JPS6115423B2 - - Google Patents

Info

Publication number: JPS6115423B2
Authority: JP; Japan
Prior art keywords: hydroxy; carbon atoms; group; naphthamide; tert
Prior art date: 1978-03-30
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.): Expired

Application number

JP3712878A

Other languages

English (en)

Japanese (ja)

Other versions

JPS54130024A (en

Inventor

Kazuhiko Kimura

Hajime Wada

Takaya Endo

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Konica Minolta Inc

Original Assignee

Konica Minolta 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.)

1978-03-30

Filing date

1978-03-30

Publication date

1986-04-24

1978-03-30 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1978-03-30 Priority to JP3712878A priority Critical patent/JPS54130024A/ja

1979-10-09 Publication of JPS54130024A publication Critical patent/JPS54130024A/ja

1986-04-24 Publication of JPS6115423B2 publication Critical patent/JPS6115423B2/ja

Status Granted legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 claims description 18
239000000463 material Substances 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 5
229910052709 silver Inorganic materials 0.000 claims description 5
239000004332 silver Substances 0.000 claims description 5
125000002252 acyl group Chemical group 0.000 claims description 3
125000003342 alkenyl group Chemical group 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
230000009102 absorption Effects 0.000 description 20
238000010521 absorption reaction Methods 0.000 description 20
239000000243 solution Substances 0.000 description 18
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
239000013078 crystal Substances 0.000 description 9
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
230000015572 biosynthetic process Effects 0.000 description 8
238000003786 synthesis reaction Methods 0.000 description 8
AOPRXJXHLWYPQR-UHFFFAOYSA-N 2-phenoxyacetamide Chemical compound NC(=O)COC1=CC=CC=C1 AOPRXJXHLWYPQR-UHFFFAOYSA-N 0.000 description 7
239000000975 dye Substances 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
238000000921 elemental analysis Methods 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 4
238000011161 development Methods 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
238000012545 processing Methods 0.000 description 4
230000035945 sensitivity Effects 0.000 description 4
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
239000002904 solvent Substances 0.000 description 4
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000007844 bleaching agent Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
239000012046 mixed solvent Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 2
235000011114 ammonium hydroxide Nutrition 0.000 description 2
229940101006 anhydrous sodium sulfite Drugs 0.000 description 2
XNSQZBOCSSMHSZ-UHFFFAOYSA-K azane;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(3+) Chemical compound [NH4+].[Fe+3].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O XNSQZBOCSSMHSZ-UHFFFAOYSA-K 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
KYQODXQIAJFKPH-UHFFFAOYSA-N diazanium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [NH4+].[NH4+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O KYQODXQIAJFKPH-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
229920000159 gelatin Polymers 0.000 description 2
239000008273 gelatin Substances 0.000 description 2
235000019322 gelatine Nutrition 0.000 description 2
235000011852 gelatine desserts Nutrition 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000011259 mixed solution Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
235000010288 sodium nitrite Nutrition 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
UBRSRFZIOKQXOI-UHFFFAOYSA-N 1,4-dihydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC=1C2=CC=CC=C2C(O)=CC=1C(=O)NC1=CC=CC=C1 UBRSRFZIOKQXOI-UHFFFAOYSA-N 0.000 description 1
GBPJOFUKOHMFPR-UHFFFAOYSA-N 1-(1,4-dihydroxy-6-tetradecoxycyclohexa-2,4-dien-1-yl)naphthalene-2-carboxamide Chemical compound CCCCCCCCCCCCCCOC1C=C(O)C=CC1(O)C1=C(C(N)=O)C=CC2=CC=CC=C12 GBPJOFUKOHMFPR-UHFFFAOYSA-N 0.000 description 1
JRVZITODZAQRQM-UHFFFAOYSA-N 1-isocyanato-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1N=C=O JRVZITODZAQRQM-UHFFFAOYSA-N 0.000 description 1
GFNKTLQTQSALEJ-UHFFFAOYSA-N 1-isocyanato-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(N=C=O)C=C1 GFNKTLQTQSALEJ-UHFFFAOYSA-N 0.000 description 1
JMAARDACHPXLOZ-UHFFFAOYSA-N 3-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1,4-dihydroxynaphthalene-2-carboxamide Chemical compound C(C)(C)(CC)C1=C(OCCCCC=2C(=C(C3=CC=CC=C3C=2O)O)C(=O)N)C=CC(=C1)C(C)(C)CC JMAARDACHPXLOZ-UHFFFAOYSA-N 0.000 description 1
CRVPAIHTIXMDQV-UHFFFAOYSA-N 3-acetamido-4-hydroxynaphthalene-2,7-disulfonic acid Chemical compound C(C)(=O)NC1=C(C2=CC=C(C=C2C=C1S(=O)(=O)O)S(=O)(=O)O)O CRVPAIHTIXMDQV-UHFFFAOYSA-N 0.000 description 1
AVDLFIONKHGQAP-UHFFFAOYSA-N 4-nitrophenoxyacetic acid Chemical compound OC(=O)COC1=CC=C([N+]([O-])=O)C=C1 AVDLFIONKHGQAP-UHFFFAOYSA-N 0.000 description 1
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
RPWFJAMTCNSJKK-UHFFFAOYSA-N Dodecyl gallate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC(O)=C(O)C(O)=C1 RPWFJAMTCNSJKK-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
238000000862 absorption spectrum Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000004450 alkenylene group Chemical group 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000012937 correction Methods 0.000 description 1
238000006193 diazotization reaction Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
SVHVEORJPVYLCT-UHFFFAOYSA-N ethanol;hexane;propan-2-one Chemical compound CCO.CC(C)=O.CCCCCC SVHVEORJPVYLCT-UHFFFAOYSA-N 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000007654 immersion Methods 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
DSSJWFWQVKAZBA-UHFFFAOYSA-N n-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1,4-dihydroxynaphthalene-2-carboxamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1OCCCCNC(=O)C1=CC(O)=C(C=CC=C2)C2=C1O DSSJWFWQVKAZBA-UHFFFAOYSA-N 0.000 description 1
150000002828 nitro derivatives Chemical class 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000010992 reflux Methods 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
QPILZZVXGUNELN-UHFFFAOYSA-M sodium;4-amino-5-hydroxynaphthalene-2,7-disulfonate;hydron Chemical class [Na+].OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S([O-])(=O)=O)=CC2=C1 QPILZZVXGUNELN-UHFFFAOYSA-M 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
JOQGJRQKCIJIDB-UHFFFAOYSA-N tin;hydrochloride Chemical compound Cl.[Sn] JOQGJRQKCIJIDB-UHFFFAOYSA-N 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
LZGVDNRJCGPNDS-UHFFFAOYSA-N trinitromethane Chemical class [O-][N+](=O)C([N+]([O-])=O)[N+]([O-])=O LZGVDNRJCGPNDS-UHFFFAOYSA-N 0.000 description 1
HERBOKBJKVUALN-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]acetate;hydrate Chemical compound O.[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O HERBOKBJKVUALN-UHFFFAOYSA-K 0.000 description 1
238000001429 visible spectrum Methods 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1
239000008096 xylene Substances 0.000 description 1
ZJVTYKZWDWVIFD-UHFFFAOYSA-N zinc;hydrochloride Chemical compound Cl.[Zn] ZJVTYKZWDWVIFD-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/333—Coloured coupling substances, e.g. for the correction of the coloured image
- G03C7/3335—Coloured coupling substances, e.g. for the correction of the coloured image containing an azo chromophore

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP3712878A 1978-03-30 1978-03-30 Silver halide color photographic material Granted JPS54130024A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP3712878A JPS54130024A (en)	1978-03-30	1978-03-30	Silver halide color photographic material

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP3712878A JPS54130024A (en)	1978-03-30	1978-03-30	Silver halide color photographic material

Publications (2)

Publication Number	Publication Date
JPS54130024A JPS54130024A (en)	1979-10-09
JPS6115423B2 true JPS6115423B2 (de)	1986-04-24

Family

ID=12488962

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP3712878A Granted JPS54130024A (en)	1978-03-30	1978-03-30	Silver halide color photographic material

Country Status (1)

Country	Link
JP (1)	JPS54130024A (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61272741A (ja) *	1985-05-28	1986-12-03	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料
US4833069A (en) *	1986-01-23	1989-05-23	Konishiroku Photo Industry Co., Ltd.	Silver halide color photographic light-sensitive material comprising a specified cyan coupler combination and total film thickness
US5364745A (en) *	1990-12-19	1994-11-15	Eastman Kodak Company	Azoaniline masking couplers for photographic materials

1978
- 1978-03-30 JP JP3712878A patent/JPS54130024A/ja active Granted

Also Published As

Publication number	Publication date
JPS54130024A (en)	1979-10-09

Publication	Publication Date	Title
JPH0152742B2 (de)	1989-11-09
JPH0240647A (ja)	1990-02-09	改良された粒状度特性を与える写真記録材料
US4052213A (en)	1977-10-04	Light-sensitive photographic material
DE69403230T2 (de)	1998-01-08	Bilderzeugung in Farbumkehrmaterialien, die starke Inhibitoren verwendet
JPS6116060B2 (de)	1986-04-28
JPS6333138B2 (de)	1988-07-04
US3271152A (en)	1966-09-06	Light-sensitive elements for color photography and process therefor
JPH0247734B2 (de)	1990-10-22
GB1564349A (en)	1980-04-10	Light-sensitive silver halide photographic materials
JPS6115423B2 (de)	1986-04-24
JPS6023855A (ja)	1985-02-06	カラ−写真感光材料
EP0125522A2 (de)	1984-11-21	Farbphotographische Materialien
JPH0322973B2 (de)	1991-03-28
JP2683001B2 (ja)	1997-11-26	カラー写真記録材料
US3658545A (en)	1972-04-25	Light-sensitive silver halide color photographic material containing cyan couplers
JPH0248097B2 (ja)	1990-10-24	Karaashashinkankozairyo
JPH0466018B2 (de)	1992-10-21
US3632347A (en)	1972-01-04	Silver halide emulsions containing cyan-forming couplers
JPS5950977B2 (ja)	1984-12-11	カラ−写真感光材料
JPS6410061B2 (de)	1989-02-21
JPS62147457A (ja)	1987-07-01	ハロゲン化銀写真感光材料の処理方法
US4504577A (en)	1985-03-12	Silver halide photographic materials
JPH0583897B2 (de)	1993-11-30
JPS5914742B2 (ja)	1984-04-05	ハロゲン化銀写真感光材料
JPH0559422B2 (de)	1993-08-31