155-25-9

Basic information

• Product Name: 3-AMINOTRIAZOLE
• Synonyms: 1H-1,2,4-Triazol-3-amin; 1H-1,2,4-Triazol-3-amine; 1H-1,2,4-Triazol-5-amine; 4H-1,2,4-triazol-3-amine
• CAS NO: 155-25-9
• Molecular Weight: 0
• EINECS: 200-521-5
• Mol File: 155-25-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 347.2°C at 760 mmHg
• Flash Point: 190.7°C
• Appearance: /
• Density: 1.488g/cm³
• Vapor Pressure: 5.45E-05mmHg at 25°C
• Refractive Index: 1.67
• CAS DataBase Reference: 3-AMINOTRIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINOTRIAZOLE(155-25-9)
• EPA Substance Registry System: 3-AMINOTRIAZOLE(155-25-9)

Safety Data

• Hazardous Substances Data: 155-25-9(Hazardous Substances Data)

Usage

Chemical Properties

Amitrole is a colorless to off-white crystalline solid or white powder. Odorless when pure.

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 

Downstream Products

• 1378233-00-1 10-benzylidene-6-phenyl-6,7,8,9,10,11-hexahydrobenzo[g][1,2,4]triazolo[3,4-a]quinazolin-5-ol 
• 1378232-97-3 10-benzylidene-6-phenyl-6,7,8,9,10,11-hexahydrobenzo[g][1,2,4]triazolo[4,3-b]quinazolin-5-ol 
• 1378232-96-2 9-benzylidene-6-phenyl-7,8,9,10-tetrahydro-6H-cyclopenta[g][1,2,4]triazolo[3,4-b]quinazolin-5-ol 
• 1378232-99-5 9-benzylidene-6-phenyl-7,8,9,10-tetrahydro-6H-cyclopenta[g][1,2,4]triazolo[3,4-a]quinazolin-5-ol 
• 89977-78-6 ethyl 4,7-dihydro-7-oxo-[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate 
• 1373425-78-5 (E)-1-(5-amino-1H-1,2,4-triazol-1-yl)-5-(5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-1-deoxy-β-D-ribofuranos-1-yl)pent-1-en-3-one 
• 89167-24-8 6-bromo[1,2,4]triazolo[1,5-α]pyrazine 

Related news

3-AMINOTRIAZOLE (cas 155-25-9) protects from CoCl2-induced ototoxicity by inhibiting the generation of reactive oxygen species and proinflammatory cytokines in mice09/30/2019

Cobalt is an essential heavy metal that is necessary for the formation of vitamin B12 (hydroxocobalamin). However, exposure to excess cobalt for a prolonged period can harm the human body, causing pulmonary fibrosis, blindness, deafness, and peripheral neuropathy. 3-Aminotriazole (3-AT) is a cat...detailed

3-AMINOTRIAZOLE (cas 155-25-9) protects against cobalt (II) chloride-induced cytotoxicity by inhibiting reactive oxygen species formation and preventing mitochondrial damage in HepG2 cells09/29/2019

Cobalt is an essential metal that is required for the generation of vitamin B12. However, exposure to excess cobalt for a prolonged period may adversely affect the human body, causing hepatotoxicity, pulmonary fibrosis, and neurotoxicity. 3-Aminotriazole (3-AT) is a catalase inhibitor that is of...detailed

Relevant articles and documents

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.]