JPWO2020003169A5 - - Google Patents

Download PDF

Info

Publication number
JPWO2020003169A5
JPWO2020003169A5 JP2020573036A JP2020573036A JPWO2020003169A5 JP WO2020003169 A5 JPWO2020003169 A5 JP WO2020003169A5 JP 2020573036 A JP2020573036 A JP 2020573036A JP 2020573036 A JP2020573036 A JP 2020573036A JP WO2020003169 A5 JPWO2020003169 A5 JP WO2020003169A5
Authority
JP
Japan
Prior art keywords
article according
meth
orthodontic article
weight
monofunctional
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.)
Pending
Application number
JP2020573036A
Other languages
Japanese (ja)
Other versions
JP2021529858A (en
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2019/055413 external-priority patent/WO2020003169A1/en
Publication of JP2021529858A publication Critical patent/JP2021529858A/en
Publication of JPWO2020003169A5 publication Critical patent/JPWO2020003169A5/ja
Priority to JP2024009850A priority Critical patent/JP2024038487A/en
Pending legal-status Critical Current

Links

Description

上記の特許出願において引用された全ての参考文献、特許文献又は特許出願は、一貫した形でその全文が参照により本明細書に組み込まれる。組み込まれた参照文献の一部と本出願との間に不一致又は矛盾がある場合、前述の記載における情報が優先するものとする。以下に例示的実施形態を示す。
[項目1]
歯科矯正物品であって、
30~70重量%(両端の値を含む)の少なくとも1つのウレタン成分と、
25~70重量%(両端の値を含む)の、少なくとも1つの単官能性(メタ)アクリレートモノマーを含む反応性希釈剤と、
少なくとも1つの、酸性官能基を有するエチレン性不飽和成分と、を含むフリーラジカル重合性樹脂の反応生成物を含む硬化組成物を含み、
前記フリーラジカル重合性樹脂が、35重量%以下の、水に対して高い親和性を有する反応性希釈剤を含む、歯科矯正物品。
[項目2]
水に対して高い親和性を有する前記反応性希釈剤が、1.5未満、又は1未満のlog Pを有する、項目1に記載の歯科矯正物品。
[項目3]
前記反応性希釈剤が、2、2.5、3、又は3.5を超えるlog Pを有する少なくとも1つの単官能性(メタ)アクリレートモノマーを含む、項目1又は2に記載の歯科矯正物品。
[項目4]
水に対して高い親和性を有する前記反応性希釈剤が、2、2.5、3、又は3.5を超えるlog Pを有する前記単官能性(メタ)アクリレートモノマーよりも少ない量で存在する、項目3に記載の歯科矯正物品。
[項目5]
前記重合性樹脂が、水に対して高い親和性を有する反応性希釈剤を、前記反応性希釈剤の50、45、30、又は25重量%以下の濃度で含む、項目1~4のいずれか一項に記載の歯科矯正物品。
[項目6]
前記反応性希釈剤が、前記ウレタン成分の分子量より小さい分子量を有する単官能性(メタ)アクリレートモノマーを含む、項目1~5のいずれか一項に記載の歯科矯正物品。
[項目7]
前記反応性希釈剤が、400g/モル未満の分子量を有する単官能性(メタ)アクリレートモノマーを含む、項目1~6のいずれか一項に記載の歯科矯正物品。
[項目8]
前記反応性希釈剤が、単官能性(メタ)アクリレートモノマーの混合物を含む、項目1~7のいずれか一項に記載の歯科矯正物品。
[項目9]
前記反応性希釈剤が、前記フリーラジカル重合性樹脂の1~30重量%の量の少なくとも1つの多官能性反応性希釈剤を含む、項目1~8のいずれか一項に記載の歯科矯正物品。
[項目10]
反応性希釈剤が、少なくとも25、30、35、40、45、又は50℃のTgを有する少なくとも1つの単官能性(メタ)アクリレートモノマーを含む、項目1~9のいずれか一項に記載の歯科矯正物品。
[項目11]
酸性官能基を有する前記エチレン性不飽和成分が、前記フリーラジカル重合性樹脂の少なくとも0.5、1、1.5、2、2.5、3、3.5、4、3.5、又は5重量%の量で存在する、項目1~10のいずれか一項に記載の歯科矯正物品。
[項目12]
酸性官能基を有する前記エチレン性不飽和成分が、前記フリーラジカル重合性樹脂の35、30、25、20、15、又は10重量%以下の量で存在する、項目1~9のいずれか一項に記載の歯科矯正物品。
[項目13]
酸性官能基を有する前記エチレン性不飽和成分が、少なくとも30、35、40、45、50、55、60、65、70、75、80、85、90、95、100℃のTgを有する、項目1~12のいずれか一項に記載の歯科矯正物品。
[項目14]
酸性官能基を有する前記エチレン性不飽和成分が、20、15、10、5、0、-5、-10、又は-15℃未満のTgを有する、項目1~12のいずれか一項に記載の歯科矯正物品。
[項目15]
酸性官能基当たりの酸性官能基を有するエチレン性不飽和成分の当量を、カルバメート官能基当たりの前記ウレタン成分の当量で割ったものが、6、5、4、3、又は2未満である、項目1~12のいずれか一項に記載の歯科矯正物品。
[項目16]
前記ウレタン成分が、アルキル、ポリアルキレン、ポリアルキレンオキシド、アリール、ポリカーボネート、ポリエステル、ポリアミド、及びこれらの組み合わせから選択される連結基を含む、項目1~15のいずれか一項に記載の歯科矯正物品。
[項目17]
前記ウレタン成分が、ポリカーボネートジオール若しくはポリエステルジオールから選択されるジオール又はポリアルキレンオキシド又はこれらの組み合わせから誘導される重合単位を含むウレタン(メタ)アクリレートポリマーである、項目1~16のいずれか一項に記載の歯科矯正物品。
[項目18]
前記ジオールが、少なくとも750、800、850、900、950、又は1000g/モルのMnを有する、項目17に記載の歯科矯正物品。
[項目19]
前記ウレタン(メタ)アクリレートポリマーが、2,000g/モル~50,000g/モルの分子量(Mw)を有する、項目17又は18に記載の歯科矯正物品。
[項目20]
前記ウレタン(メタ)アクリレートポリマーが、ポリカーボネートジオール、ポリエステルジオール、又はポリアルキレンオキシドジオールから選択される少なくとも1つのジオールに由来する、項目17~19のいずれか一項に記載の歯科矯正物品。
[項目21]
前記重合性樹脂が、10重量%を超える、そのホモポリマーが60、65、70、75、80、85、又は90℃のTgを有する単官能性(メタ)アクリレートモノマーを含む、項目1~20のいずれか一項に記載の歯科矯正物品。
[項目22]
前記重合性樹脂が、10重量%超の、少なくとも3.5のlog Pを有する単官能性(メタ)アクリレートモノマーを含む、項目1~21のいずれか一項に記載の歯科矯正物品。
[項目23]
前記重合性樹脂が、25℃未満のTgを有する単官能性(メタ)アクリレートモノマーを25、20、15、10、又は5重量%未満の量で含む、項目1~22のいずれか一項に記載の歯科矯正物品。
[項目24]
前記重合性樹脂が、25℃未満のTgを有する単官能性(メタ)アクリレートモノマーを含まない、項目1~23のいずれか一項に記載の歯科矯正物品。
[項目25]
前記組成物が、前記重合性組成物の総重量に基づいて、0.1~5重量%の光開始剤を含み、前記光開始剤が、単一の光開始剤を含むか、又は第1の光開始剤と、熱開始剤若しくは第1の光開始剤とは異なる波長範囲で十分な吸光度を有する光開始剤から選択される第2のフリーラジカル開始剤と、を含む、項目1~24のいずれか一項に記載の歯科矯正物品。
[項目26]
前記重合性組成物が、紫外線吸収剤を更に含む、項目1~25のいずれか一項に記載の歯科矯正物品。
[項目27]
前記歯科矯正物品が、5%のエタノールの水溶液中に0.1重量%未満の抽出物を含む、項目1~26のいずれか一項に記載の歯科矯正物品。
[項目28]
前記硬化組成物が、37℃の温度で24時間、pH7.4を有するリン酸緩衝生理食塩水中でのコンディショニング後に、ASTM D638-14に従って測定したときに、15%以上の破断点伸び及び少なくとも10MPaの降伏点引張強度を示す、項目1~27のいずれか一項に記載の歯科矯正物品。
[項目29]
前記硬化光重合性組成物重合組成物が、20~25℃で48時間脱イオン水中でのコンディショニング後に、2%のひずみで動的機械分析に従って測定したときに、少なくとも100MPaの3点曲げ弾性率を示す、項目1~28のいずれか一項に記載の歯科矯正物品。
[項目30]
歯科矯正物品であって、
30~70重量%(両端の値を含む)の少なくとも1つのウレタン成分と、
25~70重量%(両端の値を含む)の、少なくとも1つの単官能性(メタ)アクリレートモノマーを含む反応性希釈剤と、を含むフリーラジカル重合性樹脂の反応生成物を含む硬化組成物を含み、
前記重合性樹脂が、35重量%以下の、水に対して高い親和性を有する反応性希釈剤を含む、歯科矯正物品。
[項目31]
前記重合性樹脂が、項目2~29のいずれか一項に従って更に特徴付けられる、項目30に記載の歯科矯正物品。
[項目32]
前記ウレタン成分が、ポリエーテルジオールから誘導され、前記重合性組成物が、25℃未満のTgを有する単官能性(メタ)アクリレートモノマーを含まない、項目30に記載の歯科矯正物品。
[項目33]
前記重合性樹脂が、項目2~22及び24~29のいずれか一項に従って更に特徴付けられる、項目32に記載の歯科矯正物品。
[項目34]
前記歯科矯正物品が、歯科矯正トレイアライナ物品である、項目1~33のいずれか一項に記載の歯科矯正物品。
[項目35]
重合性組成物であって、
30~70重量%(両端の値を含む)の少なくとも1つのウレタン成分と、
25~70重量%(両端の値を含む)の、少なくとも1つの単官能性(メタ)アクリレートモノマーを含む反応性希釈剤と、
任意に、少なくとも1つの、酸性官能基を有するエチレン性不飽和成分と、を含み、
重合性樹脂が、50重量%以下の、水に対して高い親和性を有する反応性希釈剤を含む、重合性組成物。
[項目36]
前記重合性樹脂が、項目2~33のいずれか一項に従って更に特徴付けられる、項目35に記載の光重合性組成物。
All references, patent documents or patent applications cited in the above patent applications are incorporated herein by reference in their entirety in a consistent manner. In the event of any discrepancy or inconsistency between a portion of the incorporated references and this application, the information in the above description shall prevail. An exemplary embodiment is shown below.
[Item 1]
It ’s an orthodontic item,
With at least one urethane component of 30-70% by weight (including the values at both ends),
Reactive diluents comprising at least one monofunctional (meth) acrylate monomer of 25-70% by weight (including values at both ends).
A cured composition comprising a reaction product of a free radically polymerizable resin comprising at least one ethylenically unsaturated component having an acidic functional group.
An orthodontic article containing 35% by weight or less of the free radically polymerizable resin and a reactive diluent having a high affinity for water.
[Item 2]
The orthodontic article according to item 1, wherein the reactive diluent having a high affinity for water has a log P of less than 1.5 or less than 1.
[Item 3]
The orthodontic article of item 1 or 2, wherein the reactive diluent comprises at least one monofunctional (meth) acrylate monomer having a log P greater than 2, 2.5, 3, or 3.5.
[Item 4]
The reactive diluent having a high affinity for water is present in a smaller amount than the monofunctional (meth) acrylate monomer having a log P greater than 2, 2.5, 3, or 3.5. , The orthodontic article according to item 3.
[Item 5]
Any of items 1 to 4, wherein the polymerizable resin contains a reactive diluent having a high affinity for water at a concentration of 50, 45, 30, or 25% by weight or less of the reactive diluent. The orthodontic article described in paragraph 1.
[Item 6]
The orthodontic article according to any one of items 1 to 5, wherein the reactive diluent contains a monofunctional (meth) acrylate monomer having a molecular weight smaller than the molecular weight of the urethane component.
[Item 7]
The orthodontic article according to any one of items 1 to 6, wherein the reactive diluent contains a monofunctional (meth) acrylate monomer having a molecular weight of less than 400 g / mol.
[Item 8]
The orthodontic article according to any one of items 1 to 7, wherein the reactive diluent contains a mixture of monofunctional (meth) acrylate monomers.
[Item 9]
The orthodontic article according to any one of items 1 to 8, wherein the reactive diluent comprises at least one polyfunctional reactive diluent in an amount of 1 to 30% by weight of the free radically polymerizable resin. ..
[Item 10]
The item according to any one of items 1 to 9, wherein the reactive diluent comprises at least one monofunctional (meth) acrylate monomer having a Tg of at least 25, 30, 35, 40, 45, or 50 ° C. Orthodontic articles.
[Item 11]
The ethylenically unsaturated component having an acidic functional group is at least 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 3.5, or the free radically polymerizable resin of the free radically polymerizable resin. The orthodontic article according to any one of items 1 to 10, which is present in an amount of 5% by weight.
[Item 12]
Item 1 of item 1 to 9, wherein the ethylenically unsaturated component having an acidic functional group is present in an amount of 35, 30, 25, 20, 15, or 10% by weight or less of the free radically polymerizable resin. Orthodontic articles described in.
[Item 13]
The item, wherein the ethylenically unsaturated component having an acidic functional group has a Tg of at least 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 ° C. The orthodontic article according to any one of 1 to 12.
[Item 14]
Item 6. Orthodontic articles.
[Item 15]
Item that the equivalent of the ethylenically unsaturated component having an acidic functional group per acidic functional group divided by the equivalent of the urethane component per carbamate functional group is 6, 5, 4, 3, or less than 2. The orthodontic article according to any one of 1 to 12.
[Item 16]
The orthodontic article according to any one of items 1 to 15, wherein the urethane component comprises an alkyl, a polyalkylene, a polyalkylene oxide, an aryl, a polycarbonate, a polyester, a polyamide, and a linking group selected from a combination thereof. ..
[Item 17]
Item 1 to any one of items 1 to 16, wherein the urethane component is a urethane (meth) acrylate polymer containing a diol selected from a polycarbonate diol or a polyester diol, a polyalkylene oxide, or a polymerization unit derived from a combination thereof. The listed orthodontic article.
[Item 18]
The orthodontic article according to item 17, wherein the diol has at least 750, 800, 850, 900, 950, or 1000 g / mol of Mn.
[Item 19]
The orthodontic article according to item 17 or 18, wherein the urethane (meth) acrylate polymer has a molecular weight (Mw) of 2,000 g / mol to 50,000 g / mol.
[Item 20]
The orthodontic article according to any one of items 17 to 19, wherein the urethane (meth) acrylate polymer is derived from at least one diol selected from a polycarbonate diol, a polyester diol, or a polyalkylene oxide diol.
[Item 21]
Items 1-20, wherein the polymerizable resin comprises more than 10% by weight, the homopolymer comprising a monofunctional (meth) acrylate monomer having a Tg of 60, 65, 70, 75, 80, 85, or 90 ° C. The orthodontic article according to any one of the above.
[Item 22]
The orthodontic article according to any one of items 1 to 21, wherein the polymerizable resin contains a monofunctional (meth) acrylate monomer having a log P of at least 3.5, which is more than 10% by weight.
[Item 23]
Item 1 to any one of items 1 to 22, wherein the polymerizable resin contains a monofunctional (meth) acrylate monomer having a Tg of less than 25 ° C. in an amount of 25, 20, 15, 10, or less than 5% by weight. The orthodontic article described.
[Item 24]
The orthodontic article according to any one of items 1 to 23, wherein the polymerizable resin does not contain a monofunctional (meth) acrylate monomer having a Tg of less than 25 ° C.
[Item 25]
The composition comprises 0.1-5% by weight of the photoinitiator based on the total weight of the polymerizable composition and the photoinitiator comprises a single photoinitiator or a first. 1-24, comprising the photoinitiator of 1 and a second free radical initiator selected from photoinitiators having sufficient absorbance in a wavelength range different from that of the thermal initiator or the first photoinitiator. The orthodontic article according to any one of the above.
[Item 26]
The orthodontic article according to any one of items 1 to 25, wherein the polymerizable composition further contains an ultraviolet absorber.
[Item 27]
The orthodontic article according to any one of items 1 to 26, wherein the orthodontic article contains less than 0.1% by weight of an extract in a 5% aqueous solution of ethanol.
[Item 28]
When the cured composition was conditioned in a phosphate buffered physiological saline solution having a pH of 7.4 at a temperature of 37 ° C. for 24 hours and then measured according to ASTM D638-14, it had a breaking point elongation of 15% or more and at least 10 MPa. The orthodontic article according to any one of items 1 to 27, which indicates the yield point tensile strength of.
[Item 29]
Cured Photopolymerizable Composition When the polymerized composition is conditioned in deionized water at 20-25 ° C. for 48 hours and then measured by dynamic mechanical analysis at a strain of 2%, it has a three-point flexural modulus of at least 100 MPa. The orthodontic article according to any one of items 1 to 28.
[Item 30]
It ’s an orthodontic item,
With at least one urethane component of 30-70% by weight (including the values at both ends),
A cured composition comprising a reactive diluent comprising at least one monofunctional (meth) acrylate monomer of 25-70% by weight (including values at both ends) and a reaction product of a free radically polymerizable resin comprising. Including,
An orthodontic article containing 35% by weight or less of the polymerizable resin and a reactive diluent having a high affinity for water.
[Item 31]
30. The orthodontic article of item 30, wherein the polymerizable resin is further characterized according to any one of items 2-29.
[Item 32]
The orthodontic article according to item 30, wherein the urethane component is derived from a polyether diol, and the polymerizable composition does not contain a monofunctional (meth) acrylate monomer having a Tg of less than 25 ° C.
[Item 33]
32. The orthodontic article of item 32, wherein the polymerizable resin is further characterized according to any one of items 2-22 and 24-29.
[Item 34]
The orthodontic article according to any one of items 1 to 33, wherein the orthodontic article is an orthodontic tray aligner article.
[Item 35]
It is a polymerizable composition and
With at least one urethane component of 30-70% by weight (including the values at both ends),
Reactive diluents comprising at least one monofunctional (meth) acrylate monomer of 25-70% by weight (including values at both ends).
Optionally, it comprises at least one ethylenically unsaturated component having an acidic functional group.
A polymerizable composition comprising a reactive diluent in which the polymerizable resin has a high affinity for water in an amount of 50% by weight or less.
[Item 36]
35. The photopolymerizable composition of item 35, wherein the polymerizable resin is further characterized according to any one of items 2-33.

Claims (15)

歯科矯正物品であって、
30~70重量%(両端の値を含む)の少なくとも1つのウレタン成分と、
25~70重量%(両端の値を含む)の、少なくとも1つの単官能性(メタ)アクリレートモノマーを含む反応性希釈剤と、
少なくとも1つの、酸性官能基を有するエチレン性不飽和成分と、を含むフリーラジカル重合性樹脂の反応生成物を含む硬化組成物を含み、
前記フリーラジカル重合性樹脂が、35重量%以下の、水に対して高い親和性を有する反応性希釈剤を含む、歯科矯正物品。
It ’s an orthodontic item,
With at least one urethane component of 30-70% by weight (including the values at both ends),
A reactive diluent comprising at least one monofunctional (meth) acrylate monomer of 25-70% by weight (including values at both ends).
A cured composition comprising a reaction product of a free radically polymerizable resin comprising at least one ethylenically unsaturated component having an acidic functional group.
An orthodontic article containing 35% by weight or less of the free radically polymerizable resin and a reactive diluent having a high affinity for water.
水に対して高い親和性を有する前記反応性希釈剤が、1.5未満、又は1未満のlog Pを有する、請求項1に記載の歯科矯正物品。 The orthodontic article according to claim 1, wherein the reactive diluent having a high affinity for water has a log P of less than 1.5 or less than 1. 前記反応性希釈剤が、2、2.5、3、又は3.5を超えるlog Pを有する少なくとも1つの単官能性(メタ)アクリレートモノマーを含む、請求項1又は2に記載の歯科矯正物品。 The orthodontic article according to claim 1 or 2, wherein the reactive diluent comprises at least one monofunctional (meth) acrylate monomer having a log P greater than 2, 2.5, 3, or 3.5. .. 水に対して高い親和性を有する前記反応性希釈剤が、2、2.5、3、又は3.5を超えるlog Pを有する前記単官能性(メタ)アクリレートモノマーよりも少ない量で存在する、請求項3に記載の歯科矯正物品。 The reactive diluent having a high affinity for water is present in a smaller amount than the monofunctional (meth) acrylate monomer having a log P greater than 2, 2.5, 3, or 3.5. , The orthodontic article according to claim 3. 前記反応性希釈剤が、単官能性(メタ)アクリレートモノマーの混合物を含む、請求項1~のいずれか一項に記載の歯科矯正物品。 The orthodontic article according to any one of claims 1 to 4 , wherein the reactive diluent contains a mixture of monofunctional (meth) acrylate monomers. 反応性希釈剤が、少なくとも25、30、35、40、45、又は50℃のTgを有する少なくとも1つの単官能性(メタ)アクリレートモノマーを含む、請求項1~のいずれか一項に記載の歯科矯正物品。 10. One of claims 1-5 , wherein the reactive diluent comprises at least one monofunctional (meth) acrylate monomer having a Tg of at least 25, 30, 35, 40, 45, or 50 ° C. Orthodontic articles. 酸性官能基を有する前記エチレン性不飽和成分が、前記フリーラジカル重合性樹脂の少なくとも0.5、1、1.5、2、2.5、3、3.5、4、3.5、又は5重量%かつ35、30、25、20、15、又は10重量%以下の量で存在する、請求項1~のいずれか一項に記載の歯科矯正物品。 The ethylenically unsaturated component having an acidic functional group is at least 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 3.5, or the free radically polymerizable resin of the free radically polymerizable resin. The orthodontic article according to any one of claims 1 to 6 , which is present in an amount of 5% by weight and 35, 30, 25, 20, 15, or 10% by weight or less . 酸性官能基を有する前記エチレン性不飽和成分が、少なくとも30、35、40、45、50、55、60、65、70、75、80、85、90、95、100℃のTgを有し、又は、20、15、10、5、0、-5、-10、又は-15℃未満のTgを有する、請求項1~のいずれか一項に記載の歯科矯正物品。 The ethylenically unsaturated component having an acidic functional group has a Tg of at least 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 ° C. Alternatively, the orthodontic article according to any one of claims 1 to 7 , which has a Tg of less than 20, 15, 10, 5, 0, -5, -10, or -15 ° C. 酸性官能基当たりの酸性官能基を有するエチレン性不飽和成分の当量を、カルバメート官能基当たりの前記ウレタン成分の当量で割ったものが、6、5、4、3、又は2未満である、請求項1~のいずれか一項に記載の歯科矯正物品。 Claimed that the equivalent of an ethylenically unsaturated component having an acidic functional group per acidic functional group divided by the equivalent of the urethane component per carbamate functional group is 6, 5, 4, 3 or less than 2. The orthodontic article according to any one of Items 1 to 8 . 前記ウレタン成分が、ポリカーボネートジオール若しくはポリエステルジオールから選択されるジオール又はポリアルキレンオキシド又はこれらの組み合わせから誘導される重合単位を含むウレタン(メタ)アクリレートポリマーであかつ、前記ジオールが、少なくとも750、800、850、900、950、又は1000g/モルのMnを有する、請求項1~のいずれか一項に記載の歯科矯正物品。 The urethane component is a urethane (meth) acrylate polymer containing a diol selected from a polycarbonate diol or a polyester diol or a polyalkylene oxide or a polymerization unit derived from a combination thereof, and the diol is at least 750. The orthodontic article according to any one of claims 1 to 9 , which has Mn of 800, 850, 900, 950, or 1000 g / mol . 前記ウレタン(メタ)アクリレートポリマーが、2,000g/モル~50,000g/モルの分子量(Mw)を有する、請求項10に記載の歯科矯正物品。 The orthodontic article according to claim 10 , wherein the urethane (meth) acrylate polymer has a molecular weight (Mw) of 2,000 g / mol to 50,000 g / mol. 前記重合性樹脂が、10重量%を超える、そのホモポリマーが60、65、70、75、80、85、又は90℃のTgを有する単官能性(メタ)アクリレートモノマーを含む、請求項1~11のいずれか一項に記載の歯科矯正物品。 Claims 1 to 1, wherein the polymerizable resin comprises a monofunctional (meth) acrylate monomer having a Tg of more than 10% by weight, the homopolymer thereof having a Tg of 60, 65, 70, 75, 80, 85, or 90 ° C. The orthodontic article according to any one of 11 . 前記重合性樹脂が、10重量%超の、少なくとも3.5のlog Pを有する単官能性(メタ)アクリレートモノマーを含む、請求項1~12のいずれか一項に記載の歯科矯正物品。 The orthodontic article according to any one of claims 1 to 12 , wherein the polymerizable resin contains a monofunctional (meth) acrylate monomer having a log P of at least 3.5, which is more than 10% by weight. 前記重合性樹脂が、25℃未満のTgを有する単官能性(メタ)アクリレートモノマーを含まない、請求項1~13のいずれか一項に記載の歯科矯正物品。 The orthodontic article according to any one of claims 1 to 13 , wherein the polymerizable resin does not contain a monofunctional (meth) acrylate monomer having a Tg of less than 25 ° C. 前記組成物が、前記重合性組成物の総重量に基づいて、0.1~5重量%の光開始剤を含み、前記光開始剤が、単一の光開始剤を含むか、又は第1の光開始剤と、熱開始剤若しくは第1の光開始剤とは異なる波長範囲で十分な吸光度を有する光開始剤から選択される第2のフリーラジカル開始剤と、任意成分としての紫外線吸収剤と、を含む、請求項1~14のいずれか一項に記載の歯科矯正物品。 The composition comprises 0.1-5% by weight of the photoinitiator based on the total weight of the polymerizable composition and the photoinitiator comprises a single photoinitiator or a first. A second free radical initiator selected from the photoinitiators of the above, a photoinitiator having sufficient absorbance in a wavelength range different from that of the thermal initiator or the first photoinitiator, and an ultraviolet absorber as an optional component. The orthodontic article according to any one of claims 1 to 14 , which comprises.
JP2020573036A 2018-06-29 2019-06-26 Orthodontic articles containing a cured free radically polymerizable composition with improved strength in an aqueous environment Pending JP2021529858A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2024009850A JP2024038487A (en) 2018-06-29 2024-01-26 Orthodontic articles comprising cured free-radically polymerizable composition with improved strength in aqueous environment

Applications Claiming Priority (21)

Application Number Priority Date Filing Date Title
US201862692456P 2018-06-29 2018-06-29
US201862692466P 2018-06-29 2018-06-29
US62/692,456 2018-06-29
US62/692,466 2018-06-29
US201862736027P 2018-09-25 2018-09-25
US201862736031P 2018-09-25 2018-09-25
US62/736,027 2018-09-25
US62/736,031 2018-09-25
US201862769421P 2018-11-19 2018-11-19
US201862769375P 2018-11-19 2018-11-19
US201862769305P 2018-11-19 2018-11-19
US201862769434P 2018-11-19 2018-11-19
US201862769081P 2018-11-19 2018-11-19
US62/769,305 2018-11-19
US62/769,081 2018-11-19
US62/769,375 2018-11-19
US62/769,421 2018-11-19
US62/769,434 2018-11-19
US201962850658P 2019-05-21 2019-05-21
US62/850,658 2019-05-21
PCT/IB2019/055413 WO2020003169A1 (en) 2018-06-29 2019-06-26 Orthodontic articles comprising cured free-radically polymerizable composition with improved strength in aqueous environment

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2024009850A Division JP2024038487A (en) 2018-06-29 2024-01-26 Orthodontic articles comprising cured free-radically polymerizable composition with improved strength in aqueous environment

Publications (2)

Publication Number Publication Date
JP2021529858A JP2021529858A (en) 2021-11-04
JPWO2020003169A5 true JPWO2020003169A5 (en) 2022-07-05

Family

ID=67660594

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2020573036A Pending JP2021529858A (en) 2018-06-29 2019-06-26 Orthodontic articles containing a cured free radically polymerizable composition with improved strength in an aqueous environment
JP2024009850A Pending JP2024038487A (en) 2018-06-29 2024-01-26 Orthodontic articles comprising cured free-radically polymerizable composition with improved strength in aqueous environment

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2024009850A Pending JP2024038487A (en) 2018-06-29 2024-01-26 Orthodontic articles comprising cured free-radically polymerizable composition with improved strength in aqueous environment

Country Status (5)

Country Link
US (2) US11584817B2 (en)
EP (1) EP3813763A1 (en)
JP (2) JP2021529858A (en)
CN (1) CN112367959A (en)
WO (1) WO2020003169A1 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11141919B2 (en) 2015-12-09 2021-10-12 Holo, Inc. Multi-material stereolithographic three dimensional printing
US11904031B2 (en) * 2017-11-22 2024-02-20 3M Innovative Properties Company Orthodontic articles comprising polymerized composition comprising at least two free-radical initiators
US20230131633A1 (en) * 2020-03-26 2023-04-27 Mitsui Chemicals, Inc. Photocurable composition, three-dimensional modeling product, and dental product
CN116472175A (en) * 2020-09-03 2023-07-21 巴斯夫欧洲公司 Reactive polyurethane elastomers
WO2022106998A1 (en) 2020-11-20 2022-05-27 3M Innovative Properties Company Articles, methods and compositions comprising polymerizable dicarbonyl polymers
KR102499004B1 (en) * 2021-03-22 2023-02-14 오스템임플란트 주식회사 Photocurable resin composition and molded article prepared therefrom
CN113185645A (en) * 2021-04-23 2021-07-30 东莞理工学院 Photosensitive resin for 3D printing based on DLP type photocuring and preparation method thereof
EP4334402A1 (en) 2021-05-07 2024-03-13 3D Systems, Inc. Additives for build materials and associated printed 3d articles
US11998415B2 (en) * 2021-11-08 2024-06-04 Sprintray, Inc. System and method of forming a custom bleaching tray with trench and material reservoirs
DE102022110896A1 (en) * 2022-05-03 2023-11-09 Kulzer Gmbh Radiation-curable composition for use in rapid prototyping or rapid manufacturing processes
WO2024044330A1 (en) * 2022-08-24 2024-02-29 Pac-Dent, Inc. Photocurable materials for the production of dental prostheses and devices
DE102022123995A1 (en) 2022-09-19 2024-03-21 Amann Girrbach Ag Light-curable mixture of substances

Family Cites Families (132)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3429722A (en) 1965-07-12 1969-02-25 Carborundum Co Boron nitride fiber manufacture
US3795524A (en) 1971-03-01 1974-03-05 Minnesota Mining & Mfg Aluminum borate and aluminum borosilicate articles
GB1428673A (en) 1972-06-02 1976-03-17 Amalgamated Dental Co Ltd Orthodontics
JPS5224965B2 (en) 1972-06-28 1977-07-05
US4047965A (en) 1976-05-04 1977-09-13 Minnesota Mining And Manufacturing Company Non-frangible alumina-silica fibers
FR2431514A1 (en) 1978-07-19 1980-02-15 Poudres & Explosifs Ste Nale NOVEL UNSATURATED POLY (CARBONATES-URETHANNES) AND THEIR APPLICATIONS TO PHOTORETICULATION
US4264752A (en) 1979-08-08 1981-04-28 Union Carbide Corporation Radiation-curable acrylated urethane polycarbonate compositions
US4591626A (en) 1983-10-24 1986-05-27 Hitachi Chemical Company, Ltd. Polymers of tricyclo[5.2.1.02,6 ]deca-8-yl (meth)acrylate
JPS6121117A (en) * 1984-07-10 1986-01-29 Yokohama Rubber Co Ltd:The Photosetting resin composition
US4642126A (en) 1985-02-11 1987-02-10 Norton Company Coated abrasives with rapidly curable adhesives and controllable curvature
US4652274A (en) 1985-08-07 1987-03-24 Minnesota Mining And Manufacturing Company Coated abrasive product having radiation curable binder
JPH0653647B2 (en) 1986-04-18 1994-07-20 而至歯科工業株式会社 Dental restoration composition
US5185299A (en) 1987-06-05 1993-02-09 Minnesota Mining And Manufacturing Company Microcrystalline alumina-based ceramic articles
US4954462A (en) 1987-06-05 1990-09-04 Minnesota Mining And Manufacturing Company Microcrystalline alumina-based ceramic articles
CA2024379A1 (en) 1989-09-01 1991-03-02 Erwin S. Poklacki Primary coating compositions for optical glass fibers
DE59007720D1 (en) 1989-10-27 1994-12-22 Ciba Geigy Ag Method for tuning the radiation sensitivity of photopolymerizable compositions.
CA2048232A1 (en) 1990-09-05 1992-03-06 Jerry W. Williams Energy curable pressure-sensitive compositions
EP0506616B1 (en) 1991-03-27 1998-01-21 Ciba SC Holding AG Photosensitive acrylate mixture
CA2092131A1 (en) * 1992-03-27 1993-09-28 Victor Kadziela (Nmi) Low viscosity self-toughening acrylate composition
JP3301447B2 (en) 1992-12-01 2002-07-15 共栄社化学株式会社 Urethane / unsaturated organo oligomers and method for producing the same
US5780154A (en) 1994-03-22 1998-07-14 Tokuyama Corporation Boron nitride fiber and process for production thereof
DE69515310T2 (en) 1994-07-29 2000-07-27 Minnesota Mining & Mfg ACRYLIC SYRUP WHICH CAN BE CURED TO A CROSSLINKED VISCOELASTIC MATERIAL
JPH09504572A (en) * 1994-11-04 1997-05-06 ザ カー コーポレイション Radiation curable molding composition
JPH08188630A (en) 1995-01-06 1996-07-23 Daicel Chem Ind Ltd Photocurable resin composition
GB9504995D0 (en) 1995-03-11 1995-04-26 Zeneca Ltd Compositions
JP3115792B2 (en) 1995-05-15 2000-12-11 早川ゴム株式会社 Active energy ray-curable resin composition, method for producing the same, molded cured product of active energy ray-curable resin
US5981621A (en) 1996-02-29 1999-11-09 Closure Medical Corporation Monomeric compositions effective as wound closure devices
DE19603577C2 (en) 1996-02-01 2003-11-13 Heraeus Kulzer Gmbh & Co Kg adhesive
EP0802455B1 (en) 1996-04-15 2002-10-16 Teijin Seiki Co., Ltd. Use of a photocurable resin composition for the production of a stereolithographed object
EP0807853B1 (en) 1996-05-16 2003-10-08 Teijin Seiki Co., Ltd. Photocurable resin composition, method of producing photo-cured shaped object, vacuum casting mold, vacuum casting method and urethane acrylate
KR100341693B1 (en) 1996-11-08 2002-06-24 윌리암 로엘프 드 보에르 Radiation-curable optical glass fiber coating compositions, coated optical glass fibers, and optical glass fiber assemblies
WO1998039374A1 (en) 1997-03-07 1998-09-11 Dsm N.V. Radiation-curable composition having high cure speed
JPH1111986A (en) 1997-04-25 1999-01-19 Takeda Chem Ind Ltd Resin composition for coating optical fiber
US6379866B2 (en) 2000-03-31 2002-04-30 Dsm Desotech Inc Solid imaging compositions for preparing polypropylene-like articles
US6572693B1 (en) 1999-10-28 2003-06-03 3M Innovative Properties Company Aesthetic dental materials
US6183593B1 (en) 1999-12-23 2001-02-06 Closure Medical Corporation 1,1-disubstituted ethylene adhesive compositions containing polydimethylsiloxane
JP2001302744A (en) 2000-04-26 2001-10-31 Mitsubishi Rayon Co Ltd Actinic-ray curing composition
US6448301B1 (en) 2000-09-08 2002-09-10 3M Innovative Properties Company Crosslinkable polymeric compositions and use thereof
US6635690B2 (en) 2001-06-19 2003-10-21 3M Innovative Properties Company Reactive oligomers
FR2835828B1 (en) 2002-02-08 2006-07-14 Ct De Transfert De Technologie METHOD AND COMPOSITION FOR THE MANUFACTURE OF CERAMIC PIECES BY STEREO-LITHOPHOTOGRAPHY AND DENTAL FIELD APPLICATION
US7211368B2 (en) 2003-01-07 2007-05-01 3 Birds, Inc. Stereolithography resins and methods
JP2004217809A (en) 2003-01-16 2004-08-05 Mitsubishi Chemicals Corp Active energy beam-cured resin sheet
JP4526056B2 (en) 2003-08-26 2010-08-18 三菱レイヨン株式会社 Active energy ray-curable composition
EP1589040B1 (en) 2004-03-24 2008-09-10 Nippon Shokubai Co., Ltd. Method for continuous production of water absorbent resin
JP4880248B2 (en) 2004-05-17 2012-02-22 リンテック株式会社 Adhesive sheet and decorative adhesive sheet
US20050277084A1 (en) 2004-06-10 2005-12-15 3M Innovative Properties Company Orthodontic brace with polymeric arch member
JP4682544B2 (en) 2004-06-17 2011-05-11 日本ポリウレタン工業株式会社 RESIN COMPOSITION FOR PHOTOCURABLE COATING AND PROCESS FOR PRODUCING THE SAME
US7641828B2 (en) 2004-10-12 2010-01-05 Align Technology, Inc. Methods of making orthodontic appliances
KR100968670B1 (en) 2005-03-15 2010-07-06 쇼와 덴코 가부시키가이샤 Methacryloyl group-containing aromatic isocyanate compound and production process thereof
US20070031791A1 (en) 2005-08-03 2007-02-08 3M Innovative Properties Company Scanning models for digital orthodontics
US7495054B2 (en) 2005-09-19 2009-02-24 3M Innovative Properties Company Curable compositions containing dithiane monomers
JP5055764B2 (en) 2005-12-21 2012-10-24 住友ベークライト株式会社 Resin composition and semiconductor device produced using resin composition
CN101437692B (en) 2006-05-08 2011-02-02 旭化成电子材料株式会社 Cushioning material for printing
JP5068513B2 (en) 2006-11-21 2012-11-07 根上工業株式会社 Unsaturated group-containing urethane resin and active energy ray-curable resin composition containing the same
WO2008103494A2 (en) 2007-02-23 2008-08-28 Dentsply International Inc. Methods for making dental restorations using two-phase light-curing materials
EP2008636A1 (en) 2007-06-29 2008-12-31 3M Innovative Properties Company Dental composition containing a polyfunctional (meth)acrylate comprising urethane, urea or amide groups, method of production and use thereof
US20110229838A1 (en) 2007-10-01 2011-09-22 Kalgutkar Rajdeep S Orthodontic composition with polymeric fillers
US8827697B2 (en) 2008-04-09 2014-09-09 3M Innovative Properties Company Lingual orthodontic appliance with removable section
DK2299926T3 (en) 2008-06-26 2020-03-02 3M Innovative Properties Co PROCEDURE FOR PREPARING A TRANSFER TRAY FOR ORTHODONTIC DEVICES
JP5224965B2 (en) 2008-08-04 2013-07-03 三菱レイヨン株式会社 Cured resin and key sheet
JP2010043194A (en) 2008-08-13 2010-02-25 Mitsubishi Rayon Co Ltd Curable composition and optical information-recording medium
CN102209708B (en) * 2008-10-22 2015-03-11 3M创新有限公司 Dental composition comprising biphenyl di(meth)acrylate monomer comprising urethane moieties
JP5445215B2 (en) 2009-02-24 2014-03-19 三菱化学株式会社 Active energy ray-curable resin composition, cured film and laminate
CN102428112B (en) 2009-05-18 2014-01-08 爱克发印艺公司 Polymerizable Polymeric Photoinitiators And Radiation Curable Compositions
WO2011143620A2 (en) 2010-05-13 2011-11-17 Symdent, Inc. Dental appliance, dental appliance adhesive and related methods and uses
EP2603160A2 (en) 2010-08-11 2013-06-19 3M Innovative Properties Company Polymer coated dental articles and method of making the same
EP2436510A1 (en) 2010-10-04 2012-04-04 3D Systems, Inc. System and resin for rapid prototyping
EP2481390A1 (en) 2011-01-31 2012-08-01 3M Innovative Properties Company Dental composition, method of producing and use thereof
CN103370041B (en) 2011-02-15 2016-06-15 3M创新有限公司 Comprise the dental composition of the unsaturated addition-clastogen of ethylenic
JP2012184385A (en) 2011-03-08 2012-09-27 Ube Industries Ltd Polyurethane compound, composition including the same, and cured product of them
KR20120119442A (en) 2011-04-21 2012-10-31 동우 화인켐 주식회사 Pressure-sensitive adhesive composition for optical use
EP2581062A3 (en) 2011-10-12 2015-07-22 Ormco Corporation Direct manufacture of an orthodontic aligner
EP2751618B1 (en) 2012-04-11 2019-05-29 Ivoclar Vivadent AG Composite resin composition and use of it, method for producing dental components by means of stereo-lithography
WO2014078537A1 (en) 2012-11-14 2014-05-22 Dentsply International Inc. Three-dimensional fabricating material systems for producing dental products
WO2014077688A1 (en) 2012-11-16 2014-05-22 Dsm Ip Assets B.V. D1531 radiation-curable resin composition for wire coating layer formation
JP2014114444A (en) 2012-11-16 2014-06-26 Jsr Corp Radiation-curable resin composition for forming wire coating layer
JP2014116295A (en) 2012-11-16 2014-06-26 Jsr Corp Radiation-curable resin composition for forming wire coating layer
US10357435B2 (en) 2012-12-18 2019-07-23 Dentca, Inc. Photo-curable resin compositions and method of using the same in three-dimensional printing for manufacturing artificial teeth and denture base
WO2014098956A1 (en) 2012-12-18 2014-06-26 Dentca. Inc. Photo-curable resin compositions and method of using the same in three-dimensional printing for manufacturing artificial teeth and denture base
DK2956823T4 (en) 2013-02-12 2019-09-23 Carbon3D Inc CONTINUOUS PRINTING WITH LIQUID INTERMEDIATE
EP2842980B1 (en) 2013-08-09 2021-05-05 DSM IP Assets B.V. Low-viscosity liquid radiation curable dental aligner mold resin compositions for additive manufacturing
US9360757B2 (en) 2013-08-14 2016-06-07 Carbon3D, Inc. Continuous liquid interphase printing
JP2015043793A (en) 2013-08-27 2015-03-12 ディーダブルエス エス・アール・エル Method for manufacturing artificial teeth
US9580621B2 (en) 2013-09-09 2017-02-28 Dymax Corporation High temperature resistance, radiation curable maskant for metal substrates
US9096722B2 (en) 2013-10-18 2015-08-04 Hrl Laboratories, Llc Method for curing structures using a dual photoinitiator system and a structure made using the same
EP2886077A1 (en) 2013-12-18 2015-06-24 3M Innovative Properties Company Method of making a transfer tray
US9682018B2 (en) 2014-03-13 2017-06-20 Steven Sadowsky Denture tooth and material
JP6329281B2 (en) 2014-06-23 2018-05-23 アルケマ フランス Urethane acrylate polymer with unique physical properties
BR112016029755A2 (en) 2014-06-23 2017-08-22 Carbon Inc methods of producing three-dimensional objects from materials having multiple hardening mechanisms
US9574039B1 (en) 2014-07-22 2017-02-21 Full Spectrum Laser Additive use in photopolymer resin for 3D printing to enhance the appearance of printed parts
WO2016071811A1 (en) 2014-11-04 2016-05-12 Dws S.R.L. Stereolithographic method and composition
CN104765251A (en) 2014-11-06 2015-07-08 青岛科技大学 High-toughness photosensitive resin for 3D printing and preparation method thereof.
WO2016094272A1 (en) 2014-12-09 2016-06-16 3M Innovative Properties Company Dental restoration molding techniques
US20160167301A1 (en) 2014-12-12 2016-06-16 Autodesk, Inc. Polymeric photoinitiators for 3d printing applications
JP6451288B2 (en) 2014-12-17 2019-01-16 コニカミノルタ株式会社 Model material ink, ink set and method for producing 3D object
EP3240496B1 (en) 2014-12-30 2020-09-16 3M Innovative Properties Company Dental appliance providing exposed occlusal surfaces
US20180049847A1 (en) 2015-03-13 2018-02-22 3M Innovative Properties Company Orthodontic appliance including arch member
US20180014916A1 (en) 2015-03-13 2018-01-18 3M Innovative Properties Company Orthodontic appliance including arch member
JP6831333B2 (en) 2015-04-02 2021-02-17 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company A method for producing it using a polymer-based gravure printing plate and a curable composition having a polyfunctional urethane.
WO2016182444A1 (en) 2015-05-12 2016-11-17 Rijksuniversiteit Groningen 3d-printable antimicrobial composite resins, methods for manufacturing the same
CA2986029C (en) 2015-05-15 2023-05-23 Dentsply Sirona Inc. Three-dimensional fabricating method for rapidly producing objects
JP6835742B6 (en) 2015-05-28 2021-03-24 スリーエム イノベイティブ プロパティズ カンパニー Additional manufacturing method for producing ceramic articles using sol containing nano-sized particles
JP6493875B2 (en) 2015-06-08 2019-04-03 富士フイルム株式会社 Method for forming a three-dimensional structure
US10492888B2 (en) 2015-07-07 2019-12-03 Align Technology, Inc. Dental materials using thermoset polymers
JP6574980B2 (en) 2015-09-01 2019-09-18 Kjケミカルズ株式会社 Active energy ray-curable resin composition for model materials
EP3391871A4 (en) 2015-12-18 2019-08-28 Kuraray Noritake Dental Inc. Dental adhesive material kit
CN105566916B (en) 2016-02-23 2018-04-06 上海应用技术学院 A kind of quick-setting noctilucence 3D printing light-sensitive emulsion and preparation method thereof
JP2017210579A (en) 2016-05-27 2017-11-30 凸版印刷株式会社 Photocurable resin molded body using urethane acrylate
WO2017208959A1 (en) 2016-06-01 2017-12-07 三菱瓦斯化学株式会社 Urethane (meth)acrylate, method for producing urethane (meth)acrylate, curable composition, cured product and method for producing cured product
US11650498B2 (en) 2016-06-30 2023-05-16 3M Innovative Properties Company Printable compositions including highly viscous components and methods of creating 3D articles therefrom
US10941313B2 (en) 2016-11-21 2021-03-09 3M Innovative Properties Company Flexible hardcoat comprising urethane oligomer hydrogen bonded to an acrylic polymer
CN110036342A (en) 2016-12-05 2019-07-19 阿科玛股份有限公司 Initiator blend and the Photocurable composition containing such initiator blend that can be used for 3D printing
US11602412B2 (en) 2016-12-23 2023-03-14 3M Innovative Properties Company Printable compositions including polymeric and polymerizable components, articles, and methods of making articles therefrom
US20200048392A1 (en) 2017-02-17 2020-02-13 3M Innovative Properties Company Physically crosslinkable (meth)acrylate copolymer composition
CN110997744B (en) 2017-07-25 2022-06-24 3M创新有限公司 Photopolymerizable compositions, articles, and methods comprising a urethane component and a reactive diluent
WO2019023166A1 (en) 2017-07-25 2019-01-31 3M Innovative Properties Company Water-resistant polymer-based dental articles
KR102555173B1 (en) 2017-07-26 2023-07-12 쓰리엠 이노베이티브 프로퍼티즈 컴파니 Methods of manufacturing physical objects by additive manufacturing
US11553996B2 (en) 2017-09-11 2023-01-17 3M Innovative Properties Company Radiation curable compositions and composite articles made using an additive manufacturing process
CN111107804A (en) 2017-09-19 2020-05-05 3M创新有限公司 Tooth repairing mould
CN111372959B (en) 2017-11-22 2022-09-02 3M创新有限公司 Photopolymerizable compositions, articles, and methods comprising a urethane component and a monofunctional reactive diluent
WO2019104072A1 (en) 2017-11-22 2019-05-31 3M Innovative Properties Company Orthodontic articles comprising cured free-radically polymerizable composition comprising polymer or macromolecule with photoinitiator group
US11904031B2 (en) * 2017-11-22 2024-02-20 3M Innovative Properties Company Orthodontic articles comprising polymerized composition comprising at least two free-radical initiators
WO2019104079A1 (en) 2017-11-22 2019-05-31 3M Innovative Properties Company Orthodontic articles comprising polymerized composition comprising at least two free-radical initiators
WO2019175716A1 (en) 2018-03-15 2019-09-19 3M Innovative Properties Company Photopolymerizable compositions including a polypropylene oxide component, articles, and methods
US11591438B2 (en) 2018-05-22 2023-02-28 3M Innovative Properties Company Process of processing a radiation-curable thiolen based composition with additive-manufacturing technology
WO2019244007A1 (en) 2018-06-19 2019-12-26 3M Innovative Properties Company Aqueous dispersions including polyester particles, photopolymerizable compositions, articles, and methods
WO2020003197A2 (en) 2018-06-29 2020-01-02 3M Innovative Properties Company Orthodontic articles prepared using a polycarbonate diol, polymerizable compositions, and methods of making the articles
CN112118802B (en) 2018-06-29 2021-12-07 3M创新有限公司 Orthodontic articles prepared using polycarbonate diols and methods of making the same
CN112105332A (en) 2018-06-29 2020-12-18 3M创新有限公司 Photopolymerizable compositions, articles, and methods comprising urethane methacrylate polymers prepared using polycarbonate diols
WO2020104873A1 (en) 2018-11-19 2020-05-28 3M Innovative Properties Company Orthodontic articles comprising polyester urethane (meth)acrylate polymer and monofunctional (meth)acrylate monomer, methods, and polymerizable compositions
WO2020157598A1 (en) 2019-01-29 2020-08-06 3M Innovative Properties Company Orthodontic articles and methods of making and postprocessing same
WO2020234775A1 (en) 2019-05-21 2020-11-26 3M Innovative Properties Company Orthodontic articles comprising polymerized composition with pendent cyclic moieties, methods, and polymerizable compositions

Similar Documents

Publication Publication Date Title
JPWO2020003169A5 (en)
JPH09507475A (en) Urea and urethane monomers for contact lens materials
JP2007510035A5 (en)
JP3030115B2 (en) Crosslinkable polymer casting composition
JP2008542850A5 (en)
JP2003012711A5 (en)
JP2001302744A5 (en)
WO2008036117A3 (en) Nanogel contrast agents for optical molecular imaging
CA2964242A1 (en) Aqueous dental glass ionomer composition
Mehravar et al. Role of grafting on particle and film morphology and film properties of zero VOC polyurethane/poly (meth) acrylate hybrid dispersions
US20230392041A1 (en) Polymerizable composition for dental tooth and material 3d printing
AU2003237685A1 (en) Process for preparing polymer polyols
EP1593722B1 (en) An acrylic composition for use in coating applications and method of forming the same
JPH01101316A (en) Optical material
JPH04164910A (en) Polybutylene glycol di(meta)acrylate and resin composition for cast polymerization containing same
JPH04202308A (en) Composition for plastic lens
JP3362987B2 (en) Composition for plastic lens
JPH03231908A (en) Composition for plastic lens
CA2403391A1 (en) Photochromic article and method of preparation
AU601779B2 (en) Cross-linkable casting composition
JPH0699538B2 (en) Method for producing curable resin
JP2760624B2 (en) Composition for plastic lens
JP4018252B2 (en) New urethane diacrylate
JPH03255117A (en) Composition for plastic lens
JPH03215512A (en) Resin composition for cast polymerization