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T46108

1,2,4-Triazole

Name: 1,2,4-Triazole
Brand: ALDRICH

98%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):

C₂H₃N₃

CAS Number:

288-88-0

Molecular Weight:

69.07

Beilstein:

104767

EC Number:

206-022-9

MDL number:

MFCD00005228

UNSPSC Code:

12352100

PubChem Substance ID:

24900056

NACRES:

NA.22

Assay

98%

bp

260 °C (lit.)

mp

119-121 °C (lit.)

SMILES string

c1nc[nH]n1

InChI

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

InChI key

NSPMIYGKQJPBQR-UHFFFAOYSA-N

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Related Categories

Heterocyclic Building Blocks

Application

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

Pictograms

GHS08,GHS07

Signal Word

Danger

Hazard Statements

H302,H319,H360FD

Precautionary Statements

P202 - P264 - P280 - P301 + P312 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

338.0 °F

Flash Point(C)

170 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Applications of Metal-Free 1, 2, 4-Triazole Derivatives in Materials Science.

Diaz-Ortiz A

Current Organic Chemistry, 19(7), 568-584 (2015)

Mononuclear, oligonuclear and polynuclear metal coordination compounds with 1, 2, 4-triazole derivatives as ligands.

Haasnoot JG

Coordination Chemistry Reviews, 200, 131-185 (2000)

1, 2, 4-Triazoles: Synthetic approaches and pharmacological importance.

Al-Masoudi IA

Chemistry of Heterocyclic Compounds, 42(11), 1377-1403 (2006)

Small-molecule APOBEC3G DNA cytosine deaminase inhibitors based on a 4-amino-1,2,4-triazole-3-thiol scaffold.

Margaret E Olson et al.

ChemMedChem, 8(1), 112-117 (2012-11-28)

APOBEC3G (A3G) is a single-stranded DNA cytosine deaminase that functions in innate immunity against retroviruses and retrotransposons. Although A3G can potently restrict Vif-deficient HIV-1 replication by catalyzing excessive levels of G→A hypermutation, sublethal levels of A3G-catalyzed mutation may contribute to

Synthesis, characterization and preliminary anticonvulsant evaluation of some 4-alkyl-1,2,4-triazoles.

Tomasz Plech et al.

European journal of medicinal chemistry, 60, 208-215 (2013-01-08)

Designed and synthesized 4-alkyl-1,2,4-triazole-3-thione derivatives showed significant anticonvulsant activity, determined in the maximal electroshock-induced seizure (MES) test. The chemical structure of all new compounds was confirmed by spectral methods ((1)H NMR, (13)C NMR, IR, MS). A sensitive and selective method

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