Dichlorprop-dimethylammonium

Base Information

• Chemical Name: Dichlorprop-dimethylammonium
• CAS No.: 53404-32-3
• Molecular Formula: C9H8Cl2O3.C2H7N
• Molecular Weight: 280.151
• European Community (EC) Number: 258-530-5
• UNII: 3Z317V0WW0
• DSSTox Substance ID: DTXSID2034546
• Wikidata: Q27258236
• Mol file: 53404-32-3.mol

Synonyms:Dichlorprop-dimethylammonium;53404-32-3;Dichlorprop dimethylamine salt;Caswell No. 320B;Dichlorprop-dimethylammonium [ISO];Dimethylammonium 2-(2,4-dichlorophenoxy)propionate;EINECS 258-530-5;Dimethylamine 2-(2,4-dichlorophenoxy)propionate;EPA Pesticide Chemical Code 031419;UNII-3Z317V0WW0;3Z317V0WW0;EINECS 282-717-0;2-(2,4-dichlorophenoxy)propanoic acid;N-methylmethanamine;2-(2,4-Dichlorophenoxy)propionic acid dimethylamine salt;Methanamine, N-methyl-, 2-(2,4-dichlorophenoxy)propanoate;C9H8Cl2O3.C2H7N;Dimethylammonium (1)-2-(2,4-dichlorophenoxy)propionate;C9-H8-Cl2-O3.C2-H7-N;84332-88-7;SCHEMBL726618;DTXSID2034546;Dichlorprop, dimethylamine salt (1:1);LS-121357;Q27258236;Dimethylammonium (+-)-2-(2,4-dichlorophenoxy)propionate;Propanoic acid, 2-(2,4-dichlorophenoxy)-, compound with N-methylmethanamine (1:1)

Chemical Property of Dichlorprop-dimethylammonium

Chemical Property:

• Vapor Pressure: 1.9E-05mmHg at 25°C
• Boiling Point: 348.3°C at 760 mmHg
• Flash Point: 164.5°C
• PSA: 65.97000
• LogP: 0.32000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 279.0428987
• Heavy Atom Count: 17
• Complexity: 213

Purity/Quality:

99% ^*data from raw suppliers

2-(2,4-DICHLOROPHENOXY)PROPANOIC ACID DIMETHYLAMINE SALT 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)O)OC1=C(C=C(C=C1)Cl)Cl.CNC
• Uses: Dichlorprop Dimethylammonium Salt is used in herbicidal combinations along with saflufenacil and clomazone for the method of controlling weeds.

Technology Process of Dichlorprop-dimethylammonium

There total 3 articles about Dichlorprop-dimethylammonium 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: 98.81%

ethyl 2-(2,4-dichlorophenoxy)propionate (66423-06-1,66768-02-3,58048-39-8) + dimethyl amine (124-40-3) → 2-(2,4-dichlorophenoxy)propionic acid dimethylamine salt (53404-32-3,104786-87-0)

Guidance literature:

at 110 ℃;

Reference yield:

ethyl 2-phenoxypropionate (42412-84-0) → 2-(2,4-dichlorophenoxy)propionic acid dimethylamine salt (53404-32-3,104786-87-0)

Guidance literature:

Multi-step reaction with 2 steps

1: sulfuryl dichloride; 2-methylpropan-2-thiol / 0.5 h / 40 °C

2: 110 °C

With sulfuryl dichloride; 2-methylpropan-2-thiol;

Reference yield:

→ 2-(2,4-dichlorophenoxy)propionic acid dimethylamine salt (53404-32-3,104786-87-0)

Guidance literature:

upstream raw materials:

ethyl 2-phenoxypropionate

ethyl 2-(2,4-dichlorophenoxy)propionate

dimethyl amine

Refernces

• 1、 -. "PROCESS FOR PREPARATION OF HERBICIDAL SALTS". Page/Page column 8. . Retrieved 2011/12/04.