327
Table 19.1 Properties and significant information of 16 US EPA enlisted PAHs as priority pollutant
Name
Mol.
formula
Physicochemical properties
Toxicology
Biodegradation
Boiling
point (°C)
Melting
point (°C)
Vapor pressure (mm
Hg at 25 °C)
Solubility
(mg/L)
a
TEF
b
IARC
c
EPA
d
Estimated
half-lives
(days)
e
Measured
half-lives (days)
f
Naphthalene
C
10 H
8
218
80.2
8.5 × 10
−2
31
n.d. 2B
C
5.66
n.d.
Acenaphthene
C
12 H
10
279
93.4
2.5 × 10
−3
3.93
0.001 3
D
18.77
n.d.
Acenaphthylene
C
12 H
8
280
91.8
6.68 × 10
−3
1.93
0.001 n.c.
D
30.7
n.d.
Anthracene
C
14 H
10
342
216.4
6.53 × 10
−6
0.076
0.01 3
D
123
2.7
Phenanthrene
C
14 H
10
340
100.5
1.2 × 10
−4
1.20
0.001 3
D
14.97
5
Fluorene
C
13 H
10
295
116–7
6.0 × 10
−4
1.68–1.98
0.001 3
D
15.14
n.d.
Fluoranthene
C
16 H
10
375
108.8
9.22 × 10
−6
0.20–0.26
0.001 3
D
191.4
9.2
Benzo[a]anthracene C
18 H
12
438
158
4.11 × 10
−3
0.010
0.1
2B
D
343.8
>182
Chrysene
C
18 H
12
448
254
6.23 × 10
−2
1.5 × 10
−3
0.010 2B
B2
343.8
n.d.
Pyrene
C
16 H
10
150.4
393
4.5 × 10
−6
0.132
0.001 3
B2
283.4
151
Benzo[a]pyrene
C
20 H
12
495
179
5.49 × 10
−9
3.8 × 10
−3
1.0
1
D
421.6
11
Benzo[b]
fluoranthene
C
20 H
12
481
168.3
5.0 × 10
−7
0.0012
n.d. 2B
B2
284.7
n.d.
Benzo[k]
fluoranthene
C
20 H
12
480
215.7
9.7 × 10
−10
7.6 × 10
−4
0.1
2B
B2
284.7
n.d.
Dibenzo[a,h]
anthracene
C
22 H
14
524
262
9.55 × 10
−10
5.0 × 10
−4
n.d. 2A
B2
511.4
n.d.
Benzo[g,h,i]
perylene
C
22 H
12
500
277
1.0 × 10
−10
2.6 × 10
−5
n.d. 3
B2D 517.1
n.d.
Indenol[1,2,3-cd]
pyrene
C
22 H
12
536
161–3
1.25 × 10
−3
0.062
n.d. 2B
B2
349.2
n.d.
a
[93]
b
Toxic equivalent relative factor to benzo[a]pyrene
(continued)
19 Role of Polycyclic Aromatic Hydrocarbons as EDCs in Metabolic Disorders
Table 19.1 Properties and significant information of 16 US EPA enlisted PAHs as priority pollutant
Name
Mol.
formula
Physicochemical properties
Toxicology
Biodegradation
Boiling
point (°C)
Melting
point (°C)
Vapor pressure (mm
Hg at 25 °C)
Solubility
(mg/L)
a
TEF
b
IARC
c
EPA
d
Estimated
half-lives
(days)
e
Measured
half-lives (days)
f
Naphthalene
C
10 H
8
218
80.2
8.5 × 10
−2
31
n.d. 2B
C
5.66
n.d.
Acenaphthene
C
12 H
10
279
93.4
2.5 × 10
−3
3.93
0.001 3
D
18.77
n.d.
Acenaphthylene
C
12 H
8
280
91.8
6.68 × 10
−3
1.93
0.001 n.c.
D
30.7
n.d.
Anthracene
C
14 H
10
342
216.4
6.53 × 10
−6
0.076
0.01 3
D
123
2.7
Phenanthrene
C
14 H
10
340
100.5
1.2 × 10
−4
1.20
0.001 3
D
14.97
5
Fluorene
C
13 H
10
295
116–7
6.0 × 10
−4
1.68–1.98
0.001 3
D
15.14
n.d.
Fluoranthene
C
16 H
10
375
108.8
9.22 × 10
−6
0.20–0.26
0.001 3
D
191.4
9.2
Benzo[a]anthracene C
18 H
12
438
158
4.11 × 10
−3
0.010
0.1
2B
D
343.8
>182
Chrysene
C
18 H
12
448
254
6.23 × 10
−2
1.5 × 10
−3
0.010 2B
B2
343.8
n.d.
Pyrene
C
16 H
10
150.4
393
4.5 × 10
−6
0.132
0.001 3
B2
283.4
151
Benzo[a]pyrene
C
20 H
12
495
179
5.49 × 10
−9
3.8 × 10
−3
1.0
1
D
421.6
11
Benzo[b]
fluoranthene
C
20 H
12
481
168.3
5.0 × 10
−7
0.0012
n.d. 2B
B2
284.7
n.d.
Benzo[k]
fluoranthene
C
20 H
12
480
215.7
9.7 × 10
−10
7.6 × 10
−4
0.1
2B
B2
284.7
n.d.
Dibenzo[a,h]
anthracene
C
22 H
14
524
262
9.55 × 10
−10
5.0 × 10
−4
n.d. 2A
B2
511.4
n.d.
Benzo[g,h,i]
perylene
C
22 H
12
500
277
1.0 × 10
−10
2.6 × 10
−5
n.d. 3
B2D 517.1
n.d.
Indenol[1,2,3-cd]
pyrene
C
22 H
12
536
161–3
1.25 × 10
−3
0.062
n.d. 2B
B2
349.2
n.d.
a
[93]
b
Toxic equivalent relative factor to benzo[a]pyrene
(continued)
19 Role of Polycyclic Aromatic Hydrocarbons as EDCs in Metabolic Disorders
