133-90-4
Chemical Structure
Chloramben
- No. CAS: 133-90-4
- Formula:C7H5Cl2NO2
- Molecular Weight:206.03
IUPAC Name: 3-amino-2,5-dichlorobenzoic acid
InChIKey: HSSBORCLYSCBJR-UHFFFAOYSA-N
SMILES: O=C(C1=CC(Cl)=CC(N)=C1Cl)O
Biological Activity: Chloramben (3-Amino-2,5-dichlorobenzoic acid) is a pre-emergence herbicide used to control the seedlings of annual grasses and broadleaf weeds[1].
| Referencia número | Nombre del producto | Pureza | Descripciòn | Pricing | |||||||||||||||||||
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Chloramben | 97.06% | Chloramben (3-Amino-2,5-dichlorobenzoic acid) is a pre-emergence herbicide used to control the seedlings of annual grasses and broadleaf weeds. | ||||||||||||||||||||
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Chloramben (Standard) | ≥98% | Chloramben (Standard) is the analytical standard of Chloramben. This product is intended for research and analytical applications. Chloramben (3-Amino-2,5-dichlorobenzoic acid) is a pre-emergence herbicide used to control the seedlings of annual grasses and broadleaf weeds. | ||||||||||||||||||||
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Chloramben sodium | Chloramben sodium is a herbicide with anti-growth activity against plants. Chloramben sodium can be effectively removed by photo-Fenton reaction under natural pH conditions, showing good degradation performance. The removal rate of chloramben sodium is consistent with different electrodes, mainly due to the oxidation mediated by the hydroxyl ions formed in the Fenton reaction. Chloramben sodium is almost completely mineralized using IrO2-based electrodes at high current density, indicating that it can be effectively degraded under light. Chloramben sodium leads to the formation of persistent chlorine derivatives in chlorine-containing environments, so the removal rate and mineralization rate are slightly reduced. Chloramben sodium can form intermediates with a variety of aromatic compounds and organic acids, reflecting the complexity of its transformation in the environment. | |||||||||||||||||||||
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4,6-Dichloronicotinic acid | 4,6-Dichloronicotinic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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2,3-Dichlorobenzoic acid (Standard) | ≥98% | 2,3-Dichlorobenzoic acid (Standard) is the analytical standard of 2,3-Dichlorobenzoic acid. This product is intended for research and analytical applications. | ||||||||||||||||||||
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Furosemide impurity 6 | Furosemide impurity 6 is an impurity of Furosemide. | |||||||||||||||||||||
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2,5-Dichloroterephthalic acid | 98.53% | |||||||||||||||||||||
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4-Amino-2-chlorobenzoic acid | 4-Amino-2-chlorobenzoic acid (4ACB) is a biochemical reagent. | |||||||||||||||||||||
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4-Amino-5-chloro-2-methoxybenzoic acid (Standard) | ≥98% | 4-Amino-5-chloro-2-methoxybenzoic acid (Standard) is the analytical standard of 4-Amino-5-chloro-2-methoxybenzoic acid. This product is intended for research and analytical applications. | ||||||||||||||||||||
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2,3-Dichlorobenzoic acid-13C | 2,3-Dichlorobenzoic acid-13C is the 13C-labeled 2,3-Dichlorobenzoic acid. | |||||||||||||||||||||
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3,5-Dichlorobenzoic acid | 99.21% | 3,5-Dichlorobenzoic acid is a chlorinated benzoic acid-based synthetic building block that can be used as an intermediate in organic synthesis-related research. | ||||||||||||||||||||
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Mesalazine impurity 7 | Mesalazine impurity 7 (Mesalazine impurity J)?is an impurity of?Mesalazine. | |||||||||||||||||||||
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