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165252-70-0

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165252-70-0 Usage

Description

Dinotefuran is a broad-spectrum insecticide belonging to the neonicotinoid class, specifically the nitroguanidine sub-class. It is an odorless white crystalline solid with a solubility of 39.83 g/L in water and is highly soluble in dichloromethane, acetone, methanol, and ethyl acetate. Dinotefuran has a melting point of 107.5°C, a log Pow of -0.549 at 25°C, and a vapor pressure of <1.7 x 10^-6 Pa at 25°C. It is nonflammable and not explosive to thermal, shock, and frictional tests.

Uses

Used in Pest Control:
Dinotefuran is used as a contact insecticide for controlling various insect pests such as aphids, whiteflies, thrips, leafhopper, leafminer, sawfly, mole cricket, white grubs, lacebugs, billbugs, beetles, mealybugs, sawfly larvae, and cockroaches. It is effective against fleas but not against ticks, mites, or any internal parasites. It is often used in combination with a tickicide/acaricide (e.g., permethrin) or with an insect growth regulator (e.g., pyriproxyfen).
Used in Agricultural Applications:
Dinotefuran is employed as an insecticide in leafy vegetables (except Brassica), residential and commercial buildings, outdoor uses for professional turf management, turf farms, professional ornamental production, golf courses, and residential indoor, lawn, and garden use. It is not listed for use in EU countries but is actively registered in the U.S. and other countries.
Used in Cannabis Testing Kits:
Dinotefuran is used as a component of pesticide mixes in cannabis testing kits, with the product code P698240. This application helps in the detection and management of pesticide residues in cannabis products, ensuring safety and quality standards.

Flammability and Explosibility

Notclassified

Trade name

ALBARIN?; MIKEBLOCK MTI-446?; SAFARI?; SPARKLE?; VENOM?

Pharmacokinetics

After topical administration to dogs and cats dinotefuran remains mostly on the animal's surface and is not absorbed. However a certain amount can be ingested through licking and grooming. In laboratory animals ingested dinotefuran was almost completely absorbed (>90%) quickly distributed throughout the whole body and also rapidly eliminated, mostly through urine in the form of unchanged dinotefuran.

Carcinogenicity

Dinotefuran has been classified as —Not likely to be carcinogenic to humans.“ This classification is based on the lack of evidence for carcinogenicity in mice and rats.

Environmental Fate

Dinotefuran is nontoxic to birds, mammals, fish and algae, but it is highly toxic to marine/estuarine mysid shrimp.Dinotefuran is highly toxic to honey bees by all routes of administration.The mean aerobic biodegradation half-life of dinotefuran measured in 2 soils was 81.5 days. If released into water, dinotefuran is not expected to adsorb to suspended solids and sediment.Dinotefuran was stable to hydrolysis over the pH range of 4 to 9, but was rapidly photolyzed in aqueous solution with a half-life of 1.8 days.Potential for bioconcentration in aquatic organisms is low.Dinotefuran may potentially be present in drinking water, given its high water solubility, high mobility in soils.Dinotefuran does not cumulate in the environment or in the food chain.Correct use of dinotefuran in dogs and cats is unlikely to result in any significant environmental pollution.

Toxicity evaluation

LD50 acute, rats, oral 2450 mg/kgD50 acute, rabbits, dermal >2000 mg/kgAs a general rule, dogs and cats tolerate dinotefuran quite well.Dinotefuran is slightly irritant to the eyes and the skin.Dinotefuran is not carcinogenic, teratogenic or mutagenic.Seven repeated dermal administrations of dinotefuran to kittens at 1X, 3X and 5X the recommended dose were well tolerated by the animals. Dry skin as well as soft, loose or liquid feces were reported in some treated kittens bur were of transient character.

Check Digit Verification of cas no

The CAS Registry Mumber 165252-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,2,5 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 165252-70:
(8*1)+(7*6)+(6*5)+(5*2)+(4*5)+(3*2)+(2*7)+(1*0)=130
130 % 10 = 0
So 165252-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N4O3/c1-8-7(10-11(12)13)9-5-6-3-2-4-14-6/h6H,2-5H2,1H3,(H2,8,9,10)

165252-70-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dinotefuran

1.2 Other means of identification

Product number -
Other names N-methyl-N’-nitro-N″-[(tetrahydro-3-furanyl)methyl]guanidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:165252-70-0 SDS

165252-70-0Downstream Products

165252-70-0Relevant articles and documents

Preparation method of dinotefuran

-

Paragraph 0013; 0048-0053, (2021/08/07)

The invention provides a preparation method of dinotefuran, and belongs to the field of organic synthesis. The invention provides a preparation method of dinotefuran, which is characterized by comprising the following steps: step 1, adding a compound I, a compound II and a solvent into a reaction container, heating to 50 DEG C which is the reflux temperature of the solvent, reacting for 1-24 hours, then adding tetrahydrofuran-3-methylamine, and continuously reacting for 1-24 hours to obtain a reaction solution; and 2, cooling the reaction solution to 0-20 DEG C, standing, filtering, separating the solid and filtrate, and purifying the solid to obtain dinotefuran, wherein the structural formula of the compound I is shown in the specification, the structural formula of the compound II is shown in the specification, and R1 and R2 are independently selected from any one of H, C1-C5 alkyl and C1-C5 alkyl substituted by at least one halogen atom. According to the invention, a brand new dinotefuran synthesis route is developed, the synthesis route is greatly shortened, and the production efficiency is improved.

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