CA1037866A - Fongicide en dispersion - Google Patents

Fongicide en dispersion

Info

Publication number: CA1037866A
Authority: CA; Canada
Prior art keywords: weight; dispersions; bcm; polyglycol ether; fungicidal
Prior art date: 1973-10-31
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

CA212,699A

Other languages

English (en)

Other versions

CA212699S (en

Inventor

Konrad Albrecht

Heinz Frensch

Kurt Hartel

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.)

Hoechst AG

Original Assignee

Hoechst 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.)

1973-10-31

Filing date

1974-10-30

Publication date

1978-09-05

1974-10-30 Application filed by Hoechst AG filed Critical Hoechst AG

1978-09-05 Application granted granted Critical

1978-09-05 Publication of CA1037866A publication Critical patent/CA1037866A/fr

Status Expired legal-status Critical Current

Links

239000006185 dispersion Substances 0.000 title claims abstract description 29
230000000855 fungicidal effect Effects 0.000 title claims abstract description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 24
229920000151 polyglycol Polymers 0.000 claims abstract description 18
239000010695 polyglycol Substances 0.000 claims abstract description 18
239000002480 mineral oil Substances 0.000 claims abstract description 11
239000003795 chemical substances by application Substances 0.000 claims abstract description 10
235000010446 mineral oil Nutrition 0.000 claims abstract description 7
TXPYHRFTMYVSLD-UHFFFAOYSA-N 2,3,4-tris(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=C(O)C(CC(C)C)=C1CC(C)C TXPYHRFTMYVSLD-UHFFFAOYSA-N 0.000 claims abstract description 6
125000001931 aliphatic group Chemical group 0.000 claims abstract description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 4
239000011575 calcium Substances 0.000 claims abstract description 4
229910052791 calcium Inorganic materials 0.000 claims abstract description 4
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
150000001875 compounds Chemical class 0.000 claims description 7
230000009885 systemic effect Effects 0.000 abstract description 4
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 abstract 1
239000000203 mixture Substances 0.000 description 14
241000196324 Embryophyta Species 0.000 description 12
238000009472 formulation Methods 0.000 description 9
230000000052 comparative effect Effects 0.000 description 8
RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 7
MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 5
239000002245 particle Substances 0.000 description 5
239000004480 active ingredient Substances 0.000 description 4
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
240000008067 Cucumis sativus Species 0.000 description 3
238000009835 boiling Methods 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000011049 pearl Substances 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
239000010453 quartz Substances 0.000 description 3
239000011347 resin Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
244000141359 Malus pumila Species 0.000 description 2
230000002776 aggregation Effects 0.000 description 2
-1 alicyclic hydrocarbons Chemical class 0.000 description 2
159000000007 calcium salts Chemical class 0.000 description 2
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
230000016615 flocculation Effects 0.000 description 2
238000005189 flocculation Methods 0.000 description 2
238000000227 grinding Methods 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
238000011534 incubation Methods 0.000 description 2
GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
238000004062 sedimentation Methods 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
UYWWLYCGNNCLKE-UHFFFAOYSA-N 2-pyridin-4-yl-1h-benzimidazole Chemical compound N=1C2=CC=CC=C2NC=1C1=CC=NC=C1 UYWWLYCGNNCLKE-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241000896246 Golovinomyces cichoracearum Species 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical class CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
241001307210 Pene Species 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
229920004929 Triton X-114 Polymers 0.000 description 1
229920004897 Triton X-45 Polymers 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
239000000654 additive Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
238000004220 aggregation Methods 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000002542 deteriorative effect Effects 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
238000009837 dry grinding Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
230000002427 irreversible effect Effects 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
FEXWUTZBVAGRAS-UHFFFAOYSA-N methyl 4-amino-1-(butylcarbamoyl)benzimidazole-2-carboxylate Chemical compound C1=CC=C2N(C(=O)NCCCC)C(C(=O)OC)=NC2=C1N FEXWUTZBVAGRAS-UHFFFAOYSA-N 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
230000000069 prophylactic effect Effects 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000007873 sieving Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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

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)

CA212,699A 1973-10-31 1974-10-30 Fongicide en dispersion Expired CA1037866A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2354467A DE2354467C3 (de)	1973-10-31	1973-10-31	Fungizide Dispersionen auf Basis von Benzimidazolmethylcarbamat

Publications (1)

Publication Number	Publication Date
CA1037866A true CA1037866A (fr)	1978-09-05

Family

ID=5896892

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA212,699A Expired CA1037866A (fr)	1973-10-31	1974-10-30	Fongicide en dispersion

Country Status (16)

Country	Link
JP (1)	JPS5077538A (fr)
AT (1)	AT338044B (fr)
BE (1)	BE821781A (fr)
BR (1)	BR7409052D0 (fr)
CA (1)	CA1037866A (fr)
DD (1)	DD114215A5 (fr)
DE (1)	DE2354467C3 (fr)
FR (1)	FR2249617B1 (fr)
GB (1)	GB1476948A (fr)
IL (1)	IL45932A (fr)
IT (1)	IT1046794B (fr)
KE (1)	KE2866A (fr)
MX (1)	MX3679E (fr)
NL (1)	NL7413991A (fr)
OA (1)	OA04841A (fr)
ZA (1)	ZA746994B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1596380A (en)	1977-03-28	1981-08-26	Lilly Industries Ltd	Fungicidal combinations
RO66706A2 (fr) *	1977-10-01	1982-03-24	Centrala Industriala De Produse Anorganice,Ro	Composition fungicide a volume ultrareduit
FR2466952A1 (fr) *	1979-10-12	1981-04-17	Boots Co Ltd	Composition fongicide a base de prochloraz et ses applications
DE2952239A1 (de)	1979-12-22	1981-07-02	Celamerck Gmbh & Co Kg, 6507 Ingelheim	Fungizide mischungen
JPS572202A (en) *	1980-05-21	1982-01-07	Ishihara Sangyo Kaisha Ltd	Composite agricultural chemical composition

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3427388A (en) *	1966-05-06	1969-02-11	Du Pont	Esters of benzimidazolecarbamic acid as mite ovicides
CH501364A (de) *	1967-04-11	1971-01-15	Du Pont	Verfahren zur Bekämpfung von Pilzerkrankungen bei Pflanzen
DE1792687A1 (de) *	1967-05-03	1971-11-25	Du Pont	Fungicides Mittel

1973
- 1973-10-31 DE DE2354467A patent/DE2354467C3/de not_active Expired
1974
- 1974-10-24 IL IL45932A patent/IL45932A/xx unknown
- 1974-10-25 NL NL7413991A patent/NL7413991A/xx unknown
- 1974-10-29 JP JP49124010A patent/JPS5077538A/ja active Pending
- 1974-10-29 AT AT867674A patent/AT338044B/de not_active IP Right Cessation
- 1974-10-29 DD DD181999A patent/DD114215A5/xx unknown
- 1974-10-29 GB GB4675274A patent/GB1476948A/en not_active Expired
- 1974-10-29 IT IT28943/74A patent/IT1046794B/it active
- 1974-10-30 CA CA212,699A patent/CA1037866A/fr not_active Expired
- 1974-10-30 BR BR9052/74A patent/BR7409052D0/pt unknown
- 1974-10-31 ZA ZA00746994A patent/ZA746994B/xx unknown
- 1974-10-31 MX MX741401U patent/MX3679E/es unknown
- 1974-10-31 FR FR7436425A patent/FR2249617B1/fr not_active Expired
- 1974-10-31 BE BE150149A patent/BE821781A/fr unknown
- 1974-10-31 OA OA55335A patent/OA04841A/fr unknown
1978
- 1978-08-03 KE KE2866A patent/KE2866A/xx unknown

Also Published As

Publication number	Publication date
DE2354467B2 (de)	1980-09-04
BR7409052D0 (pt)	1975-08-26
KE2866A (en)	1978-08-18
BE821781A (fr)	1975-04-30
IL45932A (en)	1978-03-10
FR2249617B1 (fr)	1979-04-13
GB1476948A (en)	1977-06-16
AU7483474A (en)	1976-05-06
AT338044B (de)	1977-07-25
ZA746994B (en)	1975-11-26
FR2249617A1 (fr)	1975-05-30
ATA867674A (de)	1976-11-15
NL7413991A (nl)	1975-05-02
IL45932A0 (en)	1974-12-31
MX3679E (es)	1981-04-27
IT1046794B (it)	1980-07-31
DD114215A5 (fr)	1975-07-20
OA04841A (fr)	1980-10-31
JPS5077538A (fr)	1975-06-24
DE2354467A1 (de)	1975-07-17
DE2354467C3 (de)	1981-07-30

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