FI70180C - Maerkregistreringssystem - Google Patents

Maerkregistreringssystem Download PDF

Info

Publication number: FI70180C
Authority: FI; Finland
Prior art keywords: aliphatic; benzyl phthalate; chromogen; phthalate; solvent
Prior art date: 1978-05-31

Application number

FI791647A

Other languages

English (en)

Finnish (fi)

Other versions

FI70180B (fi

FI791647A7 (fi

Inventor

Pierre Jean Allart

Claude Andre Guillaume

Original Assignee

Monsanto Europe Sa

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.)

1978-05-31

Filing date

1979-05-24

Publication date

1986-09-15

1979-05-24 Application filed by Monsanto Europe Sa filed Critical Monsanto Europe Sa

1979-12-01 Publication of FI791647A7 publication Critical patent/FI791647A7/fi

1986-02-28 Publication of FI70180B publication Critical patent/FI70180B/fi

1986-09-15 Application granted granted Critical

1986-09-15 Publication of FI70180C publication Critical patent/FI70180C/fi

Links

239000002904 solvent Substances 0.000 claims abstract description 39
125000001931 aliphatic group Chemical group 0.000 claims abstract description 25
UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 claims abstract description 20
239000002253 acid Substances 0.000 claims abstract description 10
239000007788 liquid Substances 0.000 claims abstract description 4
DYFFAVRFJWYYQO-UHFFFAOYSA-N n-methyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(C)C1=CC=CC=C1 DYFFAVRFJWYYQO-UHFFFAOYSA-N 0.000 claims abstract 2
-1 cyanogen-diphenylmethanol Chemical compound 0.000 claims description 19
239000000463 material Substances 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 10
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 8
150000002148 esters Chemical class 0.000 claims description 7
239000000203 mixture Substances 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
125000005907 alkyl ester group Chemical group 0.000 claims description 3
239000003085 diluting agent Substances 0.000 claims description 3
230000004888 barrier function Effects 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims 1
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
239000004927 clay Substances 0.000 abstract description 15
QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical class C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 abstract description 3
239000003795 chemical substances by application Substances 0.000 abstract 2
230000001235 sensitizing effect Effects 0.000 abstract 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical class CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 14
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 7
YLZSIUVOIFJGQZ-UHFFFAOYSA-N bis[4-(dimethylamino)phenyl]methanol Chemical compound C1=CC(N(C)C)=CC=C1C(O)C1=CC=C(N(C)C)C=C1 YLZSIUVOIFJGQZ-UHFFFAOYSA-N 0.000 description 6
229940054021 anxiolytics diphenylmethane derivative Drugs 0.000 description 5
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 5
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical class C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 4
239000003350 kerosene Substances 0.000 description 4
239000003208 petroleum Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
238000005538 encapsulation Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
239000003094 microcapsule Substances 0.000 description 3
LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 2
ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 2
FXJVNINSOKCNJP-UHFFFAOYSA-M 4-methylbenzenesulfinate Chemical compound CC1=CC=C(S([O-])=O)C=C1 FXJVNINSOKCNJP-UHFFFAOYSA-M 0.000 description 2
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
125000006177 alkyl benzyl group Chemical group 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
239000002775 capsule Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
229910052625 palygorskite Inorganic materials 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000003825 pressing Methods 0.000 description 2
230000000717 retained effect Effects 0.000 description 2
ZXQVXEAZKZFEEP-UHFFFAOYSA-N 2,2-diphenylacetamide Chemical compound C=1C=CC=CC=1C(C(=O)N)C1=CC=CC=C1 ZXQVXEAZKZFEEP-UHFFFAOYSA-N 0.000 description 1
HHWGOADEDJUWSM-UHFFFAOYSA-N 2-(3-methyl-1-phenylbutoxy)carbonylbenzoic acid Chemical compound C=1C=CC=CC=1C(CC(C)C)OC(=O)C1=CC=CC=C1C(O)=O HHWGOADEDJUWSM-UHFFFAOYSA-N 0.000 description 1
WHHSHXMIKFVAEK-UHFFFAOYSA-N 2-o-benzyl 1-o-octyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 WHHSHXMIKFVAEK-UHFFFAOYSA-N 0.000 description 1
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 1
HKCCBTGBFGJZFG-UHFFFAOYSA-N 4-n-[4-(dimethylamino)phenyl]-1-n,1-n,4-n-trimethylbenzene-1,4-diamine Chemical class C1=CC(N(C)C)=CC=C1N(C)C1=CC=C(N(C)C)C=C1 HKCCBTGBFGJZFG-UHFFFAOYSA-N 0.000 description 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
206010024769 Local reaction Diseases 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000907663 Siproeta stelenes Species 0.000 description 1
229920000147 Styrene maleic anhydride Polymers 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
150000004074 biphenyls Chemical class 0.000 description 1
235000014121 butter Nutrition 0.000 description 1
238000001354 calcination Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical compound C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000005562 fading Methods 0.000 description 1
239000012530 fluid 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
150000008282 halocarbons Chemical class 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
XIKIUQUXDNHBFR-UHFFFAOYSA-N monobenzyl phthalate Chemical class OC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 XIKIUQUXDNHBFR-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 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
229920000620 organic polymer Polymers 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
125000005498 phthalate group Chemical class 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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 1
229920001059 synthetic polymer Polymers 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
150000001911 terphenyls Chemical class 0.000 description 1
238000011282 treatment Methods 0.000 description 1
239000008096 xylene Substances 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
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/165—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components characterised by the use of microcapsules; Special solvents for incorporating the ingredients
- B41M5/1655—Solvents

Landscapes

Color Printing (AREA)
Holo Graphy (AREA)
Optical Recording Or Reproduction (AREA)

FI791647A 1978-05-31 1979-05-24 Maerkregistreringssystem FI70180C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB2596078		1978-05-31
GB2596078		1978-05-31

Publications (3)

Publication Number	Publication Date
FI791647A7 FI791647A7 (fi)	1979-12-01
FI70180B FI70180B (fi)	1986-02-28
FI70180C true FI70180C (fi)	1986-09-15

Family

ID=10236113

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI791647A FI70180C (fi)	1978-05-31	1979-05-24	Maerkregistreringssystem

Country Status (7)

Country	Link
EP (1)	EP0005921B1 (fr)
JP (1)	JPS552090A (fr)
AT (1)	ATE1699T1 (fr)
AU (1)	AU528695B2 (fr)
CA (1)	CA1126026A (fr)
DE (1)	DE2963924D1 (fr)
FI (1)	FI70180C (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS57116690A (en) *	1981-01-13	1982-07-20	Ricoh Co Ltd	Thermal recording material
US5318940A (en) *	1992-12-02	1994-06-07	Koch Industries, Inc.	Carbonless paper solvent comprising diisopropylbiphenyl and triisopropylbiphenyl and products utilizing same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3016308A (en) *	1957-08-06	1962-01-09	Moore Business Forms Inc	Recording paper coated with microscopic capsules of coloring material, capsules and method of making
US3684549A (en) *	1970-10-12	1972-08-15	Joseph L Shank	Pressure sensitive transfer coating
JPS4931414A (fr) *	1972-07-05	1974-03-20
DE2334227A1 (de) *	1973-07-05	1975-01-23	Basf Ag	Griffestes, druckempfindliches durchschreibematerial
US4093278A (en) *	1976-12-27	1978-06-06	Monsanto Company	Dye solvents for pressure-sensitive copying systems

1979
- 1979-05-10 DE DE7979300801T patent/DE2963924D1/de not_active Expired
- 1979-05-10 AT AT79300801T patent/ATE1699T1/de active
- 1979-05-10 EP EP79300801A patent/EP0005921B1/fr not_active Expired
- 1979-05-24 FI FI791647A patent/FI70180C/fi not_active IP Right Cessation
- 1979-05-28 AU AU47478/79A patent/AU528695B2/en not_active Ceased
- 1979-05-29 JP JP6569279A patent/JPS552090A/ja active Pending
- 1979-05-30 CA CA328,731A patent/CA1126026A/fr not_active Expired

Also Published As

Publication number	Publication date
ATE1699T1 (de)	1982-11-15
AU4747879A (en)	1980-02-07
JPS552090A (en)	1980-01-09
EP0005921B1 (fr)	1982-10-27
FI70180B (fi)	1986-02-28
EP0005921A1 (fr)	1979-12-12
CA1126026A (fr)	1982-06-22
AU528695B2 (en)	1983-05-12
FI791647A7 (fi)	1979-12-01
DE2963924D1 (en)	1982-12-02

Legal Events

Date	Code	Title	Description
2004-08-31	MM	Patent lapsed	Owner name: MONSANTO EUROPE S.A.

Publication	Publication Date	Title
US4343652A (en)	1982-08-10	Chromogen solutions for pressure-sensitive mark-recording systems
FI62548B (fi)	1982-09-30	Saosom faergbildare anvaendbara diaminosubstituerade fluoranfoereningar
CS234013B2 (en)	1985-03-14	Chromogenic material and method of its making
FI71694C (fi)	1987-02-09	Tryckkaensligt eller vaermekaensligt uppteckningsmaterial.
EP0024898B1 (fr)	1984-06-27	Solvants, solutions et papiers copiants sensibles à la pression
FI70180B (fi)	1986-02-28	Maerkregistreringssystem
US3968320A (en)	1976-07-06	Dye solvents for pressure-sensitive record material
EP0102132A1 (fr)	1984-03-07	Matériau sensible à la chaleur réutilisable
US5476829A (en)	1995-12-19	Pressure-sensitive copying material
EP0902745B1 (fr)	2001-10-17	Composes chromogenes a base de sultine et leur utilisation dans des papiers autocopiants sans carbone
US3900217A (en)	1975-08-19	Pressure-sensitive copying paper
US4093278A (en)	1978-06-06	Dye solvents for pressure-sensitive copying systems
FI59220B (fi)	1981-03-31	Kopieringsmaterial
US3914470A (en)	1975-10-21	Capsule-carrying sheets or webs
US4411452A (en)	1983-10-25	Pressure-sensitive recording material
FI72686C (fi)	1987-07-10	Tryckkaensligt kopierpapper.
US4447075A (en)	1984-05-08	Pressure-sensitive recording material
EP0012579B1 (fr)	1983-06-22	Systèmes d'enregistrement sensibles à la pression et solutions à utiliser dans ces systèmes
JPH0325180Y2 (fr)	1991-05-31
JPS6333478B2 (fr)	1988-07-05
KR830001754B1 (ko)	1983-09-03	압력민감(Pressure-sensitive)복사지의 제조방법
JPS6361194B2 (fr)	1988-11-28
ES2102605T3 (es)	1997-08-01	Disolvente para uso en papel sin carbon que comprende diisopropil-bifenilo y triisopropil-bifenilo y productos que utilizan el mismo.
GB2099471A (en)	1982-12-08	Pressure-sensitive recording material
JPS58222880A (ja)	1983-12-24	感圧記録用顕色層