Metobromuron (CAS 3060-89-7) — formula C9H11BrN2O2, molecular weight 259.10; category organic chemicals.
| CAS Number | 3060-89-7 |
|---|---|
| Molecular Formula | C9H11BrN2O2 |
| Molecular Weight | 259.10 |
| Melting Point | 95-96 °C |
| LogP | 2.41 |
| Applications | Uses: Used as pre-emergence herbicide to control annual broad-leaved weeds and grasses in beans, soybeans, tomatoes, tobacco, potatoes, flax, and sunflowers, Not sold in the US, [HSDB] Used in the EU as herbicide on potatoes, [ExPub: EC: EFSA], Farming (Pesticides) [Category: Industry], Used on beans, and sunflowers., IT IS A, SELECTIVE PRE-EMERGENT ANNUAL BROADLEAFED WEED AND GRASS CONTROL IN POTATOES, WHITE (FIELD) AND SNAP (BUSH) BEANS, AT 1.5-2.5 KG AI, HECTARE ..., IT IS, SOMEWHAT LESS EFFECTIVE AGAINST GRASSES, PARTICULARLY AT LOW RATES., ... RECOMMENDED FOR PRE-EMERGENCE USE ON POTATOES, BEANS, GROUNDNUTS AT RATES OF 1.5-2.0 KG AI, HECTARE, ON TOBACCO PRIOR TO TRANSPLANTING AT 1.5-2.5 KG AI, HECTARE., As a herbicide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Herbicides, Methods of Manufacturing: PREPARED BY BROMINATION OF N-PHENYL-N'-METHOXY-N'-METHYLUREA: H MARTIN ET AL, SWISS PATENT 405, 821 CORRESP TO US PATENT 3, 288, 851 (BOTH 1966 TO CIBA)., BY BROMINATION OF 1-METHOXY-1-METHYL-3-PHENYLUREA OR BY REACTION OF 4-BROMOPHENYL ISOCYANATE WITH O, N-DIMETHYLHYDROXYLAMINE. ... BRITISH PATENT 965, 313, US PATENT 3, 223, 721., Reaction of p-bromoaniline with phosgene and N, O-dimethylhydroxylamine (phosgenation, isocyanate addition)., Formulations, Preparations: 50% wettable powder (BASF, Ciba-Geigy). In combination with metolachlor (Galex and Tobacron) or with terbutryn (Ingrater) Ciba-Geigy, 4 lb, gal (400 g, l) flowable (BASF), Combinations: Igrater 50 WP (metobromuron 25% and terbutryn 25%), Galex 500 EC (metobromuron + metolachlor 1:1 or 2:3), C 3126, Ciba-3126, For more Formulations, Preparations (Complete) data for METOBROMURON (6 total), please visit the HSDB record page., General Manufacturing Information: Metobromuron is the bromophenyl analog of monuron., Not marketed in USA., ..., IT, BECOMES NON-PHYTOTOXIC IN 3 MO AT RECOMMENDED DOSAGES., Substituted ureas may be hydrolyzed, whereby the end products are carbon dioxide and the corresponding amines. Hydrolysis proceeds under acid as well as alkaline conditions. This reaction is used for the quantitative analysis of active ingredients and, or residues of urea herbicide preparations by determining either the aromatic or the aliphatic amine moiety. |
| Category | Organic Chemicals |
Documented applications: Uses: Used as pre-emergence herbicide to control annual broad-leaved weeds and grasses in beans, soybeans, tomatoes, tobacco, potatoes, flax, and sunflowers, Not sold in the US, [HSDB] Used in the EU as herbicide on potatoes, [ExPub: EC: EFSA], Farming (Pesticides) [Category: Industry], Used on beans, and sunflowers., IT IS A, SELECTIVE PRE-EMERGENT ANNUAL BROADLEAFED WEED AND GRASS CONTROL IN POTATOES, WHITE (FIELD) AND SNAP (BUSH) BEANS, AT 1.5-2.5 KG AI, HECTARE ..., IT IS, SOMEWHAT LESS EFFECTIVE AGAINST GRASSES, PARTICULARLY AT LOW RATES., ... RECOMMENDED FOR PRE-EMERGENCE USE ON POTATOES, BEANS, GROUNDNUTS AT RATES OF 1.5-2.0 KG AI, HECTARE, ON TOBACCO PRIOR TO TRANSPLANTING AT 1.5-2.5 KG AI, HECTARE., As a herbicide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Herbicides, Methods of Manufacturing: PREPARED BY BROMINATION OF N-PHENYL-N'-METHOXY-N'-METHYLUREA: H MARTIN ET AL, SWISS PATENT 405, 821 CORRESP TO US PATENT 3, 288, 851 (BOTH 1966 TO CIBA)., BY BROMINATION OF 1-METHOXY-1-METHYL-3-PHENYLUREA OR BY REACTION OF 4-BROMOPHENYL ISOCYANATE WITH O, N-DIMETHYLHYDROXYLAMINE. ... BRITISH PATENT 965, 313, US PATENT 3, 223, 721., Reaction of p-bromoaniline with phosgene and N, O-dimethylhydroxylamine (phosgenation, isocyanate addition)., Formulations, Preparations: 50% wettable powder (BASF, Ciba-Geigy). In combination with metolachlor (Galex and Tobacron) or with terbutryn (Ingrater) Ciba-Geigy, 4 lb, gal (400 g, l) flowable (BASF), Combinations: Igrater 50 WP (metobromuron 25% and terbutryn 25%), Galex 500 EC (metobromuron + metolachlor 1:1 or 2:3), C 3126, Ciba-3126, For more Formulations, Preparations (Complete) data for METOBROMURON (6 total), please visit the HSDB record page., General Manufacturing Information: Metobromuron is the bromophenyl analog of monuron., Not marketed in USA., ..., IT, BECOMES NON-PHYTOTOXIC IN 3 MO AT RECOMMENDED DOSAGES., Substituted ureas may be hydrolyzed, whereby the end products are carbon dioxide and the corresponding amines. Hydrolysis proceeds under acid as well as alkaline conditions. This reaction is used for the quantitative analysis of active ingredients and, or residues of urea herbicide preparations by determining either the aromatic or the aliphatic amine moiety..
Metobromuron is a carbon-based organic compound with CAS registry number 3060-89-7 and molecular formula C9H11BrN2O2 (molecular weight 259.10), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 3060-89-7
Its molecular formula C9H11BrN2O2 comprises 9 C, 11 H, 1 Br, 2 N, 2 O atoms.
Also known as: Metobromuron · 秀谷隆
Category: organic chemicals
The CAS registry number of Metobromuron is 3060-89-7.
Molecular formula C9H11BrN2O2, molecular weight 259.10.
It is also registered under: Metobromuron, 秀谷隆.
Recorded applications: Uses: Used as pre-emergence herbicide to control annual broad-leaved weeds and grasses in beans, soybeans, tomatoes, tobacco, potatoes, flax, and sunflowers, Not sold in the US, [HSDB] Used in the EU as herbicide on potatoes, [ExPub: EC: EFSA], Farming (Pesticides) [Category: Industry], Used on beans, and sunflowers., IT IS A, SELECTIVE PRE-EMERGENT ANNUAL BROADLEAFED WEED AND GRASS CONTROL IN POTATOES, WHITE (FIELD) AND SNAP (BUSH) BEANS, AT 1.5-2.5 KG AI, HECTARE ..., IT IS, SOMEWHAT LESS EFFECTIVE AGAINST GRASSES, PARTICULARLY AT LOW RATES., ... RECOMMENDED FOR PRE-EMERGENCE USE ON POTATOES, BEANS, GROUNDNUTS AT RATES OF 1.5-2.0 KG AI, HECTARE, ON TOBACCO PRIOR TO TRANSPLANTING AT 1.5-2.5 KG AI, HECTARE., As a herbicide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Herbicides, Methods of Manufacturing: PREPARED BY BROMINATION OF N-PHENYL-N'-METHOXY-N'-METHYLUREA: H MARTIN ET AL, SWISS PATENT 405, 821 CORRESP TO US PATENT 3, 288, 851 (BOTH 1966 TO CIBA)., BY BROMINATION OF 1-METHOXY-1-METHYL-3-PHENYLUREA OR BY REACTION OF 4-BROMOPHENYL ISOCYANATE WITH O, N-DIMETHYLHYDROXYLAMINE. ... BRITISH PATENT 965, 313, US PATENT 3, 223, 721., Reaction of p-bromoaniline with phosgene and N, O-dimethylhydroxylamine (phosgenation, isocyanate addition)., Formulations, Preparations: 50% wettable powder (BASF, Ciba-Geigy). In combination with metolachlor (Galex and Tobacron) or with terbutryn (Ingrater) Ciba-Geigy, 4 lb, gal (400 g, l) flowable (BASF), Combinations: Igrater 50 WP (metobromuron 25% and terbutryn 25%), Galex 500 EC (metobromuron + metolachlor 1:1 or 2:3), C 3126, Ciba-3126, For more Formulations, Preparations (Complete) data for METOBROMURON (6 total), please visit the HSDB record page., General Manufacturing Information: Metobromuron is the bromophenyl analog of monuron., Not marketed in USA., ..., IT, BECOMES NON-PHYTOTOXIC IN 3 MO AT RECOMMENDED DOSAGES., Substituted ureas may be hydrolyzed, whereby the end products are carbon dioxide and the corresponding amines. Hydrolysis proceeds under acid as well as alkaline conditions. This reaction is used for the quantitative analysis of active ingredients and, or residues of urea herbicide preparations by determining either the aromatic or the aliphatic amine moiety..
Category: Organic Chemicals.
Independent reference data for Metobromuron (CAS 3060-89-7), compiled from public chemistry databases.
| CAS 号 | 3060-89-7 |
|---|---|
| PubChem CID | 18290 |
| 分子式 | C9H11BrN2O2 |
| IUPAC 名称 | 3-(4-bromophenyl)-1-methoxy-1-methylurea |
| UNII（FDA） | 4251089P3L |
| Molecular Weight | 259.10 |
|---|---|
| XLogP3 | 2.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 258.00039 |
| Monoisotopic Mass | 258.00039 |
| Topological Polar Surface Area | 41.6 |
| Heavy Atom Count | 14 |
| Melting Point | 95-96 °C |
|---|---|
| Vapor Pressure | 0.000003 [mmHg] |
| Vapor Pressure | 3X10-6 MM HG @ 20 °C |
| LogP | 2.41 |
| Formulations/Preparations | C 3126 |
| Formulations/Preparations | Ciba-3126 |
METOBROMURON; 3060-89-7; Metbromuron; Monobromuron; Pattonex; 3-(4-Bromophenyl)-1-methoxy-1-methylurea; N'-(4-Bromophenyl)-N-methoxy-N-methylurea; 3-(p-Bromophenyl)-1-methoxy-1-methylurea; DTXSID6042157; Urea, 3-(p-bromophenyl)-1-methoxy-1-methyl-; 3-(p-Bromophenyl)-1-methyl-1-methoxyurea; 4251089P3L; DTXCID4022157; N-(4-Bromophenyl)-N'-methyl-N'-methoxy-harnstoff; RefChem:158371; 221-301-5
| GHS 通报统计 | 5.1% (3 / 59) |
|---|
| GHS 通报统计 | 5.1% (3 / 59) |
|---|---|
| 已通报的危害声明 | H302 (93.2%), H332 (93.2%), H351 (27.1%), H373 (28.8%), H400 (27.1%), H410 (28.8%) |
秀谷隆 · CAS 3060-89-7 · C9H11BrN2O2. UNII 4251089P3L. Melting Point: 95-96 °C; Vapor Pressure: 0.000003 [mmHg]; Vapor Pressure: 3X10-6 MM HG @ 20 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 秀谷隆