Sodium 2,4-dichlorophenoxyacetate

Base Information

• Chemical Name: Sodium 2,4-dichlorophenoxyacetate
• CAS No.: 2702-72-9
• Molecular Formula: C8H5Cl2NaO3
• Molecular Weight: 243.022
• Hs Code.: 2918990090
• Mol file: 2702-72-9.mol

Synonyms:Aceticacid, (2,4-dichlorophenoxy)-, sodium salt (8CI,9CI);2,4-D Sodium salt;2,4-Dichlorophenoxyacetic acid sodium salt;Agrion;Agrion (pesticide);Dichlordon sodium;Diconirt;Diconirt D;Dikonirt;Dikonirt D;Fernoxone;Hormit;Kar D;Pielik E;Sodium (2,4-dichlorophenoxy)acetate;Sodium 2,4-D;Sodium diclordon;Spray-Hormite;Spritz-hormit;Taficide;Tornado DF;U 46D;

Chemical Property of Sodium 2,4-dichlorophenoxyacetate

Chemical Property:

• Appearance/Colour: clear brown to black liquid
• Vapor Pressure: 2.31E-05mmHg at 25°C
• Melting Point: 215 °C
• Boiling Point: 345.6 °C at 760 mmHg
• Flash Point: 162.8 °C
• PSA: 49.36000
• LogP: 1.12210
• Solubility.: H2O: soluble
• Water Solubility.: Soluble

Purity/Quality:

99% ^*data from raw suppliers

Sodium 2,4-Dichlorophenoxyacetate Monohydrate >98.0%(HPLC)(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn, N
• Hazard Codes: Xn,N
• Statements: 22-41-43-51/53
• Safety Statements: 24/25-26-36/37/39-46-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Herbicide. 2,4-Dichlorophenoxy Acetic Acid Sodium Salt is the salt form of 2,4-Dichlorophenoxyacetic Acid (D435680); herbicide. Used to increase latex output of old rubber trees.

Technology Process of Sodium 2,4-dichlorophenoxyacetate

There total 13 articles about Sodium 2,4-dichlorophenoxyacetate 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: 100.0%

→ sodium 2,4-dichlorophenoxyacetate (2702-72-9)

Guidance literature:

Reference yield: 95.0%

2-(2,4-dichlorophenoxy)ethanol (120-67-2) → 2,6-dichlorophenoxyacetic acid (575-90-6) + sodium 2,4-dichlorophenoxyacetate (2702-72-9)

Guidance literature:

With sodium hydroxide; oxygen; bismuth(III) nitrate; palladium on activated charcoal; at 90 ℃; for 1.5h; Title compound not separated from byproducts;

Reference yield:

2,4-dichlorophenoxyacetic acid n-decyl ester (67821-08-3) → sodium 2,4-dichlorophenoxyacetate (2702-72-9)

Guidance literature:

With sodium hydrogencarbonate; In water; at 80 ℃; for 2h;

upstream raw materials:

2-(2,4-dichlorophenoxy)ethanol

2,4-dichlorophenoxyacetic acid ammonium salt

sodium monochloroacetic acid

sodium 2,4-dichlorophenolate

Downstream raw materials:

2,4-Dichlorophenoxyacetic acid

2-chloroethyltrimethylammonium 2-(2,4-dichlorophenoxy)acetate

2,4-dichlorophenoxymethyl 2,4-dichlorophenoxyacetate

benzene

Refernces

• 1、 Ferenc, Wies?awa,Cristóv?o, Beata,Sarzyński, Jan,Osypiuk, Dariusz. "Complexes of some transition metal ions with selected dichlorophenoxyacetic acid: Thermal, spectral and magnetic properties". . p. 129 - 139. Retrieved 2016.
• 2、 -. "Preparation method of 2,4-dichlorophenoxyacetic acid and salt thereof". . . Retrieved 2019/01/06.