| Weight | 211.692 g/mol |
|---|---|
| Formula | C11H14ClNO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
propachlor (1918-16-7)
Ramrod · 2-chloro-N-isopropylacetanilide
Score:
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- Sigma-Aldrich - propachlor49.30 - 61.80 USD
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- Biodegradation of the Acetanilide Herbicides Alachlor, Metolachlor, and Propachlor (Critical Reviews in Microbiology, 1998)
- Oxidative degradation of propachlor by ferrous and copper ion activated persulfate (Science of The Total Environment, 2012)
- Structure and photocatalytic performance of magnetically separable titania photocatalysts for the degradation of propachlor (Applied Catalysis B-environmental, 2009)
- Metabolism of 2-chloro-N-isopropylacetanilide (propachlor) in the leaves of corn, sorghum, sugarcane, and barley. (Journal of Agricultural and Food Chemistry, 1971)
- Photocatalytic degradation of propachlor in aqueous TiO2 suspensions. Determination of the reaction pathway and identification of intermediate products by various analytical methods (Water Research, 2002)
- Heterogeneous photocatalysed reaction of three selected pesticide derivatives, propham, propachlor and tebuthiuron in aqueous suspensions of titanium dioxide (Chemosphere, 2005)
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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 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - Ramrod
- 2-chloro-N-isopropylacetanilide
-
SMILESCC(C)N(C1=CC=CC=C1)C(=O)CCl
-
InChIKeyMFOUDYKPLGXPGO-UHFFFAOYSA-N
- Pubchem - propachlor
- Wikipedia - propachlor
Propachlor (2-chloro-N-isopropylacetanilide) is an herbicide first marketed by Monsanto. It was registered for use in the United States during 1965. The preparation acts on annual grasses and on some broadleaf plants and was briefly sold in the UK as a germination inhibitor under the name Murphy Covershield.
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Areas of Application
Safety
Trends
Alternate Names
Estimated Properties
| Boiling Point | 277.61 C | EPA T.E.S.T. |
|---|---|---|
| Density | 1.08 g/cm3 | EPA T.E.S.T. |
| Flash Point | 145.22 C | EPA T.E.S.T. |
| Water Solubility | 729.77 mg/L | EPA T.E.S.T. |
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Synthesis
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propachlor
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