CH512186A - Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen - Google Patents

Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen

Info

Publication number: CH512186A
Authority: CH; Switzerland
Prior art keywords: salts; arylguanamines; arylguanamine; carbon atoms; contain
Prior art date: 1967-12-14

Application number

CH1618068A

Other languages

German (de)

English (en)

Inventor

Max Dr Schellenbaum

Max Dr Duennenberger

Original Assignee

Ciba Geigy 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.)

1967-12-14

Filing date

1968-10-30

Publication date

1971-09-15

1967-12-14 Priority claimed from CH1754667A external-priority patent/CH482404A/de

1968-10-30 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1968-10-30 Priority to CH214171A priority Critical patent/CH504837A/de

1968-10-30 Priority to CH1618068D priority patent/CH1618068A4/xx

1968-10-30 Priority to CH1618068A priority patent/CH512186A/de

1968-12-13 Priority to ES361401A priority patent/ES361401A1/es

1971-09-15 Publication of CH512186A publication Critical patent/CH512186A/de

Links

150000003839 salts Chemical class 0.000 title claims abstract description 16
230000000845 anti-microbial effect Effects 0.000 title claims abstract description 4
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
244000005700 microbiome Species 0.000 claims abstract description 5
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 5
239000004753 textile Substances 0.000 claims abstract description 5
239000002253 acid Substances 0.000 claims abstract description 3
150000007513 acids Chemical class 0.000 claims abstract description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 3
229910052760 oxygen Inorganic materials 0.000 claims abstract 2
150000001875 compounds Chemical class 0.000 claims description 11
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
150000001347 alkyl bromides Chemical class 0.000 claims description 2
150000001351 alkyl iodides Chemical class 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 2
239000000463 material Substances 0.000 claims description 2
230000001419 dependent effect Effects 0.000 claims 2
150000001242 acetic acid derivatives Chemical class 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 claims 1
150000004675 formic acid derivatives Chemical class 0.000 claims 1
150000003840 hydrochlorides Chemical class 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
150000003873 salicylate salts Chemical class 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 abstract description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 1
125000005842 heteroatom Chemical group 0.000 abstract 1
230000000266 injurious effect Effects 0.000 abstract 1
125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
229920006395 saturated elastomer Polymers 0.000 abstract 1
241000894006 Bacteria Species 0.000 description 5
229920001817 Agar Polymers 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
239000008272 agar Substances 0.000 description 4
230000008018 melting Effects 0.000 description 4
238000002844 melting Methods 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
235000001674 Agaricus brunnescens Nutrition 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
210000004556 brain Anatomy 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000835 fiber Substances 0.000 description 2
238000001802 infusion Methods 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000000203 mixture Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
238000001953 recrystallisation Methods 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
210000002268 wool Anatomy 0.000 description 2
-1 2 - acetoxyethyl Chemical group 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
ORLGPUVJERIKLW-UHFFFAOYSA-N 5-chlorotriazine Chemical class ClC1=CN=NN=C1 ORLGPUVJERIKLW-UHFFFAOYSA-N 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
241000194017 Streptococcus Species 0.000 description 1
241000223238 Trichophyton Species 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
125000001769 aryl amino group Chemical group 0.000 description 1
244000052616 bacterial pathogen Species 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000007858 starting material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pharmacology & Pharmacy (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Medicinal Chemistry (AREA)
Plant Pathology (AREA)
Epidemiology (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

CH1618068A 1967-12-14 1968-10-30 Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen CH512186A (de)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
CH214171A CH504837A (de)	1968-10-30	1968-10-30	Verwendung von Arylguanaminsalzen zur Bekämpfung schädlicher Mikroorganismen
CH1618068D CH1618068A4 (es)	1968-10-30	1968-10-30
CH1618068A CH512186A (de)	1967-12-14	1968-10-30	Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen
ES361401A ES361401A1 (es)	1967-12-14	1968-12-13	Procedimiento para la preparacion de arilguanaminas.

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH1754667A CH482404A (de)	1967-12-14	1967-12-14	Verwendung von Arylguanaminen zum antimikrobiellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen
CH1618068A CH512186A (de)	1967-12-14	1968-10-30	Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen

Publications (1)

Publication Number	Publication Date
CH512186A true CH512186A (de)	1971-09-15

Family

ID=25717473

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1618068A CH512186A (de)	1967-12-14	1968-10-30	Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen

Country Status (2)

Country	Link
CH (1)	CH512186A (es)
ES (1)	ES361401A1 (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN117024361A (zh) *	2023-07-21	2023-11-10	科莱博(江苏)科技股份有限公司	一种三氟甲磺酸衍生物及其制备方法

1968
- 1968-10-30 CH CH1618068A patent/CH512186A/de unknown
- 1968-12-13 ES ES361401A patent/ES361401A1/es not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN117024361A (zh) *	2023-07-21	2023-11-10	科莱博(江苏)科技股份有限公司	一种三氟甲磺酸衍生物及其制备方法
CN117024361B (zh) *	2023-07-21	2024-04-26	科莱博(江苏)科技股份有限公司	一种三氟甲磺酸衍生物及其制备方法

Also Published As

Publication number	Publication date
ES361401A1 (es)	1970-09-16

Legal Events

Date	Code	Title	Description
1975-07-15	PLZ	Patent of addition ceased

Publication	Publication Date	Title
DE69028461T2 (de)	1997-02-06	Triazin-derivate und unkrautvertilgungsmittel daraus
DE2609280A1 (de)	1977-09-15	Schaedlingsbekaempfungsmittel
DE1617994A1 (de)	1971-05-19	Mittel zur Bekaempfung von schaedlichen Mikroorganismen
DE1768961A1 (de)	1972-01-13	Neue Salicylsaeure-o-hydroxyphenylamide,Verfahren zu deren Herstellung und Verwendung
DE2133056C3 (de)	1980-10-23	Verwendung von NJS-di-alkyl-N'arylsubstituierten Guanidinen zur Bekämpfung von Mehltaupilzen und Grauschimmel der Pflanzen
DE2509416C2 (de)	1985-04-11	Dinitrobenzotrifluoride, Verfahren zu deren Herstellung und diese enthaltende pestizide Zusammensetzungen
DE2514402A1 (de)	1976-10-21	Insektizide mittel
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DE2921660A1 (de)	1980-01-10	5-nitroimidazolderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende antiprotozoen-mittel
DE2133049A1 (de)	1972-01-05	Heterocyclische Verbindungen,Verfahren zu deren Herstellung sowie deren Verwendung
CH512186A (de)	1971-09-15	Anwendung von Arylguanaminsalzen zum antibakteriellen Ausrüsten bzw. zum Schützen von Textilfasern gegen Mikroorganismen
DE1955894A1 (de)	1970-07-02	Herbizides und insektizides Mittel
CH504837A (de)	1971-03-31	Verwendung von Arylguanaminsalzen zur Bekämpfung schädlicher Mikroorganismen
CH515875A (de)	1971-11-30	Verfahren zur Herstellung von bakterizid wirksamen Kohlensäure-bis-(phenoxyphenyl)- estern und ihre Verwendung
DE2041732A1 (de)	1972-02-24	Acylierte Arylhydrazino-2-imidazoline,Verfahren zu ihrer Herstellung und ihre Verwendung als Ektoparasitizide
DE2242785A1 (de)	1974-03-14	1-alkylsulfonyl-2-trifluormethylbenzimidazole, verfahren zu ihrer herstellung sowie ihre verwendung als ektoparasitenmittel
DE1812784A1 (de)	1969-07-10	Arylguanamine,Verfahren zu ihrer Herstellung und Verwendung als Antimikrobika
DD265783A5 (de)	1989-03-15	Pyrazoline, ihre herstellung und ihre verwendung als mittel mit insektizider und akarizider wirkung
DE1542993C3 (de)	1974-05-16	Verwendung von N-Cyanoalkylchloracetamiden als Pflanzenfungizide
DE3134596A1 (de)	1982-08-19	Carbamatderivate, insektizide, antimilben- oder nematozide zusammensetzungen, welche diese enthalten, und verfahren zu deren herstellung
DE2033720A1 (de)	1971-02-04	Verwendung von 2 Hydroxybenzophenonen zur Bekämpfung schädlicher Mikroorganismen
AT213832B (de)	1961-03-10	Verfahren zum Schützen von organischen Materialien aller Art vor Befall und Schädigung durch Mikroorganismen
DE1770517C (de)	1972-10-12	Benzimidazolverbindungen, Verfahren zu deren Herstellung und diese enthaltende Mittel
AT221528B (de)	1962-06-12	Verfahren zur Herstellung von neuen, insektizid und bakterizid wirksamen Derivaten des Diphenylharnstoffes
AT243445B (de)	1965-11-10	Verfahren zur Herstellung von neuen, am Stickstoff substituierten 3-(Dibenzo-[a,d]-1, 4-cycloheptadien-5-yloxy)-nortropanen und von Salzen dieser Verbindungen