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T46108

Sigma-Aldrich

1,2,4-Triazole

98%

Sinonimo/i:

3,4-Diazapyrrole, 4H-1,2,4-Triazole, s-Triazole (8CI)

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25 G
CHF 33.50
100 G
CHF 88.70
500 G
CHF 210.00

CHF 33.50


Spedizione prevista il19 marzo 2025


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Cambia visualizzazione
25 G
CHF 33.50
100 G
CHF 88.70
500 G
CHF 210.00

About This Item

Formula empirica (notazione di Hill):
C2H3N3
Numero CAS:
Peso molecolare:
69.07
Beilstein:
104767
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

CHF 33.50


Spedizione prevista il19 marzo 2025


Richiedi un ordine bulk

Livello qualitativo

Saggio

98%

P. ebollizione

260 °C (lit.)

Punto di fusione

119-121 °C (lit.)

Stringa SMILE

c1nc[nH]n1

InChI

1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5)
NSPMIYGKQJPBQR-UHFFFAOYSA-N

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Applicazioni

1,2,4-triazole and its derivatives are important structural moieties of many pharmaceutical drugs.[1] Triazoles can also act as ligands to form coordination complexes with transition metal ions.[2] Due to their electron-deficient nature, they exhibit excellent electron-transport and hole-blocking properties, making them promising organic materials in material science applications.[3]

Pittogrammi

Health hazardExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

338.0 °F

Punto d’infiammabilità (°C)

170 °C

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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I clienti hanno visto anche

Slide 1 of 2

1 of 2

1, 2, 4-Triazoles: Synthetic approaches and pharmacological importance.
Al-Masoudi IA
Chemistry of Heterocyclic Compounds, 42(11), 1377-1403 (2006)
Mononuclear, oligonuclear and polynuclear metal coordination compounds with 1, 2, 4-triazole derivatives as ligands.
Haasnoot JG
Coordination Chemistry Reviews, 200, 131-185 (2000)
Applications of Metal-Free 1, 2, 4-Triazole Derivatives in Materials Science.
Diaz-Ortiz A
Current Organic Chemistry, 19(7), 568-584 (2015)
Muhammad Salman et al.
Biosensors & bioelectronics, 36(1), 236-241 (2012-05-15)
Conventional synthesis of silver nanoparticles employs a reducing agent and a capping agent. In this report water-soluble silver nanoparticles (AgNPs) were prepared facilely by chemical reduction of Ag(I) ions. 4-Amino-3-(d-gluco-pentitol-1-yl)-4,5-dihydro-1,2,4-triazole-5-thione (AGTT) was used both as reducing and stabilizing agent. Direct
Jing-Lin Chen et al.
Inorganic chemistry, 52(17), 9727-9740 (2013-08-22)
A new series of mononuclear copper(I) complexes (1-9) with functionalized 3-(2'-pyridyl)-1,2,4-triazole chelating ligands, as well as the halide and/or phosphine ancillary ligands, have been synthesized. Complexes 1-9 were fully characterized by elemental analysis, NMR spectroscopy, mass spectroscopy, electronic absorption spectroscopy

Questions

1–5 of 5 Questions  
  1. What is the solubility of 1,2,4-Triazole (Product No. T46108)?

    1 answer
    1. Triazole is appreciably soluble in water and alcohol, according to the 14th edition of the chemicals encyclopedia published by the Royal Society of Chemistry.

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  2. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  3. What type of information is available for derivatives of 1,2,4-triazole (Product No. T46108)?

    1 answer
    1. A good source for information on 1,2,4-triazoles is a review article by K.T. Potts entitled The Chemistry of 1,2,4-Triazoles. Here is the citation: Chem. Rev., 61(2), 87-127 (1961).

      Helpful?

  4. How is Product No. T46108, 1,2,4-Triazole, produced?

    1 answer
    1. Typically the exact production methods are considered proprietary; this is also true for product T46108.  The 1,2,4-Triazole preparation is outlined in this article by C. Ainsworth: Org. Synth., 40, 99 (1960).

      Helpful?

  5. How is Product No. T46108, 1,2,4-Triazole, packaged?

    1 answer
    1. Product No. T46108 is typically packaged in a high density polyethylene (HDPE) bottle with a Teflon-lined polypropylene (PP) cap.

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