TWI712424B - 乳化組合物及粉末組合物 - Google Patents
乳化組合物及粉末組合物 Download PDFInfo
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- TWI712424B TWI712424B TW106111047A TW106111047A TWI712424B TW I712424 B TWI712424 B TW I712424B TW 106111047 A TW106111047 A TW 106111047A TW 106111047 A TW106111047 A TW 106111047A TW I712424 B TWI712424 B TW I712424B
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- bitterness
- emulsified composition
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- emulsified
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Classifications
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- C11B9/00—Essential oils; Perfumes
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
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- A23L27/29—Fruit flavours
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
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- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/88—Taste or flavour enhancing agents
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/10—Foods or foodstuffs containing additives; Preparation or treatment thereof containing emulsifiers
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
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- A61K8/35—Ketones, e.g. benzophenone
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- 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
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Emergency Medicine (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Confectionery (AREA)
- General Preparation And Processing Of Foods (AREA)
- Non-Alcoholic Beverages (AREA)
- Detergent Compositions (AREA)
- Seasonings (AREA)
Abstract
Description
本發明係關於一種乳化組合物及粉末組合物,其係作為具有特異之香氣與苦味的香氣賦予或香氣調變劑或苦味賦予用之香味調變劑而有用且含有特定之薄荷基醚類。本發明亦係關於一種含有該等乳化組合物及粉末組合物之飲食品及香妝品。本發明亦係關於一種使用該等乳化組合物及粉末組合物之飲食品或香妝品之香氣賦予或香氣調變方法及飲食品之苦味賦予方法。
人除了藉由食物而攝取能量源以外,亦感受到食物帶來之身體狀況之維持、由食物之美味或食感帶來之滿足感,食物對於人發揮著重要之功能。食物之美味據說係源於飲食品之碳水化合物、脂肪等營養成分,並且其飲食品之味道與香氣亦為重要之要素。用口所感覺到之味覺、與用鼻所感覺到之嗅覺雖然為獨立之感覺,但根據近年之研究,據說於飲食時,味覺與嗅覺於腦內進行整合,作為食物之美味與食物之滿足感而被認知。 關於飲食品之香氣,據說雖然由鼻所吸入之香氣被鼻黏膜所感知之鼻腔香氣(前鼻腔香氣)亦較為重要,但飲食品經口腔刺激味覺,感知由咽喉傳入至鼻之香氣之口腔香氣(後鼻腔香氣)最為重要。 自先前,作為有氣味之物質,已知有刺激嗅覺,同時亦對味覺賦予刺激之化合物。作為此種化合物之代表性之例所知之薄荷腦具有強力之清涼香與分配至黏膜之刺激感,廣泛用於各種飲食品、香妝品中。同時,關於味覺,已知具有特有之苦味。於使用薄荷腦之情形時,對於作為對象之飲食品、香妝品,該等性質存在有利地發揮作用之情形、與不利地發揮作用之情形。 例如,於為了獲得薄荷腦之清涼感而用於飲食品之情形時,由於揮發性較高,故而指出有清涼感不持續、及其特有之苦味為不利之方面。因此,多數創作用以克服作為該薄荷腦所存在之缺點之苦味之掩蔽方法。舉一例,揭示有使用作香料之縮水甘油酸酯成為苦味之掩蔽劑(專利文獻1)。 另一方面,為了使薄荷腦之清涼感持續,同時抑制苦味,亦廣泛進行將薄荷腦之化學結構進行變更之嘗試,合成有用之衍生物。為此所開發之化合物係合成利用薄荷腦之羥基之酯衍生物、於薄荷腦之構成碳骨架中導入有羧酸之對薄荷烷羧酸衍生物。作為更具體之化合物,已知有:3-羥基丁酸薄荷酯、薄荷腦甘油醚(Coolact 10,高砂香料公司註冊商標,專利文獻2)、乳酸薄荷酯(Frescolate ML,Symrise AG公司註冊商標)、丁二酸單薄荷酯(Physcool,V.Mane fils公司註冊商標)、N-乙基對薄荷烷羧醯胺(WS-3)、2-[(5-甲基-2-丙烷-2-基環己烷羰基)胺基]乙酸乙酯(WS-5)、N-(4-甲氧基苯基)對薄荷烷羧醯胺(WS-12)、N,2,3-三甲基-2-異丙基丁醯胺(WS-23)等(專利文獻3)。該等化合物係以具有清爽之香氣、具有清涼感持續作用、無苦味為特徵,以化合物單一成分、或藉由與薄荷腦併用而用於各種製品中。 另一方面,苦味係表現食品之特徵之重要之構成要素,作為苦味成分,有:澀柿子、葡萄酒等中所含之單寧、茶中所含之兒茶素、咖啡中所含之綠原酸、蛇麻草中所含之具有啤酒之苦味之特徵之阿爾法酸等。該等成分分別具有特有之苦味,於構成包含該等之飲食品之方面,被認識為重要之化合物(非專利文獻1)。然而,源自天然之苦味原材料由於除了特有之苦味以外,亦具有源於原料之天然物特有之香味,故而僅限於在通常之飲食品之應用。因此,期待具有優良品質之苦味之化合物之開發,而不是源於原材料之天然物特有之香氣。 應用有薄荷腦特有之刺激與苦味之例較少,僅揭示有為了防止藥物之亂用而添加薄荷腦之例(專利文獻4)。又,薄荷腦由於具有強力之清涼香,故而先前為了賦予苦味而於通常之飲食品中調整較為困難。尚未知有為了克服該缺點而追求薄荷腦特有之苦味作為優良品質之苦味,同時為了抑制強力之清涼香而研究薄荷腦衍生物之嘗試。 [先前技術文獻] [專利文獻] [專利文獻1]日本專利第5198533號公報 [專利文獻2]日本專利特開昭58-88334號公報 [專利文獻3]日本專利特開昭47-16648號公報 [專利文獻4]日本專利特表2005-500364號公報 [非專利文獻] [非專利文獻1]山田恭正,「New Food Industry」2002年,44卷,2號,49~55頁
[發明所欲解決之問題] 因此,本發明者等人鑒於上述課題,對於提供具有無雜味之苦味且以抑制冰涼感及清涼感之薄荷腦衍生物作為有效成分之香味調變劑進行努力研究,其結果為,發現2-甲基-4-薄荷基氧基-2-丁醇等特定之薄荷基醚類較為有用,先前進行過專利申請(日本專利特開2016-84418號公報)。 該等化合物係抑制如薄荷腦及其衍生物中常見之冰涼感及清涼感,香氣中具有稍稍木質、辛辣且青草之香氣,且關於苦味,具有無雜味之優良品質之苦味且使該苦味持續者。然而,為了對飲食品進行苦味賦予而調配,期待藉由延遲苦味之上升,製成更清爽且溫和之苦味,而於飲食品中取得甜味、酸味等之平衡。又,該等薄荷基醚類為油溶性,故而於調配於水分較多之食品中之情形時,有難以均勻地混合,於保存中分離等問題方面。 因此,本發明所欲解決之課題在於提供一種乳化組合物及粉末組合物,其容易調配於飲食品或香妝品中,進而苦味之上升較慢,具有清爽且溫和之苦味。 [解決問題之技術方法] 本發明者等人進而對於4-薄荷基氧基-2-丁酮等特定之薄荷基醚類進行努力研究,結果發現:可藉由製成含有特定之薄荷基醚類之乳化組合物、或在製成乳化組合物後進行乾燥而成為粉末組合物之形態,而容易調配於飲食品或香妝品中,又,尤其於添加於飲食品中之情形時,一面維持尖銳之苦味特性,一面製成與不製成乳化組合物之情形相比,延遲苦味之上升且更清爽且溫和之苦味,從而完成本發明。再者,本發明者等人亦發現:可藉由將油脂調配於乳化組合物中而使苦味持續更長時間。 再者,本發明中作為薄荷基醚類所揭示之4-薄荷基氧基-2-丁酮雖然為有機化學研究中所合成之化合物,但關於其香味之特性並無任何記載,關於其衍生物亦未發現報告(Tetrahedron Lett., 47, 2905(2006))。 如此,本發明係提供以下者。 [1]一種乳化組合物,其含有下述(A)~(D): (A)下述式(1)所表示之薄荷基醚類; [化1][式(1)中,X表示部分結構式(1-a)或(1-b),R1
及R2
表示甲基、乙基、丙基或異丙基] (B)水; (C)選自糖類、一元醇或多元醇中之一種以上;及 (D)乳化劑。 [2]如[1]之乳化組合物,其進而含有(E)食用油脂類。 [3]如[1]或[2]中記載之乳化組合物,其中薄荷基醚類為下述式(2)所表示之2-甲基-4-薄荷基氧基-2-丁醇。 [化2][4]一種粉末組合物,其係使如[1]至[3]中任一項記載之乳化組合物乾燥而成。 [5]一種飲食品,其含有如[1]至[3]中任一項記載之乳化組合物或如[4]中記載之粉末組合物。 [6]一種香妝品,其含有如[1]至[3]中任一項記載之乳化組合物或如[4]中記載之粉末組合物。 [7]一種飲食品或香妝品之香氣賦予或香氣調變方法,其係藉由含有如[1]至[3]中任一項記載之乳化組合物或如[4]中記載之粉末組合物而進行。 [8]一種飲食品之苦味賦予方法,其係藉由使如[1]至[3]中任一項記載之乳化組合物或如[4]中記載之粉末組合物含有於飲食品中而進行。 [發明之效果] 含有特定之薄荷基醚類之本發明之乳化組合物或粉末組合物無雜味而優良品質且具有銳利苦味,與未進行乳化之上述薄荷基醚類相比,可製成延遲苦味之上升,更清爽且溫和之苦味。其結果為,可賦予如使人想起柚皮苷等柑橘類之苦味的苦味。 又,於本發明之較佳之態樣中,含有特定之薄荷基醚類之本發明之乳化組合物或粉末組合物具有少許之冰涼感及清涼感、與稍稍之木質、辛辣且青草之香氣。 又,於本發明之較佳之態樣中,藉由於上述乳化組合物中調配油脂,可使上述薄荷基醚類特有之苦味持續更長時間。藉由將該等本發明之乳化組合物或粉末組合物作為香氣賦予或香氣調變劑或苦味賦予用之香味調變劑而調配於香料組合物、飲食品中,可利用香氣與優良品質之苦味開發具有目前所未知之新的香味之飲食品,可擴展於新的應用範圍中。
本發明係關於一種乳化組合物及粉末組合物,其含有:(A)式(1)所表示之薄荷基醚類、(B)水、(C)選自糖類、一元醇或多元醇中之一種以上、及(D)乳化劑。式(1)所表示之薄荷基醚類係未進行乳化等,顯示出作為其自身、香氣賦予或香氣調變劑或苦味賦予用之香味調變劑、冰涼感賦予劑、苦味賦予劑之效果而具有有用性。再者,所謂「香氣賦予或香氣調變」之用語中之「或」係與「及/或」為相同意義。 然而,可藉由製成含有(A)式(1)所表示之薄荷基醚類、(B)水、(C)選自糖類、一元醇或多元醇中之一種以上、及(D)乳化劑之乳化組合物或粉末組合物,而提高於水中之分散性,容易調配於飲食品或香妝品中,同時延遲苦味之上升,使其更清爽且溫和。又,可藉由視需要於上述乳化組合物中含有食用油脂類,進而增加食用油脂類之含量,而使薄荷基醚類之苦味持續更長時間。進而,含有式(1)中所表示之薄荷基醚類之乳化組合物或粉末組合物較佳為於保存時亦穩定。 例如,於為了賦予香氣與苦味而於葡萄柚風味飲料中調配2-甲基-4-薄荷基氧基-2-丁醇之情形時,若於油溶性香料中調配並添加,則油溶性香料油脂上浮,使油中所含之2-甲基-4-薄荷基氧基-2-丁醇直接作用於口腔內。另一方面,於製成乳化組合物之情形時,2-甲基-4-薄荷基氧基-2-丁醇之微細之粒子均勻地作用於口腔內。其結果為,可進而賦予類似葡萄柚之苦味。 製成本發明之乳化組合物或粉末組合物之薄荷基醚類與未進行乳化之薄荷基醚類相比,苦味之上升變慢,使伴隨其之苦味感覺更加清爽且溫和。 作為本發明之乳化組合物或粉末組合物中所使用之式(1)所表示之薄荷基醚類,並無特別限定,具體而言,可例示:式(3)所表示之4-薄荷基氧基烷基酮,例如4-薄荷基氧基-2-丁酮。又,可例示:式(4)所表示之烷基-4-薄荷基氧基烷醇,例如式(2)所表示之2-甲基-4-薄荷基氧基-2-丁醇等,但並不限定於此。式(1)中之R1
及R2
分別獨立地表示甲基、乙基、丙基或異丙基,可相互相同亦可不同。R1
及R2
較佳為甲基。 為了獲得式(1)所表示之薄荷基醚類,可依據以下所示之反應式1,藉由步驟(1)而合成式(3)所表示之4-薄荷基氧基烷基酮,進而藉由步驟(2)而合成式(4)所表示之烷基-4-薄荷基氧基烷醇。 [化3]反應式1:[R1
及R2
表示甲基、乙基、丙基或異丙基;M表示Li或MgX,X表示鹵素原子] 若對反應式1之各步驟進行概括說明,則作為步驟(1),於觸媒之存在下使薄荷腦與烷基乙烯基酮進行麥可型加成反應,合成式(3)所表示之4-薄荷基氧基烷基酮。作為步驟(2),可藉由於步驟(1)中所獲得之式(3)所表示之4-薄荷基氧基烷基酮中,使烷基金屬試劑進行反應而合成式(4)所表示之烷基-4-薄荷基氧基烷醇。 以下,詳細地說明步驟(1)及步驟(2)。作為步驟(1)之原料所使用之薄荷腦(2-異丙基-5-甲基環己醇)雖然存在8種異構物,但較理想為使用具有優異之香氣之天然型之l-薄荷腦,但並不限定於此。作為一者之反應模塊之烷基乙烯基酮係3-丁烯-2-酮(甲基乙烯基酮)、1-戊烯-3-酮(乙基乙烯基酮)、1-己烯-3-酮(丙基乙烯基酮)或4-甲基-1-戊烯-3-酮(異丙基乙烯基酮),雖然均可自市場採購,但亦可依據已知之方法進行合成而使用。 用於步驟(1)之反應之烷基乙烯基酮只要相對於薄荷腦為當量以上,則並無特別制約,但就經濟性之觀點而言,可列舉:1.5當量至5當量,較佳為可列舉:2當量至4等量。 於麥可型加成反應中觸媒之利用較為有效,可利用酸性型或鹼性型之觸媒。關於酸性型觸媒,例如作為布忍斯特酸觸媒,可列舉:硫酸、鹽酸、磷酸、對甲苯磺酸等,較佳為使用對甲苯磺酸。又,可列舉:作為路易斯酸觸媒之三氟化硼醚錯合物、四氯化鈦、三氯化鋁等,較佳為使用三氟化硼醚錯合物。亦可使用鹼性型之觸媒,亦可使用:三級胺類、氫氧化四級烷基胺類。 步驟(1)之反應即便於無溶劑之情況下亦進行,但亦可使用溶劑,較佳為於反應原料之薄荷腦、烷基乙烯基酮及使用之觸媒中具有不活性之性質之溶劑,更佳為使用:甲苯、庚烷、己烷等烴溶劑、二乙醚等醚系觸媒、二氯甲烷等氯系溶劑,更佳為使用:二氯甲烷等氯系溶劑。 反應溫度雖然受到使用之觸媒之使用量及/或活性、及使用之溶劑之影響,但可列舉較佳為-78℃~50℃,進而較佳為0℃~30℃之溫度條件。又,反應時間雖然受到使用之觸媒之使用量及/或活性、及使用之溶劑之影響,但並無特別限制,可列舉:數小時至數天。反應時間可一面利用氣相層析法或薄層層析法等監測反應之進行一面決定反應時間。步驟(1)中所獲得之式(3)所表示之4-薄荷基氧基烷基酮可視需要使用管柱層析法、減壓蒸餾等方法進行精製。 於步驟(2)中,藉由使式(3)所表示之4-薄荷基氧基烷基酮之羰基與烷基金屬試劑進行加成反應,而合成式(4)所表示之烷基-4-薄荷基氧基烷醇。與式(3)所表示之4-薄荷基氧基烷基酮進行反應之鹼金屬化合物可使用:甲基鋰、乙基鋰、丙基鋰等烷基鋰或氯化甲基鎂、溴化甲基鎂、氯化乙基鎂、溴化乙基鎂等烷基格里納德試劑。該等烷基金屬試劑可為自市場所採購者,亦可使用自對應之金屬與鹵化烷基所製備之試劑。用於反應之烷基金屬試劑較佳為相對於式(3)所表示之4-薄荷基氧基烷基酮使用等莫耳至2倍莫耳,尤佳為使用1.05倍莫耳至1.5倍莫耳。 使用之反應溶劑雖然取決於使用之烷基金屬試劑之性質,但只要為通常於烷基金屬試劑中於不活性之狀態下使烷基金屬試劑分散於溶劑中,並使作為反應基質之式(3)所表示之4-薄荷基氧基烷基酮進行溶解之溶劑,則並無特別限制,例如較佳為使用:二乙醚、甲基第三丁醚、四氫呋喃、1,4-二㗁烷。 反應條件雖然受到使用之烷基金屬試劑之性質之影響,但由於通常羰基化合物與烷基金屬試劑之反應為發熱反應,受到溶劑中之水分、於氣體中或溶劑中溶存之氧之影響,故而較佳為於回避該等之反應條件下進行,較佳為於氮氣氣體下使用經脫水之溶劑等。 反應溫度雖然受到使用之烷基金屬試劑之種類、使用之溶劑之影響,但較佳為-78℃~40℃,進而較佳為0℃~30℃之溫度條件。又,反應時間雖然受到使用之烷基金屬試劑之種類、使用之溶劑之影響,但以數小時結束反應。較佳為一面利用氣相層析法或薄層層析法等監測反應之進行一面決定反應時間。步驟(2)中所獲得之式(4)所表示之烷基-4-薄荷基氧基烷醇較佳為視需要使用管柱層析、減壓蒸餾等方法進行精製。 式(1)所表示之薄荷基醚類可以兩種以上任意之比率進行混合而用於本發明之乳化組合物,亦可尤其利用與其他清涼感持續劑之併用,而發揮將清涼感之持續與薄荷腦之苦味進行改質之效果。 含有式(1)所表示之薄荷基醚類之本發明之乳化組合物並無特別限定,可採用利用公知之方式將式(1)所表示之薄荷基醚類進行乳化而成者,例如,可除了作為(A)之作為香味調變化合物成分之式(1)所表示之薄荷基醚類以外,亦包含(B)水、(C)選自糖類、一元醇或多元醇中之一種以上、(D)乳化劑,將該等進行混合、攪拌及乳化而獲得。 上述乳化時,例如可將(A)式(1)所表示之薄荷基醚類作為油相部,將(B)水及(C)選自糖類、一元醇或多元醇中之一種以上作為水相部,而製備為水中油型(Oil-in-water型;O/W型)乳化組合物。 藉此,使式(1)所表示之薄荷基醚類之苦味之上升與不製成乳化組合物之情形相比更慢,使伴隨其之苦味感到更清爽且溫和。再者,苦味之上升較慢之意思,係指自包含於口腔中開始稍稍遲緩地感到苦味。苦味通常為忌避之味道,當苦味物質進入至口腔中時,立即表現出苦味,賦予較強之衝擊之某種不快感之情況較多。然而,苦味物質中亦具有表現較佳之苦味者。例如,柑橘中所含之柚皮苷據說於柑橘果實或柑橘果汁中呈現出清爽且溫和之苦味。本發明之乳化組合物具有接近該柑橘中之柚皮苷之苦味之味道特性。 又,於上述油相部中,除了(A)式(1)所表示之薄荷基醚類以外,亦可含有(E)食用油脂類。藉由視需要於上述乳化組合物中含有食用油脂類,可使苦味持續更長時間。上述食用油脂類之調配量對苦味之持續時間產生影響。即,藉由增加食用油脂類之調配量,可使苦味之持續時間變成更長時間,藉由降低食用油脂類之調配量,可相對地縮短苦味之持續時間。 又進而,於用以使式(1)所表示之薄荷基醚類溶解之劑(例如油相部)中,亦可除上述食用油脂類以外,含有SAIB(蔗糖・二乙酸酯・六異丁酸酯)作為比重調整劑,或含有通常之各種香料作為式(1)所表示之薄荷基醚類以外之香味成分。 作為可使用之(E)成分之食用油脂類,較佳為容易與式(1)所表示之薄荷基醚類進行混和者,例如可列舉:大豆油、芝麻油、玉米油、菜籽油、米糠油、棉籽油、蓖麻油、花生油、橄欖油、棕櫚油、紅花油、小麥胚芽油、椰子油、葵花籽油、山茶油、可可脂、鯡魚油、鮭魚油、青花魚油、鯊魚油、鯖科金槍魚油、鯨油、海豚油、墨魚油、秋刀魚油、鯡魚油、鱈魚油、牛脂、雞油、豬油、黃油等動植物油脂類及其等之硬化油類、中鏈飽和脂肪酸甘油三酸酯(以下,稱為MCT)等。尤佳為MCT。作為該MCT,例如可列舉:己酸三甘油脂、辛酸三甘油脂、癸酸三甘油脂、月桂酸三甘油脂、及如其等之任意之混合物般之碳原子數6~12之中鏈飽和脂肪酸之甘油三酸酯,其等之中,尤佳為:辛酸三甘油脂、癸酸三甘油脂及其等之任意之混合物。該等MCT混合物可於市場上廉價且容易地獲得。本發明之乳化組合物中之食用油脂類之含量雖無特別限定,但相對於式(1)所表示之薄荷基醚類1質量份,可為通常為0.01~2000質量份,較佳為0.1~500質量份,更佳為0.5~100質量份,進而較佳為2~50質量份之範圍內。 SAIB(蔗糖・二乙酸酯・六異丁酸酯)係用以調整本發明之乳化組合物中之油相部之比重而調配者,於調配有本發明之乳化組合物之最終製品(飲食品、香妝品)為水性組合物之情形時,可調配以防止乳化組合物因比重差而分離。 作為可使用之SAIB,例如可列舉:其比重為約1.13~約1.19,較佳為約1.14~約1.15之範圍內之SAIB。本發明之乳化組合物中之SAIB之含量可根據使用之SAIB之比重、調配有乳化組合物之飲料之比重等而變化,但通常,較理想為本發明之乳化組合物中之油相部整體之比重、與作為調配有本發明之乳化組合物之最終製品之水性組合物(例如本發明之飲食品或香妝品)之比重差成為0.05以下,尤其成為0.03以下之量。若該比重差為0.05以下,則於將調配有本發明之乳化組合物之水性組合物長期保存之情形時,不易發生環圈或油脂上浮。關於油相部中之SAIB之混合比率,於將含有SAIB之油相部整體設為1質量份之情形時,通常可例示約0.2質量份~約0.6質量份,較佳為可例示約0.3質量份~約0.5質量份之範圍內。然而,較理想為最終一面測定調配有本發明之乳化組合物之水性組合物之比重及該乳化組合物中之油相部之比重一面經驗性地發現比重差成為0.05以下之SAIB之含量。 作為式(1)所表示之薄荷基醚類以外之香味成分,作為通常之各種香料(可與式(1)所表示之薄荷基醚類一同含有之其他通式之各種香料),例如作為清涼感持續劑,可列舉:3-羥基丁酸薄荷酯、薄荷腦甘油醚(Coolact 10,高砂香料公司之註冊商標)、乳酸薄荷酯(Frescolate ML,Symrise AG公司之註冊商標)、丁二酸單薄荷酯(Physcool,V.Mane fils公司之註冊商標)、N-乙基-對薄荷烷羧醯胺(WS-3)、2-[(5-甲基-2-丙烷-2-基環己烷羰基)胺基]乙酸乙酯(WS-5)、N-(4-甲氧基苯基)-對薄荷烷羧醯胺(WS-12)、N,2,3-三甲基-2-異丙基丁醯胺(WS-23)等。 又,作為可與式(1)所表示之薄荷基醚類一同含有之上述以外之通常之各種香料,可列舉:「專利廳,周知慣用技術集(香料)第II部食品香料,第8頁-87,平成12年(2000年)1月14日發行」中所記載之合成香料、天然精油、天然香料、動植物萃取物等。 作為該等香料成分,例如作為烴化合物,可列舉:α-蒎烯、β-蒎烯、月桂烯、莰烯、檸檬烯等單萜;朱欒倍半萜、雪松烯、石竹烯、長葉烯等倍半萜;1,3,5-十一碳三烯等。 作為醇化合物,可列舉:丁醇、戊醇、異戊醇、己醇等直鏈・飽和烷醇;戊烯醇、(Z)-3-己烯-1-醇、2,6-壬二烯醇等直鏈・不飽和醇;沉香醇、香葉草醇、香茅醇、四氫月桂烯醇、金合歡醇、橙花叔醇、雪松醇等萜烯醇;苄醇、苯基乙基醇、呋喃甲醇等芳香族醇。 作為醛化合物,可列舉:乙醛、異戊醛、己醛、辛醛、壬醛、癸醛等脂肪族飽和醛;(E)-2-己烯醛、2,4-辛二醛等脂肪族不飽和醛;香茅醛、檸檬醛等萜烯醛;苯甲醛、肉桂醛、香草醛、乙香草醛、糠醛、向日花香醛等芳香族醛。 作為酮化合物,可列舉:2-庚酮、2-十一酮、1-辛烯-3-酮等直鏈・飽和及不飽和酮;乙偶姻、二乙醯、2,3-戊二酮、麥芽醇、乙基麥芽醇、2,5-二甲基-4-羥基-3(2H)-呋喃酮等直鏈及環狀二酮及羥基酮;香旱芹酮、薄荷酮、諾卡酮等萜烯酮;α-紫羅蘭酮、β-紫羅蘭酮、β-突厥烯酮等源自萜烯分解物之酮;覆盆子酮等芳香族酮。 作為呋喃・醚化合物,可列舉:玫瑰醚、氧化芳樟醇、薄荷呋喃、茶螺烷等環狀醚類;甲基胡椒酚、大茴香腦等芳香族醚類。 作為酯化合物,可列舉:乙酸乙酯、乙酸異戊烷等脂肪族醇之乙酸酯;乙酸沉香酯、乙酸香葉酯、乙酸薰衣草酯等萜烯醇之乙酸酯;丁酸乙酯、己酸乙酯等脂肪酸與低級醇之酯;乙酸苄酯、水楊酸甲酯等芳香族酯。 作為內酯化合物,可列舉:γ-癸內酯、γ-十二內酯、δ-癸內酯、δ-十二內酯等飽和內酯;7-癸烯-4-內酯、2-癸烯-5-內酯等不飽和內酯。 作為酸化合物,可列舉:丁酸、4-甲基-3-戊烯酸、辛酸、硬脂酸、油酸、亞麻油酸、次亞麻油酸等飽和、不飽和脂肪酸。 作為含氮化合物,可列舉:吲哚、糞臭素、吡啶、經烷基取代之吡𠯤、鄰胺苯甲酸甲酯等。 作為含硫化合物,可列舉:甲硫醇、糠基硫醇、二甲硫醚、二甲雙硫醚、二糠基二硫醚、異硫氰酸烯丙酯等。 作為天然精油,可列舉:甜橙、酸橙、卑檸、檸檬、葡萄柚、酸橙(lime)、佛手柑、柑橘、橙花、胡椒薄荷、綠薄荷、熏衣草、黃金菊、迷迭香、桉樹、鼠尾草、羅勒、玫瑰、天竺葵、茉莉、香水樹、大茴香、小茴香、八角茴香、丁香、肉桂、薑、肉豆蔻、小豆蔻、蛇麻草、柳杉、扁柏、香根草、天竺薄荷、勞丹脂等。 又,作為各種萃取物,亦可列舉:花草茶・香辛料萃取物;咖啡・綠茶・紅茶・烏龍茶萃取物;乳或乳加工品及其等之脂肪酶・蛋白酶等酵素分解物。 於含有式(1)所表示之薄荷基醚類之乳化組合物中,視需要可含有:通常用於香料組合物中之水、乙醇等溶劑;乙二醇、1,2-丙二醇、甘油、苯甲酸苄酯、檸檬酸三乙酯、脂肪酸甘油三酸酯、脂肪酸甘油二酯等香料保留劑。 本發明中所使用之作為(B)成分之水較佳為與作為(C)成分之糖類、一元醇或多元醇一同構成上述水相部。於水相部中之含水率通常為50%以下、尤其為約0~25%之範圍內之含水狀態下使用較佳,若含水率超過50%,則有喪失防腐性之可能性。 本發明中所使用之作為(C)成分之糖類、一元醇或多元醇係為了乳化之穩定而調配。作為糖類,例如可列舉:葡萄糖、果糖、蔗糖、海藻糖、纖維雙糖、麥芽三糖、鼠李糖、乳糖、麥芽糖、核糖、木糖、阿拉伯糖及飴糖等,作為一元醇,例如可列舉:乙醇、丙醇及異丙醇等,作為多元醇,例如可列舉:甘油、丙二醇、1,3-丁二醇、山梨糖醇、麥芽糖醇及澱粉分解還原物等,可列舉:該等兩種以上之混合物。 本發明之乳化組合物中之上述水相部之使用量較佳為相對於油相部1質量份,通常為約1質量份~約10質量份,尤其為約1.5質量份~約5質量份之範圍內。又,於上述水相部中,為了提高保存性,根據所需亦可添加:乳酸、檸檬酸、蘋果酸、酒石酸等有機酸。 再者,(A)式(1)所表示之薄荷基醚類及上述各種香料只要為低濃度,則亦可為了溶解於作為(C)成分之糖類、一元醇或多元醇中,而調配於上述水相部中。 作為本發明中所使用之作為(D)成分之乳化劑,並無特別限制,可使用自先前用於飲食品等中之各種乳化劑,例如可例示:脂肪酸單甘油酯、脂肪酸甘油二酯、脂肪酸甘油三酸酯、丙二醇脂肪酸酯、蔗糖脂肪酸酯、聚甘油脂肪酸酯、卵磷脂、化工澱粉、山梨糖醇酐脂肪酸酯、皂樹萃取物、阿拉伯膠、黃耆膠、瓜爾膠、刺梧桐樹膠、三仙膠、果膠、海藻酸及其鹽類、角叉菜膠、明膠、酪蛋白等。 該等乳化劑中,尤佳為HLB為8以上之親水性界面活性劑,於該情形時,於水相部中混合乳化劑。具體而言,可列舉:聚甘油脂肪酸酯、山梨糖醇酐脂肪酸酯、蔗糖脂肪酸酯、甘油脂肪酸酯等。作為聚甘油脂肪酸酯類,例如可列舉:平均聚合度3以上之聚甘油與碳數8以上之脂肪酸之酯,例如為十甘油單油酸酯、十甘油單硬脂酸酯、十甘油單棕櫚酸酯、十甘油單肉豆蔻酸酯等且HLB為8以上、較佳為8~14之範圍內者。於使用HLB為8以上之聚甘油脂肪酸酯之情形時,通常易於製備均勻且粒徑較小之乳化粒子,又,若將乳化組合物穩定地添加於飲料中,則引起沈澱、油分離等分離現象之傾向低。 聚甘油脂肪酸酯類之含量相對於油相部1質量份,可為通常為0.05質量份~0.5質量份,較佳為0.15質量份~0.3質量份之範圍內。 若例示本發明之乳化組合物之製備法之一實施態樣,則為如下所示。首先,將上述之油相部中所使用之包含(A)式(1)所表示之薄荷基醚類之原料進行混合,製備油相部1質量份。另外,藉由製備將(B)水、(C)選自糖類、一元醇或多元醇中之一種以上、及(D)乳化劑進行混合溶解而成之溶液(水相部)約2~約50質量份(水分含量約0.5質量%~約10質量%),將油相部與水相部進行混合,使用均質攪拌機、膠體磨機、高壓均質器等進行乳化處理,可獲得粒徑約0.2 μm~約2 μm之極其微細且穩定性優異之乳化組合物。 於該乳化組合物中,可以該乳化組合物之質量作為基準,通常以0.01%~30%之濃度含有式(1)所表示之薄荷基醚類,作為下限值,較佳為可例示:0.02%,更佳為0.05%,進而較佳為可例示:0.1%,又,作為上限值,較佳為可例示:10%,更佳為可例示:5%,進而較佳為可例示:2%,該等下限值與上限值可以任意之組合設定範圍。 本發明之粉末組合物可藉由將上述乳化組合物進行乾燥而獲得。作為乾燥方法,可例示:真空乾燥、噴霧乾燥、冷凍乾燥等乾燥方法。於乾燥時,亦可於上述乳化組合物中進而添加糊精類、澱粉類、天然膠類、糖類其他賦形劑作為賦形劑。 於使用含有式(1)所表示之薄荷基醚類之乳化組合物或粉末組合物之情形時,相對於飲食品或香妝品,以質量基準計,作為式(1)所表示之薄荷基醚類,通常可以0.1 ppm~300 ppm之濃度含有,作為下限值,較佳為可例示:0.2 ppm,更佳為可例示:0.5 ppm,進而較佳為可例示:1 ppm,又,作為上限值,較佳為可例示:100 ppm,更佳為可例示:50 ppm,進而較佳為可例示:20 ppm,該等下限值與上限值可以任意之組合而設定範圍。藉由以該濃度範圍添加,可對飲食品或香妝品賦予稍稍木質、辛辣且青草之香氣,又,可對飲食品賦予柚皮苷之各種苦味,即與不製成乳化組合物之情形相比,賦予苦味之上升較慢且清爽且溫和之苦味。 作為可藉由本發明之乳化組合物或粉末組合物而賦予香味或改良、增強香味之飲食品之具體例,可列舉:可樂飲料、加入果汁之碳酸飲料、加入乳類之碳酸飲料等碳酸飲料類;果汁飲料、蔬菜飲料、運動飲料、蜂蜜飲料、豆乳、維生素補給飲料、礦物質補給飲料、營養飲料、滋養飲料、乳酸菌飲料、乳飲料等軟飲料類;綠茶、紅茶、烏龍茶、花草茶、奶茶、咖啡飲料等嗜好飲料類;燒酒摻蘇打水、雞尾酒飲料、發泡酒、果實酒、藥酒等酒精飲料類;黃油、乳酪、牛奶、酸乳酪等乳製品;冰淇淋、乳酸冰淇淋、冰點心、酸乳酪、布丁、果凍、日常甜點等甜點類及用以製造該等之混合物類;焦糖、糖果、模壓點心、脆餅、餅乾、曲奇、餡餅、巧克力、休閒點心等甜食類及用以製造該等之糕點混合物等混合物類;麵包、湯、各種即食食品等通常食品類;潔牙等口腔用組合物,但並無任何限定。 又,作為可藉由本發明之乳化組合物或粉末組合物而增強稍稍木質、辛辣且青草之香氣的香妝品之具體例,例如可列舉:香水;洗髮精、潤絲精、髮霜、髮蠟等毛髮護理製品;白粉、口紅等化妝品類;潔面用肥皂、身體用肥皂、洗滌用肥皂、洗滌用洗劑、消毒用洗劑、防臭洗劑等保健、衛生用洗劑類;衛生抽紙、衛生紙等保健、衛生材料類;室內芳香劑、車內香水等芳香製品。 [實施例] 以下,根據實施例對本發明更具體地說明。再者,本發明並不限定於該等。實施例中,只要無特別說明,則記載為「%」者為質量基準。 於實施例中,反應粗製物、精製物之測定係使用以下分析機器進行。 GC(Gas chromatography,氣相層析)測定:GC-2014(島津製作所公司製造)及積分儀C-R8A(島津製作所公司製造) GC測定用GC管柱:GL Science公司製造之TC-1(長度30 m,內徑0.53 mm,液層膜厚1.50測微計)、GL Science公司製造之TC-1701(長度30 m,內徑0.53 mm,液層膜厚1.00測微計) GC/MS(Gas chromatography-mass spectrometry,氣相層析/質譜儀)測定:5973N(Agilent公司製造) GC/MS測定用GC管柱:GL Science公司製造之TC-1701(長度30 m,內徑0.25 mm,液層膜厚0.25測微計) NMR(nuclear magnetic resonance,核磁共振)測定:ECX-400A(JEOL RESONANCE公司製造)。參考例 1 : 4- 薄荷基氧基 -2- 丁酮之製備
向經氮氣置換之100 mL燒瓶中添加l-薄荷腦(7.81 g,50 mmol)、二氯甲烷(50.0 g)、三氟化硼二乙醚錯合物(0.71 g,5 mmol)並攪拌混合後,向其中添加甲基乙烯基酮(10.51 g,,150 mmol),直接於20℃下攪拌4天。將反應液注入至5%碳酸氫鈉水溶液(30.0 g)中並停止反應。使有機層分離後,將水層利用二氯甲烷(15.0 g)提取2次,將對應之有機層利用飽和食鹽水進行洗淨,利用無水硫酸鎂進行乾燥。進行吸引過濾而將硫酸鎂去除後,利用旋轉蒸發器將溶劑蒸餾去除。藉由將所獲得之粗產物12.99 g進行減壓蒸餾,而獲得4-薄荷基氧基-2-丁酮(參考品1:產量7.28 g,產率64.3%,純度99.1%)。4- 薄荷基氧基 -2- 丁酮 ( 參考品 1) 之物性資料
沸點:85~88℃/0.1 kPa1
H NMR(CDCl3
, 400 MHz) δ 0.74(d, 3H, J=7.2 Hz), 0.81(m, 1H),0.85(d, 3H, J=7.2 Hz), 0.89(d, 3H, J=6.4 Hz), 0.95(m, 1H), 1.16(m, 1H), 1.32(m, 1H), 1.60(m, 2H), 2.09(m, 2H), 2.16(s, 3H), 2.64(m, 2H), 3.01(dt, 1H, J=4.0, 6.4 Hz), 3.54(ddd, 1H, J=9.6, 6.8, 6.0 Hz), 3.84(dt, 1H, J=9.2, 6.0 Hz).13
C NMR(CDCl3
, 100 MHz) δ 16.30, 20.97, 22.39, 23.41, 25.66, 30.57, 31.55, 34.60, 40.29, 44.24, 48.24, 63.51, 79.58, 207.69。 MS(EI, 70 eV)m/z 41(29), 43(96), 55(44), 71(100), 81(44), 83(26), 87(23), 95(39), 123(18), 138(30), 141(40), 155(25), 169(1), 211(1), 226(M+, 0.2). [α](20℃,D射線,c=2.04 in CHCl3
)=-80.8。實施例 1 :含有 4- 薄荷基氧基 -2- 丁酮之乳化組合物之製備
作為油相部,將4-薄荷基氧基-2-丁酮(1.0 g)、SAIB 9.0 g及MCT(中鏈脂肪酸甘油三酸酯)9.0 g混合溶解。另一方面,作為水相部,將甘油66 g、離子交換水11 g及十甘油單油酸酯(4.0 g)混合溶解。將水相部與油相部藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm進行攪拌混合,進行10分鐘之乳化。利用離子交換水製作如2000倍稀釋時之波長680 nm下之吸光度成為0.2 Abs之O/W型乳膠(本發明品1:4-薄荷基氧基-2-丁酮濃度1.0%)。香氣評價
於樣品瓶中準備本發明品1之1%水溶液(本說明書中,於水溶液中亦包含將本發明之乳化組合物添加於水中之水分散液),藉由5名官能檢查員,進行來自瓶口之香氣評價及對香氣評價用之含浸本發明品1之1%水溶液藉由紙進行香氣評價。 根據5名官能檢查員之平均之評價結果:稍微木質且青草之香氣苦味評價
製備將4-薄荷基氧基-2-丁酮相對於99.5%乙醇溶解10(W/W)%而成之溶液(參考品2)。將本發明品1及參考品2利用純水稀釋,製備使4-薄荷基氧基-2-丁酮成為下述表1所示之濃度之溶液。對於各溶液,藉由5名官能檢查員,對直接放入口中時、進而喝下時之苦味綜合地評價。將苦味之強度設為以下之基準(完全感覺不到苦味=0點,稍稍感覺苦味=2點,有些感覺苦味=4點,明顯感到苦味=6點,強烈感到苦味=8點,非常強烈感到苦味=10點),對於苦味之品質附上評價。將5名官能檢查員之平均之評價結果示於下述表1。 [表1]
如上述表1所示般,4-薄荷基氧基-2-丁酮之水溶液係評價為乙醇稀釋品及乳化組合物均於1 ppm~200 ppm之範圍感到苦味。於將乳化組合物稀釋於水中之情形、與將乙醇溶液稀釋於水中之情形之比較中,於同一濃度之4-薄荷基氧基-2-丁酮之水溶液中,苦味之強度雖然不那樣有差,但將乳化組合物稀釋於水中之情形者與將乙醇溶液稀釋於水中之情形相比,苦味之上升較慢,苦味更清爽且溫和。又,乳化組合物之苦味係使人想起柚皮苷之苦味的苦味之評價。實施例 2 :含有 4- 薄荷基氧基 -2- 丁酮之乳化組合物之製備
作為水相部,將甘油81 g、離子交換水14 g及十甘油單油酸酯(4.0 g)混合溶解。將水相部與4-薄荷基氧基-2-丁酮(1.0 g)藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm攪拌混合,進行10分鐘之乳化。利用離子交換水製作如2000倍稀釋時之波長680 nm下之吸光度成為0.2 Abs之O/W型乳膠(本發明品2:4-薄荷基氧基-2-丁酮濃度1.0%)。實施例 3 :調配有食用油脂類之含有 4- 薄荷基氧基 -2- 丁酮之乳化組合物之製備 (2)
作為油相部,將4-薄荷基氧基-2-丁酮(1.0 g)、SAIB 17.5 g及MCT(中鏈脂肪酸甘油三酸酯;食用油脂類)17.5 g混合溶解。另一方面,作為水相部,將甘油50 g、離子交換水8 g及十甘油單油酸酯(6.0 g)混合溶解。將水相部與油相部藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm攪拌混合,進行10分鐘之乳化。利用離子交換水製作如2000倍稀釋時之波長680 nm下之吸光度成為0.2 Abs之O/W型乳膠(本發明品3:4-薄荷基氧基-2-丁酮濃度1.0%)。苦味評價
將上述本發明品1及參考品2及本發明品2及本發明品3利用純水進行稀釋,製備使4-薄荷基氧基-2-丁酮成為10 ppm之溶液。對於各溶液,藉由5名官能檢查員,將直接含入口中時、進而喝下時之苦味之上升與持續進行比較評價。將其平均的評價結果示於下述表2。 [表2]
如上述表2所示般,確認到伴隨乳化組合物中之食用油脂類之含量之增加,苦味之持續時間變長。參考例 2 : 2- 甲基 -4- 薄荷基氧基 -2- 丁醇之 製備
使安裝有溫度計、滴液漏斗之200 mL燒瓶經氮氣置換後,注入四氫呋喃(利用分子篩5A進行乾燥,50 mL)與氯化甲基鎂之3.0 M四氫呋喃溶液(21.7 mL,65 mmol),利用水浴進行冷卻。自滴液漏斗以將內溫保持為30℃以下之速度向其中滴加將4-薄荷基氧基-2-丁酮(11.32 g,50 mmol)溶解於四氫呋喃(50 mL)中之溶液。滴加結束後,直接於室溫下攪拌3小時後,將反應液注入至25%氯化銨水溶液(100 g)中,利用分液漏斗將有機相與水相部分離。將水相部利用第三丁基甲醚(30 g)提取2次後,將對應之有機相利用飽和食鹽水洗淨。利用無水硫酸鎂進行乾燥後,利用旋轉蒸發器將溶劑蒸餾去除。藉由向所獲得之粗產物12.54 g中少量添加碳酸鈉並減壓蒸餾而獲得2-甲基-4-薄荷基氧基-2-丁醇(參考品3:產量10.25 g,產率84.6%,純度98.2%)。2- 甲基 -4- 薄荷基氧基 -2- 丁醇 ( 參考品 3) 之物性資料
沸點:87℃/0.1 kPa1
H NMR(CDCl3
, 400 MHz) δ 0.76(d, 3H, J=6.8 Hz), 0.79-0.88(m, 2H), 0.86(d, 3H, J=6.8 Hz), 0.90(d, 3H, J=6.8 Hz), 0.96(m, 1H), 1.18(m, 1H), 1.22(s, 3H), 1.22(s, 3H), 1.33(m, 1H), 1.61(m, 2H), 1.69(ddd, 1H, J=14.4, 6.8, 4.4 Hz), 1.77(ddd, 1H, J=14.4, 7.6, 4.4 Hz), 2.13(m, 2H), 3.03(dt, 1H, J=4.4, 10.8 Hz), 3.50(ddd, 1H, J=9.2, 6.8, 4.4 Hz), 3.68(s, 1H),3.89(ddd, 1H, J=9.2, 7.6, 4.4 Hz)。13
C NMR(CDCl3
, 100 MHz) δ 16.13, 21.03, 22.37, 23.25, 25.77, 29.07, 29.44, 31.57, 34.53, 40.10, 41.68, 48.23, 65.71, 70.49, 79.89。 MS(EI, 70 eV) m/z 41(63), 43(59), 55(73), 57(49), 59(55), 67(20), 69(100), 71(90), 81(50), 83(96), 87(21), 89(23), 95(37), 97(22), 101(23), 123(17), 138(39), 139(55), 155(17), 157(22), 167(1), 181(1), 224(1), 227(1), 242(M+, 0.1)。 [α](20℃,D射線,c=2.05 in CHCl3
)=-85.4。實施例 4 :含有 2- 甲基 -4- 薄荷基氧基 -2- 丁醇之 乳化組合物之製備
作為油相部,將2-甲基-4-薄荷基氧基-2-丁醇(1.0 g)、SAIB 9.0 g及MCT(中鏈脂肪酸甘油三酸酯)9.0 g混合溶解,作為水相部,將甘油66 g、離子交換水11 g及十甘油單油酸酯(4.0 g)混合溶解,將兩種溶液藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm攪拌混合,進行10分鐘之乳化。利用離子交換水製作如2000倍稀釋時之波長680 nm下之吸光度成為0.2 Abs之O/W型乳膠(本發明品4:2-甲基-4-薄荷基氧基-2-丁醇濃度1.0%)。香氣評價
於樣品瓶中準備本發明品4之1%水溶液,藉由5名官能檢查員,進行來自瓶口之香氣評價及對含浸有香氣評價液藉由紙進行香氣評價。 根據5名官能檢查員之平均之評價結果:辛辣且青草之香氣苦味評價
製備將2-甲基-4-薄荷基氧基-2-丁醇於99.5%乙醇中溶解10(W/W)%而成之溶液(參考品4)。將本發明品4及參考品4利用純水進行稀釋,製備使2-甲基-4-薄荷基氧基-2-丁醇成為下述表3所示之濃度之溶液。針對各溶液,藉由5名官能檢查員,將直接含入口中時、進而喝下時之苦味綜合地評價。將苦味之強度設為以下之基準(完全感覺不到苦味=0分,稍稍感覺苦味=2分,有些感覺苦味=4分,明顯感到苦味=6分,強烈感到苦味=8分,非常強烈感到苦味=10分),對於苦味之品質附上評價。將5名官能檢查員之平均之評價結果示於下述表3。 [表3]
如上述表3所示般,2-甲基-4-薄荷基氧基-2-丁醇之水溶液係評價為乙醇稀釋品及乳化組合物均於0.5 ppm~100 ppm之範圍感到苦味。於將乳化組合物稀釋於水中之情形、與將乙醇溶液稀釋於水中之情形之比較時,於同一濃度之4-薄荷基氧基-2-丁醇之水溶液中,苦味之強度不那樣有差,將乳化組合物稀釋於水中之情形者與將乙醇溶液稀釋於水中之情形相比,苦味之上升較慢、苦味更清爽且溫和。又,乳化組合物之苦味係讓人想起柚皮苷之苦味的苦味之評價。實施例 5 :對啤酒風味飲料之添加效果
向市售之啤酒風味飲料中,將本發明品1添加0.1%(4-薄荷基氧基-2-丁酮濃度10 ppm)或將本發明品4添加0.1%(2-甲基-4-薄荷基氧基-2-丁醇濃度10 ppm),分別藉由5名官能檢查員,就苦味、飲用口感、入喉、味道之爽口、餘味之觀點進行官能評價。其平均之官能評價結果係如下所述。 添加有本發明品1之啤酒風味飲料與無添加品相比,感到良好之苦味,又,關於入喉及味道之爽口,感到顯著之效果。又,關於飲用口感,稍許增加,餘味亦改善一些。 添加有本發明品4之啤酒風味飲料與無添加品相比,感到良好之苦味,又,關於入喉及味道之爽口,感到顯著之效果。又,關於飲用口感,稍許增加,餘味亦改善一些。實施例 6 :橘子味調製香料組合物之乳化組合物
根據下述表4,製備參考品5~7之橘子味調製香料組合物。 [表4]
製備將作為油相部之上述表4之橘子風味調製香料組合物(參考品5、參考品6或參考品7)100 g、作為水相部之甘油312.5 g、離子交換水65 g溶解於十甘油單硬脂酸酯22.5 g中者,將兩種溶液藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm攪拌混合,進行10分鐘之乳化。獲得利用離子交換水製作如2000倍稀釋時之波長680 nm下之吸光度成為0.2 Abs之O/W型乳膠之橘子味調製香料組合物之乳化組合物。將參考品5之乳化組合物設為比較品1,將參考品6之乳化組合物設為本發明品5,將參考品7之乳化組合物設為本發明品6。 將各橘子味調製香料組合物之乳化組合物(比較品1、本發明品5及本發明品6)添加於下述表5所示之配方之飲料基材中,製備橘子果汁飲料。 [表5]
於香味評價中,選定熟練之官能檢查員5名,對於飲食添加有比較品1、本發明品5或本發明品6之橘子果汁飲料時之苦味、與作為香味評價項目之橘子果汁飲料之果肉感、新鮮感、果皮感、成熟感進行評價。評價係以比較品1之香味作為基準,綜合地評價將果汁飲料直接含入口中時、進而喝下時之香味。苦味係設為以下之基準(完全未感到苦味=-分,未明確感到苦味=+/-分,感到苦味=+分,強烈感到苦味=++分,苦味過強=+++分),作為飲食時之香味評價,對於果肉感、新鮮感、果皮感、成熟感,用以下之基準(未感到=-分,未明確感到=+/-分,感到=+分,強烈感到=++分)進行評價。又,記載香味評價之評價。將其平均之香味評價結果示於下述表6。 [表6]
如上述表6所示般,添加有本發明品5或6之橘子果汁飲料係再現具有天然感之橘子之風味。即,為賦予橘子之果皮感,強調聯想到食用新鮮之生橘子時之香味之評價。實施例 7 :薄荷味調製香料組合物之乳化組合物
依據下述表7,製備參考品8~10之薄荷味調製香料組合物(薄荷香料)。 [表7]
製備於作為油相部之上述表7之薄荷味調製香料組合物(參考品8、參考品9或參考品10)100 g、作為水相部之甘油312.5 g、離子交換水65 g中溶解十甘油單硬脂酸酯22.5 g者,將兩種溶液藉由乳化機MARKII(PRIMIX公司製造)以8000 rpm攪拌混合,進行10分鐘之乳化,獲得製成O/W型乳膠之薄荷味調製香料組合物之乳化組合物。將參考品8之乳化組合物設為比較品2,將參考品9之乳化組合物設為本發明品7,將參考品10之乳化組合物設為本發明品8。 將各薄荷味調製香料組合物之乳化組合物(本發明品7、8或比較品2)添加至下述表8所示之配方之橡膠基材中,依據常法製備薄荷風味口香糖。 [表8]
於香味評價中,選定熟練之官能檢查員5名,作為咀嚼添加有本發明品7、8或比較品2之薄荷風味口香糖時之香味評價項目,對薄荷風味口香糖之苦味、清涼感、花草茶感、天然感、化學品感進行評價。評價係以添加有比較品2者作為基準,對開始咀嚼口香糖時、進而咀嚼10分鐘咀嚼時之香味綜合地評價。苦味係設為以下之基準(完全未感到苦味=-分,未明確感到苦味=+/-分,感到苦味=+分,強烈感到苦味=++分,苦味過強=+++分),作為咀嚼時之香味評價,對清涼感、花草茶感、天然感、化學品感,用以下之基準(未感到=-分,未明確感到=+/-分,感到=+分,強烈感到=++分)進行評價。將香味評價示於下述表9。 [表9]
如上述表9所示般,添加有比較品2之薄荷風味口香糖雖然清涼感較強,但苦味、花草茶感較弱,亦有化學品感,缺乏天然感。相對於此,添加有本發明品7或8之薄荷風味口香糖係清爽之苦味與薄荷之清涼感一體化,賦予天然感,抑制了比較品2中所感到之化學品感之評價。
Claims (8)
- 如請求項1之乳化組合物,其進而含有(E)食用油脂類。
- 一種粉末組合物,其係將如請求項1之乳化組合物乾燥而成。
- 一種飲食品,其含有如請求項1至3中任一項之乳化組合物或如請求項4之粉末組合物。
- 一種香妝品,其含有如請求項1至3中任一項之乳化組合物或如請求項4之粉末組合物。
- 一種飲食品或香妝品之香氣賦予或香氣調變方法,其係藉由含有如請求項1至3中任一項之乳化組合物或如請求項4之粉末組合物而進行。
- 一種飲食品之苦味賦予方法,其係藉由使如請求項1至3中任一項之乳化組合物或如請求項4之粉末組合物含有於飲食品中而進行。
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WO2005082154A1 (en) * | 2004-02-26 | 2005-09-09 | Wm. Wrigley Jr. Company | Confections containing a blend of physilogical cooling agents |
WO2010010894A1 (ja) * | 2008-07-23 | 2010-01-28 | 三栄源エフ・エフ・アイ株式会社 | メントールの風味改善剤及び風味改善方法 |
JP5546788B2 (ja) * | 2009-04-24 | 2014-07-09 | 高砂香料工業株式会社 | (3S)−3−ヒドロキシブタン酸−l−メンチルの製造方法および冷感剤組成物 |
CN102811702B (zh) * | 2010-03-19 | 2014-10-08 | 狮王株式会社 | 液体口腔用组合物及其制造方法 |
EP2620137B1 (de) * | 2012-01-30 | 2017-11-15 | Symrise AG | Zubereitungen |
JP6148892B2 (ja) * | 2013-04-12 | 2017-06-14 | 三栄源エフ・エフ・アイ株式会社 | 高濃度エチル−2−(p−メンタン−3−カルボキサミド)アセテート含有粉末香料製剤 |
BR112015029759A2 (pt) * | 2013-06-21 | 2017-07-25 | Firmenich & Cie | preparação de partículas secas que compreendem mentol |
JP6001031B2 (ja) * | 2014-10-27 | 2016-10-05 | 長谷川香料株式会社 | 香味変調剤 |
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2016
- 2016-04-01 JP JP2016074574A patent/JP6391179B2/ja active Active
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2017
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- 2017-03-09 CN CN201780017405.8A patent/CN108882737A/zh active Pending
- 2017-03-31 TW TW106111047A patent/TWI712424B/zh active
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2018
- 2018-09-28 US US16/145,500 patent/US20190093047A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103930394A (zh) * | 2011-10-27 | 2014-07-16 | 高砂香料工业株式会社 | 3-薄荷氧基丙醇的制造方法以及凉爽剂组合物 |
CN104684412A (zh) * | 2012-10-05 | 2015-06-03 | 小川香料株式会社 | 粉末状清凉剂组合物 |
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JP6391179B2 (ja) | 2018-09-19 |
TW201735898A (zh) | 2017-10-16 |
US20190093047A1 (en) | 2019-03-28 |
JP2017184636A (ja) | 2017-10-12 |
CN108882737A (zh) | 2018-11-23 |
WO2017169606A1 (ja) | 2017-10-05 |
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