Fungicide Pesticide Boscalid 400g/L + Cyproconazole 100g/L Sc

• CAS No.: 94361-06-5
• Formula: C15h18cln3o
• Appearance: Liquid
• Source: Insect Hormone
• Toxicity of High and Low: Low Toxicity of Reagents
• Mode: Systemic Insecticide
• Model NO.: SC
• Toxicological Effect: Nerve Poison
• Transport Package: 20L 200L 5L 10L
• Specification: TC WP EC
• Trademark: MOLOTUS
• Origin: China
• HS Code: 3808
• Production Capacity: 5000t

Product Description

Fungicide Pesticide Boscalid 400g/L + Cyproconazole 100g/L SC


Boscalid
Description: A fungicide active against a broad range of fungal pathogens in a wide range of crops including vegetables and other crops
Example pests controlled: Alternaria blight; Botrytis; Powdery mildew; Purple blotch; Rust; Leaf spot; Target spot; Grey mould; Stem rot
Example applications: Vegetables including beans, brassicas, onions, garlic, shallots, peas, carrots, turnips; Soybeans; Fruits including grapes, apples, pears, strawberries; Tree nuts

Chemical structure: 

Isomerism	-
Chemical formula	C18H12Cl2N2O
Canonical SMILES	C1=CC=C(C(=C1)C2=CC=C(C=C2)Cl)NC(=O)C3=C(N=CC=C3)Cl
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	WYEMLYFITZORAB-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C18H12Cl2N2O/c19-13-9-7-12(8-10-13)14-4-1-2-6-16(14)22-18(23)15-5-3-11-21-17(15)20/h1-11H,(H,22,23)/f/h22H

General status: 

Pesticide type	Fungicide
Substance group	Carboxamide
Minimum active substance purity	960 g/kg
Known relevant impurities	EU dossier - none declared
Substance origin	Synthetic
Mode of action	Protectant, foliar absorption, translocates, inhibits spore germination and germ tude elongation. Succinate DeHydrogenase Inhibitor.
CAS RN	188425-85-6
EC number	-
CIPAC number	673
US EPA chemical code	128008
PubChem CID	213013
Molecular mass (g mol^-1)	343.21
PIN (Preferred Identification Name)	2-chloro-N-(4'-chloro[1,1'-biphenyl]-2-yl)pyridine-3-carboxamide
IUPAC name	2-chloro-N-(4'-chlorobiphenyl-2-yl)nicotinamide
CAS name	2-chloro-N-(4'-chloro[1,1'-biphenyl]-2-yl)-3-pyridinecarboxamide

Cyproconazole
Cyproconazole is a commonly used fungicide approved for use in the EU and in many other countries. It is moderately soluble in water and readily soluble in many organic solvents. It is a volatile substance. Based on its physico-chemical properties, cyproconazole has a high risk of leaching to groundwater. It can be persistent in both soil and water systems. It is moderately toxic to mammals. It is highly toxic to birds and moderately toxic to most aquatic organisms, earthworms and honeybees.

Description: A broad spectrum fungicide for cereals and other field crops used to control Septoria, rust, powdery mildew and other diseases
Example pests controlled: Spetoria; Net blotch; Brown rust; Yellow rust; Eyespot; Powdery mildews; Chocolate spot; Ear disease; Glume blotch
Example applications: Cereals including wheat, barley, oats, rye; Vegetables including peas & beans, asparagus; Oilseed rape; Sugarbeet; Fruit including apples, peach; Almonds

Chemical structure: 

Isomerism	A chiral molecule that is an approximately equal mixture of the two diastereomers, each of which is exactly a 1:1 mixture of the enantiomers.
Chemical formula	C15H18ClN3O
Canonical SMILES	CC(C1CC1)C(CN2C=NC=N2)(C3=CC=C(C=C3)Cl)O
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	UFNOUKDBUJZYDE-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C15H18ClN3O/c1-11(12-2-3-12)15(20,8-19-10-17-9-18-19)13-4-6-14(16)7-5-13/h4-7,9-12,20H,2-3,8H2,1H3

General status: 

Pesticide type	Fungicide
Substance group	Triazole
Minimum active substance purity	940 g/kg
Known relevant impurities	EU dossier - may contain diastereomers of cyproconazole
Substance origin	Synthetic
Mode of action	Systemic with protective, curative and eradicant action. Disrupts membrane function. An ergosterol-biosynthesis inhibitor.
CAS RN	94361-06-5
EC number	-
CIPAC number	600
US EPA chemical code	128993
PubChem CID	86132
Molecular mass (g mol^-1)	291.78
PIN (Preferred Identification Name)	mixture of the 2 enantiomeric pairs rac-(2R,3R)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol and rac-(2R,3S)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol in the ratio 1:1
IUPAC name	(2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
CAS name	α-(4-chlorophenyl)-α-(1-cyclopropylethyl)-1H-1,2,4-triazole-1-ethanol