とする)
とは、ブドウ酒製造過程において常法によって得られた
ブドウ果実の滓を称し、一般にブドウ果実を破砕除梗機
にて果梗を除き、得られた果醪にブドウ酒酵母等を加え
て発酵せしめ、発酵終了後、残渣を圧搾機にかけて液部
を除いて得られるものであって、通常は赤ブドウ酒生産
用のものが用いられるが、これに限定されるものではな
い。Here, grape fruit fermentation residue (hereinafter referred to as "wine dregs") obtained in the grape wine manufacturing process etc. used in the present invention
refers to the dregs of grapes obtained by a conventional method during the grape wine manufacturing process, and generally the grapes are crushed and destemmed to remove the stems, and the resulting mash is fermented by adding wine yeast etc. After fermentation is complete, the residue is pressed to remove the liquid part, and is usually used for producing red grape wine, but it is not limited thereto.
また、この発明で用いられるエタノールは、特3−
に限定されるものではないが、工業用として、J IS
規格適合品であることが好ましく、所謂合成アルコール
でも発酵アルコールでもよい。In addition, the ethanol used in this invention is not limited to specific 3-
It is preferable to use a standard-compliant product, and so-called synthetic alcohol or fermented alcohol may be used.
このエタノールは、一般に無変性ものが好ましいが、化
粧品用変性アルコールを用いることもできる。Although undenatured ethanol is generally preferred, denatured alcohol for cosmetics may also be used.
次ぎに、本発明に係る香粧材用アルコールは、以下の如
くして製造することができる。Next, the alcohol for perfumery materials according to the present invention can be produced as follows.
ワイン滓1部(1重量部、以下同じ)に対し、工業用エ
タノール1〜100部を加え、室温〜80℃の温度下に
1〜10時間の間よく混和或いは攪拌するか、又は攪拌
せずに室温下に2〜3日間静置浸漬する。Add 1 to 100 parts of industrial ethanol to 1 part (1 part by weight, the same applies hereinafter) of wine dregs, and mix or stir well for 1 to 10 hours at a temperature of room temperature to 80°C, or without stirring. Leave to soak for 2 to 3 days at room temperature.
その後、上記抽出滓を濾別し、該濾液を40〜50ml
(gの減圧下にて蒸溜して沸点20〜40°Cの溜山部
を集めて完成する。減圧度は工業操作上10〜500m
m 11 gの範囲でよく、この場合上記に相当する
沸点範囲を適宜選ぶことができる。Thereafter, the extraction residue was filtered, and the filtrate was poured into 40 to 50 ml.
(It is completed by distilling under reduced pressure of 1.5 g and collecting the accumulated part with a boiling point of 20 to 40°C.The degree of reduced pressure is 10 to 500 m for industrial operation.
m 11 g, and in this case, the boiling point range corresponding to the above can be selected as appropriate.
また、別法として、ワイン滓より種子を除きこれを水分
1〜3%、アルコール分1〜2%まで乾4−
燥し、この顆粒をカラムに詰め、上方より工業エタノー
ルを徐々に滴下し、カラム下方より出たエタノールを含
む濾液を集め、前記と同様の条件下にて減圧蒸溜して製
造することもできる。Alternatively, the seeds are removed from the wine dregs and dried to a moisture content of 1-3% and alcohol content of 1-2%, the granules are packed in a column, and industrial ethanol is gradually dripped from above. It can also be produced by collecting the filtrate containing ethanol coming out from the bottom of the column and distilling it under reduced pressure under the same conditions as above.
このようにして得られる香粧材用アルコールは、エタノ
ール特有の刺激臭がマスキングされるばかりでなく、ワ
イン滓からの快い発酵臭がエタノールに付着するので香
粧材用として添加される調合香料とも極めて良好な調和
を保つことができ、理想的な香粧材用アルコールという
ことができる。The alcohol for perfumery materials obtained in this way not only masks the pungent odor peculiar to ethanol, but also has a pleasant fermentation odor from the wine dregs that adheres to the ethanol, so it can also be used as a blended fragrance added for perfumery materials. It can maintain extremely good harmony and can be said to be an ideal alcohol for cosmetics.
また、この発明では、今日のブドウ酒製造工業において
廃棄するのみであるワイン滓を有効利用することとなり
、資源の再利用となって産業上大きな利益をもたらす。Furthermore, the present invention makes effective use of wine dregs, which are only discarded in today's wine manufacturing industry, resulting in the reuse of resources, which brings great industrial benefits.
更に、上記ブドウ酒製造過程で生ずる発酵残渣は廉価に
且つ大量に人手しうろことから、この発明に係る香粧材
用アルコールのコストダウンを可能とし且つ大量生産に
も適するものとなる。Furthermore, since the fermentation residue produced in the grape wine production process can be produced manually in large quantities at low cost, it is possible to reduce the cost of the alcohol for perfumery materials according to the present invention, and it is also suitable for mass production.
この発明の香粧材用アルコールは、香水、オーデコロン
用のほか、化粧水、ヘアートニック、ヘ−5=
アーリキッド、セットローションその他エタノールを原
材料に用いる香粧材用に広汎に使用できることは言うま
でもない。Needless to say, the alcohol for cosmetics of this invention can be used not only for perfumes and colognes, but also for lotions, hair tonics, hair tonics, hair-5 liquids, setting lotions, and other cosmetics that use ethanol as a raw material. .
次に、実施例により本発明を更に詳しく説明する。Next, the present invention will be explained in more detail with reference to Examples.
尚、本実施例においては、本発明に係る香粧材用アルコ
ールの特性を示す意味で、他の調合香料に比して最もエ
タノール臭を強く感じ易いローズ系調合香料を用いた。In this example, in order to demonstrate the characteristics of the alcohol for cosmetic materials according to the present invention, a rose-based blended fragrance, which has the strongest ethanol odor compared to other blended fragrances, was used.
実施例−1
ワイン滓100gに工業用エタノール1000 gを加
え、室温で2時間、攪拌した。次いでガラスフィルター
(G3)で濾過し、紫色のエタノール含有濾液1060
gを得た。この紫色エタノール含有濾液を50mmHH
の減圧下に蒸溜し沸点20〜40℃の溜置720gを水
冷下の受器内に得た。得たる溜置(香粧利用アルコール
完成品)は比重0.8153 (15℃)で純度試験の
結果は化粧品用原料標準規格に合格した。Example-1 1000 g of industrial ethanol was added to 100 g of wine dregs, and the mixture was stirred at room temperature for 2 hours. Then, it was filtered through a glass filter (G3), and the purple ethanol-containing filtrate 1060
I got g. This purple ethanol-containing filtrate was heated to 50 mmHH.
720 g of distillate having a boiling point of 20 to 40 DEG C. was obtained in a water-cooled receiver. The resulting reservoir (finished alcohol product for use in perfumery) had a specific gravity of 0.8153 (15°C), and the purity test passed the standards for raw materials for cosmetics.
純度試験の結果は下記の通りである。The results of the purity test are as follows.
■ 溶状 上記により得られた香粧料用アルコ6−
−ル完成品(以下、本節とする) 10m1に水30m
1を加えて振りまぜ8〜10℃の恒温槽中に30分間放
置したとき澄明であった。■ Solution Finished alcohol 6--alcohol product for perfume and cosmetics obtained as above (hereinafter referred to as this section) 10 ml of water 30 ml
1 was added, shaken, and left in a constant temperature bath at 8 to 10°C for 30 minutes.The mixture was clear.
■ 酸又はアルカリ 本節20m1に蒸溜水20m l
及びフェノールフタレン試薬3滴を加えたときに変色せ
ず、これに0.IN水酸化ナトリウム液0.1mlを加
えたとき、紅色を呈した。■ Acid or alkali: 20ml of main section, 20ml of distilled water
There was no discoloration when 3 drops of phenolphthalene reagent was added, and 0. When 0.1 ml of IN sodium hydroxide solution was added, a red color appeared.
■ 塩化物 本節101に硝酸銀試液2滴を加えて5分
間放置したが何等変化は認められなかった。■ Chloride Two drops of silver nitrate test solution were added to Section 101 and left for 5 minutes, but no change was observed.
■ 重金属 本節30m1に希酢酸2ml及び水を加え
て50m1とし、これを試験溶液として第4法により試
験を行った結果、重金属量は0.9ppmであった。■ Heavy metals 2 ml of dilute acetic acid and water were added to 30 ml of this section to make 50 ml, and this was used as a test solution for testing according to method 4, and the amount of heavy metals was 0.9 ppm.
■ フーゼル油及び類似不純物 本節10m1に水5m
l及びグリセリン1mlを加え、濾紙上に滴加し、常温
で放置して揮散せしめても異臭を残さなかった。■ Fusel oil and similar impurities 10m1 of this section and 5m of water
1 and 1 ml of glycerin were added, added dropwise onto a filter paper, and left at room temperature to evaporate without leaving any odor.
本節5mlを、硫酸5mlを入れた試験管内に注意して
層積したが、その接界面は紅色を呈しなかった。5 ml of this section was carefully layered in a test tube containing 5 ml of sulfuric acid, but the contact surface did not turn red.
■ アルデヒド又はその他の還元性物質 本節7−
7−1Oに15℃で0.IN過マンガン酸カリウム液0
.3mlを加え、同温で20分間放置しても紅色は消失
しなかった。■ Aldehyde or other reducing substance This section 7-7-1 O at 15°C. IN potassium permanganate solution 0
.. Even after adding 3 ml of the solution and leaving it for 20 minutes at the same temperature, the red color did not disappear.
本節10m1に水酸化ナトリウム試液5mlを加えて5
分間放置しても黄色を呈さなかった。Add 5 ml of sodium hydroxide test solution to 10 ml of this section.
It did not turn yellow even after being left for a minute.
■ メタノール及びアセトン メタノール及びアセトン
試験に適合した。■ Methanol and acetone Passed the methanol and acetone test.
■ 蒸発残留物 本節40m1を水浴上で蒸発し、残留
物を105℃で1時間乾燥した時の残渣は0.8mgで
あった・
■ 匂い 無色透明な液体でかすかに甘い発酵臭を感す
る。■ Evaporation residue When 40ml of this section was evaporated on a water bath and the residue was dried at 105°C for 1 hour, the residue was 0.8mg. ■Odor A colorless and transparent liquid with a slightly sweet fermented odor.
実施例−2
ワイン滓200gに工業用エタノール2000 gを加
え、攪拌下にて1時間70〜80℃で煮沸還流した。そ
の後冷却して、濾過して紫色のエタノール含有濾液を得
た。次いで実施例−1と同様な操作により溶分1420
gを得た。この溶分(香粧材用アルコール完成品)の
品質は実施例1とほぼ同様であった。Example 2 2000 g of industrial ethanol was added to 200 g of wine dregs, and the mixture was boiled and refluxed at 70 to 80° C. for 1 hour while stirring. It was then cooled and filtered to obtain a purple ethanol-containing filtrate. Then, by the same operation as in Example-1, the solubilities 1420
I got g. The quality of this dissolved component (finished alcohol product for perfumery materials) was almost the same as in Example 1.
−8=
実施例−3
ワイン滓100gに工業用エタノール1.000gを加
え、よく攪拌して均一とした後、室温(約20’C)に
て2昼夜放置した。その後、これを濾過し、この濾液を
実施例−1と同様な操作により溶分715gを得た。こ
の溶分(香粧材用アルコール完成品)の品質は実施例−
1とほぼ同様であった。-8= Example-3 1.000 g of industrial ethanol was added to 100 g of wine dregs, stirred well to make it homogeneous, and then left at room temperature (approximately 20'C) for 2 days and nights. Thereafter, this was filtered, and the filtrate was subjected to the same operation as in Example-1 to obtain 715 g of a solvate. The quality of this dissolved content (alcohol finished product for perfumery materials) is shown in Example-
It was almost the same as 1.
実施例−4
ワイン滓1 kgを挽肉機でミンチとし糸状に押出し、
これを天火で2日間乾燥し、水分2.2%(カールフィ
シャー法)アルコール分1.4%(蒸発水分比重測定法
)の顆粒を得、該顆粒を下方を直径1cmに絞り、その
上に03のフィルターをつけた直径5c111のガラス
製円筒管に詰め、上方より5kgの工業用エタノールを
毎分10〜50m1の速度で注いだ。下方より流出する
着色エタノール含有濾液を合計3.7kg集めた。これ
を実施例−1と同様の操作により溶分2.59Kgを得
た。この得られた溶分(香粧材用アルコール完成品)の
品質は実施例1とほぼ同様であった。Example-4 1 kg of wine dregs was minced using a meat grinder and extruded into threads.
This was dried in the open fire for 2 days to obtain granules with a water content of 2.2% (Karl Fischer method) and an alcohol content of 1.4% (evaporation water specific gravity measurement method).The lower part of the granules was squeezed to a diameter of 1 cm, and then It was packed in a glass cylindrical tube with a diameter of 5c111 equipped with a No. 03 filter, and 5kg of industrial ethanol was poured from above at a rate of 10 to 50ml per minute. A total of 3.7 kg of colored ethanol-containing filtrate flowing out from the bottom was collected. This was subjected to the same operation as in Example-1 to obtain 2.59 kg of soluble matter. The quality of the obtained dissolved substance (finished alcohol product for perfumery materials) was almost the same as in Example 1.
9−
実施例−5
下記の処方に従って香水を作り、その比較官能テストを
行った。9- Example-5 A perfume was made according to the following recipe and a comparative sensory test was conducted.
処方:ローズ系調合香料 BP−147320重量%(
高砂香料工業@製)
エタノール*80重量%
*エタノールA:化粧品用原料標準規格品、未処理の工
業用エタノール
エタノールB:実施例−1により製造されたこの発明の
香粧材用アルコー
ル
10人の熟練した官能パネラ−(以下、単にパネラとす
る)を用い、エタノールの刺激臭につき4段階法による
官能テストを行った結果、下記の表■に示す如くこの発
明の香粧材用アルコールを使用した香水は、エタノール
の刺激臭が少な(且つ、調合香料との調和もよく、望ま
しい結果を得た。Prescription: Rose-based blended fragrance BP-147320% by weight (
(manufactured by Takasago Fragrance Industry @) Ethanol*80% by weight *Ethanol A: Standard raw material for cosmetics, untreated industrial ethanol Ethanol B: Alcohol for perfumery materials of this invention produced according to Example-1 10 samples Using a skilled sensory panelist (hereinafter simply referred to as Panela), we conducted a sensory test on the pungent odor of ethanol using a four-step method, and as a result, the alcohol for perfumery materials of the present invention was used as shown in Table 1 below. The perfume had less pungent odor from ethanol (and harmonized well with the blended perfume, giving desirable results).
10−
表■
一11一
実施例−6
下記の処方に従ってオーデコロンを作り、その比較官能
テストを行った。10-Table ■-111-Example-6 Eau de cologne was prepared according to the following recipe and a comparative sensory test was conducted.
処方二ローズ系調合香料 BP−30025重量%(高
砂香料工業■製)
エタノール*95重量%
*エタノールA:化粧品用原料標準規格品、未処理の工
業用エタノール
エタノールB:実施例−1により製造されたこの発明の
香粧材用アルコー
ル
8人の熟練した官能パネラ−を用い官能テストを行った
結果、下記の表Hに示す如くこの発明に係る香粧材用ア
ルコールを使用したオーデコロンはエタノールの刺激臭
が少なく且つ調合香料との調和も優れている、との評価
を得た。Prescription Two-rose compound fragrance BP-300 25% by weight (manufactured by Takasago International Co., Ltd.) Ethanol*95% by weight *Ethanol A: Standard raw material for cosmetics, untreated industrial ethanol Ethanol B: Manufactured according to Example-1 Alcohol for perfumery according to this invention As a result of a sensory test conducted using eight experienced sensory panelists, as shown in Table H below, the cologne using the alcohol for perfumery according to this invention has the same irritation as ethanol. It was evaluated as having little odor and blending well with blended fragrances.
尚、エタノールの刺激臭の評価法は実施例−5と同じで
ある。The method for evaluating the pungent odor of ethanol was the same as in Example-5.
12− 表■ 出願人 高砂香料工業株式会社 代理人 西 良 久 13−12- Table ■ Applicant: Takasago Fragrance Industries Co., Ltd. Agent Yoshihisa Nishi 13-
Claims (1)
るブドウ果実発酵残渣のエタノール可溶成分からなる香
粧材用アルコール。(1) An alcohol for perfumery materials consisting of ethanol and ethanol-soluble components of grape fruit fermentation residue obtained in the grape wine manufacturing process.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58182494A JPS6075426A (en) | 1983-09-30 | 1983-09-30 | Alcohol for cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58182494A JPS6075426A (en) | 1983-09-30 | 1983-09-30 | Alcohol for cosmetic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6075426A true JPS6075426A (en) | 1985-04-27 |
Family
ID=16119265
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58182494A Pending JPS6075426A (en) | 1983-09-30 | 1983-09-30 | Alcohol for cosmetic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6075426A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02169510A (en) * | 1988-12-23 | 1990-06-29 | T Hasegawa Co Ltd | Flavor composition containing alcoholic beverage aroma concentrate and/or cosmetics |
| FR2804864A1 (en) * | 2000-02-11 | 2001-08-17 | Serobiologiques Lab Sa | RESIDUE EXTRACTS FROM WINE MANUFACTURING AND THEIR USE IN COSMETICS OR PHARMACOLOGY |
| JP2006001932A (en) * | 2004-06-15 | 2006-01-05 | Botica Comercial Farmaceutica Ltda | Composition for personal care product, cosmetic and perfume |
-
1983
- 1983-09-30 JP JP58182494A patent/JPS6075426A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02169510A (en) * | 1988-12-23 | 1990-06-29 | T Hasegawa Co Ltd | Flavor composition containing alcoholic beverage aroma concentrate and/or cosmetics |
| FR2804864A1 (en) * | 2000-02-11 | 2001-08-17 | Serobiologiques Lab Sa | RESIDUE EXTRACTS FROM WINE MANUFACTURING AND THEIR USE IN COSMETICS OR PHARMACOLOGY |
| WO2001058412A3 (en) * | 2000-02-11 | 2002-01-17 | Cognis France Sa | Extracts from residues left in the production of wine |
| JP2006001932A (en) * | 2004-06-15 | 2006-01-05 | Botica Comercial Farmaceutica Ltda | Composition for personal care product, cosmetic and perfume |
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