| Weight | 297.483 g/mol |
|---|---|
| Formula | C18H35NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Spiroxamine (118134-30-8)
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- Residues of spiroxamine in grapes following field application and their fate from vine to wine. (Journal of Agricultural and Food Chemistry, 2005)
- Sensitivity of California isolates of Uncinula necator to trifloxystrobin and spiroxamine, and update on triadimefon sensitivity (Plant Disease, 2004)
- Dissipation and metabolism of 14C-spiroxamine in soil under laboratory condition (Environmental Pollution, 2010)
- Determination of spiroxamine residues in grapes, must, and wine by gas chromatography/ion trap-mass spectrometry. (Journal of AOAC International, 2005)
- Hydrolysis study and extraction of spiroxamine from soils of different physico-chemical properties (Chemosphere, 2009)
- Assignment of the stereochemistry of spiroxamine by two-dimensional NMR spectroscopy and stereoselective chemical synthesis (Magnetic Resonance in Chemistry, 1998)
-
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 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCCCN(CC)CC1COC2(O1)CCC(CC2)C(C)(C)C
-
InChIKeyPUYXTUJWRLOUCW-UHFFFAOYSA-N
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Spiroxamine
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