FI65190C - Uppteckningsmaterial - Google Patents

Uppteckningsmaterial Download PDF

Info

Publication number: FI65190C
Authority: FI; Finland
Prior art keywords: color; agent according; labeling agent; group; excipient
Prior art date: 1977-12-15

Application number

FI783739A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI65190B (fi

FI783739A7 (fi

Inventor

Henry Helmut Baum

Original Assignee

Appleton Paper Inc

Priority date (The priority date 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 date listed.)

1977-12-15

Filing date

1978-12-05

Publication date

1984-04-10

1978-12-05 Application filed by Appleton Paper Inc filed Critical Appleton Paper Inc

1979-06-16 Publication of FI783739A7 publication Critical patent/FI783739A7/fi

1983-12-30 Publication of FI65190B publication Critical patent/FI65190B/fi

1984-04-10 Application granted granted Critical

1984-04-10 Publication of FI65190C publication Critical patent/FI65190C/fi

Links

239000000546 pharmaceutical excipient Substances 0.000 claims description 38
239000006185 dispersion Substances 0.000 claims description 34
239000003795 chemical substances by application Substances 0.000 claims description 31
239000000203 mixture Substances 0.000 claims description 29
239000010410 layer Substances 0.000 claims description 28
239000002243 precursor Substances 0.000 claims description 27
-1 fluorane compound Chemical class 0.000 claims description 14
239000004372 Polyvinyl alcohol Substances 0.000 claims description 13
230000015572 biosynthetic process Effects 0.000 claims description 13
238000000354 decomposition reaction Methods 0.000 claims description 13
229920002451 polyvinyl alcohol Polymers 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 12
239000011230 binding agent Substances 0.000 claims description 12
239000002356 single layer Substances 0.000 claims description 10
WNZQDUSMALZDQF-UHFFFAOYSA-N isobenzofuranone Natural products C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims description 9
239000003550 marker Substances 0.000 claims description 9
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 8
XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
150000001768 cations Chemical class 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 5
AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
150000002596 lactones Chemical group 0.000 claims description 5
150000002989 phenols Chemical class 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
150000001450 anions Chemical class 0.000 claims description 4
125000003435 aroyl group Chemical group 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
SHWZFQPXYGHRKT-FDGPNNRMSA-N (z)-4-hydroxypent-3-en-2-one;nickel Chemical group [Ni].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O SHWZFQPXYGHRKT-FDGPNNRMSA-N 0.000 claims description 2
POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims description 2
XMOWAIVXKJWQBJ-UHFFFAOYSA-N 1-ethyl-2-methylindole Chemical compound C1=CC=C2N(CC)C(C)=CC2=C1 XMOWAIVXKJWQBJ-UHFFFAOYSA-N 0.000 claims description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 2
125000004104 aryloxy group Chemical group 0.000 claims description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
125000005841 biaryl group Chemical group 0.000 claims description 2
230000015556 catabolic process Effects 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
229910017052 cobalt Inorganic materials 0.000 claims description 2
239000010941 cobalt Substances 0.000 claims description 2
229910052802 copper Inorganic materials 0.000 claims description 2
239000010949 copper Substances 0.000 claims description 2
238000006731 degradation reaction Methods 0.000 claims description 2
230000000694 effects Effects 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
229910052742 iron Inorganic materials 0.000 claims description 2
239000011133 lead Substances 0.000 claims description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 2
229910052753 mercury Inorganic materials 0.000 claims description 2
UIEKYBOPAVTZKW-UHFFFAOYSA-L naphthalene-2-carboxylate;nickel(2+) Chemical compound [Ni+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 UIEKYBOPAVTZKW-UHFFFAOYSA-L 0.000 claims description 2
125000005609 naphthenate group Chemical group 0.000 claims description 2
229910052759 nickel Inorganic materials 0.000 claims description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
229940049964 oleate Drugs 0.000 claims description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
238000002372 labelling Methods 0.000 claims 24
238000001035 drying Methods 0.000 claims 3
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims 1
IPAJDLMMTVZVPP-UHFFFAOYSA-N Crystal violet lactone Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C=CC(=CC=2)N(C)C)C2=CC=C(N(C)C)C=C2C(=O)O1 IPAJDLMMTVZVPP-UHFFFAOYSA-N 0.000 claims 1
241000721662 Juniperus Species 0.000 claims 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
125000005506 phthalide group Chemical group 0.000 claims 1
125000001391 thioamide group Chemical group 0.000 claims 1
229940075466 undecylenate Drugs 0.000 claims 1
239000003086 colorant Substances 0.000 description 12
239000000126 substance Substances 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
238000002844 melting Methods 0.000 description 10
230000008018 melting Effects 0.000 description 10
239000011248 coating agent Substances 0.000 description 8
238000000576 coating method Methods 0.000 description 8
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical class F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 7
239000000463 material Substances 0.000 description 7
239000000155 melt Substances 0.000 description 6
230000002378 acidificating effect Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 4
238000002845 discoloration Methods 0.000 description 4
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
238000002156 mixing Methods 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
150000003556 thioamides Chemical class 0.000 description 3
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
SSIZLKDLDKIHEV-UHFFFAOYSA-N 2,6-dibromophenol Chemical compound OC1=C(Br)C=CC=C1Br SSIZLKDLDKIHEV-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
CONFUNYOPVYVDC-UHFFFAOYSA-N 3,3-bis(1-ethyl-2-methylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C3=C(C)N(C4=CC=CC=C43)CC)=C(C)N(CC)C2=C1 CONFUNYOPVYVDC-UHFFFAOYSA-N 0.000 description 2
TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
230000002411 adverse Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
125000004926 indolenyl group Chemical group 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
239000002245 particle Substances 0.000 description 2
125000006239 protecting group Chemical group 0.000 description 2
239000000700 radioactive tracer Substances 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
PKKDWPSOOQBWFB-UHFFFAOYSA-N 2,4-dichloro-6-[(3,5-dichloro-2-hydroxyphenyl)methyl]phenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1CC1=CC(Cl)=CC(Cl)=C1O PKKDWPSOOQBWFB-UHFFFAOYSA-N 0.000 description 1
QHCDYIRWTPEABF-UHFFFAOYSA-N 2-(4-chlorophenyl)ethanethioamide Chemical compound NC(=S)CC1=CC=C(Cl)C=C1 QHCDYIRWTPEABF-UHFFFAOYSA-N 0.000 description 1
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
UABVUROTLVCZSU-UHFFFAOYSA-N 2-phenoxypropanethioamide Chemical compound NC(=S)C(C)OC1=CC=CC=C1 UABVUROTLVCZSU-UHFFFAOYSA-N 0.000 description 1
WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
SVOBELCYOCEECO-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-methylphenyl)cyclohexyl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(C2(CCCCC2)C=2C=C(C)C(O)=CC=2)=C1 SVOBELCYOCEECO-UHFFFAOYSA-N 0.000 description 1
229940073735 4-hydroxy acetophenone Drugs 0.000 description 1
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
229920003043 Cellulose fiber Polymers 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
229920000881 Modified starch Polymers 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
206010057040 Temperature intolerance Diseases 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
IMHDGJOMLMDPJN-UHFFFAOYSA-N biphenyl-2,2'-diol Chemical group OC1=CC=CC=C1C1=CC=CC=C1O IMHDGJOMLMDPJN-UHFFFAOYSA-N 0.000 description 1
JFIOVJDNOJYLKP-UHFFFAOYSA-N bithionol Chemical compound OC1=C(Cl)C=C(Cl)C=C1SC1=CC(Cl)=CC(Cl)=C1O JFIOVJDNOJYLKP-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000004927 clay Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000006103 coloring component Substances 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000975 dye Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 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
230000005484 gravity Effects 0.000 description 1
150000002357 guanidines Chemical class 0.000 description 1
230000008543 heat sensitivity Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000012535 impurity Substances 0.000 description 1
125000001041 indolyl group Chemical group 0.000 description 1
235000000396 iron Nutrition 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
235000019426 modified starch Nutrition 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229920003986 novolac Polymers 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000013047 polymeric layer Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000010703 silicon Substances 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
238000003860 storage Methods 0.000 description 1
229910052712 strontium Inorganic materials 0.000 description 1
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000003232 water-soluble binding agent Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/34—Multicolour thermography
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/34—Multicolour thermography
- B41M5/345—Multicolour thermography by thermal transfer of dyes or pigments

Landscapes

Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Heat Sensitive Colour Forming Recording (AREA)
Color Printing (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

FI783739A 1977-12-15 1978-12-05 Uppteckningsmaterial FI65190C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US05/861,046 US4151748A (en)	1977-12-15	1977-12-15	Two color thermally sensitive record material system
US86104677		1977-12-15

Publications (3)

Publication Number	Publication Date
FI783739A7 FI783739A7 (fi)	1979-06-16
FI65190B FI65190B (fi)	1983-12-30
FI65190C true FI65190C (fi)	1984-04-10

Family

ID=25334724

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI783739A FI65190C (fi)	1977-12-15	1978-12-05	Uppteckningsmaterial

Country Status (20)

Country	Link
US (1)	US4151748A (de)
JP (1)	JPS5822357B2 (de)
AT (1)	AT373827B (de)
AU (1)	AU512720B2 (de)
BE (1)	BE872635A (de)
BR (1)	BR7808195A (de)
CA (1)	CA1121158A (de)
CH (1)	CH628574A5 (de)
DE (1)	DE2853120C2 (de)
DK (1)	DK561678A (de)
ES (1)	ES476050A1 (de)
FI (1)	FI65190C (de)
FR (1)	FR2415009B1 (de)
GB (2)	GB2011105B (de)
HK (2)	HK74484A (de)
IE (1)	IE47515B1 (de)
LU (1)	LU80650A1 (de)
NL (1)	NL170827C (de)
SE (1)	SE443535B (de)
ZA (1)	ZA786661B (de)

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JPS6043318B2 (ja) *	1978-07-18	1985-09-27	富士写真フイルム株式会社	感熱記録紙
JPS5527253A (en) *	1978-08-18	1980-02-27	Fuji Photo Film Co Ltd	Heat sensitizing recording sheet
US4286017A (en) *	1978-09-25	1981-08-25	Honshu Seishi Kabushiki Kaisha	Heat-sensitive recording paper
US4339207A (en) *	1978-09-28	1982-07-13	Akzona Incorporated	Temperature indicating compositions of matter
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JPS5581194A (en) *	1978-12-14	1980-06-18	Ricoh Co Ltd	Polychromic heat sensitive recording material
US4363664A (en) *	1980-01-25	1982-12-14	Sterling Drug Inc.	Novel compositions and processes
US4424990A (en)	1980-01-30	1984-01-10	Raychem Corporation	Thermochromic compositions
JPS5736694A (en) *	1980-08-15	1982-02-27	Mitsui Toatsu Chem Inc	Heat-sensitive recording material
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US4450023A (en) *	1981-06-12	1984-05-22	N.V. Raychem S.A.	Thermochromic composition
GB2116735B (en) *	1982-02-27	1986-11-26	Arthur R Zingher	Optically annotatable recording film
US4533640A (en) *	1984-02-21	1985-08-06	Shafer Jules A	Accumulated thermal exposure responder and method of use
US4711815A (en) *	1985-03-07	1987-12-08	Matsushita Electric Industrial Co., Ltd.	Recording medium
JP2566628B2 (ja) *	1988-08-24	1996-12-25	保土谷化学工業株式会社	フレオラン化合物および記録材料
JPH0647464B2 (ja) *	1990-03-20	1994-06-22	工業技術院長	示温材料及びその製造方法
GB9116626D0 (en) *	1991-08-01	1991-09-18	Univ Strathclyde	Improvements in and relating to ropes
US5290704A (en) *	1993-03-19	1994-03-01	Valence Technology, Inc.	Method of detecting organic solvent vapors
US5441418A (en) *	1993-05-20	1995-08-15	Binney & Smith Inc.	Thermochromic drawing device
US5514635A (en) *	1993-12-29	1996-05-07	Optum Corporation	Thermal writing surface and method for making the same
US5601867A (en) *	1995-06-22	1997-02-11	The United States Of America As Represented By The Secretary Of The Navy	Method and apparatus for generating fingerprints and other skin prints
US6294502B1 (en)	1998-05-22	2001-09-25	Bayer Aktiengesellschaft	Thermally-responsive record material
US6737274B1 (en)	1999-02-04	2004-05-18	United States Of America As Represented By The Secretary Of The Army	Comparator for time-temperature indicator
US6937153B2 (en) *	2002-06-28	2005-08-30	Appleton Papers Inc.	Thermal imaging paper laminate
US7094732B2 (en)	2002-10-02	2006-08-22	General Data Company, Inc.	Direct thermal imaging on plastic film
US7108190B2 (en) *	2003-02-28	2006-09-19	Appleton Papers Inc.	Token array and method employing authentication tokens bearing scent formulation information
US20040251309A1 (en) *	2003-06-10	2004-12-16	Appleton Papers Inc.	Token bearing magnetc image information in registration with visible image information
US20040259975A1 (en) *	2003-06-18	2004-12-23	Robillard Jean J.	System and method for forming photobleachable ink compositions
US7923412B1 (en) *	2004-02-12	2011-04-12	Kazdin Richard H	Creating background colors on thermal printing material
JP4851465B2 (ja)	2004-11-08	2012-01-11	フレッシュポイント・ホールディングス・ソシエテ・アノニム	時間温度指示装置
US8500895B2 (en)	2006-05-22	2013-08-06	Marken-Imaje Corporation	Methods of marking and related structures and compositions
US9418576B2 (en) *	2008-05-14	2016-08-16	Avery Dennison Corporation	Dissolvable thermal direct adhesive label and label assembly including the same
AU2009256212B2 (en)	2008-06-04	2015-12-10	Jp Laboratories Inc.	A monitoring system based on etching of metals
CN102077060B (zh)	2008-06-04	2014-10-29	G·帕特尔	一种基于腐蚀金属的监测系统
US9034790B2 (en)	2013-03-14	2015-05-19	Appvion, Inc.	Thermally-responsive record material
US9126451B2 (en)	2013-12-18	2015-09-08	Appvion, Inc.	Thermal recording materials
US9534156B2 (en)	2014-09-17	2017-01-03	Appvion, Inc.	Linerless record material
USD785287S1 (en) *	2015-08-04	2017-05-02	Dana Ronci	Backless bathing suit
KR102404989B1 (ko)	2018-03-23	2022-06-07	압비온 오퍼레이션즈, 인크.	상태의 선택적인 변화를 기초로 하는 직접적인 열적 기록 매체
US20200019077A1 (en)	2018-07-11	2020-01-16	Appvion Operations, Inc.	Media Adapted for Both Direct Thermal Recording and Memjet-Type Printing
EP4021734A1 (de)	2019-09-25	2022-07-06	Appvion, LLC	Direkte thermische aufzeichnungsmedien mit perforierten partikeln
US11376879B2 (en)	2019-11-22	2022-07-05	Appvion, Llc	Water-dispersible direct thermal or inkjet printable media
US12115803B2 (en)	2020-12-10	2024-10-15	Appvion, Llc	Fade-resistant water-dispersible phenol-free direct thermal media
US12151498B2 (en)	2020-12-10	2024-11-26	Appvion, Llc	Multi-purpose phenol-free direct thermal recording media
KR102945498B1 (ko)	2020-12-10	2026-03-30	압비온, 엘엘씨	다목적 무-페놀 직접 감열 기록 매체
DE202020006063U1 (de)	2020-12-10	2024-08-27	Appvion, Llc	Phenol-freie Mehrzweck-Thermodirekt-Aufzeichnungsmedien
JP2025528105A (ja)	2022-08-10	2025-08-26	アプヴィオンエルエルシー	耐油性のためのジアリール尿素の組合せを用いた直接感熱記録媒体

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US3471422A (en) *	1961-05-22	1969-10-07	Tempil Corp	Time-temperature responsive color changing typographic printing ink composition
BE623057A (de) *	1961-10-05
FR1373659A (fr) *	1961-10-05	1964-10-02	Ncr Co	Feuille de reproduction colorée thermiquement
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GB1337757A (en) *	1970-10-19	1973-11-21	Columbia Ribbon Carbon Mfg	Thermographic copy sheets
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US4010033A (en) *	1973-08-03	1977-03-01	Agence Nationale De Valorisation De La Recherche (Anvar)	Photosensitive layer and method of forming a photographic image therefrom
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FR2271938A1 (en) *	1974-05-24	1975-12-19	Issec	Thermochromic compsns. for thermographic recording - giving variety of colours with phenolic cpds. and chelating cpds.
JPS5223806B2 (de) *	1974-05-30	1977-06-27
JPS515792A (ja) *	1974-07-05	1976-01-17	Mitsubishi Heavy Ind Ltd	Mekanikarudoraibushikihansosochi
JPS5211231A (en) *	1975-07-16	1977-01-28	Matsushita Electric Ind Co Ltd	Thermoplastic resin composition
GB1563175A (en) *	1977-03-04	1980-03-19	Lawton W	Heat-sensitive recording composition with mixed colour precursors

1977
- 1977-12-15 US US05/861,046 patent/US4151748A/en not_active Expired - Lifetime
1978
- 1978-11-23 IE IE2316/78A patent/IE47515B1/en unknown
- 1978-11-27 ZA ZA00786661A patent/ZA786661B/xx unknown
- 1978-12-01 GB GB7846938A patent/GB2011105B/en not_active Expired
- 1978-12-01 GB GB8041273A patent/GB2064153B/en not_active Expired
- 1978-12-05 FI FI783739A patent/FI65190C/fi not_active IP Right Cessation
- 1978-12-06 SE SE7812551A patent/SE443535B/sv unknown
- 1978-12-07 AU AU42280/78A patent/AU512720B2/en not_active Expired
- 1978-12-08 DE DE2853120A patent/DE2853120C2/de not_active Expired
- 1978-12-08 BE BE192221A patent/BE872635A/xx not_active IP Right Cessation
- 1978-12-11 JP JP53152133A patent/JPS5822357B2/ja not_active Expired
- 1978-12-11 CA CA000317723A patent/CA1121158A/en not_active Expired
- 1978-12-12 AT AT0884278A patent/AT373827B/de not_active IP Right Cessation
- 1978-12-13 LU LU80650A patent/LU80650A1/xx unknown
- 1978-12-13 CH CH1267678A patent/CH628574A5/fr not_active IP Right Cessation
- 1978-12-14 DK DK561678A patent/DK561678A/da not_active Application Discontinuation
- 1978-12-14 NL NLAANVRAGE7812167,A patent/NL170827C/xx not_active IP Right Cessation
- 1978-12-14 FR FR7835233A patent/FR2415009B1/fr not_active Expired
- 1978-12-14 BR BR7808195A patent/BR7808195A/pt unknown
- 1978-12-15 ES ES476050A patent/ES476050A1/es not_active Expired
1984
- 1984-09-27 HK HK744/84A patent/HK74484A/xx unknown
- 1984-09-27 HK HK736/84A patent/HK73684A/xx unknown

Also Published As

Publication number	Publication date
SE7812551L (sv)	1979-06-16
IE782316L (en)	1979-06-15
DE2853120C2 (de)	1983-06-09
CA1121158A (en)	1982-04-06
NL170827C (nl)	1983-01-03
IE47515B1 (en)	1984-04-04
GB2011105A (en)	1979-07-04
AT373827B (de)	1984-02-27
NL7812167A (nl)	1979-06-19
GB2064153A (en)	1981-06-10
FI65190B (fi)	1983-12-30
DK561678A (da)	1979-06-16
FR2415009A1 (fr)	1979-08-17
US4151748A (en)	1979-05-01
FI783739A7 (fi)	1979-06-16
AU4228078A (en)	1979-06-21
ATA884278A (de)	1983-07-15
FR2415009B1 (fr)	1985-11-22
ES476050A1 (es)	1979-06-16
LU80650A1 (fr)	1979-04-13
BR7808195A (pt)	1979-07-31
JPS5822357B2 (ja)	1983-05-09
DE2853120A1 (de)	1979-06-21
AU512720B2 (en)	1980-10-23
CH628574A5 (fr)	1982-03-15
SE443535B (sv)	1986-03-03
BE872635A (fr)	1979-03-30
GB2064153B (en)	1983-01-12
NL170827B (nl)	1982-08-02
HK73684A (en)	1984-10-05
GB2011105B (en)	1982-05-26
JPS5492264A (en)	1979-07-21
HK74484A (en)	1984-10-05
ZA786661B (en)	1979-10-31

Legal Events

Date	Code	Title	Description
1996-07-11	MM	Patent lapsed
2004-08-31	MM	Patent lapsed	Owner name: APPLETON PAPERS INC.

Publication	Publication Date	Title
FI65190C (fi)	1984-04-10	Uppteckningsmaterial
US3244550A (en)	1966-04-05	Manifold sheets coated with lactone and related chromogenous compounds and reactive phenolics and method of marking
US3244549A (en)	1966-04-05	Manifold sheets coated with lactone and related chromogenous compounds and reactive phenolics and method of marking
US4246318A (en)	1981-01-20	Thermally-responsive record material
GB2171531A (en)	1986-08-28	Thermosensitive recording materials
FI93333B (fi)	1994-12-15	Lämpöherkkä tallennusmateriaali
FI62548C (fi)	1983-01-10	Saosom faergbildare anvaendbara diaminosubstituerade fluoranfoereningar
FI71694B (fi)	1986-10-31	Tryckkaensligt eller vaermekaensligt uppteckningsmaterial
FI87763C (fi)	1993-02-25	Som faergframkallare anvaenbara metallsalicylater och deras anvaendning
EP0112710B1 (de)	1987-08-26	Fluoranderivate
US4283458A (en)	1981-08-11	Heat-sensitive recording paper containing a novel electron accepting compound
US4289535A (en)	1981-09-15	Heat sensitive coating
FI68069B (fi)	1985-03-29	Tryck- eller vaermekaensligt uppteckningsmaterial
US5670446A (en)	1997-09-23	Sultine color-former compounds and their use in cabonless copy paper
GB2178440A (en)	1987-02-11	Fluoran derivatives and sensitive recording materials containing them
US4835133A (en)	1989-05-30	Recording material
US4520379A (en)	1985-05-28	Thermally-responsive record material
IE47516B1 (en)	1984-04-04	Record material
JPH01190484A (ja)	1989-07-31	記録材料
EP0997315A1 (de)	2000-05-03	Polycyclische Phenolen und wärmeempfindliche Aufzeichnungsmaterialien, die diese Verbindungen verwenden
JPH0346473B2 (de)	1991-07-16
JPH0775910B2 (ja)	1995-08-16	感熱記録体、フタリド誘導体、その製造方法およびその誘導体を用いた記録体
JPH0225369A (ja)	1990-01-26	記録材料
JPH0471891A (ja)	1992-03-06	記録材料
JPS58183755A (ja)	1983-10-27	フルオラン誘導体、その製造方法およびその誘導体を用いた記録体