| Weight | 206.028 g/mol |
|---|---|
| Formula | C7H5Cl2NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Chloramben (133-90-4)
Amiben · Amiben, ammonium salt · Amiben, monopotassium salt
Score:
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- Sigma-Aldrich - Chloramben56.40 - 135.00 USD
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- Photocatalytic and photolytic transformation of chloramben in aqueous solutions (Applied Catalysis B-environmental, 1999)
- Herbicide Metabolism: N-Glycoside of Amiben Isolated from Soybean Plants (Science, 1965)
- Chloramben metabolism in plants: isolation and identification of glucose ester (Journal of Agricultural and Food Chemistry, 1978)
- Photodegradation of Chloramben on a Soil Surface: A Laboratory-Controlled Study (Journal of Agricultural and Food Chemistry, 1997)
- Mechanism for the Differential Translocation of Amiben in Plants (Plant Physiology, 1970)
- Photolysis of Amiben (3-Amino-2,5-dichlorbenzoic Acid) and Its Methyl Ester (Journal of Agricultural and Food Chemistry, 1969)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Amiben
- Amiben, ammonium salt
- Amiben, monopotassium salt
- Amiben, aluminum salt
- Amiben, sodium salt
-
SMILESC1=C(C=C(C(=C1N)Cl)C(=O)O)Cl
-
InChIKeyHSSBORCLYSCBJR-UHFFFAOYSA-N
- Pubchem - Chloramben
- Wikipedia - chloramben
Chloramben is a selective herbicide used to control the seedlings of broadleaf weeds and annual grasses. It is mostly used for soybeans, but also for dry beans, peanuts, sunflowers, peppers, cotton, sweet potatoes, squash, hardwood trees, shrubs, and some conifers. Chloramben is considered practically nontoxic.
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Chloramben
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