Phenol

Phenol
Names
Preferred IUPAC name
Phenol
Systematic IUPAC name
Benzenol
Other names
  • Carbolic acid
  • Phenolic acid
  • Phenylic acid
  • Hydroxybenzene
  • Phenic acid
  • Phenyl alcohol
  • Phenyl hydroxide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.303
KEGG
RTECS number
  • SJ3325000
UNII
UN number 2821 (solution)
2312 (molten)
1671 (solid)
  • InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H Y
    Key: ISWSIDIOOBJBQZ-UHFFFAOYSA-N Y
  • InChI=1/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H
  • Oc1ccccc1
Properties
C6H6O
Molar mass 94.113 g/mol
Appearance Transparent crystalline solid
Odor Sweet and tarry
Density 1.07 g/cm3
Melting point 40.5 °C (104.9 °F; 313.6 K)
Boiling point 181.7 °C (359.1 °F; 454.8 K)
8.3 g/100mL (20 °C)
log P 1.48
Vapor pressure 0.4 mmHg (20 °C)
Acidity (pKa)
  • 9.95 (in water),
  • 18.0 (in DMSO),
  • 29.1 (in acetonitrile)
Conjugate base Phenoxide
UV-vismax) 270.75 nm
1.224 D
Pharmacology
C05BB05 (WHO) D08AE03 (WHO), N01BX03 (WHO), R02AA19 (WHO)
Hazards
GHS labelling:
Danger
H301, H311, H314, H331, H341, H373
P261, P280, P301+P310, P305+P351+P338, P310
NFPA 704 (fire diamond)
3
2
0
Flash point 79 °C (174 °F; 352 K)
Explosive limits 1.8–8.6%
Lethal dose or concentration (LD, LC):
  • 317 mg/kg (rat, oral)
  • 270 mg/kg (mouse, oral)
  • 420 mg/kg (rabbit, oral)
  • 500 mg/kg (dog, oral)
  • 80 mg/kg (cat, oral)
  • 19 ppm (mammal)
  • 81 ppm (rat)
  • 69 ppm (mouse)
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 5 ppm (19 mg/m3) [skin]
REL (Recommended)
  • TWA 5 ppm (19 mg/m3)
  • C 15.6 ppm (60 mg/m3) [15-minute] [skin]
IDLH (Immediate danger)
250 ppm
Safety data sheet (SDS)
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C6H5OH. It is a white crystalline solid that is volatile and can catch fire.

The molecule consists of a phenyl group (−C6H5) bonded to a hydroxy group (−OH). Mildly acidic, it requires careful handling because it can cause chemical burns. It is acutely toxic and is considered a health hazard.

Phenol was first extracted from coal tar, but today is produced on a large scale (about 7 million tonnes a year) from petroleum-derived feedstocks. It is an important industrial commodity as a precursor to many materials and useful compounds, and is a liquid when manufactured. It is primarily used to synthesize plastics and related materials. Phenol and its chemical derivatives are essential for production of polycarbonates, epoxies, explosives such as picric acid, Bakelite, nylon, detergents, herbicides such as phenoxy herbicides, and numerous pharmaceutical drugs.