About This Item
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Assay
97%
form
solid
reaction suitability
reaction type: C-C Bond Formation
mp
285 °C (dec.) (lit.)
functional group
sulfonic acid
SMILES string
OS(=O)(=O)c1cccc2[nH]nnc12
InChI
1S/C6H5N3O3S/c10-13(11,12)5-3-1-2-4-6(5)8-9-7-4/h1-3H,(H,7,8,9)(H,10,11,12)
InChI key
WVKWKEWFTVEVCF-UHFFFAOYSA-N
Application
- A precursor for the preperation of 4-hydroxy-benzotriazole via hydrolysis using a strong alkali.[1]
- A reactant to synthesize copper benzotriazolesulfonate phenanthroline supramolecular complex by the reaction with 1,10-phenanthroline ligand.[2]
- A corrosion inhibitor in preparation of polystyrene nanosphere-templated cerium molybdate nanocontainers.[3]
- Reactant for preparation of copper benzotriazolesulfonate phenanthroline supramolecular complex
- Used as a corrosion inhibitor in preparation of polystyrene nanosphere-templated cerium molybdate nanocontainers loaded with corrosion inhibitors
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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