(2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate

Base Information

• Chemical Name: (2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate
• CAS No.: 3599-58-4
• Molecular Formula: C10H13Cl2NO4
• Molecular Weight: 282.124
• Hs Code.: 2923900090
• European Community (EC) Number: 222-752-0
• DSSTox Substance ID: DTXSID9058367
• Mol file: 3599-58-4.mol

Synonyms:3599-58-4;(2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate;2-aminoethanol;2-(2,4-dichlorophenoxy)acetic acid;2,4-D ethanolammonium salt;DTXSID9058367;LWEGPOVUIQAHBP-UHFFFAOYSA-N;2,4-D, ETHANOLAMINE SALT;2-aminoethanol 2-(2,4-dichlorophenoxy)acetate

Chemical Property of (2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate

Chemical Property:

• Vapor Pressure: 2.31E-05mmHg at 25°C
• Boiling Point: 345.6°Cat760mmHg
• Flash Point: 162.8°C
• PSA: 92.78000
• Density: g/cm³
• LogP: 2.09450
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 281.0221633
• Heavy Atom Count: 17
• Complexity: 196

Purity/Quality:

99% ^*data from raw suppliers

2,4-DEthanolammoniumSalt ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi,N,Xn
• Statements: 36/37/38-51/53-43-41-40-22
• Safety Statements: 26-61-46-36/37/39-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1Cl)Cl)OCC(=O)O.C(CO)N
• Uses: 2,4-D ethanolammonium salt can be used in agricultural use and biological study of selection of pesticide mixture ingredients using mathematical modeling and cluster analysis.

Technology Process of (2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate

There total 3 articles about (2-Hydroxyethyl)ammonium (o,p-dichlorophenoxy)acetate 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:

ethanolamine (141-43-5) → ethanolamine salt of 2,4-D (3599-58-4)

Guidance literature:

In Methylated soybean oil; at 20 ℃; for 1h; Nonionic emulsifier;

Reference yield:

2,4-dichlorophenol (120-83-2,40477-79-0) → ethanolamine salt of 2,4-D (3599-58-4)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydroxide / water / 3 h / 60 - 70 °C

2: acetone / 0.5 h / Reflux

With sodium hydroxide; In water; acetone;

Reference yield:

2,4-Dichlorophenoxyacetic acid (94-75-7,89300-30-1) + ethanolamine (141-43-5) → ethanolamine salt of 2,4-D (3599-58-4)

Guidance literature:

In acetone; for 0.5h; Reflux;

upstream raw materials:

ethanolamine

2,4-Dichlorophenoxyacetic acid

2,4-dichlorophenol

Refernces

• 1、 -. "Manufacture and use of herbicide chlorinated phenoxy formulation". Page/Page column 2. . Retrieved 2008/06/13.