Fungicide Pesticide & Metabolite Carbendazim 12.5% + Mancozeb 63% Wp

• CAS No.: 10605-21-7
• Formula: C9h9n3o2
• Application: Fungicide, Bactericide, Viricide/Virucide
• Usage Mode: Therapeutic Agent
• Raw Material: Inorganic Fungicide
• Application Fields: Agricultural Fungicide
• Model NO.: WP
• Conductivity: Systemic Fungicide
• Composition: Organic
• Transport Package: 25kg 1kg 100g
• Specification: TC WP EC
• Trademark: MOLOTUS
• Origin: China
• HS Code: 3808
• Production Capacity: 5000t

Product Description

Fungicide Pesticide & Metabolite Carbendazim 12.5% + Mancozeb 63% WP

Carbendazim
Carbendazim is a fungicide that is not approved for use in the EU. It has a low aqueous solubility, is volatile and moderately mobile. It is moderately persistent in soil and can be very persistent in water systems under certain conditions. Carbendazim has a low mammalian toxicity and is not expected to bioaccumulate. It is, however, reported as a reproduction/developmental toxicant. It is moderately toxic to honeybees and most aquatic organisms. It is highly toxic to earthworms but non-toxic to birds.

Description: A fungicide used to control a a range of diseases including Septoria, Fusarium and Sclerotina. Can also be a pesticide transformation product
Example pests controlled: Husk spot; Chocolate spot; Grey mould; Green mould; Crown rot
Example applications: Beans; Macademia nuts; Lentils; Chickpeas; Strawberries; Sugarcane; Cereals

Chemical structure: 

Isomerism	None
Chemical formula	C9H9N3O2
Canonical SMILES	COC(=O)NC1=NC2=CC=CC=C2N1
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	TWFZGCMQGLPBSX-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C9H9N3O2/c1-14-9(13)12-8-10-6-4-2-3-5-7(6)11-8/h2-5H,1H3,(H2,10,11,12,13)

General status: 

Pesticide type	Fungicide, Metabolite
Metabolite Type	Soil
Substance group	Benzimidazole
Minimum active substance purity	960 g/kg
Known relevant impurities	EU dossier - 3-amino-2-hydroxyphenazine 0.0005 g/kg; 2,3-diamino-phenazine 0.0006 g/kg
Substance origin	Synthetic
Mode of action	Systemic with curative and protectant activity. Inhibition of mitosis and cell division (Beta-tubulin assembly in mitosis).
CAS RN	10605-21-7
EC number	234-323-0
CIPAC number	263
US EPA chemical code	115001/128872
PubChem CID	25429
CLP index number	613-048-00-8
Molecular mass (g mol^-1)	191.21
PIN (Preferred Identification Name)	methyl 1H-1,3-benzimidazol-2-ylcarbamate
IUPAC name	methyl benzimidazol-2-ylcarbamate
CAS name	methyl 1H-benzimidazol-2-ylcarbamate
Other status information	Marine Pollutant
Relevant Environmental Water Quality Standards	Environment Agency UK non-statutory standard for the protection of aquatic life: freshwater and saltwater annual average 0.1 ug/L; max acceptable conc: 1.0 ug/L

Mancozeb
Manacozeb is a commonly used fungicide approved for use in the EU and in manny other countries. It has a low aqueous solubility, is quite volatile and not expected to leach to groundwater. It is not persistent in soil systems but may be persistent in water under certain conditions. Mancozeb has a low mammalian toxicity by has been associated with adverse reproduction/development effects. It is highly toxic to fish and aquatic invertebrates, and moderately toxic to birds and earthworms. The toxicity of mancozeb to honeybees is low.

Description: A fungicide for control of a wide range of pathogens including blights and scabs on crops
Example pests controlled: Potato blight; Leaf spot; Scab; Rust
Example applications: Potatoes; Fruit including apples, pears, grapes; Cotton; Corn; Sunflowers; Peanuts; Tomatoes; Cereals; Ornamental shrubs including roses

Chemical structure: 

Isomerism	-
Chemical formula	(C4H6MnN2S4)x(Zn)y
Canonical SMILES	C(CNC(=S)[S-])NC(=S)[S-].C(CNC(=S)[S-])NC(=S)[S-].[Mn+2].[Zn+2]
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	CHNQZRKUZPNOOH-UHFFFAOYSA-J
International Chemical Identifier (InChI)	InChI=1S/2C4H8N2S4.Mn.Zn/c2*7-3(8)5-1-2-6-4(9)10;;/h2*1-2H2,(H2,5,7,8)(H2,6,9,10);;/q;;2*+2/p-4

General status: 

Pesticide type	Fungicide
Substance group	Carbamate
Minimum active substance purity	85% w/w
Known relevant impurities	EU dossier - Ethylene thiourea
Substance origin	Synthetic
Mode of action	Broad spectrum, non-systemic, contact with protective action, acts by distrupting lipid metabolism. Multi-site activity.
CAS RN	8018-01-7
Alternative/old CAS RN	formerly 8065-67-6
EC number	006-076-00-1
CIPAC number	34
US EPA chemical code	014504
PubChem CID	13307026
Molecular mass (g mol^-1)	271.3
PIN (Preferred Identification Name)	-
IUPAC name	manganese ethylenebis(dithiocarbamate) (polymeric) complex with zinc salt
CAS name	((2-((dithiocarboxy)amino)ethyl)carbamodithioato))(2-)-kS,kS')manganese mixture with((2-((dithiocarboxy)amino)ethyl)carbamodithioato))(2-)-kS,kS')zinc
Other status information	Marine Pollutant
Relevant Environmental Water Quality Standards	UK Environment Agency non-statutory standard for the protection of aquatic life in freshwater and saltwater annual average 2 ug/L, max acceptable conc 20 ug/L