Vydate

Base Information

• Chemical Name: Vydate
• CAS No.: 23135-22-0
• Molecular Formula: C7H13N3O3S
• Molecular Weight: 219.265
• Hs Code.: 2930909052
• European Community (EC) Number: 245-445-3
• UN Number: 2991,2757
• UNII: SWV4D62X9E
• DSSTox Substance ID: DTXSID6021086
• Wikipedia: Oxamyl
• Wikidata: Q409836
• NCI Thesaurus Code: C163684
• ChEMBL ID: CHEMBL3187175
• Mol file: 23135-22-0.mol

Synonyms:DPX 1410;N',N'-dimethyl-N-((methylcarbamoyl)oxy)-1- thiooxamimidate;oxamyl;Oxamyl 1211;Oxamyl 4509;Vydate

Chemical Property of Vydate

Chemical Property:

• Appearance/Colour: White Solid
• Vapor Pressure: 5.1×10-5Pa (25 °C)
• Melting Point: 100 °C
• Refractive Index: 1.6630 (estimate)
• PKA: 10.48±0.46(Predicted)
• PSA: 96.30000
• Density: 1.23 g/cm³
• LogP: 0.49800
• Storage Temp.: 0-6°C
• Water Solubility.: 28 g/100 mL
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 219.06776246
• Heavy Atom Count: 14
• Complexity: 253
• Transport DOT Label: Poison Flammable Liquid

Purity/Quality:

Oxamyl ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T+, N
• Hazard Codes: T+;N,N,T+
• Statements: 21-26/28-51/53
• Safety Statements: 36/37-45-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Carbamate Insecticides
• Canonical SMILES: CNC(=O)ON=C(C(=O)N(C)C)SC
• Description: Oxamyl, is also called N,N-dimethyl-2-methylcarbamoyloxyimino- 2-(methylthio)acetamide (IUPAC), consists of colorless crystals, which are readily soluble in water, methanol, ethanol, acetone, and fairly soluble in toluene. Oxamyl is produced by chlorination of the oxime of methylglycolate, reaction with methanethiol and alkali, and conversion to the carbamate with methyl isocyanate.
• Uses: Oxamyl is a pesticide used in the treatment and protection of crops from parasites and insects. Insecticide, nematocide, acaricide. Oxamyl is a broad spectrum systemic insecticide/nematicide. It exhibits both oral and contact toxicity to control both sucking and chewing insects and mites in a wide variety of row crops, fruits, vegetables and ornamentals.

Technology Process of Vydate

There total 2 articles about Vydate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

methyl 2-(dimethylamino)-N-hydroxy-2-oxoethanimidothioate (30558-43-1) + methyl isocyanate (624-83-9) → oxamyl (23135-22-0)

Guidance literature:

With triethylamine; In water; at 42 ℃; Inert atmosphere;

Reference yield:

→ oxamyl (23135-22-0)

Guidance literature:

/BRN= 929813/, CH3-NCO;

Reference yield:

oxamyl (23135-22-0) → carbon dioxide (124-38-9,18923-20-1) + methyl 2-(dimethylamino)-N-hydroxy-2-oxoethanimidothioate (30558-43-1) + methylamine (74-89-5)

Guidance literature:

With borate buffer; cetyltrimethylammonim bromide; In water; at 100 ℃; for 0.00833333h; pH=9.0; Further Variations:; Temperatures; Product distribution;

DOI:10.1021/ac990928d

upstream raw materials:

methyl 2-(dimethylamino)-N-hydroxy-2-oxoethanimidothioate

methyl isocyanate

Downstream raw materials:

methylamine

carbon dioxide

methyl 2-(dimethylamino)-N-hydroxy-2-oxoethanimidothioate

Refernces