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3-Amino-1,2,4-Triazole

CAS No.
61-82-5
Chemical Name:
3-Amino-1,2,4-Triazole
Synonyms
3-AMINO-1,2,4-TRIAZOLE;AMITROLE;3-AT;AT;1H-1,2,4-Triazol-3-amine;AMINOTRIAZOLE;3-AMINO-1H-1,2,4-TRIAZOLE;3-Aminotriazole;1H-1,2,3-triazol-4-amine;3-amino-s-triazole
CBNumber:
CB6767936
Molecular Formula:
C2H4N4
Molecular Weight:
84.08
MDL Number:
MFCD00005230
MOL File:
61-82-5.mol
MSDS File:
SDS
Last updated:2024-03-25 15:20:08

3-Amino-1,2,4-Triazole Properties

Melting point 150-153 °C(lit.)
Boiling point 144.35°C (rough estimate)
Density 1.138
vapor pressure <0.1 hPa (20 °C)
refractive index 1.6260 (estimate)
storage temp. Store below +30°C.
solubility 280g/l
form Powder or Flakes
pka 11.14±0.20(Predicted)
color White to off-white or yellow
PH 6.4-7.4 (100g/l, H2O, 20℃)
Water Solubility 280 g/L (20 ºC)
Merck 14,489
BRN 107687
Exposure limits NIOSH REL: TWA 0.2 mg/m3; ACGIH TLV: TWA 0.2 mg/m3.
Stability Stable. Incompatible with iron, copper, aluminium, acids, alkalies, strong oxidizing agents, acid chlorides, acid anhydrides. Forms chelates with some metals. Moisture sensitive.
LogP -0.860
CAS DataBase Reference 61-82-5(CAS DataBase Reference)
EWG's Food Scores 7
FDA UNII ZF80H5GXUF
NIST Chemistry Reference 3-Amino-s-triazole(61-82-5)
Proposition 65 List Amitrole
IARC 3 (Vol. 79, Sup 7) 2001
EPA Substance Registry System Amitrole (61-82-5)
Pesticides Freedom of Information Act (FOIA) Amitrole

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H360D
Precautionary statements  P202-P264-P280-P302+P352-P305+P351+P338-P308+P313
Hazard Codes  Xn,N,T
Risk Statements  48/22-51/53-63-40-61
Safety Statements  13-36/37-61-45-53
RIDADR  UN 3077 9/PG 3
WGK Germany  2
RTECS  XZ3850000
Autoignition Temperature >225 °C
TSCA  Yes
HazardClass  9
PackingGroup  III
HS Code  29339990
Toxicity LD50 in mice, rats (g/kg): 14.7, 25.0 orally (Krller)
NFPA 704
0
1 0

3-Amino-1,2,4-Triazole price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A8056 3-Amino-1,2,4-triazole ≥95% (TLC) 61-82-5 10g $51.6 2024-03-01 Buy
Sigma-Aldrich SAB1304379 ANTI-TAS1R2 (C-TERM) antibody produced in rabbit IgG fraction of antiserum, buffered aqueous solution 61-82-5 400μl $481 2024-03-01 Buy
Sigma-Aldrich 8.14495 3-Amino-1H-1,2,4-triazole for synthesis 61-82-5 100g $49.8 2024-03-01 Buy
Sigma-Aldrich 8.14495 3-Amino-1H-1,2,4-triazole for synthesis 61-82-5 500g $176 2024-03-01 Buy
Sigma-Aldrich 45324 Amitrol PESTANAL 61-82-5 250mg $64.4 2024-03-01 Buy
Product number Packaging Price Buy
A8056 10g $51.6 Buy
SAB1304379 400μl $481 Buy
8.14495 100g $49.8 Buy
8.14495 500g $176 Buy
45324 250mg $64.4 Buy

3-Amino-1,2,4-Triazole Chemical Properties,Uses,Production

Chemical Properties

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

Chemical Properties

white powder or crystals

Uses

catalase inhibitor

Uses

Nonselective, foliage-applied, systemic, triazole herbicide used in uncropped land and orchards to control certain grasses and to kill annual and perennial grasses and weeds. It is also effective on poison ivy, poison oak and aquatic weeds

Uses

Herbicide; plant regulator.

Definition

A powerful plant growth suppressant and cotton defoliant that is readily absorbed by leaves and roots. 3-Amino-1,2,4-Triazole inhibits many aspects of growth and differentiation including cell division in the primary root meristems in some plants.

Production Methods

3-Amino-1,2,4-Triazole(Amitrole) is synthesized by condensing formic acid with aminoguanidine and can be purified by recrystallization from methanol.

General Description

Odorless white crystals or white powder. Bitter taste. Melting point 147-159°C. Sublimes undecomposed at reduced pressure. Used as a post-emergence herbicide.

Air & Water Reactions

Water soluble. Aqueous solutions are neutral. Dust may form an explosive mixture in air.

Reactivity Profile

3-Amino-1,2,4-Triazole is a triazole derivative. The triazoles are a group that contain several derivatives that are highly explosive materials. They are sensitive to heat, friction, and impact. Sensitivity varies with the type substitution to the triazole ring. Metal chelated and halogen substitution of the triazol ring make for a particularly heat sensitive material. Azido and nitro derivatives have been employed as high explosives. No matter the derivative these materials should be treated as explosives. It forms chelates with some metals. 3-Amino-1,2,4-Triazole is corrosive to iron, copper and aluminum. Forms salts with most acids and alkalis. It is incompatible with strong oxidizers, strong acids, acid chlorides and acid anhydrides .

Hazard

Toxic; carcinogen.

Health Hazard

Amitrole (3-Amino-1,2,4-Triazole) has low acute toxicity; in experimental animal studies subchronic exposures were associated with changes in the thyroid and chronic exposures were carcinogenic.
Intentional ingestion of a mixture that contained 20 mg/kg amitrole did not cause any signs of intoxication.1 In one reported case study, inhalation of a large amount of amitrolecontaining herbicide was associated with acute toxic reaction of the lungs.2 Lung injury was thought to be secondary to direct toxic damage to the alveolar lining cells. The remarkable lack of any other reports describing pulmonary toxicity of this herbicide was noted, in addition to the presence of other chemicals in the herbicide solution.

Fire Hazard

Literature sources indicate that Triazol-3-amine is non-combustible.

Agricultural Uses

Herbicide, Plant growth regulator: A non-food use herbicide for control of grasses, woody plants and broad-leaf weeds on hard surface and in areas where crops are not normally grown.

Trade name

AMITRIL®; ATLAZIN®; ATLAZINE® FLOWABLE; AT®; 3-AT®; AT-90®; ATRAFLOW PLUS®; AZAPLANT®; AZAPLANT KOMBI®; AZOLAN®; AZOLE®; BOROFLOW® A/ATA; CAMPAPRIM® A 1544; CDA SIMFLOW PLUS®; CHIPMAN® PATH; CYTROLE®; DIUROL® AMITROLE; DOMATOL®; ELMASIL®; EMISOL®; FARMCO®; HERBAZIN PLUS SC®; HERBICIDE® TOTAL; MASCOT HIGHWAY®; MSS AMINOTRIAZOLE®; MSS SIMAZINE®; ORGA-414®; RADOXONE® TL; RAMIZOL®; RASSAPRON®; SIMAZOL®; SIMFLOW PLUS®; SOLUTION CNCENTREE T271®; SYNCHEMICALS® TOTAL WEED KILLER; SYNTOX®; TORAPRON®; VOROX®; WEEDAR®; WEEDAZIN®; WEEDAZOL TL ®; WEEDOCLOR®

Biochem/physiol Actions

BTK (also known as Bruton tyrosine kinase) plays a crucial role in B-lymphocyte differentiation and activation. BTK interacts with SRC homology 3 domains of FYN, LYN and HCK that are activated upon stimulation of B- and T-cell receptors.Defects in the BTK gene cause Agammaglobulinemia, an X-linked immunodeficiency characterized by failure to produce mature B lymphocyte cells and associated with a failure of Ig heavy chain rearrangement. The unique role of BTK makes it a desirable target for potential anti-cancer, anti-inflammatory and anti-viral agents as well as other treatments.

Safety Profile

Confirmed carcinogen with experimental carcinogenic, tumorigenic, and neoplastigenic data. Poison by intraperitoneal route. Moderately toxic by ingestion. An experimental teratogen. Other experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,. An herbicide and plant growth regulator

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.

Carcinogenicity

Amitrole is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

Environmental Fate

Soil. When radiolabeled amitrole-5-14C was incubated in a Hagerstown silty clay loam, 50 and 70% of the applied amount evolved as 14CO2 after 3 and 20 days, respectively. In autoclaved soil, however, no 14CO2 was detected. The chemical degradation in soil was probably via hydroxyl radicals (Kaufman et al., 1968). The average persistence in soils is 2–4 weeks (Hartley and Kidd, 1987)
Plant.Amitrole is transformed in plants to form the conjugate β-(3-amino-1,2,4-triazol- 1-yl)-α-alanine (Humburg et al., 1989) and/or 3-(3-amino-s-triazole-1-yl)-2-aminopropionic acid (Duke et al., 1991). Amitrole is metabolized in Canada thistl
Surface Water. In pond water, adsorption to suspended sediments was an important process. The initial half-life was reported to be no more than 68 days. After 120 days, 20% of the applied amount remained (Grzenda et al., 1966). The biodegradation
Photolytic. Direct photolysis of amitrole is not expected to occur since the herbicide shows little or no absorption greater than 295 nm (Gore et al., 1971)
Chemical/Physical. Reacts with acids and bases forming soluble salts (Hartley and Kidd, 1987). Emits toxic fumes of nitrogen oxides when heated to decomposition (Sax and Lewis, 1987); however, incineration with polyethylene results in more than 9

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.

Purification Methods

It crystallises from EtOH (charcoal), then three times from dioxane [Williams et al. J Phys Chem 61 261 1957]. [Beilstein 26 H 137.] Possible carcinogen. [Beilstein 26 H 137, Temple & Montgomery 1,2,4-Triazoles —The Chemistry of Heterocyclic Compounds Vol 37 (Weissberger & Taylor eds.). Wiley & Sons NY 1981, ISBN 0-471-0656-6.]

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.

75232-02-9
1118-03-2
71831-21-5
61-82-5
Synthesis of 3-Amino-1,2,4-Triazole from 5-MERCAPTO-1,2,3-TRIAZOLE MONOSODIUM SALT and AZIDOTRIMETHYLTIN and 4-BROMO METHYLBENZYL ALCOHOL
Global( 540)Suppliers
Supplier Tel Email Country ProdList Advantage
Jiaxing Dongliang Pharmaceutical Technology Co.,Ltd.
+86-0573-84772883 +86-18905731109 hujidong@hailunchem.com China 7 58
Wuwei hailun New Material Technology Co., Ltd.
+86-0935-5322366 +86-13605736198 hailunchem@vip.163.com China 7 58
Jinan Finer Chemical Co., Ltd
+86-531-88989536 +86-15508631887 sales@finerchem.com China 2966 58
hebei hongtan Biotechnology Co., Ltd
+86-86-1913198-3935 +8617331935328 sales03@chemcn.cn China 951 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
NINGBO INNO PHARMCHEM CO., LTD.
13867897135 sales@nbinno.com CHINA 925 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293 sales@sdzschem.com China 2931 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58

View Lastest Price from 3-Amino-1,2,4-Triazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Triazol-3-amine pictures 2024-04-16 Triazol-3-amine
61-82-5
US $5.00 / KG 1KG 99% 500mt/year Jinan Finer Chemical Co., Ltd
Triazol-3-amine pictures 2024-04-12 Triazol-3-amine
61-82-5
US $30.00 / kg 1kg 98% 2000kg hebei hongtan Biotechnology Co., Ltd
Triazol-3-Amine pictures 2023-03-06 Triazol-3-Amine
61-82-5
US $19.00 / KG 1KG 99.% 50 ton Hebei Guanlang Biotechnology Co,.LTD
  • Triazol-3-amine pictures
  • Triazol-3-amine
    61-82-5
  • US $30.00 / kg
  • 98%
  • hebei hongtan Biotechnology Co., Ltd
  • Triazol-3-Amine pictures
  • Triazol-3-Amine
    61-82-5
  • US $19.00 / KG
  • 99.%
  • Hebei Guanlang Biotechnology Co,.LTD
Vorox Vorox AA Vorox AS voroxaa voroxas AMITROL PESTANAL (1,2,4-TRIAZOL- 3-YLAMI Amitrol=Aminotriazole=3-Aminotriazole 3-Amino-1,2,4-Triazole 61-82-5 1H-3-AMINO-1,2,4-TRIAZOLE Amitrole (ATA) CYTROLAMITROLE-T 1H-1,2,4-Triazol-3-amine, Amitrol CYTROL(R) ATA(R) AZOLAN AURORA KA-678 ORIFLAM SUPERZOL 1H-1,2,4-TRIAZOL-3-YLAMINE amitrole (ISO) 1,2,4-triazol-3-ylamine 1,2,4-Triazol-3-amine, 3-Amino-1,2,4-triazole, 3-AT, Amitrol 1,2,4-Triazol-3-amine, 3-AT, Amitrol 3-AMINO-1H-1,2,4-TRIAZOLE 99% 3-Amino-3H-1,2,4-triazole 3-Amino-1,2,4-triazole,1,2,4-Triazol-3-amine, 3-AT, Amitrol 3-Amino-1,2,4-triazole ,95% 4-triazole 3-Amino-1H-1,2,4-triazole,95% 3-AMino-1H-1,2,4-triazole, 95% 100GR 3-AMino-1H-1,2,4-triazole, 95% 10GR 3-AMINO-1H-1,2,4-TRIAZOLE FOR SYNTHESIS 1H-1,2,3-triazol-1-aMine 1,2,4-triazol-3-ylamine 1,2,4-triazole,3-amino- 1H-1,2,4-Triazole-3-amine 2-aminotriazole 3-amino-11,2,4-triazole 3-amino-s-triazol Amitril T.L. amitriltl Amitrol 90 amitrol90 Amitrol-T Amizol Amizol D Amizol DP NAU Amizol F amizold amizoldpnau amizolf Azaplant Azaplant kombi azaplantkombi Boroflow S/ATA Campaprim A 1544 campaprima1544 Cytrol Cytrole