GB890461A - New 1:3:4-oxdiazole compounds and process for their manufacture - Google Patents

New 1:3:4-oxdiazole compounds and process for their manufacture

Info

Publication number
GB890461A
GB890461A GB433559A GB433559A GB890461A GB 890461 A GB890461 A GB 890461A GB 433559 A GB433559 A GB 433559A GB 433559 A GB433559 A GB 433559A GB 890461 A GB890461 A GB 890461A
Authority
GB
United Kingdom
Prior art keywords
substituted
carbon atoms
residue
protect
resins
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
GB433559A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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.)
Filing date
Publication date
Application filed by Ciba AG filed Critical Ciba AG
Publication of GB890461A publication Critical patent/GB890461A/en
Expired legal-status Critical Current

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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
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/815Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
    • G03C1/8155Organic compounds therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/35Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0042Preserving by using additives, e.g. anti-oxidants containing nitrogen
    • C11B5/0064Heterocyclic compounds containing nitrogen in the ring
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/422Hydrazides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Textile Engineering (AREA)
  • Dermatology (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

1.3.4-Oxdiazoles, free from hydroxyl groups and acid groups imparting solubility in water, and substituted in each of the 2- and 5- positions by a residue of the benzene series, at least one of these residues being substituted by at least one aliphatic hydrocarbon group containing at least 4 carbon atoms, are used as light-screening agents for incorporating in various substrata to protect them from ultra-violet light or for incorporation in films which are used to protect the substrata. Among the substances which may be so protected are oils, fats and waxes, such as edible oils and fats; candles; floor polishes; floor stains or other wood stains; furniture polishes; dyed or natural soaps; and shampoos. Specification 816,750 is referred to.ALSO:1,3,4-Oxdiazoles, free from hydroxyl groups and acid groups imparting solubility in water, and substituted in each of the 2- and 5-positions by a residue of the benzene series, at least one of these residues being substituted by at least one aliphatic hydrocarbon group containing at least 4 carbon atoms, are used as light-screening agents for incorporating in various substrata to protect them from ultra-violet light or for incorporation in films which are used to protect substrata from ultra-violet light. They may be added, for example, to the spinning mass of acetylcellulose (including cellulose triacetate) or to the mass from which fully synthetic fibres are made, e.g. polyamide melts or polyacrylonitrile spinning masses, prior to, in the course of, or subsequently to the polycondensation or polymerization respectively. They may also be added to lacquers and films, e.g. those made from acetyl cellulose, cellulose propionate, cellulose butyrate, nitrocellulose, vinyl acetate, polyvinyl chloride, copolymers of vinyl chloride and vinylidene chloride, alkyd lacquers, polyethylene, polyamides, polyacrylonitrile, polyesters and in transparent foils of regenerated cellulose or acetylcellulose. They may also be added to natural or synthetic resins, e.g. epoxy resins, polyester resins, vinyl resins, polystyrene resins, alkyd resins, phenol-, urea- and melaminealdehyde resins, emulsions of synthetic resins, synthetic resins reinforced with glass fibres and natural or synthetic rubber-like materials such as rubber, balata gum, gutta-percha, polychloroprene, olefinic polysulphides, polybutadiene, butadiene-styrene copolymers and butadiene-acrylonitrile copolymers. Specification 816,750 is referred to.ALSO:The invention comprises 1,3,4-oxdiazoles which are free from hydroxyl groups and acid groups imparting solubility in water and are substituted in each of the 2- and 5-positions by a residue of the benzene series and contain at least one aliphatic hydrocarbon residue containing at least 4 carbon atoms. They may be prepared by treating a diacylhydrazine of formula <FORM:0890461/IV (b)/1> in which R1 and R2 each represent a residue of the benzene series at least one being substituted by an aliphatic hydrocarbon residue having at least 4 carbon atoms, with a nonsulphonating agent capable of eliminating water. The diacyl hydrazines used as starting materials may be obtained by condensing hydrazine at both nitrogen atoms, or a monoacyl hydrazine of formula <FORM:0890461/IV (b)/2> at the -NH2 groups, with an acid halide of formula <FORM:0890461/IV (b)/3> The residues R1 and R2 may contain several of the aliphatic residues containing at least 4 carbon atoms. These aliphatic residues may be branched or unbranched. The preferred diacylhydrazines for use as starting materials are those of formula <FORM:0890461/IV (b)/4> in which R is an aliphatic hydrocarbon radical containing at least 4 carbon atoms, A is hydrogen or an alkoxy group containing not more than 3 carbon atoms and B is hydrogen, a chlorine atom, or an alkyl group, e.g. methyl or tertiary butyl, an alkoxy group containing not more than 3 carbon atoms or a phenyl residue. Non-sulphonating agents capable of eliminating water from the diacyl hydrazines are, for example, anhydrous aluminium chloride, phosgene, phosphorus trichloride, pentachloride or oxychloride, and, preferably, thionyl chloride. The dehydration may be carried out by heating the diacylhydrazine with the water-eliminating agent in an inert organic solvent. The new compounds may be used as light-screening agents for various materials. Examples are given of the preparation of compounds of formula <FORM:0890461/IV (b)/5> and <FORM:0890461/IV (b)/6> Specification 816,750 is referred to.ALSO:1,3,4-Oxdiazoles, free from hydroxyl groups and acid groups imparting solubility in water, and substituted in each of the 2- and 5-positions by a residue of the benzene series at least one of such residues being substituted by at least one aliphatic hydrocarbon group containing at least 4 carbon atoms, are used as light-screening agents for a variety of materials. These compounds may be incorporated with the substratum to protect it from attacks by ultra-violet rays, by way of a dyeing process; or they may be incorporated with a "filter coating" to protect a substratum placed immediately underneath the filter or some distance from it. Materials that can be protected are textile materials in general, e.g. fibres, filaments, yarns, woven or knitted fabrics or felt and finished products made therefrom, consisting of natural materials of animal or vegetable origin, semi-synthetic materials such as regenerated cellulose, rayon or spun rayon, or synthetic materials obtained by polymerization or copolymerization. The protective compounds may also be added to coating and dressing agents for textiles, e.g. those based on starches, casein or synthetic resins made from vinyl acetate or derivatives of acrylic acid. Specification 816,750 is referred to.ALSO:1.3.4-Oxdiazoles, free from hydroxyl groups and acid groups imparting solubility in water, and substituted in each of the 2- and 5-positions by a residue of the benzene series, at least one of these residues being substituted by at least one aliphatic hydrocarbon group containing at least 4 carbon atoms, are used as light-screening agents for incorporating in various substrata to protect them from ultra-violet light or for incorporation in films which are used to protect substrata from ultra-violet light. They may be used for the protection of butter, feathers, hairs, pelts, hides, straw and wood, for example, or for incorporation in cosmetics such as perfumes, bath salts, skin and face creams, lipsticks, powder, brilliantines, hair sprays, insect repellents and sunburn lotions and oils. Examples are given of the preparation of sunburn preparations and insect repellents containing one of the substituted 1.3.4-oxdiazoles defined above with (a) adipic acid isopropyltetrahydrofurfuryl ester and glycerol monostearate in alcoholic solution; (b) trichloromonofluoromethane, dichlorodifluoromethane, ethanol and perfume oil; (c) adipic acid isopropyltetrahydrofurfuryl ester, benzoic acid diethyl amide and dimethyl phthalate dissolved in peanut oil and paraffin oil; (d) glycerol monostearate, cetyl alcohol, sodium cetyl sulphate, stearic acid and glycerol; and (e) adipic acid isopropyltetrahydrofurfuryl ester, toluic acid diethylamide, cetyl alcohol, petroleum oil, beeswax, lanolin, cocoa butter, water and sodium benzoate. Specification 816,750 is referred to.
GB433559A 1958-02-07 1959-02-06 New 1:3:4-oxdiazole compounds and process for their manufacture Expired GB890461A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH5560658A CH364790A (en) 1958-02-07 1958-02-07 Process for the preparation of new 1,3,4-oxdiazoles

Publications (1)

Publication Number Publication Date
GB890461A true GB890461A (en) 1962-02-28

Family

ID=4520004

Family Applications (2)

Application Number Title Priority Date Filing Date
GB297259A Expired GB881537A (en) 1958-02-07 1959-01-27 New 1:3:4-oxadiazoles and their manufacture and use
GB433559A Expired GB890461A (en) 1958-02-07 1959-02-06 New 1:3:4-oxdiazole compounds and process for their manufacture

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB297259A Expired GB881537A (en) 1958-02-07 1959-01-27 New 1:3:4-oxadiazoles and their manufacture and use

Country Status (3)

Country Link
CH (1) CH364790A (en)
DE (3) DE1094754B (en)
GB (2) GB881537A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3246007A (en) * 1963-12-13 1966-04-12 Parke Davis & Co 2-halo-5-(1, 3, 4-oxadiazolin-2-yl)-benzene-sulfonamide compounds
JP2008545767A (en) * 2005-06-08 2008-12-18 ノバルティス アクチエンゲゼルシャフト Polycyclic oxadiazoles or isoxazoles and their use as SIP receptor ligands

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL291628A (en) * 1962-04-17

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2464831A (en) * 1947-09-16 1949-03-22 Du Pont Compounds of the oxdiazole series
DE932184C (en) * 1952-05-21 1955-10-27 Ciba Geigy Process for the preparation of new 1, 3, 4-oxdiazole compounds
FR1127243A (en) * 1954-07-07 1956-12-11 Ciba Geigy Novel oxdiazoles and process for their preparation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3246007A (en) * 1963-12-13 1966-04-12 Parke Davis & Co 2-halo-5-(1, 3, 4-oxadiazolin-2-yl)-benzene-sulfonamide compounds
JP2008545767A (en) * 2005-06-08 2008-12-18 ノバルティス アクチエンゲゼルシャフト Polycyclic oxadiazoles or isoxazoles and their use as SIP receptor ligands

Also Published As

Publication number Publication date
GB881537A (en) 1961-11-08
DE1094755B (en) 1960-12-15
DE1094753B (en) 1960-12-15
DE1094754B (en) 1960-12-15
CH364790A (en) 1962-10-15

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