Substance
ID:336097
Names and Identifiers
IUPAC name
1H-1,2,3-benzotriazol-1-ylmethanol
IUPAC Traditional name
1,2,3-benzotriazol-1-ylmethanol
Synonyms
1-(Hydroxymethyl)benzotriazole1H-Benzotriazole-1-methanol1H-苯并三唑-1-甲醇1-BenzotriazolemethanolNSC 12463
Properties
Safety Information
GHS Signal Word
Warning
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
European Hazard Symbols
Irritant (Xi)German water hazard class
3
GHS Hazard statements
H315-H319-H335
GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
36/37/38
Safety Statements
26-36
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Physical Property
Melting Point
150-152 °C(lit.)
Product Information
Empirical Formula (Hill Notation)
C7H7N3O
Purity
98%
Molecule Details
Application
Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents.8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
Packaging
10, 50 g in glass bottle
Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents.8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
Packaging
10, 50 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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