JP5613980B2 - Oil composition for chocolate - Google Patents
Oil composition for chocolate Download PDFInfo
- Publication number
- JP5613980B2 JP5613980B2 JP2008514439A JP2008514439A JP5613980B2 JP 5613980 B2 JP5613980 B2 JP 5613980B2 JP 2008514439 A JP2008514439 A JP 2008514439A JP 2008514439 A JP2008514439 A JP 2008514439A JP 5613980 B2 JP5613980 B2 JP 5613980B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- chocolate
- oils
- fats
- fat
- 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.)
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Links
- 235000019219 chocolate Nutrition 0.000 title claims description 136
- 239000000203 mixture Substances 0.000 title claims description 64
- 239000003925 fat Substances 0.000 claims description 219
- 239000003921 oil Substances 0.000 claims description 218
- 235000019198 oils Nutrition 0.000 claims description 218
- 235000019197 fats Nutrition 0.000 claims description 204
- 244000299461 Theobroma cacao Species 0.000 claims description 161
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 82
- 229910052740 iodine Inorganic materials 0.000 claims description 82
- 239000011630 iodine Substances 0.000 claims description 82
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 39
- 229930195729 fatty acid Natural products 0.000 claims description 39
- 239000000194 fatty acid Substances 0.000 claims description 39
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 26
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 claims description 26
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims description 26
- 238000005809 transesterification reaction Methods 0.000 claims description 22
- 238000002156 mixing Methods 0.000 claims description 21
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims description 19
- 229930006000 Sucrose Natural products 0.000 claims description 17
- 239000005720 sucrose Substances 0.000 claims description 17
- -1 sucrose fatty acid ester Chemical class 0.000 claims description 17
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 9
- 239000003346 palm kernel oil Substances 0.000 claims description 9
- 235000019865 palm kernel oil Nutrition 0.000 claims description 9
- 235000019482 Palm oil Nutrition 0.000 claims description 8
- 239000002540 palm oil Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims 1
- 238000002844 melting Methods 0.000 description 28
- 230000008018 melting Effects 0.000 description 28
- 150000004665 fatty acids Chemical class 0.000 description 22
- 235000019868 cocoa butter Nutrition 0.000 description 21
- 229940110456 cocoa butter Drugs 0.000 description 21
- 240000002791 Brassica napus Species 0.000 description 20
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 20
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 20
- 125000004432 carbon atom Chemical group C* 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 17
- 230000000630 rising effect Effects 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 16
- 238000003860 storage Methods 0.000 description 16
- 238000012360 testing method Methods 0.000 description 16
- 150000004671 saturated fatty acids Chemical class 0.000 description 14
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 13
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 13
- 235000001046 cacaotero Nutrition 0.000 description 13
- 238000005496 tempering Methods 0.000 description 13
- 235000009470 Theobroma cacao Nutrition 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 12
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 12
- 239000000796 flavoring agent Substances 0.000 description 12
- 235000019634 flavors Nutrition 0.000 description 12
- 239000000843 powder Substances 0.000 description 12
- 235000000346 sugar Nutrition 0.000 description 12
- 235000010692 trans-unsaturated fatty acids Nutrition 0.000 description 12
- 235000019864 coconut oil Nutrition 0.000 description 11
- 239000003240 coconut oil Substances 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 238000007796 conventional method Methods 0.000 description 10
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 10
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 10
- 238000012790 confirmation Methods 0.000 description 9
- 235000003441 saturated fatty acids Nutrition 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 7
- 239000000787 lecithin Substances 0.000 description 7
- 229940067606 lecithin Drugs 0.000 description 7
- 235000010445 lecithin Nutrition 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000007670 refining Methods 0.000 description 7
- 235000021357 Behenic acid Nutrition 0.000 description 6
- 229940116226 behenic acid Drugs 0.000 description 6
- 235000009508 confectionery Nutrition 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 235000014593 oils and fats Nutrition 0.000 description 4
- 235000010724 Wisteria floribunda Nutrition 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000008164 mustard oil Substances 0.000 description 3
- 150000008163 sugars Chemical class 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000021323 fish oil Nutrition 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 235000021243 milk fat Nutrition 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000008939 whole milk Nutrition 0.000 description 2
- SBMYBOVJMOVVQW-UHFFFAOYSA-N 2-[3-[[4-(2,2-difluoroethyl)piperazin-1-yl]methyl]-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group FC(CN1CCN(CC1)CC1=NN(C=C1C=1C=NC(=NC=1)NC1CC2=CC=CC=C2C1)CC(=O)N1CC2=C(CC1)NN=N2)F SBMYBOVJMOVVQW-UHFFFAOYSA-N 0.000 description 1
- DCVGCQPXTOSWEA-UHFFFAOYSA-N 4-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]pyrazol-3-yl]methyl]-1-methylpiperazin-2-one Chemical group CN1CCN(CC2=NN(CC(=O)N3CCC4=C(C3)N=NN4)C=C2C2=CN=C(NC3CC4=C(C3)C=CC=C4)N=C2)CC1=O DCVGCQPXTOSWEA-UHFFFAOYSA-N 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 235000003301 Ceiba pentandra Nutrition 0.000 description 1
- 244000146553 Ceiba pentandra Species 0.000 description 1
- 235000003901 Crambe Nutrition 0.000 description 1
- 241000220246 Crambe <angiosperm> Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000019774 Rice Bran oil Nutrition 0.000 description 1
- 241000282849 Ruminantia Species 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical group N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 208000011775 arteriosclerosis disease Diseases 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000019221 dark chocolate Nutrition 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000008524 evening primrose extract Nutrition 0.000 description 1
- 239000010475 evening primrose oil Substances 0.000 description 1
- 229940089020 evening primrose oil Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000013020 final formulation Substances 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019860 lauric fat Nutrition 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 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
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000008165 rice bran oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 125000005457 triglyceride group Chemical group 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000019222 white chocolate Nutrition 0.000 description 1
- 235000019220 whole milk chocolate Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/10—Ester interchange
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings, cooking oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/36—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds characterised by the fats used
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/36—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds characterised by the fats used
- A23G1/38—Cocoa butter substitutes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/56—Cocoa products, e.g. chocolate; Substitutes therefor making liquid products, e.g. for making chocolate milk drinks and the products for their preparation, pastes for spreading, milk crumb
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G2200/00—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents
- A23G2200/08—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents containing cocoa fat if specifically mentioned or containing products of cocoa fat or containing other fats, e.g. fatty acid, fatty alcohol, their esters, lecithin, paraffins
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Confectionery (AREA)
- Edible Oils And Fats (AREA)
Description
本発明は、炭素数12以下の脂肪酸を30%以上含む油脂と炭素数20以上の飽和脂肪酸を30%以上含む油脂をエステル交換してなる油脂であって、更にこのエステル交換された油脂にアセチル化蔗糖脂肪酸エステルを配合してなるチョコレート用油脂組成物であって、テンパリング操作しないでココアバターを含む風味に優れたチョコレートを製造することの出来るチョコレート用油脂組成物に関する。 The present invention is an oil obtained by transesterifying an oil containing 30% or more of a fatty acid having 12 or less carbon atoms and an oil containing 30% or more of a saturated fatty acid having 20 or more carbon atoms. It is the oil-fat composition for chocolates formed by mix | blending the sucrose fatty acid ester, Comprising: It is related with the oil-fat composition for chocolates which can manufacture the chocolate excellent in the flavor containing cocoa butter, without tempering operation.
チョコレートは使用する油脂成分によりテンパリング操作を必要とするものと、必要としないものに大別される。前者はココアバターに代表されるSUS型トリグリセリドを(S:飽和脂肪酸、U:不飽和脂肪酸)主要成分として含む油脂からなる。一方後者は多くの場合トランス型不飽和脂肪酸を含む油脂又はヤシ油やパーム核油等のラウリン系油脂からなる。 Chocolates are roughly classified into those that require tempering operations and those that do not require, depending on the oil and fat components used. The former consists of fats and oils containing SUS triglycerides represented by cocoa butter as the main component (S: saturated fatty acid, U: unsaturated fatty acid). On the other hand, the latter often consists of fats and oils containing trans-unsaturated fatty acids or lauric fats such as coconut oil and palm kernel oil.
近年、消費者の嗜好性の多様化でチョコレートと焼き菓子などの組合せ商品が増えている。チョコレートと焼き菓子を組み合わせても、チョコレートをテンパリング操作できれば、トランス型不飽和脂肪酸を含む油脂を主成分とするトリグリセリドを使用しなくても良好な製品は作れるが、テンパリング操作が出来ない場合がある。例えば焼き菓子が熱い状態でチョコレートと組み合わせる場合や、中空の焼き菓子の中にチョコレートを充填する場合などである。前者では焼き菓子を一旦冷却した後、チョコレートのテンパリング操作を行えば良いが、この場合生産性が悪く、経済的ではない。後者の場合、一般にテンパリング操作を行ったチョコレートは粘度が高くなるため、充填操作が出来ず、結果粘度の低い状態で充填する必要がある。従ってテンパリング操作が実質できないことが多い。 In recent years, combined products such as chocolate and baked confectionery are increasing due to diversification of consumer preferences. Even if chocolate and baked confectionery are combined, if chocolate can be tempered, good products can be made without using triglycerides based on fats and oils containing trans-unsaturated fatty acids, but tempering may not be possible. . For example, when baked confectionery is combined with chocolate in a hot state, or when chocolate is filled into a hollow baked confectionery. In the former case, the baked confectionery may be cooled once, and then the chocolate tempering operation may be performed. However, in this case, the productivity is low and it is not economical. In the latter case, the chocolate that has been subjected to the tempering operation generally has a high viscosity. Therefore, the filling operation cannot be performed, and it is necessary to fill the chocolate with a low viscosity. Therefore, the tempering operation is often impossible.
従来よりチョコレートに使用される油脂中のココアバターが5%以下であれば、ヤシ油やパーム核油、又はそれらの分別油など、トランス型不飽和脂肪酸からなる油脂を使用しなくとも、品質の安定なチョコレートは製造できる。しかし、ココアバター、もしくはカカオマスが使用できないためチョコレート本来の良好な風味を出すことは出来ない。この場合はココアパウダーを使用する事になるため、チョコレート本来の風味と言うより、ココア風味の強いものとなってしまう。
風味に優れたチョコレートを製造するために、ココアバターもしくはカカオマスを使用し、テンパリング操作をしないで良好な品質のチョコレートを得るためには、トランス型不飽和脂肪酸を含む油脂を使用する場合が多い。このトランス型不飽和脂肪酸を含む油脂中のトランス型不飽和脂肪酸の含量は一般的には40〜50%程度である。例えば特許文献1では高トランス型不飽和脂肪酸含有油脂とアセチル化蔗糖脂肪酸エステルの組合せで、カカオ脂含量が高い非テンパリング型チョコレートが例示されている。If cocoa butter in fats and oils conventionally used in chocolate is 5% or less, quality oil can be used without using fats made of trans-unsaturated fatty acids such as palm oil, palm kernel oil, or fractionated oils thereof. Stable chocolate can be manufactured. However, since cocoa butter or cocoa mass cannot be used, the original good flavor of chocolate cannot be obtained. In this case, since cocoa powder is used, the cocoa flavor is stronger than the original flavor of chocolate.
In order to produce chocolate with excellent flavor, cocoa butter or cacao mass is used, and in order to obtain good quality chocolate without tempering operation, fats and oils containing trans-type unsaturated fatty acids are often used. The content of the trans unsaturated fatty acid in the fat and oil containing the trans unsaturated fatty acid is generally about 40 to 50%. For example, Patent Document 1 exemplifies non-tempering chocolate having a high cocoa butter content by a combination of a highly trans unsaturated fatty acid-containing oil and fat and an acetylated sucrose fatty acid ester.
トランス型不飽和脂肪酸の含量の低い硬化油もあるが、トランス型不飽和脂肪酸含量が低ければそれだけチョコレートに使用する油脂中のココアバターの使用量も低くなる。
トランス型不飽和脂肪酸を含む油脂は一般に水素添加(硬化とも呼ばれる)によって製造される。この水素添加とは不飽和脂肪酸の2重結合の部分に水素を付加して飽和脂肪酸を作製する工程である。一般に不飽和脂肪酸はその水素の付いている位置がシス型であるが、水素添加の工程でトランス型になる。天然では反芻動物の微生物により作られる為、乳脂や肉中に含まれる。
近年、このトランス型不飽和脂肪酸は取りすぎると動脈硬化などの心臓病になるリスクを高めるとの研究結果が得られ、欧米諸国では消費者に注意を喚起している。例えば、米国では製品ラベルにトランス型不飽和脂肪酸の含有量を表示する義務を2006年1月より実施しているし、デンマークでは更にトランス型不飽和脂肪酸を2%以上含む加工油脂の販売を禁止している。
日本では従来よりトランス型不飽和脂肪酸の摂取量が欧米より低い為、現時点では特に健康上の問題となることは無いとの見方であるが、それでもよりトランス型不飽和脂肪酸の低い油脂が要望されている。Some hardened oils have a low content of trans-unsaturated fatty acids, but the lower the trans-unsaturated fatty acid content, the lower the amount of cocoa butter used in the fats and oils used in chocolate.
Oils and fats containing trans unsaturated fatty acids are generally produced by hydrogenation (also called hardening). This hydrogenation is a process for preparing saturated fatty acids by adding hydrogen to the double bond portion of unsaturated fatty acids. In general, unsaturated fatty acids are cis-type at the position where hydrogen is attached, but become trans-type in the hydrogenation process. It is naturally produced by ruminant microorganisms, so it is contained in milk fat and meat.
In recent years, research has shown that excessive use of trans-unsaturated fatty acids increases the risk of heart disease such as arteriosclerosis, and has attracted consumers in Western countries. For example, the United States has been obligated to display the content of trans-unsaturated fatty acids on product labels since January 2006, and Denmark has also banned the sale of processed fats and oils containing more than 2% trans-unsaturated fatty acids. doing.
In Japan, the intake of trans-unsaturated fatty acids has been lower than in Europe and the United States, so it seems that there is no particular health problem at present, but there is still a demand for oils with lower trans-unsaturated fatty acids. ing.
従来、炭素数の短い脂肪酸又はそれらを含む油脂と炭素数の長い脂肪酸又はそれらを含む油脂をエステル交換することにより、それぞれの油脂の持つ特徴を改質する方法は一般的に知られている。例えば特許文献2ではヤシ油50部と高エルシン酸の菜種極度硬化油50部をランダムエステル交換した油脂や、特許文献3でもヤシ油50部と高エルシン酸の菜種極度硬化油50部とをアルカリ触媒によってエステル交換した油脂や、特許文献4では炭素数14以下の飽和脂肪酸2〜50重量%及び炭素数20以上の飽和脂肪酸1〜50重量%を含有する油脂のランダムエステル交換油脂が記載され、実施例としてヤシ油40%、高エルシン酸の菜種極度硬化油30%、大豆油30%をナトリウムメチラートを用いてランダムエステル交換油脂を製造している。しかし、これらの油脂組成物はマーガリンやショートニングなどの焼き菓子煉り込み用途に使用するものであり、油脂の可塑性を得るために急冷可塑化されている。 2. Description of the Related Art Conventionally, a method for modifying the characteristics of each oil / fat by transesterifying a fatty acid having a short carbon number or an oil / fat containing them with a fatty acid having a long carbon number or an oil / fat containing them is generally known. For example, in Patent Document 2, 50 parts of coconut oil and 50 parts of high erucic acid rapeseed extremely hardened oil are randomly transesterified. In Patent Document 3, 50 parts of coconut oil and 50 parts of high erucic acid rapeseed extremely hardened oil are alkalinized. Fats and oils transesterified with a catalyst, and Patent Document 4 describes random transesterified fats and oils containing 2 to 50% by weight of saturated fatty acids having 14 or less carbon atoms and 1 to 50% by weight of saturated fatty acids having 20 or more carbon atoms, As an example, random transesterified oils and fats are produced using 40% coconut oil, 30% rapeseed extremely hardened oil of high erucic acid, and 30% soybean oil using sodium methylate. However, these oil and fat compositions are used for baked confectionery embedding applications such as margarine and shortening, and are quenched and plasticized to obtain oil and fat plasticity.
本発明の目的は、チョコレートを製造するに際して、テンパリング操作しないで、ココアバターを含む風味、口溶けに優れたチョコレートが得られ、経時保存で品質劣化が防止されているチョコレート及び当該チョコレートに使用する油脂組成物を提供することにある。 The object of the present invention is to produce a chocolate containing cocoa butter and excellent in melting in the mouth without tempering when producing chocolate, and to prevent deterioration in quality by storage over time, and fats and oils used in the chocolate It is to provide a composition.
本発明者らは、鋭意研究を重ねた結果、特定の脂肪酸種に由来する油脂の選択とエステル交換による油脂加工法が上記課題に対して有効であるという知見、更にはこの油脂加工法と特定の乳化剤を組み合わせる事が上記課題に対して有効であるという知見に基づいて、本発明を完成するに至った。
即ち、本発明の第1は、炭素数12以下の脂肪酸を30%以上含む油脂と炭素数20以上の飽和脂肪酸を30%以上含む油脂をエステル交換してなる油脂組成物であって、炭素数12以下の脂肪酸を30%以上含む油脂がヤシ油、パーム核油の非硬化油、極度硬化油であり、これらの単独又は組み合わせたものであり、トランス型不飽和脂肪酸が5%以下であるチョコレート用油脂組成物である。第2は、ヨウ素価が28以下である、第1記載のチョコレート用油脂組成物である。第3は、第1に記載のエステル交換してなる油脂組成物に更にベヘン酸を30%以上含む油脂を配合してなるチョコレート用油脂組成物である。第4は、エステル交換がランダムエステル交換である、第1又は第2記載のチョコレート用油脂組成物である。第5は、炭素数20以上の飽和脂肪酸を30%以上含む油脂が高エルシン酸の菜種油、からし油、クランベ油、魚油を極度硬化(ヨウ素価1以下まで水素添加した油)したものである、第1〜4何れか1に記載のチョコレート用油脂組成物である。第6は、第1〜5何れか1に記載の油脂組成物を使用してなるチョコレートである。第7は、第1又は第2に記載の油脂組成物をチョコレート全体に対して20〜68重量%使用するチョコレートの製造法である。第8は、第1に記載の油脂組成物にアセチル化蔗糖脂肪酸エステルを配合してなるチョコレート用油脂組成物である。第9は、ヨウ素価が5〜30である、第9記載のチョコレート用油脂組成物である。第10は、第8又は第9に記載の油脂組成物を使用してなるチョコレートである。第11は、第8又は第9に記載の油脂組成物をチョコレート全体に対して20〜68重量%使用するチョコレートの製造法である。
As a result of intensive studies, the present inventors have found that the selection of fats and oils derived from specific fatty acid species and the fats and oils processing method by transesterification are effective for the above-mentioned problems, and further, the fats and oils processing method and the specifics The present invention has been completed on the basis of the knowledge that the combination of these emulsifiers is effective for the above problems.
That is, the first of the present invention is an oil and fat composition obtained by transesterifying an oil or fat containing 30% or more of a fatty acid having 12 or less carbon atoms and an oil or fat containing 30% or more of a saturated fatty acid having 20 or more carbon atoms, Fats and oils containing 30% or more of 12 or less fatty acids are coconut oil, palm kernel oil non-hardened oil, extremely hardened oil, these are used alone or in combination, and the chocolate having a trans unsaturated fatty acid of 5% or less is the use fats and oils group formed products. The second is the fat composition for chocolate according to the first aspect, which has an iodine value of 28 or less. 3rd is the fat composition for chocolate formed by mix | blending the fats and oils formed by transesterification as described in 1 with the fats and oils which contain 30% or more of behenic acid further. 4th is the fat composition for chocolate of the 1st or 2nd description whose transesterification is random transesterification. Fifth, oils containing 30% or more of saturated fatty acids having 20 or more carbon atoms are hardened rapeseed oil of high erucic acid, mustard oil, crambo oil, and fish oil (oil hydrogenated to an iodine value of 1 or less). And any one of the first to fourth oil / fat compositions for chocolate. 6th is chocolate which uses the oil-fat composition of any one of 1st-5th. 7th is the manufacturing method of the chocolate which uses 20 to 68weight% of the oil-fat composition as described in 1st or 2nd with respect to the whole chocolate. The eighth is an oil / fat composition for chocolate formed by blending an acetylated sucrose fatty acid ester with the oil / fat composition described in the first. Ninth is the fat composition for chocolate according to ninth, wherein the iodine value is 5-30. 10th is chocolate which uses the oil-fat composition as described in 8th or 9th. The 11th is the manufacturing method of the chocolate which uses 20 to 68weight% of the oil-fat composition as described in 8th or 9th with respect to the whole chocolate.
本発明の油脂組成物はトランス型不飽和脂肪酸を10%以下しか含まないにも拘らず、油脂中ココアバターが5%以上含むチョコレートでもテンパリング操作することなしで、風味、口溶けに優れ、経時保存でブルーム、グレーニング、艶等の品質劣化が防止されているチョコレートを製造することができるチョコレート用油脂組成物である。 Even though the fat composition of the present invention contains only 10% or less of a trans-unsaturated fatty acid, the chocolate containing 5% or more of cocoa butter in fats and oils is excellent in flavor and meltability without tempering, and stored over time. It is a fat composition for chocolate that can produce chocolate in which quality deterioration such as bloom, graining, and gloss is prevented.
本発明のチョコレート用油脂組成物は炭素数12以下の脂肪酸を30%以上含む油脂と炭素数20以上の飽和脂肪酸を30%以上含む油脂をエステル交換して得ることが出来、得られたチョコレート用油脂組成物のヨウ素価が28以下であり、好ましくはヨウ素価が0〜27であり、更に0〜26である。 更にこのエステル交換された油脂にアセチル化蔗糖脂肪酸エステルを配合するのが好ましく、量としては油脂組成物全体に対して0.4〜7.5重量%配合するのが好ましい。得られたチョコレート用油脂組成物のヨウ素価が5〜30であり、好ましくはヨウ素価が7〜25である。
チョコレート用油脂組成物に更にベヘン酸を30%以上含む油脂を配合するのがチョコレートの艶の点で好ましい。
炭素数12以下の脂肪酸を30%以上含む油脂としては、ヤシ油、パーム核油及びそれらの分別油、硬化油又はエステル交換油などを単独又は組み合わせて使用することが出来る。
一方炭素数20以上の飽和脂肪酸を30%以上含む油脂としては、例えば高エルシン酸の菜種油、からし油、クランベ油、魚油などの油脂を極度硬化(通常ヨウ素価1以下まで水素添加した油)したものが挙げられる。ベヘン酸を30%以上含む油脂も同様に、例えば高エルシン酸の菜種油を極度硬化(不飽和のエルシン酸を硬化すれば、飽和のベヘン酸を得ることが出来る)した油脂、からし油、クランベ油、魚油などを極度硬化したものが挙げられるが、容易に入手可能な高エルシン酸の菜種油が好ましい。The oil composition for chocolate of the present invention can be obtained by transesterifying an oil containing 30% or more of a fatty acid having 12 or less carbon atoms and an oil or fat containing 30% or more of a saturated fatty acid having 20 or more carbon atoms. The iodine value of the oil and fat composition is 28 or less, preferably the iodine value is 0 to 27, and more preferably 0 to 26. Furthermore, it is preferable to mix | blend acetylated sucrose fatty acid ester with this transesterified fat and oil, and it is preferable to mix | blend 0.4 to 7.5 weight% with respect to the whole fats and oils composition as an amount. The obtained oil and fat composition for chocolate has an iodine value of 5 to 30, preferably an iodine value of 7 to 25.
It is preferable from the point of gloss of chocolate to mix | blend the fats and oils which contain behenic acid 30% or more into the fats and oils composition for chocolates.
As fats and oils containing 30% or more of fatty acids having 12 or less carbon atoms, coconut oil, palm kernel oil and fractionated oils thereof, hardened oil or transesterified oil can be used alone or in combination.
On the other hand, as fats and oils containing 30% or more of saturated fatty acids having 20 or more carbon atoms, for example, oils such as rapeseed oil of high erucic acid, mustard oil, crambe oil, fish oil, etc. are extremely hardened (usually hydrogenated to an iodine value of 1 or less) The thing which was done is mentioned. Similarly, fats and oils containing 30% or more of behenic acid are oils and fats obtained by extremely curing rapeseed oil of high erucic acid (saturated behenic acid can be obtained by curing unsaturated erucic acid), mustard oil, Oils, fish oils, and the like that are extremely hardened can be mentioned, and rapeseed oils with high erucic acid that are readily available are preferred.
チョコレート用油脂組成物に使用する炭素数12以下の脂肪酸を30%以上含む油脂並びに炭素数20以上の飽和脂肪酸を30%以上含む油脂及びベヘン酸を30%以上含む油脂以外の油脂としては例えば、大豆油、ひまわり種子油、綿実油、落花生油、米糠油、コーン油、サフラワー油、オリーブ油、カポック油、ゴマ油、月見草油、パーム油等の植物性油脂ならびに乳脂、牛脂、豚脂等の動物性油脂が例示でき、上記油脂類の単独または混合油あるいはそれらの硬化油、分別油、硬化分別油、分別硬化油ならびにエステル交換等を施した加工油脂が使用できる。
このようにして得られた油脂組成物は、トランス型不飽和脂肪酸を10%以下、更に5%以下が好ましい。トランス型不飽和脂肪酸が多いと本発明の目的を達成し難くなる。Examples of fats and oils other than fats and oils containing 30% or more of fatty acids having 12 or less carbon atoms and fats and oils containing 30% or more of saturated fatty acids having 20 or more carbon atoms and fats and oils containing 30% or more of behenic acid used in the fat composition for chocolate, Vegetable oils such as soybean oil, sunflower seed oil, cottonseed oil, peanut oil, rice bran oil, corn oil, safflower oil, olive oil, kapok oil, sesame oil, evening primrose oil, palm oil, and other animal oils such as milk fat, beef tallow, pork fat Fats and oils can be exemplified, and the above fats and oils can be used alone or as a mixed oil, or hardened oils, fractionated oils, hardened fractionated oils, fractionated hardened oils, and processed fats and oils subjected to transesterification.
The oil and fat composition thus obtained preferably has a trans-type unsaturated fatty acid of 10% or less, more preferably 5% or less. When there are many trans type unsaturated fatty acids, it will become difficult to achieve the objective of this invention.
エステル交換としては、トリグリセリドの1位と3位に結合する脂肪酸のみを酵素(リパーゼ)を用いて特異的に交換する方法(1、3位特異的エステル交換)と、酵素若しくは金属触媒(例えばナトリウムメチラート)を用いて結合する位置に関係なくランダムに交換する方法(ランダムエステル交換)に分けられる。本発明におけるエステル交換とは、後者のランダムエステル交換が好ましい。これはより多くのトリグリセリドの種類が生成するランダムエステル交換の方が、テンパリングをしないチョコレートでは長期にわたる品質の安定化に優れるため好ましい。 The transesterification includes a method of specifically exchanging only fatty acids bound to the 1st and 3rd positions of triglyceride using an enzyme (lipase) (1,3rd specific transesterification), and an enzyme or a metal catalyst (for example, sodium). Methylate) is a random exchange method (random transesterification) regardless of the bonding position. The transesterification in the present invention is preferably the latter random transesterification. Random transesterification, in which more types of triglycerides are generated, is preferable because chocolate without tempering is excellent in stabilizing quality over a long period of time.
本発明におけるアセチル化蔗糖脂肪酸エステルは、蔗糖脂肪酸エステル中の残存水酸基をアセチル基にて置換したタイプの蔗糖脂肪酸エステルで、脂肪酸としてはステアリン酸やパルミチン酸などの炭素数16以上の長鎖飽和酸が好ましく、またエステル化度は3以上のものが好ましい。アセチル化蔗糖脂肪酸エステルの配合量は油脂中0.4〜7.5重量%の範囲で実施されるが、これはチョコレート中に換算した場合のアセチル化蔗糖脂肪酸エステルの配合量が0.4〜2.0重量%に相当する量が望ましい。チョコレート中のアセチル化蔗糖脂肪酸エステルの含有量が少ない場合は、経時的に品質劣化(粗大化)を起こす危険があり、多すぎると、コスト的に高くなる割には効果の増大が少ないので、2.0重量%以下が好ましい。 The acetylated sucrose fatty acid ester in the present invention is a sucrose fatty acid ester of the type in which the remaining hydroxyl group in the sucrose fatty acid ester is substituted with an acetyl group, and the fatty acid is a long chain saturated acid having 16 or more carbon atoms such as stearic acid or palmitic acid. The degree of esterification is preferably 3 or more. The blending amount of acetylated sucrose fatty acid ester is carried out in the range of 0.4 to 7.5% by weight in fats and oils, and this is the blending amount of acetylated sucrose fatty acid ester when converted into chocolate is 0.4 to 0.4%. An amount corresponding to 2.0% by weight is desirable. If the content of the acetylated sucrose fatty acid ester in the chocolate is low, there is a risk of quality deterioration (coarse) over time, and if it is too much, there is little increase in effect for the higher cost, It is preferably 2.0% by weight or less.
上記で得られた油脂組成物をチョコレートに使用するのであるが、一般的にチョコレートとは、例えば原料としてカカオマス、ココアパウダー、砂糖などの糖類、ココアバター等の油脂、乳化剤、香料等を使用して作られるダークチョコレート、例えば原料としてカカオマス、ココアパウダー、砂糖などの糖類、ココアバター等の油脂、全粉乳等の乳製品類、乳化剤、香料等を使用して作られるミルクチョコレート、例えば砂糖などの糖類、ココアバター等の油脂、全粉乳等の乳製品類、乳化剤、香料等を使用して作られるホワイトチョコレートに区別されたり、またカカオ分の含量によりチョコレート(カカオ分35%以上)や準チョコレート(カカオ分15%以上)に区別されるが、本発明のチョコレートとはこれらに限定されるものではなく、何れにおいても使用することが出来る。またこれらチョコレート中の油脂分としては30〜60重量%が一般的である。 The fat composition obtained above is used for chocolate. Generally, chocolate is, for example, cacao mass, cocoa powder, sugars such as sugar, fats and oils such as cocoa butter, emulsifiers, fragrances, etc. Dark chocolate made by using, for example, cacao mass, cocoa powder, sugars such as sugar, fats and oils such as cocoa butter, milk products such as whole milk powder, milk chocolate made using emulsifiers, flavors, etc. Differentiated into white chocolate made using sugars, cocoa butter and other fats and oils such as whole milk powder, emulsifiers, fragrances, etc. Depending on the content of cacao, chocolate (cacao content 35% or more) and semi-chocolate (The cacao content is 15% or more), but the chocolate of the present invention is limited to these. Without also it can be used in any. Moreover, 30-60 weight% is common as fat and oil in these chocolates.
本発明のチョコレートは上記油脂組成物を使用するものであるが、第1〜第2又は第8〜第9に記載の油脂組成物をチョコレート全体に対して20〜68重量%使用するのが好ましく、より好ましくは24〜60重量%であり、更に好ましくは28〜51重量%である。油脂組成物が少ない場合はチョコレートの品質を長期にわたり維持し難くなる(ブルームやグレーニングなどのチョコレートの品質劣化)。逆に多い場合には本発明の油脂組成物以外の成分の比率が下がりすぎて風味の良いチョコレートが作製し難くなる。
また、チョコレートに使用される油脂中のココアバターの含有量が25重量%以下、更に20重量%以下が好ましい。油脂中のココアバターの含有量が25重量%を超えると、本発明の油脂組成物を使用してもテンパリングすることなしに、風味や品質に優れるチョコレートを作製し難くなる。Although the chocolate of this invention uses the said oil-and-fat composition, it is preferable to use 20 to 68 weight% of the oil-and-fat composition of the 1st-2nd or 8th-9th with respect to the whole chocolate. More preferably, it is 24-60 weight%, More preferably, it is 28-51 weight%. When there are few oil-fat compositions, it becomes difficult to maintain the quality of chocolate over a long period of time (degradation of chocolate quality such as bloom and graining). On the other hand, when the amount is large, the ratio of components other than the oil and fat composition of the present invention is too low, and it becomes difficult to produce a chocolate with good flavor.
Moreover, the content of cocoa butter in fats and oils used for chocolate is preferably 25% by weight or less, and more preferably 20% by weight or less. If the content of cocoa butter in the fat exceeds 25% by weight, it is difficult to produce a chocolate excellent in flavor and quality without tempering even if the fat composition of the present invention is used.
以下、実施例を例示して本発明の効果を明瞭にするが、本発明の精神は以下の実施例に限定されるものではない。なお、例中、%及び部は重量基準を意味する。
実験例1(油脂の調製)
ヤシ油(ヨウ素価8)50部、パーム分別ステアリン(ヨウ素価31)40部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行い油脂Aとした。ヨウ素価は17であり、上昇融点は35℃であった。Examples The following examples illustrate the effects of the present invention, but the spirit of the present invention is not limited to the following examples. In the examples,% and part mean weight basis.
Experimental Example 1 (Preparation of fat / oil)
A metal catalyst (sodium methoxide) 0 in an oil and fat mixed with 50 parts of coconut oil (iodine value 8), 40 parts of palm fractionated stearin (iodine value 31) and 10 parts of high erucic acid rapeseed rapeseed oil (iodine value 1 or less) .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were refined according to a conventional method to obtain fats and oils A. The iodine value was 17, and the rising melting point was 35 ° C.
実験例2(油脂の調製)
実験例1で作製したエステル交換脂99.6部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)0.4部を混合し油脂Bとした。ヨウ素価は17であり、上昇融点は35℃であった。
実験例3(油脂の調製)
実験例1で作製したエステル交換脂98部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)2部を混合し油脂Cとした。ヨウ素価は17であり、上昇融点は36℃であった。Experimental Example 2 (Preparation of fats and oils)
The transesterified fat 99.6 parts prepared in Experimental Example 1 was mixed with 0.4 part of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less) to obtain fat B. The iodine value was 17, and the rising melting point was 35 ° C.
Experimental Example 3 (Preparation of fats and oils)
2 parts of high erucic acid rapeseed extremely hardened oil (iodine value of 1 or less) was mixed with 98 parts of transesterified fat prepared in Experimental Example 1 to obtain Oil C. The iodine value was 17, and the rising melting point was 36 ° C.
実験例4(油脂の調製)
ヤシ油(ヨウ素価8)40部、パーム分別ステアリン(ヨウ素価31)55部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)5部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られたエステル交換脂99.5部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)0.5部を混合し油脂Dとした。ヨウ素価は20であり、上昇融点は38℃であった。Experimental Example 4 (Preparation of fats and oils)
A metal catalyst (sodium methoxide) 0 in an oil / fat mixed with 40 parts of coconut oil (iodine value 8), 55 parts of palm fractionated stearin (iodine value 31), and 5 parts of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less). .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The transesterified fat (99.5 parts) was mixed with 0.5 part of a high erucic acid rapeseed extremely hardened oil (iodine value of 1 or less) to obtain fat D. The iodine value was 20, and the rising melting point was 38 ° C.
実験例5(油脂の調製)
ヤシ油(ヨウ素価8)50部、パーム分別ステアリン(ヨウ素価31)20部、硬化パームオレイン(ヨウ素価55)20部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂に、金属触媒0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行った。得られたエステル交換脂99部と高エルシン酸菜種極度硬化油(ヨウ素価1以下)1部を混合し油脂Eとした。ヨウ素価は21であり、上昇融点は32℃であった。Experimental Example 5 (Preparation of fats and oils)
50 parts of coconut oil (iodine value 8), 20 parts of palm fractionated stearin (iodine value 31), 20 parts of hardened palm olein (iodine value 55), 10 parts of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less) were mixed. 0.3 parts of a metal catalyst was added to the oil and fat, and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were purified according to a conventional method. 99 parts of the obtained transesterified fat and 1 part of a high erucic acid rapeseed extremely hardened oil (iodine value of 1 or less) were mixed to obtain a fat E. The iodine value was 21 and the rising melting point was 32 ° C.
実験例6(油脂の調製)
パーム核油(ヨウ素価17)95部とパーム油(ヨウ素価52)5部を混合し極度硬化した。この極度硬化した油脂(ヨウ素価1以下)70部、パーム分別ステアリン(ヨウ素価31)15部、ハイオレイックヒマワリ油(ヨウ素価84)5部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合し、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行い油脂Fとした。ヨウ素価は9であり、上昇融点は36℃であった。Experimental Example 6 (Preparation of fats and oils)
95 parts of palm kernel oil (iodine number 17) and 5 parts of palm oil (iodine number 52) were mixed and extremely hardened. 70 parts of this extremely hardened oil (iodine value of 1 or less), 15 parts of palm fractionated stearin (iodine value of 31), 5 parts of high oleic sunflower oil (iodine value of 84), high erucic acid rapeseed extremely hardened oil (iodine value of 1 or less) ) 10 parts were mixed, 0.3 part of a metal catalyst (sodium methoxide) was added, and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were refined according to a conventional method to obtain fats and oils F. The iodine value was 9, and the rising melting point was 36 ° C.
実験例7(油脂の調製)
パーム核油(ヨウ素価17)95部とパーム油(ヨウ素価52)5部を混合し極度硬化した。この極度硬化した油脂(ヨウ素価1以下)70部、パーム分別ステアリン(ヨウ素価31)25部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)5部を混合し、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行い油脂Gとした。ヨウ素価は7であり、上昇融点は38℃であった。Experimental Example 7 (Preparation of fat / oil)
95 parts of palm kernel oil (iodine number 17) and 5 parts of palm oil (iodine number 52) were mixed and extremely hardened. 70 parts of this extremely hardened oil (iodine value of 1 or less), 25 parts of palm fractionated stearin (iodine value of 31) and 5 parts of high erucic acid rapeseed extremely hardened oil (iodine value of 1 or less) were mixed to form a metal catalyst (sodium methoxide). ) 0.3 part was added, and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were refined according to a conventional method to obtain fats and oils G. The iodine value was 7, and the rising melting point was 38 ° C.
以下油脂A、油脂B、油脂C、油脂D、油脂E、油脂F、油脂Gの脂肪酸組成を表1に纏めた。
脂肪酸の測定は以下のように行った。先ず脂肪酸の調製は「基準油脂分析法の2.4.1.2−1996」に従い実施した。得られた脂肪酸調製液はガスクロマトグラフ法で分析した。
The measurement of fatty acid was performed as follows. First, the fatty acid was prepared according to “Reference Oil Analysis Method 2.4.1.2-1996”. The obtained fatty acid preparation was analyzed by gas chromatography.
比較実験例1(油脂の調製)
ヤシ油(ヨウ素価8)50部、パーム分別ステアリン(ヨウ素価31)40部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂を作製し、油脂Hとした。ヨウ素価は17であり、上昇融点は54℃であった。Comparative Experimental Example 1 (Preparation of fats and oils)
An oil and fat was prepared by mixing 50 parts of palm oil (iodine value 8), 40 parts of palm fractionated stearin (iodine value 31) and 10 parts of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less). The iodine value was 17, and the rising melting point was 54 ° C.
比較実験例2(油脂の調製)
パーム油(ヨウ素価52)31部、パーム分別ステアリン(ヨウ素価31)66部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)3部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行い油脂Iとした。ヨウ素価は37であり、上昇融点は46℃であった。Comparative Experimental Example 2 (Preparation of fats and oils)
A metal catalyst (sodium methoxide) 0 in an oil / fat mixed with 31 parts palm oil (iodine value 52), 66 parts palm fractionated stearin (iodine value 31) and 3 parts high erucic acid rapeseed extremely hardened oil (iodine value 1 or less) .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were refine | purified according to the usual method, and it was set as fats and oils I. The iodine value was 37 and the rising melting point was 46 ° C.
比較実験例3(油脂の調製)
パーム核油(ヨウ素価17)65部、パーム分別オレイン(ヨウ素価62)35部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた後、ヨウ素価1以下になるまで硬化した油脂を定法に従い精製を行い油脂Jとした。ヨウ素価は1であり、上昇融点は42℃であった。Comparative Experimental Example 3 (Preparation of fats and oils)
A metal catalyst (sodium methoxide) 0.3 part is added to fat and oil obtained by mixing 65 parts of palm kernel oil (iodine number 17) and 35 parts of palm fractionated olein (iodine number 62), and random ester at 80 ° C. for 60 minutes under vacuum. After the replacement, the oil and fat cured until the iodine value became 1 or less was refined according to a conventional method to obtain an oil J. The iodine value was 1, and the rising melting point was 42 ° C.
比較実験例4(油脂の調製)
ヨウ素価69のパームオレインをヨウ素価55まで異性化硬化し、定法に従い脱色、脱臭を行った。得られた硬化油脂を油脂Kとした。油脂Kのトランス脂肪酸含量は42.7%であった。ヨウ素価は55であり、上昇融点は39℃であった。Comparative Experimental Example 4 (Preparation of fats and oils)
Palm olein having an iodine value of 69 was isomerized and cured to an iodine value of 55, and decolorized and deodorized according to a conventional method. The obtained hardened fat was named fat K. The trans fatty acid content of fat K was 42.7%. The iodine value was 55 and the rising melting point was 39 ° C.
比較実験例5(油脂の調製)
ヨウ素価45のパーム中融点部(PMF)をヨウ素価40まで硬化し、定法に従い脱色、脱臭を行った。得られた硬化油脂を油脂Lとする。油脂Lのトランス脂肪酸含量は6.7%であった。ヨウ素価は40であり、上昇融点は36℃であった。Comparative Experimental Example 5 (Preparation of fats and oils)
A palm middle melting point (PMF) having an iodine value of 45 was cured to an iodine value of 40, and decolorization and deodorization were performed according to a conventional method. Let the obtained hardened fats and oils be the fats and oils L. The trans fatty acid content of the fat L was 6.7%. The iodine value was 40 and the rising melting point was 36 ° C.
以下油脂H、油脂I、油脂J、油脂K、油脂Lの脂肪酸組成を表2に纏めた。
実験例1〜7及び比較実験例1〜5で調製した油脂A〜Lについて、炭素数12以下の脂肪酸の合計量、炭素数20以上の飽和脂肪酸の合計量、全飽和脂肪酸の合計量、ヨウ素価、上昇融点を表3に纏めた。
実施例1
カカオマス8部、ココアパウダー15部、砂糖43部、実験例1で得られた油脂A20部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂A14部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表4に記載した。
8 parts of cacao mass, 15 parts of cocoa powder, 43 parts of sugar, and 20 parts of fat and oil A obtained in Experimental Example 1 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 14 parts of the remaining fat / oil A and 0.4 part of lecithin were added to prepare chocolate. The final formulation of chocolate is listed in Table 4.
実施例2〜実施例7及び比較例1〜比較例5
実施例1において、油脂Aを油脂Bに替えた以外は実施例1と同様な配合、同様な処理を行い実施例2に基づくチョコレートを得た。
同様に油脂Aを油脂Cに替え、実施例3に基づくチョコレートを得、同様にして、実施例4〜実施例7及び比較例1〜比較例5に基づくチョコレートを得た。Examples 2 to 7 and Comparative Examples 1 to 5
In Example 1, except having changed fats and oils A into fats and oils B, the same mixing | blending and the same process as Example 1 were performed, and the chocolate based on Example 2 was obtained.
Similarly, fats and oils A were replaced with fats and oils C to obtain chocolates based on Example 3, and similarly, chocolates based on Examples 4 to 7 and Comparative Examples 1 to 5 were obtained.
チョコレートの保存性確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15〜20℃で冷却固化した。固化したチョコレートは以下の方法と評価で保存性確認試験を行った。
項目としては、口溶け感、ブルーム若しくはグレーニングの程度、艶の確認試験を行った。
チョコレートにおける口溶け感確認試験
各油脂で作製したチョコレートの口溶け感をパネラー(6名)により評価した。評価として口溶け感が良いと感じた物を○、悪いと感じた物を×とした。
結果を表5に纏めた。
As items, a mouth melting feeling, the degree of bloom or graining, and a gloss check test were conducted.
Mouth melt feeling confirmation test in chocolate The panel melt feeling was evaluated by the panelists (six persons). As evaluation, the thing which felt that the mouth melted feeling was good was set as (circle), and the thing which felt bad was set as x.
The results are summarized in Table 5.
チョコレートにおけるブルーム若しくはグレーニングの程度の確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15〜20℃で冷却固化した。固化したチョコレートは20℃で1週間熟成(エージング)した後、1日で17℃を10時間、28℃を10時間保持できる恒温器(温度を17℃から28℃に変えるのに2時間、同様に28℃から17℃に変えるのに2時間)に交互にチョコレートを保管しサイクルテストを行った(サイクルは90回の結果)。また、室温20℃に温調されている部屋でチョコレートを保管して(保管日数90日の結果)、経時的なチョコレートの品質変化(ブルームやグレーニングの発生など)を目視により確認した。
結果を表6に纏めた。
The results are summarized in Table 6.
結果は油脂A〜Gでは保存中ブルーム若しくはグレーニングの発生は認められなかった。油脂H、I、J及びLは保存中ブルーム若しくはグレーニングが認められた。油脂Hは保存中ブルーム若しくはグレーニングの発生が認められただけではなく、チョコレートとして非常に口溶けが悪く、商品的な価値が認められなかった。油脂Kは保存中ブルーム若しくはグレーニングの発生は認められないが、トランス脂肪酸を10%以上含むため、本発明の範囲外である。一方油脂Lはトランス脂肪酸が10%以下であるが、保存中にブルーム若しくはグレーニングが発生した。 As a result, in the fats and oils A to G, no bloom or graining was observed during storage. Oils and fats H, I, J and L showed bloom or graining during storage. The fats and oils H were not only recognized to generate bloom or graining during storage, but also very poorly melted as chocolate, and no commercial value was recognized. The fats and oils K do not show bloom or graining during storage, but contain 10% or more of trans fatty acids, which is outside the scope of the present invention. On the other hand, the fat L has 10% or less trans fatty acid, but bloom or graining occurred during storage.
チョコレートの艶の確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15℃、20℃、25℃の各温度で冷却固化した。固化したチョコレートは20℃で1週間熟成(エージング)した後、目視によりその艶の状態を確認した。
結果を表7に纏めた。
The results are summarized in Table 7.
実施例1及び6、7はランダムエステル交換脂のみで作製したチョコレートであるが、チョコレートの艶は良好であった。実施例2〜5はランダムエステル交換脂にベヘン酸を30%以上含む油脂を0.4〜2.0重量%配合した油脂からなるチョコレートであり、添加量が多いほど、またチョコレートの固化条件が高い温度ほどチョコレートの艶が良好であり、チョコレートを急冷固化することの出来ない条件ではより機能を発揮した。これに対し、比較例1〜3では冷却温度の如何に拘らず艶の悪い物であった。また比較例4〜5は比較的低温(15℃)で冷却したチョコレートでは艶は良好であったが、20℃以上の温度で冷却した物は艶の悪いものであった。 Examples 1 and 6 and 7 are chocolates made only with random transesterified fat, but the gloss of the chocolate was good. Examples 2 to 5 are chocolates composed of fats and oils in which 0.4 to 2.0% by weight of fats and oils containing 30% or more of behenic acid are blended with random transesterified fats. The higher the temperature, the better the gloss of the chocolate, and it performed more under conditions where the chocolate could not be rapidly cooled and solidified. On the other hand, in Comparative Examples 1-3, it was a thing with poor gloss irrespective of the cooling temperature. In Comparative Examples 4 to 5, the gloss of the chocolate cooled at a relatively low temperature (15 ° C.) was good, but the product cooled at a temperature of 20 ° C. or more had a poor gloss.
実験例8(油脂の調製)
ヤシ油(ヨウ素価8)50部、パーム分別ステアリン(ヨウ素価31)40部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行った。このエステル交換脂99.6部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)0.4部を混合した。更にこの混合油脂100部に対してアセチル化蔗糖脂肪酸エステル(DKエステルFA10−E/第一工業製薬株式会社製:エステル化度4.9)を1.5部配合し油脂Mとした。ヨウ素価は17であり、上昇融点は35℃であった。Experimental Example 8 (Preparation of fat / oil)
A metal catalyst (sodium methoxide) 0 in an oil and fat mixed with 50 parts of coconut oil (iodine value 8), 40 parts of palm fractionated stearin (iodine value 31) and 10 parts of high erucic acid rapeseed rapeseed oil (iodine value 1 or less) .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were purified according to a conventional method. 0.4 part of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less) was mixed with 99.6 parts of this transesterified fat. Further, 1.5 parts of acetylated sucrose fatty acid ester (DK Ester FA10-E / Daiichi Kogyo Seiyaku Co., Ltd .: Degree of esterification 4.9) was blended with 100 parts of this mixed fat to make fat M. The iodine value was 17, and the rising melting point was 35 ° C.
実験例9(油脂の調製)
ヤシ油(ヨウ素価8)50部、パーム分別ステアリン(ヨウ素価31)40部、高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂を定法に従い精製を行った。このエステル交換脂99.6部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)0.4部を混合した。更にこの混合油脂100部に対してアセチル化蔗糖脂肪酸エステル(DKエステルFA10−E/第一工業製薬株式会社製:エステル化度4.9)を6.3部配合し油脂Nとした。ヨウ素価は16であり、上昇融点は35℃であった。Experimental Example 9 (Preparation of fats and oils)
A metal catalyst (sodium methoxide) 0 in an oil and fat mixed with 50 parts of coconut oil (iodine value 8), 40 parts of palm fractionated stearin (iodine value 31) and 10 parts of high erucic acid rapeseed rapeseed oil (iodine value 1 or less) .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fats and oils were purified according to a conventional method. 0.4 part of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less) was mixed with 99.6 parts of this transesterified fat. Furthermore, 6.3 parts of acetylated sucrose fatty acid ester (DK Ester FA10-E / Daiichi Kogyo Seiyaku Co., Ltd .: Degree of esterification 4.9) was blended with 100 parts of this mixed fat to obtain fat N. The iodine value was 16, and the rising melting point was 35 ° C.
実験例10(油脂の調製)
実験例8で作製したエステル交換脂99.6部に高エルシン酸菜種極度硬化油(ヨウ素価1以下)0.4部を混合した油脂95部にベヘン酸含有エステル交換脂(不二製油製:商品名「EBFW」:融点58℃/ヨウ素価26)5部を混合し、更にこの混合油脂100部に対してアセチル化蔗糖脂肪酸エステルを1.5部配合し油脂Oとした。ヨウ素価は18であり、上昇融点は38℃であった。Experimental Example 10 (Preparation of fats and oils)
Behenic acid-containing transesterified fat (manufactured by Fuji Oil Co., Ltd.) was added to 95 parts of fat and oil mixed with 99.6 parts of transesterified fat prepared in Experimental Example 8 and 0.4 part of high erucic acid rapeseed extremely hardened oil (iodine value 1 or less). Product name “EBFW”: Melting point 58 ° C./iodine value 26) 5 parts were mixed, and 1.5 parts of acetylated sucrose fatty acid ester was blended with 100 parts of this mixed oil and fat to obtain fat O. The iodine value was 18 and the rising melting point was 38 ° C.
実験例11(油脂の調製)
パーム核油(ヨウ素価17)85部とパーム油(ヨウ素価52)5部と高エルシン酸菜種極度硬化油(ヨウ素価1以下)10部を混合した油脂に、金属触媒(ナトリウムメトキシド)0.3部を加え、真空下80℃で60分ランダムエステル交換させた。得られた油脂をヨウ素価0まで硬化した後、定法に従い精製を行った。この油脂78部に別のエステル交換脂(不二製油製「パーキッドY:融点33℃/ヨウ素価39」)10部、硬化油脂(不二製油製「メラノF−11:融点36℃/ヨウ素価60」)12部を混合し、更にこの混合油脂100部に対してアセチル化蔗糖脂肪酸エステルを1.5部配合し油脂Pとした。ヨウ素価は12であり、上昇融点は38℃であった。Experimental Example 11 (Preparation of fats and oils)
A metal catalyst (sodium methoxide) 0 in an oil and fat obtained by mixing 85 parts of palm kernel oil (iodine number 17), 5 parts of palm oil (iodine number 52) and 10 parts of high erucic acid rapeseed extremely hardened oil (iodine number 1 or less). .3 parts were added and random transesterification was performed at 80 ° C. for 60 minutes under vacuum. The obtained fat was cured to an iodine value of 0 and then purified according to a conventional method. 10 parts of another transesterified fat (Fuji Oil “Perkyd Y: melting point 33 ° C./iodine 39”) and hardened oil (Fuji Oil “Melano F-11: melting point 36 ° C./iodine value) 60 ") 12 parts were mixed, and 1.5 parts of acetylated sucrose fatty acid ester was blended with 100 parts of this mixed fat to make fat P. The iodine value was 12, and the rising melting point was 38 ° C.
実験例8〜11で調製した油脂M〜Pについて、炭素数12以下の脂肪酸の合計量、炭素数20以上の飽和脂肪酸の合計量、ヨウ素価、上昇融点、アセチル化蔗糖脂肪酸エステル量、トランス脂肪酸含有量を表8に纏めた。
実施例8
カカオマス8部、ココアパウダー15部、ココアバター2部、砂糖43部、実験例8で得られた油脂M 18部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂M 14部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表9に記載した。
8 parts of cacao mass, 15 parts of cocoa powder, 2 parts of cocoa butter, 43 parts of sugar, and 18 parts of fats and oils M obtained in Experimental Example 8 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 14 parts of the remaining fat and oil M and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 9.
実施例9〜実施例10、参考例11
実施例8において、油脂Mを油脂Nに替えた以外は実施例8と同様な配合、同様な処理を行い実施例9に基づくチョコレートを得た。同様に油脂Mを油脂Oに替え、実施例10に基づくチョコレートを得、同様にして、参考例11に基づくチョコレートを得た。
Examples 9 to 10 and Reference Example 11
In Example 8, except having changed fats and oils M to fats and oils N, the same mixing | blending and the same process as Example 8 were performed, and the chocolate based on Example 9 was obtained. Similarly, fats and oils M were replaced with fats and oils O to obtain chocolates based on Example 10, and similarly, chocolates based on Reference Example 11 were obtained.
チョコレートの保存性確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15〜20℃で冷却固化した。固化したチョコレートは以下の方法と評価で保存性確認試験を行った。
項目としては、口溶け感、ブルーム若しくはグレーニングの程度の確認試験を行った。 チョコレートにおける口溶け感確認試験
各油脂で作製したチョコレートの口溶け感をパネラー(6名)により評価した。評価として口溶け感が良いと感じた物を○、悪いと感じた物を×とした。 結果を表10に纏めた。
Chocolate storage stability confirmation test The chocolate prepared as described above was poured into a mold at a temperature (50 ° C) at which the fats and oils were melted, and then cooled and solidified at 15 to 20 ° C. The solidified chocolate was subjected to a storage stability confirmation test by the following method and evaluation.
As items, a test for confirming the degree of mouth melting, bloom or graining was conducted. Mouth melt feeling confirmation test in chocolate The panel melt feeling was evaluated by the panelists (six persons). As evaluation, the thing which felt that the mouth melted feeling was good was set as (circle), and the thing which felt bad was set as x. The results are summarized in Table 10.
チョコレートにおけるブルーム若しくはグレーニングの程度の確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15〜20℃で冷却固化した。固化したチョコレートは20℃で1週間熟成(エージング)した後、1日で17℃を10時間、28℃を10時間保持できる恒温器(温度を17℃から28℃に変えるのに2時間、同様に28℃から17℃に変えるのに2時間)に交互にチョコレートを保管しサイクルテストを行った(サイクルは90回の結果)。また、室温20℃に温調されている部屋でチョコレートを保管して(保管日数90日の結果)、経時的なチョコレートの品質変化(ブルームやグレーニングの発生など)を目視により確認した。
結果を表11に纏めた。
The results are summarized in Table 11.
結果は油脂M〜Pでは保存中ブルーム若しくはグレーニングの発生は認められなかった。 As a result, in the fats and oils M to P, no bloom or graining was observed during storage.
実施例12
カカオマス8部、ココアパウダー15部、ココアバター1部、砂糖38部、実験1例で得られた油脂A 15部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂A 23部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表12に記載した。Example 12
8 parts of cacao mass, 15 parts of cocoa powder, 1 part of cocoa butter, 38 parts of sugar and 15 parts of fats and oils A obtained in one experiment were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 23 parts of the remaining fat / oil A and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 12.
実施例13
カカオマス8部、ココアパウダー15部、ココアバター3部、砂糖23部、実験例1で得られた油脂A 7部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂A 44部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表12に記載した。Example 13
8 parts of cacao mass, 15 parts of cocoa powder, 3 parts of cocoa butter, 23 parts of sugar and 7 parts of fat A obtained in Experimental Example 1 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 44 parts of the remaining fat / oil A and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 12.
実施例14
カカオマス8部、ココアパウダー15部、ココアバター1部、砂糖48部、実験例8で得られた油脂M 18部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂M 10部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表12に記載した。Example 14
8 parts of cacao mass, 15 parts of cocoa powder, 1 part of cocoa butter, 48 parts of sugar, and 18 parts of fats and oils M obtained in Experimental Example 8 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 10 parts of the remaining fat and oil M and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 12.
比較例11
カカオマス9部、ココアパウダー17部、砂糖45部、実験例1で得られた油脂A 24部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂A 11部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表12に記載した。Comparative Example 11
9 parts of cacao mass, 17 parts of cocoa powder, 45 parts of sugar and 24 parts of fats and oils A obtained in Experimental Example 1 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 11 parts of the remaining fat and oil A and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 12.
比較例12
ココアパウダー13部、砂糖52部、実験例8で得られた油脂M 19部をミキサーで混合し、ドウを調製した(ミキシング)。これをリファイナーに通し、粒度を約20マイクロメーターに調製した(リファイニング)。得られたフレークをコンチングした。尚コンチングの最終段階で残りの油脂M 6部とレシチン0.4部を加え、チョコレートを作製した。チョコレートの最終的な配合は表12に記載した。Comparative Example 12
13 parts of cocoa powder, 52 parts of sugar, and 19 parts of fats and oils M obtained in Experimental Example 8 were mixed with a mixer to prepare a dough (mixing). This was passed through a refiner to adjust the particle size to about 20 micrometers (refining). The obtained flakes were conching. In the final stage of conching, 6 parts of the remaining fat and oil M and 0.4 part of lecithin were added to prepare chocolate. The final chocolate formulation is listed in Table 12.
表12に、実施例12〜実施例14及び比較例11、12の配合、総油分、チョコレート中の本願発明の油脂組成物量及びチョコレートに使用される油脂中のココアバター量を纏めた。
チョコレートにおけるブルーム若しくはグレーニングの程度の確認試験
上記のように調製したチョコレートを油脂が融解している温度(50℃)で型に流し込み、15〜20℃で冷却固化した。固化したチョコレートは20℃で1週間熟成(エージング)した後、1日で17℃を10時間、28℃を10時間保持できる恒温器(温度を17℃から28℃に変えるのに2時間、同様に28℃から17℃に変えるのに2時間)に交互にチョコレートを保管しサイクルテストを行った(サイクルは90回の結果)。また、室温20℃に温調されている部屋でチョコレートを保管して(保管日数90日の結果)、経時的なチョコレートの品質変化(ブルームやグレーニングの発生など)を目視により確認した。
結果を表13に纏めた。
The results are summarized in Table 13.
結果は実施例12〜14及び比較例11では保存期間中にチョコレートにブルーム若しくはグレーニングの発生は見られなかった。しかし、比較例11ではカカオマスを配合していないものであるため風味的には劣るものであり、本発明が解決する目的とはそぐわない。一方比較例12はココアバターの配合量が多いため、風味的には優れるものであったが、サイクル保存テストでチョコレートに激しくブルーム若しくはグレーニングが発生し、商品価値が著しく劣るものであった。 As a result, in Examples 12 to 14 and Comparative Example 11, no bloom or graining was observed in the chocolate during the storage period. However, since Comparative Example 11 does not contain cacao mass, it is inferior in flavor and is not suitable for the purpose of the present invention. On the other hand, Comparative Example 12 was excellent in flavor due to the large amount of cocoa butter, but in the cycle storage test, the chocolate was intensely bloomed or grained, and the commercial value was remarkably inferior.
本発明は、炭素数12以下の脂肪酸を30%以上含む油脂と炭素数20以上の飽和脂肪酸を30%以上含む油脂をエステル交換してなる油脂であって、更にこのエステル交換された油脂にアセチル化蔗糖脂肪酸エステルを配合してなるチョコレート用油脂組成物であって、テンパリング操作しないでココアバターを含む風味に優れたチョコレートを製造することの出来るチョコレート用油脂組成物に関する。 The present invention is an oil obtained by transesterifying an oil containing 30% or more of a fatty acid having 12 or less carbon atoms and an oil containing 30% or more of a saturated fatty acid having 20 or more carbon atoms. It is the oil-fat composition for chocolates which mix | blends a sucrose fatty acid ester, Comprising: It is related with the oil-fat composition for chocolates which can manufacture the chocolate excellent in the flavor containing cocoa butter, without tempering operation.
Claims (9)
(A)ヤシ油又はパーム核油の、非硬化油又は極度硬化油であり、これらの単独又は組み合わせた油脂
(B)高エルシン酸の菜種油を極度硬化した油脂
(C)パーム分別ステアリン An oil / fat composition obtained by random transesterification of an oil / fat mixed with the following (A) to (C), wherein the trans-unsaturated fatty acid is 5% or less.
(A) Non-hardened oil or extremely hardened oil of palm oil or palm kernel oil, and these fats and oils (B) Highly hardened rapeseed oil of high erucic acid (C) Palm fractionated stearin
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KR (1) | KR101367014B1 (en) |
CN (1) | CN101478884B (en) |
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JP4515470B2 (en) * | 2007-01-30 | 2010-07-28 | 花王株式会社 | Hard butter |
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WO2012161105A1 (en) * | 2011-05-25 | 2012-11-29 | 不二製油株式会社 | Fat composition for chocolate |
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JP6052423B2 (en) | 2013-10-06 | 2016-12-27 | 不二製油株式会社 | No tempering type chocolate oil and fat composition and tempering type chocolate fat and oil composition |
KR102591200B1 (en) | 2015-02-17 | 2023-10-18 | 닛신 오일리오그룹 가부시키가이샤 | Transesterified fat and oil and chocolate using the transesterified fat and oil |
CN107613779B (en) * | 2015-05-28 | 2021-06-11 | 日清奥利友集团株式会社 | Chocolate |
RU2017144106A (en) * | 2015-06-10 | 2019-07-10 | ААК АБ (публ) | METHOD OF OBTAINING FILLING MASS AND RELATED DEVICE |
CN105475517B (en) * | 2016-01-08 | 2017-07-04 | 广州南侨食品有限公司 | A kind of human body easily absorbs baking basic oil and preparation method thereof |
MY170228A (en) * | 2016-03-31 | 2019-07-10 | Fuji Oil Holdings Inc | Fat composition for low-trans fat, non-tempered chocolate and chocolate |
MY190071A (en) * | 2016-04-07 | 2022-03-24 | Adeka Corp | Method for manufacturing no-temper-type hard butter composition |
EP3603409B1 (en) * | 2017-03-31 | 2023-09-06 | Fuji Oil Holdings Inc. | Transesterified fat or oil |
WO2019176963A1 (en) * | 2018-03-12 | 2019-09-19 | 株式会社カネカ | Cocoa butter compatibility improver and method for producing same, and non-tempered chocolate and food containing same |
CN118511925A (en) | 2018-03-26 | 2024-08-20 | 不二制油集团控股株式会社 | Transesterification fat, fat for chocolate, and chocolate |
JP7444061B2 (en) * | 2018-07-24 | 2024-03-06 | 不二製油株式会社 | chocolate-like food |
JP2022076026A (en) * | 2019-03-20 | 2022-05-19 | 株式会社J-オイルミルズ | Method for producing transesterified fat |
JP7085146B2 (en) * | 2019-03-27 | 2022-06-16 | 不二製油株式会社 | Bloom-suppressing oil-and-fat composition and oil-based confectionery using this |
JP7294957B2 (en) * | 2019-08-30 | 2023-06-20 | 株式会社カネカ | No-tempering type chocolate with high laurin fat content and food containing the same |
JP2021052686A (en) * | 2019-09-30 | 2021-04-08 | 株式会社明治 | Fat composition and fatty food product |
JP6936901B1 (en) * | 2020-06-19 | 2021-09-22 | 不二製油株式会社 | Oil and fat composition for filling |
BR112023014874A2 (en) * | 2021-01-27 | 2023-10-10 | Aak Ab Publ | A VEGETABLE FAT COMPOSITION FOR EDIBLE APPLICATIONS |
WO2022209887A1 (en) * | 2021-03-30 | 2022-10-06 | 不二製油グループ本社株式会社 | Oil and fat composition for chocolate |
WO2023176337A1 (en) * | 2022-03-16 | 2023-09-21 | 不二製油グループ本社株式会社 | Oil and fat composition for chocolate |
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CN101478884A (en) | 2009-07-08 |
KR20090008312A (en) | 2009-01-21 |
JPWO2007129590A1 (en) | 2009-09-17 |
CN101478884B (en) | 2012-12-26 |
WO2007129590A1 (en) | 2007-11-15 |
KR101367014B1 (en) | 2014-02-24 |
SG160347A1 (en) | 2010-04-29 |
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