CA1280003C - Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides - Google Patents

Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides

Info

Publication number: CA1280003C
Authority: CA; Canada
Prior art keywords: solution; solution according; haloacetamide; alkylthio; weight
Prior art date: 1985-11-26
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 - Lifetime

Application number

CA000521984A

Other languages

English (en)

Inventor

Joseph Synek

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.)

Bayer Corp

Original Assignee

Mobay 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.)

1985-11-26

Filing date

1986-11-03

Publication date

1991-02-12

1986-11-03 Application filed by Mobay Corp filed Critical Mobay Corp

1986-11-03 Priority to CA000521984A priority Critical patent/CA1280003C/fr

1991-02-12 Application granted granted Critical

1991-02-12 Publication of CA1280003C publication Critical patent/CA1280003C/fr

2008-02-12 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000007788 liquid Substances 0.000 title claims abstract description 13
QMNWYGTWTXOQTP-UHFFFAOYSA-N 1h-triazin-6-one Chemical compound O=C1C=CN=NN1 QMNWYGTWTXOQTP-UHFFFAOYSA-N 0.000 claims abstract description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
239000003995 emulsifying agent Substances 0.000 claims abstract description 8
239000000203 mixture Substances 0.000 claims abstract description 6
239000002904 solvent Substances 0.000 claims abstract description 6
150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 4
230000002363 herbicidal effect Effects 0.000 claims abstract description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
239000008096 xylene Substances 0.000 claims description 6
239000005583 Metribuzin Substances 0.000 claims description 5
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims description 5
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical group CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 4
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
AFTQZZLFNGNUPC-UHFFFAOYSA-N 3-butyl-2h-1,2,4-triazin-5-one Chemical compound CCCCC1=NC(=O)C=NN1 AFTQZZLFNGNUPC-UHFFFAOYSA-N 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
239000006185 dispersion Substances 0.000 abstract description 3
239000004009 herbicide Substances 0.000 description 6
239000004615 ingredient Substances 0.000 description 5
239000004480 active ingredient Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
150000003869 acetamides Chemical class 0.000 description 2
239000011149 active material Substances 0.000 description 2
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000009977 dual effect Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
CQQHIHSXNUGDTF-UHFFFAOYSA-N 2-chloro-4,6-diethyl-2h-1,3,5-triazin-1-amine Chemical compound CCC1=NC(Cl)N(N)C(CC)=N1 CQQHIHSXNUGDTF-UHFFFAOYSA-N 0.000 description 1
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
239000005510 Diuron Substances 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
241001579678 Panthea coenobita Species 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000003466 anti-cipated effect Effects 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
239000000725 suspension Substances 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CA000521984A 1985-11-26 1986-11-03 Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides Expired - Lifetime CA1280003C (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000521984A CA1280003C (fr)	1985-11-26	1986-11-03	Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US801,885		1985-11-26
CA000521984A CA1280003C (fr)	1985-11-26	1986-11-03	Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides

Publications (1)

Publication Number	Publication Date
CA1280003C true CA1280003C (fr)	1991-02-12

Family

ID=4134270

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000521984A Expired - Lifetime CA1280003C (fr)	1985-11-26	1986-11-03	Solution de 3-alkylthio-4-amino-6-tert-butyl-1, 2, 4, -triazin-5-ones dans des n-aryl-n-alkoxyalkylbaloacetamides normalement liquides

Country Status (1)

Country	Link
CA (1)	CA1280003C (fr)

1986
- 1986-11-03 CA CA000521984A patent/CA1280003C/fr not_active Expired - Lifetime

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Legal Events

Date	Code	Title	Description
2008-02-12	MKEX	Expiry