155-25-9

Usage

Uses

Used in Chemical Industry:
3-AMINOTRIAZOLE is used as a chemical intermediate for the synthesis of various compounds, including pharmaceuticals, dyes, and pesticides. Its versatile chemical structure allows it to be a key component in the production of a wide range of products.
Used in Pharmaceutical Industry:
3-AMINOTRIAZOLE is used as an active pharmaceutical ingredient for the development of drugs targeting specific medical conditions. Its unique chemical properties enable it to interact with biological systems, making it a valuable asset in the creation of novel therapeutic agents.
Used in Agricultural Industry:
3-AMINOTRIAZOLE is used as a herbicide to control the growth of unwanted plants in agricultural fields. Its effectiveness in controlling a broad spectrum of weeds makes it a popular choice for farmers looking to improve crop yields and protect their investments.
Used in Research and Development:
3-AMINOTRIAZOLE is used as a research compound in various scientific studies, particularly in the fields of chemistry, biology, and materials science. Its unique properties make it an interesting subject for exploration and potential applications in new technologies and innovations.

Potential Exposure

A potential danger to those involved in the manufacture, formulation, and application of this postemergence herbicide, which is now limited to noncrop applications as a herbicide and plant growth regulator. Some triazoles have been used as rubber components.

Shipping

UN2588 Pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Incompatibilities

Dust may be explosive in air. Keep away from strong oxidizers; strong acids; light and heat (decomposes). Corrosive to iron, aluminum, and copper. Sublimes undecomposed at reduced pressure.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Amitrol is resistant to hydrolysis and the action of oxidizing agents. Burning the compound with polyethylene is reported to result in .99% decomposition.

InChI:InChI=1/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)

Upstream product

• 78158-91-5 N,N-dimethyl-N'-(4H-1,2,4-triazol-3-yl) formamidine 

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Relevant academic research and scientific papers

Kinetics and mechanism of uncatalyzed and ruthenium(III)-catalyzed oxidation of formamidine derivative by hexacyanoferrate(III) in aqueous alkaline medium

The catalytic effect of ruthenium(III) on the oxidation of N, N-dimethyl- N′-(4H-1,2,4-triazol- 3-yl) formamidine (ATF) by hexacyanoferrate(III) (HCF) was studied spectrophotometrically in aqueous alkaline medium. Both uncatalyzed and catalyzed reactions showed first order kinetics with respect to [HCF], whereas the reaction orders with respect to [ATF] and [OH ?] were apparently less than unity over the concentration range studied. A first order dependence with respect to [RuIII] was obtained. Increasing ionic strength increased the rate of uncatalyzed reaction and decreased the rate of the catalyzed one Plausible mechanistic schemes of oxidation reactions have been proposed. In both cases, the final oxidation products are identified as aminotriazole, dimethyl amine and carbon dioxide. The rate laws associated with the reaction mechanisms are derived. The reaction constants involved in the different steps of the mechanisms were calculated. The activation and thermodynamic parameters have been computed and discussed. [Figure not available: see fulltext.]

Kinetic and Mechanistic Aspects of Oxidation of Aminotriazole Formamidine by Cerium(IV) in Aqueous Perchloric and Sulfuric Acid Solutions: A Comparative Study

The kinetics of the oxidation of an aminotriazole formamidine derivative, N,N-dimethyl-N′-(4H-1,2,4-triazol-3-yl) formamidine (ATF) by cerium(IV) has been studied spectrophotometrically in aqueous perchloric and sulfuric acid solutions at constant ionic strength of 1.0 mol·dm-3. In both acids, the reaction shows first order kinetics with respect to [Ce(IV)], whereas the orders with respect to [ATF] are less than unity. The reaction exhibits negative fractional order kinetics with respect to [H+]. The rates of reaction are not significantly affected by variations of either ionic strength or relative permittivity of the reaction's media. Addition of cerium(III) product does not affect the rates. Plausible mechanistic schemes for the reactions have been proposed. In both cases, the final oxidation products were identified as aminotriazole, dimethyl amine and carbon dioxide. Under comparable experimental conditions, the oxidation rate in perchloric acid solution is about sixfold higher than that in sulfuric acid solution. The effect of temperature on the rates has also been studied and activation parameters have been evaluated and discussed. The rate laws associated with the reaction mechanisms are derived.