JPS5951256B2 - Sweetening method - Google Patents

Sweetening method

Info

Publication number
JPS5951256B2
JPS5951256B2 JP51034810A JP3481076A JPS5951256B2 JP S5951256 B2 JPS5951256 B2 JP S5951256B2 JP 51034810 A JP51034810 A JP 51034810A JP 3481076 A JP3481076 A JP 3481076A JP S5951256 B2 JPS5951256 B2 JP S5951256B2
Authority
JP
Japan
Prior art keywords
stevioside
taste
sweetness
sweetening
sweet
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.)
Expired
Application number
JP51034810A
Other languages
Japanese (ja)
Other versions
JPS52117474A (en
Inventor
悦雄 守田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Morita Kagaku Kogyo Co Ltd
Original Assignee
Morita Kagaku Kogyo Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Morita Kagaku Kogyo Co Ltd filed Critical Morita Kagaku Kogyo Co Ltd
Priority to JP51034810A priority Critical patent/JPS5951256B2/en
Publication of JPS52117474A publication Critical patent/JPS52117474A/en
Publication of JPS5951256B2 publication Critical patent/JPS5951256B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は、食品、医薬品、医薬部外品の製造に際して、
ステビオサイド100部に対してジテルペン骨格でグル
コース4分子を有し、分子式C44H7oO23、分子
量966で表わされる配糖体甘味物質A3を70部(重
量比)以上共存させた甘味組成物を使用することにより
甘味を付与することを特徴とする甘味付与法に関するも
のである。
[Detailed Description of the Invention] The present invention provides for the production of foods, drugs, and quasi-drugs.
By using a sweetening composition in which 70 parts (weight ratio) or more of a glycoside sweet substance A3 having a diterpene skeleton and having 4 molecules of glucose and having a molecular formula of C44H7oO23 and a molecular weight of 966 coexists with respect to 100 parts of stevioside, sweetness can be obtained. The present invention relates to a method for imparting sweetness characterized by imparting.

サッカリンナトリウム、サッカリンナトリウム等の合成
甘味料の安全性が論議され、法的に規制されるに従い、
天然甘味料による甘味付与法が益々活発化している。
As the safety of synthetic sweeteners such as saccharin sodium and sodium saccharin is being debated and legally regulated,
Sweetening methods using natural sweeteners are becoming increasingly popular.

特に、甘味付与に主として使用される蔗糖、ブドウ糖等
は、良質の甘味と糖度を得る為に最も適したものである
が、その使用の増加は、糖害が社会問題となっている命
取また資源問題が論しられている時だけに、歓迎すべき
ものではない。
In particular, sucrose, glucose, etc., which are mainly used for sweetening, are the most suitable for obtaining high-quality sweetness and sugar content, but their increased use is due to the fact that sugar damage has become a social problem and has become a life-threatening and This is not something that should be welcomed only when resource issues are being discussed.

昨今では、ステビア・レバウディアナ・ボルトニー(S
tevia Rebaudiana Bertoni)
(7)抽出濃縮エキス液若しくはその粉末が使用され
始めたが、香り、色調、不純物起因のニゴリ、オリ、不
快味が呈される為、むしろ上記エキス液から採取したス
テビオサイドが使用される傾向にある。
Nowadays, Stevia rebaudiana bortonii (S
tevia Rebaudiana Bertoni)
(7) Concentrated extract liquid or its powder has begun to be used, but because of its aroma, color tone, and unpleasant taste due to impurities, there is a tendency to use stevioside extracted from the above liquid extract instead. be.

しかし、ステビオサイドによる甘味付与法は、ステビオ
サイドが水に対して難溶性であり、甘味ノ度及び合成甘
味料サッカリンの様な苦味、嫌味等の不快味を有するこ
とと、甘味が後味に尾を引く呈味質上の欠点を有してい
ることから、自ずから限度があり、食品、医薬品、医薬
部外品の甘味付与に使用する、蔗糖、麦芽糖、異性化糖
、ブドウi糖、果糖、及びソルビット、マルチット、マ
ンニット、キシリット等の糖質甘味料の代替物としては
余り期待することが出来ない。
However, the sweetening method using stevioside is difficult because stevioside is poorly soluble in water, has a high degree of sweetness, and has an unpleasant taste such as bitterness and sarcastic taste similar to the synthetic sweetener saccharin, and the sweetness leaves a trailing aftertaste. Sucrose, maltose, isomerized sugar, glucose, fructose, and sorbitol are used to sweeten foods, medicines, and quasi-drugs because of their flaws in taste quality. It cannot be expected to serve as a substitute for carbohydrate sweeteners such as malt, mannitol, xylit, etc.

本発明者は、この実情に鑑み、蔗糖の味に近似し、溶解
性及び呈味質の問題が呈されることな1 く、十分なる
甘味を付与する方法について鋭意研究した結果、ステビ
オサイドに対して、ジテルペン骨格でグルコース4分子
を有し、分子式C44H7oO23、分子量966で表
わされる、ステビア・レバウディアナ・ボルトニーに含
まれる配糖体せ1味物質A3(レバウテ゛イオサイドA
とも呼ばれる。
In view of this fact, the inventor of the present invention has conducted intensive research on a method of imparting a sufficient sweetness that approximates the taste of sucrose without causing problems in solubility and taste quality, and has found that stevioside It has a diterpene skeleton, has 4 molecules of glucose, has a molecular formula of C44H7oO23, and has a molecular weight of 966.The glycoside contained in Stevia rebaudiana bortonii is a taste substance A3 (rebautioside A3).
Also called.

以下甘味物質A3と略す。)をステビオサイドに対して
一定の割合以上で共存させ、食品、医薬品、医薬部外品
の製造に際して添加、使用することにより、溶解性及び
呈味質の問題を呈することノがなく、蔗糖の味に極めて
近似した満足な甘味を経済的に付与出来ることを知見し
、本発明を完成したのである。
Hereinafter, it will be abbreviated as sweet substance A3. ) can coexist with stevioside in a certain proportion or more, and by adding and using it in the production of foods, medicines, and quasi-drugs, there will be no problems with solubility or taste quality, and the taste of sucrose can be improved. They discovered that it is possible to economically impart a satisfying sweetness that is extremely similar to that of sucrose, and have completed the present invention.

本発明に於てステビオサイドに対して一定の割合以上に
共存させ使用する甘味物質A3は、蔗糖テの300倍程
倍程甘味度を有するステビオサイドよりもさらに甘味度
が強く、蔗糖の450倍程鹿の強い甘味度を有し、且つ
水に易溶性の、苦味、嫌味等の不快味のない甘味質を有
する甘味物質で夕る。
In the present invention, the sweet substance A3 used in coexistence with stevioside at a certain ratio or more has a sweetness that is even stronger than stevioside, which is about 300 times sweeter than sucrose, and about 450 times sweeter than sucrose. It is a sweet substance that has a strong degree of sweetness, is easily soluble in water, and has sweet qualities without unpleasant tastes such as bitterness and sarcastic taste.

本発明は、この甘味度の強い甘味物質A3をステビオサ
イドに単に共存させ、これを甘味付与に使用するもので
はなく、ステビオサイド100部に対して甘味物質A3
を70部(重量比)以上の割合で共存させることにより
、ステビオサイド及び士味物質A3の単独甘味物質では
得られない、蔗稈の味に近似した強い甘味度が得られ、
良質の甘味を経済的に付与することが出来るのである。
The present invention does not simply make the sweet substance A3 with a strong sweetness coexist with stevioside and use it for imparting sweetness, but rather
By coexisting in a ratio of 70 parts (weight ratio) or more, a strong sweetness similar to the taste of cane culm, which cannot be obtained with the individual sweetening substances of stevioside and Shimi substance A3, can be obtained.
It is possible to provide high-quality sweetness economically.

即ち、ステビオサイド100部に対して甘味物質A3を
70部(重量比)以上共存させ、甘味物質A3の共存比
を増加させるに従い、より一層易溶性の著しく蔗糖の味
に近似した甘味となり、甘味源として満足な甘味を付与
することが出来るが、ステビオサイド100部に対して
甘味物質A3を70部以下にし、甘味物質A3の共存比
を減少させるに従い蔗糖の味に近似したものではなくな
り、良質の甘味及び満足なる甘味付与効果に欠けるもの
となる。
That is, as the coexistence ratio of sweet substance A3 is 70 parts or more (weight ratio) to 100 parts of stevioside, and the coexistence ratio of sweet substance A3 is increased, the sweetness becomes even more easily soluble and extremely similar in taste to sucrose, and the sweetness source However, as the sweetening substance A3 is reduced to 70 parts or less per 100 parts of stevioside, and the coexistence ratio of sweetening substance A3 is reduced, the taste no longer resembles that of sucrose, resulting in a high-quality sweetness. and lacks a satisfactory sweetening effect.

本発明の甘味付与法を採用することによって、蔗糖、ブ
ドウ糖、果糖等による従来の甘味付与法、また、ステビ
オサイド及び甘味物質A3の単独による甘味付与法に比
較して、天然物甘味成分間の相乗効果による従来では得
られないすぐれた甘味付与効果が得られる。
By adopting the sweetening method of the present invention, compared to conventional sweetening methods using sucrose, glucose, fructose, etc., or sweetening methods using stevioside and sweet substance A3 alone, the synergy between natural sweetening components can be improved. As a result, an excellent sweetening effect that cannot be obtained conventionally can be obtained.

したがって、本発明の甘味付与法は、ダイエツト食品、
漬物、佃煮、醤油、味噌、海藻加工品、煮豆、マヨネー
ズ、ケチャツプ、スープの素、だれの素、だしの素、魚
肉練り製品、魚介加工品、酢、清涼飲料水、ソース、乳
飲料、醗酵孔、乳酸飲料、氷菓、アイスクリーム、あん
、ジャム、菓子、菓子パン、洋菓子及びクリーム、かん
詰、ビン詰等の一般食品及び調味料、天然甘味料により
甘味を付与する必要がる医薬品、医薬部外品の製造に際
して使用することか゛出来る。
Therefore, the sweetening method of the present invention can be applied to diet foods,
Pickles, tsukudani, soy sauce, miso, processed seaweed products, boiled beans, mayonnaise, ketchup, soup base, sauce base, dashi base, fish paste products, processed seafood products, vinegar, soft drinks, sauces, milk drinks, fermentation holes , lactic acid drinks, frozen confectionery, ice cream, bean paste, jam, confectionery, sweet bread, Western confectionery and cream, canned goods, bottled food and seasonings, medicines that need to be sweetened with natural sweeteners, and non-medicinal products. It can be used in the manufacture of products.

尚、本発明の甘味付与に際して、蔗糖、ブ才つ糖、果糖
、麦芽糖、乳糖、水あめ、ソルビット、マルチツ1〜、
マンニット、キシリソ1一等の天然甘味料、または必要
に応じてステビオールバイオサイド(分子式C3゜H5
oO13、分子量642)、レバウディオサイドC(分
子式C44H7oO22、分子量950)、ス゛ルコサ
イドA(分子式C38H6oO17、分子量788)、
レバウディオサイドE (分子式C44H680゜3、
分子量964)、レバウテ゛イオサイドD(分子式C3
oH8oO38、分子量1128)等の配糖体甘味物質
を併用することも出来、更にはサツカリンナI・リウム
、サイクラミン酸すトリウム、アスパラチル フェニル
アラニン メチルエステル、グリチルリチン酸及びその
塩類等をも併用することが出来る。
In addition, when imparting sweetness according to the present invention, sucrose, butyl sugar, fructose, maltose, lactose, starch syrup, sorbitol, maltose 1 to 1,
Natural sweeteners such as mannitol, xyliso 1, or steviol biocide (molecular formula C3゜H5
oO13, molecular weight 642), Rebaudioside C (molecular formula C44H7oO22, molecular weight 950), Sulcoside A (molecular formula C38H6oO17, molecular weight 788),
Rebaudioside E (molecular formula C44H680°3,
molecular weight 964), rebate ioside D (molecular formula C3
Glycoside sweet substances such as oH8oO38, molecular weight 1128) can be used in combination, and further, saccharinna I.lium, sodium cyclamate, asparatyl phenylalanine methyl ester, glycyrrhizic acid and its salts, etc. can also be used in combination.

本発明の甘味付与法に於て、ステビア・レバウテ゛イア
ナ・ボルトニー (Stevia Rebaudian
aBertoni)に含有されるステビオサイド及び甘
味物質A3を本発明に示す一定の割合以上に共存させる
様に抽出精製した抽出物を使用する場合、その抽出精製
物中に他の成分が共存しても、上記一定の割合以上に共
存させているものであれば、本発明の効果を妨げるもの
でない為、本発明の目的が達成することが出来る。
In the sweetening method of the present invention, Stevia Rebaudian
When using an extract that has been extracted and purified so that stevioside and sweet substance A3 contained in A. aBertoni coexist at a certain ratio or more shown in the present invention, even if other components coexist in the extracted and purified product, As long as they are allowed to coexist in amounts above the above-mentioned certain proportion, they will not impede the effects of the present invention, and therefore the purpose of the present invention can be achieved.

以下本発明の効果を実施例により説明する。The effects of the present invention will be explained below using examples.

実施例 1 クエン酸340g、リンゴ酸100g、黄色5号色素4
g、115濃縮用かんきつ混合果汁3.6リツ1ヘル、
オレンジベース200m1、オレンジフレーバー100
m1、合成保存料 法的規制量、 ステビオサイド10
0部に対して甘味物質A370部(重量比)を共存させ
た甘味組成物66gを使用し、常法により清涼飲料水1
80リツトルを製造した。
Example 1 340 g of citric acid, 100 g of malic acid, Yellow No. 5 dye 4
g, 115 citrus mixed fruit juice for concentration 3.6 liters 1 health,
Orange base 200ml, orange flavor 100
m1, synthetic preservative legally regulated amount, stevioside 10
Using 66 g of a sweet composition containing 370 parts (weight ratio) of sweet substance A to 0 parts, 1 part of a soft drink was prepared by a conventional method.
80 liters were produced.

実施例 2 クエン酸340g、リンゴ酸100g、黄色5号色素4
g、115濃縮用かんきつ混合果汁3.6リツトル、オ
レンジベース200m1、オレンジフレーバー100m
1、合成保存料 法的規制量、ステビオサイド100部
に対して甘味物質A3150部(重量比)を共存させた
甘味組成物61gを使用し、常法により清涼飲料水18
0リツトルを製造した。
Example 2 340 g of citric acid, 100 g of malic acid, Yellow No. 5 dye 4
g, 115 citrus mixed fruit juice for concentration 3.6 liters, orange base 200ml, orange flavor 100ml
1. Synthetic preservatives Using 61 g of a sweetening composition in which 100 parts of stevioside coexists with 3150 parts of sweet substance A (weight ratio), the legally regulated amount is used to prepare a soft drink by a conventional method.
0 liters were produced.

比較例として、本発明甘味組成物の代りにステビオサイ
ド80gを使用した清涼飲料水(比較例1)、及びステ
ビオサイド100部に対して甘味物質A360部(重量
比)を共存させた甘味組成vlJ67gを使用した清涼
飲料水(比較例2)を同様に、製造した。
As a comparative example, a soft drink using 80 g of stevioside instead of the sweet composition of the present invention (Comparative Example 1) and a sweet composition vlJ 67 g in which 360 parts (weight ratio) of sweet substance A coexisted with 100 parts of stevioside were used. A soft drink (Comparative Example 2) was produced in the same manner.

上で得られた、アミノ酸を使用せずに、甘味付与効果を
端的に考察することが出来る清涼飲料水を対象として1
3名のパネルにより、嗜好呈味テストを行った結果、表
の通りであった。
1 for soft drinks, where the sweetening effect obtained above can be directly examined without using amino acids.
A taste preference test was conducted by a panel of three people, and the results were as shown in the table.

本発明により甘味が付与された清涼飲料水は、比較例よ
りも優れていることが認められた。
The soft drink sweetened according to the invention was found to be superior to the comparative example.

更に甘味物質A3の共存比を増大させた甘味組成物が、
より効果があることも認められた。
Furthermore, a sweet composition in which the coexistence ratio of sweet substance A3 is increased,
It was also found to be more effective.

実施例 3 常法により得られた中漬奈良漬原料15kgに対して、
みりん粕2に500g、酒粕10kg、砂糖1kg、水
あめ500g、3%アルコール300cc、コハク酸す
トリウム4g、天然アミノ酸調味料30g、ステビオサ
イド30%及び甘味物質A323%を含有するステビア
・レバウディアナ・ボルトニーの抽出精製甘味組成物7
1g、ソルビン酸カリウム 法的規定量を用いて常法に
より奈良漬を製造した。
Example 3 For 15 kg of Nakazuke Narazuke raw materials obtained by a conventional method,
Extraction of Stevia rebaudiana bortonii containing 500g of mirin lees 2, 10kg of sake lees, 1kg of sugar, 500g of starch syrup, 300cc of 3% alcohol, 4g of succinate, 30g of natural amino acid seasoning, 30% stevioside and 323% sweet substance A. Purified sweet composition 7
Narazuke was produced by a conventional method using 1 g of potassium sorbate in the legally prescribed amount.

比較例として、抽出精製甘味組成物71gの代りにステ
ビオサイド45gを使用し、同様に、奈良漬を製造した
As a comparative example, Narazuke was produced in the same manner using 45 g of stevioside instead of 71 g of the extracted and purified sweet composition.

この両奈良漬製品をパネルにより嗜好呈味テストした結
果、本発明実施奈良漬製品が甘味的にも甘く、比較品よ
りも甘味が原料に浸透し、呈味質に優れていたのに比べ
、比較品は甘味的にも劣り、甘味が原料に浸透したもの
ではなく、不快な甘味が残味に感じられることが認めら
れた。
As a result of a panel taste test of both Narazuke products, it was found that the Narazuke product of the present invention had a sweeter taste, and the sweetness penetrated into the ingredients more than the comparative product, and the taste quality was superior. The comparative product was also inferior in sweetness, and it was observed that the sweetness did not penetrate into the raw material, and an unpleasant sweetness was felt as a residual taste.

実施例 4 生揚66.6リツトル、アミノ酸濃口60.8リツトル
、食塩5に300g、天然調味料350g、コハク酸ナ
トリウム30g、ステビオサイド20%及び甘味物質A
370%を含有するステビア・レバウテ゛イアナ・ボル
トニーの抽出精製甘味組成物27gからなる調味剤を水
で薄めて180リツトルとして、アミノ酸混合醤油を製
造した。
Example 4 66.6 liters of fresh fried rice, 60.8 liters of concentrated amino acids, 300 g of salt 5, 350 g of natural seasoning, 30 g of sodium succinate, 20% stevioside, and sweet substance A
An amino acid mixed soy sauce was prepared by diluting a seasoning consisting of 27 g of an extracted and purified sweet composition of Stevia reboutiana bortonii containing 370% with water to make 180 liters.

比較例として、抽出精製甘味組成物の代りにステビオサ
イド20gとグリチルリチン20gを使用し、同様に、
アミノ酸混合醤油を製造した。
As a comparative example, 20 g of stevioside and 20 g of glycyrrhizin were used instead of the extracted and purified sweet composition, and similarly,
Amino acid mixed soy sauce was produced.

この両醤油を10倍希釈して、パネルにより嗜好呈味テ
スl−した結果、本発明実施醤油は苦味、嫌味の不快味
を感じなかったのに比べ、比較例は苦味、嫌味等の不快
味を感じられ、後味にも感じられた。
Both soy sauces were diluted 10 times and subjected to a taste test using a panel. As a result, the soy sauce of the present invention had no unpleasant taste such as bitterness or sarcastic taste, whereas the comparative example had no unpleasant taste such as bitterness or sarcastic taste. I could feel it, and I could also feel it in the aftertaste.

これは使用したステビオサイドとグリチルリチンの苦味
等が相乗的に呈されたためであると考えられる。
This is thought to be due to the synergistic bitterness of the stevioside and glycyrrhizin used.

また、本発明実施醤油は製造に際して発泡性、保泡性が
なくビン詰作業も容易であったのに比べ、比較例の製造
に際しては発泡性、保泡性が強くビン詰作業に障害とな
り、時間を要した。
In addition, the soy sauce of the present invention had no foaming or foam-retaining properties during production and was easy to bottle, whereas the comparative example had strong foaming and foam-retaining properties that hindered the bottling process. It took time.

実施例 5 複合ビタミン錠剤 1銑中ビタミンA
500OUSP単位ビタミン
D 100OUSP単位ビタミ
ンC(アスコルビン酸) 60mgビタ
ミンB11mg ビタミンB21.5mg ビタミンB60.5mg ビタミンB1゜ 1m
gパン1〜テン酸カルシウム 3m
gニコチン酸アミド 10m
g甘味組成物(ステビオサイド0.29mg 甘味物
質A30.21mg)
0.5mgオオレンシフレ−バー
7mgマンニトール 234.
8mgアカシア粉末 6.
5mgステアリン酸マグネシウム 6.
5mgタルク 7
mg上記の処方にて、ビタミンA、D、C及びステアリ
ン酸マグネシウムを除いたビタミン類を混合した甘味組
成物2.5gを精製水300m1に溶かした。
Example 5 Multivitamin tablet 1 Vitamin A in pig iron
500 OUSP units Vitamin D 100 OUSP units Vitamin C (ascorbic acid) 60 mg Vitamin B 11 mg Vitamin B 21.5 mg Vitamin B 60.5 mg Vitamin B1° 1m
g bread 1~calcium thenate 3m
gNicotinic acid amide 10m
g Sweet composition (stevioside 0.29 mg, sweet substance A 30.21 mg)
0.5mg oranges flavor
7mg mannitol 234.
8mg acacia powder 6.
5mg magnesium stearate 6.
5mg talc 7
2.5 g of a sweet composition prepared by mixing vitamins except vitamins A, D, C and magnesium stearate according to the above formulation was dissolved in 300 ml of purified water.

この溶液と上記5倍量の処方の粉末成分を配合して顆粒
を作った。
Granules were prepared by blending this solution with the powder components of the above-mentioned formula in an amount five times the amount.

これを40℃にて乾燥し、8メツシユで振るった。This was dried at 40°C and shaken with 8 meshes.

次いで、ビタミンA、D、C及びステアリン酸マグネシ
ウムを混合し、タルクと共に前記混合物と良く混合した
のち打錠し、複合ビタミン錠を得た。
Next, vitamins A, D, C and magnesium stearate were mixed, and the mixture was thoroughly mixed with talc and then tableted to obtain a multivitamin tablet.

この錠剤は、不快味がなく、優れた甘味を有することが
認められた。
This tablet was found to have no unpleasant taste and excellent sweetness.

実施例 6 リン酸水素カルシウム42%、不溶性メタリン酸すI・
リウム23%、グリセリン12%、ナI・リウム・ラウ
ロイルザルコシーネ−1−1,4%、メント−ル1.1
%、甘味組成’jh (ステビオサイド20%、甘味物
質A370%)1%に水を加えて100%として均質練
合し、歯磨を製造した。
Example 6 Calcium hydrogen phosphate 42%, insoluble metaphosphoric acid I.
23% glycerin, 12% sodium chloride, 1-1.4% sodium lauroyl sarcocine, 1.1 menthol
%, sweetness composition 'jh (20% stevioside, 370% sweet substance A) was mixed homogeneously by adding water to 1% to make 100% to produce a toothpaste.

なお、必要に応じて薬効成分、香料、酵素、ビタミン類
、食塩、葉緑素等を加えることができる。
Note that medicinal ingredients, fragrances, enzymes, vitamins, salt, chlorophyll, etc. can be added as necessary.

この歯磨は、甘味質のすぐれた甘味を有し、不快な残味
がなかった。
This toothpaste had an excellent sweet taste and no unpleasant aftertaste.

Claims (1)

【特許請求の範囲】[Claims] 1 食品、医薬品、医薬部外品の製造に際して、ステビ
オサイド100部に対してジテルペン骨格でグルコース
4分子を有し、分子式C44H7oO23、分子量96
6で表わされる配糖体甘味物質A3を70部(重量比)
以上共存させた甘味組成物を使用することを特徴とする
甘味付与法。
1 In the production of foods, pharmaceuticals, and quasi-drugs, it has a diterpene skeleton with 4 glucose molecules per 100 parts of stevioside, a molecular formula of C44H7oO23, and a molecular weight of 96.
70 parts (weight ratio) of glycoside sweet substance A3 represented by 6
A sweetening method characterized by using a sweetening composition in which the above components coexist.
JP51034810A 1976-03-29 1976-03-29 Sweetening method Expired JPS5951256B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51034810A JPS5951256B2 (en) 1976-03-29 1976-03-29 Sweetening method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51034810A JPS5951256B2 (en) 1976-03-29 1976-03-29 Sweetening method

Publications (2)

Publication Number Publication Date
JPS52117474A JPS52117474A (en) 1977-10-01
JPS5951256B2 true JPS5951256B2 (en) 1984-12-13

Family

ID=12424561

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51034810A Expired JPS5951256B2 (en) 1976-03-29 1976-03-29 Sweetening method

Country Status (1)

Country Link
JP (1) JPS5951256B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5060674A (en) * 1990-01-12 1991-10-29 Kimberly-Clark Corporation Sidestream smoke reducing cigarette paper with improved physicals and improved sidestream odor/aroma

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6075252A (en) * 1983-09-30 1985-04-27 Sekisui Chem Co Ltd Low-calorie sweetener composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5816863A (en) * 1975-06-26 1983-01-31 イング・チイ・オリベツチ・アンド・チイ・エス・ピ−・ア Point printer

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5816863A (en) * 1975-06-26 1983-01-31 イング・チイ・オリベツチ・アンド・チイ・エス・ピ−・ア Point printer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5060674A (en) * 1990-01-12 1991-10-29 Kimberly-Clark Corporation Sidestream smoke reducing cigarette paper with improved physicals and improved sidestream odor/aroma

Also Published As

Publication number Publication date
JPS52117474A (en) 1977-10-01

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