![]() Desmedipham structure
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Common Name | Desmedipham | ||
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CAS Number | 13684-56-5 | Molecular Weight | 300.309 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 495.4±55.0 °C at 760 mmHg | |
Molecular Formula | C16H16N2O4 | Melting Point | 120 °C | |
MSDS | Chinese USA | Flash Point | 253.4±31.5 °C | |
Symbol |
![]() GHS09 |
Signal Word | Warning |
Use of DesmediphamDesmedipham is a selective systemic phenyl-carbamate herbicide. Desmedipham acts by disrupting CO2 fixation and the production of intermediary energy components-ATP and NADPH2 and inhibition of Hill reaction[1]. |
Name | desmedipham |
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Synonym | More Synonyms |
Description | Desmedipham is a selective systemic phenyl-carbamate herbicide. Desmedipham acts by disrupting CO2 fixation and the production of intermediary energy components-ATP and NADPH2 and inhibition of Hill reaction[1]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 495.4±55.0 °C at 760 mmHg |
Melting Point | 120 °C |
Molecular Formula | C16H16N2O4 |
Molecular Weight | 300.309 |
Flash Point | 253.4±31.5 °C |
Exact Mass | 300.110992 |
PSA | 76.66000 |
LogP | 4.49 |
Vapour Pressure | 0.0±1.3 mmHg at 25°C |
Index of Refraction | 1.568 |
Storage condition | 0-6°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
![]() GHS09 |
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Signal Word | Warning |
Hazard Statements | H410 |
Precautionary Statements | P273-P391-P501 |
Personal Protective Equipment | Eyeshields;Gloves |
Hazard Codes | N:Dangerousfortheenvironment; |
Risk Phrases | R50/53 |
Safety Phrases | S60-S61 |
RIDADR | UN 3077 |
RTECS | FD0425000 |
HS Code | 2924299038 |
~99% Desmedipham CAS#:13684-56-5 |
Literature: Kemisk Vaerk Koge A/S Patent: US4748265 A1, 1988 ; |
Precursor 2 | |
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DownStream 0 |
HS Code | 2924299038 |
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Summary | 2924299038 2-chloro-n-(ethoxymethyl)-n-(2-ethyl-6-methylphenyl)acetamide。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% |
Expression of a bacterial gene in transgenic plants confers resistance to the herbicide phenmedipham.
Plant Mol. Biol. 25(6) , 977-87, (1994) Tobacco plants were genetically engineered to express a detoxifying pathway for the herbicide phenmedipham. A gene from Arthrobacter oxidans strain P52 that encodes an enzyme catalysing the hydrolytic... |
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Acute and chronic toxicity of Betanal(®)Expert and its active ingredients on nontarget aquatic organisms from different trophic levels.
Environ. Toxicol. 27(9) , 537-48, (2012) As a way to improve the efficacy to target organisms, new pesticide generation is based on technologically advanced coformulations of two or more active ingredients. One example is Betanal(®)Expert, a... |
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Liquid chromatographic/mass spectrometric determination of desmedipham and phenmedipham and their metabolites in soil.
J. AOAC Int. 84(5) , 1407-12, (2001) A simple method is described for the simultaneous determination of residues of 2 carbamate herbicides (phenmedipham and desmedipham) and related metabolites (m-aminophenol, aniline, and m-toluidine) i... |
Ethyl (3-((phenylcarbamoyl)oxy)phenyl)carbamate |
[3-[[(Phenylamino)carbonyl]oxy]phenyl]carbamic acid ethyl ester |
EINECS 237-198-5 |
3-{(E)-[Ethoxy(hydroxy)methylene]amino}phenyl hydrogen phenylcarbonimidate |
Methanol, 1-ethoxy-1-[[3-[[(E)-hydroxy(phenylimino)methyl]oxy]phenyl]imino]-, (E)- |
MFCD00055462 |
3-[(Ethoxycarbonyl)amino]phenyl phenylcarbamate |
ethyl N-[3-[[(phenylamino)carbonyl]oxy]phenyl]carbamate |
ethyl 3-phenylcarbamoyloxycarbanilate |
3-[(ethoxycarbonyl)amino]phenyl phenylcarbamate (non-preferred name) |
Carbamic acid, [3-[[(phenylamino)carbonyl]oxy]phenyl]-, ethyl ester |
Carbamic acid, N-[3-[[(phenylamino)carbonyl]oxy]phenyl]-, ethyl ester |
Desmedipham |
ethyl {3-[(phenylcarbamoyl)oxy]phenyl}carbamate |