Linuron
- CAS No.
- 330-55-2
- Chemical Name:
- Linuron
- Synonyms
- Liron;LOROX;LINEX;Lorex;AFALON;LINNET;Laroks;Afolan;Norunil;Sarclex
- CBNumber:
- CB2749714
- Molecular Formula:
- C9H10Cl2N2O2
- Molecular Weight:
- 249.09
- MOL File:
- 330-55-2.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/11/22 20:27:16
| Melting point | 93-94°C |
|---|---|
| Boiling point | 180-190°C |
| Density | 1.4909 (rough estimate) |
| refractive index | 1.6100 (estimate) |
| Flash point | 11 °C |
| storage temp. | APPROX 4°C |
| solubility | DMSO : 100 mg/mL (401.46 mM; Need ultrasonic) |
| form | Crystalline Solid |
| pka | 12.13±0.70(Predicted) |
| color | White |
| Water Solubility | 0.0075 g/100 mL |
| BRN | 2128725 |
| CAS DataBase Reference | 330-55-2(CAS DataBase Reference) |
| NIST Chemistry Reference | N'-(3,4-Dichlorophenyl)-N-methoxy-N-methylurea(330-55-2) |
| EPA Substance Registry System | Linuron (330-55-2) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |    GHS07,GHS08,GHS09 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H302-H351-H360FD-H373-H410 | |||||||||
| Precautionary statements | P202-P260-P264-P273-P301+P312-P308+P313 | |||||||||
| Hazard Codes | T;N,N,T,F | |||||||||
| Risk Statements | 61-22-40-48/22-50/53-62-39/23/24/25-23/24/25-11 | |||||||||
| Safety Statements | 53-45-60-61-36/37-16-7 | |||||||||
| RIDADR | UN 3077 | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | YS9100000 | |||||||||
| HS Code | 29280000 | |||||||||
| Toxicity | LD50 orally in rats: 1500 mg/kg (Bailey, White) | |||||||||
| NFPA 704 |
|
Linuron Chemical Properties,Uses,Production
Description
Linuron is found as white crystals that have no smell. It is very slightly soluble in water. Linuron can enter the body either by ingestion of contaminated food or water or by dermal contact. Linuron can cause nausea, vomiting, and diarrhea. Eye contact can cause irritation. There is little evidence available as to the effects of exposure to linuron on human health. However, exposure to linuron at normal background levels is unlikely to have any adverse effect on human health.
Chemical Properties
White crystalline solid or powder. Odorless. Commercial product may be available a water soluble or emulsifiable concentrate.
Uses
Linuron is used to control annual and perennial broadleaf and grassy weeds on crop and noncrop sites. It is used as a pre- and post-emergent herbicide. It works by inhibiting photosynthesis in target weed plants. It is used in soybean, cotton, potato, corn, bean, pea, winter wheat, asparagus, carrot, and fruit crops. It is also used on crops stored in warehouses and storerooms. Linuron is classified by the US Environmental Protection Agency (EPA) as a Restricted Use Pesticide (RUP).
Definition
ChEBI: A member of the class of ureas that is N-methyl urea substituted by a methoxy group at position 1 and a 3,4-dichlorophenyl group at position 3.
General Description
Colorless crystals. Non corrosive. Used as an herbicide.
Air & Water Reactions
Hydrolyzed slowly by acids and bases.
Reactivity Profile
A urea derivative.
Health Hazard
Lowtomoderatelytoxicbyingestion—LD50varying with experimental animals; 4-hourexposure to its vapors at 48 mg/m3 was lethalto rats; toxic properties similar to those ofMonuron.
LD50 oral (rat): 1146 mg/kg
LD50 oral (mouse): 2400 mg/kg
LD50 inhalation (rat): 48 mg/m3 /4 h.
Agricultural Uses
Herbicide: Inhibits photosynthesis. Linuron is a selective, pre-emergence herbicide used to control grasses and broadleaf weeds in carrots, beans, peas, asparagus, maize, potatoes, soybeans, sorghum, wheat, bananas, coffee, cotton and ornamentals. It is also used for control of annual weeds in storehouses, roadsides, fence rows and other noncrop lands. Linuron is frequently used in formulations with other herbicides, insecticides and fungicides.
Trade name
AFALON®; ALIBI®; ALISTELL®; BROADCIDE 20EC®; BRONOX®; CERTOLLIN ONIONS®; CLOVACORN EXTRA®; CROP WEEDSTOP®; DU PONT 326®[C]; FF6135' HERBICIDE 326®; GARNITAN®; H 326®; GEMINI®[C]; HERBICIDE 326®; HOE 2810®; JANUS®; LANDSIDE®; LINNET®; LINEX®; LINOROX®; LINUREX®; LOREX®; LOROX®[C]; MARKSMAN 1®; NEMINFEST®; ONSLAUGHT®; PRE-EMPT®; PREMALIN®; PROFALON®; ROTILIN®; SARCLEX®; SCARCLEX®; SINURON®; STAY KLEEN®; TEMPO®; TRIFARMON FL®; TRIFLURON®; TRILIN®; URANUS® (trifluralin + linuron); WARRIOR®
Safety Profile
Poison by inhalation. Moderately toxic by ingestion. Mutation data reported. A selective herbicide used in farming. Vlihen heated to decomposition it emits very toxic fumes of Cl and NOx. See also 3-@-CHLOROPHENYL)-1,1 DIMETHYLUREA.
Potential Exposure
Inhibits photosynthesis. Linuron is a selective, pre-emergence urea herbicide used to control grasses and broadleaf weeds in carrots, beans, peas, asparagus, maize, potatoes, soybeans, sorghum, wheat, bananas, coffee, cotton, and ornamentals. It is also used for control of annual weeds in storehouses, roadsides, fence rows and other noncrop lands. Linuron is frequently used in formulations with other herbicides, insecticides, and fungicides
Environmental Fate
Soil. Linuron degraded in soil forming the common metabolite 3,4-dichloroaniline
(Duke et al., 1991). In an aerobic, biologically active, organic-rich, pond sediment, linuron
was converted to the intermediate 3-(3-chlorophenyl)-1-methoxymethylurea. This compound
further degraded to unidentified compounds (Stepp et al., 1985).
Linuron was degraded by Bacillus sphaericus in soil forming N,O-dimethylhydroxylamine
and carbon dioxide (Engelhardt et al., 1972). Only 1 ppm 3,4-dichloroaniline was
identified in soils after incubation of soils containing 500 ppm linuron (Belasco and Pe
The half-lives for linuron in soil incubated in the laboratory under aerobic conditions
ranged from 56 to 88 days with an average of 75 days (Moyer et al., 1972; Hance, 1974;
Usorol and Hance, 1974). In field soils, the average half-life for linuron was 8
Plant. Undergoes demethylation and demethoxylation in plants (Hartley and Kidd,
1987). Metabolites identified in carrots 117 days after treatment were 3,4-dichlorophenylurea,
3-(3,4-dichlorophenyl)-1-methylurea and 3,4-dichloroaniline. About 87% of the
linuron remained unreacted (Loekke, 1974).
Photolytic. When an aqueous solution of linuron was exposed to summer sunlight for
2 months, 3-(3-chloro-4-hydroxyphenyl)-1-methoxy-1-methylurea, 3,4-dichlorophenylurea
and 3-(3,4-dichlorophenyl)-1-methylurea formed at yields of 13, 10 and 2%, re
Metabolic pathway
The main photoproducts initially formed in the phototransformation of linuron and chlorbromuron in aqueous solution result from photolysis, i.e. hydroxylation with release of the halide ion, and from elimination of a methoxy group. The orientation of the reaction depends on the wavelength: short wavelengths (254 nm) favor demethoxylation and photolysis in the meta position,whereas, with black light longer than 330 nm, photolysis in the para position is the main reaction observed. In soils, 4-bromo-3-chloroaniline is identified as a soil degradation product of chlorbromuron.
Shipping
UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.
Incompatibilities
Amides are incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides. Similar organic amides react with azo and diazo compounds, releasing toxic gases. Contact with reducing agents can release flammable gases. Amides are very weak bases but they can react as acids, forming salts. Mixing amides with dehydrating agents such as such as phosphorus pentoxide or thionyl chloride generates the corresponding nitrile
Waste Disposal
Incinerate in a unit operating at 850C equipped with off-gas scrubbing equipment. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office
Linuron Preparation Products And Raw materials
Raw materials
1of2
chevron_rightPreparation Products
| Supplier | Tel | Country | ProdList | Advantage | Inquiry |
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| CLEARSYNTH LABS LTD. | +91-22-45045900 | Hyderabad, India | 6257 | 58 | Inquiry |
| Pharmaffiliates Analytics and Synthetics P. Ltd | +91-172-5066494 | Haryana, India | 6739 | 58 | Inquiry |
| AS WATER CO., LTD. | +86-18994963526 +8618994963526 | United Kingdom | 176 | 58 | Inquiry |
| Hebei Weibang Biotechnology Co., Ltd | +8615531157085 | China | 8810 | 58 | Inquiry |
| Hebei Mojin Biotechnology Co., Ltd | +86 13288715578 +8613288715578 | China | 12839 | 58 | Inquiry |
| Henan Bao Enluo International TradeCo.，LTD | +86-17331933971 +86-17331933971 | China | 2472 | 58 | Inquiry |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | China | 21634 | 55 | Inquiry |
| career henan chemical co | +86-0371-86658258 +8613203830695 | China | 29881 | 58 | Inquiry |
| Chongqing Chemdad Co., Ltd | +86-023-6139-8061 +86-86-13650506873 | China | 39894 | 58 | Inquiry |
| CONIER CHEM AND PHARMA LIMITED | +8618523575427 | China | 49374 | 58 | Inquiry |