JPS60133863A - Production of rapidly solving food product - Google Patents
Production of rapidly solving food productInfo
- Publication number
- JPS60133863A JPS60133863A JP58242093A JP24209383A JPS60133863A JP S60133863 A JPS60133863 A JP S60133863A JP 58242093 A JP58242093 A JP 58242093A JP 24209383 A JP24209383 A JP 24209383A JP S60133863 A JPS60133863 A JP S60133863A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- fatty acid
- ester
- powder
- hydrophobic
- 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
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- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Formation And Processing Of Food Products (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は速溶性食品製剤の製法に関する。詳しく述べる
と本発明ば加水性の食品添加物たとえばアジピン酸、安
息香酸、ソルビン酸、フマール酸のような水に難溶性の
有機酸に対し湿潤性を賦与し、水に速やかに溶解する食
品製剤の製法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a fast-dissolving food formulation. Specifically, the present invention provides a food preparation that imparts wettability to hydrophilic food additives, such as organic acids that are poorly soluble in water, such as adipic acid, benzoic acid, sorbic acid, and fumaric acid, and quickly dissolves in water. Concerning the manufacturing method.
食品添加物には、調味料、酸味料、着香料、保存料、酸
化防止剤など10種余シに分類された化合物が規定され
ておシ、これらの中には疎水性のため水に溶解しにくい
化合物、とくに有機酸が数多く含まれている。たとえば
、アジピン酸、安息香酸、ソルビン酸、デヒドロ酢酸、
フマール酸が挙げられる。これらのうちでもとくにフマ
ール酸は酸性度も高く、その酸味もクエン酸やリンゴ酸
よシかなり強く少量の使用量で有効であシ、かつ比較的
安価である。しかし吸湿性がほとんどないため、取扱い
上は有利であるものの溶解速度が小さくかつ溶解度も比
較的低く、さらに比重も小さいため、水に添加されたと
き、水面に浮上し溶解させるのに長時間を要する欠点を
有する。このため優れた特性を持ちながら敬遠され、他
の高価なりエン酸やリンゴ酸に代替されているのが現状
である。Food additives are defined as compounds classified into more than 10 categories, including seasonings, acidulants, flavoring agents, preservatives, and antioxidants. Some of these are hydrophobic and cannot be dissolved in water. It contains many compounds that are difficult to treat, especially organic acids. For example, adipic acid, benzoic acid, sorbic acid, dehydroacetic acid,
Examples include fumaric acid. Among these, fumaric acid has particularly high acidity, and its sour taste is much stronger than that of citric acid and malic acid, and it is effective when used in small amounts, and is relatively inexpensive. However, since it has almost no hygroscopicity, it is advantageous in terms of handling, but its dissolution rate is low and its solubility is relatively low, and its specific gravity is also small, so when it is added to water, it takes a long time to rise to the surface and dissolve. It has some disadvantages. For this reason, although it has excellent properties, it is now avoided and replaced by other expensive enoic acids and malic acids.
また、安息香酸、ソルビン酸、デヒドロ酢酸なども保存
料として有用であるが、これら酸型の保存料の有効性は
そのpHによシ著しく左右されpH値が低いほど効果が
大きいとされる。したがってこれらが酸の形で用いられ
るのが望ましいが、これらは疎水性であり、やむな(p
H値の高いナトリウム塩やカリウム塩の形で用いられる
ことが多い。Furthermore, benzoic acid, sorbic acid, dehydroacetic acid, and the like are also useful as preservatives, but the effectiveness of these acid-type preservatives is significantly influenced by their pH, and the lower the pH value, the greater the effect. Therefore, it is desirable to use these in acid form, but they are hydrophobic and unavoidable (p
It is often used in the form of sodium and potassium salts, which have a high H value.
こうした疎水性を改善することを目的とした試みはこれ
までにもなされている。たとえば、フマール酸やソルビ
ン酸に蔗糖脂肪酸エステルを担持させた例がある。しか
しこの方法ではそれが水に添加されたとき蔗糖脂肪酸エ
ステルが完全に溶解せず濁った状態となシ、食品に利用
したとき外観を著しく損うという欠点がある。Attempts have been made to improve such hydrophobicity. For example, there are examples in which sucrose fatty acid esters are supported on fumaric acid or sorbic acid. However, this method has the disadvantage that when added to water, the sucrose fatty acid ester does not completely dissolve and becomes cloudy, which significantly impairs the appearance when used in foods.
まだマルトデキストリンを担持せしめたフマール酸顆粒
も知られているが、これは湿潤効力が弱いだめ5重量係
という大量を担持せねばならず、経済性に欠けかつ味覚
を損うといった欠点がある。Fumaric acid granules loaded with maltodextrin are also known, but they have a weak wetting effect and must support a large amount of 5 parts by weight, which is disadvantageous in that they are uneconomical and impair taste.
本発明は、こうした従来技術の欠点を克服し、疎水性の
食品添加物、とくに有機酸に対し、少量の担持量でも速
やかに溶解させかつ水に添加したとき濁シも生じない湿
潤性を賦与しうる、ポリグリセリン脂肪酸エステルを混
合担持せしめることを特徴とするものである。The present invention overcomes these drawbacks of the prior art, and provides wettability to hydrophobic food additives, especially organic acids, that allows them to dissolve quickly even in small amounts and does not cause cloudiness when added to water. It is characterized by supporting a mixture of polyglycerol fatty acid esters.
すなわち、本発明は、以下の如く特定される。That is, the present invention is specified as follows.
(1)疎水性粉末の食品添加物にポリグリセリン脂肪酸
エステルを混合担持させることを特徴とする速溶性食品
製剤の製法。(1) A method for producing a fast-dissolving food preparation, which is characterized in that a hydrophobic powdered food additive is mixed and supported with a polyglycerin fatty acid ester.
(2)食品添加物が有機酸である上記(1)記載の方法
。(2) The method according to (1) above, wherein the food additive is an organic acid.
(3)有機酸がアジピン酸、安息香酸、ソルビン酸、デ
ヒドロ酢酸および7マール酸よりなる群から選ばれた少
なくとも1種である上記(2)記載の方法。(3) The method according to (2) above, wherein the organic acid is at least one selected from the group consisting of adipic acid, benzoic acid, sorbic acid, dehydroacetic acid, and hexamaric acid.
(4)ポリグリセリン脂肪酸エステルは、重合度が3以
上のポリグリセリンとアルキル基の炭素数が5〜17で
ある飽和または不飽和の脂肪酸とのエステルであシ、そ
のHLBが7〜18の範囲にあるものを主要成分として
なる上記(1)、(2)または(3)記載の方法。(4) Polyglycerin fatty acid ester is an ester of polyglycerin with a degree of polymerization of 3 or more and a saturated or unsaturated fatty acid whose alkyl group has 5 to 17 carbon atoms, and its HLB is in the range of 7 to 18. The method according to (1), (2) or (3) above, wherein the main component is one of the following.
(5)ポリグリセリン脂肪酸エステルの担持量が疎水性
粉末に対しo、oos〜2重量−の範囲であることを特
徴とする上記(1)、(2)、(3)または(4)記載
の方法。(5) The method according to (1), (2), (3) or (4) above, characterized in that the amount of polyglycerin fatty acid ester supported is in the range of o, oos to 2 weight - based on the hydrophobic powder. Method.
(6)疎水性粉末の粒度が20メツシユ以下である上記
(1)、(2)、(3)、(4)または(5)記載の方
法。(6) The method according to (1), (2), (3), (4) or (5) above, wherein the hydrophobic powder has a particle size of 20 mesh or less.
本発明で用いられる疎水性食品添加物、とくに有機酸は
上述したものが挙げられるが、これらはその使用の場合
を考慮して粉末の形で上記湿潤剤と混合担持処理される
。とくに溶解処理を経ず、粒状を維持したまま湿潤剤で
の処理を受ける場合、粉末の粒径は20メツシユ以下に
粉砕されている必要がある。The hydrophobic food additives used in the present invention, particularly the organic acids, include those mentioned above, but these are mixed and supported in powder form with the above-mentioned wetting agent in consideration of the use case. In particular, when the powder is treated with a wetting agent while maintaining its granular form without undergoing dissolution treatment, the particle size of the powder must be pulverized to 20 mesh or less.
ポリグリセリン脂肪酸エステルは、上述した如きエステ
ルを主要成分とするものが使用され、具体的には、テト
ラグリセリンモノラウレート、ヘキサグリセリンモノオ
レート、へキサグリセリンモノラウレート、デカグリセ
リンモノオレート、デカグリセリンモノステアレート、
デカグリセリンモノラウレートなどである。The polyglycerin fatty acid ester used is one containing the above-mentioned ester as a main component, and specifically, tetraglycerin monolaurate, hexaglycerin monooleate, hexaglycerin monolaurate, decaglycerin monooleate, decaglycerin monostearate,
These include decaglycerin monolaurate.
担持量は上記疎水性粉末に対し0.005〜2重量−の
範囲で適宜選ばれ、とくに001〜1重量%が好ましい
結果を与える。少なすぎると均一な混合担持が困難であ
り、水面に浮上する恐れが生ずる。逆に多過ぎると経済
性はもとよシ風味にも影響が出てくる恐れがある。担持
法としてはポリグリセリン脂肪酸エステルが疎水性粉末
の粒子表面を被覆処理しうる方法であればあらゆる方法
が採用される。好適な例としては浸漬法があげられる。The supported amount is appropriately selected within the range of 0.005 to 2% by weight based on the hydrophobic powder, and particularly preferably 0.001 to 1% by weight gives preferable results. If it is too small, it will be difficult to mix and support the particles uniformly, and there is a risk that they will float to the surface of the water. On the other hand, if there is too much, it may affect not only the economy but also the flavor. As the supporting method, any method that can coat the surface of the particles of the hydrophobic powder with polyglycerin fatty acid ester can be employed. A suitable example is a dipping method.
その場合、水、エタノールなど該エステルに変質をきた
さない溶媒中に該エステルを溶解して浸漬液とする。こ
れに疎水性粉末を浸漬し沢過乾燥する。まだこの浸漬液
を該粉末に噴霧して粒子表面に均一に混合し担持せしめ
る方法も採用され、さらに浸漬液と粉末とを混合して、
そのまま濃縮加熱乾燥せしめる方法も採用される。In that case, the ester is dissolved in a solvent such as water or ethanol that does not cause deterioration of the ester to prepare an immersion liquid. Hydrophobic powder is immersed in this and thoroughly dried. A method is also adopted in which this immersion liquid is sprayed onto the powder to be uniformly mixed and supported on the particle surface, and the immersion liquid and powder are further mixed,
A method of directly concentrating and heating and drying is also adopted.
浸漬液には上記ポリグリセリン脂肪酸エステルのほか他
の添加剤、たとえばトリポIJ IJン酸ナトリウムな
どが少量添加されていてもよい。In addition to the polyglycerol fatty acid ester described above, other additives such as sodium tripo-IJ phosphate may be added in small amounts to the immersion liquid.
乾燥条件は、常温〜150℃、好ましくは50〜120
℃が適当である。Drying conditions are room temperature to 150°C, preferably 50 to 120°C.
°C is appropriate.
上記担持方法は、いずれも疎水性粉末の溶解をほとんど
行なわず、添加された粒径をほとんど変えない捷ま被覆
処理された顆粒とすることのできるものであるが、溶解
部分が無視しえない場合には、上記方法のうち噴霧方法
または濃縮方法の採用が好ましくなる。In any of the above supporting methods, the hydrophobic powder is hardly dissolved, and it is possible to form granules that are coated by rolling and hardly changing the particle size of the added particles, but the dissolved portion is not negligible. In this case, it is preferable to use the spray method or the concentration method among the above methods.
かくしてえられる速溶性食品製剤、とくに有機酸類を主
要成分とするものは、溶解性が犬l〕に改善され、しか
もpH値を低くすることができ、酸味についても保存性
についても比較的少量の使用で所望の目的を達すること
を可能にする。The fast-dissolving food preparations obtained in this way, especially those containing organic acids as the main ingredients, have improved solubility to 100%, can lower the pH value, and have a relatively small amount of acidity and storage stability. Enables its use to reach the desired purpose.
以下、本発明を実施例および比較例にてさらに具体的に
説明する。なお、本発明で性能評価の基準となる溶解性
試験は以下の如くである。Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. In addition, the solubility test that serves as a standard for performance evaluation in the present invention is as follows.
300m1のビーカーに20°Cの水300m1を入れ
スタラーにて25 Orpmで撹拌している中に、試料
o、 s o yを添加する。添加時の水面浮」ニ状態
を観察し、粉末が浮上していないもの◎、わずかに浮上
しているもの○、かなり浮上しているもの△、はとんど
全部浮上しているもの×と認定する。また水中に沈降し
た粒子が完全に溶解するまでの時間も測定した。5分経
過しても水面または水中に不溶分が残っている場合、G
4ガラスフィルターで沢過し70℃で24時間乾燥して
残存重量とした。Samples o and so y are added to a 300 ml beaker filled with 300 ml of water at 20°C and stirred at 25 Orpm using a stirrer. Observe the state of the powder floating on the water surface when adding it, and find that the powder is not floating ◎, the powder is slightly floating ○, the powder is floating a lot △, and almost all of it is floating × Certify. The time taken for the particles that had settled in the water to completely dissolve was also measured. If insoluble matter remains on the water surface or in the water after 5 minutes,
The residue was filtered through a 4-glass filter and dried at 70°C for 24 hours to calculate the residual weight.
実施例1
200メツシユで篩ったフマール酸粉末10.01をデ
カグリセリンモノラウレートの5重量%水溶液50m1
!に室温下10分間撹拌浸漬した。Example 1 10.0ml of fumaric acid powder sieved through 200 mesh was added to 50ml of 5% by weight aqueous solution of decaglycerol monolaurate.
! The sample was stirred and immersed for 10 minutes at room temperature.
このスラリーを03ガラスフイルターでf過し9.61
のケーキをえた。これを70℃で一晩乾燥し9.21の
粉末をえた。これを60メツシユで篩い製品とした。デ
カグリセリンモノラウレートの担持量は高速液体クロマ
ドグ2フイを用いて測定したところ、0.22重量%で
あった。This slurry was passed through a 03 glass filter and 9.61
I got a cake. This was dried at 70°C overnight to obtain a powder of 9.21. This was made into a sieved product with 60 mesh. The amount of decaglycerol monolaurate supported was 0.22% by weight as measured using a high performance liquid chroma dog 2 filter.
溶解性試験の結果を表1に示す。The results of the solubility test are shown in Table 1.
実施例2
テトラグリセリンモノラウレートの1重量%水溶液50
dを用いるほかは実施例1におけると同様に行々い、ケ
ーキ10.1 ? 、乾燥粉末9,7Vをえ、あとは実
施例1におけると同様に行ない表1に示す結果をえた。Example 2 1% by weight aqueous solution of tetraglycerol monolaurate 50
Proceed as in Example 1 except for using d, and prepare cake 10.1? , dry powder 9.7V was obtained, and the rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
実施例3 ′
デカグリセリンモノステアレートの5重量%水溶液50
m1を用いるほかは実施例1におけると同様に行ない、
ケーキ11.:IM、乾燥粉末9.42をえた。あとは
実施例1におけると同様に行ない表1に示す結果をえた
。Example 3' 5% by weight aqueous solution of decaglycerol monostearate 50
The same procedure as in Example 1 was carried out except for using m1,
Cake 11. :IM, dry powder yield 9.42. The rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
比較例1
グリセリンモノオレートの11重量%エタノール溶液s
omeを用いるほかは実施例1におけると同様に行ない
ケーキ10.25’、乾燥粉末901をえた。あとは実
施例1におけると同様に行ない表1に示す結果をえた。Comparative Example 1 11% by weight ethanol solution of glycerin monooleate
A cake 10.25' and a dry powder 901 were obtained in the same manner as in Example 1 except that ome was used. The rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
比較例2
グリセリンモノステアレートの4重量%エタノール溶液
someを用いるほかは実施例1におけると同様に行な
いケーキ9.8f、乾燥粉末8.07をえた。あとは実
施例1におけると同様に行ない表1に示す結果をえた。Comparative Example 2 The same procedure as in Example 1 was carried out except that some 4% by weight ethanol solution of glycerin monostearate was used, yielding 9.8 f of cake and 8.07 g of dry powder. The rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
比較例3
蔗糖脂肪酸エステルとして第−工業製薬製のDKエステ
ルF−160(商品名)の4重量%イソプロピルアルコ
ール溶液50m1を用いるほかは実施例1におけると同
様に行ないケーキ10.0?、乾燥粉末8.49をえた
。あとは実施例1におけると同様に行ない表1に示した
結果をえた。Comparative Example 3 The same procedure as in Example 1 was conducted except that 50 ml of a 4% by weight isopropyl alcohol solution of DK Ester F-160 (trade name) manufactured by Dai-Kogyo Seiyaku Co., Ltd. was used as the sucrose fatty acid ester, and a cake of 10.0% was prepared. , 8.49% of dry powder was obtained. The rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
実施例4
48メツシユで篩ったアジピン酸粉末10.Ofをデカ
グリセリンモノラウレートの5重量%水溶液50m1に
室温下3分間撹拌浸漬した。このスラリーを03ガラス
フイルターでf過し、8.82のケーキをえた。Example 4 Adipic acid powder sieved through 48 mesh 10. Of was immersed in 50 ml of a 5% by weight aqueous solution of decaglycerol monolaurate under stirring for 3 minutes at room temperature. This slurry was passed through a 03 glass filter to yield a cake of 8.82 mm.
これを70℃で一晩乾燥し8.52の粉末をえた。これ
を48メツシユで篩い製品とした。あとは実施例1にお
けると同様に行ない表1に示す結果をえた。This was dried at 70° C. overnight to obtain a powder of 8.52. This was made into a product by sieving with 48 mesh. The rest was carried out in the same manner as in Example 1, and the results shown in Table 1 were obtained.
比較例4
48メツシユで篩ったアジピン酸粉末をそのまま試料と
して用い、表1に示す結果をえた。Comparative Example 4 Adipic acid powder sieved through a 48-mesh sieve was used as a sample as it was, and the results shown in Table 1 were obtained.
実施例5 48メツシユで篩った安息香酸粉末を用い。Example 5 Use benzoic acid powder sieved through 48 mesh.
あとは実施例4におけると同様に行ない、ケーキ10.
1 ?、乾燥粉末9.42をえた。あとは実施例4にお
けると同様に行ない表1に示す結果をえた。The rest is carried out in the same manner as in Example 4, and cake 10.
1? , 9.42% of dry powder was obtained. The rest was carried out in the same manner as in Example 4, and the results shown in Table 1 were obtained.
比較例5
48メツシユで篩った安息香酸粉末をそのまま試料とし
て用い、表1に示す結果をえた。Comparative Example 5 Benzoic acid powder sieved through a 48-mesh sieve was used as a sample as it was, and the results shown in Table 1 were obtained.
Claims (6)
エステルを混合担持させることを特徴とする速溶性食品
製剤の製法。(1) A method for producing a fast-dissolving food preparation, which is characterized in that a hydrophobic powdered food additive is mixed and supported with a polyglycerin fatty acid ester.
記載の方法。(2) Claim (1) in which the food additive is an organic acid
Method described.
ヒドロ酢酸およびフマール酸よりたる群から選ばれた少
なくとも1種である特許請求の範囲(2)記載の方法。(3) The method according to claim (2), wherein the organic acid is at least one selected from the group consisting of adipic acid, benzoic acid, sorbic acid, dehydroacetic acid, and fumaric acid.
上のポリグリセリンとアルキル基の炭素数が5〜17で
ある飽和または不飽和の脂肪酸とのエステルであシ、そ
のHLBが7〜18の範囲にあるものを主要成分として
なる特許請求の範囲(1)、(2)まだは(3)記載の
方法。(4) Polyglycerin fatty acid ester is an ester of polyglycerin with a degree of polymerization of 3 or more and a saturated or unsaturated fatty acid whose alkyl group has 5 to 17 carbon atoms, and its HLB is in the range of 7 to 18. The method according to claim (1), (2) or (3), which comprises as a main component one or more of the following.
粉末に対し0.005〜2重量−の範囲であることを特
徴とする特許請求の範囲(1) 、 +2)、(3)ま
だは(4)記載の方法。(5) Claims (1), +2), (3) and (4) characterized in that the amount of polyglycerin fatty acid ester supported is in the range of 0.005 to 2 weight - based on the hydrophobic powder. ) method described.
請求の範囲(1)、(2)、(3)、(4)または(5
)記載の方法。(6) Claims (1), (2), (3), (4) or (5) in which the particle size of the hydrophobic powder is 20 mesh or less.
) method described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58242093A JPS60133863A (en) | 1983-12-23 | 1983-12-23 | Production of rapidly solving food product |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58242093A JPS60133863A (en) | 1983-12-23 | 1983-12-23 | Production of rapidly solving food product |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60133863A true JPS60133863A (en) | 1985-07-17 |
JPS6219146B2 JPS6219146B2 (en) | 1987-04-27 |
Family
ID=17084189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58242093A Granted JPS60133863A (en) | 1983-12-23 | 1983-12-23 | Production of rapidly solving food product |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60133863A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61216671A (en) * | 1985-03-23 | 1986-09-26 | Kyokuto Shibousan Kk | Adipic acid composition |
JPS6279763A (en) * | 1985-08-03 | 1987-04-13 | Kiyokutoo Internatl:Kk | Adipic acid composition |
JPS6356261A (en) * | 1986-08-25 | 1988-03-10 | Kiyokutoo Internatl:Kk | Preparation of raw bread crumb |
JPH01120267A (en) * | 1987-11-05 | 1989-05-12 | Saraya Kk | Germicidal and detergent composition for food |
GB2358971A (en) * | 2000-02-01 | 2001-08-08 | Strix Ltd | Control of a liquid heating apparatus |
WO2018003965A1 (en) * | 2016-07-01 | 2018-01-04 | 株式会社林原 | Method for producing fumaric acid powder formulation |
-
1983
- 1983-12-23 JP JP58242093A patent/JPS60133863A/en active Granted
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61216671A (en) * | 1985-03-23 | 1986-09-26 | Kyokuto Shibousan Kk | Adipic acid composition |
JPH0563148B2 (en) * | 1985-03-23 | 1993-09-09 | Kyokuto Int | |
JPS6279763A (en) * | 1985-08-03 | 1987-04-13 | Kiyokutoo Internatl:Kk | Adipic acid composition |
JPS6356261A (en) * | 1986-08-25 | 1988-03-10 | Kiyokutoo Internatl:Kk | Preparation of raw bread crumb |
JPH01120267A (en) * | 1987-11-05 | 1989-05-12 | Saraya Kk | Germicidal and detergent composition for food |
JPH0585600B2 (en) * | 1987-11-05 | 1993-12-08 | Saraya Kk | |
GB2358971A (en) * | 2000-02-01 | 2001-08-08 | Strix Ltd | Control of a liquid heating apparatus |
WO2018003965A1 (en) * | 2016-07-01 | 2018-01-04 | 株式会社林原 | Method for producing fumaric acid powder formulation |
Also Published As
Publication number | Publication date |
---|---|
JPS6219146B2 (en) | 1987-04-27 |
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