Structure via PubChem · Public domain (PubChem)
امسیپیبی
Sign in to saveAlso known as 4-(4-chloro-o-tolyloxy)butyric acid
MCPB, 2,4-MCPB, 4-(4-chloro-o-tolyloxy)butyric acid (IUPAC), or 4-(4-chloro-2-methylphenoxy)butanoic acid (CAS) is a selective phenoxybutyric herbicide. In the United States it is registered for use on pea crops before flowering, for post-emergence control of broadleaf annual and perennial weeds including Canadian thistle, buttercup, mustard, purslane, ragweed, common lambsquarters, pigweed, smartweed, sowthistle, and morning glory. It has low to moderate acute toxicity, with kidney and liver effects as the main hazard concerns.
Chemical data
- Formula
- C11H13ClO3
- Molecular weight
- 228.67 g/mol
- IUPAC name
- 4-(4-chloro-2-methylphenoxy)butanoic acid
- SMILES
- CC1=C(C=CC(=C1)Cl)OCCCC(=O)O
- InChIKey
- LLWADFLAOKUBDR-UHFFFAOYSA-N
- XLogP
- 3.6
- Polar surface area
- 46.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
131 papers- MCPB.py: A Python Based Metal Center Parameter Builder.Journal of chemical information and modeling · 2016
- The involvement of McpB chemoreceptor from Pseudomonas aeruginosa PAO1 in virulence.Scientific reports · 2019
- Parameterization of a Dioxygen Binding Metal Site Using the MCPB.py Program.Methods in molecular biology (Clifton, N.J.) · 2021
- CheY-dependent methylation of the asparagine receptor, McpB, during chemotaxis in Bacillus subtilis.The Journal of biological chemistry · 1999
- The role of heterologous receptors in McpB-mediated signalling in Bacillus subtilis chemotaxis.Molecular microbiology · 2002
via PubMed
Wikidata facts
- Subclass of
- carboxylic acid
- Mass
- 228.055
- Has use
- herbicide
Show 3 more facts
- canonical SMILES
- CC1=C(C=CC(=C1)Cl)OCCCC(=O)O
- chemical formula
- C₁₁H₁₃ClO₃
- Commons category
- MCPB
Sources (2)
via Wikidata · CC0