GB689930A - Synthetic polypeptides of amino acids as photographic restrainers - Google Patents

Synthetic polypeptides of amino acids as photographic restrainers

Info

Publication number
GB689930A
GB689930A GB769/51A GB76951A GB689930A GB 689930 A GB689930 A GB 689930A GB 769/51 A GB769/51 A GB 769/51A GB 76951 A GB76951 A GB 76951A GB 689930 A GB689930 A GB 689930A
Authority
GB
United Kingdom
Prior art keywords
mixture
polypeptide
amino acids
synthetic polypeptides
acid
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
GB769/51A
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.)
GAF Chemicals Corp
Original Assignee
General Aniline and Film Corp
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 General Aniline and Film Corp filed Critical General Aniline and Film Corp
Publication of GB689930A publication Critical patent/GB689930A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G5/00Compounds of silver
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/04Polyamides derived from alpha-amino carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Inorganic Chemistry (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Synthetic polypeptides are produced by allowing the anhydride of an N-carboxy-a -amino acid to polymerize in a water-miscible alcohol, e.g. methanol, ethanol, or propanol, containing some water to catalyse the reaction. A mixture of two or more anhydrides may be polymerized, and such mixture may be obtained by converting a mixture of two or more amino acids into the anhydrides of their N-carboxy derivatives. The polypeptide of leucine is prepared by warming together N-carbomethoxyleucine, benzene, and thionyl chloride, distilling off the excess thionyl chloride, and allowing a 1 per cent solution in 95 per cent ethanol to stand. The polypeptides of proline, arginine, histidine, glutamic acid, and e -carbobenzyloxylysine, and the copolypeptide of leucine and lysine are similarly prepared. The e -carbobenzyloxy group may be removed from the polypeptide of e -carbobenzyloxylysine by adding red phosphorus to a mixture of the polypeptide, glacial acetic acid, and hydriodic acid.
GB769/51A 1950-01-11 1951-01-10 Synthetic polypeptides of amino acids as photographic restrainers Expired GB689930A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US689930XA 1950-01-11 1950-01-11

Publications (1)

Publication Number Publication Date
GB689930A true GB689930A (en) 1953-04-08

Family

ID=22086012

Family Applications (1)

Application Number Title Priority Date Filing Date
GB769/51A Expired GB689930A (en) 1950-01-11 1951-01-10 Synthetic polypeptides of amino acids as photographic restrainers

Country Status (2)

Country Link
BE (1) BE500537A (en)
GB (1) GB689930A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1217436A2 (en) * 2000-12-19 2002-06-26 Eastman Kodak Company Color photographic element with improved developability
CN103087313A (en) * 2013-02-06 2013-05-08 三角轮胎股份有限公司 Amino acid oligomer preparation method

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB721067A (en) * 1952-10-09 1954-12-29 Ilford Ltd Improvements in or relating to the production of silver halide photographic emulsions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1217436A2 (en) * 2000-12-19 2002-06-26 Eastman Kodak Company Color photographic element with improved developability
EP1217436A3 (en) * 2000-12-19 2003-12-03 Eastman Kodak Company Color photographic element with improved developability
CN103087313A (en) * 2013-02-06 2013-05-08 三角轮胎股份有限公司 Amino acid oligomer preparation method
CN103087313B (en) * 2013-02-06 2015-12-09 三角轮胎股份有限公司 Prepare the method for oligomeric aminobenzoic acid

Also Published As

Publication number Publication date
BE500537A (en)

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