JPH01137939A - Production of chocolate - Google Patents
Production of chocolateInfo
- Publication number
- JPH01137939A JPH01137939A JP62295053A JP29505387A JPH01137939A JP H01137939 A JPH01137939 A JP H01137939A JP 62295053 A JP62295053 A JP 62295053A JP 29505387 A JP29505387 A JP 29505387A JP H01137939 A JPH01137939 A JP H01137939A
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- chocolate
- ingredient
- ester
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 235000019219 chocolate Nutrition 0.000 title claims abstract description 57
- 238000004519 manufacturing process Methods 0.000 title claims description 33
- 244000299461 Theobroma cacao Species 0.000 claims abstract description 91
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 67
- 229930195729 fatty acid Natural products 0.000 claims abstract description 67
- 239000000194 fatty acid Substances 0.000 claims abstract description 67
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 46
- 150000002148 esters Chemical class 0.000 claims abstract description 38
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims abstract description 34
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 claims abstract description 28
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 claims abstract description 28
- 235000001046 cacaotero Nutrition 0.000 claims abstract description 28
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 238000006467 substitution reaction Methods 0.000 claims abstract description 25
- 239000000126 substance Substances 0.000 claims abstract description 23
- -1 fatty acid ester Chemical class 0.000 claims abstract description 22
- 239000005639 Lauric acid Substances 0.000 claims abstract description 17
- 238000001816 cooling Methods 0.000 claims abstract description 15
- 239000008267 milk Substances 0.000 claims abstract description 13
- 235000013336 milk Nutrition 0.000 claims abstract description 12
- 210000004080 milk Anatomy 0.000 claims abstract description 12
- 229920000728 polyester Polymers 0.000 claims abstract description 11
- 229930006000 Sucrose Natural products 0.000 claims description 21
- 239000005720 sucrose Substances 0.000 claims description 21
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 46
- 239000004615 ingredient Substances 0.000 abstract description 24
- 239000000796 flavoring agent Substances 0.000 abstract description 15
- 235000019634 flavors Nutrition 0.000 abstract description 15
- 235000000346 sugar Nutrition 0.000 abstract description 11
- 235000014593 oils and fats Nutrition 0.000 abstract description 9
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 abstract description 6
- 235000021360 Myristic acid Nutrition 0.000 abstract description 6
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 abstract description 6
- 235000009508 confectionery Nutrition 0.000 abstract description 3
- 125000004185 ester group Chemical group 0.000 abstract 3
- 235000013305 food Nutrition 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 28
- 235000019198 oils Nutrition 0.000 description 28
- 239000003925 fat Substances 0.000 description 27
- 235000019197 fats Nutrition 0.000 description 27
- 235000014121 butter Nutrition 0.000 description 25
- 239000000843 powder Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 18
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 18
- 229940110456 cocoa butter Drugs 0.000 description 10
- 235000019868 cocoa butter Nutrition 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 235000009470 Theobroma cacao Nutrition 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 235000020183 skimmed milk Nutrition 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 6
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 6
- 150000005690 diesters Chemical class 0.000 description 6
- ZAZKJZBWRNNLDS-UHFFFAOYSA-N methyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC ZAZKJZBWRNNLDS-UHFFFAOYSA-N 0.000 description 6
- 150000005691 triesters Chemical class 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 5
- 230000036760 body temperature Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 235000020186 condensed milk Nutrition 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000009991 scouring Methods 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 2
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- AOFUBOWZWQFQJU-SNOJBQEQSA-N (2r,3s,4s,5r)-2,5-bis(hydroxymethyl)oxolane-2,3,4-triol;(2s,3r,4s,5s,6r)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O.OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O AOFUBOWZWQFQJU-SNOJBQEQSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 101100150045 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) spe-3 gene Proteins 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
- 102000007544 Whey Proteins Human genes 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 235000015155 buttermilk Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 235000019879 cocoa butter substitute Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000015140 cultured milk Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000504 effect on taste Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000020187 evaporated milk Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000021552 granulated sugar Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960004903 invert sugar Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000002366 lipolytic effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
Landscapes
- Edible Oils And Fats (AREA)
- Confectionery (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はチョコレートの製造法に関するものである。詳
しくは低カロリーで、風味と艶が良好であり、かつ適度
の固さを有するチョコレートの製造法に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for manufacturing chocolate. Specifically, the present invention relates to a method for producing chocolate that is low in calories, has good flavor and gloss, and has an appropriate hardness.
(従来の技術と問題点)
チョコレートは一般に、所謂カカオ成分に甘味成分とカ
カオ脂(カカオバター)とを加え、さらに場合により乳
成分を加えた原料成分を溶融状態で混合して任意の形状
とした後、冷却固化することによって製造されている。(Conventional technology and problems) Chocolate is generally made by mixing raw ingredients in a molten state, such as cacao ingredients, sweetening ingredients and cacao butter (cocoa butter), and in some cases milk ingredients. After that, it is manufactured by cooling and solidifying it.
これ等従来のチョコレート原料のうち、油脂成分のカカ
オ脂は、室温ては適度の硬度を有し体温付近の温度では
急激に溶融する、可塑性範囲が極めて狭い性質を有する
ため、チョコレート原料として不可欠のものであるが、
高価で品薄傾向にあるため、これに代る油脂成分として
、カカオ脂と類似する性質を有する所謂ハートバターが
検討され使用されている。Among these conventional chocolate ingredients, cacao butter, which is an oil component, has a moderate hardness at room temperature, melts rapidly at temperatures around body temperature, and has an extremely narrow plasticity range, making it an essential ingredient for chocolate. Although it is a thing,
Because it is expensive and tends to be in short supply, so-called heart butter, which has properties similar to cacao butter, has been studied and used as an alternative fat and oil component.
ハートバターとしては、例えは、
(イ)天然又は合成による油脂原料から、物理性がカカ
オ脂の特徴的成分である1、3−ジ飽和脂肪酸−2−不
飽和脂肪酸トリグリセライトを採取したもの、
(ロ)脂肪酸成分として不飽和脂肪酸を含む油脂原料を
、調整された条件下で水素添加処理して得られる、不飽
和脂肪酸のトランス型異性体を含むトリグリセライド(
高トランス酸型ハートバター)、(ハ)ヤシ油、パーム
核油等の脂肪酸成分がラウリン酸を主体とする油脂をそ
のまま、あるいは水素添加したもの(ラウリン酸型ハー
トバター)等が知られている。Examples of heart butter include: (a) 1,3-disaturated fatty acid-2-unsaturated fatty acid triglycerite, which is a characteristic component of cocoa butter, is collected from natural or synthetic oil and fat raw materials; (b) Triglycerides containing trans isomers of unsaturated fatty acids obtained by hydrogenating oil and fat raw materials containing unsaturated fatty acids as fatty acid components under controlled conditions (
(c) Coconut oil, palm kernel oil, and other fats and oils whose fatty acid component is mainly lauric acid, either as they are or hydrogenated (lauric acid heart butter) are known. .
これ等のハードバター及びカカオ脂は、何れも化学構造
上トリグリセライド、即ちグリセリンの脂肪酸トリエス
テル体であり、それ等の構造を適宜制御して得られたも
のであるため、体内に摂取された場合に、脂質分解酵素
により分解され、代謝されて、栄養源となり、肥満等の
健康管理上好ましくない問題を招く恐れがある。Both hard butter and cocoa butter have a chemical structure of triglycerides, that is, fatty acid triesters of glycerin, and are obtained by appropriately controlling their structures, so when ingested into the body, In addition, it is degraded and metabolized by lipolytic enzymes and becomes a source of nutrients, which may lead to unfavorable health management problems such as obesity.
以上のトリグリセライドの外、パルミチン酸又は酢酸の
ソルビタンエステルが、カカオ脂の代替として使用し得
ることも知られているが、風味に欠け、安定性にも問題
があり実用性に乏しい。In addition to the above triglycerides, it is also known that sorbitan esters of palmitic acid or acetic acid can be used as substitutes for cocoa butter, but these lack flavor and have problems with stability, making them impractical.
(問題点を解決するための手段)
本発明者等は、チョコレート原料中の油脂成分として、
従来知られているカカオ脂や、ハートバターの代りに、
チョコレート原料成分として優れた性質及び風味を付与
すると共に、非カロリー性で健康管理上好ましいカカオ
脂代替物を得ることを目的として探索中のところ、ショ
糖脂肪酸エステルにおいて、ショ糖に対する脂肪酸のエ
ステル結合数(置換度)が4以上のものは、体内に摂取
された場合に、脂質代謝系に取り込まれず、実質的に非
カロリー性の物質であることが知られていることに着目
し、種々検討した結果、特定の脂肪酸成分からなり、か
つ特定のエステル置換度の組成を有するショ糖脂肪酸エ
ステルが上記の目的に適合することを確認し本発明を達
成した。(Means for solving the problem) The present inventors have discovered that as fat and oil components in chocolate raw materials,
Instead of the conventionally known cocoa butter and heart butter,
We are currently searching for a cocoa butter substitute that has excellent properties and flavor as a chocolate raw ingredient, is non-caloric, and is preferable for health management. Focusing on the fact that substances with a number (degree of substitution) of 4 or more are not taken into the lipid metabolic system and are essentially non-caloric substances when ingested into the body, various studies were conducted. As a result, it was confirmed that a sucrose fatty acid ester consisting of a specific fatty acid component and having a composition with a specific degree of ester substitution was compatible with the above object, and the present invention was achieved.
即ち、本発明の要旨は、カカオ成分、油脂成分及び甘味
成分を含み、あるいはこれ等に更に乳成分を加えた成分
を主体とする溶融状態のチョコレート原料を任意形状と
した後、冷却固化してチョコレートを製造する方法にお
いて、油脂成分として、ラウリン系油脂由来の脂肪酸、
ラウリン酸又はミリスチン酸を主構成脂肪酸とするショ
糖脂肪酸のポリエステルであって、置換度が1〜3のエ
ステル体が20重量%以下であり、残余のエステルの平
均置換度が5以上であるショ糖脂肪酸ポリエステル体か
らなるハートバター様物質を用いることを特徴とするチ
ョコレートの製造法に存する。That is, the gist of the present invention is to form a molten chocolate raw material containing a cacao component, an oil and fat component, and a sweetening component, or a milk component into an arbitrary shape, and then cool and solidify it. In the method for manufacturing chocolate, fatty acids derived from lauric oils and fats are used as oil components.
A polyester of sucrose fatty acid whose main fatty acid is lauric acid or myristic acid, in which esters with a degree of substitution of 1 to 3 account for 20% by weight or less, and the average degree of substitution of the remaining esters is 5 or more. A method for producing chocolate characterized by using a heart butter-like substance made of a sugar fatty acid polyester.
以下に本発明の詳細な説明する。The present invention will be explained in detail below.
チョコレートは一般に、カカオ成分に、甘味成分及び油
脂成分としてカカオ脂(カカオバター)を加え、さらに
場合により乳成分を加えた原料成分を溶融状態で混合し
て任意形状とした後、冷却固化することによって製造さ
れている。Generally, chocolate is made by mixing the raw ingredients in a molten state by adding cocoa butter as a sweetening ingredient and oil/fat ingredient to the cacao ingredient, and in some cases adding a milk ingredient to form an arbitrary shape, and then cooling and solidifying. Manufactured by.
本発明方法においては、これ等チョコレート原料成分の
うち油脂成分として、後に詳細に述べるような、その性
質がカカオ脂に類似し、かつ低カロリー性のショ糖脂肪
酸ポリエステルからなるハートバター様物質が使用され
る。In the method of the present invention, a heart butter-like substance made of sucrose fatty acid polyester, which has properties similar to cacao butter and is low in calories, is used as the fat and oil component among these chocolate raw ingredients, as will be described in detail later. be done.
油脂成分以外の成分は、従来一般に使用されているもの
が適用される。例えは、カカオ成分とし= 4−
では、カカオ豆を焙焼して微粒子状にすり潰して得られ
るカカオマスと、このカカオマスを搾油してカカオ脂を
除いた残固形分との混合物が使用される。As for the components other than the oil and fat components, those commonly used in the past are applicable. For example, when the cacao component is 4-, a mixture of cacao mass obtained by roasting and grinding cacao beans into fine particles and residual solid content obtained by extracting oil from this cacao mass to remove cacao fat is used.
また、甘味成分としては、ショ糖、葡萄糖、果糖、粉糖
、妻芽糖、転化糖、乳糖等の食品用甘味物質が挙げられ
、さらに乳成分としては、クリーム、バター、チーズ、
濃縮乳、無糖練乳、無糖脱脂練乳加糖練乳、加糖脱脂練
乳、全粉乳、脱脂粉乳、クリームパウダー、ホエイパウ
ダー、バターミルクパウダー、発酵乳、牛乳等が用いら
れる。In addition, sweet ingredients include food-use sweet substances such as sucrose, glucose, fructose, powdered sugar, gable sugar, invert sugar, and lactose, and milk ingredients include cream, butter, cheese,
Concentrated milk, unsweetened condensed milk, unsweetened skim condensed milk, sweetened condensed milk, sweetened skim condensed milk, whole milk powder, skim milk powder, cream powder, whey powder, buttermilk powder, fermented milk, milk, etc. are used.
油脂成分、カカオ成分、甘味成分及び乳成分の混合割合
も従来のチョコレートとの場合と同様であり、例えは、
準チョコレート(公正取引委員会による規格)の場合は
、油脂成分18〜50%、カカオ成分7〜50%、甘味
成分10〜60%、乳成分0〜30%の配合が好ましく
、また準ミルクチョコレートの場合は、油脂成分18〜
50%、カカオ成分7〜50%、甘味成分10〜60%
、乳成分12.5〜30%の配合が好ましく、さらにチ
ョコレート生地の場合は、油脂成分10〜50%、カカ
オ成分1〜50%、甘味成分10〜60%、乳成分0〜
30%の配合が好ましい。The mixing proportions of fat and oil components, cacao components, sweetness components, and milk components are also the same as in conventional chocolate; for example,
In the case of quasi-chocolate (standards by the Fair Trade Commission), it is preferable to have a blend of 18-50% oil and fat components, 7-50% cacao components, 10-60% sweetness components, and 0-30% milk components, and quasi-milk chocolate. In the case of , oil and fat components 18~
50%, cacao component 7-50%, sweetness component 10-60%
, a milk component of 12.5 to 30% is preferable, and in the case of chocolate dough, an oil and fat component of 10 to 50%, a cacao component of 1 to 50%, a sweetness component of 10 to 60%, and a milk component of 0 to 30%.
A loading of 30% is preferred.
本発明の特異とするところは、チョコレート原料の油脂
成分として、その性質がカカオ脂に類似し、かつ低カロ
リー性のショ糖脂肪酸ポリエステルからなるハートバタ
ー様物質を用いることである。The unique feature of the present invention is that a heart butter-like substance made of sucrose fatty acid polyester, which has properties similar to cacao butter and is low in calories, is used as the fat and oil component of the chocolate raw material.
一般に、ある油脂がカカオ脂に類似する所謂ハードバタ
ーとして有用であるためには、種々の温度に対する固体
脂の含有割合の変化が、カカオ脂の温度に対する固体脂
の含有割合の変化と類似していること、換言すれは、常
温では適度の硬度を有し、体温付近の温度では急激に溶
融するという、可塑性範囲が極めて狭い性質を有するこ
とが必要である。Generally, in order for a certain fat to be useful as a so-called hard butter similar to cacao butter, the change in solid fat content with respect to various temperatures must be similar to the change in the solid fat content with respect to temperature of cacao butter. In other words, it is necessary that the plasticity range is extremely narrow, that is, it has moderate hardness at room temperature and rapidly melts at temperatures around body temperature.
本発明に使用される油脂成分は、種々の温度に対する固
体脂の含有割合の変化が、カカオ脂のそれと類似するよ
うに調整され、体内に摂取された場合に脂質代謝系に取
り込まれず、低カロリー性であって、しかも風味を損な
うことのないハードバター様物質であって、ラウリン系
油脂由来の脂肪酸、ラウリン酸又はミリスチン酸を主構
成脂肪酸とするショ糖脂肪酸のポリエステルからなるも
のである。The oil and fat components used in the present invention are adjusted so that the change in solid fat content ratio with respect to various temperatures is similar to that of cacao butter, and when ingested into the body, is not taken into the lipid metabolic system and has a low calorie content. It is a hard butter-like substance that is soft and does not impair flavor, and is made of a polyester of sucrose fatty acids whose main constituent fatty acids are fatty acids derived from lauric oils and fats, lauric acid, or myristic acid.
上記ラウリン系油脂由来の脂肪酸とは、ヤシ油、パーム
油等の所謂ラウリン系油脂又はその水素添加物から得ら
れる脂肪酸を指示するもので、ラウリン酸とミリスチン
酸の合計量が50%(重量)以上であって、該合計量中
ラウリン酸が80〜20%、ミリスチン酸が20〜80
%の混合物を指示するものである。The fatty acids derived from lauric oils and fats mentioned above refer to fatty acids obtained from so-called lauric oils and fats such as coconut oil and palm oil, or their hydrogenated products, and the total amount of lauric acid and myristic acid is 50% (by weight). or more, and in the total amount, lauric acid is 80 to 20% and myristic acid is 20 to 80%.
% mixture.
脂肪酸成分としては、上記のラウリン系油脂由来の脂肪
酸に限られず、それぞれ別途に調製されたラウリン酸又
はミリスチン酸を主構成成分とするものであってもよい
。The fatty acid component is not limited to the above-mentioned fatty acids derived from lauric oils and fats, but may also be one containing separately prepared lauric acid or myristic acid as a main component.
このようなショ糖脂肪酸エステルは、脂肪酸成分が上記
特定のものであることの外に、エステル置換度1〜3の
エステルが20重量%以下であり、残余のエステルの平
均置換度が5以上の組成のものであることが必要である
。Such sucrose fatty acid esters contain not only the above-specified fatty acid components but also 20% by weight or less of esters with a degree of ester substitution of 1 to 3, and an average degree of substitution of the remaining esters of 5 or more. It is necessary that the composition be of the same composition.
ショ糖脂肪酸エステルには、ショ糖1分子に対する脂肪
酸の置換度によって、モノエステルからオクタエステル
までの8種類が存在するが、これ等のうち、体内に摂取
された場合に、脂質代謝系に取り込まれず、実質的に非
カロリー性の物質であるのは、テトラエステル以上のも
の、即ち脂肪酸の置換度が4以上のものである。There are eight types of sucrose fatty acid esters, ranging from monoesters to octaesters, depending on the degree of substitution of fatty acid per molecule of sucrose. Substantially non-caloric substances are tetraesters or higher, ie, those with a degree of fatty acid substitution of 4 or higher.
また味覚上、脂肪酸の呈味の懸念を払拭するためには、
ショ糖脂肪酸エステル中のモノエステル体が実質的に存
在しないレベルとすることが肝要である。その理由は、
脂肪酸成分の種類によって程度は異なるものの、モノエ
ステル体は親水性が極めて高く、味覚に大きな影響を与
えるからである。その程度は、脂肪酸成分の炭素数の少
ない程著しく、例えばミリスチン酸(炭素数14)以下
の炭素数の脂肪酸成分のモノエステル体では、1%程度
存在しても苦味を感じるようになる。In addition, in order to eliminate concerns about the taste of fatty acids,
It is important that the monoester form in the sucrose fatty acid ester be at a level that is substantially absent. The reason is,
Although the degree differs depending on the type of fatty acid component, monoesters have extremely high hydrophilicity and have a large effect on taste. The degree of this is more pronounced as the number of carbon atoms in the fatty acid component decreases; for example, a monoester of a fatty acid component with a carbon number of less than myristic acid (14 carbon atoms) will taste bitter even if it is present at about 1%.
以上に述べた低カロリー性であり、しかも風味を損なう
ことのない性質に加えて、前述の常温では適度の硬度を
有し、体温付近の温度では急激に溶融する可塑性範囲が
極めて狭いという、ハードバターとして要求される性質
を具備するために、本発明の油脂成分として使用される
ハードバター様物質は、ショ糖脂肪酸エステルの脂肪酸
成分として、前記のラウリン酸又はラウリン酸を主とす
る脂肪酸を選択するとともに、エステル置換度1〜3の
エステルが20重量%以下、好ましくは10重量%以下
、特に好ましくは5重量%以下で0%に近い程望ましく
、また残余のエステルの平均置換度は5以上であること
が必要である。In addition to the above-mentioned properties of low calorie content and no loss of flavor, it has a hardness that is moderately hard at room temperature and melts rapidly at temperatures around body temperature, and has an extremely narrow plasticity range. In order to have the properties required for butter, the hard butter-like substance used as the oil and fat component of the present invention is selected from the above-mentioned lauric acid or a fatty acid mainly composed of lauric acid as the fatty acid component of the sucrose fatty acid ester. At the same time, esters with a degree of ester substitution of 1 to 3 are preferably 20% by weight or less, preferably 10% by weight or less, particularly preferably 5% by weight or less, as close to 0% as possible, and the average degree of substitution of the remaining esters is 5 or more. It is necessary that
即ち、エステル置換度1〜3のエステルを含有しないか
、含有してもそれ等の合計量が全体の20重量%以下で
あることが必要であり、20重量%より多い場合には、
風味並びに非カロリー性の点において、ハードバター様
物質として不適当である。That is, it is necessary that esters with a degree of ester substitution of 1 to 3 are not contained, or even if they are contained, the total amount thereof is 20% by weight or less of the whole, and if it is more than 20% by weight,
It is unsuitable as a hard butter-like substance in terms of flavor and non-caloric properties.
また、エステル置換度1〜3のエステルが20重量%以
下であって、残余のエステルの平均置換度が5以上とな
る組成であっても、脂肪酸成分が、前記のラウリン系油
脂由来の脂肪酸、ラウリン酸又はミリスチン酸を主構成
とするもの以外の場合には、後記比較例に示すように、
ハードバターとして要求される、常温では適度の硬度を
有し体温付近の温度では急激に溶融する性質のものが得
られない。Furthermore, even if the composition has a composition in which esters with a degree of ester substitution of 1 to 3 are 20% by weight or less and the average degree of substitution of the remaining esters is 5 or more, the fatty acid component may be the fatty acid derived from the lauric oil or fat, In cases other than those mainly composed of lauric acid or myristic acid, as shown in the comparative example below,
It is not possible to obtain the property required for hard butter, which has moderate hardness at room temperature and rapidly melts at temperatures near body temperature.
なお、ラウリン系油脂由来の脂肪酸、ラウリン酸又はミ
リスチン酸を主構成とするもの以外の脂肪酸成分、例え
ばパルミチン酸(炭素数16)やステアリン酸(炭素数
18)のような高級脂肪酸と、例えば酢酸のような極く
低級の脂肪酸(炭素数が6以下のもの)とを適当な割合
で使用したショ糖脂肪酸エステルでも、本発明に使用さ
れるハードバター様物質と同様に、常温では適度の硬度
を有し体温付近の温度では急激に溶融する性質のものと
することは可能であるが、前述のように風味や香りの点
てチョコレート原料の油脂成分としては不適当である。In addition, fatty acids derived from lauric oils, fatty acids other than those mainly composed of lauric acid or myristic acid, such as higher fatty acids such as palmitic acid (16 carbon atoms) and stearic acid (18 carbon atoms), and acetic acid, for example. Similar to the hard butter-like substance used in the present invention, even sucrose fatty acid esters containing extremely low fatty acids (those with 6 or fewer carbon atoms) in an appropriate ratio have a moderate hardness at room temperature. Although it is possible to have a substance that has a property of rapidly melting at a temperature near body temperature, as mentioned above, it is unsuitable as an oil or fat component for chocolate raw materials due to the flavor and aroma.
上述の本発明の油脂成分として使用されるハードバター
様物質は、ショ糖脂肪酸エステルの製造法として周知の
種々の方法によって製造することができる。The hard butter-like substance used as the fat/oil component of the present invention described above can be produced by various methods well known as methods for producing sucrose fatty acid esters.
例えば、(a)ショ糖と、前記の脂肪酸の低級アルコー
ルエステルとを、適当な有機溶媒中において、アルカリ
性触媒を使用し、減圧上加熱してエステル交換反応させ
、反応の進行に伴って溶媒を留去し、最終的に有機溶媒
を残存させない条件で反応を完結させる方法、(b)シ
ョ糖と、前記の脂肪酸の低級アルコールエステルとを、
石鹸の存在下で、溶媒を使用し又は使用せずに、溶融混
合状態とし、アルカリ性触媒を使用して減圧上加熱して
エステル交換反応させる方法、あるいは(C)ショ糖と
前記の脂肪酸のクロライドとを、有機溶媒を使用し又は
使用せずに、アルカリ性触媒の存在下でエステル化する
方法等が挙げられるが、製造に当っては、原料によって
反応条件を選択することが必要である。また場合により
、これ等の方法で得られたショ糖脂肪酸エステルを適宜
配合することによっても調製される。For example, (a) sucrose and the above lower alcohol ester of fatty acid are transesterified in an appropriate organic solvent by heating under reduced pressure using an alkaline catalyst, and as the reaction progresses, the solvent is removed. (b) a method in which sucrose and the lower alcohol ester of fatty acid are distilled off and the reaction is finally completed under conditions that do not leave any organic solvent;
In the presence of soap, with or without the use of a solvent, the mixture is melted and mixed and heated under reduced pressure using an alkaline catalyst to carry out a transesterification reaction, or (C) a chloride of sucrose and the above-mentioned fatty acid. Examples include a method of esterifying and in the presence of an alkaline catalyst with or without an organic solvent, but during production, it is necessary to select reaction conditions depending on the raw materials. In some cases, it may also be prepared by appropriately blending sucrose fatty acid esters obtained by these methods.
以上に述べた本発明の油脂成分として使用されるハード
バター様物質の詳細は、本発明者等の一部がさきに発明
した特願昭62−236259号に記載されている。Details of the hard butter-like substance used as the oil and fat component of the present invention described above are described in Japanese Patent Application No. 62-236259, which was previously invented by some of the present inventors.
なお、チョコレートの固さを調整するため、本発明の上
記ハードバター様物質に加えて、他の油脂成分、例えは
カカオ脂を併用することができるが、この場合両者の相
溶性が十分でないので、ハードバター様物質に対するカ
カオ脂の量を10重量%以下、好ましくは5重量%以下
とすることが、常温で固形状であり、日溜は性が良く、
しかも表面に艶のあるチョコレートを製造する上で必要
である。In addition, in order to adjust the hardness of chocolate, in addition to the hard butter-like substance of the present invention, other oil and fat components, such as cacao butter, can be used in combination, but in this case, the compatibility between the two is insufficient. , the amount of cacao butter relative to the hard butter-like substance is 10% by weight or less, preferably 5% by weight or less, so that it is solid at room temperature, has good daily retention,
Moreover, it is necessary for producing chocolate with a glossy surface.
また、他の油脂成分として、前記のラウリン酸型ハード
バターは、本発明のハードバター様物質との相溶性が良
好であるため、チョコレートの常温での固さの調整用と
して、本発明のハードバター様物質と併用することがで
きるが、多量に使用すると、チョコレート表面にブルー
ムを生じ(結晶が表面に析出し)、チョコレート固有の
色光沢が無くなり、灰色の粉に覆われた外観を呈するよ
うになるので、本発明のハートバター様物質に対するラ
ウリン酸型バートバターの量は20重量%以−12=
下、好ましくは10重量%以下とすることが好ましい。In addition, as other fat and oil components, the lauric acid type hard butter has good compatibility with the hard butter-like substance of the present invention, so it can be used as a hard butter of the present invention for adjusting the hardness of chocolate at room temperature. It can be used in combination with a butter-like substance, but if used in large quantities, it may cause blooming on the chocolate surface (crystals precipitate on the surface), which may cause the chocolate to lose its characteristic color and luster and appear covered in gray powder. Therefore, it is preferable that the amount of lauric acid-type burt butter relative to the heart butter-like substance of the present invention is 20% by weight or less -12 = or less, preferably 10% by weight or less.
以上の事項に加えて1.カカオ脂及びラウリン酸型ハー
ドバター等は何れも代謝性があり、カロリー源となるも
のであるから、低カロリー性で健康管理上好ましいチョ
コレートを製造する点において、これらの添加は自から
制限される。In addition to the above, 1. Cocoa butter, lauric acid type hard butter, etc. are both metabolizable and serve as calorie sources, so their addition is self-limited in order to produce chocolate that is low in calories and good for health management. .
本発明方法によりチョコレートを製造するには、周知の
方法に従って、所定配合割合の前記チョコレート原料成
分をニーダ−で混合した後、粒度が20μn程度になる
ようにロール掛けし、50〜70°Cで20時間精練す
る。ついで、この溶融状のチョコレートを一定量づつ金
型へ流し込み、シェーキングマシンを用いて脱泡した後
、クーリングトンネル(5〜10°C)を所定の速度で
通過させて10℃以下に急速冷却し、固化したチョコレ
ートを金型から脱離する。To produce chocolate by the method of the present invention, according to a well-known method, the chocolate raw ingredients in a predetermined proportion are mixed in a kneader, then rolled so that the particle size is about 20 μm, and heated at 50 to 70°C. Refine for 20 hours. Next, a certain amount of this molten chocolate is poured into a mold, defoamed using a shaking machine, and then passed through a cooling tunnel (5 to 10°C) at a predetermined speed to be rapidly cooled to below 10°C. Then, the solidified chocolate is released from the mold.
本発明の方法においては、チョコレート原料の油脂成分
として、上記のハートバター様物質を使用することの外
に、溶融状態のチョコレート原料を任意の形状に冷却固
化する際に、チョコレートの温度が15℃、好ましくは
10°Cに達するまでは、急速冷却することが好ましい
。具体的には、例えは、冷却速度を0.38C/分以上
とするのが好ましく、遅い冷却速度では適度に固いチョ
コレートを得ることが困難である。In the method of the present invention, in addition to using the above-mentioned heart butter-like substance as the oil and fat component of the chocolate raw material, when cooling and solidifying the molten chocolate raw material into an arbitrary shape, the temperature of the chocolate is 15 ° C. Rapid cooling is preferred until the temperature reaches , preferably 10°C. Specifically, for example, it is preferable to set the cooling rate to 0.38 C/min or more, as it is difficult to obtain appropriately hard chocolate at a slow cooling rate.
(発明の効果)
本発明の方法によれは、原料の油脂成分として、特定の
脂肪酸成分からなり、かつ特定のエステル置換度の組成
を有するショ糖脂肪酸ポリエステルを使用することによ
って、カカオ脂を使用した従来のチョコレートと類似す
る優れた風味と艶があり、かつ適度の硬さを有し、加え
て低カロリー性で健康管理上好ましいチョコレートを得
ることが)きる
(実施例)
以下本発明を実施例について更に詳細に説明するが、本
発明はその要旨を超えない限りこれ等の実施例に限定さ
れるものではない。また、実施例中「部」とあるは「重
量部」を表わす。(Effects of the Invention) According to the method of the present invention, cacao butter is used by using a sucrose fatty acid polyester consisting of a specific fatty acid component and having a composition with a specific degree of ester substitution as a raw material oil component. It is possible to obtain chocolate that has an excellent flavor and luster similar to those of conventional chocolate, and has an appropriate hardness, and is also low in calories and favorable for health management (Example) The present invention will be carried out as follows. Examples will be explained in more detail, but the present invention is not limited to these examples unless it exceeds the gist thereof. In addition, "parts" in the examples represent "parts by weight."
ショ糖脂肪酸ポリエステル(以下SPEと略記する)の
製造例1
グラニユー糖977部及びジメチルスルホキシド(DM
SO)4000部を仕込み、23 Torrの減圧下で
沸騰させながら20分間溶媒を還流させ後、DMSOを
留出させ脱水した。留出量が1000部に達した点で留
出を止め、系内の水分を測定したところ、残存水分は0
.06重量%てあった。Production example 1 of sucrose fatty acid polyester (hereinafter abbreviated as SPE) 977 parts of granulated sugar and dimethyl sulfoxide (DM
After refluxing the solvent for 20 minutes while boiling under reduced pressure of 23 Torr, DMSO was distilled off and dehydrated. When the distillation amount reached 1000 parts, the distillation was stopped and the moisture in the system was measured, and the residual moisture was 0.
.. 06% by weight.
次いで無水炭酸カリウム43.7部及びラウリン酸メチ
ル(純度98%、2%のカプリン酸を含む)4370部
を仕込み、23 Torrの減圧下で沸騰させながら溶
媒を還流させ、メタノールは留去した。反応液が実質的
に均一になった時点で溶媒の留去を開始し、7 Tor
rの減圧下で液温を110°Cに保持して10時間反応
を行なった後、生成物を中和精製することによって、9
8%のラウリン酸(炭素数12)及び2%のカプリン酸
(炭素数10)からなる脂肪酸組成で、次のエステル体
組成を有するSPEを得た。Next, 43.7 parts of anhydrous potassium carbonate and 4370 parts of methyl laurate (98% purity, containing 2% capric acid) were charged, and the solvent was refluxed while boiling under reduced pressure of 23 Torr, and methanol was distilled off. When the reaction solution became substantially homogeneous, the solvent was distilled off and heated to 7 Torr.
After carrying out the reaction for 10 hours under reduced pressure of r and maintaining the liquid temperature at 110 °C, the product was neutralized and purified.
An SPE having the following ester composition was obtained with a fatty acid composition consisting of 8% lauric acid (12 carbon atoms) and 2% capric acid (10 carbon atoms).
エステル体組成
このSPEにおけるモノエステル体、ジエステル体及び
トリエステ、ル体の合計含量は2.9重量(%)であり
、残余のエステルの平均置換度は6.4であった。Ester Composition The total content of monoesters, diesters, triesters, and esters in this SPE was 2.9% by weight, and the average degree of substitution of the remaining esters was 6.4.
SPEの製造例2
製造例1において使用したラウリン酸メチルの使用量を
4500部とし、反応時間を1o、5時間とじた以外は
製造例1と同様な処理を行なった。Production Example 2 of SPE The same process as in Production Example 1 was carried out, except that the amount of methyl laurate used in Production Example 1 was 4500 parts, and the reaction time was 1 o, 5 hours.
上記方法によって、製造例1と同一の脂肪酸組成を有し
、次のエステル体組成を有するSPEを製造した。By the above method, SPE having the same fatty acid composition as Production Example 1 and the following ester composition was produced.
エステル体組成
このSPEにおける、モノエステル体、ジエステル体及
びトリエステル体の合計含量は3.5重量(%)であり
、残余のエステルの平均置換度は6.6であつた・
SPEの製造例3
製造例1において使用したラウリン酸メチルの代りに、
70%のラウリン酸メチル、10%のミリスチン酸メチ
ル、5%のパルミチン酸メチル、3%のカプリン酸メチ
ル及び3%のカプリル酸メチルを含む脂肪酸メチル35
00部を使用し、他は製造例1と全く同様の処理を行な
った。Ester composition In this SPE, the total content of monoester, diester, and triester was 3.5 weight (%), and the average degree of substitution of the remaining ester was 6.6. Production example of SPE 3 Instead of methyl laurate used in Production Example 1,
Methyl fatty acids 35 including 70% methyl laurate, 10% methyl myristate, 5% methyl palmitate, 3% methyl caprate and 3% methyl caprylate
00 parts was used, and the other processes were performed in exactly the same manner as in Production Example 1.
上記方法によって、次の脂肪酸組成及びエステル体組成
を有するSPEを製造した。By the above method, SPE having the following fatty acid composition and ester composition was produced.
脂肪酸組成
エステル体組成
このSPEにおける、モノエステル体、ジエステル体及
びトリエステル体の合計含量は16.8重量(%)であ
り、残余のエステルの平均置換度は5.4であった。Fatty acid composition Ester composition In this SPE, the total content of monoesters, diesters, and triesters was 16.8 weight (%), and the average degree of substitution of the remaining esters was 5.4.
’)SPEの製造例4
ノ製造例1において使用したラウリン酸メチルの代りこ
こ、ラウリン系油脂から調製された、78.7%のラウ
リン酸メチル、21.2%のミリスチン酸メチル及び0
.1%のパルミチン酸メチルを含む脂肪酸メチル350
0部を使用し、かつ反応時間を10時間とし、他は製造
例1と全く同様の処理を行なった。') Production Example 4 of SPE In place of the methyl laurate used in Production Example 1, 78.7% methyl laurate, 21.2% methyl myristate and 0
.. Fatty acid methyl 350 containing 1% methyl palmitate
The same treatment as in Production Example 1 was carried out except that 0 parts of the product was used and the reaction time was 10 hours.
上記方法によって、次の脂肪酸組成及びエステル体組成
を有するSPEを製造した。By the above method, SPE having the following fatty acid composition and ester composition was produced.
脂肪酸組成
エステル体組成
このSPEζこおける、モノエステル体、ジエステル体
及びトリエステル体の合計含量は3.5重量(%)であ
り、残余のエステルの平均置換度は6.3であった・
SPEの製造例5
製造例1において使用したラウリン酸メチルの代りに、
49.7%のラウリン酸メチル、49.9%のミリスチ
ン酸メチル及びQ、4%のパルミチン酸メチルを含む脂
肪酸メチル3500部を使用し、かつ反応時間を10時
間とし、他は製造例1と全く同様の処理を行なった。Fatty acid composition Ester composition The total content of monoesters, diesters, and triesters in this SPEζ was 3.5 weight (%), and the average degree of substitution of the remaining esters was 6.3. Production Example 5 Instead of methyl laurate used in Production Example 1,
3,500 parts of fatty acid methyl containing 49.7% methyl laurate, 49.9% methyl myristate and Q, 4% methyl palmitate were used, and the reaction time was 10 hours, and the rest was as in Production Example 1. Exactly the same treatment was performed.
上記方法によって、次の脂肪酸組成及びエステル体組成
を有するSPEを製造した。By the above method, SPE having the following fatty acid composition and ester composition was produced.
脂肪酸組成
エステル体組成
このSPEにおける、モノエステル体、ジエステル体及
びトリエステル体の合計含量は4.4重量(%)であり
、残余のエステルの平均置換度は6.3であった。Fatty acid composition Ester composition In this SPE, the total content of monoesters, diesters, and triesters was 4.4 weight (%), and the average degree of substitution of the remaining esters was 6.3.
SPEの比較製造例1
製造例1において使用したラウリン酸メチル(純度98
%、2%のカプリン酸を含む)の使用量を3000部と
し、反応時間を5時間とした以外は製造例1と同様な処
理を行ない、製造例1と同一の脂肪M組成を有し、次の
エステル体組成を有するSPEを製造した。Comparative production example 1 of SPE Methyl laurate (purity 98
%, containing 2% capric acid), the amount used was 3000 parts, the reaction time was 5 hours, the same treatment as in Production Example 1 was carried out, and the fat M composition was the same as Production Example 1. An SPE having the following ester composition was produced.
エステル体組成
このSPEにおける、モノエステル体、ジエステル体及
びトリエステル体の合計含量は90.2重量(%)であ
り、残余のエステルの平均置換度は4.2てあった。Ester Composition In this SPE, the total content of monoesters, diesters, and triesters was 90.2% by weight, and the average degree of substitution of the remaining esters was 4.2.
試験例1
製造例1て得たSPEと、カカオ脂とを、表1及び表2
に示す種々の比率で混合して60℃で溶融し、表1及び
表2に示す各温度で2時間放置し、次いで20°Cて1
日間放置した試料について、固さ、均−性及び表面の状
態を観察した。その評価結果を表1及び表2に示す。Test Example 1 The SPE obtained in Production Example 1 and cacao butter were listed in Tables 1 and 2.
The mixture was mixed at various ratios shown in Table 1 and melted at 60°C, left for 2 hours at each temperature shown in Tables 1 and 2, and then heated to 20°C for 1 hour.
The hardness, uniformity, and surface condition of the samples left for days were observed. The evaluation results are shown in Tables 1 and 2.
表 1
表1における、固さの状態を示す記号○は適度の固さを
意味し、×は軟らかいことを意味する。Table 1 In Table 1, the symbol ○ indicating the state of hardness means moderate hardness, and × means soft.
均一性の状態を示す記号○は均一なことを意味し、×は
不均一を意味する。また、表面の状態を示す記号○は、
表面が滑らかで艶が−あることを意味し、×は表面がザ
ラザラであることを意味する。なお、後記表2〜4にお
ける記号も同一の意味を示す。The symbol ○ indicating the state of uniformity means uniformity, and the symbol × means nonuniformity. In addition, the symbol ○ indicating the surface condition is
It means that the surface is smooth and glossy, and × means that the surface is rough. Note that the symbols in Tables 2 to 4 below also have the same meaning.
表 2
試験例2
製造例2で得たSPEと、パルケナ]1[不二製油例製
のラウリン酸型ハードバターコとを、表3及び表4に示
す種々の比率で混合して60 ℃で溶融し、表3及び表
4に示す各温度で2時間放置し、次いで25℃で1日間
放置した試料について、固さ、均−性及び表面の状態を
観察した。その評価結果を表3及び表4に示す。Table 2 Test Example 2 The SPE obtained in Production Example 2 and Parquena] 1 [Lauric acid type hard butterco manufactured by Fuji Oil Co., Ltd. were mixed at various ratios shown in Tables 3 and 4 and heated at 60 °C. The samples were melted and left at each temperature shown in Tables 3 and 4 for 2 hours, and then at 25°C for 1 day, and the hardness, uniformity, and surface condition were observed. The evaluation results are shown in Tables 3 and 4.
表 3
表 4
実施例1
[原料の配合組成]
ココアパウダー6部 脱脂粉乳 20部粉 糖
42部 カカオ脂 2部製造例1のSP
E 30部
(注)ココアパウダー:カカオ豆を焙煎し、すり消した
泥状のココアケーキをプレスに掛けてカカオ脂を搾出し
、残渣を粉砕したもの。Table 3 Table 4 Example 1 [Raw material composition] 6 parts cocoa powder 20 parts skim milk powder Sugar
42 parts cocoa butter 2 parts SP of Production Example 1
E 30 parts (Note) Cocoa powder: Cocoa powder is made by roasting cacao beans, grinding the slurry cocoa cake through a press to extract the cacao fat, and pulverizing the residue.
上記配合組成の原料をニーダ−で混合し、粒度が20μ
m程度になるようにロール掛けして50〜70℃で20
時間精練した。ついて、この溶融状のチョコレートを一
定量づつ金型へ流し込み、シェーキングマシンを用いて
脱泡した後、クーリングトンネル(5〜10℃)を通過
させて、5℃/分の速度で10℃以下に急速冷却し、固
化したチョコレートを金型から取出した。得られた製品
は、固さ、風味及び艶ともに良好なものであった。The raw materials with the above composition are mixed in a kneader, and the particle size is 20μ.
Roll it to a thickness of about m and heat it at 50-70℃ for 20
Time spent scouring. Then, pour a certain amount of this molten chocolate into a mold, degas it using a shaking machine, and then pass it through a cooling tunnel (5 to 10°C) at a rate of 5°C/min to below 10°C. The chocolate was rapidly cooled and the solidified chocolate was taken out from the mold. The obtained product had good hardness, flavor, and gloss.
実施例2
[原料の配合組成]
ココアパウダー6部 脱脂粉乳 20部粉 糖
42部 カカオ脂 2部製造例3のSP
E 30部
上記配合組成の原料を、実施例1と同様にニーダ−で混
合し、ロール掛けして50〜70℃で20時間精練した
後、溶融状のチョコレートを一定量づつ金型へ流し込み
、シェーキングマシンを用いて脱泡した後、クーリング
トンネルを通過させて、5℃/分の速度で10℃以下に
急速冷却し、固化したチョコレートを金型から取出した
。得られた製品は、固さ、風味及び艶ともに良好なもの
であった。Example 2 [Composition of raw materials] 6 parts cocoa powder 20 parts skim milk powder Powder Sugar
42 parts Cocoa butter 2 parts SP of Production Example 3
E 30 parts The raw materials having the above composition were mixed in a kneader in the same manner as in Example 1, rolled and refined at 50 to 70°C for 20 hours, and then a fixed amount of molten chocolate was poured into a mold. After defoaming using a shaking machine, the chocolate was passed through a cooling tunnel and rapidly cooled to 10°C or less at a rate of 5°C/min, and the solidified chocolate was taken out from the mold. The obtained product had good hardness, flavor, and gloss.
実施例3
[原料の配合組成コ
ココアパウダー6部 脱脂粉乳 20部粉 糖
42部 カカオ脂 2部製造例2のSP
E 30部 パルケナ■3部上記配合組成の原料を
、実施例1と同様にニーダ−で混合し、ロール掛けして
50〜70℃で20時間精練した後、溶融状のチョコレ
ートを一定量づつ金型へ流し込み、シェーキングマシン
を用いて脱泡した後、クーリングトンネルを通過させて
、5°C/分の速度で10℃以下に急速冷却し、固化し
たチョコレートを金型から取出した。得られた製品は、
固さ、風味及び艶ともに良好なものであった。Example 3 [Raw material composition: 6 parts of cocoa powder, 20 parts of skim milk powder, sugar
42 parts Cocoa butter 2 parts Production example 2 SP
E 30 parts Parquena ■ 3 parts The raw materials with the above composition were mixed in a kneader in the same manner as in Example 1, rolled and refined at 50 to 70°C for 20 hours. After pouring into a mold and defoaming using a shaking machine, the chocolate was passed through a cooling tunnel and rapidly cooled to below 10°C at a rate of 5°C/min, and the solidified chocolate was taken out from the mold. The obtained product is
The hardness, flavor and gloss were all good.
実施例4
[原料の配合組成コ
ココアパウダー6部 脱脂粉乳 20部粉 糖
41部 バルケナ113部製造例4のSPE
30部
上記配合組成の原料を、実施例1と同様にニーダ−で混
合し、ロール掛けして50〜70°Cて20時間精練し
た後、溶融状のチョコレートを一定量づつ金型へ流し込
み、シェーキングマシンを用いて脱泡した後、クーリン
グトンネルを通過させて、5℃/分の速度で10℃以下
に急速冷却し、固化したチョコレートを金型から取出し
た。得られた製品は、固さ、風味及び艶ともに良好なも
のであった。Example 4 [Raw material composition: 6 parts of cocoa powder, 20 parts of skim milk powder, sugar
41 parts Balkena 113 parts SPE of manufacturing example 4
30 parts The raw materials having the above composition were mixed in a kneader in the same manner as in Example 1, rolled and refined at 50 to 70°C for 20 hours, and then a fixed amount of molten chocolate was poured into a mold. After defoaming using a shaking machine, the chocolate was passed through a cooling tunnel and rapidly cooled to 10°C or less at a rate of 5°C/min, and the solidified chocolate was taken out from the mold. The obtained product had good hardness, flavor, and gloss.
実施例5
[原料の配合組成]
粉 糖 50部 脱脂粉乳 20部製造
例5のSPE 30部
上記配合組成の原料を、実施例1と同様にニーダ−で混
合し、ロール掛けして50〜70℃で20時間精練した
後、溶融状のチョコレートを一定量づつ金型へ流し込み
、シェーキングマシンを用いて脱泡した後、クーリング
トンネルを通過させて、5= 31−
℃/分の速度で10℃以下に急速冷却し、固化したチョ
コレートを金型から取出した。得られた製品は、固さ、
風味及び艶ともに良好なものであった。Example 5 [Composition of raw materials] Powdered sugar 50 parts Skimmed milk powder 20 parts SPE of Production Example 5 30 parts The raw materials having the above composition were mixed in a kneader in the same manner as in Example 1, and rolled to give a powder of 50 to 70 parts. After scouring at ℃ for 20 hours, molten chocolate was poured into a mold in fixed amounts, defoamed using a shaking machine, passed through a cooling tunnel, and heated at a rate of 5 = 31-℃/min to 10 The chocolate was rapidly cooled to below 0.degree. C. and the solidified chocolate was taken out from the mold. The resulting product has hardness,
Both flavor and gloss were good.
比較例1
[原料の配合組成コ
粉 糖 50部 脱脂粉乳 20部比
較製造例1のSPE 30部
上記配合組成の原料を、実施例1と同様にニーダ−で混
合し、ロール掛けして50〜70℃で20時間精練した
後、溶融状のチョコレートを一定量づつ金型へ流し込み
、シェーキングマシンを用いて脱ン包した後、クーリン
グトンネルを通過させて、5℃/分の速度で10℃以下
に急速冷却し、固化したチョコレートを金型から取出し
た。得られた製品は、固く、風味及び口溶けが悪いもの
であった。Comparative Example 1 [Blend composition of raw materials Co-flour Sugar 50 parts Skim milk powder 20 parts SPE of Comparative Production Example 1 30 parts The raw materials having the above composition were mixed in a kneader in the same manner as in Example 1, and rolled to give a After scouring at 70°C for 20 hours, molten chocolate was poured into a mold in fixed amounts, unwrapped using a shaking machine, passed through a cooling tunnel, and heated to 10°C at a rate of 5°C/min. Following rapid cooling, the solidified chocolate was taken out from the mold. The obtained product was hard and had poor flavor and meltability in the mouth.
Claims (1)
いはこれ等に更に乳成分を加えた成分を主体とする溶融
状態のチョコレート原料を任意形状とした後、冷却固化
してチョコレートを製造する方法において、油脂成分と
して、ラウリン系油脂由来の脂肪酸、ラウリン酸又はミ
リスチン酸を主構成脂肪酸とするシヨ糖脂肪酸のポリエ
ステルであって、置換度が1〜3のエステル体が20重
量%以下であり、残余のエステルの平均置換度が5以上
であるショ糖脂肪酸ポリエステル体からなるハードバタ
ー様物質を用いることを特徴とするチョコレートの製造
法。(1) A method of manufacturing chocolate by shaping a molten chocolate raw material containing a cacao component, an oil/fat component, and a sweetening component, or further adding a milk component into an arbitrary shape, and then cooling and solidifying the raw material. The oil component is a polyester of sucrose fatty acid whose main constituent fatty acid is fatty acid derived from lauric oil, lauric acid or myristic acid, and the ester form with a degree of substitution of 1 to 3 is 20% by weight or less, A method for producing chocolate, comprising using a hard butter-like substance made of a sucrose fatty acid polyester in which the average degree of substitution of the remaining esters is 5 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62295053A JPH07108184B2 (en) | 1987-11-25 | 1987-11-25 | Manufacturing method of chicorylate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62295053A JPH07108184B2 (en) | 1987-11-25 | 1987-11-25 | Manufacturing method of chicorylate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01137939A true JPH01137939A (en) | 1989-05-30 |
JPH07108184B2 JPH07108184B2 (en) | 1995-11-22 |
Family
ID=17815709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62295053A Expired - Lifetime JPH07108184B2 (en) | 1987-11-25 | 1987-11-25 | Manufacturing method of chicorylate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07108184B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007097418A (en) * | 2005-09-30 | 2007-04-19 | Morinaga & Co Ltd | Chocolate, method for producing the same, and agent for inhibiting rise of viscosity of chocolate dough |
WO2009081916A1 (en) | 2007-12-20 | 2009-07-02 | Fuji Oil Company, Limited | Oily food and method for producing the same |
US7866596B2 (en) | 2008-05-14 | 2011-01-11 | Sony Corporation | Recording-paper-roll supporting device and printer |
JP2012100601A (en) * | 2010-11-11 | 2012-05-31 | Tanizawa Kaki Kogyo Kk | Method and system for processing food |
JP2020129989A (en) * | 2019-02-14 | 2020-08-31 | 第一工業製薬株式会社 | Oil and fat composition for food, chocolate product and fat blooming inhibitor |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52120131A (en) * | 1976-02-12 | 1977-10-08 | Procter & Gamble | Treating composition for rercholesterol disease |
JPS62192395A (en) * | 1986-02-19 | 1987-08-22 | ユニリ−バ− ナ−ムロ−ゼ ベンノ−トシヤ−プ | Fatty acid ester of sugar and sugar alcohol |
-
1987
- 1987-11-25 JP JP62295053A patent/JPH07108184B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52120131A (en) * | 1976-02-12 | 1977-10-08 | Procter & Gamble | Treating composition for rercholesterol disease |
JPS62192395A (en) * | 1986-02-19 | 1987-08-22 | ユニリ−バ− ナ−ムロ−ゼ ベンノ−トシヤ−プ | Fatty acid ester of sugar and sugar alcohol |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007097418A (en) * | 2005-09-30 | 2007-04-19 | Morinaga & Co Ltd | Chocolate, method for producing the same, and agent for inhibiting rise of viscosity of chocolate dough |
WO2009081916A1 (en) | 2007-12-20 | 2009-07-02 | Fuji Oil Company, Limited | Oily food and method for producing the same |
US7866596B2 (en) | 2008-05-14 | 2011-01-11 | Sony Corporation | Recording-paper-roll supporting device and printer |
JP2012100601A (en) * | 2010-11-11 | 2012-05-31 | Tanizawa Kaki Kogyo Kk | Method and system for processing food |
JP2020129989A (en) * | 2019-02-14 | 2020-08-31 | 第一工業製薬株式会社 | Oil and fat composition for food, chocolate product and fat blooming inhibitor |
Also Published As
Publication number | Publication date |
---|---|
JPH07108184B2 (en) | 1995-11-22 |
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