Benzene

Benzene is an organic chemical compoond wi the molecular formula C6H6. The benzene molecule is componed o sax caurbon atoms jynt in a ring wi ane hydrogen atom attached tae ilk. As it conteens anerly caurbon an hydrogen atoms, benzene is clessed as a hydrocaurbon.

Benzene
Skeletal formula detail o benzene
Skeletal formula detail o benzene
Stack o benzene baw-an-stick model
Stack o benzene baw-an-stick model
Frozen benzene
Names
IUPAC name
Benzene
Seestematic IUPAC name
Cyclohexa-1,3,5-triene
Ither names
1,3,5-Cyclohexatriene, Benzol, Phene
Identifiers
CAS Nummer
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
EC Nummer200-753-7
KEGG
RTECS nummerCY1400000
UNII
Properties
C6H6
Molar mass78.11 g·mol−1
AppearanceColourless liquid
OdourAromatic, petrol-like
Density0.8765(20) g/cm3[1]
Meltin pynt 5.53 °C (41.95 °F; 278.68 K)
Bylin pynt 80.1 °C (176.2 °F; 353.2 K)
Solubility in watter
1.53 g/L (0 °C)
1.81 g/L (9 °C)
1.79 g/L (15 °C)[2][3][4]
1.84 g/L (30 °C)
2.26 g/L (61 °C)
3.94 g/L (100 °C)
21.7 g/kg (200 °C, 6.5 MPa)
17.8 g/kg (200 °C, 40 MPa)[5]
SolubilitySoluble in alcohol, CHCl3, CCl4, diethyl ether, acetone, acetic acid[5]
Solubility in ethanediol5.83 g/100 g (20 °C)
6.61 g/100 g (40 °C)
7.61 g/100 g (60 °C)[5]
Solubility in ethanol20 °C, solution in water:
1.2 mL/L (20% v/v)[6]
Solubility in acetone20 °C, solution in water:
7.69 mL/L (38.46% v/v)
49.4 mL/L (62.5% v/v)[6]
Solubility in diethylene glycol52 g/100 g (20 °C)[5]
log P2.13
Vapour pressur12.7 kPa (25 °C)
24.4 kPa (40 °C)
181 kPa (100 °C)[7]
λmax255 nm
Magnetic susceptibility54.8·10−6 cm3/mol
Refractive index (nD)1.5011 (20 °C)
1.4948 (30 °C)[5]
Viscosity0.7528 cP (10 °C)
0.6076 cP (25 °C)
0.4965 cP (40 °C)
0.3075 cP (80 °C)
Structur
Molecular shapeTetrahedral
Dipole moment
0 D
Thermochemistry
Speceefic heat capacity, C134.8 J/mol·K
Staundart molar
entropy So298
173.26 J/mol·K[7]
Std enthalpy o
formation ΔfHo298
48.7 kJ/mol
Std enthalpy o
combustion ΔcHo298
3267.6 kJ/mol[7]
Hazards
GHS pictogramsThe flame pictogram in the Globally Harmonized Seestem o Classification an Labelling o Chemicals (GHS)The skull-an-crossbones pictogram in the Globally Harmonized Seestem o Classification an Labellin o Chemicals (GHS)The health hazard pictogram in the Globally Harmonized Seestem o Classification an Labellin of Chemicals (GHS)[8]
GHS signal wirdDanger
GHS hazard statementsH225, H304, H315, H319, H340, H350, H372[8]
GHS precautionary statementsP201, P210, P301+310, P305+351+338, P308+313, P331[8]
NFPA 704
NFPA 704 four-colored diamondFlammability code 3: Liquids an solids that can be ignited unner awmaist ae ambient temperature condeetions. Flash pynt atween 23 an 38 °C (73 an 100 °F). E.g., gasoline)Health code 3: Short exposur could cause serious temporary or residual injury. E.g., chlorine gasReactivity code 0: Normally stable, even unner fire exposur condeetions, an is nae reactive wi watter. E.g., liquid nitrogenSpecial hazards (white): no code
3
3
0
Flash pynt −11.63 °C (11.07 °F; 261.52 K)
Autoigneetion
temperatur
497.78 °C (928.00 °F; 770.93 K)
Explosive leemits1.2–7.8%
Lethal dose or concentration (LD, LC):
LD50 (Median dose)
930 mg/kg (rat, oral)
Relatit compoonds
Except whaur itherwise notit, data are gien for materials in thair staundart state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Benzene is a naitural constituent o crude ile an is ane o the elementar petrochemicals. Due tae the cyclic conteenous pi bond atween the caurbon atoms, benzene is clessed as an aromatic hydrocarbon, the seicont [n]-annulene ([6]-annulene). It is whiles abbreviatit PhH. Benzene is a colourless an heichly flammable liquid wi a sweet smell, an is responsible for the aroma aroond petrol stations. It is uised primarily as a precursor tae the manufacture o chemicals wi mair complex structur, uic as ethylbenzene an cumene, o that billions o kilogrammes are produced annually. As benzene haes a heich octane nummer, aromatic derivatives lik toluene an xylene teepically comprise up tae 25% o petrol. Benzene itsel haes been leemitit tae less nor 1% in petrol acause it is a kent human carcinogen. Most nan-industrial applications hae been leemitit as weel for the same raison.

References