69409-94-5 Usage
Description
TAU-FLUVALINATE, also known as Fluvalinate, is a viscous amber oil with a moderate or weak sweetish odor, typically found in its technical grade form. It is a synthetic pyrethroid insecticide that belongs to the class of chemicals known as pyrethroids, which are modeled after the natural pyrethrins found in chrysanthemum flowers. TAU-FLUVALINATE is known for its effectiveness in controlling a wide range of insect pests and has been widely used in various applications across different industries.
Uses
Used in Agricultural Industry:
TAU-FLUVALINATE is used as an insecticide for controlling various insect pests that damage crops and reduce agricultural productivity. Its application helps protect plants from infestations and ensures a healthy and abundant harvest.
Used in Veterinary Medicine:
In the veterinary medicine industry, TAU-FLUVALINATE is used as a pesticide to protect animals from insect-borne diseases and parasites. It is applied to livestock to control pests such as ticks, mites, and lice, which can cause discomfort and transmit diseases to animals.
Used in Public Health:
TAU-FLUVALINATE is also used in public health applications to control insect populations that transmit diseases to humans. By reducing the number of disease-carrying insects, such as mosquitoes, it helps to minimize the spread of vector-borne illnesses and protect public health.
Used in Home and Garden:
For home and garden use, TAU-FLUVALINATE is employed as a pesticide to control insects that infest residential areas and gardens. It is used to eliminate pests such as ants, cockroaches, and flies, which can be a nuisance and pose health risks.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
TAU-FLUVALINATE is a trifluoromethyl pyrethroid. May react with acids to liberate heat. Strong oxidizing acids may cause a reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated in contact with caustic solutions. Flammable or toxic gases may be generated by mixing with alkali metals and hydrides.
Trade name
APISTAN?; KARTAN?; KLARTAN?;
MAVRIK?; MAVRIK AQUAFLOW?; SPUR?[C];
TAUFLUALINATE?; YARDER?; ZEOCON?; ZR
3210?
Metabolic pathway
Metabolism of 14C-fluvalinate by chickens produces
3-phenoxybenzoic acid, which is further degraded by
two pathways. The first pathway involves
O-dephenylation and is the major metabolic route. The
second pathway converts the carboxylic metabolites
into four conjugates of benzoylornithine together with
the conjugate of acetylornithine. The predominant
conjugate is 2N-(3-hydroxybenzoyl)-5N-
benzoylornithine.
Toxicity evaluation
Acute oral LD50 for rats: >3,000 mg/kg
Waste Disposal
Incineration would be an
effective disposal procedure where permitted. If an efficient
incinerator is not available, the product should be mixed
with large amounts of combustible material and contact
with the smoke should be avoided. In accordance with
40CFR165, follow recommendations for the disposal of
pesticides and pesticide containers.
Check Digit Verification of cas no
The CAS Registry Mumber 69409-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,0 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69409-94:
(7*6)+(6*9)+(5*4)+(4*0)+(3*9)+(2*9)+(1*4)=165
165 % 10 = 5
So 69409-94-5 is a valid CAS Registry Number.
69409-94-5Relevant articles and documents
Method for fighting against arthropods destructive of crops and compositions therefor
-
, (2008/06/13)
The present invention relates to processes for controlling arthropods, particularly processes for controlling insects and especially processes for controlling insects which ravage crops, particularly rice crops or market-garden crops; as well as to processes for protecting crops, particularly rice crops or market-garden crops; as well as to processes directed towards improving the yield of the treated crops; as well as to compositions or products which may be used in such processes.
Preparation of alpha-cyanobenzyl esters
-
, (2008/06/13)
A process for the preparation of α-cyanobenzyl esters of cyclopropane carboxylic acids and substituted alkanoic acids by treating a carboxylic acid and a benzaldehyde with a metal cyanide, followed by treatment with a sulfonyl halide.
Nitro- and cyanoguanidines as selective preemergence herbicides and plant defoliants
-
, (2008/06/13)
There are provided novel nitroguanidine and cyanoguanidine compounds. A method of dessicating and defoliating plants by applying to the foliage thereof certain nitroguanidine or cyanoguanidine compounds and a method for the selective preemergence control of undesirable broadleaf weeds and grasses in the presence of graminaceous crops are disclosed.
