Pesticide Herbicide 2, 4-Dichlorophenoxyacetic Acid SL Agrochemical

• Customization: Available
• CAS No.: 2008-39-1
• Formula: C8h6cl2o3
• Model NO.: 2 4-dinitrophenylhydrazine
• EINECS: 202-361-1
• Appearance: Liquid
• Method of Application: Cauline Leaf, Soil Treatment Agent
• Usage: Selective

Product Description

Basic Info.

Model NO.

SL

Chemical Formula 1

C8h6cl2o3

CAS 2

1918-02-1

Ec No. 2

217-636-1

Chemical Formula 2

C6h3cl3n2o2

Origin

China

Product Description

2,4-D is a selective, systemic  approved for use in the EU and used for the control of broad-leaved weeds. It is highly soluble in water, volatile and has a low potential to leach to groundwater based on its chemical properties. It is non-persistent in soil but may persist in aquatic systems under certain conditions. It is moderately toxic to mammals but should not bioaccumulate. It may have negeative effects on reproduction, development and is considered to be a neurotoxin and an irritant. It is moderately toxic to birds and most aquatic species as well as honeybees and earthworms.

Description: A translocated phenoxy herbicide for use in cereals, grass and amenity use. Can also be a pesticide transformation product
Example pests controlled: Broad-leaved weeds, Evasive weeds in aquatic situations
Example applications: Turf grass & pastures; Non-cropping situations; Amenity sites; Orchards; Cereals including barley, wheat and oats; Lucerne

Chemical structure: 

Isomerism	None
Chemical formula	C8H6Cl2O3
Canonical SMILES	C1=CC(=C(C=C1Cl)Cl)OCC(=O)O
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	OVSKIKFHRZPJSS-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C8H6Cl2O3/c9-5-1-2-7(6(10)3-5)13-4-8(11)12/h1-3H,4H2,(H,11,12)

General status: 

Pesticide type	Herbicide, Plant growth regulator, Metabolite
Metabolite Type	Soil
Substance group	Alkylchlorophenoxy
Minimum active substance purity	960 g/kg
Known relevant impurities	EU dossier - dioxins & furans; 2,4-dichlorophenol
Substance origin	Synthetic
Mode of action	Selective, systemic, absorbed through roots and increases biosynthesis and production of ethylene causing uncontrolled cell division and so damages vascular tissue. Synthetic auxin.
CAS RN	94-75-7
EC number	202-361-1
CIPAC number	1
US EPA chemical code	030001
PubChem CID	1486
Molecular mass (g mol^-1)	221.04
PIN (Preferred Identification Name)	(2,4-dichlorophenoxy)acetic acid
IUPAC name	(2,4-dichlorophenoxy)acetic acid
CAS name	(2,4-dichlorophenoxy)acetic acid
Other status information	Potential groundwater contaminant
Relevant Environmental Water Quality Standards	UK statutory standard for protection of aquatic life for inland, coastal & territorial surface waters as annual average: 40 ug/L