CAS Number330-55-2
SynonymsLorex; EINECS 206-356-5; 3-(3,4-Dichlorophenyl)-1-methoxy-1-methylurea; Linuron; Laroks; AFALON; LOROX; MFCD00055249; Afolan; Liron; LINEX; LINNET; N'-(3,4-dichlorophenyl)-N-methoxy-N-methylurea; LINUREX
Molecular FormulaC9H10Cl2N2O2
Molecular Weight249.09
Purity98%
Density1.3±0.1 g/cm3
Boiling Point361.7±52.0 °C at 760 mmHg
Melting Point93-94°C
Appearancesolid
EINECS206-356-5
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 330-55-2 |
| Catalog No. | 2A-9011198 |
| Chinese Name | 利谷隆 |
| Synonyms | Lorex; EINECS 206-356-5; 3-(3,4-Dichlorophenyl)-1-methoxy-1-methylurea; Linuron; Laroks; AFALON; LOROX; MFCD00055249; Afolan; Liron; LINEX; LINNET; N'-(3,4-dichlorophenyl)-N-methoxy-N-methylurea; LINUREX |
| Molecular Formula | C9H10Cl2N2O2 |
| Molecular Weight | 249.09 |
| Purity | 98 |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 361.7±52.0 °C at 760 mmHg |
| Melting Point | 93-94°C |
| Appearance | solid |
| Water Solubility | 0.0075 g/100 mL |
| Storage Condition | The warehouse is ventilated and dried at low tempe |
| Application | Linuron is a phenylurea herbicide widely used to control the growth of grasses and weeds in a variety of crops and orchards. Linuron is a photosystem II inhibitor. Linuron is also a competitive androg |
| EINECS | 206-356-5 |
| HTC | 2928000032 |
| PubChem ID | 329755289 |
| MDL Number | MFCD00055249 |
| SMILES | CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1 |
| 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) |
| InChI Key | XKJMBINCVNINCA-UHFFFAOYSA-N |
| Beilstein/REAXYS | 2128725 |
| NACRES Code | NA.24 |
| UNSPSC | 41116107 |
| MSDS | msds/11198_1_330_55_2.pdf |
| Bioactivity | Linuron is a phenylurea herbicide that is widely used to control the growth of grass and weeds in various agriculture crops and in orchards. Linuron is a photosystem II inhibitor. Linuron is also a competitive androgen receptor (AR) antagonist with a Ki of 100 μM. Linuron shows reproductive toxicity in animals that acts as an endocrine disruptor[1][2][3][4]. Related Catalog Research Areas >> Endocrinology Signaling Pathways >> Others >> Androgen Receptor Target Ki: 100 μM (Androgen receptor)[2] Photosystem II[4] References [1]. Benjamin Horemans, et al. Functional Redundancy of Linuron Degradation in Microbial Communities in Agricultural Soil and Biopurification Systems. Appl Environ Microbiol. 2016 Apr 18;82(9):2843-2853. [2]. C Lambright, et al. Cellular and Molecular Mechanisms of Action of Linuron: An Antiandrogenic Herbicide That Produces Reproductive Malformations in Male Rats. Toxicol Sci. 2000 Aug;56(2):389-99. [3]. Hongwei Ding, et al. Reproductive Toxicity of Linuron Following Gestational Exposure in Rats and Underlying Mechanisms. Toxicol Lett. 2017 Jan 15;266:49-55. [4]. Elżbieta G Magnucka, et al. Various Effects of the Photosystem II--inhibiting Herbicides on 5-n-alkylresorcinol Accumulation in Rye Seedlings. Pestic Biochem Physiol. 2014 Nov;116:56-62. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 361.7±52.0 °C at 760 mmHg Melting Point 93-94°C Molecular Formula C9H10Cl2N2O2 Molecular Weight 249.094 Flash Point 172.6±30.7 °C Exact Mass 248.011932 PSA 41.57000 LogP 3.33 Vapour Pressure 0.0±0.9 mmHg at 25°C Index of Refraction 1.556 InChIKey XKJMBINCVNINCA-UHFFFAOYSA-N SMILES CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1 Water Solubility 0.0075 g/100 mL |
| Use of | Linuron is a phenylurea herbicide that is widely used to control the growth of grass and weeds in various agriculture crops and in orchards. Linuron is a photosystem II inhibitor. Linuron is also a competitive androgen receptor (AR) antagonist with a Ki of 100 μM. Linuron shows reproductive toxicity in animals that acts as an endocrine disruptor[1][2][3][4]. Properties Articles38 Name linuron Synonym More Synonyms Linuron Biological Activity Description Linuron is a phenylurea herbicide that is widely used to control the growth of grass and weeds in various agriculture crops and in orchards. Linuron is a photosystem II inhibitor. Linuron is also a competitive androgen receptor (AR) antagonist with a Ki of 100 μM. Linuron shows reproductive toxicity in animals that acts as an endocrine disruptor[1][2][3][4]. Related Catalog Research Areas >> Endocrinology Signaling Pathways >> Others >> Androgen Receptor Ki: 100 μM (Androgen receptor)[2] Photosystem II[4] References [1]. Benjamin Horemans, et al. Functional Redundancy of Linuron Degradation in Microbial Communities in Agricultural Soil and Biopurification Systems. Appl Environ Microbiol. 2016 Apr 18;82(9):2843-2853. [2]. C Lambright, et al. Cellular and Molecular Mechanisms of Action of Linuron: An Antiandrogenic Herbicide That Produces Reproductive Malformations in Male Rats. Toxicol Sci. 2000 Aug;56(2):389-99. [3]. Hongwei Ding, et al. Reproductive Toxicity of Linuron Following Gestational Exposure in Rats and Underlying Mechanisms. Toxicol Lett. 2017 Jan 15;266:49-55. [4]. Elżbieta G Magnucka, et al. Various Effects of the Photosystem II--inhibiting Herbicides on 5-n-alkylresorcinol Accumulation in Rye Seedlings. Pestic Biochem Physiol. 2014 Nov;116:56-62. Chemical & Physical Properties Exact Mass 248.011932 PSA 41.57000 Index of Refraction 1.556 InChIKey XKJMBINCVNINCA-UHFFFAOYSA-N |
| Tax Rebate | 9.0% |
| Supervision | S (Import and export pesticide registration certificate) |
| Transport Info | Product name: Chemical name |
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