Claims
- 1. A stabilizing solution for a light-sensitive silver halide color photographic material which comprises a compound represented by the following Formula F, and has a pH of from 7.5 to 10.0; ##STR61## wherein Z represents a group of atoms necessary to form a substituted or unsubstituted cyclic hydrocarbon, X represents an aldehyde group, ##STR62## wherein R.sub.1 and R.sub.2 each represent a lower alkyl group; and n is an integer of 1 to 3.
- 2. The solution of claim 1, wherein Z represents a group of atoms necessary to form a substituted cyclic hydrocarbon.
- 3. The solution of claim 1, wherein said stabilizing solution for a light-sensitive silver halide color photographic material comprises substantially no formaldehyde.
- 4. The solution of claim 1, wherein said stabilizing solution for a light-sensitive silver halide color photographic material comprises a water-soluble surface active agent and an amount of a water-soluble surface active agent is within the range of 0.1 to 40 g.
- 5. The solution of claim 1, wherein said stabilizing solution for a light-sensitive silver halide color photographic material comprises a anti fungal agent.
- 6. The solution of claim 1, wherein said compound represented by Formula F, is a compound selected from the group consisting of No. 1 to No. 48, and Structural formulas of Exemplary compounds 1 to 48 are each completed by inserting the following substituents or atoms 1 to 6 to the positions 1 to 6 of the following formula;
- __________________________________________________________________________ ##STR63##No. 1 2 3 4 5 6__________________________________________________________________________ 1 CHO H H H H H 2 CHO H H OH H H 3 CHO H OH H H H 4 CHO OH H H H H 5 CHO OH H OH H H 6 CHO H OH H OH H 7 CHO OH OH H H H 8 CHO H CHO H OH H 9 CHO H CHO H H OH10 CHO OH CHO H H H11 CHO H CHO H CHO H12 CHO OH CHO H CHO H13 CH(OCH.sub.3).sub.2 H OH H H H14 CH(OCH.sub.3).sub.2 H H OH H H15 CH(OCH.sub.3).sub.2 H OH H OH H16 CHO H NO.sub.2 H H H17 CHO H H NO.sub.2 H H18 CHO NO.sub.2 H H H H19 CHO H NO.sub.2 H NO.sub.2 H20 CHO H H OCH.sub.3 H H21 CHO H OCH.sub.3 H OH H22 CHO H OH OCH.sub.3 H H23 CHO H OCH.sub.3 OH H H24 CHO H OH OCH.sub.3 OH H25 CHO H Cl H H H26 CHO H H Cl H H27 CHO H Cl H Cl H28 CHO H COOH COOH H H29 CHO H Br H H H30 CHO H H Br H H31 CHO H OH SO.sub.3 H H H32 CHO H H NH.sub.2 H H33 CHO H H N(CH.sub.3).sub.2 H H34 CHO H H N(C.sub.2 H.sub.6).sub.2 H H35 CHO H H CONH.sub.2 H H36 CHO H H SO.sub.2 NH.sub.2 H H37 CHO H H SO.sub.3 H H H38 CHO H H CN H H39 CHO H H COOCH.sub.3 H H40 CHO H H COOH H H41 CHO H SO.sub.3 H H H H42 CHO H COOH H H H43 CHO H CN H H H44 CHO H COOCH.sub.3 H H H45 CHO H CONH.sub.2 H H H46 ##STR64## H OH H H H47 ##STR65## H H OH H H48 CHO H OH CH.sub.3 H H__________________________________________________________________________
- 7. The solution of claim 4, wherein said water-soluble surface active agent is a member selected from the group consisting of Formula SI, SII, and SU-I; Formula SI:
- R.sup.1 --X--(E.sup.1).sub.l1 --(E.sup.2).sub.m1 --(E.sup.3).sub.n1 --R.sup.2
- wherein R.sup.1 represents a hydrogen atom, an aliphatic group or an acyl group, R.sup.2 represents a hydrogen atom or an aliphatic group, E.sup.1 represents an ethylene oxide group, E.sup.2 represents a propylene oxide group, E.sup.3 represents an ethylene oxide group, X represents an oxygen atom or an --R.sup.3 N-- group, wherein R.sup.3 represents an aliphatic group, a hydrogen atom or (E.sup.1).sub.12 --(E.sup.2).sub.m2 --(E.sup.3).sub.n2 --R.sup.4, wherein R.sup.4 represents a hydrogen atom or an aliphatic group, l.sub.1, l.sub.2, m.sub.1, m.sub.2, n.sub.1, n.sub.2 each represents a value of 0 to 300; Formula SII:
- A.sub.2 --O--(B).sub.m --(C).sub.n --X.sup.1
- wherein A.sub.2 represents a monovalent organic group as exemplified by an alkyl group having 6 to 50 carbon atoms, B and C represents each an ethylene oxide group, a propylene oxide group, or ##STR66## wherein n1, m1 and 11 each represents 0, 1, 2 or 3, m and n each represents an integer of 0 to 100, X.sup.1 represents a hydrogen atom, or an alkyl group, an aralkyl group or an aryl group, ##STR67## wherein R.sub.9 represents a hydrogen atom, a hydroxyl group, a lower alkyl group, an alkoxy group, ##STR68## wherein R.sub.1, R.sub.11 and R.sub.12 each represents a hydrogen atom or a lower alkyl group, and R.sub.1, R.sub.11 and R.sub.12 are the same or different from each other, l.sub.1, to l.sub.3 each represents an integer of 0 or 1 to 30, p, q1 and q2 each represents an integer of 0 or 1 to 30, X.sub.1 and X.sub.2 each represent --CH.sub.2 CH.sub.2 --, --CH.sub.2 CH.sub.2 CH.sub.2 --, ##STR69##
- 8. The solution of claim 5, wherein said antifungal agent is a member selected from the group consisting of Formula B-1, B-2, and B-3, ##STR70## wherein R.sub.1 represents an alkyl group, a cycloalkyl group, an aryl group, a hydroxyl group, an alkoxycarbonyl group, an amino group, a carboxyl group (including its salt) or a sulfo group (including its salt);
- R.sup.2 and R.sup.3 independently represent a hydrogen atom, a halogen atom, an amino group, a nitro group, a hydroxyl group, an alkoxycarbonyl group, a carboxyl group (including its salt) or a sulfo group (including its salt), M represents a hydrogen atom, an alkali metal or an ammonium group; ##STR71## wherein R.sup.4 represents a halogen atom, an alkyl group, an aryl group, a halogenated alkyl group, --R.sup.12 --OR.sup.13, --CONHR.sup.14 (where R.sup.12 represents a alkylene group, R.sub.13 and R.sub.14 each represent a hydrogen atom, an alkyl group or an arylalkyl group) or an arylalkyl group; R.sup.5 and R.sup.6 each represent a hydrogen atom, a halogen atom, a halogenated alkyl group or alkyl group; R7 represents a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a halogenated alkyl group, an arylalkyl group, --R.sup.15 --OR.sup.16, --CONHR.sup.17 (where R.sup.15 represents a alkylene group, R.sub.16 and R.sub.17 each represent a hydrogen atom, an alkyl group); and R.sub.8, R.sub.9, R.sub.10 and R.sub.11 each represent a hydrogen atom, a halogen atom, a hydroxyl group, an alkyl group, an amino group or a nitro group.
- 9. The solution of claim 1, wherein a processing method of said material comprising the steps of:
- processing with a processing solution having a bleaching ability;
- processing with a processing solution having a fixing ability;
- processing with said stabilizing solution.
- 10. The solution of claim 1, wherein a processing method of said material comprising the steps of:
- processing with a processing solution having a fixing ability;
- processing with said stabilizing solution.
Priority Claims (1)
| Number |
Date |
Country |
Kind |
| 3-245912 |
Sep 1991 |
JPX |
|
Parent Case Info
This application is a continuation, of application Ser. No. 07/932,259, filed Aug. 19, 1992 (abandoned).
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Continuations (1)
|
Number |
Date |
Country |
| Parent |
932259 |
Aug 1992 |
|
Patent Grant
5362609
