CH654173A5 - Composizioni liquide stabili di meta-bis-carbammati erbicidi. - Google Patents

Composizioni liquide stabili di meta-bis-carbammati erbicidi. Download PDF

Info

Publication number: CH654173A5
Authority: CH; Switzerland
Prior art keywords: bis; herbicide; compositions; formula; weight
Prior art date: 1982-07-16

Application number

CH3818/83A

Other languages

English (en)

Italian (it)

Inventor

Moro Anacleto Dal

Sergio Maccone

Original Assignee

Montedison Spa

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.)

1982-07-16

Filing date

1983-07-12

Publication date

1986-02-14

1983-07-12 Application filed by Montedison Spa filed Critical Montedison Spa

1986-02-14 Publication of CH654173A5 publication Critical patent/CH654173A5/it

Links

239000000203 mixture Substances 0.000 title claims description 66
239000004009 herbicide Substances 0.000 title claims description 34
239000007788 liquid Substances 0.000 title description 3
230000002363 herbicidal effect Effects 0.000 claims description 26
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 24
239000004094 surface-active agent Substances 0.000 claims description 24
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 16
235000011007 phosphoric acid Nutrition 0.000 claims description 13
239000005594 Phenmedipham Substances 0.000 claims description 9
IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
239000003960 organic solvent Substances 0.000 claims description 7
-1 alkyl aromatic hydrocarbons Chemical class 0.000 claims description 6
239000005503 Desmedipham Substances 0.000 claims description 4
WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
150000001733 carboxylic acid esters Chemical class 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
150000003016 phosphoric acids Chemical class 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 22
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 11
229910000147 aluminium phosphate Inorganic materials 0.000 description 11
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 8
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000008096 xylene Substances 0.000 description 6
239000002253 acid Substances 0.000 description 5
230000015556 catabolic process Effects 0.000 description 5
238000006731 degradation reaction Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
238000004128 high performance liquid chromatography Methods 0.000 description 4
239000000758 substrate Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000004996 alkyl benzenes Chemical class 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
229960001760 dimethyl sulfoxide Drugs 0.000 description 3
238000007046 ethoxylation reaction Methods 0.000 description 3
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000011575 calcium Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000000034 method Methods 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000009333 weeding Methods 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N25/22—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 containing ingredients stabilising the active ingredients
- 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH3818/83A 1982-07-16 1983-07-12 Composizioni liquide stabili di meta-bis-carbammati erbicidi. CH654173A5 (it)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT22428/82A IT1195941B (it)	1982-07-16	1982-07-16	Composizioni liquide stabili di meta-bis-carbammati erbicidi

Publications (1)

Publication Number	Publication Date
CH654173A5 true CH654173A5 (it)	1986-02-14

Family

ID=11196176

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH3818/83A CH654173A5 (it)	1982-07-16	1983-07-12	Composizioni liquide stabili di meta-bis-carbammati erbicidi.

Country Status (16)

Country	Link
JP (1)	JPS5931703A (ro)
BE (1)	BE897299A (ro)
CH (1)	CH654173A5 (ro)
CS (1)	CS235047B2 (ro)
DD (1)	DD209953A5 (ro)
DE (1)	DE3325444A1 (ro)
DK (1)	DK318483A (ro)
FI (1)	FI832524L (ro)
FR (1)	FR2530122A1 (ro)
GR (1)	GR79327B (ro)
IL (1)	IL69215A0 (ro)
IT (1)	IT1195941B (ro)
NL (1)	NL8302464A (ro)
PL (1)	PL135928B1 (ro)
RO (1)	RO88069A (ro)
SE (1)	SE8303926L (ro)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SK278523B6 (en) *	1984-02-29	1997-08-06	Erik Nielsen	A stabilised liquid herbicidal agent and method for killing weed plants
FR2590119B1 (fr) *	1985-03-14	1988-07-29	Rhone Poulenc Agrochimie	Compositions herbicides liquides stabilisees, a base de biscarbamate
FR2596618B1 (fr) *	1986-04-02	1988-07-15	Rhone Poulenc Agrochimie	Compositions herbicides a base de biscarbamate et le procede de traitement herbicide les utilisant
FR2597720A1 (fr) *	1986-04-29	1987-10-30	Rhone Poulenc Agrochimie	Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation.
FR2599593A1 (fr) *	1986-06-06	1987-12-11	Rhone Poulenc Agrochimie	Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation
IT1199818B (it) *	1986-12-19	1989-01-05	Agrimont Spa	Composizioni di metil-3-(3'-metilfenil-carbamoilossi)feniclcarbammato stabili in emulsione acquosa
JPH01290605A (ja) *	1988-05-18	1989-11-22	Dai Ichi Kogyo Seiyaku Co Ltd	水中崩壊性良好な農薬粒剤
JP2005145901A (ja) *	2003-11-17	2005-06-09	Hokko Chem Ind Co Ltd	茎葉散布用の農薬製剤
CN103501598B (zh) *	2011-05-03	2016-02-03	巴斯夫欧洲公司	包含二甲亚砜和磷酸酯的助剂

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3898075A (en) *	1970-01-20	1975-08-05	Freund Heinz Eberhard	Stabilized liquid compositions
IT1163687B (it) *	1979-07-27	1987-04-08	Montedison Spa	Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature
HU177590B (en) *	1979-10-26	1981-11-28	Chinoin Gyogyszer Es Vegyeszet	Stable liquid herbicide preparation

1982
- 1982-07-16 IT IT22428/82A patent/IT1195941B/it active
1983
- 1983-07-11 DK DK318483A patent/DK318483A/da not_active Application Discontinuation
- 1983-07-11 FI FI832524A patent/FI832524L/fi not_active Application Discontinuation
- 1983-07-11 NL NL8302464A patent/NL8302464A/nl not_active Application Discontinuation
- 1983-07-11 SE SE8303926A patent/SE8303926L/xx not_active Application Discontinuation
- 1983-07-12 RO RO83111611A patent/RO88069A/ro unknown
- 1983-07-12 CH CH3818/83A patent/CH654173A5/it not_active IP Right Cessation
- 1983-07-13 FR FR8311687A patent/FR2530122A1/fr not_active Withdrawn
- 1983-07-13 IL IL69215A patent/IL69215A0/xx unknown
- 1983-07-14 GR GR71940A patent/GR79327B/el unknown
- 1983-07-14 DE DE19833325444 patent/DE3325444A1/de not_active Withdrawn
- 1983-07-15 PL PL1983243030A patent/PL135928B1/pl unknown
- 1983-07-15 CS CS835357A patent/CS235047B2/cs unknown
- 1983-07-15 BE BE0/211180A patent/BE897299A/fr not_active IP Right Cessation
- 1983-07-15 DD DD83253118A patent/DD209953A5/de not_active IP Right Cessation
- 1983-07-15 JP JP58128081A patent/JPS5931703A/ja active Pending

Also Published As

Publication number	Publication date
NL8302464A (nl)	1984-02-16
PL243030A1 (en)	1984-07-16
IT8222428A1 (it)	1984-01-16
GR79327B (ro)	1984-10-22
FI832524A0 (fi)	1983-07-11
DK318483D0 (da)	1983-07-11
DK318483A (da)	1984-01-17
IL69215A0 (en)	1983-11-30
DD209953A5 (de)	1984-05-30
IT8222428A0 (it)	1982-07-16
RO88069B (ro)	1985-10-31
FI832524L (fi)	1984-01-17
SE8303926D0 (sv)	1983-07-11
JPS5931703A (ja)	1984-02-20
CS235047B2 (en)	1985-04-16
IT1195941B (it)	1988-11-03
BE897299A (fr)	1984-01-16
RO88069A (ro)	1985-11-30
SE8303926L (sv)	1984-01-17
PL135928B1 (en)	1986-01-31
DE3325444A1 (de)	1984-01-19
FR2530122A1 (fr)	1984-01-20

Legal Events

Date	Code	Title	Description
1992-03-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

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CA3172234A1 (en)	2021-10-21	Agricultural formulations