JPS61282032A - Method for preventing discoloration of red cabbage pigment - Google Patents
Method for preventing discoloration of red cabbage pigmentInfo
- Publication number
- JPS61282032A JPS61282032A JP60124950A JP12495085A JPS61282032A JP S61282032 A JPS61282032 A JP S61282032A JP 60124950 A JP60124950 A JP 60124950A JP 12495085 A JP12495085 A JP 12495085A JP S61282032 A JPS61282032 A JP S61282032A
- Authority
- JP
- Japan
- Prior art keywords
- red cabbage
- cabbage pigment
- rutin
- red
- quercetin
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B61/00—Dyes of natural origin prepared from natural sources, e.g. vegetable sources
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、食品赤キャベツ色素に係るものである。こ
とに、重要なアンドンアニン系色素である赤キャベツ色
素による赤ないし赤紫色着色の退色を防止する方法に係
るものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] This invention relates to food red cabbage pigment. In particular, the present invention relates to a method for preventing fading of red to reddish-purple colors caused by red cabbage pigment, which is an important andonanine pigment.
赤キャベツ色素は、赤ないし赤紫色を呈する無害の天然
系色素として著名であるが、この色素から着色したもの
は退色が著しいという欠点がある。Red cabbage pigment is well-known as a harmless natural pigment that exhibits a red to reddish-purple color, but products colored with this pigment have the disadvantage of significant fading.
この欠点の克服即ち、退色防止の方法として、種々の手
段が講じられている。例えば、色素溶液のI)Hはでき
るだけ 、 酸性溶液を使用する、あるいは抗
酸化剤例えば、ビタミンCを添加する。あるいは、糸か
ら浴存酸素を除去する。Various measures have been taken to overcome this drawback, that is, to prevent discoloration. For example, for the dye solution I), use an acidic solution as much as possible, or add an antioxidant such as vitamin C. Alternatively, the bath oxygen is removed from the thread.
あるいは遮光性容器に充填して日光を遮断する等である
が、これらはいずれも、初期の目的を達成しがたい。Alternatively, it is difficult to achieve the initial objective by filling it in a light-shielding container to block sunlight.
その故は、着色溶液のp)Iが変動し易いこと、遮光性
容器を使用できない場合が多いこと、溶存酸素の除去に
有効な手段が適用できない場合が多いこと等である。This is because the p)I of the colored solution tends to fluctuate, it is often impossible to use light-shielding containers, and effective means for removing dissolved oxygen cannot be applied in many cases.
発明者は、永年の研究により退色の原因である光、熱及
びpHの変動への対応を考えて、退色を有効・に防止す
るには、赤キャベツ色素と他の特定の物質との併用が有
効であることを発見して、この発明を創出した。以下に
、この発明の詳細な説明する。After many years of research, the inventor considered how to deal with light, heat, and pH fluctuations that cause discoloration, and found that in order to effectively prevent discoloration, it is necessary to use red cabbage pigment in combination with other specific substances. discovered that it was effective and created this invention. The present invention will be explained in detail below.
この発明は、赤キャベツ色素に特定の退色防止剤を添加
ないし、併用することを骨子とするものである。The gist of this invention is to add or use a specific anti-fading agent to red cabbage pigment.
特定の退色防止剤は、ルチン及び又はケルセチンとフィ
チン及び又はフィチン酸とである。これ等を赤キャベツ
色素の粉末ないしその水及び又はアルコール溶液であっ
て酸性系のものに添加する。Particular anti-fade agents are rutin and/or quercetin and phytin and/or phytic acid. These are added to an acidic red cabbage pigment powder or its water and/or alcohol solution.
赤キャベツの水及び又はアルコール溶液は、そのpHを
酸性にする必要がある。その場合、酸度は任意である。The water and/or alcohol solution of red cabbage needs to have an acidic pH. In that case, the acidity is arbitrary.
即ちI)Hが6.9でもよいし、2でもよい。そして、
その温度は、赤キャベツ色素の熱分解温度(概ね120
°C)以下氷点までの温度でよい。That is, I)H may be 6.9 or 2. and,
The temperature is the thermal decomposition temperature of red cabbage pigment (approximately 120
°C) or below the freezing point.
ルチン及びケルセチンを使用する。その液中濃度は、室
温基準で約600ppm以下とする。この際約6oop
pmを越える場合には、ルチン及び又はケルセチンの使
用量に無駄を生じる。そして、ルチン単独でもよいし、
ケルセチン単独でもよいし、ケルセチンとルチンとの併
用でもよい。Using rutin and quercetin. Its concentration in the liquid is about 600 ppm or less based on room temperature. At this time, about 6 oop
If the amount exceeds pm, the amount of rutin and/or quercetin used will be wasted. Also, rutin alone may be used,
Quercetin may be used alone or in combination with quercetin and rutin.
ただ両者を併用する場合、これ等のものの価格との関係
で生産性が異なってくるという相違点がある。However, when both are used together, there is a difference in that the productivity will differ depending on the price of these items.
フィ/4−ン及び又はフィチン酸を併用する。その液中
濃度は、約iooppm以下でよい。そして、フィチン
及び又はフィチン酸のいずれを使用するかは、ルチン及
び又はケルセチンの場合と同様、生産性と基準に決定す
ればよい。Combined use of fine/4-fin and/or phytic acid. Its concentration in the liquid may be about iooppm or less. As in the case of rutin and/or quercetin, which of phytin and/or phytic acid to use may be determined based on productivity and criteria.
赤キャベツ色素溶液にだいし、ルチン及び又はケルセチ
ンをフィチン及び又はフィチン酸より先に添加してもよ
いし逆にフィチン及びフィチン酸を添加し後にルチン及
び又はケルセチンを添加してもよいし、あるいは、両者
を同時に添加してもよい。Rutin and/or quercetin may be added to the red cabbage pigment solution before phytin and/or phytic acid, or conversely, rutin and/or quercetin may be added after phytic acid and phytic acid are added, or, Both may be added at the same time.
このようにして収得した赤キャベツ液を食品、例えば、
各秤飲料、水産ねり製品、ソース類、菓子類、その他に
塗布あるいは混合する。また、この着色溶液を乾個して
得た粉末あるいは赤キャベツ色素粉末にルチン及び又は
ケルセチンとフィチン及び又はフィチン酸との水溶液を
添加してなる粉末を相手食品に使用する。The red cabbage liquid obtained in this way can be used as food, e.g.
Apply to or mix with various types of beverages, seafood paste products, sauces, confectionery, and others. Further, a powder obtained by drying this coloring solution or a powder obtained by adding an aqueous solution of rutin and/or quercetin and phytin and/or phytic acid to red cabbage pigment powder is used for the target food.
ここに、この発明はこの目的を達しおえる。Here, the present invention achieves this objective.
この発明は、次の作用及び効果を有する。■退色防止効
果(耐熱、耐光性)がきわめて高い。■食品の味におい
を殆んど阻害しない。■赤キャベツ色素の発色がなんら
阻害されない。これ等を次の実例に1り証明す6・
(実験例)(説明)
1、供試物溶液を酸性にするため添加したクエン酸10
%
21、赤キャベツ色素0.35 ? (色価E 6
0cIn
pl(。3バ壕衝液)ビタミンC0,25?を清水(2
0″C)で全量を1gとした物。ただし、退色剤無添加
のものは、クエン酸、ビタミンCをも含有していない。This invention has the following functions and effects. ■Extremely high anti-fading effect (heat resistance, light resistance). ■It hardly interferes with the taste and smell of food. ■The color development of red cabbage pigment is not inhibited in any way. We will prove these using the following example.6.
(Experiment example) (Explanation) 1. Citric acid 10 added to make the sample solution acidic
% 21, red cabbage pigment 0.35? (color value E 6
0cIn pl (.3 bath solution) Vitamin C0,25? Shimizu (2
0''C) with a total amount of 1 g.However, those without fading agents do not contain citric acid or vitamin C.
2、耐光性は、次の条件で比較した。2. Light resistance was compared under the following conditions.
紫外線カーボンアーク耐光試験機使用(スガイ試験機製
、型式FA−2)
波長領域 ;紫外部(主波長380 nm)試料
面エネルギー ; 383mW−mm/cJ試験器容
器 ;透明ジュース瓶
照射時間 ;7時間
温 度 ; 40°C
3、耐熱性は、次の条件で比較した。Using ultraviolet carbon arc light resistance tester (manufactured by Sugai Test Instruments, model FA-2) Wavelength range: Ultraviolet (main wavelength 380 nm) Sample surface energy: 383 mW-mm/cJ Tester container: Transparent juice bottle Irradiation time: 7 hours at temperature degree; 40°C 3. Heat resistance was compared under the following conditions.
20°C20°Cl力月間
38〃 38ノ/ 1 η
80〃 80〃 3時間
実施例1
クエン酸(結晶) 3.0 ?、クエン酸ナトリウム1
0%
0、flu’、赤キャベツ色素(色価E 80)I
)H1口
3.0緩衝液) 1.5 F、コーン色素(色価E1¥
’!40 )■、52、ルチン0.05 (熱湯400
2にルチンを溶解しておく)、フィチン0.11清水で
全量を100(1’としだ。攪拌混合後、容器に小分し
充填80’C・30分間加熱殺菌をした。このものは、
赤色で室温に10ケ月間放置しだが、はとんど変化がな
く、安定性に優れていた。20°C20°Cl force per month 38〃 38 no/1 η 80〃 80〃 3 hours Example 1 Citric acid (crystal) 3.0 ? , sodium citrate 1
0% 0, flu', red cabbage pigment (color value E 80) I
) H1 port 3.0 buffer) 1.5 F, Cohn dye (color value E1¥
'! 40) ■, 52, Rutin 0.05 (boiling water 400
Dissolve rutin in 2), phytin 0.11 and bring the total amount to 100 (1') with clear water. After stirring and mixing, divide into containers and heat sterilize at 80'C for 30 minutes.
The color was red and was left at room temperature for 10 months, but the color showed almost no change and was excellent in stability.
このものに甘味料例えば、砂糖及び香料各若干量を添加
したものは溶解清涼飲料水として好適であった。This product to which a certain amount of sweetener, for example, sugar and flavoring agent was added, was suitable as a dissolved soft drink.
実施例2
カラギーナン125’、ケルセチン0.04 F、フィ
チン酸0.12を約4002の水(20’C)に攪拌し
ながら上記粉体を添加、全量を100(1’に水で補正
して後、80°C・10分間加熱、その後、クエン酸(
結晶)2!?、赤キャベツ色素(色価E10%
□、、80)0.5P、ベリー色素(色価E10966
0 ) 0.59を添加し、カップに小分は殺菌して清
涼飲料を得た。このものは、赤色で室温に6力月間放置
で殆んど変化なく、安定性に優れていた。Example 2 Carrageenan 125', quercetin 0.04 F, and phytic acid 0.12 were added to approximately 4002 ml of water (20' C) with stirring, and the total amount was adjusted to 100 (1' with water). After that, heat at 80°C for 10 minutes, then add citric acid (
Crystal) 2! ? , red cabbage pigment (color value E10% □,,80) 0.5P, berry pigment (color value E10966
0) 0.59 was added and the small portions were sterilized in a cup to obtain a soft drink. This product was red in color and showed almost no change after being left at room temperature for 6 months, indicating excellent stability.
実施例3
塩實梅5001の水洗脱水したものを、4%氷錯酸水1
000P、グルタミン酸ナトリウム2f!。Example 3 Washed and dehydrated Shiozaneume 5001 was mixed with 1 part of 4% ice complex acid water.
000P, monosodium glutamate 2f! .
赤キャベツ色素(色価E17二80)3 F、ルチン0
、2 W 、フィチン酸0,22の混合調味液に7日間
常温で浸漬着色した後、液切り、小分は包装した。Red cabbage pigment (color value E17280) 3 F, rutin 0
, 2 W, and a mixed seasoning solution of 0.22 phytic acid for 7 days at room temperature for coloring, the liquid was drained, and the small portions were packaged.
とのものは、赤色で室温に6力月間放置したが、殆んど
変化がなく、安定性に優れていた。The red color was left at room temperature for 6 months, but there was almost no change and it was excellent in stability.
Claims (1)
ルセチンとフィチン及び又はフィチン酸とを添加するこ
とを特徴とする赤キャベツ色素の退色防止法。A method for preventing fading of red cabbage pigment, which comprises adding rutin and/or quercetin and phytin and/or phytic acid to red cabbage pigment powder or acidic solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12495085A JPH0622465B2 (en) | 1985-06-07 | 1985-06-07 | Prevention method of red cabbage pigment fading |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12495085A JPH0622465B2 (en) | 1985-06-07 | 1985-06-07 | Prevention method of red cabbage pigment fading |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61282032A true JPS61282032A (en) | 1986-12-12 |
JPH0622465B2 JPH0622465B2 (en) | 1994-03-30 |
Family
ID=14898220
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12495085A Expired - Lifetime JPH0622465B2 (en) | 1985-06-07 | 1985-06-07 | Prevention method of red cabbage pigment fading |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0622465B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06234935A (en) * | 1993-02-09 | 1994-08-23 | Sanei Gen F F I Inc | Method for stabilizing coloring matter |
JP2006174832A (en) * | 2004-11-26 | 2006-07-06 | Okuno Chem Ind Co Ltd | Discoloration inhibitor for vegetable and fruit |
JP2007302751A (en) * | 2006-05-09 | 2007-11-22 | Musashino Chemical Laboratory Ltd | Fading inhibitor of natural pigment or food and drink comprising the same |
JP2009112270A (en) * | 2007-11-08 | 2009-05-28 | National Agriculture & Food Research Organization | Purple-like colored potato-containing food and drink, and method for producing the same |
JP2010024230A (en) * | 2008-06-19 | 2010-02-04 | Glico Dairy Products Co Ltd | Composition for promoting biological absorption of flavonoid, food and drink for promoting biological absorption of flavonoid using the same and method for producing the same |
CN110305497A (en) * | 2019-07-12 | 2019-10-08 | 天津宏顺科生物科技有限公司 | Method for converting fat-soluble natural pigment into water-soluble pigment and protecting fading of water-soluble pigment |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4563186B2 (en) * | 2004-02-16 | 2010-10-13 | 理研ビタミン株式会社 | Anthocyanin dyes with improved heat resistance |
-
1985
- 1985-06-07 JP JP12495085A patent/JPH0622465B2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06234935A (en) * | 1993-02-09 | 1994-08-23 | Sanei Gen F F I Inc | Method for stabilizing coloring matter |
JP2006174832A (en) * | 2004-11-26 | 2006-07-06 | Okuno Chem Ind Co Ltd | Discoloration inhibitor for vegetable and fruit |
JP2007302751A (en) * | 2006-05-09 | 2007-11-22 | Musashino Chemical Laboratory Ltd | Fading inhibitor of natural pigment or food and drink comprising the same |
JP2009112270A (en) * | 2007-11-08 | 2009-05-28 | National Agriculture & Food Research Organization | Purple-like colored potato-containing food and drink, and method for producing the same |
JP2010024230A (en) * | 2008-06-19 | 2010-02-04 | Glico Dairy Products Co Ltd | Composition for promoting biological absorption of flavonoid, food and drink for promoting biological absorption of flavonoid using the same and method for producing the same |
CN110305497A (en) * | 2019-07-12 | 2019-10-08 | 天津宏顺科生物科技有限公司 | Method for converting fat-soluble natural pigment into water-soluble pigment and protecting fading of water-soluble pigment |
Also Published As
Publication number | Publication date |
---|---|
JPH0622465B2 (en) | 1994-03-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |