Structure via PubChem · Public domain (PubChem)
pirogallolo
Sign in to saveAlso known as Fouramine Brown AP, Fourrine 85, 2,3-Dihydroxyphenol, Benzene-1,2,3-triol, 1,2,3-Trihydroxy-Benzene, Pyro, Fourrine PG, C.I. Oxidation Base 32
composto chimico
Chemical data
- Formula
- C6H6O3
- Molecular weight
- 126.11 g/mol
- IUPAC name
- benzene-1,2,3-triol
- SMILES
- C1=CC(=C(C(=C1)O)O)O
- InChIKey
- WQGWDDDVZFFDIG-UHFFFAOYSA-N
- XLogP
- 0.5
- Polar surface area
- 60.7 Ų
- H-bond donors
- 3
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
2,773 papers- Pyrogallol Toxicosis in Horses.The Veterinary clinics of North America. Equine practice · 2024
- Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase.European journal of biochemistry · 1974
- Pyrogallol-mediated toxicity and natural antioxidants: triumphs and pitfalls of preclinical findings and their translational limitations.Chemico-biological interactions · 2010
- Synthesis of biologically derived poly(pyrogallol) nanofibers for antibacterial applications.Journal of materials chemistry. B · 2023
- Pyrogallol impairs staphylococcal biofilm formation via induction of bacterial oxidative stress.Journal of applied microbiology · 2023
via PubMed
Wikidata facts
- Subclass of
- benzenetriol
- Has part
- carbon
- Mass
- 126.032
- Image
- Pyrogallol powder.jpg
Show 12 more facts
- Commons category
- Pyrogallol
- described by source
- Brockhaus and Efron Encyclopedic Dictionary
- chemical formula
- C₆H₆O₃
- density
- 1.453
- canonical SMILES
- C1=CC(=C(C(=C1)O)O)O
- found in taxon
- Crocus sativus
- melting point
- 133.0
- boiling point
- 171
- subject has role
- antioxidant
- solubility
- 400
- median lethal dose (LD50)
- 1600
- minimal lethal dose
- 28
via Wikidata · CC0
Article · Italiano
Il pirogallolo (chiamato anche acido pirogallico, anche se nella sua struttura non sono presenti gruppi carbossilici) è un fenolo. Si può ottenere per denaturazione di tannini idrolizzabili portati ad elevate temperature. A temperatura ambiente si presenta come un solido incolore dall'odore tenue caratteristico. È un composto nocivo citotossico, pericoloso per l'ambiente. Trova impiego in fotografia come rivelatore. Il pirogallolo è in grado di inibire l'enzima COMT, dando come effetto iperstimolazione adrenergica.
Abstract from DBpedia / Wikipedia · CC BY-SA