CA1050880A - Composes a proprietes microbicides et algacides - Google Patents

Composes a proprietes microbicides et algacides

Info

Publication number: CA1050880A
Authority: CA; Canada
Prior art keywords: alkyl; composition; group; weight; quaternary ammonium
Prior art date: 1974-12-23
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

CA240,918A

Other languages

English (en)

Other versions

CA240918S (en

Inventor

Roger C. Hollenbach

Harry M. Castrantas

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.)

FMC Corp

Original Assignee

FMC 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.)

1974-12-23

Filing date

1975-12-02

Publication date

1979-03-20

1975-12-02 Application filed by FMC Corp filed Critical FMC Corp

1979-03-20 Application granted granted Critical

1979-03-20 Publication of CA1050880A publication Critical patent/CA1050880A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 74
238000011012 sanitization Methods 0.000 title abstract description 5
230000002353 algacidal effect Effects 0.000 title abstract description 3
239000000460 chlorine Substances 0.000 claims abstract description 50
229910052801 chlorine Inorganic materials 0.000 claims abstract description 49
150000003242 quaternary ammonium salts Chemical class 0.000 claims abstract description 18
239000003619 algicide Substances 0.000 claims abstract description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
PYILKOIEIHHYGD-UHFFFAOYSA-M sodium;1,5-dichloro-4,6-dioxo-1,3,5-triazin-2-olate;dihydrate Chemical compound O.O.[Na+].[O-]C1=NC(=O)N(Cl)C(=O)N1Cl PYILKOIEIHHYGD-UHFFFAOYSA-M 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 12
-1 diisobutylphenoxyethoxyethyl Chemical group 0.000 claims description 9
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
150000001875 compounds Chemical class 0.000 claims description 2
229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
125000006839 xylylene group Chemical group 0.000 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
239000005909 Kieselgur Substances 0.000 claims 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
239000011734 sodium Substances 0.000 abstract description 7
229910052708 sodium Inorganic materials 0.000 abstract description 7
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 abstract description 6
238000004880 explosion Methods 0.000 abstract description 4
239000007864 aqueous solution Substances 0.000 abstract description 3
230000009182 swimming Effects 0.000 abstract description 3
150000004683 dihydrates Chemical class 0.000 abstract description 2
230000002085 persistent effect Effects 0.000 abstract description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 45
239000003795 chemical substances by application Substances 0.000 description 24
238000000354 decomposition reaction Methods 0.000 description 15
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 12
230000000052 comparative effect Effects 0.000 description 9
CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical class [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 7
229910052799 carbon Inorganic materials 0.000 description 7
CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 description 6
230000014759 maintenance of location Effects 0.000 description 5
235000019270 ammonium chloride Nutrition 0.000 description 4
238000003556 assay Methods 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
125000001453 quaternary ammonium group Chemical group 0.000 description 4
230000000717 retained effect Effects 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
239000002655 kraft paper Substances 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000000243 solution Substances 0.000 description 3
ZYFORHCCOXYZKB-UHFFFAOYSA-M (2,6-dimethyl-4-phenylheptan-4-yl)-dimethyl-[2-(2-phenoxyethoxy)ethyl]azanium chloride hydrate Chemical compound O.[Cl-].C=1C=CC=CC=1OCCOCC[N+](C)(C)C(CC(C)C)(CC(C)C)C1=CC=CC=C1 ZYFORHCCOXYZKB-UHFFFAOYSA-M 0.000 description 2
ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 2
UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 2
ABONIXOLZDCGIG-UHFFFAOYSA-N calcium;dihypochlorite;dihydrate Chemical compound O.O.[Ca+2].Cl[O-].Cl[O-] ABONIXOLZDCGIG-UHFFFAOYSA-N 0.000 description 2
150000001805 chlorine compounds Chemical class 0.000 description 2
230000000875 corresponding effect Effects 0.000 description 2
239000011521 glass Substances 0.000 description 2
ISMYGHVVCUTUFB-UHFFFAOYSA-N hypochlorous acid dihydrate Chemical compound O.O.ClO ISMYGHVVCUTUFB-UHFFFAOYSA-N 0.000 description 2
238000003780 insertion Methods 0.000 description 2
230000037431 insertion Effects 0.000 description 2
229910001120 nichrome Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
IFIDXBCRSWOUSB-UHFFFAOYSA-N potassium;1,3-dichloro-1,3,5-triazinane-2,4,6-trione Chemical compound [K+].ClN1C(=O)NC(=O)N(Cl)C1=O IFIDXBCRSWOUSB-UHFFFAOYSA-N 0.000 description 2
230000002269 spontaneous effect Effects 0.000 description 2
JWSQWXWJDSOPDU-UHFFFAOYSA-N (2,6-dimethyl-4-phenylheptan-4-yl)-dimethyl-[2-(2-phenoxyethoxy)ethyl]azanium Chemical compound C=1C=CC=CC=1OCCOCC[N+](C)(C)C(CC(C)C)(CC(C)C)C1=CC=CC=C1 JWSQWXWJDSOPDU-UHFFFAOYSA-N 0.000 description 1
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
230000004913 activation Effects 0.000 description 1
230000005791 algae growth Effects 0.000 description 1
229960001040 ammonium chloride Drugs 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
150000003841 chloride salts Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
125000006182 dimethyl benzyl group Chemical group 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
125000006178 methyl benzyl group Chemical group 0.000 description 1
239000006082 mold release agent Substances 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 1
230000001902 propagating effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
239000010959 steel Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
YFYABWXIJBTAAM-UHFFFAOYSA-M trimethyl(2-phenyltetradecan-2-yl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCC(C)([N+](C)(C)C)C1=CC=CC=C1 YFYABWXIJBTAAM-UHFFFAOYSA-M 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/76—Treatment of water, waste water, or sewage by oxidation with halogens or compounds of halogens
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Inorganic Chemistry (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Hydrology & Water Resources (AREA)
Environmental & Geological Engineering (AREA)
Water Supply & Treatment (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CA240,918A 1974-12-23 1975-12-02 Composes a proprietes microbicides et algacides Expired CA1050880A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US53573974A	1974-12-23	1974-12-23

Publications (1)

Publication Number	Publication Date
CA1050880A true CA1050880A (fr)	1979-03-20

Family

ID=24135563

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA240,918A Expired CA1050880A (fr)	1974-12-23	1975-12-02	Composes a proprietes microbicides et algacides

Country Status (11)

Country	Link
JP (1)	JPS5186122A (fr)
AU (1)	AU498154B2 (fr)
BE (1)	BE837038A (fr)
CA (1)	CA1050880A (fr)
DE (1)	DE2558181A1 (fr)
ES (1)	ES443783A1 (fr)
FR (1)	FR2295761A1 (fr)
GB (1)	GB1494869A (fr)
IT (1)	IT1051851B (fr)
NZ (1)	NZ179533A (fr)
ZA (1)	ZA757978B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0032357B1 (fr) *	1979-12-18	1983-09-21	Ciba-Geigy Ag	Utilisation de 2-chloro-4,6-diamino-s-triazines comme algicides
JPH0243989A (ja) *	1988-08-03	1990-02-14	Otsuka Chem Co Ltd	用水系の微生物抑制方法
AT413980B (de) *	2004-10-08	2006-08-15	Maximilian Babeluk	Tablette
JP2017506653A (ja) *	2014-02-27	2017-03-09	ブローミンコンパウンズリミテッド	殺生物性組成物、その調製および使用方法

1975
- 1975-12-02 CA CA240,918A patent/CA1050880A/fr not_active Expired
- 1975-12-03 AU AU87231/75A patent/AU498154B2/en not_active Expired
- 1975-12-12 NZ NZ179533A patent/NZ179533A/xx unknown
- 1975-12-16 JP JP50149221A patent/JPS5186122A/ja active Pending
- 1975-12-18 FR FR7538861A patent/FR2295761A1/fr active Granted
- 1975-12-19 IT IT30580/75A patent/IT1051851B/it active
- 1975-12-19 GB GB52124/75A patent/GB1494869A/en not_active Expired
- 1975-12-23 ZA ZA00757978A patent/ZA757978B/xx unknown
- 1975-12-23 DE DE19752558181 patent/DE2558181A1/de not_active Withdrawn
- 1975-12-23 BE BE163083A patent/BE837038A/fr unknown
- 1975-12-23 ES ES443783A patent/ES443783A1/es not_active Expired

Also Published As

Publication number	Publication date
NZ179533A (en)	1978-06-02
DE2558181A1 (de)	1976-07-01
AU8723175A (en)	1977-06-09
ES443783A1 (es)	1977-04-16
JPS5186122A (en)	1976-07-28
GB1494869A (en)	1977-12-14
ZA757978B (en)	1976-12-29
FR2295761A1 (fr)	1976-07-23
FR2295761B1 (fr)	1980-03-28
AU498154B2 (en)	1979-02-15
BE837038A (fr)	1976-06-23
IT1051851B (it)	1981-05-20

Publication	Publication Date	Title
CA1098250A (fr)	1981-03-24	Traduction non-disponible
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US7695639B2 (en)	2010-04-13	Calcium hypochlorite compositions
EP0427517A1 (fr)	1991-05-15	Composition oxydante N-halogénée et oxydant N-halogéné qui contient un pigment bleu stable
CN100522136C (zh)	2009-08-05	次氯酸钙混合物片
BRPI0620502A2 (pt)	2011-11-16	composição de tratamento de água
CA1050880A (fr)	1979-03-20	Composes a proprietes microbicides et algacides
US5049385A (en)	1991-09-17	Solid halogen-containing composition and method for producing same
JPH11505245A (ja)	1999-05-18	ガス発生が減じられたクロロイソシアヌル酸組成物
US5498415A (en)	1996-03-12	Disinfectant for the treatment of water systems
CA2221252C (fr)	2004-08-17	Assainissant et clarificateur multifonction a dissolution lente
US5015643A (en)	1991-05-14	Disinfectant for the treatment of water systems
US7431863B2 (en)	2008-10-07	Calcium hypochlorite composition
BRPI0717966B1 (pt)	2018-08-14	Composição sólida de tratamento de água
US4058618A (en)	1977-11-15	Certain hydantoin containing bactericides which are resistant to self-heating
JP2006522805A (ja)	2006-10-05	固体殺生物剤
JP3323197B2 (ja)	2002-09-09	水系処理のための殺菌剤
US3919103A (en)	1975-11-11	Trichloroisocyanuric acid stabilized with hydrated sodium dichloroisocyanurate
US3853867A (en)	1974-12-10	Method of stabilizing dichlorocyanuric acid salts
GB2094799A (en)	1982-09-22	Stabilised succinyl peroxide composition
WO2009060246A2 (fr)	2009-05-14	Liquide ignifugeant, production et utilisation de ce dernier
JPS6297692A (ja)	1987-05-07	高溶解性及び持続性を有する殺菌清浄剤
US4145543A (en)	1979-03-20	Alkali metal dichloroisocyanurate compositions
GB1307125A (en)	1973-02-14	Chlorine-containing compositions
JPS61130203A (ja)	1986-06-18	安定化された殺虫剤