PL95290B1 - Zwilzalny proszek biocydowy - Google Patents

Zwilzalny proszek biocydowy Download PDF

Info

Publication number: PL95290B1
Authority: PL; Poland
Prior art keywords: wetting agent; weight; so3na; roocch2ch; wetting
Prior art date: 1973-06-29

Application number

PL17225674A

Other languages

English (en)

Polish (pl)

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.)

1973-06-29

Filing date

1974-06-28

Publication date

1977-10-31

1974-06-28 Application filed filed Critical

1977-10-31 Publication of PL95290B1 publication Critical patent/PL95290B1/pl

Links

239000000843 powder Substances 0.000 title claims description 11
239000000080 wetting agent Substances 0.000 claims description 20
239000002270 dispersing agent Substances 0.000 claims description 14
230000003115 biocidal effect Effects 0.000 claims description 8
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 5
239000004480 active ingredient Substances 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000000945 filler Substances 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
238000009736 wetting Methods 0.000 description 11
239000003139 biocide Substances 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
230000000694 effects Effects 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
238000005187 foaming Methods 0.000 description 5
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 3
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 3
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
238000000034 method Methods 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
239000000126 substance Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
229930003836 cresol Natural products 0.000 description 2
239000006260 foam Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
235000010265 sodium sulphite Nutrition 0.000 description 2
JMYXGQXAPBYULT-UHFFFAOYSA-N 1,10,11,12,13,13-hexachloro-3,4,6,8-tetraoxa-5lambda4-thiatricyclo[8.2.1.02,9]tridec-11-ene 5-oxide Chemical compound S1(=O)OOC2C3(C(=C(C(C2OCO1)(C3(Cl)Cl)Cl)Cl)Cl)Cl JMYXGQXAPBYULT-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
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 1
239000005949 Malathion Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
-1 alkylether sulphates Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001702 camphene derivatives Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
229950006824 dieldrin Drugs 0.000 description 1
NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
RAVGVZKLFHNYBZ-UHFFFAOYSA-N dihydroxy-(4-nitrophenoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound OP(O)(=S)OC1=CC=C([N+]([O-])=O)C=C1 RAVGVZKLFHNYBZ-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003906 humectant Substances 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
229960000453 malathion Drugs 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
239000000047 product Substances 0.000 description 1
239000013558 reference substance Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
125000004436 sodium atom Chemical group 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007921 spray Substances 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PL17225674A 1973-06-29 1974-06-28 Zwilzalny proszek biocydowy PL95290B1 (pl)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19732333050 DE2333050C3 (de)	1973-06-29	1973-06-29	Netzmittel für biocide Spritzpulver

Publications (1)

Publication Number	Publication Date
PL95290B1 true PL95290B1 (pl)	1977-10-31

Family

ID=5885410

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL17225674A PL95290B1 (pl)	1973-06-29	1974-06-28	Zwilzalny proszek biocydowy

Country Status (7)

Country	Link
BE (1)	BE817123A (fr)
DE (1)	DE2333050C3 (fr)
FR (1)	FR2234864A1 (fr)
HU (1)	HU169201B (fr)
IT (1)	IT1015404B (fr)
NL (1)	NL7408460A (fr)
PL (1)	PL95290B1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4082537A (en) *	1977-03-23	1978-04-04	American Cyanamid Company	2,6-dinitroaniline herbicidal compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2028091A (en) *	1933-07-28	1936-01-14	American Cyanamid & Chem Corp	Esters of sulphodicarboxylic acids

1973
- 1973-06-29 DE DE19732333050 patent/DE2333050C3/de not_active Expired
1974
- 1974-06-24 NL NL7408460A patent/NL7408460A/xx not_active Application Discontinuation
- 1974-06-25 IT IT2443074A patent/IT1015404B/it active
- 1974-06-26 HU HUHO001685 patent/HU169201B/hu not_active IP Right Cessation
- 1974-06-28 PL PL17225674A patent/PL95290B1/pl unknown
- 1974-07-01 BE BE146112A patent/BE817123A/fr unknown
- 1974-07-01 FR FR7422846A patent/FR2234864A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
FR2234864A1 (en)	1975-01-24
DE2333050A1 (de)	1975-01-23
DE2333050B2 (de)	1980-08-14
HU169201B (fr)	1976-10-28
IT1015404B (it)	1977-05-10
BE817123A (fr)	1975-01-02
DE2333050C3 (de)	1981-06-04
NL7408460A (fr)	1974-12-31

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