JPS5924128B2 - dental cement curing liquid - Google Patents
dental cement curing liquidInfo
- Publication number
- JPS5924128B2 JPS5924128B2 JP56011492A JP1149281A JPS5924128B2 JP S5924128 B2 JPS5924128 B2 JP S5924128B2 JP 56011492 A JP56011492 A JP 56011492A JP 1149281 A JP1149281 A JP 1149281A JP S5924128 B2 JPS5924128 B2 JP S5924128B2
- Authority
- JP
- Japan
- Prior art keywords
- cement
- acid
- weight
- curing liquid
- dental cement
- 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
Links
- 239000007788 liquid Substances 0.000 title claims description 21
- 239000003479 dental cement Substances 0.000 title claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 11
- 239000010452 phosphate Substances 0.000 claims description 11
- UFOIOXZLTXNHQH-UHFFFAOYSA-N oxolane-2,3,4,5-tetracarboxylic acid Chemical compound OC(=O)C1OC(C(O)=O)C(C(O)=O)C1C(O)=O UFOIOXZLTXNHQH-UHFFFAOYSA-N 0.000 claims description 10
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 239000000843 powder Substances 0.000 description 22
- 239000004568 cement Substances 0.000 description 20
- 235000021317 phosphate Nutrition 0.000 description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 230000000704 physical effect Effects 0.000 description 7
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 235000010724 Wisteria floribunda Nutrition 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000005354 aluminosilicate glass Substances 0.000 description 4
- ROBFUDYVXSDBQM-UHFFFAOYSA-N hydroxymalonic acid Chemical compound OC(=O)C(O)C(O)=O ROBFUDYVXSDBQM-UHFFFAOYSA-N 0.000 description 4
- 229920000554 ionomer Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 4
- 239000002672 zinc phosphate cement Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 2
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical class OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 150000004673 fluoride salts Chemical class 0.000 description 2
- 239000003178 glass ionomer cement Substances 0.000 description 2
- YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- IQVLXQGNLCPZCL-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate Chemical compound CC(C)(C)OC(=O)NCCCCC(NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O IQVLXQGNLCPZCL-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- QNSOHXTZPUMONC-UHFFFAOYSA-N benzene pentacarboxylic acid Natural products OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O QNSOHXTZPUMONC-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- QQFLQYOOQVLGTQ-UHFFFAOYSA-L magnesium;dihydrogen phosphate Chemical compound [Mg+2].OP(O)([O-])=O.OP(O)([O-])=O QQFLQYOOQVLGTQ-UHFFFAOYSA-L 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- BECVLEVEVXAFSH-UHFFFAOYSA-K manganese(3+);phosphate Chemical compound [Mn+3].[O-]P([O-])([O-])=O BECVLEVEVXAFSH-UHFFFAOYSA-K 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- -1 oxides Chemical class 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
Landscapes
- Dental Preparations (AREA)
Description
【発明の詳細な説明】
本発明は新規な歯科用セメント硬化液に関するものであ
り、更に詳述するとテトラヒドロフランテトラカルボン
酸を使用し練和操作性が良く、且つ硬化時間を自由に調
節することが可能で物理的性質に優れた新規な歯科用セ
メント硬化液に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel dental cement curing liquid, and more specifically, it uses tetrahydrofurantetracarboxylic acid, has good kneading operability, and can freely adjust the curing time. The present invention relates to a novel dental cement curing liquid that is flexible and has excellent physical properties.
従来よりクラウン、インレー、矯正用バンドなどの合着
の目的で広範に使用されている歯科用セメントにはリン
酸亜鉛セメント、グラスアイオノマーセメント、カルボ
キシレートセメントなどがある。Dental cements that have been widely used for the purpose of bonding crowns, inlays, orthodontic bands, etc. include zinc phosphate cement, glass ionomer cement, and carboxylate cement.
之等のセメント硬化液の主成分はリン酸亜鉛セメントは
リン酸、グラスアイオノマーセメント及びカルボキシレ
ートセメントはアクリル酸のホモポリマー若しくはコポ
リマーであるが、之等の硬化液については種々の問題点
を有しており、改良されなげればならない点の多いこと
が知られている。The main components of these cement hardening solutions are phosphoric acid for zinc phosphate cement, and acrylic acid homopolymer or copolymer for glass ionomer cement and carboxylate cement, but these hardening solutions have various problems. It is known that there are many points that need to be improved.
例えばポリアクリル酸は高分子電解質であり、一般にポ
リアクリル酸を主成分とする硬化液は1000 cps
以上の高粘度であるため、練和操作性に難点があると言
える。For example, polyacrylic acid is a polymer electrolyte, and generally a curing liquid containing polyacrylic acid as a main component has a power consumption of 1000 cps.
Because of the above high viscosity, it can be said that there are difficulties in kneading operability.
一方、リン酸亜鉛セメントの硬化液に使用されているリ
ン酸は強酸であり、セメント粉末と練和したとき可成り
の発熱を示す。On the other hand, phosphoric acid used in the curing solution of zinc phosphate cement is a strong acid and generates considerable heat when mixed with cement powder.
そこでセメント本来の物理的性質を具現させるためには
粉末を分割して練和し、反応熱を抑制しなければならな
い。Therefore, in order to realize the physical properties inherent to cement, the powder must be divided and kneaded to suppress the heat of reaction.
またリン酸は生体組織に対する刺激作用も大きい。Phosphoric acid also has a strong stimulating effect on living tissues.
そこで之等の練和操作性を改善し、物理的性質に優れた
新規なセメント硬化液を作製するべく鋭意検討を重ねた
結果、テトラヒドロフランテトラカルボン酸を使用した
歯科用セメント硬化液は低粘度の水溶液であり硬化特性
も自由に調節することが可能であって破砕抗力、溶解度
にも優れ、歯科用セメントとして臨床に便利に使用でき
得るものであることを見出し本発明を完成した。Therefore, as a result of intensive studies to improve the kneading operability and create a new cement hardening liquid with excellent physical properties, we have developed a dental cement hardening liquid using tetrahydrofuran tetracarboxylic acid with a low viscosity. We have completed the present invention by discovering that it is an aqueous solution, which allows the curing properties to be freely adjusted, has excellent crushing resistance and solubility, and can be conveniently used clinically as a dental cement.
本発明で使用するテトラヒドロフランテトラカルボン酸
(T、HoF、T、C)の代表的なものはテトラヒドロ
フラン−2・3・4・5−テトラカルボン酸であり、そ
れは(1)式の構造式を有する4塩基酸である。A typical example of tetrahydrofuran tetracarboxylic acid (T, HoF, T, C) used in the present invention is tetrahydrofuran-2,3,4,5-tetracarboxylic acid, which has the structural formula (1). It is a tetrabasic acid.
このテトラヒドロフランテトラカルボン酸は水溶性であ
り、室温で加熱することなく水に可溶であり、容易に水
溶液が作製出来る。This tetrahydrofuran tetracarboxylic acid is water-soluble, and is soluble in water at room temperature without heating, so an aqueous solution can be easily prepared.
但し70重量%を超える高濃度の硬化液によって練和さ
れた硬化体の物性は低下する。However, the physical properties of a cured product kneaded with a hardening liquid at a high concentration of more than 70% by weight deteriorate.
このことはTHFTCが溶液中で過飽和となって析出し
、未反応の酸が硬化体に残存するためと考えられる。This is thought to be because THFTC becomes supersaturated in the solution and precipitates, leaving unreacted acid in the cured product.
また30重量%未満の低濃度の硬化液は含有水分量が過
多となるため硬化体の物性が劣悪となり耐久性に欠ける
。Furthermore, a curing liquid with a low concentration of less than 30% by weight will contain too much moisture, resulting in poor physical properties of the cured product and lack of durability.
このためTHFTCが単独の場合は、その濃度が30〜
70重量%の範囲にあるとき歯科用セメント硬化液とし
て適当なものとして使用することが可能となり、通常は
この範囲外にある硬化液は適当ではない。Therefore, when THFTC is used alone, its concentration is 30~
When the content is in the range of 70% by weight, it can be suitably used as a dental cement hardening fluid, and hardening fluids outside this range are usually not suitable.
更にセメント硬化液としてTHFTCと第一リン酸塩と
の両方を含んだものは、より優れた性能を示す。Furthermore, a cement hardening liquid containing both THFTC and primary phosphate exhibits even better performance.
この場合、第一リン酸塩としては水溶性第一リン酸塩が
特に好ましい。In this case, the primary phosphate is particularly preferably a water-soluble primary phosphate.
水溶性第一リン酸塩とは例えば第一リン酸アルミニウム
、第一リン酸マクネシウム、第一リン酸マンガン、第一
リン酸ナトリウムなどのことである。Water-soluble primary phosphates include, for example, aluminum monophosphate, magnesium monophosphate, manganese monophosphate, sodium monophosphate, and the like.
なお第一リン酸塩が溶液に含まれているということは、
第一リン酸塩を溶解させてもよいが、そればかりでなく
第一リン酸イオンと金属イオンとが共存していることを
示す。Furthermore, the fact that primary phosphate is contained in the solution means that
Although the primary phosphate may be dissolved, this also indicates that primary phosphate ions and metal ions coexist.
例えば、金属、酸化物、塩などと共にリン酸を混合し、
該硬化液中で第一リン酸塩が多少なりとも生成する可能
性があるならば本発明の範囲内にある。For example, mixing phosphoric acid with metals, oxides, salts, etc.
It is within the scope of the present invention if there is a possibility that primary phosphate may be formed to some extent in the curing liquid.
また第ニリン酸塩や第ニリン酸塩とリン酸とを硬化液中
に含ませて第一リン酸塩を生成させてもよい。Alternatively, a diphosphate salt or a diphosphate salt and phosphoric acid may be included in the curing liquid to generate a primary phosphate salt.
従って該硬化液中に含まれるリン酸塩は第一リン酸塩に
制限されるものではなく、他のリン酸塩であっても第一
リン酸塩が多少なりとも生成する可能性があるならばよ
い。Therefore, the phosphates contained in the curing liquid are not limited to primary phosphates, and other phosphates may also be used if primary phosphates may be generated to some extent. Bye.
なお本発明に準じてリン酸塩をセメント粉末中に混合し
ても差支えない。Note that phosphate may be mixed into cement powder according to the present invention.
特に不溶性のリン酸塩を用いる場合はこの方法が好まし
い。This method is particularly preferred when using an insoluble phosphate.
またリン酸塩及びTHFTCを用いた硬化液の濃度は、
THFTCとリン酸塩との合計が30〜70重量%の水
溶液濃度であるものが好ましい。In addition, the concentration of the curing solution using phosphate and THFTC is
Preferably, the total aqueous concentration of THFTC and phosphate is 30 to 70% by weight.
本発明で使用する水溶性の多塩基性カルボン酸とはカル
ボキシル基が1分子内に2つ以上あるカルボン酸で水溶
性のものを表わし、例えばリンゴ酸、タルトロン酸、酒
石酸、ベンゼンペンタカルボン酸、ベンゼンヘキサカル
ボン酸などが挙げられる。The water-soluble polybasic carboxylic acid used in the present invention refers to a water-soluble carboxylic acid having two or more carboxyl groups in one molecule, such as malic acid, tartronic acid, tartaric acid, benzenepentacarboxylic acid, Examples include benzenehexacarboxylic acid.
之等の多塩基性カルボン酸の1種以上をTHFTCと共
に水中に溶解させることにより、セメント硬化液として
優れたものが作製できる。By dissolving one or more polybasic carboxylic acids such as these in water together with THFTC, an excellent cement hardening solution can be prepared.
このとき、多塩基性カルボン酸とTHFTCとの合計濃
度が30〜70重量%である水溶液が好ましい濃度範囲
にある。At this time, an aqueous solution in which the total concentration of polybasic carboxylic acid and THFTC is 30 to 70% by weight is in a preferable concentration range.
歯科用セメントとしてはセメント硬化液と共に練和され
た場合、硬化するセメント粉末を必要とする。Dental cements require cement powders that harden when mixed with a cement hardening solution.
このセメント粉末は本発明では特に限定するものではな
いが、粉と液とを練和した場合、硬化体を形成するもの
でなげればならない。This cement powder is not particularly limited in the present invention, but it must be able to form a hardened product when the powder and liquid are kneaded together.
例えば金属酸化物、水酸化物、ケイ酸塩、フッ化物など
が通常は使用され得るが、特に好ましいセメント粉末と
しては酸化亜鉛を主成分とし、他の酸化物やフン化物と
共に焼成して粉砕した粉末やフルオロアルミノシリケー
トガラス粉末が挙げられる。For example, metal oxides, hydroxides, silicates, fluorides, etc. can usually be used, but particularly preferred cement powders are those containing zinc oxide as the main component, calcined and ground together with other oxides and fluorides. Examples include powder and fluoroaluminosilicate glass powder.
之等のセメント粉末は80メツシユ篩を通過する粉末が
望ましく、特に150メツシユ篩を通過する微粉末が適
当である。Such cement powders are preferably powders that pass through an 80-mesh sieve, and particularly fine powders that pass through a 150-mesh sieve are suitable.
なおTHFTCを含む硬化液は必ずしも液体である必要
はなくペーストの形で供給されてもよい。Note that the curing liquid containing THFTC does not necessarily have to be a liquid and may be supplied in the form of a paste.
以下、実施例を挙げて本発明の詳細な説明する。Hereinafter, the present invention will be explained in detail by giving Examples.
実施例 1
テトラヒドロフラン−2・3・4・5−テトラカルボン
酸50グを室温で純水50グに溶解させTHFTCの5
0重量%水溶液を作製した。Example 1 50 g of tetrahydrofuran-2,3,4,5-tetracarboxylic acid was dissolved in 50 g of pure water at room temperature, and 50 g of THFTC was added.
A 0% by weight aqueous solution was prepared.
この水溶液0.4?とアルミノシリケートガラス粉末(
G、C1社製、商品名、フジアイオノマータイプIの粉
末)1.1’を練和し、セメント硬化体を作製した。This aqueous solution 0.4? and aluminosilicate glass powder (
G, manufactured by C1, trade name, Fuji Ionomer Type I powder) 1.1' was kneaded to prepare a hardened cement body.
なお、歯科用リン酸亜鉛セメントに関するJIS規格T
6602に従って1日後の破砕抗力及び硬化時間を測定
した結果、780 kg/c4及び4分50秒であり、
この硬化液は臨床的に適格な物性であることが判った。In addition, JIS standard T regarding dental zinc phosphate cement
6602, the crushing force and curing time after one day were measured to be 780 kg/c4 and 4 minutes 50 seconds,
This curing liquid was found to have clinically acceptable physical properties.
実施例 2
実施例1で得た50重量%のTHFTC水溶液302と
50重量%第一リン酸アルミニウム水溶液70グを室温
で混合しセメント硬化液を作製した。Example 2 A cement hardening solution was prepared by mixing the 50% by weight THFTC aqueous solution 302 obtained in Example 1 and 70 g of the 50% by weight monoaluminum phosphate aqueous solution at room temperature.
この水溶液0.4L?をアルミノシリケートガラス粉末
(G、C1社製、商品名、フジアイオノマータイプ■の
粉末)1.1と練和し実施例1に準じて破砕抗力及び硬
化時間を測定した処、1680kg/crA及び3分O
秒の値を得た。0.4L of this aqueous solution? was kneaded with aluminosilicate glass powder (G, manufactured by C1 company, trade name, Fuji ionomer type ■ powder) 1.1, and the crushing force and curing time were measured according to Example 1, and the result was 1680 kg/crA and 3. Minute O
I got the value of seconds.
之等は臨床的に適格な物性である。These are clinically relevant physical properties.
実施例 3
テトラヒドロフラン−2・3・4・5−テトラカルボン
酸25グ及びタルトロン酸30y′を水40?に室温で
溶解させ、セメント硬化液を作製した。Example 3 25 g of tetrahydrofuran-2,3,4,5-tetracarboxylic acid and 30 g of tartronic acid were mixed with 40 g of water. A cement hardening solution was prepared by dissolving the cement at room temperature.
この硬化液04y′をアルミノシリケートガラス粉末(
G、 C,社製、商品名、フジアイオノマータイプ■の
粉末)1.1’と練和し実施例1に準じて破砕抗力及び
硬化時間を測定した処、850kg/c4及び4分10
秒であった。This curing liquid 04y' was mixed with aluminosilicate glass powder (
G, C, company, trade name, powder of Fuji ionomer type ■) 1.1' was kneaded and the crushing resistance and curing time were measured according to Example 1, 850 kg/c4 and 4 minutes 10
It was seconds.
之等は臨床的に適格なものであった。These were clinically qualified.
実施例 4
実施例3で得たセメント硬化液0.41を、ZnOを主
成分としたセメント粉末(G、C,社製、商品名、カー
ボリット100の粉末)とアルミノシリケートガラス粉
末(G、C,社製、商品名、フジアイオノマータイプ■
の粉末)を1:1に混合した粉末1.01と練和し実施
例1に準じ破砕抗力及び硬化時間を測定した処、970
kg/ca、及び2分O秒であった。Example 4 0.41% of the cement hardening liquid obtained in Example 3 was mixed with cement powder containing ZnO as the main component (product name: Carbolyt 100 powder, manufactured by G, C) and aluminosilicate glass powder (G, C). , manufactured by company, product name, Fuji ionomer type■
) was kneaded with powder 1.01 mixed at a ratio of 1:1, and the crushing resistance and curing time were measured according to Example 1.
kg/ca, and 2 minutes O seconds.
Claims (1)
0重量%を超え70重量%までの水溶液であることを特
徴とする歯科用セメント硬化液。 2 テトラヒドロフランテトラカルボン酸と水溶性第一
リン酸塩とを計30重量%を超え70重量%までを含む
水溶液であることを特徴とする歯科用セメント硬化液。 3 テトラヒドロフランテトラカルボン酸と水溶性多塩
基性カルボン酸とを計30重量%を超え70重量%まで
を含む水溶液であることを特徴とする歯科用セメント硬
化液。[Claims] 1. The content of tetrahydrofuran tetracarboxylic acid is 3.
A dental cement curing liquid characterized by being an aqueous solution containing more than 0% by weight and up to 70% by weight. 2. A dental cement curing liquid, which is an aqueous solution containing a total of more than 30% by weight and up to 70% by weight of tetrahydrofuran tetracarboxylic acid and water-soluble primary phosphate. 3. A dental cement curing liquid, which is an aqueous solution containing a total of more than 30% by weight and up to 70% by weight of tetrahydrofuran tetracarboxylic acid and a water-soluble polybasic carboxylic acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56011492A JPS5924128B2 (en) | 1981-01-30 | 1981-01-30 | dental cement curing liquid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56011492A JPS5924128B2 (en) | 1981-01-30 | 1981-01-30 | dental cement curing liquid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57126406A JPS57126406A (en) | 1982-08-06 |
| JPS5924128B2 true JPS5924128B2 (en) | 1984-06-07 |
Family
ID=11779533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56011492A Expired JPS5924128B2 (en) | 1981-01-30 | 1981-01-30 | dental cement curing liquid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5924128B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0699181B2 (en) * | 1985-05-25 | 1994-12-07 | 株式会社はいる | Tetracalcium phosphate curable composition |
| JP4794201B2 (en) | 2005-04-25 | 2011-10-19 | 株式会社松風 | 2 paste type glass ionomer cement |
-
1981
- 1981-01-30 JP JP56011492A patent/JPS5924128B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57126406A (en) | 1982-08-06 |
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