Propachlor structure
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Common Name | Propachlor | ||
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CAS Number | 1918-16-7 | Molecular Weight | 211.688 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 290.4±23.0 °C at 760 mmHg | |
Molecular Formula | C11H14ClNO | Melting Point | 67-76°C | |
MSDS | Chinese USA | Flash Point | 129.4±22.6 °C | |
Symbol |
GHS07, GHS09 |
Signal Word | Warning |
Use of PropachlorPropachlor is a specific ALDH1A1 inhibitor. It is sometimes used as an herbicide. |
Name | propachlor |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 290.4±23.0 °C at 760 mmHg |
Melting Point | 67-76°C |
Molecular Formula | C11H14ClNO |
Molecular Weight | 211.688 |
Flash Point | 129.4±22.6 °C |
Exact Mass | 211.076385 |
PSA | 20.31000 |
LogP | 2.28 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.551 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS07, GHS09 |
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Signal Word | Warning |
Hazard Statements | H302-H317-H319-H410 |
Precautionary Statements | P273-P280-P305 + P351 + P338-P501 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful;N:Dangerousfortheenvironment; |
Risk Phrases | R22;R36;R43;R50/53 |
Safety Phrases | S24-S37-S60-S61 |
RIDADR | UN 2811 |
RTECS | AE1575000 |
HS Code | 2924299014 |
HS Code | 2924299014 |
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Summary | 2924299014 2-chloro-n-isopropyl-n-phenylacetamide。supervision conditions:s(import or export registration certificate for pesticides)。VAT:17.0%。tax rebate rate:9.0%。MFN tarrif:6.5%。general tariff:30.0% |
Glutathione-dependent cytotoxicity of the chloroacetanilide herbicides alachlor, metolachlor, and propachlor in rat and human hepatoma-derived cultured cells.
Cell Biol. Toxicol. 15(5) , 325-32, (1999) Alachlor, metolachlor, and propachlor are widely used chloroacetanilide herbicides. Their cytotoxicity in rat (Fa32) and human (Hep G2) hepatoma-derived cells was investigated, in connection with thei... |
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Kinetics and mechanism of propachlor reductive transformation through nucleophilic substitution by dithionite
Chemosphere 85(9) , 1438-43, (2011) Highlights ► The reductive dechlorination of propachlor was efficiently achieved by dithionite. ► The transformation of propachlor initiated by dithionite follows second-order kinetics. ► Dechlorinati... |
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Characterization of glutathione conjugates of chloroacetanilide pesticides using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry and liquid chromatography/ion trap mass spectrometry.
Rapid Commun. Mass Spectrom. 21(24) , 4017-22, (2007) Glutathione S-transferases (GSTs) isolated from maize were used to catalyze the conjugation of glutathione (GSH) with chloroacetanilide herbicides, producing stable conjugates that were structurally c... |
2-Chloro-N-isopropylacetanilide |
Satecid |
N-isopropyl-2-chloroacetanilide |
2-Chloro-N-isopropyl-N-phenyl-acetamide |
Niticid |
N-isopropyl-N-phenyl-chloroacetamide |
2-Chloro-N-isopropyl-N-phenylacetamide |
Prolex |
Propachlore |
2-Chloro-N-(1-methylethyl)-N-phenylacetamide (9CI) |
Nitacid |
α-chloro-N-isopropylacetanilide |
MFCD00078731 |
EINECS 217-638-2 |
Bexton |
2-chloro-N-(1-methylethyl)-N-phenylacetamide |
2-chloro-N-phenyl-N-(propan-2-yl)acetamide |
n-isopropyl-a-chloroacetanilide |
Bexton 4L |
2-chloro-N-phenyl-N-propan-2-ylacetamide |
Acetamide, 2-chloro-N-(1-methylethyl)-N-phenyl- |
Ramrod |
Propachlor |