isoxaben structure
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Common Name | isoxaben | ||
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CAS Number | 82558-50-7 | Molecular Weight | 332.39 | |
Density | 1.138g/cm3 | Boiling Point | 427.8ºC at 760 mmHg | |
Molecular Formula | C18H24N2O4 | Melting Point | 175-179ºC | |
MSDS | Chinese USA | Flash Point | 212.6ºC |
Use of isoxabenIsoxaben, a herbicide, inhibits incorporation of radiolabeled glucose into an acid insoluble cell wall fraction. Isoxaben is also a specific inhibitor of cell wall biosynthesis[1]. |
Name | isoxaben |
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Synonym | More Synonyms |
Description | Isoxaben, a herbicide, inhibits incorporation of radiolabeled glucose into an acid insoluble cell wall fraction. Isoxaben is also a specific inhibitor of cell wall biosynthesis[1]. |
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Related Catalog | |
References |
Density | 1.138g/cm3 |
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Boiling Point | 427.8ºC at 760 mmHg |
Melting Point | 175-179ºC |
Molecular Formula | C18H24N2O4 |
Molecular Weight | 332.39 |
Flash Point | 212.6ºC |
Exact Mass | 332.17400 |
PSA | 73.59000 |
LogP | 3.61400 |
Index of Refraction | 1.544 |
Storage condition | 0-6°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Hazard Statements | H413 |
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Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn: Harmful; |
Risk Phrases | 53-40 |
Safety Phrases | S36 |
RIDADR | NONH for all modes of transport |
RTECS | CV4370300 |
~91% isoxaben CAS#:82558-50-7 |
Literature: Eli Lilly and Company Patent: US4416683 A1, 1983 ; |
Precursor 1 | |
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DownStream 0 |
Coupling passive sampling and time of flight mass spectrometry for a better estimation of polar pesticide freshwater contamination: Simultaneous target quantification and screening analysis.
J. Chromatogr. A. 1387 , 75-85, (2015) The aim of this study was first to develop and validate an analytical method for the quantification of 35 polar pesticides and 9 metabolites by ultra-high-performance-liquid chromatography combined wi... |
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A fluorescent hormone biosensor reveals the dynamics of jasmonate signalling in plants.
Nat. Commun. 6 , 6043, (2015) Activated forms of jasmonic acid (JA) are central signals coordinating plant responses to stresses, yet tools to analyse their spatial and temporal distribution are lacking. Here we describe a JA perc... |
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Toxicity of herbicides in highway runoff.
Environ. Toxicol. Chem. 24(9) , 2336-40, (2005) Previous field monitoring at two highway sites found highway-applied herbicides in storm water runoff at maximum concentrations ranging from 10 microg/L for glyphosate and diuron to as high as 200 mic... |
2,6-dimethoxy-N-[3-(3-methylpentan-3-yl)-1,2-oxazol-5-yl]benzamide |
Caswell No. 419F |
N-[3-(1-ethyl-1-methylpropyl)-5-isoxazolyl]-2,6-dimethoxybenzamide |
benzamizole |
Cent 7 |
Isoxaben |
EINECS 407-190-8 |
Flexidor |
MFCD00078687 |
X-Pand |
Gallery |
N-[3-(1-ethyl-1-methylpropyl)-1,2-oxazol-5-yl]-2,6-dimethoxybenzamide |
ixoxaben |