- METOXURON
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- $1.00 / 1KG
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2020-01-01
- CAS:19937-59-8
- Min. Order: 1KG
- Purity: 95-99%
- Supply Ability: 1ton
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| | METOXURON Basic information |
| | METOXURON Chemical Properties |
| Melting point | 124-127 °C | | Boiling point | 391.6±42.0 °C(Predicted) | | density | 1.3100 (rough estimate) | | refractive index | 1.5500 (estimate) | | Fp | 2 °C | | storage temp. | APPROX 4°C | | solubility | Chloroform (Slightly), DMSO (Slightly) | | form | Solid | | pka | 13.83±0.70(Predicted) | | color | White to Off-White | | Water Solubility | 678mg/L(23 ºC) | | Major Application | agriculture
environmental | | InChI | 1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14) | | InChIKey | DSRNRYQBBJQVCW-UHFFFAOYSA-N | | SMILES | COc1ccc(NC(=O)N(C)C)cc1Cl | | EPA Substance Registry System | Metoxuron (19937-59-8) |
| Hazard Codes | N,Xn,F | | Risk Statements | 50/53-36-20/21/22-11 | | Safety Statements | 60-61-36-26-16-36/37 | | RIDADR | UN3077 9/PG 3 | | WGK Germany | WGK 2 | | RTECS | YS5775000 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1 | | Toxicity | mouse,LD50,oral,2542mg/kg (2542mg/kg),ENDOCRINE: OTHER CHANGESBLOOD: OTHER CHANGES,Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 47(2), Pg. 13, 1982. |
| | METOXURON Usage And Synthesis |
| Uses | Metoxuron is used as a herbicide. | | Definition | ChEBI: Metoxuron is a member of the class of 3-(3,4-substituted-phenyl)-1,1-dimethylureas that is urea in which one of the nitrogens is substituted by a 3-chloro-4-methoxyphenyl group while the other is substituted by two methyl groups. It is a plant growth regulator and a pre- and post-emergence herbicide used for the control of grasses and broad-leaved weeds in carrots and cereals (e.g. wheat, barley and rye). It has a role as an agrochemical, an environmental contaminant, a herbicide, a xenobiotic, a photosystem-II inhibitor and a plant growth regulator. It is a 3-(3,4-substituted-phenyl)-1,1-dimethylurea, a monomethoxybenzene and a member of monochlorobenzenes. | | Metabolic pathway | Photodegradation of metoxuron with UV irradiation in
the presence of UV-H2O2 and -TiO2 primarily proceeds
with the replacement of the chlorine atom with the
hydroxy group and the attack of OH radicals at the
6-position on the phenyl ring. The principal
photoproducts identified are 3-(4-methoxy-2,5-
paraquinone)-1,1-dimethylurea, hydroxymetoxuron,
3-(3-hydroxy-4-methoxyphenyl)-1,1-dimethylurea,
3-(3-chloro-4-hydroxyphenyl)-1,1-dimethylurea, and
3-(3-chloro-4-methoxyphenyl)-1,1dimethylurea. |
| | METOXURON Preparation Products And Raw materials |
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