CH605662A5 - - Google Patents
Info
- Publication number
- CH605662A5 CH605662A5 CH1594873A CH1594873A CH605662A5 CH 605662 A5 CH605662 A5 CH 605662A5 CH 1594873 A CH1594873 A CH 1594873A CH 1594873 A CH1594873 A CH 1594873A CH 605662 A5 CH605662 A5 CH 605662A5
- Authority
- CH
- Switzerland
- Prior art keywords
- fabric
- sub
- dispersion
- dihalohydrin
- acyl residue
- Prior art date
Links
- 239000004744 fabric Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 26
- 239000001913 cellulose Substances 0.000 claims description 9
- 229920002678 cellulose Polymers 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- 239000006185 dispersion Substances 0.000 claims description 8
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 238000001704 evaporation Methods 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 239000002562 thickening agent Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 238000004132 cross linking Methods 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims 1
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 150000003944 halohydrins Chemical class 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- -1 halohydrin acetate Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 2,3-dichloropropan-1-ol Chemical compound OCC(Cl)CCl ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pulmonology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31700572A | 1972-12-20 | 1972-12-20 | |
| US05/382,762 US3993679A (en) | 1972-12-20 | 1973-07-26 | Cyano phenylene dioxamic molecules |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH605662A5 true CH605662A5 (ru) | 1978-10-13 |
Family
ID=26980710
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1594873A CH605662A5 (ru) | 1972-12-20 | 1973-11-13 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3993679A (ru) |
| JP (1) | JPS5761028B2 (ru) |
| CA (1) | CA1030156A (ru) |
| CH (1) | CH605662A5 (ru) |
| DE (1) | DE2362409C3 (ru) |
| ES (1) | ES421536A1 (ru) |
| FR (1) | FR2211230B1 (ru) |
| GB (2) | GB1454777A (ru) |
| HK (1) | HK10982A (ru) |
| HU (1) | HU168135B (ru) |
| NL (1) | NL177487C (ru) |
| SE (1) | SE410965B (ru) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4191840A (en) * | 1973-03-23 | 1980-03-04 | American Home Products Corporation | Oxamic acid derivatives |
| CA1058209A (en) * | 1974-06-10 | 1979-07-10 | John B. Wright | Cyano phenylene-dioxamates |
| US4011337A (en) * | 1975-07-07 | 1977-03-08 | The Upjohn Company | Oxamide-oxamic compounds, compositions and methods of use |
| US4055414A (en) * | 1976-03-11 | 1977-10-25 | Monsanto Company | Herbicidal composition and method of use |
| US4057556A (en) * | 1976-06-17 | 1977-11-08 | Ayerst, Mckenna & Harrison Ltd. | Troponyl-oxamic acid derivatives |
| US4119783A (en) * | 1977-02-18 | 1978-10-10 | The Upjohn Company | 3'Lower alkylcarbonyl oxanilic acid esters |
| US4089974A (en) * | 1977-06-13 | 1978-05-16 | American Cyanamid Company | 5-Carboxy-phenylenebis(carbonylimino)benzene carboxylic and dicarboxylic acids and salts |
| EP0000152B1 (en) * | 1977-06-28 | 1981-09-09 | Sandoz Ag | Oxaminic acids and esters, process for their preparation and pharmaceutical compositions containing them |
| US4204970A (en) * | 1978-12-07 | 1980-05-27 | Standard Oil Company (Indiana) | Lubricant compositions containing alkylated aromatic amino acid antioxidants |
| EP0018100B1 (en) * | 1979-04-12 | 1984-01-18 | Imperial Chemical Industries Plc | Substituted aromatic biologically active compound, a process for its preparation and its use as biocide |
| CA1181070A (en) * | 1979-11-28 | 1985-01-15 | Kiyoshi Murase | Process of producing 2-hydroxyoxanilic acid derivatives |
| US4296129A (en) * | 1980-10-29 | 1981-10-20 | Pfizer, Inc. | (Carboxyacylamino)phenylalkenamides and esters thereof as SRS-A antagonists |
| US4342781A (en) * | 1981-05-29 | 1982-08-03 | Pfizer Inc. | Diphenylpropenamides as SRS-A antagonists |
| US4584315A (en) * | 1981-11-16 | 1986-04-22 | The Upjohn Company | Method of treating ischemic states |
| US4447449A (en) * | 1981-11-16 | 1984-05-08 | The Upjohn Company | Methods of treating ischemic states |
| DE3229539A1 (de) * | 1982-08-07 | 1984-02-09 | Basf Ag, 6700 Ludwigshafen | Neue oxamidsaeure-derivate, verfahren zu ihrer herstellung und diese enthaltende therapeutische mittel |
| US4788198A (en) * | 1983-09-01 | 1988-11-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | Diazine-ethyenylphenyl oxamic acids and esters and salts thereof |
| DE3474817D1 (en) * | 1983-09-01 | 1988-12-01 | Boehringer Ingelheim Ltd | Diazine-ethenylphenyl oxamic acids and esters and salts thereof |
| US4681884A (en) * | 1983-09-01 | 1987-07-21 | Boehringer Ingelheim Pharmaceuticals, Inc. | Diazine-ethenylphenyl oxamic acids and esters and salts thereof |
| US5457126A (en) * | 1986-11-18 | 1995-10-10 | Alcon Laboratories, Inc. | Use of lodoxamide to treat ophthalmic allergic conditions |
| US6225327B1 (en) | 1996-04-18 | 2001-05-01 | Alcon Laboratories, Inc. | Compounds which inhibit human conjunctival mast cell degranulation for treating ocular allergic-type complications |
| US6225332B1 (en) | 1997-10-21 | 2001-05-01 | Alcon Laboratories, Inc. | Compositions containing histamine H2 agonists and methods of use in treating allergy and inflammation |
| US6596284B1 (en) | 2002-04-30 | 2003-07-22 | Thomas E. Fleming | Treating eczema with a combination of isotonic saline ocean® and nasal mast cell stabilizers |
| ATE454415T1 (de) * | 2002-07-05 | 2010-01-15 | Sabic Innovative Plastics Ip | Witterungsbeständige polycarbonate enthaltend oxanilid-struktureinheinten, verfahren und daraus hergestellte gegenstände |
| CN108863846B (zh) * | 2017-05-09 | 2020-11-06 | 武汉先路医药科技股份有限公司 | 一种洛度沙胺氨丁三醇中间体的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH485485A (de) * | 1966-02-07 | 1970-02-15 | Ciba Geigy | Verwendung von Oxalsäure-esteramiden als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
| US3532737A (en) * | 1967-02-02 | 1970-10-06 | Sterling Drug Inc | Esters of arylglyoxylic acids |
| CH500260A (de) * | 1967-05-16 | 1971-01-29 | Ciba Geigy Ag | Verwendung von Bis-oxalsäure-esteramiden als Stabilisierungsmittel ausserhalb der Textilindustrie |
| US3781329A (en) * | 1971-12-23 | 1973-12-25 | American Cyanamid Co | Electronegatively substituted carboxy-phenyl oxalates as superior chemiluminescent materials |
| US3852324A (en) * | 1972-12-20 | 1974-12-03 | Upjohn Co | N,n-(cyano-phenylene) dioxamic acids |
-
1973
- 1973-07-26 US US05/382,762 patent/US3993679A/en not_active Expired - Lifetime
- 1973-11-13 CH CH1594873A patent/CH605662A5/fr not_active IP Right Cessation
- 1973-11-19 CA CA186,095A patent/CA1030156A/en not_active Expired
- 1973-11-28 GB GB5520873A patent/GB1454777A/en not_active Expired
- 1973-11-28 GB GB4817075A patent/GB1454778A/en not_active Expired
- 1973-12-11 NL NLAANVRAGE7316916,A patent/NL177487C/xx not_active IP Right Cessation
- 1973-12-15 ES ES421536A patent/ES421536A1/es not_active Expired
- 1973-12-15 DE DE2362409A patent/DE2362409C3/de not_active Expired
- 1973-12-17 JP JP48139732A patent/JPS5761028B2/ja not_active Expired
- 1973-12-17 SE SE7316994A patent/SE410965B/sv unknown
- 1973-12-19 FR FR7345462A patent/FR2211230B1/fr not_active Expired
- 1973-12-19 HU HUUO98A patent/HU168135B/hu unknown
-
1982
- 1982-03-11 HK HK109/82A patent/HK10982A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPS49108029A (ru) | 1974-10-14 |
| DE2362409C3 (de) | 1980-05-14 |
| NL177487C (nl) | 1985-10-01 |
| SE410965B (sv) | 1979-11-19 |
| FR2211230B1 (ru) | 1977-04-15 |
| US3993679A (en) | 1976-11-23 |
| NL7316916A (ru) | 1974-06-24 |
| FR2211230A1 (ru) | 1974-07-19 |
| HU168135B (ru) | 1976-02-28 |
| DE2362409A1 (de) | 1974-06-27 |
| HK10982A (en) | 1982-03-19 |
| CA1030156A (en) | 1978-04-25 |
| AU6298073A (en) | 1975-05-29 |
| NL177487B (nl) | 1985-05-01 |
| DE2362409B2 (de) | 1979-08-09 |
| ES421536A1 (es) | 1976-07-16 |
| JPS5761028B2 (ru) | 1982-12-22 |
| GB1454777A (en) | 1976-11-03 |
| GB1454778A (en) | 1976-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |