438545
4-Amino-5-(4-pyridyl)-4H-1,2,4-triazole-3-thiol
97%
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About This Item
Empirical Formula (Hill Notation):
C7H7N5S
CAS Number:
Molecular Weight:
193.23
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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![5-Amino-1H-[1,2,4]-triazole-3-carboxylic acid methyl ester 96%](/deepweb/assets/sigmaaldrich/product/structures/343/124/fed9a51c-601d-495f-8ded-bd63502da7ca/640/fed9a51c-601d-495f-8ded-bd63502da7ca.png)
Assay
97%
mp
250-254 °C (lit.)
SMILES string
Nn1c(S)nnc1-c2ccncc2
InChI
1S/C7H7N5S/c8-12-6(10-11-7(12)13)5-1-3-9-4-2-5/h1-4H,8H2,(H,11,13)
InChI key
LHSIJUVRXSETDR-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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A Silsesquioxane Organically Modified with 4-Amino-5-(4-pyridyl)-4H-1,2,4-triazole-3-thiol: Thermal Behavior and Its Electrochemical Detection of Sulfhydryl Compounds.
Do Carmo DR, et al.
Journal of Nanomaterials, 2014 (2014)
Raghad Haddad et al.
SpringerPlus, 2, 510-510 (2013-10-18)
Series of coordination complexes of Ni(II), Cu(II), Zn(II), Cd(II) and Sn(II) metal with 4-amino-5-(pyridyl)-4H-1,2,4-triazole-3-thiol, as a ligand has been successfully prepared in alcoholic medium. The prepared complexes were characterized quantitatively and qualitatively by using: microelemental analysis, FTIR spectroscopy, UV-visible spectroscopy
Generalized approach to SERS-active nanomaterials via controlled nanoparticle linking, polymer encapsulation, and small-molecule infusion.
Braun GB, et al.
The Journal of Physical Chemistry C, 113(31), 13622-13629 (2009)
A new hybrid polyhedral cubic silsesquioxane chemically modified with 4-amino-5-(4-pyridyl)-4H-1, 2, 4-triazole-3-thiol (APTT) and copper hexacyanoferrate (III) for voltammetric determination of nitrite.
Soares LA, et al.
International Journal of Electrochemical Science, 8, 4654-4669 (2013)
Qiaoshu Chen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(70), 16659-16665 (2020-10-08)
Peroxidase-mimicking nanozymes such as Fe3 O4 nanoparticles are promising substitutes for natural enzymes like horseradish peroxidase. However, most such nanozymes work efficiently only in acidic conditions. In this work, the influence of various liposomes on nanozyme activity was studied. By
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