Methylthio Acetaldoxime
Senrial Chemical Co., Limited
Methylthio-Acetaldoxime
Specifications
Item Index
Appearance Colorless transparent liquid
Acetaldehyde oxime content 50±2%
Color (Pt-Co) ≤10
Ferric ions≤ ≤1ppm
PH 8-9
Basicity (mgNH3/g) ≤0.2%
Packing & Storage
Packing in 25kg drum
Storage Sealed, cool
Shipping Store separately, do not mix
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General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Common Names (Methylthio)acetaldoxime
Structure
CAS No. 10533-67-2 Boiling Point (℃) 209.2±23.0 °C
Molecular Weight 105.159 Melting Point (℃)
Appearance Colorless transparent liquid Vapor Specific Gravity
HS Code 2930909090 Flash Point (℃) 80.3±22.6 °C
Solubility Autoignition Temperature (℃)
Safety Phrases
RIDADR
WGK Germany
Packaging Group
Hazard Class


SYMPTOMS PREVENTION FIRST AID
Inhalation Cough. Sore throat. Use local exhaust or breathing protection. Fresh air, rest.
Skin Redness. Burning sensation. Itching. Protective gloves. Remove contaminated clothes. Rinse and then wash skin with water and soap.
Eyes Redness. Pain. Wear safety goggles. First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Ingestion Abdominal pain. Nausea. Vomiting. Do not eat, drink, or smoke during work. Wash hands before eating. Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention.
CH3CHO+NH2OH·HCl+NaOH→CH3CH=NOH+NaCl十H2O CH3CH=NOH+Cl2→CH3CCl=NOH+HCl CH3CCl=NOH+NaSCH3→CH3-(SCH3)C=NOH+NaCl
Frequently Asked Questions
Is methylthioacetaldehyde oxime really an intermediate in the synthesis of methomyl?
Methylthioacetaldehyde oxime is indeed an intermediate in the synthesis of methomyl, which is a widely used insecticide. Methomyl is a carbamate insecticide that works by inhibiting the activity of the enzyme acetylcholinesterase in insects, leading to the accumulation of the neurotransmitter acetylcholine and ultimately causing paralysis and death in the targeted pests.
The synthesis of methomyl involves several steps, and methylthioacetaldehyde oxime is one of the key intermediates in this process. Here is a simplified overview of the synthesis:
1. Starting Materials: The synthesis typically starts with the reaction of methyl isocyanate and thioacetamide to form methylthioacetaldehyde oxime.
2. Conversion to Methomyl: Methylthioacetaldehyde oxime is further processed through a series of chemical reactions to eventually yield methomyl. These reactions may involve the introduction of additional functional groups and the formation of the carbamate structure characteristic of methomyl.