Pyrogallol

A phenol, C6H6O3, 126.111 g/mol. Boiling point 309 °C, melting point 133 °C, as published.

verified recordOrganic — phenol7 measured properties

Identifiers

Molecular formula: C₆H₆O₃
Molecular weight: 126.111 g/mol
Exact mass: 126.031694 g/mol
IUPAC name: benzene-1,2,3-triol
SMILES: Oc1cccc(O)c1O
InChI: InChI=1S/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9H
InChIKey: WQGWDDDVZFFDIG-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Measured properties

Published measurements, each with its source. Two readings of one property are both shown, in the units each used.

Boiling Point: 588 °F at 760 mmHg (Decomposes at 559 °F) (NTP, 1992)measured · CAMEO Chemicals; 309 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Melting Point: 271 to 273 °F (NTP, 1992)measured · CAMEO Chemicals; 133 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Density: 1.45 at 68 °F (USCG, 1999) - Denser than water; will sinkmeasured · CAMEO Chemicals; 1.453 g/cu cm at 4 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Solubility: greater than or equal to 100 mg/mL at 77 °F (NTP, 1992)measured · CAMEO Chemicals; Very soluble in ethanol, diethyl ethermeasured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure: 10 mmHg at 333.9 °F (NTP, 1992)measured · CAMEO Chemicals; 0.000479 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
LogP: 0.970 (estimated)measured · ILO-WHO International Chemical Safety Cards (ICSCs); 1.19measured · SangsterLogP
Refractive Index: Index of refraction: 1.561 at 134 °C/Dmeasured · Weast, R.C. (ed.). Handbook of Chemistry and Physics. 60th ed. Boca Raton, Florida: CRC Press Inc., 1979., p. C-171

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

Molecular weight: 126.11 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 126.031694049 Dacalculated · reference compound database; Mass of the most common isotopic form.
XLogP3: 0.5calculated · reference compound database; Estimated oil/water partition, computed by reference compound database.
Polar surface area: 60.7 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 84calculated · reference compound database; A rough measure of how intricate the structure is.
H-bond donors: 3calculated · reference compound database
H-bond acceptors: 3calculated · reference compound database
logP: 0.8034calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 60.69 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 3calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 3calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 0calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 31.4364 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.4505calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon6 atoms · 57.1% by mass
O Oxygen3 atoms · 38.1% by mass
H Hydrogen6 atoms · 4.8% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 9
Total atoms, hydrogen included: 15
Rings: 1
Aromatic rings: 1
Stereocentres: 0
Formal charge: 0

Functional groups

Phenol
An –OH group attached to an aromatic ring.
Aromatic ring
A flat six-membered ring with delocalised electrons.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Pyrogallol yet.

Other names for it

The systematic name on this record is benzene-1,2,3-triol.

The sources also call it benzene-1,2,3-triol, 1,2,3-trihydroxybenzene, pyrogallic acid, 1,2,3-benzenetriol, fourrine PG, Fouramine Brown AP, fourrine 85, Pyro, C.I. Oxidation Base 32, fouramine base ap, 1,2,3-Trihydroxybenzen.

Structurally related

Molecules sharing this formula, or whose fingerprint is at least 40% similar to this one. Similarity is Tanimoto on Morgan fingerprints over this library only — it is a measure of structural overlap, not of how alike they behave.

1,2,4-Benzenetriol

C6H6O3

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Pyrogallol. This says nothing about structure: most of them are the bases, solvents, ligands and catalysts the chemistry needed, and they are here because somebody put them in the same flask.

1,2-Dichlorobenzene

used as a reactant

C₆H₄Cl₂, 147.004 g/mol.

1,8-Dinitro-4,5-dihydroxyanthraquinone

used as a reactant

C₁₄H₆N₂O₈, 330.208 g/mol.

Where these values came from

reference compound database1057
compound record
chemistry engine
structure perception

compound record.

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.