Structure via PubChem · Public domain (PubChem)
رزورسینول
Sign in to saveAlso known as resorcinol, 1,3-benzenediol, m-benzenediol, 1,3-dihydroxybenzene, m-dihydroxybenzene, 3-hydroxyphenol, m-hydroxyphenol, 1,3-Benzenediol
Resorcinol (or resorcin) is a phenolic compound. It is an organic compound with the formula C6H4(OH)2. It is one of three isomeric benzenediols, the 1,3-isomer (or meta-isomer). Resorcinol crystallizes from benzene as colorless needles that are readily soluble in water, alcohol, and ether, but insoluble in chloroform and carbon disulfide.
OverviewAI-generated
Resorcin, also known as benzene-1,3-diol, is a chemical compound with the formula C₆H₆O₂. Its molecular mass is 110.037, and it has a density of 1.27. The substance melts at 228 and boils at 531. It exhibits a vapor pressure of 1 and a solubility of 1400. Resorcin has a flash point of 261 and a lower flammable limit of 1.4. Its ionization energy is 8.63.
Safety data for resorcin includes a time-weighted average exposure limit of 45 and a short-term exposure limit of 90. The median lethal dose (LD50) is 301, while the minimal lethal dose is 29. The compound has two hydrogen bond donors and two hydrogen bond acceptors, with a topological polar surface area of 40.5 and an xlogp of 0.8. It carries a charge of 0.
Literature references for resorcin number 4056. The compound is referenced by 199 other encyclopedia articles.
Synthesized by Vinony from 32 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C6H6O2
- Molecular weight
- 110.11 g/mol
- IUPAC name
- benzene-1,3-diol
- SMILES
- C1=CC(=CC(=C1)O)O
- InChIKey
- GHMLBKRAJCXXBS-UHFFFAOYSA-N
- XLogP
- 0.8
- Polar surface area
- 40.5 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
- Indications
- acne, eye infection
via ChEMBL · EBI
Research
4,056 papers- Biomimetic tail-to-head terpene cyclizations using the resorcin[4]arene capsule catalyst.Nature protocols · 2024
- Anion-Based Self-assembly of Resorcin[4]arenes and Pyrogallol[4]arenes.Journal of the American Chemical Society · 2022
- Resorcin poisoning.Archives of disease in childhood · 1956
- Resorcinol.IARC monographs on the evaluation of carcinogenic risks to humans · 1999
- [Resorcin hypersensitivity].Dermatologische Wochenschrift · 1958
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 110.037
- Has use
- polymer stabilizer
Show 20 more facts
- flash point
- 261
- described by source
- Encyclopædia Britannica 11th edition
- found in taxon
- Lupinus albus
- Commons category
- Resorcinol
- topic's main category
- Category:Resorcinols
- NIOSH Pocket Guide ID
- 0543
- density
- 1.27
- melting point
- 111
- boiling point
- 280
- vapor pressure
- 1
- solubility
- 1400
- lower flammable limit
- 1.4
- ionization energy
- 8.63
- time-weighted average exposure limit
- 45
- short-term exposure limit
- 90
- canonical SMILES
- C1=CC(=CC(=C1)O)O
- chemical formula
- C₆H₆O₂
- median lethal dose (LD50)
- 301
- NCI Thesaurus ID
- C77056
- minimal lethal dose
- 29
via Wikidata · CC0