JP2745598B2 - Sucrose fatty acid ester composition - Google Patents
Sucrose fatty acid ester compositionInfo
- Publication number
- JP2745598B2 JP2745598B2 JP30842688A JP30842688A JP2745598B2 JP 2745598 B2 JP2745598 B2 JP 2745598B2 JP 30842688 A JP30842688 A JP 30842688A JP 30842688 A JP30842688 A JP 30842688A JP 2745598 B2 JP2745598 B2 JP 2745598B2
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- acid ester
- sucrose
- sucrose fatty
- carbon atoms
- 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 - Lifetime
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Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、蛋白質可溶化剤として、あるいは液体洗剤
用に使用されるショ糖脂肪酸エステル組成物に関するも
のであり、詳しくは構成脂肪酸の炭素数が8のショ糖脂
肪酸エステルと、特定の脂肪酸及び特定の平均置換度を
有するショ糖脂肪酸エステルからなるショ糖脂肪酸エス
テル組成物であって、水に溶解したとき、透明に溶解
し、かつ、安定性に優れた水溶液が調製できるショ糖脂
肪酸エステル組成物に関するものである。Description: TECHNICAL FIELD The present invention relates to a sucrose fatty acid ester composition used as a protein solubilizing agent or for a liquid detergent, and more particularly to a carbon number of a constituent fatty acid. Is a sucrose fatty acid ester composition comprising a sucrose fatty acid ester of 8 and a sucrose fatty acid ester having a specific fatty acid and a specific average degree of substitution, and when dissolved in water, dissolves transparently and is stable The present invention relates to a sucrose fatty acid ester composition from which an aqueous solution having excellent properties can be prepared.
ショ糖脂肪酸エステル(以下SEと記す)は安全性の高
い界面活性剤であり、食品、化粧品、医薬品、農薬等の
広範囲の分野にわたって利用されているが、水に対し不
溶性あるいは難溶性の物質を水中に溶解させる可溶化剤
としても利用されている。特に構成脂肪酸の炭素数8の
SEは蛋白質に対する作用が穏やかであるため生体膜の蛋
白質可溶化剤として、あるいはその低起泡性を利用して
低起泡性液体洗剤等に使用されている。SEをこれらの用
途に用いるには水に対し透明に溶解させる必要があるた
め、その透明な水溶液は、一旦60℃以上に攪拌下に加温
溶解後、室温まで冷却することによって製造される。Sucrose fatty acid ester (hereinafter referred to as SE) is a highly safe surfactant and is used in a wide range of fields such as food, cosmetics, pharmaceuticals, and agricultural chemicals. It is also used as a solubilizer to dissolve in water. In particular, the constituent fatty acids with 8 carbon atoms
SE is mildly acting on proteins, and is therefore used as a protein solubilizer for biological membranes or as a low foaming liquid detergent utilizing its low foaming properties. Since SE needs to be transparently dissolved in water to be used for these applications, the transparent aqueous solution is produced by temporarily dissolving under stirring at a temperature of 60 ° C. or higher and then cooling to room temperature.
ショ糖1分子には脂肪酸を最大8分子エステル結合さ
せることが可能であり、通常得られるSEはこれらエステ
ル結合数の異なったものの混合物である。SEの水溶性
は、構成脂肪酸の炭素数が少なく、平均置換度(平均置
換度とは、ショ糖1分子にエステル化された脂肪酸の平
均結合数をいう。)が低いものほど大である。Up to eight fatty acids can be ester-bonded to one molecule of sucrose, and the SE usually obtained is a mixture of those having different numbers of ester bonds. The water solubility of SE increases as the number of carbon atoms in the constituent fatty acids decreases and the average degree of substitution (the average degree of substitution refers to the average number of bonds of the fatty acid esterified to one sucrose molecule) increases.
一般に構成脂肪酸の炭素数が8のSEは、平均置換度が
1.1〜1.5のSEで、通常、水溶液濃度0.01〜5重量%の範
囲で使用される。In general, SE with 8 carbon atoms in the constituent fatty acids has an average degree of substitution.
An SE of 1.1 to 1.5 is usually used in an aqueous solution concentration range of 0.01 to 5% by weight.
しかしながら上記水溶液は、0.2〜4重量%の濃度に
おいて著しい白濁を生じ実用上適さなくなる。この白濁
の原因は、少量含まれるジエステル、トリエステル、あ
るいはオクタエステルまでのポリエステル等が水中で著
しく凝集するためと考えられる。However, the above aqueous solution becomes extremely cloudy at a concentration of 0.2 to 4% by weight, and is not practically suitable. It is considered that the cause of the white turbidity is that polyesters such as diester, triester, and octaester contained in a small amount are remarkably aggregated in water.
本発明は、水に溶解したときに透明であって、得られ
た溶液の安定性の優れたSE組成物の提供を目的とする。An object of the present invention is to provide an SE composition that is transparent when dissolved in water and has excellent stability in the obtained solution.
本発明は、構成脂肪酸の炭素数が8のSEと、 A:構成脂肪酸の炭素数が10〜14で平均置換度1〜1.6のS
Eの5重量%以上と、 又は B:構成脂肪酸の炭素数が16〜18で平均置換度1〜1.2のS
Eの2重量%以上と、 からなる、蛋白質可溶化剤もしくは液体洗剤用のショ糖
脂肪酸エステル組成物であって、この組成物を水に溶解
したときに透明な溶液を与えるショ糖脂肪酸エステル組
成物を要旨とする。The present invention relates to an SE having 8 carbon atoms of a constituent fatty acid, and A: a C having 10 to 14 carbon atoms of a constituent fatty acid and an average degree of substitution of 1 to 1.6.
5% by weight or more of E, or B: S having 16 to 18 carbon atoms in the constituent fatty acid and an average degree of substitution of 1 to 1.2
A sucrose fatty acid ester composition for a protein solubilizer or a liquid detergent, comprising 2% by weight or more of E, wherein the sucrose fatty acid ester composition gives a transparent solution when the composition is dissolved in water. Make the object a summary.
即ち、本発明のSE組成物は、構成脂肪酸の炭素数が8
のSEと、構成脂肪酸の炭素数が10〜14で平均置換度1〜
1.6好ましくは1〜1.5のSE又は、構成脂肪酸の炭素数が
16〜18で平均置換度1〜1.2好ましくは1〜1.1のSEいず
れか一方とからなるSE組成物に関するものである。That is, the SE composition of the present invention has a constituent fatty acid having 8 carbon atoms.
SE, the number of carbon atoms of the constituent fatty acids is 10 to 14 and the average degree of substitution is 1 to 1
1.6 preferably SE of 1 to 1.5 or carbon number of the constituent fatty acid
The present invention relates to an SE composition comprising 16 to 18 and an average degree of substitution of 1 to 1.2, preferably 1 to 1.1.
本発明の構成脂肪酸の炭素数が10〜14及び16〜18のSE
は含有量が、少なすぎると透明化が充分でない。このた
め各々の場合の含有量は構成脂肪酸の炭素数8のSEに対
し、構成脂肪酸の炭素数が10〜14のSEの場合は5重量%
以上、好ましくは7重量%以上、構成脂肪酸の炭素数が
16〜18のSEの場合は2重量%以上、好ましくは3重量%
以上混合したほうがよい。また、これらの構成脂肪酸
は、飽和または不飽和の脂肪酸あるいは、それらの混合
物であってもよい。SE having 10 to 14 and 16 to 18 carbon atoms of the constituent fatty acids of the present invention.
If the content is too small, transparency is not sufficient. Therefore, in each case, the content is 5% by weight in the case of the SE having 10 to 14 carbon atoms, based on the SE having 8 carbon atoms of the constituent fatty acid.
Or more, preferably 7% by weight or more, the carbon number of the constituent fatty acid is
For SE of 16-18, 2% by weight or more, preferably 3% by weight
It is better to mix them. Further, these constituent fatty acids may be saturated or unsaturated fatty acids, or a mixture thereof.
本発明のSE組成物を水等の系に溶解するときは、水ま
たは目的とする系の溶媒の一部で60℃以上加温溶解ある
いは分散後系内へ添加混合してもよい。When dissolving the SE composition of the present invention in a system such as water, it may be heated and dissolved or dispersed in water or a part of the solvent of the target system after heating at 60 ° C. or higher, and then mixed into the system.
〔実施例〕 第1表に、実施例及び比較例において使用したショ糖
脂肪酸エステルを記載した。[Examples] Table 1 shows sucrose fatty acid esters used in Examples and Comparative Examples.
実施例1 ショ糖カプリル酸エステル(リョトーシュガーエステ
ルCE-1695:構成脂肪酸炭素数8、平均置換度1.2)100g
とショ糖カプリン酸エステル(同、CT-1695、構成脂肪
酸炭素数10、平均置換度1.2)7gとを充分混合し、本発
明のショ糖脂肪酸エステル組成物(ショ糖カプリル酸エ
ステルに対してショ糖カプリン酸エステルが7重量%)
を製造した。 Example 1 100 g of sucrose caprylate (ryoto sugar ester CE-1695: constituent fatty acid carbon number 8, average degree of substitution 1.2)
And 7 g of sucrose capric acid ester (same as above, CT-1695, constituent fatty acid carbon number 10, average degree of substitution 1.2), and sufficiently mixed, and the sucrose fatty acid ester composition of the present invention (sucrose caprylate ester to sucrose caprylate ester) 7% by weight of sugar caprate ester)
Was manufactured.
上記で製造したショ糖脂肪酸エステル組成物を60℃の
水に溶解して、濃度0.5、1.0及び2.0重量%の各水溶液
1を製造した。製造した水溶液は何れも透明な溶液で
あり、7日間室温に保存したが、何れも透明度を失わな
かった。The sucrose fatty acid ester composition prepared above was dissolved in water at 60 ° C. to prepare aqueous solutions 1 having concentrations of 0.5, 1.0 and 2.0% by weight. All prepared aqueous solutions were clear solutions and were stored at room temperature for 7 days, but none of them lost transparency.
実施例2〜8 実施例1で使用したショ糖カプリン酸エステルに代え
て、第1表のd〜g及びiのショ糖脂肪酸エステルを使
用し、実施例1と同様にしてショ糖脂肪酸エステル組成
物を製造した。但し、実施例6及び実施例8において
は、ショ糖カプリル酸エステルの100gとショ糖パルミチ
ン酸エステルの3gとを、そしてショ糖ステアリン酸エス
テルの3gとをそれぞれ混合した。Examples 2 to 8 In place of the sucrose caprate used in Example 1, sucrose fatty acid esters of d to g and i in Table 1 were used, and sucrose fatty acid ester composition was obtained in the same manner as in Example 1. Was manufactured. However, in Examples 6 and 8, 100 g of sucrose caprylate, 3 g of sucrose palmitate, and 3 g of sucrose stearate were mixed.
これら実施例により製造したショ糖脂肪酸エステル組
成物を水に溶解して、濃度0.5、1.0及び2.0重量%の各
水溶液1を製造した。The sucrose fatty acid ester compositions prepared according to these examples were dissolved in water to prepare aqueous solutions 1 having concentrations of 0.5, 1.0 and 2.0% by weight.
上記により製造したショ糖脂肪酸エステル組成物は、
何れも透明な溶液であり、7日間室温に保存しても透明
度を失わなかった。The sucrose fatty acid ester composition produced by the above,
All were clear solutions and did not lose their transparency even after being stored at room temperature for 7 days.
実施例9 ショ糖カプリル酸エステルCE-1695の2.0重量%水溶液
100gにショ糖カプリン酸エステルCT-1695の2.0重量%水
溶液7gを混合してショ糖カプリル酸エステルとショ糖カ
プリン酸エステルとの混合水溶液を製造した。Example 9 2.0% by weight aqueous solution of sucrose caprylate CE-1695
100 g was mixed with 7 g of a 2.0% by weight aqueous solution of sucrose caprate CT-1695 to prepare a mixed aqueous solution of sucrose caprylate and sucrose caprate.
上記により製造したショ糖脂肪酸エステル組成物水溶
液は、何れも透明な溶液であり、7日間室温に保存して
も透明度を失わなかった。Each of the aqueous sucrose fatty acid ester composition aqueous solutions produced as described above was a transparent solution, and did not lose its transparency even after being stored at room temperature for 7 days.
比較例1〜16 実施例1で使用したショ糖カプリン酸エステルに代え
て、第1表のb〜iのショ糖脂肪酸エステルの3又は1g
を使用し実施例1と同様にして、ショ糖脂肪酸エステル
組成物を製造した。Comparative Examples 1 to 16 In place of the sucrose caprate used in Example 1, 3 or 1 g of the sucrose fatty acid ester of b to i in Table 1 was used.
In the same manner as in Example 1 to produce a sucrose fatty acid ester composition.
これら比較例により製造したショ糖脂肪酸エステル組
成物を水に溶解して、濃度0.5、1.0及び2.0重量%の各
水溶液1を製造した。The sucrose fatty acid ester compositions produced according to these comparative examples were dissolved in water to produce aqueous solutions 1 having concentrations of 0.5, 1.0 and 2.0% by weight.
上記実施例及び比較例により得られた結果を第2表に
示した。Table 2 shows the results obtained by the above Examples and Comparative Examples.
実施例により得られた水溶液は何れも透明な水溶液で
あり、長期にわたり安定した透明性を保持した。 Each of the aqueous solutions obtained in the examples was a transparent aqueous solution, and maintained stable transparency for a long period of time.
本発明によれば、透明安定性の優れた構成脂肪酸の炭
素数が8のSE水溶液を容易に得ることができ、かつ構成
脂肪酸の炭素数が8のSEを蛋白質可溶剤あるいは液体洗
剤等に利用することが可能である。ADVANTAGE OF THE INVENTION According to this invention, the SE aqueous solution with 8 carbon atoms of the constituent fatty acid excellent in transparency stability can be easily obtained, and the SE with 8 carbon atoms of the constituent fatty acid is used as a protein solvent or a liquid detergent. It is possible to
Claims (1)
ステルと、 A:構成脂肪酸の炭素数が10〜14で平均置換度 1〜1.6のショ糖脂肪酸エステルの5重量%以上と、 又は B:構成脂肪酸の炭素数が16〜18で平均置換度 1〜1.2のショ糖脂肪酸エステルの5重量%以上と、 からなる、蛋白質可溶化剤もしくは液体洗剤用のショ糖
脂肪酸エステル組成物であって、この組成物を水に溶解
したときに透明な溶液を与えるショ糖脂肪酸エステル組
成物。1. A sucrose fatty acid ester having 8 carbon atoms of a constituent fatty acid, and A: 5% by weight or more of a sucrose fatty acid ester having 10 to 14 carbon atoms and an average degree of substitution of 1 to 1.6, or B: a sucrose fatty acid ester composition for a protein solubilizer or liquid detergent, comprising: 5% by weight or more of a sucrose fatty acid ester having 16 to 18 carbon atoms and an average degree of substitution of 1 to 1.2. A sucrose fatty acid ester composition which gives a clear solution when the composition is dissolved in water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30842688A JP2745598B2 (en) | 1988-12-06 | 1988-12-06 | Sucrose fatty acid ester composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30842688A JP2745598B2 (en) | 1988-12-06 | 1988-12-06 | Sucrose fatty acid ester composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02157288A JPH02157288A (en) | 1990-06-18 |
JP2745598B2 true JP2745598B2 (en) | 1998-04-28 |
Family
ID=17980912
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30842688A Expired - Lifetime JP2745598B2 (en) | 1988-12-06 | 1988-12-06 | Sucrose fatty acid ester composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2745598B2 (en) |
-
1988
- 1988-12-06 JP JP30842688A patent/JP2745598B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH02157288A (en) | 1990-06-18 |
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