JP2006192268A - ゴルフボール用の配合物 - Google Patents
ゴルフボール用の配合物 Download PDFInfo
- Publication number
- JP2006192268A JP2006192268A JP2006001975A JP2006001975A JP2006192268A JP 2006192268 A JP2006192268 A JP 2006192268A JP 2006001975 A JP2006001975 A JP 2006001975A JP 2006001975 A JP2006001975 A JP 2006001975A JP 2006192268 A JP2006192268 A JP 2006192268A
- Authority
- JP
- Japan
- Prior art keywords
- golf ball
- carbon atoms
- layer
- polyamine
- organic
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 113
- 239000010410 layer Substances 0.000 claims abstract description 147
- 239000000463 material Substances 0.000 claims abstract description 57
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 37
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 37
- 229920001971 elastomer Polymers 0.000 claims abstract description 19
- 239000012792 core layer Substances 0.000 claims abstract description 15
- 239000000806 elastomer Substances 0.000 claims abstract description 14
- 229920000768 polyamine Polymers 0.000 claims description 177
- 229920005862 polyol Polymers 0.000 claims description 105
- 150000003077 polyols Chemical class 0.000 claims description 103
- 125000004432 carbon atom Chemical group C* 0.000 claims description 98
- -1 n-phenyl Chemical group 0.000 claims description 95
- 238000009472 formulation Methods 0.000 claims description 57
- 229910052757 nitrogen Inorganic materials 0.000 claims description 51
- 239000004952 Polyamide Substances 0.000 claims description 34
- 229920002647 polyamide Polymers 0.000 claims description 34
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 32
- 229920006395 saturated elastomer Polymers 0.000 claims description 32
- 239000002253 acid Substances 0.000 claims description 25
- 229920000554 ionomer Polymers 0.000 claims description 25
- 239000004814 polyurethane Substances 0.000 claims description 25
- 229910052736 halogen Inorganic materials 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 24
- 229920002635 polyurethane Polymers 0.000 claims description 23
- 229920000642 polymer Polymers 0.000 claims description 22
- 150000001414 amino alcohols Chemical class 0.000 claims description 21
- 229920002396 Polyurea Polymers 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 229920000728 polyester Polymers 0.000 claims description 17
- 229910052710 silicon Inorganic materials 0.000 claims description 17
- 239000004202 carbamide Substances 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 15
- 150000002431 hydrogen Chemical class 0.000 claims description 14
- 229920001169 thermoplastic Polymers 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 13
- 229920001187 thermosetting polymer Polymers 0.000 claims description 13
- 239000004416 thermosoftening plastic Substances 0.000 claims description 13
- 239000004417 polycarbonate Substances 0.000 claims description 12
- 229920000515 polycarbonate Polymers 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 10
- 229920000098 polyolefin Polymers 0.000 claims description 10
- 239000004593 Epoxy Substances 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- 229920001897 terpolymer Polymers 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- 229920002292 Nylon 6 Polymers 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 claims description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 229920000831 ionic polymer Polymers 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 229920001955 polyphenylene ether Polymers 0.000 claims description 2
- 229920006132 styrene block copolymer Polymers 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims 23
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 claims 1
- 238000006735 epoxidation reaction Methods 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 abstract description 32
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 28
- 239000007795 chemical reaction product Substances 0.000 abstract description 17
- 229920006250 telechelic polymer Polymers 0.000 abstract description 2
- 238000009987 spinning Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 42
- 235000019589 hardness Nutrition 0.000 description 40
- 239000012948 isocyanate Substances 0.000 description 34
- 239000011162 core material Substances 0.000 description 33
- 150000002513 isocyanates Chemical class 0.000 description 33
- 125000001931 aliphatic group Chemical group 0.000 description 27
- 125000003118 aryl group Chemical group 0.000 description 25
- 150000001412 amines Chemical group 0.000 description 22
- 229920000570 polyether Polymers 0.000 description 20
- 150000001875 compounds Chemical class 0.000 description 19
- 150000004985 diamines Chemical class 0.000 description 17
- 150000002148 esters Chemical group 0.000 description 16
- 239000000376 reactant Substances 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 14
- 125000004122 cyclic group Chemical group 0.000 description 14
- 150000002009 diols Chemical class 0.000 description 14
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 14
- 239000004721 Polyphenylene oxide Substances 0.000 description 13
- 125000002947 alkylene group Chemical group 0.000 description 13
- 125000000623 heterocyclic group Chemical group 0.000 description 13
- 239000000654 additive Substances 0.000 description 11
- 150000001336 alkenes Chemical class 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- 125000000962 organic group Chemical group 0.000 description 11
- 239000002243 precursor Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 125000004429 atom Chemical group 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 238000007906 compression Methods 0.000 description 10
- 230000006835 compression Effects 0.000 description 10
- 238000004132 cross linking Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 9
- 125000002723 alicyclic group Chemical group 0.000 description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
- 125000002950 monocyclic group Chemical group 0.000 description 9
- 229920000058 polyacrylate Polymers 0.000 description 9
- 125000003367 polycyclic group Chemical group 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 8
- 239000000539 dimer Substances 0.000 description 8
- 150000008282 halocarbons Chemical group 0.000 description 8
- 125000003010 ionic group Chemical group 0.000 description 8
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 239000013638 trimer Substances 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 238000007710 freezing Methods 0.000 description 7
- 230000008014 freezing Effects 0.000 description 7
- 125000005842 heteroatom Chemical group 0.000 description 7
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 7
- 150000003335 secondary amines Chemical group 0.000 description 7
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 6
- 235000013877 carbamide Nutrition 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 150000004292 cyclic ethers Chemical class 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 description 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 229920001281 polyalkylene Polymers 0.000 description 5
- 239000005060 rubber Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 125000003003 spiro group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 240000002636 Manilkara bidentata Species 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- 229920002614 Polyether block amide Polymers 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 235000016302 balata Nutrition 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- OYQYHJRSHHYEIG-UHFFFAOYSA-N ethyl carbamate;urea Chemical compound NC(N)=O.CCOC(N)=O OYQYHJRSHHYEIG-UHFFFAOYSA-N 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 239000012968 metallocene catalyst Substances 0.000 description 4
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 239000012815 thermoplastic material Substances 0.000 description 4
- 150000004072 triols Chemical class 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 3
- ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 3
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 3
- 229960004050 aminobenzoic acid Drugs 0.000 description 3
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 3
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 235000015278 beef Nutrition 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 230000000994 depressogenic effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 3
- 229940043276 diisopropanolamine Drugs 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 150000001261 hydroxy acids Chemical class 0.000 description 3
- 239000011229 interlayer Substances 0.000 description 3
- 239000004611 light stabiliser Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920001610 polycaprolactone Polymers 0.000 description 3
- 239000004632 polycaprolactone Substances 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 229920005604 random copolymer Polymers 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 3
- 125000004149 thio group Chemical group *S* 0.000 description 3
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 3
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 2
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- GCUZEVZQPKKYLN-UHFFFAOYSA-N 1-n-(2-aminoethyl)hexane-1,2,6-triamine Chemical compound NCCCCC(N)CNCCN GCUZEVZQPKKYLN-UHFFFAOYSA-N 0.000 description 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 2
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 2
- UVLSCMIEPPWCHZ-UHFFFAOYSA-N 3-piperazin-1-ylpropan-1-amine Chemical compound NCCCN1CCNCC1 UVLSCMIEPPWCHZ-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229930195725 Mannitol Natural products 0.000 description 2
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 2
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229920005603 alternating copolymer Polymers 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- UKTKFEKWFZLRSK-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate Chemical compound C=CC=C.COC(=O)C(C)=C.COC(=O)C(C)=C UKTKFEKWFZLRSK-UHFFFAOYSA-N 0.000 description 2
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical compound OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 150000002429 hydrazines Chemical class 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 239000000594 mannitol Substances 0.000 description 2
- 235000010355 mannitol Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- WVJKHCGMRZGIJH-UHFFFAOYSA-N methanetriamine Chemical compound NC(N)N WVJKHCGMRZGIJH-UHFFFAOYSA-N 0.000 description 2
- GVOWHGSUZUUUDR-UHFFFAOYSA-N methyl N-methylanthranilate Chemical compound CNC1=CC=CC=C1C(=O)OC GVOWHGSUZUUUDR-UHFFFAOYSA-N 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- DTSDBGVDESRKKD-UHFFFAOYSA-N n'-(2-aminoethyl)propane-1,3-diamine Chemical compound NCCCNCCN DTSDBGVDESRKKD-UHFFFAOYSA-N 0.000 description 2
- KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 2
- RAWJTXJPOXFMLG-UHFFFAOYSA-N n-(dicyclohexylmethyl)butan-2-amine Chemical compound C1CCCCC1C(NC(C)CC)C1CCCCC1 RAWJTXJPOXFMLG-UHFFFAOYSA-N 0.000 description 2
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000002898 organic sulfur compounds Chemical class 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- SCHTXWZFMCQMBH-UHFFFAOYSA-N pentane-1,3,5-triamine Chemical compound NCCC(N)CCN SCHTXWZFMCQMBH-UHFFFAOYSA-N 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920003226 polyurethane urea Polymers 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229920006301 statistical copolymer Polymers 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 2
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- QBNSDCDYOGZSDP-ZXFLCMHBSA-N (1r,3r,4r)-2,2-dimethylbicyclo[2.2.1]heptane-3,4-diamine Chemical compound C1C[C@]2(N)[C@H](N)C(C)(C)[C@H]1C2 QBNSDCDYOGZSDP-ZXFLCMHBSA-N 0.000 description 1
- IFNWESYYDINUHV-OLQVQODUSA-N (2s,6r)-2,6-dimethylpiperazine Chemical compound C[C@H]1CNC[C@@H](C)N1 IFNWESYYDINUHV-OLQVQODUSA-N 0.000 description 1
- ZBUAAIKWLHWSPO-UHFFFAOYSA-N (Z)-20-aminoicos-11-en-1-ol Chemical compound OCCCCCCCCCCC=C/CCCCCCCCN ZBUAAIKWLHWSPO-UHFFFAOYSA-N 0.000 description 1
- UKGJZDSUJSPAJL-YPUOHESYSA-N (e)-n-[(1r)-1-[3,5-difluoro-4-(methanesulfonamido)phenyl]ethyl]-3-[2-propyl-6-(trifluoromethyl)pyridin-3-yl]prop-2-enamide Chemical compound CCCC1=NC(C(F)(F)F)=CC=C1\C=C\C(=O)N[C@H](C)C1=CC(F)=C(NS(C)(=O)=O)C(F)=C1 UKGJZDSUJSPAJL-YPUOHESYSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-butanediol Substances OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- PVXVWWANJIWJOO-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine Chemical compound CCNC(C)CC1=CC=C2OCOC2=C1 PVXVWWANJIWJOO-UHFFFAOYSA-N 0.000 description 1
- CWKVFRNCODQPDB-UHFFFAOYSA-N 1-(2-aminoethylamino)propan-2-ol Chemical compound CC(O)CNCCN CWKVFRNCODQPDB-UHFFFAOYSA-N 0.000 description 1
- DOJHEVQGYQYOSP-UHFFFAOYSA-N 1-(3-piperazin-1-ylpropyl)piperazine Chemical compound C1CNCCN1CCCN1CCNCC1 DOJHEVQGYQYOSP-UHFFFAOYSA-N 0.000 description 1
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 description 1
- FKOMNQCOHKHUCP-UHFFFAOYSA-N 1-[n-(2-hydroxypropyl)anilino]propan-2-ol Chemical compound CC(O)CN(CC(C)O)C1=CC=CC=C1 FKOMNQCOHKHUCP-UHFFFAOYSA-N 0.000 description 1
- NILQLFBWTXNUOE-UHFFFAOYSA-N 1-aminocyclopentanecarboxylic acid Chemical compound OC(=O)C1(N)CCCC1 NILQLFBWTXNUOE-UHFFFAOYSA-N 0.000 description 1
- DLSMMGKXYMQDMN-UHFFFAOYSA-N 1-cyclohexyl-2-methylhydrazine Chemical compound CNNC1CCCCC1 DLSMMGKXYMQDMN-UHFFFAOYSA-N 0.000 description 1
- MNZGWEVNYBSBHA-UHFFFAOYSA-N 1-ethyl-2-phenylhydrazine Chemical compound CCNNC1=CC=CC=C1 MNZGWEVNYBSBHA-UHFFFAOYSA-N 0.000 description 1
- HYWXQFOMMUKUAV-UHFFFAOYSA-N 1-methyl-1-(4-nitrophenyl)hydrazine Chemical compound CN(N)C1=CC=C([N+]([O-])=O)C=C1 HYWXQFOMMUKUAV-UHFFFAOYSA-N 0.000 description 1
- WDKZAGLJEFIVOR-UHFFFAOYSA-N 1-n,1-n-bis(2-aminoethyl)propane-1,2-diamine Chemical compound CC(N)CN(CCN)CCN WDKZAGLJEFIVOR-UHFFFAOYSA-N 0.000 description 1
- LIQNYLUOMSQISE-UHFFFAOYSA-N 1-n,4-n-di(butan-2-yl)cyclohexane-1,4-diamine Chemical compound CCC(C)NC1CCC(NC(C)CC)CC1 LIQNYLUOMSQISE-UHFFFAOYSA-N 0.000 description 1
- XDCMXOFKBHKHGP-UHFFFAOYSA-N 1-n,4-n-dimethylcyclohexane-1,4-diamine Chemical compound CNC1CCC(NC)CC1 XDCMXOFKBHKHGP-UHFFFAOYSA-N 0.000 description 1
- WOFPSIYWQQSWHC-UHFFFAOYSA-N 1-n-(10-aminodecyl)hexane-1,2,6-triamine Chemical compound NCCCCCCCCCCNCC(N)CCCCN WOFPSIYWQQSWHC-UHFFFAOYSA-N 0.000 description 1
- LCMYIHQLACAQQC-UHFFFAOYSA-N 1-n-(6-aminohexyl)hexane-1,2,6-triamine Chemical compound NCCCCCCNCC(N)CCCCN LCMYIHQLACAQQC-UHFFFAOYSA-N 0.000 description 1
- RBPFFCYPDGLOKM-UHFFFAOYSA-N 1-n-[3-[4-(3-aminopropylamino)butylamino]propyl]hexane-1,2,6-triamine Chemical compound NCCCCC(N)CNCCCNCCCCNCCCN RBPFFCYPDGLOKM-UHFFFAOYSA-N 0.000 description 1
- GXSXWRGSVNWTCR-UHFFFAOYSA-N 1-n-[4-(3-aminopropylamino)butyl]hexane-1,2,6-triamine Chemical compound NCCCCC(N)CNCCCCNCCCN GXSXWRGSVNWTCR-UHFFFAOYSA-N 0.000 description 1
- TXJUTRJFNRYTHH-UHFFFAOYSA-N 1h-3,1-benzoxazine-2,4-dione Chemical compound C1=CC=C2C(=O)OC(=O)NC2=C1 TXJUTRJFNRYTHH-UHFFFAOYSA-N 0.000 description 1
- DDHUNHGZUHZNKB-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diamine Chemical compound NCC(C)(C)CN DDHUNHGZUHZNKB-UHFFFAOYSA-N 0.000 description 1
- NDYJEAUUNHDJMC-UHFFFAOYSA-N 2,2-diphenylpropane-1,3-diol Chemical compound C=1C=CC=CC=1C(CO)(CO)C1=CC=CC=C1 NDYJEAUUNHDJMC-UHFFFAOYSA-N 0.000 description 1
- JYKLTPIGDOBKIA-UHFFFAOYSA-N 2,3,5,6-tetramethylcyclohexane-1,4-diamine Chemical compound CC1C(C)C(N)C(C)C(C)C1N JYKLTPIGDOBKIA-UHFFFAOYSA-N 0.000 description 1
- DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical compound NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-UHFFFAOYSA-N 0.000 description 1
- FWMCOYLFUCBELR-UHFFFAOYSA-N 2,4,6-tris[[hydroxymethyl(methyl)amino]methyl]phenol Chemical compound OCN(C)CC1=CC(CN(C)CO)=C(O)C(CN(C)CO)=C1 FWMCOYLFUCBELR-UHFFFAOYSA-N 0.000 description 1
- HGXVKAPCSIXGAK-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine;4,6-diethyl-2-methylbenzene-1,3-diamine Chemical compound CCC1=CC(CC)=C(N)C(C)=C1N.CCC1=CC(C)=C(N)C(CC)=C1N HGXVKAPCSIXGAK-UHFFFAOYSA-N 0.000 description 1
- NPNWQHCXLCJOIK-UHFFFAOYSA-N 2,5-dimethylheptane-1,4,7-triamine Chemical compound NCC(C)CC(N)C(C)CCN NPNWQHCXLCJOIK-UHFFFAOYSA-N 0.000 description 1
- OQYKKQQLTKPGSG-UHFFFAOYSA-N 2,5-dimethylhexane-1,6-diol Chemical compound OCC(C)CCC(C)CO OQYKKQQLTKPGSG-UHFFFAOYSA-N 0.000 description 1
- ZWNMRZQYWRLGMM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diol Chemical compound CC(C)(O)CCC(C)(C)O ZWNMRZQYWRLGMM-UHFFFAOYSA-N 0.000 description 1
- NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 1
- SFOBILRNTDKDSK-UHFFFAOYSA-N 2,6,11-trimethyldodecane-2,6,11-triamine Chemical compound CC(C)(N)CCCCC(C)(N)CCCC(C)(C)N SFOBILRNTDKDSK-UHFFFAOYSA-N 0.000 description 1
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-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
- XOISOAJGMXHXPL-UHFFFAOYSA-N 2-(aminomethyl)cyclohexane-1-carboxylic acid Chemical compound NCC1CCCCC1C(O)=O XOISOAJGMXHXPL-UHFFFAOYSA-N 0.000 description 1
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
- MGUMZJAQENFQKN-UHFFFAOYSA-N 2-(cyclohexylamino)ethanol Chemical compound OCCNC1CCCCC1 MGUMZJAQENFQKN-UHFFFAOYSA-N 0.000 description 1
- MCIKGVLBLIZYRY-UHFFFAOYSA-N 2-(hexylamino)ethanol Chemical compound CCCCCCNCCO MCIKGVLBLIZYRY-UHFFFAOYSA-N 0.000 description 1
- UVYBWDBLVDZIOX-UHFFFAOYSA-N 2-(octylamino)ethanol Chemical compound CCCCCCCCNCCO UVYBWDBLVDZIOX-UHFFFAOYSA-N 0.000 description 1
- QJXHPFHKGPEMAM-UHFFFAOYSA-N 2-(pentadecylamino)ethanol Chemical compound CCCCCCCCCCCCCCCNCCO QJXHPFHKGPEMAM-UHFFFAOYSA-N 0.000 description 1
- UCANFCXAKYMFGA-UHFFFAOYSA-N 2-Propenyl 2-aminobenzoate Chemical compound NC1=CC=CC=C1C(=O)OCC=C UCANFCXAKYMFGA-UHFFFAOYSA-N 0.000 description 1
- GFIWSSUBVYLTRF-UHFFFAOYSA-N 2-[2-(2-hydroxyethylamino)ethylamino]ethanol Chemical compound OCCNCCNCCO GFIWSSUBVYLTRF-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- GOZCAZWSEYCAPZ-UHFFFAOYSA-N 2-[2-(hexylamino)ethoxy]ethanol Chemical compound CCCCCCNCCOCCO GOZCAZWSEYCAPZ-UHFFFAOYSA-N 0.000 description 1
- HYYXWPRMMXSTCZ-UHFFFAOYSA-N 2-[2-[2-[3-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]cyclohexyl]oxyethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCOC1CCCC(OCCOCCOCCO)C1 HYYXWPRMMXSTCZ-UHFFFAOYSA-N 0.000 description 1
- XQFZOYSPPFLGEZ-UHFFFAOYSA-N 2-[2-[2-[3-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]phenoxy]ethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCOC1=CC=CC(OCCOCCOCCO)=C1 XQFZOYSPPFLGEZ-UHFFFAOYSA-N 0.000 description 1
- KTTZPZXHYJYUHY-UHFFFAOYSA-N 2-[2-[3-[2-(2-hydroxyethoxy)ethoxy]cyclohexyl]oxyethoxy]ethanol Chemical compound OCCOCCOC1CCCC(OCCOCCO)C1 KTTZPZXHYJYUHY-UHFFFAOYSA-N 0.000 description 1
- VQTAPEISMWLANM-UHFFFAOYSA-N 2-[2-[3-[2-(2-hydroxyethoxy)ethoxy]phenoxy]ethoxy]ethanol Chemical compound OCCOCCOC1=CC=CC(OCCOCCO)=C1 VQTAPEISMWLANM-UHFFFAOYSA-N 0.000 description 1
- CYOIAXUAIXVWMU-UHFFFAOYSA-N 2-[2-aminoethyl(2-hydroxyethyl)amino]ethanol Chemical compound NCCN(CCO)CCO CYOIAXUAIXVWMU-UHFFFAOYSA-N 0.000 description 1
- QVLYTZPREKNPDH-UHFFFAOYSA-N 2-[3-(2-hydroxyethoxy)cyclohexyl]oxyethanol Chemical compound OCCOC1CCCC(OCCO)C1 QVLYTZPREKNPDH-UHFFFAOYSA-N 0.000 description 1
- IAXFZZHBFXRZMT-UHFFFAOYSA-N 2-[3-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=CC(OCCO)=C1 IAXFZZHBFXRZMT-UHFFFAOYSA-N 0.000 description 1
- WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
- HLZQZSVQCJMCJE-UHFFFAOYSA-N 2-[amino(propyl)amino]ethanol Chemical compound CCCN(N)CCO HLZQZSVQCJMCJE-UHFFFAOYSA-N 0.000 description 1
- GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 description 1
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- LZDXRPVSAKWYDH-UHFFFAOYSA-N 2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical compound CCC(CO)(CO)COCC=C LZDXRPVSAKWYDH-UHFFFAOYSA-N 0.000 description 1
- VNAWKNVDKFZFSU-UHFFFAOYSA-N 2-ethyl-2-methylpropane-1,3-diol Chemical compound CCC(C)(CO)CO VNAWKNVDKFZFSU-UHFFFAOYSA-N 0.000 description 1
- BPOSPHPRYDVTFU-UHFFFAOYSA-N 2-ethylheptane-1,3-diol Chemical compound CCCCC(O)C(CC)CO BPOSPHPRYDVTFU-UHFFFAOYSA-N 0.000 description 1
- BRAJXWGTZHCUJA-UHFFFAOYSA-N 2-ethylpropane-1,2,3-triamine Chemical compound CCC(N)(CN)CN BRAJXWGTZHCUJA-UHFFFAOYSA-N 0.000 description 1
- MWCBGWLCXSUTHK-UHFFFAOYSA-N 2-methylbutane-1,4-diol Chemical compound OCC(C)CCO MWCBGWLCXSUTHK-UHFFFAOYSA-N 0.000 description 1
- KHBBRIBQJGWUOW-UHFFFAOYSA-N 2-methylcyclohexane-1,3-diamine Chemical compound CC1C(N)CCCC1N KHBBRIBQJGWUOW-UHFFFAOYSA-N 0.000 description 1
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 description 1
- JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 description 1
- KCIASSMHRZGLCT-UHFFFAOYSA-N 2-methylprop-1-ene oxepan-2-one Chemical compound CC(C)=C.O=C1CCCCCO1 KCIASSMHRZGLCT-UHFFFAOYSA-N 0.000 description 1
- VGUXXYXSILZEMR-UHFFFAOYSA-N 2-n,2-n-bis(2-aminoethyl)propane-1,2-diamine Chemical compound NCC(C)N(CCN)CCN VGUXXYXSILZEMR-UHFFFAOYSA-N 0.000 description 1
- ASGOOCMKHNKTQP-UHFFFAOYSA-N 2-n-(2,2-diaminoethyl)ethane-1,1,1,2-tetramine Chemical compound NC(N)CNCC(N)(N)N ASGOOCMKHNKTQP-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 description 1
- AJHPGXZOIAYYDW-UHFFFAOYSA-N 3-(2-cyanophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)=O)CC1=CC=CC=C1C#N AJHPGXZOIAYYDW-UHFFFAOYSA-N 0.000 description 1
- OENOEHZCGVEKHK-UHFFFAOYSA-N 3-(2-hydroxyethyl)-3-methylpentane-1,5-diol Chemical compound OCCC(C)(CCO)CCO OENOEHZCGVEKHK-UHFFFAOYSA-N 0.000 description 1
- IFPJFPROEPHIMI-UHFFFAOYSA-N 3-(2-hydroxyethylamino)propan-1-ol Chemical compound OCCCNCCO IFPJFPROEPHIMI-UHFFFAOYSA-N 0.000 description 1
- SORYQVTVJSQUPM-UHFFFAOYSA-N 3-(4-methylphenyl)-1,3-benzoxazine-2,4-dione Chemical compound C1=CC(C)=CC=C1N1C(=O)C(C=CC=C2)=C2OC1=O SORYQVTVJSQUPM-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- LYRQHZCLXXBANV-UHFFFAOYSA-N 3-(aminomethyl)cyclohexane-1-carboxylic acid Chemical compound NCC1CCCC(C(O)=O)C1 LYRQHZCLXXBANV-UHFFFAOYSA-N 0.000 description 1
- XNLUYEOBGUSDOZ-UHFFFAOYSA-N 3-[2-aminoethyl(3-hydroxypropyl)amino]propan-1-ol Chemical compound OCCCN(CCN)CCCO XNLUYEOBGUSDOZ-UHFFFAOYSA-N 0.000 description 1
- XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical compound NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 description 1
- FDGAEAYZQQCBRN-UHFFFAOYSA-N 3-amino-4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1N FDGAEAYZQQCBRN-UHFFFAOYSA-N 0.000 description 1
- XKFIFYROMAAUDL-UHFFFAOYSA-N 3-amino-4-methylbenzoic acid Chemical compound CC1=CC=C(C(O)=O)C=C1N XKFIFYROMAAUDL-UHFFFAOYSA-N 0.000 description 1
- YHFYRVZIONNYSM-UHFFFAOYSA-N 3-aminocyclopentan-1-ol Chemical compound NC1CCC(O)C1 YHFYRVZIONNYSM-UHFFFAOYSA-N 0.000 description 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- KDHWOCLBMVSZPG-UHFFFAOYSA-N 3-imidazol-1-ylpropan-1-amine Chemical compound NCCCN1C=CN=C1 KDHWOCLBMVSZPG-UHFFFAOYSA-N 0.000 description 1
- UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- NPFSLDXBLIZWGQ-UHFFFAOYSA-N 4-(4-aminobutylamino)butan-2-ol Chemical compound CC(O)CCNCCCCN NPFSLDXBLIZWGQ-UHFFFAOYSA-N 0.000 description 1
- HMJBXEZHJUYJQY-UHFFFAOYSA-N 4-(aminomethyl)octane-1,8-diamine Chemical compound NCCCCC(CN)CCCN HMJBXEZHJUYJQY-UHFFFAOYSA-N 0.000 description 1
- DLYLVPHSKJVGLG-UHFFFAOYSA-N 4-(cyclohexylmethyl)cyclohexane-1,1-diamine Chemical compound C1CC(N)(N)CCC1CC1CCCCC1 DLYLVPHSKJVGLG-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- HCFRWBBJISAZNK-UHFFFAOYSA-N 4-Hydroxycyclohexylcarboxylic acid Chemical compound OC1CCC(C(O)=O)CC1 HCFRWBBJISAZNK-UHFFFAOYSA-N 0.000 description 1
- IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 1
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
- KZTROCYBPMKGAW-UHFFFAOYSA-N 4-[[4-amino-3,5-di(propan-2-yl)phenyl]methyl]-2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=C(N)C(C(C)C)=CC(CC=2C=C(C(N)=C(C(C)C)C=2)C(C)C)=C1 KZTROCYBPMKGAW-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- KMVPXBDOWDXXEN-UHFFFAOYSA-N 4-nitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1 KMVPXBDOWDXXEN-UHFFFAOYSA-N 0.000 description 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
- KGWBKWFJRZTJSV-UHFFFAOYSA-N 5-[[3,5-bis(ethylamino)cyclohexyl]methyl]-1-n,3-n-diethylcyclohexane-1,3-diamine Chemical compound C1C(NCC)CC(NCC)CC1CC1CC(NCC)CC(NCC)C1 KGWBKWFJRZTJSV-UHFFFAOYSA-N 0.000 description 1
- RUCHWTKMOWXHLU-UHFFFAOYSA-N 5-nitroanthranilic acid Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C(O)=O RUCHWTKMOWXHLU-UHFFFAOYSA-N 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- DESUDZIADGQZIJ-UHFFFAOYSA-N 6-amino-2-bromo-3-methylbenzoic acid Chemical compound CC1=CC=C(N)C(C(O)=O)=C1Br DESUDZIADGQZIJ-UHFFFAOYSA-N 0.000 description 1
- WOVXZBSJJJIRBI-UHFFFAOYSA-N 6-ethyl-3,9-dimethylundecane-3,6,9-triamine Chemical compound CCC(C)(N)CCC(N)(CC)CCC(C)(N)CC WOVXZBSJJJIRBI-UHFFFAOYSA-N 0.000 description 1
- WWUBAHSWMPFIQZ-UHFFFAOYSA-N 6-nitro-1h-3,1-benzoxazine-2,4-dione Chemical compound N1C(=O)OC(=O)C2=CC([N+](=O)[O-])=CC=C21 WWUBAHSWMPFIQZ-UHFFFAOYSA-N 0.000 description 1
- 241000226585 Antennaria plantaginifolia Species 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- MPOXBLGUTAXAMQ-UHFFFAOYSA-N C(C(=C)C)(=O)OC(C)(C)C.CC(C)=C Chemical compound C(C(=C)C)(=O)OC(C)(C)C.CC(C)=C MPOXBLGUTAXAMQ-UHFFFAOYSA-N 0.000 description 1
- STQUCVHZTUYETO-UHFFFAOYSA-N C(CN)N.OC=CC Chemical compound C(CN)N.OC=CC STQUCVHZTUYETO-UHFFFAOYSA-N 0.000 description 1
- PCKIJMDRHBCHHE-UHFFFAOYSA-N CC(C)(CC(C)O)O.CC(CC(C)O)O Chemical compound CC(C)(CC(C)O)O.CC(CC(C)O)O PCKIJMDRHBCHHE-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical class NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- KFEZETDKFSMLMG-UHFFFAOYSA-N Cyclohexyl 2-aminobenzoate Chemical compound NC1=CC=CC=C1C(=O)OC1CCCCC1 KFEZETDKFSMLMG-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- TWLLPUMZVVGILS-UHFFFAOYSA-N Ethyl 2-aminobenzoate Chemical compound CCOC(=O)C1=CC=CC=C1N TWLLPUMZVVGILS-UHFFFAOYSA-N 0.000 description 1
- FDCOHGHEADZEGF-OCEACIFDSA-N Glycerol 1,3-dihexadecanoate 2-(9Z-octadecenoate) Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C\CCCCCCCC FDCOHGHEADZEGF-OCEACIFDSA-N 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 229920005479 Lucite® Polymers 0.000 description 1
- QMMZSJPSPRTHGB-UHFFFAOYSA-N MDEA Natural products CC(C)CCCCC=CCC=CC(O)=O QMMZSJPSPRTHGB-UHFFFAOYSA-N 0.000 description 1
- 241001112258 Moca Species 0.000 description 1
- VRPPEXGZBZBARW-UHFFFAOYSA-N N-(2-aminoethyl)butane-1,4-diamine Chemical compound NCCCCNCCN VRPPEXGZBZBARW-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- KJMRWDHBVCNLTQ-UHFFFAOYSA-N N-methylisatoic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)N(C)C2=C1 KJMRWDHBVCNLTQ-UHFFFAOYSA-N 0.000 description 1
- XNJODAJXVOZTAQ-QGAMPUOQSA-N NC(C1CCCCC1)C1CCCCC1.C(C)/C(/C(=O)O)=C/C(=O)O Chemical compound NC(C1CCCCC1)C1CCCCC1.C(C)/C(/C(=O)O)=C/C(=O)O XNJODAJXVOZTAQ-QGAMPUOQSA-N 0.000 description 1
- KEIXAJPOCIXHRG-QGAMPUOQSA-N NC1(CCCCC1)C(C1CCCCC1)(C)C.C(C)/C(/C(=O)O)=C/C(=O)O Chemical compound NC1(CCCCC1)C(C1CCCCC1)(C)C.C(C)/C(/C(=O)O)=C/C(=O)O KEIXAJPOCIXHRG-QGAMPUOQSA-N 0.000 description 1
- MKLQDVIRROCWKX-UHFFFAOYSA-N NN.ClC1=CC=C(C=C1)O Chemical compound NN.ClC1=CC=C(C=C1)O MKLQDVIRROCWKX-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- GNVQOBONVDMFSV-UHFFFAOYSA-N OCCCC(CCNN)CCCO Chemical compound OCCCC(CCNN)CCCO GNVQOBONVDMFSV-UHFFFAOYSA-N 0.000 description 1
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- YXEBFFWTZWGHEY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohex-3-en-1-yl]methanol Chemical compound OCC1(CO)CCC=CC1 YXEBFFWTZWGHEY-UHFFFAOYSA-N 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- OTKFKCIRTBTDKK-UHFFFAOYSA-N [3-(aminomethyl)-5-bicyclo[2.2.1]heptanyl]methanamine Chemical compound C1C(CN)C2C(CN)CC1C2 OTKFKCIRTBTDKK-UHFFFAOYSA-N 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- OXIKYYJDTWKERT-UHFFFAOYSA-N [4-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCC(CN)CC1 OXIKYYJDTWKERT-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- FQCJBRVTYJVAEF-UHFFFAOYSA-N [6-(hydroxymethyl)cyclohex-3-en-1-yl]methanol Chemical compound OCC1CC=CCC1CO FQCJBRVTYJVAEF-UHFFFAOYSA-N 0.000 description 1
- LONQTZORWVBHMK-UHFFFAOYSA-N [N].NN Chemical compound [N].NN LONQTZORWVBHMK-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 125000002015 acyclic group Chemical group 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- OFHCOWSQAMBJIW-AVJTYSNKSA-N alfacalcidol Chemical group C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C OFHCOWSQAMBJIW-AVJTYSNKSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000005103 alkyl silyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
- XXRGLCKZBCIEKO-DLMDZQPMSA-N azocine Chemical compound C/1=C/C=C\N=C/C=C\1 XXRGLCKZBCIEKO-DLMDZQPMSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- OTBHHUPVCYLGQO-UHFFFAOYSA-N bis(3-aminopropyl)amine Chemical compound NCCCNCCCN OTBHHUPVCYLGQO-UHFFFAOYSA-N 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- ASOSVKWACJAYKE-UHFFFAOYSA-N butan-2-yl 2-(methylamino)benzoate Chemical compound CCC(C)OC(=O)C1=CC=CC=C1NC ASOSVKWACJAYKE-UHFFFAOYSA-N 0.000 description 1
- KODVEKZCSDEPTL-UHFFFAOYSA-N butane-1,2,4-triamine Chemical compound NCCC(N)CN KODVEKZCSDEPTL-UHFFFAOYSA-N 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical group 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 150000003950 cyclic amides Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
- XMWRRBYSHRYNFR-UHFFFAOYSA-N decane-1,5,10-triamine Chemical compound NCCCCCC(N)CCCCN XMWRRBYSHRYNFR-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 125000006159 dianhydride group Chemical group 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- NZIJLQZOCMBLDE-UHFFFAOYSA-N heptadecane-1,8,17-triamine Chemical compound NCCCCCCCCCC(N)CCCCCCCN NZIJLQZOCMBLDE-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- MHIBEGOZTWERHF-UHFFFAOYSA-N heptane-1,1-diol Chemical compound CCCCCCC(O)O MHIBEGOZTWERHF-UHFFFAOYSA-N 0.000 description 1
- GDRJDUSGGPSMEI-UHFFFAOYSA-N heptane-1,4,7-triamine Chemical compound NCCCC(N)CCCN GDRJDUSGGPSMEI-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RPDQDBRTJIPWMJ-UHFFFAOYSA-N hexane-1,2,6-triamine Chemical compound NCCCCC(N)CN RPDQDBRTJIPWMJ-UHFFFAOYSA-N 0.000 description 1
- AXEYWFGSQDLHDX-UHFFFAOYSA-N hexane-1,3,6-triamine Chemical compound NCCCC(N)CCN AXEYWFGSQDLHDX-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- OHMBHFSEKCCCBW-UHFFFAOYSA-N hexane-2,5-diol Chemical compound CC(O)CCC(C)O OHMBHFSEKCCCBW-UHFFFAOYSA-N 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- NGXVMFCGYYHEGC-UHFFFAOYSA-N methyl 2-amino-3,5-dibromobenzoate Chemical compound COC(=O)C1=CC(Br)=CC(Br)=C1N NGXVMFCGYYHEGC-UHFFFAOYSA-N 0.000 description 1
- VZDNXXPBYLGWOS-UHFFFAOYSA-N methyl 3-aminobenzoate Chemical compound COC(=O)C1=CC=CC(N)=C1 VZDNXXPBYLGWOS-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 229940100573 methylpropanediol Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical group CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 1
- VHCPBLNDTKVHTI-UHFFFAOYSA-N n',n'-bis(2-aminoethyl)propane-1,3-diamine Chemical compound NCCCN(CCN)CCN VHCPBLNDTKVHTI-UHFFFAOYSA-N 0.000 description 1
- HIIFXBBGRNTKSC-UHFFFAOYSA-N n',n'-bis(aminomethyl)methanediamine Chemical compound NCN(CN)CN HIIFXBBGRNTKSC-UHFFFAOYSA-N 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- ZKKMLXOYLORBLV-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-ethylpropane-1,3-diamine Chemical compound NCCCN(CC)CCCN ZKKMLXOYLORBLV-UHFFFAOYSA-N 0.000 description 1
- RQSHNRYXVUXSJC-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-hexylpropane-1,3-diamine Chemical compound CCCCCCN(CCCN)CCCN RQSHNRYXVUXSJC-UHFFFAOYSA-N 0.000 description 1
- INAQHJUDGSEXDR-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-octylpropane-1,3-diamine Chemical compound CCCCCCCCN(CCCN)CCCN INAQHJUDGSEXDR-UHFFFAOYSA-N 0.000 description 1
- AEBNSTBDWXUNIE-UHFFFAOYSA-N n'-(3-aminopropyl)hexane-1,6-diamine Chemical compound NCCCCCCNCCCN AEBNSTBDWXUNIE-UHFFFAOYSA-N 0.000 description 1
- SCZVXVGZMZRGRU-UHFFFAOYSA-N n'-ethylethane-1,2-diamine Chemical compound CCNCCN SCZVXVGZMZRGRU-UHFFFAOYSA-N 0.000 description 1
- QHJABUZHRJTCAR-UHFFFAOYSA-N n'-methylpropane-1,3-diamine Chemical compound CNCCCN QHJABUZHRJTCAR-UHFFFAOYSA-N 0.000 description 1
- ODBJKENDOPPIFT-UHFFFAOYSA-N n,n'-bis(2-aminoethyl)butane-1,4-diamine Chemical compound NCCNCCCCNCCN ODBJKENDOPPIFT-UHFFFAOYSA-N 0.000 description 1
- DYUCNAMTUNGLAB-UHFFFAOYSA-N n,n'-bis(2-aminoethyl)hexane-1,6-diamine Chemical compound NCCNCCCCCCNCCN DYUCNAMTUNGLAB-UHFFFAOYSA-N 0.000 description 1
- FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-UHFFFAOYSA-N 0.000 description 1
- RYKLPZKUOJMKPR-UHFFFAOYSA-N n,n-bis(propylamino)methanamine Chemical compound CCCNN(C)NCCC RYKLPZKUOJMKPR-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- YZZTZUHVGICSCS-UHFFFAOYSA-N n-butan-2-yl-4-[[4-(butan-2-ylamino)phenyl]methyl]aniline Chemical compound C1=CC(NC(C)CC)=CC=C1CC1=CC=C(NC(C)CC)C=C1 YZZTZUHVGICSCS-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- FVXBCDWMKCEPCL-UHFFFAOYSA-N nonane-1,1-diol Chemical compound CCCCCCCCC(O)O FVXBCDWMKCEPCL-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XVDOIUGRNCYAJA-UHFFFAOYSA-N octadecane-1,9,10-triamine Chemical compound CCCCCCCCC(N)C(N)CCCCCCCCN XVDOIUGRNCYAJA-UHFFFAOYSA-N 0.000 description 1
- RGQVEMVVEFTMJD-UHFFFAOYSA-N octadecane-1,9,10-triol Chemical compound CCCCCCCCC(O)C(O)CCCCCCCCO RGQVEMVVEFTMJD-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- WPRDEDGZJLTOFJ-UHFFFAOYSA-N oxadiazin-4-imine Chemical class N=C1C=CON=N1 WPRDEDGZJLTOFJ-UHFFFAOYSA-N 0.000 description 1
- HXSACZWWBYWLIS-UHFFFAOYSA-N oxadiazine-4,5,6-trione Chemical class O=C1ON=NC(=O)C1=O HXSACZWWBYWLIS-UHFFFAOYSA-N 0.000 description 1
- 125000005702 oxyalkylene group Chemical class 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 0.000 description 1
- JCKCYPSMCQDSHT-UHFFFAOYSA-N pentyl 2-aminobenzoate Chemical compound CCCCCOC(=O)C1=CC=CC=C1N JCKCYPSMCQDSHT-UHFFFAOYSA-N 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- GHAIYFTVRRTBNG-UHFFFAOYSA-N piperazin-1-ylmethanamine Chemical compound NCN1CCNCC1 GHAIYFTVRRTBNG-UHFFFAOYSA-N 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- XNYADZUHUHIGRZ-UHFFFAOYSA-N propane-1,1,3-triamine Chemical compound NCCC(N)N XNYADZUHUHIGRZ-UHFFFAOYSA-N 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- PZZICILSCNDOKK-UHFFFAOYSA-N propane-1,2,3-triamine Chemical compound NCC(N)CN PZZICILSCNDOKK-UHFFFAOYSA-N 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical compound NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 description 1
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003512 tertiary amines Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- ZMCBYSBVJIMENC-UHFFFAOYSA-N tricaine Chemical compound CCOC(=O)C1=CC=CC(N)=C1 ZMCBYSBVJIMENC-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- NDFDKKKMPXHSJA-UHFFFAOYSA-N undecane-1,5,11-triamine Chemical compound NCCCCCCC(N)CCCCN NDFDKKKMPXHSJA-UHFFFAOYSA-N 0.000 description 1
- DQWFTGPZPKZMAB-UHFFFAOYSA-N undecane-1,6,11-triamine Chemical compound NCCCCCC(N)CCCCCN DQWFTGPZPKZMAB-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Polyurethanes Or Polyureas (AREA)
Abstract
【解決手段】エラストマー配合物を含むゴルフボールが開示される。エラストマー配合物は、ポリイソシアネートおよびテレチェリックポリマーの反応生成物であり、テレチェリックポリマーはイソシアネート反応性末端基、例えばヒドロキシル基および/またはアミン基を有する。このエラストマー配合物は、ゴルフボールの任意の1または複数の部分、例えば、内側コア層、中間コア層、外側コア層、中間層、カバー、内側カバー層、中間カバー層、および/または外側カバー層に用いることができる。
【選択図】なし
Description
ここでは、用語「アラリファチック」(araliphatic)、「アリール脂肪族」または「芳香族脂肪族」は、すべて、1または複数の芳香族部分と1または複数の脂肪族部分とを含む化合物を指す。ただし、反応可能な官能基、例えば、これに限定されないが、イソシアネート基、アミン基、およびヒドロキシ基が、直接に脂肪族部分に結合して芳香族部分には直接には結合しない。アラリファチック化合物の説明的な例は、o−、m−、およびp−テトラメチルキシレンジイソシアネート(TMXDI)である。
N,N’−1,2−エタンジイルビス−(1,3−プロパンジアミン)、1,5,8,12−テトラザドデカン)、ビス(アミノエチル)プロピレンジアミン、ビス(アミノエチル)ブチレンジアミン、ビス(アミノプロピル)ブチレンジアミン、ビス(アミノエチル)ヘキサメチレンジアミン、ビス(アミノプロピル)エキサメチレンジアミンを含む。他の高次の説明的な例は、テトラエチレンペンタミン(飽和も)、ペンタエチレンヘキサミン、ポリメチレン−ポリフェニルアミンを含む。
(i)トリオール、例えば、グリセロール、トリメチロールプロパンおよび/またはペンタエリトリトール;それらアルコールの低分子量アルコキシレート化生成物(例えばエトキシレート化またはポロパキシレート化トリメチロールプロパン、より具体的には、エチレンオキシドを550のOH数のトリメチロールプロパンに付加した生成物);または少なくともトリオールにジオールを混合したもの(例えば、エチレングリコールまたはプロプレングリコール)、および
(ii)上述のモル比の(メタ)アクリル酸。上記化合物の分子量は116から1000、例えば116から750または116から158である。
ジオールは、アルコキシレート化生成物(エチレンオキシド、プロピレンオキシドおよびC4−エーテルユニット)の形態で用いても良い。ポリエステルジオールを用いても良い。こららは、ジカルボン酸および/またはその無水物、エチレン系不飽和ジカルボン酸および/またはその無水物、およびラクトン(例えばε−カプロラクトン)を上述のジオールと反応させた反応生成物を含む。cc、co−ジヒドロキシポリアクリレート(例えば、GoldschmidtのTegomer(商標)BD1000)も適切である。
この開示内容のコアは、特定のゴルフボール構造に少なくとも一部依存して、種々の硬度を有し得る。コア硬度は、形成させた球体において測定したとき、少なくとも約15ショアA、好ましくは約30ショアA、約50ショアA−約90ショアD、約80ショアD以下、約30−約65ショアD、または約35−約60ショアDであってよい。この開示内容の中間層(1層以上)の硬度も、ボールの特定の構造に少なくとも一部依存して変化する。中間層の硬度は、約30ショアD以上、例えば50ショアD以上、約55ショアD以上、または約65ショアD以上であり、かつ、約90ショアD以下、例えば約80ショアD以下、または約70ショアD以下、または約55ショアD−約65ショアDであってよい。中間層がコア層よりも硬質であるようにできる。中間層硬度対コア硬度の比は、約2以下、例えば、約1.8以下または約1.3以下である。中間層の硬度はコア層の硬度と、ショアA、CまたはDで少なくとも1単位、例えば少なくとも3単位、または少なくとも5単位、または少なくとも8単位、または少なくとも10単位、または20単位未満、または10単位未満、または5単位未満だけ、異なるようにしても良い。
コアは、外側カバーよりも軟質であってよい。例えば、カバー硬度は約50−約80ショアDであってよく、コア硬度は約30−約50ショアDであってよく、硬度比は約1.55以下、または約1.25以下であってよい。
カバー層(例えば外側カバー層、内側カバー層、中間カバー層)の曲げ弾性率は任意の値でよく、例えば、上述の中間層について示した数値範囲であってよい。カバー層が50−60ショアDの硬度を有する場合、その曲げ弾性率は、55000−65000psi(3.792×105kPa−4.482×105kPa)であってよい。多層カバーでは、カバー層は実質的に同一の高度を有するが、曲げ弾性率は異なる。任意のカバー層の間の曲げ弾性率の差は10000psi以下、5000psi以下、または500psi以上、例えば、1000から2500psiであってよい。中間層対カバー層の曲げ弾性率の比は、約0.003−約50、例えば、0.006−4.5または0.11−4.5であってよい。
ゴルフボール部分の耐水性は、吸収(すなわち、特定の温度および湿度差のもとに所定期間さらしたのち増えた重量)および透過(すなわちASTM E96−00に従う水蒸気透過率(WVTR)、これは所定の厚さの材料中に単位面積当たり単位時間で特定の温度、湿度差の下で拡散した水蒸気の質量を指す)により把握できる。100%相対湿度および72°F(22.2℃)で7週間に亘ってモニターしたゴルフボール部分の質量増加は、0.15グラム以下、例えば、0.13グラム、0.09グラム、0.06グラム、0.03グラム、またはこれ以下である。ゴルフボール部分例えば外側または内側カバー層のWVTRは、38°C、90%相対湿度で、2g/(m2×日)以下、例えば0.45−0.95g/(m2×日)、0.01−0.9g/(m2×日)、またはそれ以下である。
Claims (20)
- 有機ラジカルはメチル、エチル、n−プロピル、n−ブチル、n−フェニル、n−ペンチル、n−ヘキシル、イソ−プロピル、イソ−ブチル、sec−ブチル、t−ブチル、ネオ−ペンチル、プロパンニトリル、またはマレエート基を有する請求項1記載のゴルフボール。
- 上記有機ラジカルはシクロペンチルまたはシクロヘキシル基を有する請求項1記載のゴルフボール。
- 上記有機ラジカルは、約1−20の炭素原子を有するハロゲン化または非ハロゲン化炭化水素ラジカル、あるいは、少なくとも1つのO、N、SまたはSiおよび1−12の炭素原子を有するハロゲン化または非ハロゲン化有機部分を有する請求項1記載のゴルフボール。
- 上記有機ラジカルは、−SCH3である請求項1記載のゴルフボール。
- 上記配合物は、ポリイソシアネートと、ポリオールテレチェリック、ポリアミンテレチェリックまたはアミノアルコールテレチェリックとから生成した少なくとも1つのプレポリマーを含む請求項1記載のゴルフボール。
- 上記配合物は、ポリイソシアネートおよびポリアミンから生成されたプレポリマーを含む請求項1記載のゴルフボール。
- 上記プレポリマーは実質的に飽和している請求項7記載のゴルフボール。
- 上記層は外側カバー層である請求項1記載のゴルフボール。
- 上記層は、上記コアおよび外側コア層の間の中間層である請求項1記載のゴルフボール。
- 上記層の厚さは0.005インチから0.125インチである請求項1記載のゴルフボール。
- 上記層の硬度は、20から80ショアDである請求項1記載のゴルフボール。
- 上記材料は熱可塑性である請求項1記載のゴルフボール。
- 上記材料は熱硬化性である請求項1記載のゴルフボール。
- コア、上記コアの回りに配される中間層、および上記中間層のまわりに配され0.005インチ以上の厚さの外側カバー層を具備するゴルフボールにおいて、
上記中間層は、1または複数の、酸コポリマー、酸ターポリマー、アイオノマー状コポリマー、アイオノマー状ターポリマー、改変アイオノマー、ポリウレタン、ポリ−エーテル−エステル、ポリ−アミド−エーテル、ポリエーテル−尿素、シチレン−ブタジエン−スチレンブロックコポリマー、スチレン(エチレン−ブチレン)−スチレンブロックコポリマー、ポリアミド、ポリエステル、ポリオレフィン、ビニルアセテートまたはエポキシ官能化したモノマーをともなうエチレンコポリマー、マレイン酸無水物グラフト化またはエポキシ化を伴う官能化ポリマー、エラストマー、熱硬化性エラストマーの粉砕粉末、コポリエーテルエステル、コポリエステルエステル、コポリエーテルアミド、エラストマー状ポリオレフィン、スチレンジエンブロックコポリマー、およびこれらの水素化誘導体、コポリステルアミド、コポリエーテルウレタン、コポリエステルウレタン、コポリ尿素エタン、エポキシベースのポリウレタン、ポリカプロラクタムベースのポリウレタン、ポリ尿素、ポリカーボネートベースのポリウレタンフィラー、ポリアミド、ポリアミドブレンド、グラフト化および非グラフト化メタローセン触媒ポリオレフィンまたはポリアミド、ポリアミド/アイオノマーブレンド、ポリアミド/非アイオノマーブレンド、ポリフェニレンエーテル/アイオノマーブレンド、非メタローセンシングルサイト触媒を用いて生成した非イオンポリマー、またはこれらの混合物を有し;
上記カバー層はつぎの構造式のいずれかを有する少なくとも1つのポリアミンを有する配合物から製造された材料を有することを特徴とするゴルフボール。
Z1、Z2およびZ4は同一または異なるラジカルであって、ハロゲンまたは約1−60の炭素原子の有機ラジカルを有するもの;
Z3は水素、ハロゲン、または約1−60の炭素原子の有機ラジカルである。 - 上記層の厚さは0.005インチから0.125インチであり、あるいは、上記層の硬度は、20から80ショアDである請求項16記載のゴルフボール。
- コアおよび上記コアの回りに配される少なくとも1つの層を具備するゴルフボールであって、上記層はつぎの構造式のいずれかを有する少なくとも1つのポリアミンを有する配合物から製造される材料を有することを特徴とするゴルフボール。
Z1からZ4がつぎの1)−5)のいずれかを満たす同一または異なるラジカルである。1)Z1およびZ4は、同一または異なる、ハロゲンまたは約1−60の炭素原子の有機ラジカルである。
2)Z1、Z2およびZ4は、同一または異なる、ハロゲンまたは約1−60の炭素原子の有機ラジカルである。
3)Z1、Z2およびZ3は、同一または異なる、ハロゲンまたは約1−60の炭素原子の有機ラジカルである。
4)Z2、Z3およびZ4は、同一または異なる、ハロゲンまたは約1−60の炭素原子の有機ラジカルである。
5)Z1、Z2、Z3およびZ4は、同一または異なる、ハロゲンまたは約1−60の炭素原子の有機ラジカルである。 - 上記層の厚さは0.005インチから0.125インチである請求項18記載のゴルフボール。
- 上記層の硬度は、20から80ショアDである請求項1記載のゴルフボール。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/032411 | 2005-01-10 | ||
US11/032,411 US7259222B2 (en) | 2002-08-27 | 2005-01-10 | Compositions for use in golf balls |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2006192268A true JP2006192268A (ja) | 2006-07-27 |
JP2006192268A5 JP2006192268A5 (ja) | 2009-02-19 |
JP4934320B2 JP4934320B2 (ja) | 2012-05-16 |
Family
ID=36798769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006001975A Active JP4934320B2 (ja) | 2005-01-10 | 2006-01-10 | ゴルフボール用の配合物 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4934320B2 (ja) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008114069A (ja) * | 2006-11-01 | 2008-05-22 | Acushnet Co | 湿気耐性を増強させたカバー層を具備する多層ゴルフボール |
JP2010088797A (ja) * | 2008-10-10 | 2010-04-22 | Sri Sports Ltd | ゴルフボール |
JP2010094298A (ja) * | 2008-10-16 | 2010-04-30 | Sri Sports Ltd | ゴルフボール |
JP2010148536A (ja) * | 2008-12-24 | 2010-07-08 | Sri Sports Ltd | ゴルフボール |
JP2010148553A (ja) * | 2008-12-24 | 2010-07-08 | Sri Sports Ltd | ゴルフボール |
JP2012011171A (ja) * | 2010-06-30 | 2012-01-19 | Nike Internatl Ltd | 架橋結合熱可塑性ポリウレタンを含むゴルフボール |
US8366568B2 (en) | 2008-12-24 | 2013-02-05 | Sri Sports Limited | Golf ball |
US8399563B2 (en) | 2008-10-08 | 2013-03-19 | Sri Sports Limited | Golf ball |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4849544A (en) * | 1988-04-13 | 1989-07-18 | Ethyl Corporation | 1,3-Diaminocyclohexanes |
US20020098915A1 (en) * | 1997-05-27 | 2002-07-25 | Christopher Cavallaro | Thin, thermoset, polyurethane-covered golf ball with a dual core |
US20030144087A1 (en) * | 2001-06-26 | 2003-07-31 | Murali Rajagopalan | Golf balls comprising highly-neutralized acid polymers |
-
2006
- 2006-01-10 JP JP2006001975A patent/JP4934320B2/ja active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4849544A (en) * | 1988-04-13 | 1989-07-18 | Ethyl Corporation | 1,3-Diaminocyclohexanes |
US20020098915A1 (en) * | 1997-05-27 | 2002-07-25 | Christopher Cavallaro | Thin, thermoset, polyurethane-covered golf ball with a dual core |
US20030144087A1 (en) * | 2001-06-26 | 2003-07-31 | Murali Rajagopalan | Golf balls comprising highly-neutralized acid polymers |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008114069A (ja) * | 2006-11-01 | 2008-05-22 | Acushnet Co | 湿気耐性を増強させたカバー層を具備する多層ゴルフボール |
US8399563B2 (en) | 2008-10-08 | 2013-03-19 | Sri Sports Limited | Golf ball |
JP2010088797A (ja) * | 2008-10-10 | 2010-04-22 | Sri Sports Ltd | ゴルフボール |
JP2010094298A (ja) * | 2008-10-16 | 2010-04-30 | Sri Sports Ltd | ゴルフボール |
JP2010148536A (ja) * | 2008-12-24 | 2010-07-08 | Sri Sports Ltd | ゴルフボール |
JP2010148553A (ja) * | 2008-12-24 | 2010-07-08 | Sri Sports Ltd | ゴルフボール |
US8366568B2 (en) | 2008-12-24 | 2013-02-05 | Sri Sports Limited | Golf ball |
US8574097B2 (en) | 2008-12-24 | 2013-11-05 | Sri Sports Limited | Golf ball |
JP2012011171A (ja) * | 2010-06-30 | 2012-01-19 | Nike Internatl Ltd | 架橋結合熱可塑性ポリウレタンを含むゴルフボール |
Also Published As
Publication number | Publication date |
---|---|
JP4934320B2 (ja) | 2012-05-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4934320B2 (ja) | ゴルフボール用の配合物 | |
US7105624B2 (en) | Golf balls comprising polyaspartic esters | |
US8039573B2 (en) | Dual cured castable polyurethane system for use in golf balls | |
US8791224B2 (en) | Castable hydrophobic polyurea compositions for use in golf balls | |
US20070093317A1 (en) | Compositions for Golf Equipment | |
US7964668B2 (en) | Dual cured castable polyurea system for use in golf balls | |
US9643058B2 (en) | Dual cured castable hybrid polyurethane/polyurea system for use in golf balls | |
US20050143525A1 (en) | Compositions for golf balls | |
JP2000513595A (ja) | ゴルフボールカバー | |
JP2012011171A (ja) | 架橋結合熱可塑性ポリウレタンを含むゴルフボール | |
US20120080824A1 (en) | Cast polyurethane and polyurea covers for golf balls | |
JP4387605B2 (ja) | ゴルフボール | |
US20070173348A1 (en) | Compositions for Golf Equipment | |
US9206280B2 (en) | Dual cured castable system for use in golf balls | |
US20040220356A1 (en) | Compositions for golf equipment | |
US6949617B2 (en) | Golf balls comprising chiral diols or chiral cyclic ethers | |
US7259222B2 (en) | Compositions for use in golf balls | |
US20110136587A1 (en) | Golf balls comprising thermoplastic or thermoset composition having controlled gel time | |
US9018295B2 (en) | Cationic polyurea cover compositions for a multi-layer golf ball | |
US8927653B2 (en) | Cationic polyurea cover compositions for a multi-layer golf ball | |
US8455609B2 (en) | Castable polyurea formulation for golf ball covers | |
US20050272899A1 (en) | Compositions for golf equipment | |
US7534849B2 (en) | Compositions for use in golf balls | |
JP2010274115A (ja) | 脂環式イソシアネートに基づくゴルフボール用ポリ尿素カバー | |
US20200197753A1 (en) | Golf ball |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090105 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090105 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20120207 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20120220 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 4934320 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20150224 Year of fee payment: 3 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |