GB1069052A - Polyhydroxyamide derivatives - Google Patents

Polyhydroxyamide derivatives

Info

Publication number
GB1069052A
GB1069052A GB37152/66A GB3715266A GB1069052A GB 1069052 A GB1069052 A GB 1069052A GB 37152/66 A GB37152/66 A GB 37152/66A GB 3715266 A GB3715266 A GB 3715266A GB 1069052 A GB1069052 A GB 1069052A
Authority
GB
United Kingdom
Prior art keywords
compounds
esters
methane
sulphonate
group
Prior art date
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
GB37152/66A
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of GB1069052A publication Critical patent/GB1069052A/en
Expired legal-status Critical Current

Links

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
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Polyethers (AREA)
  • Epoxy Compounds (AREA)

Abstract

The invention comprises compounds of the formula <F\1> in which R is a C1- 20 alkyl group, R7 is an ethylene group, Y is a hydroxy group and q and q1 each represent an integer such that the total of the 4q's and q1 has an average value of 6-100. The compounds are made by reacting the appropriate N-methyl-gluconamine with ethylene oxide or a polyethylene glycol. The pentahydroxy compounds can be converted to the corresponding penta-methane-sulphonate esters by reaction with methylsulphonyl chloride and these esters further reacted with tertiary bases to give compounds in which Y is <FORM:1069052/C2/1> where R2-4 are C1- 4 alkyl groups and X- is an acid anion. The examples relate to compounds in which R is lauryl and the methane sulphonate esters and pyridinium methane sulphonate salts thereof.ALSO:The invention comprises compounds of the formula <FORM:1069052/C3/1> in which R is a C1- 20 alkyl group, R7 is an ethylene group, Y is a hydroxy group and q and q1 each represent an integer such that the total of the 4q's and q1 has an average value of 6-100. The compounds are made by reacting the appropriate N-methyl-gluconamine with ethylene oxide or a polyethylene glycol. The pentahydroxy compounds can be converted to the corresponding penta-methane-sulphonate esters by reaction with methylsulphonyl chloride and these esters further reacted with tertiary bases to give compounds in which Y is <FORM:1069052/C3/2> where R2-4 are C1- 4 alkyl groups and X(-) is an acid anion. The example relate to compounds in which R is lauryl and the methane sulphonate esters and pyridinium methane sulphonate salts thereof.
GB37152/66A 1962-06-12 1963-06-11 Polyhydroxyamide derivatives Expired GB1069052A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201788A US3253919A (en) 1962-06-12 1962-06-12 Sensitizers for photographic silver halide emulsions

Publications (1)

Publication Number Publication Date
GB1069052A true GB1069052A (en) 1967-05-17

Family

ID=22747297

Family Applications (3)

Application Number Title Priority Date Filing Date
GB37153/66A Expired GB1069053A (en) 1962-06-12 1963-06-11 Polyamino alcohol derivatives
GB23159/63A Expired GB1069051A (en) 1962-06-12 1963-06-11 Photographic silver halide emulsions
GB37152/66A Expired GB1069052A (en) 1962-06-12 1963-06-11 Polyhydroxyamide derivatives

Family Applications Before (2)

Application Number Title Priority Date Filing Date
GB37153/66A Expired GB1069053A (en) 1962-06-12 1963-06-11 Polyamino alcohol derivatives
GB23159/63A Expired GB1069051A (en) 1962-06-12 1963-06-11 Photographic silver halide emulsions

Country Status (3)

Country Link
US (1) US3253919A (en)
DE (1) DE1294187B (en)
GB (3) GB1069053A (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1281842B (en) * 1964-06-22 1968-10-31 Du Pont Photographic recording material with a photo-soluble layer
JPS5125340B2 (en) * 1972-05-30 1976-07-30
US4664848A (en) * 1982-12-23 1987-05-12 The Procter & Gamble Company Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
EP0112593B1 (en) * 1982-12-23 1989-07-19 THE PROCTER &amp; GAMBLE COMPANY Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
EP0111965B1 (en) * 1982-12-23 1989-07-26 THE PROCTER &amp; GAMBLE COMPANY Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
JPH06105346B2 (en) 1986-11-07 1994-12-21 富士写真フイルム株式会社 Processing method of silver halide color photographic light-sensitive material
JPH04445A (en) 1990-04-17 1992-01-06 Fuji Photo Film Co Ltd Processing method for silver halide color photosensitive material
EP0720049B1 (en) 1990-05-09 1999-08-04 Fuji Photo Film Co., Ltd. Photographic processing composition and processing method using the same
JP3038416B2 (en) * 1991-10-28 2000-05-08 コニカ株式会社 Photographic processing agents
EP0540990B1 (en) * 1991-11-06 1998-07-15 Konica Corporation Tablet-shaped processing agent and method for processing silver halide photographic light sensitive materials
JPH0627619A (en) * 1992-05-13 1994-02-04 Fuji Photo Film Co Ltd Color photographic bleach-fixing composition
US5452045A (en) * 1992-10-30 1995-09-19 Konica Corporation Apparatus for processing a light-sensitive silver halide photographic material
JP3372994B2 (en) 1993-06-11 2003-02-04 富士写真フイルム株式会社 Processing method of silver halide color photographic light-sensitive material
US5409805A (en) * 1993-07-29 1995-04-25 Konica Corporation Solid processing agent for silver halide photographic light-sensitive materials
US5534395A (en) 1994-06-09 1996-07-09 Fuji Photo Film Co., Ltd. Method of processing silver halide color photographic materials
JPH0854716A (en) * 1994-08-12 1996-02-27 Konica Corp Silver halide photographic sensitive material and its processing method
EP0704756B1 (en) * 1994-09-09 2000-03-22 Konica Corporation Photographic processing method for processing a silver halide photographic light-sensitive material
DE59802105D1 (en) 1998-06-18 2001-12-06 Ilford Imaging Ch Gmbh Inkjet printing materials
US6071688A (en) * 1998-07-29 2000-06-06 Eastman Kodak Company Providing additives to a coating composition by vaporization

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2428353A (en) * 1943-06-21 1947-10-07 Frederick C Bersworth Lower aliphatic esters of ethylene-and propylene-diamine n,n'-tetracetic acids
US2423549A (en) * 1945-01-10 1947-07-08 Du Pont Silver halide photographic emulsions sensitized by polyalkylene glycols
US2441389A (en) * 1946-12-12 1948-05-11 Du Pont Silver halide emulsions sensitized by mixtures of high polyalkylene glycols and low polyhydric alcohols
US2524219A (en) * 1947-09-16 1950-10-03 Frederick C Bersworth Germicidally active deionizing agents for alkaline ph solutions
US2666700A (en) * 1950-09-06 1954-01-19 Du Pont Process of preparing a light sensitive silver halide emulsion
BE530063A (en) * 1953-07-01
US2704716A (en) * 1954-06-17 1955-03-22 Eastman Kodak Co Melonate and cyamelurate stabilizers for photographic emulsions sensitized with alkylene oxide polymers
BE553032A (en) * 1955-12-01
US3017271A (en) * 1955-12-01 1962-01-16 Eastman Kodak Co Photographic emulsions sensitized with alkylene oxide polymers and quaternary ammonium salts
BE590553A (en) * 1959-05-07
BE597144A (en) * 1959-11-16
BE585940A (en) * 1959-12-23
BE604938A (en) * 1960-06-17

Also Published As

Publication number Publication date
GB1069051A (en) 1967-05-17
GB1069053A (en) 1967-05-17
DE1294187B (en) 1969-04-30
US3253919A (en) 1966-05-31

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