Plant Growth Regulator Tebuconazole 250g/L Ew

Min.Order: 100

Product origin: Shanghai, China

Infringement complaint:

Complaint

US$ 1 ~ 8

Description

Imidacloprid 233g/l + Tebuconazole 13g/l FS of Insecticide & Fungicide Pesticide

Insecticide + Fungicide

Imidacloprid
Imidacloprid is an insecticide approved for use in the EU with certain restrictions for flowering crops. It is highly soluble, non-volatile and persistent in soil. It is moderately mobile. It has a low risk of bioaccumulating. It is highly toxic to birds and honeybees. Moderately toxic to mammals and earthworms. It is non-toxic to fish.

Description: A chloronicotine insecticide used to control sucking and soil insects. Also used as a flea treatment for domestic pets.
Example pests controlled: Plant hoppers, Aphids, Termites, Colorado bettle, Fleas, White grups, Craneflies; Crickets, Ants
Example applications: Lawns and turf; Domestic pets; Rice, Cereals; Maize; Potatoes; Sugar beet

Chemical structure:

Isomerism	Isomeric - existing as both the E- and Z- forms however many commerical products are comprised of almost entirely the (E)-isomer
Chemical formula	C₉H₁₀ClN₅O₂
Canonical SMILES	C1CN(C(=N1)N[N+](=O)[O-])CC2=CN=C(C=C2)Cl
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	YWTYJOPNNQFBPC-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2,5H,3-4,6H2,(H,11,13)

General status:

Pesticide type	Insecticide, Veterinary substance
Substance group	Neonicotinoid
Minimum active substance purity	970 g/kg
Known relevant impurities	EU dossier - None declared
Substance origin	Synthetic
Mode of action	Systemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist.
CAS RN	138261-41-3
EC number	-
CIPAC number	582
US EPA chemical code	129099
PubChem CID	86418
Molecular mass (g mol^-1)	255.66
PIN (Preferred Identification Name)	-
IUPAC name	(E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine
CAS name	(2E)-1-((6-chloro-3-pyridinyl)methyl)-N-nitro-2-imidazolidinimine
Other status information	NOTE ban or usage restriction may be in place for use on flowering crops in some Member States

Tebuconazole
Description: A fungicide effective against various foliar diseases in cereals and other field crops
Example pests controlled: Smut; Bunt; Stripe rust; Yellow leaf spot; Powdery mildew; Scelerotinia rot; Black spot; Net blotch
Example applications: Cereals including wheat, barley, oat, rye; Grapes; Peanuts; Vegetables including onions, peas, pepper; Bananas; Sugarcane

Chemical structure:

Isomerism	A chiral molecule. The technical material is an isomeric mixture of the (S-) and (R-) isomers. The R-form is more biologically active than the S-form.
Chemical formula	C₁₆H₂₂ClN₃O
Canonical SMILES	CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	PXMNMQRDXWABCY-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C16H22ClN3O/c1-15(2,3)16(21,10-20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7,11-12,21H,8-10H2,1-3H3

General status:

Pesticide type	Fungicide, Plant growth regulator
Substance group	Triazole
Minimum active substance purity	950 g/kg
Known relevant impurities	EU dossier - None declared
Substance origin	Synthetic
Mode of action	Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor.
CAS RN	107534-96-3
EC number	403-640-2
CIPAC number	494
US EPA chemical code	128997
PubChem CID	86102
Molecular mass (g mol^-1)	307.82
PIN (Preferred Identification Name)	rac-(3R)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol
IUPAC name	(RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol
CAS name	α-(2-(4-chlorophenyl)ethyl)-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol