CH423470A - Diazotypie-Kopierschicht, insbesondere zur Herstellung von Zwischenoriginalen - Google Patents

Diazotypie-Kopierschicht, insbesondere zur Herstellung von Zwischenoriginalen

Info

Publication number: CH423470A
Authority: CH; Switzerland
Prior art keywords: parts; weight; phenol; hydroxymethyl; sep
Prior art date: 1962-08-15

Application number

CH991963A

Other languages

German (de)

English (en)

Inventor

Heinz Dr Schlesinger

Johannes Dr Munder

Original Assignee

Kalle Ag

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.)

1962-08-15

Filing date

1963-08-12

Publication date

1966-10-31

1962-08-15 Priority claimed from DEK47504A external-priority patent/DE1242450B/de

1963-08-12 Application filed by Kalle Ag filed Critical Kalle Ag

1966-10-31 Publication of CH423470A publication Critical patent/CH423470A/de

Links

238000004519 manufacturing process Methods 0.000 title description 5
230000008878 coupling Effects 0.000 claims description 8
238000010168 coupling process Methods 0.000 claims description 8
238000005859 coupling reaction Methods 0.000 claims description 8
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
239000000306 component Substances 0.000 description 17
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
229940081735 acetylcellulose Drugs 0.000 description 5
229920002301 cellulose acetate Polymers 0.000 description 5
NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 4
BNPKZBJRGYESKG-UHFFFAOYSA-N 2-(hydroxymethyl)-3,5-dimethylphenol Chemical compound CC1=CC(C)=C(CO)C(O)=C1 BNPKZBJRGYESKG-UHFFFAOYSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 4
239000000203 mixture Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
-1 2-hydroxymethyl-3-methyl-5-isopropyl phenol Chemical compound 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 3
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
239000004327 boric acid Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000001035 drying Methods 0.000 description 3
QWBBPBRQALCEIZ-UHFFFAOYSA-N 2,3-dimethylphenol Chemical compound CC1=CC=CC(O)=C1C QWBBPBRQALCEIZ-UHFFFAOYSA-N 0.000 description 2
CIAYVZSVPJJMRU-UHFFFAOYSA-N 2,4-bis(hydroxymethyl)-3-methyl-6-propan-2-ylphenol Chemical compound CC(C)C1=CC(CO)=C(C)C(CO)=C1O CIAYVZSVPJJMRU-UHFFFAOYSA-N 0.000 description 2
NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
SKCXVVPAQZXSBM-UHFFFAOYSA-N 2-(hydroxymethyl)-3-methyl-6-propan-2-ylphenol Chemical compound CC(C)C1=CC=C(C)C(CO)=C1O SKCXVVPAQZXSBM-UHFFFAOYSA-N 0.000 description 2
TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 description 2
ZVXBWEIAIZEPGR-UHFFFAOYSA-N 4-(hydroxymethyl)-2,6-dimethylphenol Chemical compound CC1=CC(CO)=CC(C)=C1O ZVXBWEIAIZEPGR-UHFFFAOYSA-N 0.000 description 2
MYKSJJKGFCGVMF-UHFFFAOYSA-N 6-(hydroxymethyl)-2,3-dimethylphenol Chemical compound CC1=CC=C(CO)C(O)=C1C MYKSJJKGFCGVMF-UHFFFAOYSA-N 0.000 description 2
150000008049 diazo compounds Chemical class 0.000 description 2
239000011888 foil Substances 0.000 description 2
239000008098 formaldehyde solution Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
RIQXULCAEXVXDY-UHFFFAOYSA-N 2,5-dimethyl-4-(morpholin-4-ylmethyl)phenol Chemical compound C1=C(O)C(C)=CC(CN2CCOCC2)=C1C RIQXULCAEXVXDY-UHFFFAOYSA-N 0.000 description 1
MMGPIADYJSPEJI-UHFFFAOYSA-N 2-(hydroxymethyl)-3,6-dimethylphenol Chemical compound CC1=CC=C(C)C(CO)=C1O MMGPIADYJSPEJI-UHFFFAOYSA-N 0.000 description 1
HCEVEUBXZBBHOX-UHFFFAOYSA-N 2-(hydroxymethyl)-4,5-dimethylphenol Chemical compound CC1=CC(O)=C(CO)C=C1C HCEVEUBXZBBHOX-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 1
YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 1
AKYPSKXBHUGOHU-UHFFFAOYSA-N 3,6-dihydroxynaphthalene-2,7-disulfonic acid Chemical compound OC1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(O)=CC2=C1 AKYPSKXBHUGOHU-UHFFFAOYSA-N 0.000 description 1
ZDUIHRJGDMTBEX-UHFFFAOYSA-N 3-methyl-5-propan-2-ylphenol Chemical compound CC(C)C1=CC(C)=CC(O)=C1 ZDUIHRJGDMTBEX-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
CCIAVEMREXZXAK-UHFFFAOYSA-M 4-(dimethylamino)benzenediazonium;chloride Chemical compound [Cl-].CN(C)C1=CC=C([N+]#N)C=C1 CCIAVEMREXZXAK-UHFFFAOYSA-M 0.000 description 1
MENVYKGTKUQIGQ-UHFFFAOYSA-N 4-(hydroxymethyl)-2-methyl-5-propan-2-ylphenol Chemical compound CC(C)C1=CC(O)=C(C)C=C1CO MENVYKGTKUQIGQ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000005844 Thymol Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 1
HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 description 1
235000007746 carvacrol Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
235000019646 color tone Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
230000031700 light absorption Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/11—Alkylated hydroxy benzenes containing also acyclically bound hydroxy groups, e.g. saligenol
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/58—Coupling substances therefor

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

CH991963A 1962-08-15 1963-08-12 Diazotypie-Kopierschicht, insbesondere zur Herstellung von Zwischenoriginalen CH423470A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEK47504A DE1242450B (de)	1962-08-15	1962-08-15	Diazotypieschicht

Publications (1)

Publication Number	Publication Date
CH423470A true CH423470A (de)	1966-10-31

Family

ID=7224585

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH991963A CH423470A (de)	1962-08-15	1963-08-12	Diazotypie-Kopierschicht, insbesondere zur Herstellung von Zwischenoriginalen

Country Status (4)

Country	Link
AT (1)	AT243076B (da)
CH (1)	CH423470A (da)
DK (1)	DK107076C (da)
SE (1)	SE304681B (da)

1963
- 1963-08-12 SE SE882363A patent/SE304681B/xx unknown
- 1963-08-12 CH CH991963A patent/CH423470A/de unknown
- 1963-08-14 DK DK387763A patent/DK107076C/da active
- 1963-08-14 AT AT656263A patent/AT243076B/de active

Also Published As

Publication number	Publication date
SE304681B (da)	1968-09-30
DK107076C (da)	1967-04-17
AT243076B (de)	1965-10-25

Publication	Publication Date	Title
DE1015679B (de)	1957-09-12	Einkomponenten-Diazotypiematerial, das wenigstens zwei lichtempfindliche Diazoverbindungen enthaelt
DE1068556B (da)	1959-11-05
DE1900468A1 (de)	1969-07-31	Verfahren zur Entwicklung von Flachdruckplatten
DE2014775A1 (de)	1971-01-21	Diazotypie Material
DE864657C (de)	1953-01-26	Material fuer die Herstellung von Diazotypien
DE1172952B (de)	1964-06-25	Diazotypiematerial
CH423470A (de)	1966-10-31	Diazotypie-Kopierschicht, insbesondere zur Herstellung von Zwischenoriginalen
DE1772980A1 (de)	1971-11-25	Lichtempfindliches,photographisches Aufzeichnungsmaterial
DE1092767B (de)	1960-11-10	Verfahren zur Herstellung von positiven Diazotypie-Kopien und fuer dieses Verfahren geeignetes lichtempfindliches Material
DE871667C (de)	1953-03-26	Diazotypieverfahren
DE876951C (de)	1953-05-18	Lichtempfindliches Material zur Herstellung von Druckformen
DE2123554C2 (de)	1982-07-29	Zweikomponenten-Diazotypiematerial
DE2018908B2 (de)	1975-03-13	Wärmeentwickelbares Diazotypiematerial
DE1242450B (de)	1967-06-15	Diazotypieschicht
DE2000819C3 (de)	1975-01-30	Zweikomponenten-Dlazotyplematerial
DE571692C (de)	1933-03-03	Verfahren zum UEbersensibilisieren von photographischen Filmen
DE1772017A1 (de)	1972-01-13	Diazotypie-Materialien
DE694078C (de)	1940-07-25	Lichtempfindliche Schichten
DE3938763C1 (da)	1991-01-31
DE2553136B2 (de)	1978-09-21	Zweikomponenten-Diazotypiematerial
DE1230669B (de)	1966-12-15	Lichtempfindliche Diazoschicht
DE1572197C3 (de)	1976-04-15	Verfahren zur Herstellung negativer Diazotypiekopien
AT224442B (de)	1962-11-26	Verfahren zur Herstellung von Diazotypien nach dem Ein- und Zweikomponenten-Verfahren
DE1572020C3 (de)	1974-01-24	Verfahren zur Erzeugung von Diazotypiekopien
DE605553C (de)	1934-11-14	Verfahren zur Herstellung von lichtempfindlichen Schichten mittels Diazoverbindungen