| Weight | 228.675 g/mol |
|---|---|
| Formula | C11H13ClO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
MCPB (94-81-5)
4-(4-chloro-2-methylphenoxy)butyric acid · Tropotox · 2-methyl-4-chlorophenoxy gamma-butyric acid, sodium salt
Score:
#162 in Microbiology
,
#597 in Biochemistry
,
#1741 in Biology
,
#2059 in Chemistry
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- Selective Methylation Changes on the Bacillus subtilis Chemotaxis Receptor McpB Promote Adaptation (Journal of Biological Chemistry, 2000)
- CheY-dependent Methylation of the Asparagine Receptor, McpB, during Chemotaxis in Bacillus subtilis* (Journal of Biological Chemistry, 1999)
- A pas domain binds asparagine in the chemotaxis receptor MCPB in bacillus subtilis (Journal of Biological Chemistry, 2010)
- The role of heterologous receptors in McpB-mediated signalling in Bacillus subtilis chemotaxis (Molecular Microbiology, 2002)
- Relative persistence of MCPA, MCPB and mecoprop in Saskatchewan soils, and the identification of MCPA in MCPB-treated soils (Weed Research, 1981)
- Hypermetallation is ubiquitous: MX6 molecules (MCPb, XLiK) (Chemical Physics Letters, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - 4-(4-chloro-2-methylphenoxy)butyric acid
- Tropotox
- 2-methyl-4-chlorophenoxy gamma-butyric acid, sodium salt
- 2-methyl-4-chlorophenoxy gamma-butyric acid
-
SMILESCC1=C(C=CC(=C1)Cl)OCCCC(=O)O
-
InChIKeyLLWADFLAOKUBDR-UHFFFAOYSA-N
- Pubchem - MCPB
- Wikipedia - MCPB
MCPB, 2,4-MCPB, 4-(4-chloro-o-tolyloxy)butyric acid (IUPAC), or 4-(4-chloro-2-methylphenoxy)butanoic acid (CAS) is a 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.
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