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Detail of "3060-89-7"

  • MSDS Download
  • CAS Number:
  • 3060-89-7
  • Name:
  • Urea,N'-(4-bromophenyl)-N-methoxy-N-methyl-

  • Superlist Name:
  • Metobromuron
  • Molecular Structure:
  • Formula:
  • C9H11 Br N2 O2
  • Molecular Weight:
  • 259.0998
  • Synonyms:
  • Urea,3-(p-bromophenyl)-1-methoxy-1-methyl- (7CI,8CI);1-(p-Bromophenyl)-3-methoxy-3-methylurea; 1-Methoxy-1-methyl-3-(4-bromophenyl)urea;1-Methoxy-1-methyl-3-(p-bromophenyl)urea;3-(4-Bromophenyl)-1-methyl-1-methoxyurea;3-(p-Bromophenyl)-1-methoxy-1-methylurea;3-(p-Bromophenyl)-1-methyl-1-methoxyurea; C 3126; Metbromuron; Metobromuron;Monobromuron; N-(4-Bromophenyl)-N'-methoxy-N'-methylurea;N-(4-Bromophenyl)-N'-methyl-N'-methoxyurea;N-(p-Bromophenyl)-N'-methyl-N'-methoxyurea; Patoran
  • EINECS:
  • 221-301-5
  • Density:
  • 1.534 g/cm3
  • Melting Point:
  • 95.5-96 ºC
  • Boiling Point:
  • °Cat760mmHg
  • Flash Point:
  • °C
  • Solubility:
  • Solubility: In water 330 mg/l (20 ℃). In acetone 500, dichloromethane 550, methanol 240, toluene 100, octanol 70, chloroform 62.5, hexane 2.6 (all in g/l, 20 ℃).
  • Appearance:
  • White to brown powder
  • Hazard Symbols:
  • HarmfulXnFlammableF
  • Risk Codes:
  • 22-36-20/21/22-11
  • Safety:
  • 16-26-36 Details
  • Transport Information:
  • UN 1648 3

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CAS No.3060-89-7 Metobromuron

Metobromuron

Supplier:NEOCHEMA [ Germany]

910Integral
910

Address:we offer only solutions for the organic residue analysis

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CAS No.3060-89-7 Metobromuron

100 mg

Supplier:Crescent Chemical Company [ United States]

570Integral
570

Tel:(800) 877-3225

Address:2 Oval Dr,Islandia, New York

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CAS No.3060-89-7 Metobromuron

Supplier:China Surchem International [ China (Mainland)]

600Integral
600

Tel:+86-517-83905829

Address:A23006 Jinma Square, No. 39 North Huaihai Rd, Huai An 223001, Jiangsu, China

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Reference

Water toxicity of selected urea herbicides and their classification as water pollutants
Water toxicity of selected urea herbicides and their classification as water pollutants. Tscheu-Schlueter, M.; Winter, W. (Inst. Wasserwirtsch., Berlin DDR-1190, Ger. Dem. Rep.). Acta Hydrochim. Hydrobiol., 13(4), 489-97 (German) 1985. CODEN: AHCBAU. ISSN: 0323-4320. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Section cross-reference(s): 5 The 96-h LD50 value of 8 urea herbicides to Poecilia reticulata were: fenuron [101-42-8] 610, defenuron [1007-36-9] 174, bromfenuron [3408-97-7] 112, monuron [150-68-5] 159, diuron [330-54-1] 17.5, metobromuron [3060-89-7] 44, monolinuron [1746-81-2] 46, linuron [330-55-2] 8.6 mg/L. Even higher toxicity was shown to Ankistrodesmus falcatus. Dose-activity graphs are presented. The urea herbicides are dangerous water pollutants.
Detection of halogenated biphenyls from sunlight photolysis of chlorinated herbicides in aqueous solution
Detection of halogenated biphenyls from sunlight photolysis of chlorinated herbicides in aqueous solution. Tanaka, Fred S.; Hoffer, Barry L.; Wien, Ronald G. (Agric. Res. Serv., US Dep. Agric., Fargo, ND 58105, USA). Pestic. Sci., 16(3), 265-70 (English) 1985. CODEN: PSSCBG. ISSN: 0031-613X. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Section cross-reference(s): 22 A survey study was conducted to det. the generality of chlorinated biphenyl formation from the photolysis of chlorine-contg. herbicides in aq. soln. Seven herbicides from the phenylurea, anilide and carbamate classes were examd. The photoreaction under investigation proceeded via the coupling of 2 herbicide mols. to yield a chlorinated biphenyl with concomitant loss of HCl. In preliminary studies using UV lamps, 4-chlorophenyl methylcarbamate (PPG-124) [2620-53-3] gave a chlorinated biphenyl with only 1 carbamate side chain, and chlorpropham [101-21-3] gave no chlorinated biphenyl, but rather a hydroxylated biphenyl. Employing UV lamps or natural sunlight, photolysis of monuron [150-68-5], diuron [330-54-1], linuron [330-55-2], metobromuron [3060-89-7] and propanil [709-98-8] produced halogenated biphenyls according to the photocoupling reaction under investigation. All yields of chlorinated biphenyls from sunlight photolysis were approx. £1%.
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