Aminocarb

Base Information

• Chemical Name: Aminocarb
• CAS No.: 2032-59-9
• Molecular Formula: C11H16 N2 O2
• Molecular Weight: 208.26
• Hs Code.: 29224999
• European Community (EC) Number: 217-990-7
• ICSC Number: 0097
• UN Number: 2757
• UNII: 767M03K32Y
• DSSTox Substance ID: DTXSID7022172
• Nikkaji Number: J55.517G
• Wikipedia: Aminocarb
• Wikidata: Q3120938
• NCI Thesaurus Code: C163585
• Metabolomics Workbench ID: 52960
• ChEMBL ID: CHEMBL1079605
• Mol file: 2032-59-9.mol

Synonyms:4-dimethylamino-3-tolyl-N-methylcarbamate;aminocarb;Matacil

Chemical Property of Aminocarb

Chemical Property:

• Vapor Pressure: 0.00073mmHg at 25°C
• Melting Point: 93-94℃
• Refractive Index: 1.5000 (estimate)
• Boiling Point: 307.3°Cat760mmHg
• PKA: 12.25±0.46(Predicted)
• Flash Point: 139.7°C
• PSA: 41.57000
• Density: 1.095g/cm³
• LogP: 2.17010
• Storage Temp.: 0-6°C
• Water Solubility.: 915mg/L(20 oC)
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 208.121177757
• Heavy Atom Count: 15
• Complexity: 219

Purity/Quality:

Aminocarb ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T,N
• Statements: 24/25-50/53
• Safety Statements: 28-36/37-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Carbamate Insecticides
• Canonical SMILES: CC1=C(C=CC(=C1)OC(=O)NC)N(C)C
• Inhalation Risk: A harmful concentration of airborne particles can be reached quickly on spraying.
• Effects of Short Term Exposure: Cholinesterase inhibition. The substance may cause effects on the nervous system. Exposure could cause death. The effects may be delayed. Medical observation is indicated.
• Effects of Long Term Exposure: The substance may have effects on the nervous system.
• Uses: Nonsystemic, broad-spectrum insecticide used to control the spruce budworm in forests; molluscicide Insecticide. Aminocarb is a carbamate insecticide.

Technology Process of Aminocarb

There total 1 articles about Aminocarb 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:

→ aminocarb (2032-59-9)

Guidance literature:

4-Dimethylamino-3-methyl-phenol, Methylisocyanat, Triaethylamin, Ae.;

Reference yield:

aminocarb (2032-59-9) → carbon dioxide (124-38-9,18923-20-1) + 6-dimethylamino-3-hydroxytoluene (14143-25-0) + 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

Downstream raw materials:

carbon dioxide

6-dimethylamino-3-hydroxytoluene

methylamine