ALDICARB-OXIME
- Product Name
- ALDICARB-OXIME
- CAS No.
- 1646-75-9
- Chemical Name
- ALDICARB-OXIME
- Synonyms
- Temik Oxime;ALDICARB-OXIME;2-methyl-2-(methylthio)-propanal oxime;2-methyl-2-(methylsulfanyl)propanaldoxime;Propanal, 2-methyl-2-(methylthio)-, oxime;Aldicarb-oxime, 10 μg /μL in acetonitrile;2-methyl-2-(methylthio)propionaldehydeoxime;Propionaldehyde, 2-methyl-2-(methylthio)-, oxime.;N-[2-methyl-2-(methylsulfanyl)propylidene]hydro xylamine;TIANFU-CHEM_Propanal,2-methyl-2-(methylthio)-, oxime 1646-75-9
- CBNumber
- CB7258255
- Molecular Formula
- C5H11NOS
- Formula Weight
- 133.21
- MOL File
- 1646-75-9.mol
ALDICARB-OXIME Property
- Melting point:
- 21.1°C
- Boiling point:
- 210°C
- Density
- 1.037 (estimate)
- refractive index
- 1.5216 (estimate)
- storage temp.
- 0-6°C
- form
- liquid
- EPA Substance Registry System
- Aldicarb oxime (1646-75-9)
Safety
- Hazardous Substances Data
- 1646-75-9(Hazardous Substances Data)
N-Bromosuccinimide Price
- Product number
- T164670
- Product name
- TemikOxime
- Packaging
- 10mg
- Price
- $780
- Updated
- 2021/12/16
- Product number
- T164670
- Product name
- TemikOxime
- Packaging
- 25mg
- Price
- $1710
- Updated
- 2021/12/16
ALDICARB-OXIME Chemical Properties,Usage,Production
Uses
Temik Oxime is an intermediate in the synthesis of Aldicarb-d3 Sulfoxide (A514667), which is a labeled Aldicarb Sulfoxide (A514665). Aldicarb Sulfoxide is an analog of Aldicarb (A514650) detected in agricultural products as pesticide residue.
Definition
ChEBI: The oxime resulting from the formal condensation of 2-methyl-2-(methylsulfanyl)propanal with hydroxylamine. Addition of the oxime group to methyl isocyanate forms the final step in the synthesis of the systemic insecticide aldicarb.
General Description
Clear colorless,viscous liquid with an unpleasant sulfurous or musty odor.
Air & Water Reactions
Sensitive to heat. Water soluble. May decompose with prolonged exposure to moisture.
Reactivity Profile
ALDICARB-OXIME is incompatible with oxidizers, acids and alkalis [(NTP, 1992]. Several explosions or violent decompositions have occurred during distillation of alkoxides, which may be attributable to the formation of peroxides of various types. This is especially the case in the presence of acid, Chem. Eng. News, 1974, 52(35), 3. A nickel catalyzed aldoxime rearrangement to an amide, went out of control after changing the solvent employed, J. Loss Prev., 1993, 6(2), 69.
Fire Hazard
ALDICARB-OXIME is combustible.