MODIFIED BETA-AMINO ACID ESTER (ASPARATE) CURING AGENTS AND THE USE THEREOF IN POLYUREA TISSUE ADHESIVES
The present invention relates to a compound of a formula (I) in which R 1 , R 2 , R 3 are respectively independent equal or various organic radicals that have no Zerewitinoff active hydrogen, R 4 are independently hydrogen, equal or different organic radicals, having no Zerewitinoff active hydrogen, or together form an unsaturated or aromatic ring, which can potentially contain heteroatoms, wherein R 4 have no Zerewitinoff active hydrogen, X is a linear or branched, potentially even a substituted organic radical in the chain with heteroatom, which does not have Zerewitinoff active hydrogen, n 0<n≦2 and m 0≦m<2, wherein n+m=2. The invention also relates to a process for producing a compound of said formula (I) as well as a polyurea system containing such a compound.
1 - 15 . (canceled)
16 . A compound of a formula (I)
in which
R 1 , R 2 , R 3 are respectively independent equal or various organic radicals that have no Zerewitinoff active hydrogen,
R 4 are independently hydrogen, equal or different organic radicals, having no Zerewitinoff active hydrogen, or together form an unsaturated or aromatic ring, which can potentially contain heteroatoms, wherein R 4 have no Zerewitinoff active hydrogen,
X is a linear or branched organic radical, potentially substituted by a heteroatom in the chain, which does not have Zerewitinoff active hydrogen,
n 0<n≦2 and
m 0≦m<2,
wherein n+m=2.
17 . The compound according to claim 16 , wherein said radicals R 1 , R 2 , R 3 are respectively independently linear or branched, aliphatic C1 to C10 hydrocarbon radicals.
18 . The compound according to claim 16 , wherein the radical X is a linear, branched or cyclical, organic C2 to C 16 radical.
19 . The compound according to claim 16 , wherein said radicals R 1 and R 2 are equal.
20 . The compound according to claim 16 , wherein 0<n<2 and 0<m<2.
21 . A process for producing the compound according to claim 16 , comprising reacting a diamine compound of a general formula (II)
H 2 N—X—NH 2 (II)
with an acrylic acid ester of a general formula (III)
and, optionally, with a diester of an unsaturated dicarboxylic acid of a general formula (IV)
wherein n mol of acrylic acid ester and m mol of diester is used per mol of diamine compound, and wherein
R 1 , R 2 , R 3 are respectively independent equal or various organic radicals that have no Zerewitinoff active hydrogen,
R 4 are independently hydrogen, equal or different organic radicals, having no Zerewitinoff active hydrogen, or form an unsaturated or aromatic ring, which can potentially contain heteroatoms, wherein R 4 have no Zerewitinoff active hydrogen,
X is a linear or branched organic radical, potentially substituted by a heteroatom in the chain, which does not have Zerewitinoff active hydrogen,
n 0<n≦2,
m 0≦m<2
and n+m=2.
22 . A polyurea system comprising
an isocyanate functional prepolymer as a component A) obtained by reaction of
an aliphatic polyisocyanate A1) with polyol A2),
a compound according to claim 16 as a component B),
obtionally organic fillers as a component C),
reaction products of isocyanate functional prepolymers according to component A) having compounds according to component B) and/or organic filler according to component C) potentially as component D), and
potentially water and/or a tertiary amine as a component E).
23 . The polyurea system according to claim 22 , wherein said polyol A2) comprise polyester polyols and/or polyester-polyether polyols and/or polyether polyols, particularly polyester-polyether polyols and/or polyether polyols having an ethylene oxide share of between 60 and 90% by weight.
24 . The polyurea system according to claim 22 , wherein said organic filler of a component C) are hydroxy functional compounds.
25 . The polyurea system according to claim 22 , wherein component E) comprises a tertiary amine of a general formula (V)
in which
R 5 , R 6 , R 7 may independently be alkyl or heteroalkyl radicals having heteroatoms in an alkyl chain or at their ends, or R 5 and R 6 can form an aliphatic, unsaturated or aromatic heterocycle together with the nitrogen atom bearing them, which can potentially contain additional heteroatoms.
26 . The polyurea system according to claim 22 , wherein said tertiary amine is selected from a group consisting of triethanolamine, tetrakis (2-hydroxyethyl) ethylenediamine, N,N-dimethyl-2-(4-methylpiperazine-1-yl)ethanamine, 2-{[2-(dimethylamino)ethyl](methyl)amino} ethanol, and 3,3′,3″-(1,3,5-Triazinan-1,3,5-triyl)tris(N,N-dimethyl-propane-1-amine).
27 . The polyurea system according to claim 22 , wherein said component E) contains 0.2 to 2.0% by weight of water and/or 0.1 to 1.0% by weight of tertiary amine.
28 . A method comprising utilizing the polyurea system according to claim 22 for closing, bonding, adhering or covering cell tissue, or for closing leakages in cell tissue.
29 . The method according to claim 28 wherein the cell tissue is human or animal cell tissue.
30 . A dispensing system having two chambers for the polyurea/polyurethane system according to claim 22 , wherein said component A) is contained in one chamber and said components B) and potentially said components C), D), and E) in another of said polyurea system.