3766-60-7

Basic information

• Product Name: BUTURON
• Synonyms: 3-(4-CHLOROPHENYL)-1-METHYL-1-(1-METHYL-2-PROPEN-1-YL)UREA;BUTURON;3-(4-chlorophenyl)-1-methyl-1-(1-methylprop-2-ynyl)urea;3-(4-chlorphenyl)-1-methyl-1-isobutinylharnstoff;3-(p-chlorophenyl)-1-methyl-1-(1-methyl-2-propynyl)-ure;3-(p-chlorophenyl)-1-methyl-1-(1-methyl-2-propynyl)urea;arisan;butyron
• CAS NO: 3766-60-7
• Molecular Formula: C₁₂H₁₃ClN₂O
• Molecular Weight: 236.7
• EINECS: 223-187-2
• Product Categories: A-BAlphabetic;Alpha sort;B;BI - BZPesticides&Metabolites;Herbicides;Pesticides&Metabolites;Urea structure
• Mol File: 3766-60-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 149℃
• Boiling Point: 394.9°Cat760mmHg
• Flash Point: >100 °C
• Appearance: /
• Density: 1.233
• Vapor Pressure: 1.91E-06mmHg at 25°C
• Refractive Index: 1.6000 (estimate)
• Storage Temp.: 0-6°C
• PKA: 13.69±0.70(Predicted)
• Water Solubility: 30mg/L(20 oC)
• BRN: 2941811
• CAS DataBase Reference: BUTURON(CAS DataBase Reference)
• NIST Chemistry Reference: BUTURON(3766-60-7)
• EPA Substance Registry System: BUTURON(3766-60-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• RTECS: YS6475000
• Hazardous Substances Data: 3766-60-7(Hazardous Substances Data)

Usage

General Description

Buturon is a chemical compound that is commonly used as a herbicide in agricultural settings to control the growth of weeds. It belongs to the class of chemicals known as the thiocarbamate herbicides, and works by inhibiting the growth of undesirable plants by interfering with their cell division process. Buturon is typically applied to the soil and is absorbed by the roots of the target plants, where it disrupts their normal growth and eventually leads to their death. It is considered to have low toxicity to humans and animals, but care should be taken during its application to prevent accidental ingestion or inhalation. Additionally, it is important to follow the recommended safety guidelines to minimize any potential environmental impact.

InChI:InChI=1/C12H13ClN2O/c1-4-9(2)15(3)12(16)14-11-7-5-10(13)6-8-11/h1,5-9H,2-3H3,(H,14,16)

Relevant articles and documents

Herbicidal composition for upland farming and weeding method

A herbicidal composition for upland farming which can control weeds that have been difficult to control, for example, cleavers, chickweed, birdseye speedwell and violet, said composition containing as active ingredients a 3-substituted phenylpyrazole derivative represented by the general formula (I): STR1 (wherein R is a hydrogen atom, a C1-6 alkyl group, a C3-6 cycloalkyl group, a C1-6 haloalkyl group, a C2-6 alkenyl group or a C2-6 alkynyl group, R1 is a C1-6 alkyl group, X1 and X2, which may be the same or different, are halogen atoms, and Y is an oxygen atom or a sulfur atom) and at least one compound selected from the group consisting of sulfonylurea derivatives, phenylurea derivatives and phenoxy fatty acid derivatives; and a weeding method using said composition.

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.