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Linuron

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Name

Linuron

EINECS 206-356-5
CAS No. 330-55-2 Density 1.41 g/cm3
PSA 41.57000 LogP 3.09150
Solubility 0.0075 g/100 mL in water Melting Point 93-94 °C
Formula C9H10Cl2N2O2 Boiling Point 180-190 °C
Molecular Weight 249.097 Flash Point 11 °C
Transport Information N/A Appearance colorless crystals
Safety 53-45-60-61-36/37 Risk Codes 61-22-40-48/22-50/53-62-39/23/24/25-23/24/25-11
Molecular Structure Molecular Structure of 330-55-2 (Linuron) Hazard Symbols ToxicT, DangerousN
Synonyms

Urea,3-(3,4-dichlorophenyl)-1-methoxy-1-methyl- (6CI,7CI,8CI);1-(3,4-Dichlorophenyl)-3-methoxy-3-methylurea;1-Methoxy-1-methyl-3-(3,4-dichlorophenyl)urea;3-(3,4-Dichlorophenyl)-1-methoxy-1-methylurea;3-(3,4-Dichlorophenyl)-1-methyl-1-methoxyurea;Afalon;Afalon inuron;Alfalon;Aphalon;Cephalon;Du Pont 326;Du Pont Herbicide 326;Herbicide 326;Linex;Linurex;Linuron;Liron;Lorex;Lorox;Methoxydiuron;N-(3,4-Dichlorophenyl)-N'-methoxy-N'-methylurea;N'-(3,4-Dichlorophenyl)-N-methoxy-N-methylurea;Sarclex;Sinuron;

Article Data 26

Linuron Consensus Reports

Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.

Linuron Specification

The 3-(3,4-Dichlorophenyl)-1-methoxy-methylurea, with the CAS registry number 330-55-2, is also known as 1-Methoxy-1-methyl-3-(3,4-dichlorophenyl)urea. It belongs to the product categories of Herbicide; Alpha sort; Endocrine Disruptors (Draft)Pesticides&Metabolites; H-MAnalytical Standards; LPesticides&Metabolites; Urea structureMethod Specific; 2000/60/EC; Alphabetic; Endocrine Disruptors (Draft)Analytical Standards; EPA; European Community: ISO and DIN; Herbicides; Method Specific. Its EINECS registry number is 206-356-5. Its IUPAC name is called 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea. This chemical's classification codes are Agricultural Chemical; Herbicide; Herbicides; Mutation data; Pesticides. It is colorless crystals.

Physical properties of 3-(3,4-Dichlorophenyl)-1-methoxy-methylurea: (1)ACD/LogP: 3.20; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.2; (4)ACD/LogD (pH 7.4): 3.2; (5)ACD/BCF (pH 5.5): 159.44; (6)ACD/BCF (pH 7.4): 159.43; (7)ACD/KOC (pH 5.5): 1312.87; (8)ACD/KOC (pH 7.4): 1312.84; (9)#H bond acceptors: 4; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Index of Refraction: 1.6; (13)Molar Refractivity: 60.41 cm3; (14)Molar Volume: 176.5 cm3; (15)Surface Tension: 49.3 dyne/cm; (16)Density: 1.41 g/cm3; (17)Melting Point: 93-94 °C; (18)Flash Point: 11 °C °C; (19)Boiling Point: 180-190°C at 760 mmHg.

Preparation: this chemical can be prepared by hydroxylurea and dimethyl sulfate. This reaction will need 20% NaOH. The reaction time is 4 hours with reaction temperature of 20-30 ℃. The yield is about 90%.

Uses of 3-(3,4-Dichlorophenyl)-1-methoxy-methylurea: The 3-(3,4-Dichlorophenyl)-1-methoxy-methylurea can be used to prevent body-load single and double cotyledons weeds and some this perennial weeds in corn, wheat and cotton, soybeans, sorghum, peanut, peas, potatoes, sunflower, sugarcane, flax, as well as various vegetables and fruit trees, forest nursery and other crops. Rat oral LD for 4000mg/kg.

When you are using this chemical, please be cautious about it as the following:
This chemical that at low levels may cause damage to health and may present an immediate or delayed danger to one or more components of the environment. It is toxic by inhalation, in contact with skin and if swallowed. This chemical may cause harm to the unborn child. It is possible risk of impaired fertility. When using it, please wear suitable protective clothing and gloves. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible). This material and its container must be disposed of as hazardous waste.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CN(C(=O)NC1=CC(=C(C=C1)Cl)Cl)OC
(2)InChI: InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)
(3)InChIKey: XKJMBINCVNINCA-UHFFFAOYSA-N

The toxicity data is as follows:
 

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
chicken LD50 oral 3765mg/kg (3765mg/kg)   Veterinariya. Veterinary Science. Vol. 58(7), Pg. 63, 1982.
dog LD50 oral 500mg/kg (500mg/kg)   Guide to the Chemicals Used in Crop Protection. Vol. 6, Pg. 317, 1973.
mouse LD50 oral 1500mg/kg (1500mg/kg)   Yakkyoku. Pharmacy. Vol. 36, Pg. 387, 1985.
rabbit LD50 oral 2250mg/kg (2250mg/kg)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A248, Pg. 1984,
rabbit LD50 skin > 5gm/kg (5000mg/kg)   Pesticide Manual. Vol. 9, Pg. 520, 1991.
rat LC50 inhalation 48mg/m3/4H (48mg/m3)   "Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 48, 1982.
rat LD50 oral 1146mg/kg (1146mg/kg)   Fundamental and Applied Toxicology. Vol. 7, Pg. 299, 1986.
rat LD50 skin > 2500mg/kg (2500mg/kg)   Fundamental and Applied Toxicology. Vol. 7, Pg. 299, 1986.

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