JP6385098B2 - Method for producing flavor oil - Google Patents
Method for producing flavor oil Download PDFInfo
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- JP6385098B2 JP6385098B2 JP2014066760A JP2014066760A JP6385098B2 JP 6385098 B2 JP6385098 B2 JP 6385098B2 JP 2014066760 A JP2014066760 A JP 2014066760A JP 2014066760 A JP2014066760 A JP 2014066760A JP 6385098 B2 JP6385098 B2 JP 6385098B2
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- oil
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- flavor oil
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- 239000000796 flavoring agent Substances 0.000 title claims description 54
- 235000019634 flavors Nutrition 0.000 title claims description 54
- 238000004519 manufacturing process Methods 0.000 title claims description 27
- 239000003921 oil Substances 0.000 claims description 106
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 69
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 66
- 235000002639 sodium chloride Nutrition 0.000 claims description 51
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 48
- 239000003925 fat Substances 0.000 claims description 34
- 150000007524 organic acids Chemical class 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 27
- 239000000284 extract Substances 0.000 claims description 25
- 239000011780 sodium chloride Substances 0.000 claims description 24
- 235000015165 citric acid Nutrition 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 17
- 238000002156 mixing Methods 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 9
- 235000017858 Laurus nobilis Nutrition 0.000 claims description 7
- 244000178231 Rosmarinus officinalis Species 0.000 claims description 7
- 244000125380 Terminalia tomentosa Species 0.000 claims description 7
- 235000005212 Terminalia tomentosa Nutrition 0.000 claims description 7
- 239000008157 edible vegetable oil Substances 0.000 claims description 7
- 241000873224 Capparaceae Species 0.000 claims description 6
- 235000017336 Capparis spinosa Nutrition 0.000 claims description 6
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
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- 240000001851 Artemisia dracunculus Species 0.000 claims description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 3
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- 241000269333 Caudata Species 0.000 claims description 3
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- 240000000171 Crataegus monogyna Species 0.000 claims description 3
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- 235000009840 Crataegus x incaedua Nutrition 0.000 claims description 3
- 235000015655 Crocus sativus Nutrition 0.000 claims description 3
- 244000124209 Crocus sativus Species 0.000 claims description 3
- 240000004784 Cymbopogon citratus Species 0.000 claims description 3
- 235000017897 Cymbopogon citratus Nutrition 0.000 claims description 3
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
- 244000004281 Eucalyptus maculata Species 0.000 claims description 3
- 235000005206 Hibiscus Nutrition 0.000 claims description 3
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 claims description 3
- 244000284380 Hibiscus rosa sinensis Species 0.000 claims description 3
- 235000010650 Hyssopus officinalis Nutrition 0.000 claims description 3
- 235000010254 Jasminum officinale Nutrition 0.000 claims description 3
- 240000005385 Jasminum sambac Species 0.000 claims description 3
- 235000013628 Lantana involucrata Nutrition 0.000 claims description 3
- 240000005183 Lantana involucrata Species 0.000 claims description 3
- 244000165082 Lavanda vera Species 0.000 claims description 3
- 235000010663 Lavandula angustifolia Nutrition 0.000 claims description 3
- 235000007232 Matricaria chamomilla Nutrition 0.000 claims description 3
- 235000010654 Melissa officinalis Nutrition 0.000 claims description 3
- 244000062730 Melissa officinalis Species 0.000 claims description 3
- 235000006679 Mentha X verticillata Nutrition 0.000 claims description 3
- 235000002899 Mentha suaveolens Nutrition 0.000 claims description 3
- 235000001636 Mentha x rotundifolia Nutrition 0.000 claims description 3
- 235000006677 Monarda citriodora ssp. austromontana Nutrition 0.000 claims description 3
- 235000017879 Nasturtium officinale Nutrition 0.000 claims description 3
- 240000005407 Nasturtium officinale Species 0.000 claims description 3
- 235000010676 Ocimum basilicum Nutrition 0.000 claims description 3
- 240000007926 Ocimum gratissimum Species 0.000 claims description 3
- 235000011203 Origanum Nutrition 0.000 claims description 3
- 240000000783 Origanum majorana Species 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 235000004347 Perilla Nutrition 0.000 claims description 3
- 244000124853 Perilla frutescens Species 0.000 claims description 3
- 240000006086 Petroselinum crispum Neapolitanum Group Species 0.000 claims description 3
- 235000006038 Petroselinum crispum Neapolitanum Group Nutrition 0.000 claims description 3
- 240000007651 Rubus glaucus Species 0.000 claims description 3
- 235000011034 Rubus glaucus Nutrition 0.000 claims description 3
- 235000009122 Rubus idaeus Nutrition 0.000 claims description 3
- 244000228451 Stevia rebaudiana Species 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- 240000000785 Tagetes erecta Species 0.000 claims description 3
- 240000001949 Taraxacum officinale Species 0.000 claims description 3
- 235000005187 Taraxacum officinale ssp. officinale Nutrition 0.000 claims description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- 235000007303 Thymus vulgaris Nutrition 0.000 claims description 3
- 240000002657 Thymus vulgaris Species 0.000 claims description 3
- 235000011054 acetic acid Nutrition 0.000 claims description 3
- 235000011399 aloe vera Nutrition 0.000 claims description 3
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 3
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- 239000001110 calcium chloride Substances 0.000 claims description 3
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- 235000011087 fumaric acid Nutrition 0.000 claims description 3
- 239000000174 gluconic acid Substances 0.000 claims description 3
- 235000012208 gluconic acid Nutrition 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 239000001102 lavandula vera Substances 0.000 claims description 3
- 235000018219 lavender Nutrition 0.000 claims description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 3
- 239000001630 malic acid Substances 0.000 claims description 3
- 235000011090 malic acid Nutrition 0.000 claims description 3
- 235000011197 perejil Nutrition 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 3
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 claims description 3
- 238000011084 recovery Methods 0.000 claims description 3
- 235000013974 saffron Nutrition 0.000 claims description 3
- 239000004248 saffron Substances 0.000 claims description 3
- 235000002020 sage Nutrition 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- 239000001585 thymus vulgaris Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 235000004055 Clinopodium vulgare Nutrition 0.000 claims description 2
- 244000136995 Clinopodium vulgare Species 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 240000000782 Anisomeles indica Species 0.000 claims 1
- 240000009164 Petroselinum crispum Species 0.000 claims 1
- 235000004789 Rosa xanthina Nutrition 0.000 claims 1
- 241000109329 Rosa xanthina Species 0.000 claims 1
- 235000014593 oils and fats Nutrition 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 90
- 235000019197 fats Nutrition 0.000 description 27
- 238000003756 stirring Methods 0.000 description 24
- 240000008415 Lactuca sativa Species 0.000 description 20
- 235000012045 salad Nutrition 0.000 description 20
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000000926 separation method Methods 0.000 description 12
- 239000003205 fragrance Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 235000013305 food Nutrition 0.000 description 9
- 235000008216 herbs Nutrition 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 6
- 235000009566 rice Nutrition 0.000 description 6
- 240000009215 Nepeta cataria Species 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 235000007575 Calluna vulgaris Nutrition 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000208317 Petroselinum Species 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000001256 steam distillation Methods 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 241000207836 Olea <angiosperm> Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 244000040738 Sesamum orientale Species 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- PPWHTZKZQNXVAE-UHFFFAOYSA-N Tetracaine hydrochloride Chemical compound Cl.CCCCNC1=CC=C(C(=O)OCCN(C)C)C=C1 PPWHTZKZQNXVAE-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 235000011148 calcium chloride Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
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- ZDKZHVNKFOXMND-UHFFFAOYSA-N epinepetalactone Chemical compound O=C1OC=C(C)C2C1C(C)CC2 ZDKZHVNKFOXMND-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
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- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
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- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
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Landscapes
- Fats And Perfumes (AREA)
- Seasonings (AREA)
Description
本発明は、ハーブ類の香味成分を有する香味オイルの製造方法に関する。 The present invention relates to a method for producing a flavor oil having herbal flavor components.
ハーブ等の植物は、様々な香気成分を含有しており、植物から抽出された香気成分は、アロマオイルや、香料、化粧品、食品添加物として、広く用いられている。植物から香気成分を取る方法は、植物の種類や抽出部位、用途によって異なり、様々な抽出方法が検討されている。 Plants such as herbs contain various aroma components, and aroma components extracted from plants are widely used as aroma oils, fragrances, cosmetics, and food additives. The method for removing aroma components from plants varies depending on the type of plant, the extraction site, and the use, and various extraction methods have been studied.
例えば、特許文献1には、水蒸気蒸留によって、香気成分を捕集する方法が開示されている。特許文献2には、植物を破砕および撹拌しながら減圧蒸留して、香気成分を抽出する方法が開示されている。特許文献3には、香気成分をアルコールで抽出した後、アルコールを加熱蒸発させて、香気成分を濃縮する方法が開示されている。特許文献4には、超臨界状態の二酸化炭素を抽出剤とする、香気成分の抽出法が開示されている。特許文献5には、ビールの香り付けに用いられるホップから、香気成分をアルコールで抽出した後、青臭さやヤニ臭の元になる天然由来の有機酸をエステル化して不快臭成分を低減する抽出方法が開示されている。特許文献6には、魚節類に含まれる香味成分を、塩分を含有するアルコール水溶液で抽出して、生臭みのない香味オイルを製造する方法が開示されている。 For example, Patent Document 1 discloses a method for collecting aroma components by steam distillation. Patent Document 2 discloses a method for extracting aroma components by distillation under reduced pressure while crushing and stirring plants. Patent Document 3 discloses a method in which an aromatic component is extracted with alcohol, and then the alcohol is heated and evaporated to concentrate the aromatic component. Patent Document 4 discloses a method for extracting an aroma component using carbon dioxide in a supercritical state as an extractant. Patent Document 5 discloses an extraction method for reducing an unpleasant odor component by extracting a fragrance component with alcohol from a hop used for scenting beer and then esterifying a natural organic acid that is a source of blue odor or crab odor. Is disclosed. Patent Document 6 discloses a method for producing a flavor oil free from a raw odor by extracting a flavor component contained in fish buns with an aqueous alcohol solution containing salt.
しかしながら、特許文献1の水蒸気蒸留法、特許文献2の減圧蒸留法、特許文献3の蒸発濃縮法、特許文献4の超臨界流体抽出法は、高価な装置を必要とし、加熱工程に要するランニングコストも高いことから、日常食品のように、消費者に低価格で多量に商品を提供する分野において、好適とは言えない。 However, the steam distillation method of Patent Document 1, the vacuum distillation method of Patent Document 2, the evaporation concentration method of Patent Document 3, and the supercritical fluid extraction method of Patent Document 4 require expensive equipment and the running cost required for the heating process. Therefore, it is not suitable in the field of providing a large amount of goods to consumers at a low price like daily foods.
一方、アルコールを加えて香気成分を抽出する方法は、装置価格とランニングコストを低く抑えることができるが、香りが想定よりも薄くなってしまう場合、もしくは、好ましくない臭気成分まで抽出してしまう場合があり、これらの課題を改善する必要があった。 On the other hand, the method of extracting fragrance components by adding alcohol can keep the device price and running cost low, but if the fragrance becomes thinner than expected, or when extracting even unpleasant odor components There was a need to improve these issues.
したがって、本発明の目的は、香味のよい香味オイルを、低コスト、かつ簡単に製造する方法を提供することにある。 Accordingly, an object of the present invention is to provide a method for easily producing a flavor oil having a good flavor at low cost.
上記目的を達成するため、本発明の香味オイルの製造方法は、ハーブをアルコール水溶液で抽出して抽出液を得る抽出工程と、前記抽出液と食用油脂と有機酸及び/又は塩類とを混合する油脂混合工程と、前記混合液を静置して油層と水層とを分離して、油層を回収する油層回収工程とを含むことを特徴とする。 In order to achieve the above object, the method for producing a flavor oil according to the present invention comprises an extraction step of extracting an herb with an aqueous alcohol solution to obtain an extract, and the extract, edible oil and fat, and an organic acid and / or salt are mixed. It includes an oil / fat mixing step, and an oil layer recovery step of recovering the oil layer by allowing the mixed solution to stand to separate the oil layer and the aqueous layer.
本発明の香味オイルの製造方法においては、前記油脂混合工程において、前記抽出液と食用油脂と有機酸及び塩類とを混合することが好ましい。 In the method for producing flavor oil according to the present invention, it is preferable that the extract, the edible fat and oil, the organic acid and the salt are mixed in the fat and oil mixing step.
本発明の香味オイルの製造方法においては、前記油脂混合工程において、前記アルコール水溶液のアルコール濃度が20〜60容量%であることが好ましい。 In the method for producing a flavor oil of the present invention, in the oil and fat mixing step, the alcohol concentration of the aqueous alcohol solution is preferably 20 to 60% by volume.
本発明の香味オイルの製造方法においては、前記油脂混合工程において、前記抽出液と前記食用油脂との合計量100質量部に対して、前記有機酸を1〜20質量部添加することが好ましい。 In the manufacturing method of the flavor oil of this invention, it is preferable to add 1-20 mass parts of said organic acids with respect to 100 mass parts of total amounts of the said extract and the said edible fat in the said oil-fat mixing process.
本発明の香味オイルの製造方法においては、前記油脂混合工程において、前記抽出液と前記食用油脂との合計量100質量部に対して、前記塩類を1〜20質量部添加することが好ましい。 In the method for producing flavor oil according to the present invention, it is preferable that 1 to 20 parts by mass of the salts are added to 100 parts by mass of the total amount of the extract and the edible oil and fat in the oil and fat mixing step.
本発明の香味オイルの製造方法においては、前記油脂混合工程において、前記抽出液に前記油脂を添加した後、10〜50℃の条件で、2〜20時間、撹拌混合し、次いで、前記有機酸及び/又は塩類を添加して、更に1〜20時間、撹拌混合することが好ましい。 In the method for producing flavor oil of the present invention, in the oil and fat mixing step, after adding the oil and fat to the extract, the mixture is stirred and mixed for 2 to 20 hours at 10 to 50 ° C., and then the organic acid And / or salts are preferably added and further stirred and mixed for 1 to 20 hours.
本発明の香味オイルの製造方法においては、前記ハーブは、アニスヒソップ、アロエ、イタリアンパセリ、イヌハッカ、エゴマ、オリーブ、オレガノ、カモミール、キャットミント、キャラウェイ、ケッパー、コリアンダー、クレソン、サフラワー、サフラン、サンザシ、サンショウ、ジキタリス、シソ、ジャスミン、ステビア、セージ、セイヨウタンポポ、タイム、タラゴン、チコリ、ニラ、バジル、ハイビスカス、パセリ、ヒース、ヒソップ、ファンネル、ミント、ミツバ、マジョラム、マリーゴールド、ユーカリ、ラズベリー、ラベンダー、レモングラス、レモンバーム、ローレル、ローズマリー、ケッパー、ローズ、ローズヒップ又はこれらの混合物から少なくとも1種以上を選ぶことができる。 In the method for producing a flavor oil of the present invention, the herbs include anise hyssop, aloe, italian parsley, dog mint, egoma, olive, oregano, chamomile, cat mint, caraway, capers, coriander, watercress, safflower, saffron, Hawthorn, salamander, jittaris, perilla, jasmine, stevia, sage, dandelion, thyme, tarragon, chicory, leek, basil, hibiscus, parsley, heather, hyssop, funnel, mint, honeybee, marjoram, marigold, eucalyptus, raspberry, At least one or more kinds can be selected from lavender, lemongrass, lemon balm, laurel, rosemary, capers, rose, rosehip or a mixture thereof.
本発明の香味オイルの製造方法においては、前記アルコールが、エタノール、プロパノール、ブタノール、イソプロピルアルコール又はこれらの混合物から選ばれた少なくとも1種以上であることが好ましい。 In the method for producing a flavor oil of the present invention, the alcohol is preferably at least one selected from ethanol, propanol, butanol, isopropyl alcohol, or a mixture thereof.
本発明の香味オイルの製造方法においては、前記有機酸が、クエン酸、リンゴ酸、フマル酸、酢酸、コハク酸、グルコン酸、酒石酸、乳酸又はこれらの混合物から選ばれた少なくとも1種以上であることが好ましい。 In the method for producing a flavor oil of the present invention, the organic acid is at least one selected from citric acid, malic acid, fumaric acid, acetic acid, succinic acid, gluconic acid, tartaric acid, lactic acid, or a mixture thereof. It is preferable.
本発明の香味オイルの製造方法においては、前記塩類が、塩化ナトリウム、塩化カリウム、塩化マグネシウム、塩化カルシウム、リン酸塩もしくは上記記載の有機酸の塩又はこれらの混合物から選ばれた少なくとも1種以上であることが好ましい。 In the method for producing a flavor oil of the present invention, the salt is at least one selected from sodium chloride, potassium chloride, magnesium chloride, calcium chloride, phosphate, a salt of the organic acid described above, or a mixture thereof. It is preferable that
本発明によれば、香味のよい香味オイルを、低コスト、かつ簡単な方法で製造できる。 ADVANTAGE OF THE INVENTION According to this invention, flavor oil with a sufficient flavor can be manufactured by a low-cost and simple method.
本発明の香味オイルの製造方法は、ハーブをアルコール水溶液で抽出して抽出液を得る抽出工程と、前記抽出液と食用油脂と有機酸及び/又は塩類とを混合する油脂混合工程と、前記混合液を油層と水層とに分離して、油層を回収する油層回収工程からなる。以下詳しく説明する。 The method for producing flavor oil of the present invention comprises an extraction step of extracting an herb with an aqueous alcohol solution to obtain an extract, an oil and fat mixing step of mixing the extract, edible fat and oil, and an organic acid and / or salts, and the mixing The liquid consists of an oil layer recovery step of separating the liquid into an oil layer and an aqueous layer and recovering the oil layer. This will be described in detail below.
本発明で用いるハーブ類とは、香味成分を有する植物のことをいう。このようなハーブ類であれば、特に制限はなく、例えばアニスヒソップ、アロエ、イタリアンパセリ、イヌハッカ、エゴマ、オリーブ、オレガノ、カモミール、キャットミント、キャラウェイ、ケッパー、コリアンダー、クレソン、サフラワー、サフラン、サンザシ、サンショウ、ジキタリス、シソ、ジャスミン、ステビア、セージ、セイヨウタンポポ、タイム、タラゴン、チコリ、ニラ、バジル、ハイビスカス、パセリ、ヒース、ヒソップ、ファンネル、ミント、ミツバ、マジョラム、マリーゴールド、ユーカリ、ラズベリー、ラベンダー、レモングラス、レモンバーム、ローレル、ローズマリー、ケッパー、ローズ、ローズヒップ等から選ばれた1種以上を原料とすることができる。 The herbs used in the present invention refer to plants having a flavor component. If it is such herbs, there is no particular limitation, for example, anise hyssop, aloe, Italian parsley, catnip, sesame, olives, oregano, chamomile, cat mint, caraway, capers, coriander, watercress, safflower, saffron, Hawthorn, salamander, jittaris, perilla, jasmine, stevia, sage, dandelion, thyme, tarragon, chicory, leek, basil, hibiscus, parsley, heather, hyssop, funnel, mint, honeybee, marjoram, marigold, eucalyptus, raspberry, One or more selected from lavender, lemongrass, lemon balm, laurel, rosemary, capers, rose, rose hips and the like can be used as a raw material.
本発明において、上記ハーブは、生、原形乾燥又は粉末乾燥の状態で、利用できる。抽出効率から考えると、ハーブは乾燥状態のものが好ましい。ハーブの細断及び粉末化の方法は、特に制限されず、カッターミキサー、ミル、フードプロセッサー、乳鉢等を用いることができる。
本発明で用いるアルコール水溶液のアルコール濃度は20〜60容量%が好ましく、25〜35容量%がより好ましい。アルコール濃度が20%よりも低くなると抽出能力が下がり、アルコール濃度が60容量%よりも高くなるとアルコール臭が出てきてしまい好ましくない。アルコールとしては、食品製造に使用可能なものであれば特に制限はないが、エタノール、プロパノール、ブタノール、イソプロピルアルコールが好ましく、特にエタノールが好ましい。
In the present invention, the above herbs can be used in a raw, dry state or dry state. Considering the extraction efficiency, the herb is preferably in a dry state. The method of shredding and pulverizing herbs is not particularly limited, and a cutter mixer, a mill, a food processor, a mortar or the like can be used.
The alcohol concentration of the aqueous alcohol solution used in the present invention is preferably 20 to 60% by volume, and more preferably 25 to 35% by volume. When the alcohol concentration is lower than 20%, the extraction ability is lowered, and when the alcohol concentration is higher than 60% by volume, an alcohol odor is generated, which is not preferable. The alcohol is not particularly limited as long as it can be used for food production, but ethanol, propanol, butanol, and isopropyl alcohol are preferable, and ethanol is particularly preferable.
本発明で用いる食用油脂は、10〜50℃で液体状の食用油脂であれば特に制限はなく、例えば米サラダ油、大豆油、パーム油、コーン油、白絞油、ヤシ油、菜種油、サフラワー油、ひまわり油、オリーブ油等を用いることができる。本発明では、油脂自体の匂いが少ないものが好ましく、中でも米サラダ油、大豆油が特に好ましい。 The edible fat used in the present invention is not particularly limited as long as it is a liquid edible fat at 10 to 50 ° C., for example, rice salad oil, soybean oil, palm oil, corn oil, white squeezed oil, coconut oil, rapeseed oil, safflower Oil, sunflower oil, olive oil and the like can be used. In the present invention, those with less odor of fats and oils are preferable, and rice salad oil and soybean oil are particularly preferable.
本発明で用いる有機酸は、食品製造に使用可能なものであれば特に制限はないが、クエン酸、リンゴ酸、フマル酸、酢酸、コハク酸、グルコン酸、酒石酸、乳酸又はこれらの混合物から選ばれた1種以上を用いることができる。中でもクエン酸が特に好ましい。本発明において、有機酸の添加量はその種類により異なるが、アルコール水溶液と食用油脂の合計量100質量部に対して、1〜20質量部添加することが好ましく、5〜10質量部添加することがより好ましい。有機酸の添加量が1質量部よりも少なくなると、抽出液を静置分離する際に、油層と水層の分離が悪くなって白濁し、香味オイルの品質が下がる。有機酸の添加量を増やすと、油水分離が改善される。同時に、香味がアルコール水溶液から食用油脂に移動し易くなり、香味の良い香味オイルが得られる。ただし、有機酸の添加量が20質量部よりも多くなると、ハーブの好ましくない香りが出てきてしまい好ましくない。 The organic acid used in the present invention is not particularly limited as long as it can be used for food production, but is selected from citric acid, malic acid, fumaric acid, acetic acid, succinic acid, gluconic acid, tartaric acid, lactic acid or a mixture thereof. One or more of them can be used. Of these, citric acid is particularly preferred. In this invention, although the addition amount of an organic acid changes with the kinds, it is preferable to add 1-20 mass parts with respect to 100 mass parts of total amounts of aqueous alcohol solution and edible fats, and adding 5-10 mass parts. Is more preferable. When the amount of the organic acid added is less than 1 part by mass, when the extract is allowed to stand and separate, the separation of the oil layer and the aqueous layer becomes poor and white turbidity, and the quality of the flavor oil decreases. Increasing the amount of organic acid added improves oil / water separation. At the same time, the flavor is easily transferred from the aqueous alcohol solution to the edible fat and oil, and a flavor oil having a good flavor is obtained. However, when the addition amount of the organic acid is more than 20 parts by mass, an unfavorable scent of the herb comes out, which is not preferable.
本発明で用いる塩類は、食品製造に使用可能なものであれば特に制限はないが、塩化ナトリウム、塩化カリウム、塩化マグネシウム、塩化カルシウム、リン酸塩もしくは上記記載の有機酸の塩又はこれらの混合物から選ばれた1種以上を用いることができる。中でも、塩化ナトリウムが特に好ましい。本発明において、塩類の濃度は、アルコール水溶液と食用油脂の合計量100質量部に対して、1〜20質量部添加することが好ましく、5〜10質量部添加することがより好ましい。塩類の添加量が1質量部よりも少なくなると、香味がアルコール水溶液から食用油脂に移動し難くなり、香味オイルの香味が下がる。塩類の濃度を増やすと、香味オイルの香味は増すが、塩類の添加量が20質量部よりも多くなると、ハーブの好ましくない香りが出てきてしまい好ましくない。 The salts used in the present invention are not particularly limited as long as they can be used for food production, but sodium chloride, potassium chloride, magnesium chloride, calcium chloride, phosphates, salts of the organic acids described above, or mixtures thereof 1 or more types selected from can be used. Of these, sodium chloride is particularly preferable. In this invention, it is preferable to add 1-20 mass parts with respect to 100 mass parts of total amounts of alcohol aqueous solution and edible fats, and, as for the density | concentration of salt, adding 5-10 mass parts is more preferable. When the added amount of the salt is less than 1 part by mass, the flavor becomes difficult to move from the aqueous alcohol solution to the edible fat and oil, and the flavor of the flavor oil is lowered. Increasing the concentration of the salt increases the flavor of the flavor oil, but if the amount of the salt added exceeds 20 parts by mass, an unfavorable scent of the herb comes out, which is not preferable.
本発明において、ハーブのアルコール抽出液に食用油脂を加えて撹拌混合する際に、有機酸又は塩類を単体で添加してもよいが、有機酸及び塩類を共に添加してもよい。有機酸と塩類を共に添加すると、相乗効果によって、香味が濃厚となり、油水分離性も大きく改善される。有機酸と塩類を共に添加する場合は、アルコール水溶液と食用油脂の合計量100質量部に対して、有機酸の添加量は1〜20質量部が好ましく、塩類の添加量は1〜20質量部が好ましい。このうち、有機酸の添加量は5〜10質量部が好ましく、塩類の添加量は5〜10質量部が特に好ましい。有機酸と塩類を共に添加する場合、クエン酸と塩化ナトリウムの組み合わせが特に好ましい。 In the present invention, when an edible oil / fat is added to the herbal alcohol extract and mixed with stirring, the organic acid or salt may be added alone, or both the organic acid and the salt may be added. When organic acids and salts are added together, a synergistic effect results in a rich flavor and greatly improves oil / water separation. When adding both an organic acid and a salt, the addition amount of the organic acid is preferably 1 to 20 parts by mass and the addition amount of the salt is 1 to 20 parts by mass with respect to 100 parts by mass of the total amount of the aqueous alcohol solution and the edible fat / oil. Is preferred. Among these, the addition amount of the organic acid is preferably 5 to 10 parts by mass, and the addition amount of the salts is particularly preferably 5 to 10 parts by mass. When organic acids and salts are added together, a combination of citric acid and sodium chloride is particularly preferred.
本発明では、ハーブにアルコール水溶液を接触させる抽出工程において、タンク式の撹拌槽を使用することができる。このタンク式の撹拌槽は、食品工業において一般的に使用されるものでよく、特に限定はない。ハーブとアルコール水溶液を混合撹拌する温度は、10〜50℃が好ましく、15〜30℃がより好ましい。この温度条件下で1〜20時間、撹拌混合することが好ましい。 In the present invention, a tank-type stirring tank can be used in the extraction process in which an alcohol aqueous solution is brought into contact with the herb. This tank-type stirring tank may be generally used in the food industry, and is not particularly limited. 10-50 degreeC is preferable and, as for the temperature which mixes and stirs herb and alcohol aqueous solution, 15-30 degreeC is more preferable. It is preferable to stir and mix under this temperature condition for 1 to 20 hours.
本発明では、前記抽出液と食用油脂の混合工程においても、タンク式の撹拌槽を使用することができる。このタンク式の撹拌槽は、食品工業において一般的に使用されるものでよく、特に限定はない。前記食用油脂を混合撹拌する温度は、10〜50℃が好ましく、15〜30℃がより好ましい。この温度条件下で2時間〜20時間、撹拌混合することが好ましい。また、前記食用油脂に、有機酸及び/又は塩類を加えて、1時間〜20時間、混合撹拌することが好ましい。 In the present invention, a tank type agitation tank can also be used in the mixing step of the extract and edible fats and oils. This tank-type stirring tank may be generally used in the food industry, and is not particularly limited. 10-50 degreeC is preferable and, as for the temperature which mixes and stirs the said edible oil and fat, 15-30 degreeC is more preferable. It is preferable to stir and mix for 2 to 20 hours under this temperature condition. Moreover, it is preferable to add an organic acid and / or salts to the edible oil and fat and to mix and stir for 1 to 20 hours.
本発明における一つの実施形態では、上記抽出工程と、前記食用油脂混合工程は、同じ撹拌槽で、連続して行うことができる。また、本発明における別の実施形態では、ハーブとアルコール水溶液を混合撹拌して抽出液を得た後、濾過して抽出液を単離し、別の撹拌槽にて食用油脂と接触させることができる。 In one Embodiment in this invention, the said extraction process and the said edible fat and oil mixing process can be continuously performed in the same stirring tank. In another embodiment of the present invention, the herb and the aqueous alcohol solution are mixed and stirred to obtain an extract, and then the extract can be isolated by filtration and contacted with edible fats and oils in another stirring tank. .
また、本発明においては、前記アルコール水溶液と食用油脂を含む抽出液を、油層と水層とに分離する。油層と水層との分離は、静置して行うことができるが、遠心分離機を用いて分離してもよい。 Moreover, in this invention, the extract containing the said alcohol aqueous solution and edible fats and oils is isolate | separated into an oil layer and a water layer. Separation of the oil layer and the water layer can be performed by standing, but may be performed using a centrifuge.
油層と水層とに分離した後、油層を回収することによって、本発明の香味オイルを製造することができる。 After separating into an oil layer and an aqueous layer, the flavor oil of the present invention can be produced by collecting the oil layer.
本発明の製造方法によって得られた香味オイルは、ハーブのフレッシュな香りを有しており、例えば、ドレッシング、ソース、マーガリン、パン等の食品や調味料の香味付与などの風味増強として様々な用途に好適に用いることができる。また、食品の他、石鹸、クリーム、ローション等にも用いることが出来る。 The flavor oil obtained by the production method of the present invention has a fresh scent of herbs, for example, various uses for flavor enhancement such as flavoring of foods such as dressing, sauce, margarine, bread and seasonings. Can be suitably used. In addition to food, it can also be used in soaps, creams, lotions and the like.
<実施例1>
下記工程によって香味オイルを製造した。
(工程1):撹拌槽に、ハーブ原形(ローレル・タイム・ローズマリー)9.0gと、容量濃度25%のエタノール水溶液120.0gを投入し、25〜30℃にて2時間、撹拌混合した。
(工程2):撹拌槽に、サラダ油(米サラダ油)360.0g(エタノール水溶液の3倍量)を投入し、25〜30℃にて2時間、撹拌混合した。
(工程3−1):エタノール水溶液とサラダ油の合計量100質量部に対して、クエン酸8質量部と、塩化ナトリウム5質量部を加え、15時間、撹拌混合した。
(工程4):撹拌槽の内容物を濾過して、抽出液を得た。
(工程5):上記抽出液を静置して油層と水層を分離し、油層を回収して香味オイルを得た。
<Example 1>
A flavor oil was produced by the following steps.
(Step 1): 9.0 g of herb original form (Laurel Time Rosemary) and 120.0 g of an aqueous ethanol solution having a volume concentration of 25% were put into a stirring tank, and stirred and mixed at 25 to 30 ° C. for 2 hours. .
(Step 2): 360.0 g (three times the amount of ethanol aqueous solution) of salad oil (rice salad oil) was added to the stirring tank, and the mixture was stirred and mixed at 25 to 30 ° C. for 2 hours.
(Step 3-1): 8 parts by mass of citric acid and 5 parts by mass of sodium chloride were added to 100 parts by mass of the ethanol aqueous solution and the salad oil, and the mixture was stirred and mixed for 15 hours.
(Step 4): The contents of the stirring tank were filtered to obtain an extract.
(Step 5): The extract was allowed to stand to separate an oil layer and an aqueous layer, and the oil layer was recovered to obtain a flavor oil.
以下の参考例2、3、実施例4、5においては、実施例1における(工程3−1)を、各々(工程3−2)〜(工程3−5)に、変更した。その他の工程は、実施例1の方法にしたがった。 In the following Reference Examples 2 and 3, and Examples 4 and 5, (Step 3-1) in Example 1 was changed to (Step 3-2) to (Step 3-5), respectively. Other steps were in accordance with the method of Example 1.
<参考例2>
(工程3−2):エタノール水溶液とサラダ油の合計量100質量部に対して、塩化ナトリウム5質量部を加え、15時間、撹拌混合した。
< Reference Example 2>
(Step 3-2): 5 parts by mass of sodium chloride was added to 100 parts by mass of the total amount of the aqueous ethanol solution and the salad oil, and the mixture was stirred and mixed for 15 hours.
<参考例3>
(工程3−3):エタノール水溶液とサラダ油の合計量100質量部に対して、クエン酸8質量部を加え、15時間、撹拌混合した。
< Reference Example 3>
(Step 3-3): 8 parts by mass of citric acid was added to 100 parts by mass of the total amount of the ethanol aqueous solution and the salad oil, and the mixture was stirred and mixed for 15 hours.
<実施例4>
(工程3−4):エタノール水溶液とサラダ油の合計量100質量部に対して、クエン酸1質量部と、塩化ナトリウム1質量部を加え、15時間、撹拌混合した。
<Example 4>
(Step 3-4): 1 part by mass of citric acid and 1 part by mass of sodium chloride were added to 100 parts by mass of the ethanol aqueous solution and the salad oil, and the mixture was stirred and mixed for 15 hours.
<実施例5>
(工程3−5):エタノール水溶液とサラダ油の合計量100質量部に対して、クエン酸20質量部と、塩化ナトリウム20質量部を加え、15時間、撹拌混合した。
<Example 5>
(Step 3-5): 20 parts by mass of citric acid and 20 parts by mass of sodium chloride were added to 100 parts by mass of the total amount of ethanol aqueous solution and salad oil, and the mixture was stirred and mixed for 15 hours.
<比較例1>
比較例1では、エタノール水溶液による抽出工程を省略した。すなわち、撹拌槽に、ハーブ原形(ローレル・タイム・ローズマリー)9.0gと、サラダ油(米サラダ油)360.0gを投入し、25〜30℃にて2時間、撹拌混合した後、サラダ油100質量部に対して、クエン酸8質量部と、塩化ナトリウム5質量部を加え、更に15時間、撹拌混合した。最後に、撹拌槽の内容物を濾過して、香味オイルを得た。
<Comparative Example 1>
In Comparative Example 1, the extraction step using an aqueous ethanol solution was omitted. That is, 9.0 g of herb original form (Laurel, Time, Rosemary) and 360.0 g of salad oil (rice salad oil) are added to a stirring tank, and after stirring and mixing at 25-30 ° C. for 2 hours, 100 mass of salad oil To the part, 8 parts by mass of citric acid and 5 parts by mass of sodium chloride were added and further stirred and mixed for 15 hours. Finally, the contents of the stirring tank were filtered to obtain a flavor oil.
<比較例2>
比較例2では、25容量%のエタノール水溶液120.0gに、エタノール水溶液100質量部に対して、クエン酸8質量部と、塩化ナトリウム5質量部を加えて、ハーブの抽出に使用した。すなわち、撹拌槽に、ハーブ原形(ローレル・タイム・ローズマリー)9.0gと、上記のクエン酸及び塩化ナトリウムを含有するエタノール水溶液にサラダ油(米サラダ油)360.0gを投入し、25〜30℃にて17時間、撹拌混合した後、撹拌槽の内容物を濾過して、抽出液を得た。最後に、上記抽出液を静置して油層と水層を分離し、油層を回収して香味オイルを得た。
<Comparative example 2>
In Comparative Example 2, 8 parts by mass of citric acid and 5 parts by mass of sodium chloride were added to 120.0 g of a 25% by volume ethanol aqueous solution with respect to 100 parts by mass of the ethanol aqueous solution, and used for herbal extraction. Specifically, 9.0 g of herb original form (Laurel Time Rosemary) and 360.0 g of salad oil (rice salad oil) were added to the ethanol aqueous solution containing the above citric acid and sodium chloride in a stirring tank, and the temperature was 25-30 ° C. After stirring for 17 hours, the contents of the stirring tank were filtered to obtain an extract. Finally, the extract was allowed to stand to separate an oil layer and an aqueous layer, and the oil layer was recovered to obtain a flavor oil.
<比較例3>
比較例3では、クエン酸及び塩化ナトリウムは一切添加しなかった。すなわち、撹拌槽に、ハーブ原形(ローレル・タイム・ローズマリー)9.0gと、エタノール水溶液120.0gを投入し、25〜30℃にて2時間、撹拌混合した後、サラダ油(米サラダ油)360.0gを投入して更に17時間撹拌混合した。次に、撹拌槽の内容物を濾過して、抽出液を得た。最後に、上記抽出液を静置して油層と水層を分離し、油層を回収して香味オイルを得た。
<Comparative Example 3>
In Comparative Example 3, no citric acid and sodium chloride were added. That is, 9.0 g of herb original form (Laurel Time Rosemary) and 120.0 g of an aqueous ethanol solution are added to a stirring tank, and after stirring and mixing at 25 to 30 ° C. for 2 hours, salad oil (rice salad oil) 360 0.0 g was added and further stirred and mixed for 17 hours. Next, the contents of the stirring tank were filtered to obtain an extract. Finally, the extract was allowed to stand to separate an oil layer and an aqueous layer, and the oil layer was recovered to obtain a flavor oil.
実施例1、参考例2、3、実施例4、5、比較例1〜3で調製した香味オイルについて、下記に示す項目と評価基準にしたがって、評価した。 The flavor oils prepared in Example 1 , Reference Examples 2, 3, Example 4, 5, and Comparative Examples 1 to 3 were evaluated according to the following items and evaluation criteria.
[香り]
4名の検査員が香味オイルの香りを直接嗅いで判定した。
[fragrance]
Four inspectors judged the scent of the flavor oil directly.
◎:力価が強く、フレッシュな香りが非常に強い。 (Double-circle): A titer is strong and a fresh fragrance is very strong.
○:力価が強く、フレッシュな香りがある。 ○: Strong titer and fresh scent.
△:力価は強いが、フレッシュな香りが弱い。 (Triangle | delta): Although a titer is strong, a fresh fragrance is weak.
×:力価が弱く、フレッシュな香りがない。 X: A titer is weak and there is no fresh fragrance.
[分離性]
4名の検査員が香味オイルの濁りを目視して判定した。
[Separability]
Four inspectors judged the turbidity of the flavor oil visually.
◎:油水分離が、非常に良好である。 A: Oil-water separation is very good.
○:油水分離が良好である。 ○: Oil-water separation is good.
△:油水分離がやや悪く、やや濁っている。 (Triangle | delta): Oil-water separation is a little bad and it is a little muddy.
×:油水分離が悪く、白濁している。 X: Oil-water separation is poor and cloudy.
結果をまとめて表1及び2に示す。 The results are summarized in Tables 1 and 2.
上記表1に示されるように、抽出にエタノール水溶液を使用し、サラダ油投入後にクエン酸及び塩化ナトリウムを添加する、実施例1によれば、油水分離性が非常に良好で、力価が強く、フレッシュなハーブの香りを有する香味オイルが得られた。 As shown in Table 1 above, using an aqueous ethanol solution for extraction, adding citric acid and sodium chloride after adding salad oil, according to Example 1, the oil-water separation property is very good, the titer is strong, A flavor oil having a fresh herbal scent was obtained.
しかし、抽出にエタノール水溶液を使用せず、サラダ油投入後にクエン酸及び塩化ナトリウムを添加する、比較例1は、力価が弱く、フレッシュな香りが得られなかった。 However, in Comparative Example 1, in which an aqueous ethanol solution was not used for extraction and citric acid and sodium chloride were added after addition of salad oil, the titer was weak and a fresh fragrance could not be obtained.
また、抽出にクエン酸と塩化ナトリウムを含有するエタノール水溶液を使用し、サラダ油投入後にクエン酸及び塩化ナトリウムを添加しなかった、比較例2は、油水分離性は良かったが、ハーブのフレッシュな香りは弱かった。 Moreover, the aqueous solution containing citric acid and sodium chloride was used for the extraction, and citric acid and sodium chloride were not added after the salad oil was added. Was weak.
また、抽出にエタノール水溶液を使用し、サラダ油投入後にクエン酸及び塩化ナトリウムを添加しなかった、比較例3は、油水分離性が悪く白濁しており、ハーブのフレッシュな香りは弱かった。 Moreover, the ethanol aqueous solution was used for extraction, and after adding salad oil, citric acid and sodium chloride were not added, Comparative Example 3 was poor in oil / water separation and white turbidity, and the fresh aroma of herbs was weak.
上記表2は、実施例1、参考例2、3、実施例4、5のクエン酸と、塩化ナトリウムの添加量を変えた評価結果を示す。 Table 2 above shows the evaluation results obtained by changing the amounts of citric acid and sodium chloride of Example 1 , Reference Examples 2, 3, and Examples 4 and 5.
塩化ナトリウムを単独で加えた参考例2は、フレッシュな香りが弱く、クエン酸を単独で加えた参考例3では、フレッシュな香りは得られるが、クエン酸及び塩化ナトリウムを両方加えた実施例1のよりも弱かった。また、塩化ナトリウムを単独で加えた参考例2は、油水分離があまり良くなく、やや濁っていた。
In Reference Example 2 in which sodium chloride was added alone, the fresh fragrance was weak, and in Reference Example 3 in which citric acid was added alone, a fresh scent was obtained, but Example 1 in which both citric acid and sodium chloride were added. It was weaker than Further, in Reference Example 2 in which sodium chloride was added alone, oil-water separation was not so good and it was slightly cloudy.
クエン酸と塩化ナトリウムの添加量を共に1質量部とする、実施例4でも、フレッシュな香りは得られるが、油水分離があまり良くなく、やや濁っていた。 In Example 4 where the addition amounts of citric acid and sodium chloride were both 1 part by mass, a fresh scent was obtained, but the oil-water separation was not so good and it was somewhat cloudy.
クエン酸と塩化ナトリウムの添加量を共に20質量部とする、実施例5は、油水分離性が非常に良好で、実施例1と同等なハーブの香りを有する香味オイルが得られた。 In Example 5, in which the addition amounts of citric acid and sodium chloride were both 20 parts by mass, oil-water separability was very good, and a flavor oil having a herbal scent equivalent to Example 1 was obtained.
Claims (9)
The said salt is at least 1 sort (s) chosen from sodium chloride, potassium chloride, magnesium chloride, calcium chloride, a phosphate, the salt of the said organic acid, or these mixtures, The any one of Claims 1-8. The manufacturing method of the flavor oil as described in 2.
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