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The solubility in water of about 580 organic compounds, including many compounds of environmental interest, is tabulated here. Values are given
at 25C or at the nearest temperature to this where data are available. In some cases solubility values are given at other temperatures as well.
Solubility of solids is defined as the concentration of the compound in a solution that is in equilibrium with the solid phase at the specified
temperature and one atmosphere pressure. For liquids whose water mixtures separate into two phases, the solubility given here is the concentration
of the compound in the water-rich phase at equilibrium. In the case of gases (i.e., compounds whose vapor pressure at the specified temperature exceeds
one atmosphere) the solubility is defined here as the concentration in the water phase when the partial pressure of the compound above the solution
is 101.325 kPa (1 atm). Values for gases are marked with an asterisk.
All solubility values are expressed as mass percent of solute, S = 100 w2, where the mass fraction w2 is given by w2 = m2/(m1 + m2). In these equations
m2 is the mass of solute and m1 the mass of water. This quantity is related to other common measures of solubility as follows:
Molality: m2 = 1000w2/M2(1-w2)
Mole fraction: x2 = (w2/M2)/{(w2/M2) + (1-w2)/M1}
Mass of solute per 100 g of H2O: r2 = 100w2/(1-w2)
Here M2 is the molar mass of the solute and M1 = 18.015 g/mol is the molar mass of water. For small values of S the amount of substance concentration
c2 in moles per liter is approximately 10S/M2.
Data have been selected from evaluated sources wherever possible, in particular the IUPAC Solubility Data Series (References 1-4). The primary
source for each value is listed in the column following the solubility values. The user is cautioned that wide variations of data are found in the literature
for the lower solubility compounds.
The table also contains values of the Henrys Law constant kH, which provides a measure of the partition of a substance between the atmosphere
and the aqueous phase. Here kH is defined as the limit of p2/c2 as the concentration approaches zero, where p2 is the partial pressure of the solute above
the solution and c2 is the concentration in the solution at equilibrium (other formulations of Henrys Law are often used; see Reference 5). The values
of kH listed here are based on direct experimental measurement whenever available, but many of them are simply calculated as the ratio of the pure
compound vapor pressure to the solubility. This approximation is reliable only for compounds of very low solubility. In fact, values of kH found in
the literature frequently differ by a factor of two or three, and variations over an order of magnitude are not unusual (Reference 5). Therefore the data
given here should be taken only as a rough indication of the true Henrys Law constant, which is difficult to measure precisely.
All values of kH refer to 25C. If the vapor pressure of the compound at 25C is greater than one atmosphere, it can be assumed that the kH value
has been calculated as 101.325/c2 kPa m3/mol. The source of the Henrys Law data is given in the last column. The air-water partition coefficient
(i.e., ratio of air concentration to water concentration when both are expressed in the same units) is equal to kH/RT or kH/2.48 in the units used here.
Compounds are listed by molecular formula following the Hill convention. To locate a compound by name or CAS Registry Number when the
molecular formula is not known, use the table Physical Constants of Organic Compounds in Section 3 and its indexes to determine the molecular
formula.
* Indicates a value of S for a gas at a partial pressure of 101.325 kPa (1 atm) in equilibrium with the solution.
PRZYPISY
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
Solubility Data Series, International Union of Pure and Applied Chemistry, Vol. 15, Pergamon Press, Oxford, 1982.
Solubility Data Series, International Union of Pure and Applied Chemistry, Vol. 20, Pergamon Press, Oxford, 1985.
Solubility Data Series, International Union of Pure and Applied Chemistry, Vol. 37, Pergamon Press, Oxford, 1988.
Solubility Data Series, International Union of Pure and Applied Chemistry, Vol. 38, Pergamon Press, Oxford, 1988.
Mackay, D., and Shiu, W.Y., J. Phys. Chem. Ref. Data, 10, 1175, 1981.
Pearlman, R.S., and Yalkowsky, S.H., J. Phys. Chem. Ref. Data, 13, 975, 1984.
Shiu, W.Y., and Mackay, D., J. Phys. Chem. Ref. Data, 15, 911, 1986.
Varhanickova, D., Lee, S.C., Shiu, W. Y., and Mackay, D., J. Chem. Eng. Data, 40, 620, 1995.
Miller, M.M., Ghodbane, S., Wasik, S. P., Tewari, Y.B., and Martire, D.E., J. Chem. Eng. Data, 29, 184, 1984.
Riddick, J.A., Bunger, W.B., and Sakano, T.K., Organic Solvents, Fourth Edition, John Wiley & Sons, New York, 1986.
Mackay, D., Shiu, W.Y., and Ma, K.C., Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic
Chemicals, Vol. I, Lewis Publishers/CRC Press, Boca Raton, FL, 1992.
Mackay, D., Shiu, W.Y., and Ma, K.C., Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic
Chemicals, Vol. II, Lewis Publishers/CRC Press, Boca Raton, FL, 1992.
Mackay, D., Shiu, W.Y., and Ma, K.C., Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic
Chemicals, Vol. III, Lewis Publishers/CRC Press, Boca Raton, FL, 1993.
Horvath, A.L., Halogenated Hydrocarbons, Marcel Dekker, New York, 1982.
Howard, P.H., Handbook of Environmental Fate and Exposure Data for Organic Chemicals, Vol. I, Lewis Publishers/CRC Press, Boca Raton,
FL, 1989.
Howard, P.H., Handbookof Environmental Fateand Exposure Data for Organic Chemicals, Vol. II, Lewis Publishers/CRC Press, Boca Raton,
FL, 1990.
Banergee, S., Yalkowsky, S.H., and Valvani, S.C., Environ. Sci. Technol., 14, 1227, 1980.
Gevantman, L., in CRC Handbook of Chemistry and Physics, 77th Edition, p. 6-3, CRC Press, Boca Raton, FL, 1996.
Wilhelm, E., Battino, R., and Wilcock, R.J., Chem. Rev., 77, 219, 1977.
Stephenson, R.M., J. Chem. Eng. Data, 37, 80, 1992.
Stephenson, R.M., Stuart, J., and Tabak, M., J. Chem. Eng. Data, 29, 287, 1984.
-1-
Nazwa
Bromotrifluorometan
Tribromofluorometan
Tetrabromometan
Chlorotrifluorometan
Dichlorodifluorometan
Trichlorofluorometan
Tetrachlorometan
Tetrafluorometan
Tribromometan
Chlorodifluorometan
Dichlorofluorometan
Trichlorometan
Trifluorometan
Trijodometan
Bromochlorometan
Dibromometan
Chlorofluorometan
Dichlorometan
Dijodometan
Bromometan
Chlorometan
Fluorometan
Jodometan
Nitrometan
Metan
Tlenek wgla
Dwutlenek wgla
Disiarczek wgla
Chloropentafluoroetan
1,2-Dichlorotetrafluoroetan
1,1,2-trichlorotrifluoroetan
Tetrachloroetylen
1,1,2,2-Tetrachloro-1,2-difluoroetan
Heksachloroetan
Tetrafluoroetylen
Trichloroetylen
Pentachloroetan
Acetylen
1,1,2,2-Tetrabromoetan
1,1-Dichloroetylen
cis-1,2-Dichloroetylen
trans-1,2-Dichloroetylen
1,1,1,2-Tetrachloroetan
1,1,2,2-Tetrachloroetan
Chloroetylen
1,1,1-Trichloroetan
1,1,2-Trichloroetan
Etylen
1-Bromo-2-chloroetan
1,2-Dibromoetan
1,1-Dichloroetan
1,2-Dichloroetan
Mrwczan metylu
Bromoetan
Chloroetan
Fluoroetan
Jodoetan
Acetamid
Nitroetan
Etan
t/C
S/mas %
Przyp
25
25
30
25
20
20
25
25
25
25
25
25
25
25
25
25
25
25
30
20
25
30
20
25
25
25
25
20
25
25
25
25
25
25
25
25
25
25
30
25
25
25
25
25
25
25
25
25
30
25
25
25
25
20
20
25
30
20
25
25
0.032*
0.040
0.024
0.009*
0.028*
0.11
0.065
0.00187*
0.30
0.30*
0.95*
0.80
0.09*
0.012
1.7
1.14
1.05*
1.73
0.124
1.80*
0.535*
0.177*
1.4
11.1
0.00227*
0.00276*
0.1501
0.210
0.006*
0.013*
0.017
0.026
0.012
0.0050
0.0158*
0.11
0.048
0.1081*
0.0651
0.040
0.35
0.63
0.11
0.30
0.27*
0.072
0.442
0.01336*
0.683
0.17
0.51
0.75
23
0.91
0.57*
0.216*
3.88
40.8
4.68
0.00568*
14
14
14
10
5
5
20
19
5
10
10
20
14
14
10
14
14
20
10
5
5
5
10
10
18
18
18
10
10
10
10
20
10
5
19
5
5
19
10
5
5
5
5
5
5
5
5
19
10
5
5
20
10
10
5
14
10
10
10
18
-2-
kH/kPa m3 mol1
6.9
41
10.2
2.99
Przyp.
13
13
13
13
0.047
3.0
13
13
0.43
13
0.18
0.086
13
13
0.30
0.032
0.63
0.98
13
13
13
13
0.54
13
67.4
260
127
32
1.73
13
13
13
13
0.85
13
1.03
0.25
13
13
2.62
0.46
0.96
0.24
0.026
2.68
1.76
0.092
21.7
13
13
13
13
13
13
13
13
5
0.066
0.63
0.14
13
13
13
1.23
1.02
13
13
0.52
13
50.6
Nazwa
Eter dimetylowy
Dimetylosulfotlenek
Siarczek dimetylu
Heksachloropropen
Perfluoropropen
Perfluoropropan
2-Propenonitryl
Propyn
cis-1,3-Dichloropropen
trans-1,3-Dichloropropen
2,3-Dichloropropen
Akroleina
3-Chloropropen
Epichlorohydryna
1,2,3-Trichloropropan
Propanonitryl
Propen
Cyklopropan
1,2-Dibromopropan
1,2-Dichloropropan
Heksahydro-1,3,5-trinitro-1,3,5-triazina
Propanal
Methyloksiran
Mrwczan etylu
Octan metylu
1-Bromopropan
2-Bromopropan
1-Chloropropan
2-Chloropropan
1-Fluoropropan
2-Fluoropropan
1-Jodopropan
2-Jodopropan
1-Nitropropan
2-Nitropropan
Propan
Dimethoksymetan
Perfluorocyklobutan
Sukcynonitryl
Furan
Metyloakrylonitryl
Pirol
1,3-Butadien
1-Butyn
trans-2-Butenal
Kwas metakrylowy
Kwas trans-krotonowy
Octan winylu
Akrylan metylu
1-Chloro-2-metylopropen
Butanonitryl
1-Buten
Izobuten
Eter bis(2-chloroetylowy)
Alkohol cis-krotonylowy
Eter etylo-winylowy
Butanal
Izobutanal
2-Butanon
Kwas 2-metylopropanowy
t/C
S/mas %
Przyp
24
25
25
25
25
15
20
25
25
20
25
20
25
20
20
25
25
25
25
25
25
25
20
25
20
30
18
20
12
14
15
30
20
25
25
25
16
21
25
25
20
25
25
25
20
20
25
20
25
25
20
25
25
25
20
20
25
20
25
20
35.3*
25.3
2
0.00170
0.0194*
0.0015*
7.35
0.364*
0.27
0.28
0.215
20.8
0.33
6.58
0.19
10.3
0.0200*
0.0484*
0.143
0.247
0.0060
30.6
40.5
11.8
24.5
0.230
0.286
0.271
0.342
0.386*
0.366
0.104
0.140
1.50
1.71
0.00669*
24.4
0.014*
11.5
1
2.57
4.5
0.0735*
0.287*
15.6
8.9
9
2.0
4.94
0.916
3.3
0.0222*
0.0263*
1.03
16.6
0.9
7.1
9.1
25.9
22.8
10
10
10
14
14
14
10
5
5
5
5
10
5
10
10
10
5
19
10
10
17
10
10
10
10
10
10
10
10
14
14
10
10
10
10
18
10
14
10
10
10
10
5
5
10
10
10
10
10
5
10
5
5
20
10
10
10
10
20
10
-3-
kH/kPa m3 mol1
Przyp.
0.077
13
1.11
0.24
0.18
0.36
5
5
5
5
1.10
0.003
0.038
5
13
13
21.3
0.29
13
0.0087
13
3.8
1.27
1.41
13
13
13
0.93
13
71.6
0.54
13
20.7
1.91
13
5
0.12
25.6
21.6
0.003
13
13
13
Nazwa
C4H8O2
C4H8O2
C4H9Br
C4H9Cl
C4H9Cl
C4H9I
C4H10
C4H10
C4H10O
C4H10O
Mrwczan propylu
Octan etylu
1-Bromobutan
1-Chlorobutan
1-Chloro-2-metylopropan
1-Jodobutan
Butan
Izobutan
Eter dietylowy
1-Butanol
C4H10O
2-Butanol
C4H10O
2-Metylo-1-propanol
C4H10S
C4H11NO2
C4H12Si
C5H4O2
C5H6
C5H7NO2
C5H8
C5H8
1-Butanotiol
Dietanolamina
Tetrametylosilan
Furfural
1,3-Cyklopentadien
Cyjanooctan etylu
1,4-Pentadien
2-Metylo-1,3-butadien
C5H8
C5H8
C5H8O2
C5H8O2
C5H8O2
C5H10
C5H10
C5H10
C5H10
C5H10
C5H10O
C5H10O
C5H10O
C5H10O2
C5H10O2
C5H10O2
C5H10O2
C5H10O2
C5H10O2
C5H11Br
C5H11Cl
C5H12
C5H12
C5H12
C5H12O
1-Pentyn
Cyklopenten
Akrylan etylu
Metakrylan metylu
2,4-Pentanodion
1-Penten
cis-2-Penten
3-Metylo-1-buten
2-Metylo-2-buten
Cyklopentan
2-Pentanon
3-Pentanon
2-Metyoltetrahydrofuran
Kwas pentanowy
Kwas 3-metylobutanoic
Mrwczan izobutylu
Octan propylu
Octan izopropylu
Propanian etylu
1-Bromopentan
1-Chloropentan
Pentan
Izopentan
Neopentan
1-Pentanol
C5H12O
C5H12O
C5H12O
C5H12O
C5H12O
C5H12O
2-Pentanol
3-Pentanol
2-Metylo-1-butanol
3-Metylo-1-butanol
2-Methlo-2-butanol
3-Methlo-2-butanol
t/C
S/mas %
Przyp
22
25
30
20
12
17
25
25
25
0
25
50
10
25
50
0
25
50
20
20
25
20
25
20
25
25
50
25
25
25
20
20
25
25
25
25
25
25
25
25
20
21
22
20
20
20
25
25
25
25
25
0
25
50
25
25
25
25
25
25
2.05
8.08
0.0608
0.11
0.092
0.012
0.00724*
0.00535*
6.04
10.4
7.4
6.4
23.9
18.1
14.0
11.5
8.1
6.5
0.0597
95.4
0.00196
8.2
0.068
25.9
0.056
0.061
0.076*
0.157
0.054
1.50
1.56
16.6
0.0148
0.0203
0.013*
0.041
0.0157
5.5
4.72
13.9
2.4
4.1
1.0
2.3
2.9
1.92
0.0127
0.02
0.0041
0.00485
0.00332*
3.1
2.20
1.8
4.3
5.6
3.0
2.7
11.0
5.6
10
10
10
10
10
10
18
18
10
1
1
1
1
1
1
1
1
1
10
10
10
10
3
10
3
3
3
3
3
10
10
10
3
3
3
3
3
20
20
10
10
10
10
10
10
10
10
10
3
3
3
1
1
1
21
21
3
1
1
1
-4-
kH/kPa m3 mol1
Przyp.
1.2
1.54
13
13
1.87
95.9
120
0.088
13
5
5
13
12
7.78
5
5
2.5
6.56
5
13
40.3
22.8
54.7
5
5
5
19.1
13
0.67
13
2.37
128
479
220
13
13
13
13
Nazwa
C5H12O
C5H12O
C6Cl6
C6HCl5
C6HCl5O
C6H2Br4
C6H2Cl4
C6H2Cl4
C6H2Cl4
C6H2Cl4O
C6H2Cl4O2
C6H3Br3
C6H3Br3
C6H3Br3O
C6H3Cl3
C6H3Cl3
C6H3Cl3
C6H3Cl3O
C6H3Cl3O
C6H3Cl3O2
C6H4BrCl
C6H4BrCl
C6H4BrCl
C6H4BrI
C6H4Br2
C6H4Br2
C6H4Br2
C6H4Br2O
C6H4ClI
C6H4ClI
C6H4ClI
C6H4Cl2
2,2-Dimetylp-1-propanol
Eter methyl-tert-butylowy
Heksachlorobenzen
Pentachlorobenzen
Pentachlorofenol
1,2,4,5-Tetrabromobenzen
1,2,3,4-Tetrachlorobenzen
1,2,3,5-Tetrachlorobenzen
1,2,4,5-Tetrachlorobenzen
2,3,4,6-Tetrachlorofenol
3,4,5,6-Tetrachloro-1,2-benzenodiol
1,2,4-Tribromobenzen
1,3,5-Tribromobenzen
2,4,6-Tribromofenol
1,2,3-Trichlorobenzen
1,2,4-Trichlorobenzen
1,3,5-Trichlorobenzen
2,4,5-Trichlorofenol
2,4,6-Trichlorofenol
3,4,5-Trichloro-1,2-benzenodiol
1-Bromo-2-chlorobenzen
1-Bromo-3-chlorobenzen
1-Bromo-4-chlorobenzen
1-Bromo-4-jodobenzen
o-Dibromobenzen
m-Dibromobenzen
p-Dibromobenzen
2,4-Dibromofenol
1-Chloro-2-jodobenzen
1-Chloro-3-jodobenzen
1-Chloro-4-jodobenzen
o-Dichlorobenzen
C6H4Cl2
m-Dichlorobenzen
C6H4Cl2
p-Dichlorobenzen
C6H4Cl2O
C6H4Cl2O2
C6H4Cl2O2
C6H4F2
C6H4F2
C6H4F2
C6H4I2
C6H4I2
C6H4I2
C6H5Br
2,4-Dichlorofenol
3,5-Dichloro-1,2-benzenodiol
4,5-Dichloro-1,2-benzenodiol
o-Difluorobenzen
m-Difluorobenzen
p-Difluorobenzen
o-Dijodobenzen
m-Dijodobenzen
p-Dijodobenzen
Bromobenzen
C6H5BrO
C6H5Cl
p-Bromofenol
Chlorobenzen
C6H5ClO
C6H5ClO
C6H5ClO
C6H5F
o-Chlorofenol
m-Chlorofenol
p-Chlorofenol
Fluorobenzen
t/C
25
25
25
25
25
25
25
25
25
25
25
25
25
15
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
0
25
50
10
25
50
10
25
50
20
25
25
25
25
25
25
25
25
10
25
40
25
10
25
50
25
25
25
27
S/mas %
3.5
3.62
0.0000005
0.000055
0.0010
0.00000434
0.0000433
0.000346
0.0000606
1.8
0.071
0.0010
0.0000789
0.0007
0.00309
0.00379
0.000655
0.1
0.04
0.051
0.0124
0.0118
0.00442
0.000794
0.00748
0.0064
0.0020
0.2
0.00689
0.00674
0.00311
0.0142
0.0147
0.0212
0.0103
0.0106
0.0165
0.00512
0.00829
0.0167
0.45
0.78
1.19
0.114
0.114
0.122
0.00192
0.000185
0.000893
0.0387
0.0445
0.0516
1.86
0.0387
0.0495
0.0882
2.0
2.2
2.7
0.154
-5-
Przyp
1
20
2
2
2
2
2
2
2
2
8
2
2
2
2
2
2
2
2
8
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
8
8
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
kH/kPa m3 mol1
Przyp.
0.070
0.131
0.085
13
11
11
0.144
0.59
0.122
11
11
11
0.242
0.277
1.1
11
11
11
0.244
11
0.376
11
0.160
11
0.21
0.38
11
0.70
11
Nazwa
C6H5I
Jodobenzen
C6H5NO2
C6H6
Nitrobenzen
Benzen
C6H6ClN
C6H6O
C6H7N
C6H8
C6H8N2
C6H8O4
C6H10
C6H10
C6H10
C6H10O
C6H10O
C6H10O3
C6H11NO
C6H12
C6H12
C6H12
C6H12
C6H12
C6H12
C6H12
C6H12O
C6H12O
C6H12O
o-Chloroanilina
Fenol
Anilina
1,4-Cycloheksadien
Adyponitryl
Maleinian dimetylu
1,5-Heksadien
1-Heksyn
Cykloheksen
Cykloheksanon
Tlenek mezytylu
Acetooctan etylu
Kaprolaktamu
1-Heksen
trans-2-Heksen
2-Metylo-1-penten
4-Metylo-1-penten
2,3-Dimetylo-1-buten
Cykloheksan
Metylocyklopentan
1-Heksen-3-ol
4-Heksen-2-ol
Cykloheksanol
C6H12O
C6H12O
C6H12O
C6H12O2
C6H12O2
C6H12O2
C6H12O2
C6H12O2
C6H14
Eter butylo-winylowy
2-Heksanon
4-Metylo-2-pentanon
Kwas heksanowy
Octan butylu
Octan izobutylu
Octan sec-butylu
Butanian etylu
Heksan
C6H14
C6H14
C6H14
C6H14
C6H14O
2-Metylopentan
3-Metylopentan
2,2-Dimetylobutan
2,3-Dimetylbutan
1-Heksanol
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O
2-Heksanol
3-Heksanol
Eter dipropylowy
2-Metylo-1-pentanol
4-Metylo-1-pentanol
2-Metylo-2-pentanol
3-Metylo-2-pentanol
4-Metylo-2-pentanol
2-Metylo-3-pentanol
3-Metylo-3-pentanol
2-Etylo-1-butanol
t/C
S/mas %
Przyp
10
25
45
25
10
25
50
25
25
25
25
20
25
25
25
25
25
20
25
25
25
25
25
25
30
25
25
25
25
10
25
40
20
20
25
20
20
20
20
20
25
60
25
25
25
25
0
25
50
25
25
25
25
25
25
25
27
25
25
25
0.0193
0.0226
0.0279
0.21
0.178
0.177
0.208
0.876
8.66
3.38
0.08
0.80
8.0
0.017
0.036
0.016
8.8
2.89
12
84.0
0.0053
0.0067
0.0078
0.0048
0.046
0.0058
0.0043
2.52
3.81
4.62
3.8
3.30
0.3
1.75
1.7
0.958
0.68
0.63
0.62
0.49
0.0011
0.00136
0.00137
0.00129
0.0021
0.0021
0.79
0.60
0.51
1.4
1.6
0.49
0.81
0.76
3.2
1.9
1.5
2.0
4.3
1.0
2
2
2
17
3
3
3
10
10
10
3
16
10
3
3
3
20
10
10
10
3
3
3
3
3
3
3
1
1
1
1
1
10
10
10
10
10
10
10
10
3
3
3
3
3
3
1
1
1
1
1
10
1
1
1
1
1
1
1
1
-6-
kH/kPa m3 mol1
Przyp.
0.078
11
0.557
11
14
1.03
15
13
4.14
4.57
13
13
41.8
28.1
63.2
5
5
19.4
36.7
13
5
183
13
176
170
199
144
13
13
13
13
0.26
13
Nazwa
C6H14O
C6H14O
C6H14O
C6H14O
C6H14O2
C6H15N
C6H15N
C7H4Cl4O
C7H5Cl3
C7H5Cl3O
C7H5N
C7H5NO
C7H6Cl2
C7H6Cl2O
C7H6Cl2O
C7H6N2
C7H6N2
C7H6O
C7H6O2
C7H7Br
C7H7Cl
C7H7ClO
C7H7ClO
C7H7ClO
C7H7NO3
C7H8
2,2-Dimetylo-1-butanol
Eter diizopropylowy
2,3-Dimetylo-2-butanol
3,3-Dimetylo-2-butanol
1,1-Dietoksyetan
Dipropyloamina
Trietyloamina
2,3,4,6-Tetrachloro-5-metylofenol
(Trichlorometylo)benzen
2,4,6-Trichloro-3-metylofenol
Benzonitryl
Benzoksazol
(Dichlorometylo)benzen
2,6-Dichloro-4-metylfenol
2,4-Dichloro-6-metylfenol
1H-Benzimidazol
1H-Indazol
Benzaldehyd
Salicyloaldehyd
p-Bromotoluen
(Chloromethlo)benzen
4-Chloro-2-metylofenol
4-Chloro-3-metylofenol
2-Chloro-6-metylofenol
2-Nitroanizol
Toluen
C7H8
C7H8
C7H8O
C7H8O
C7H8O
C7H8O
C7H8O
C7H9N
C7H9N
C7H12
C7H12
C7H12
C7H14
C7H14
C7H14
C7H14
1,3,5-Cykloheptatrien
1,6-Heptadiyn
Alkohol benzylowy
o-Krezol
m-Krezol
p-Krezol
Anizol
o-Metylpanilina
p-Metyloanilina
1-Heptyn
Cyklohepten
1-Metylocykloheksen
1-Hepten
trans-2-Hepten
Cykloheptan
Metylocykloheksan
C7H14
C7H14O
C7H14O
C7H14O
C7H14O2
C7H14O2
C7H14O2
C7H16
Etylocyklopentan
2-Heptanon
3-Heptanon
2,4-Dimetylo-3-pentanon
Octan pentylu
Octan izopentylu
3-metylobutanian etylu
Heptan
C7H16
C7H16
C7H16
C7H16
C7H16
C7H16
2-Methylhexane
3-Methylhexane
2,2-Dimethylpentane
2,3-Dimethylpentane
2,4-Dimethylpentane
3,3-Dimethylpentane
t/C
S/mas %
25
20
25
25
25
20
20
25
5
25
25
20
30
25
25
20
20
20
86
25
20
25
25
25
30
5
25
25
25
20
40
40
40
25
20
21
25
25
25
25
25
25
25
50
20
25
20
20
20
20
20
0
25
40
25
25
25
25
25
25
0.8
1.2
4.2
2.4
5
2.5
5.5
0.00061
0.0053
0.0112
0.2
0.834
0.025
0.0673
0.0283
0.201
0.0827
0.3
1.68
0.011
0.0493
0.68
0.40
0.36
0.619
0.063
0.053
0.064
0.125
0.08
3.08
2.51
2.26
0.19
1.66
7.35
0.0094
0.0066
0.0052
0.032
0.015
0.0030
0.00151
0.0019
0.012
0.43
1.43
0.59
0.17
0.2
0.2
0.0003
0.00024
0.00025
0.00025
0.00026
0.00044
0.00052
0.00042
0.00059
-7-
Przyp
1
10
1
1
10
10
10
2
10
2
10
6
10
2
2
6
6
10
10
2
10
2
2
2
10
3
3
3
3
10
10
10
10
20
10
10
3
3
3
3
3
3
3
3
3
10
10
10
10
10
10
3
3
3
3
3
3
3
3
3
kH/kPa m3 mol1
Przyp.
0.26
13
0.680
0.47
13
13
0.025
13
4.47
4.9
13
13
40.3
42.2
9.59
43.3
13
13
13
13
209
13
346
249
318
175
323
186
5
13
5
5
13
5
Nazwa
C7H16O
1-Heptanol
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C7H16O
C8H4F6
C8H6N2
C8H6S
C8H7ClO3
C8H7Cl3O
C8H7N
C8H8
2-Heptanol
3-Heptanol
4-Heptanol
2-Metylo-2-heksanol
5-Metylo-2-heksanol
3-Metylo-3-heksanol
2,3-Dimetylo-2-pentanol
2,4-Dimetylo-2-pentanol
3-Etylo-3-pentanol
2,2-Dimetylo-3-pentanol
2,3-Dimetylo-3-pentanol
2,4-Dimetylo-3-pentanol
2,3,3-Trimethyl-2-butanol
1,3-Bis(trifluorometylo)benzen
Chinoksalina
Benzo[b]tiofen
3-Chloro-4-hydroksy-5metoksybenzaldehyd
2-Chloro-4-hydroksy-5metoksybenzaldehyd
2,4,6-Trichloro-3,5-dimetylofenol
Indol
Styren
C8H8N2
C8H8O
C8H8O2
C8H8O3
C8H8O3
C8H9ClO
C8H9ClO
C8H9ClO
C8H10
2-Metylo-1H-benzoimidazol
Acetofenon
Benzoesan metylu
Salicylan metylu
4-Hydroksy-3-metoksybenzaldehyd
4-Chloro-2,5-dimetylofenol
4-Chloro-2,6-dimetylofenol
4-Chloro-3,5-dimetylofenol
Etylobenzen
C8H10
o-Ksylen
C8H10
m-Ksylen
C8H10
p-Ksylen
C8H10O
C8H10O
C8H10O
C8H12
C8H14
C8H16
C8H16
C8H16
C8H16
C8H16
C8H16
C8H16
C8H16O
C8H16O2
Fenetol
2,4-Ksylenol
3,5-Ksylenol
4-Winylocykloheksen
1-Oktyn
1-Okten
Cyklooktan
Etylocykloheksan
cis-1,2-Dimetylocykloheksan
trans-1,4-Dimetylocykloheksan
Propylocyklopentan
1,1,3-Trimetylocyklopentan
2-Oktanon
Kwas oktanowy
C8H7ClO3
t/C
S/mas %
10
25
50
30
25
25
25
25
25
25
25
25
25
25
25
40
25
50
20
0.25
0.174
0.12
0.33
0.43
0.47
1.0
0.49
1.2
1.5
1.3
1.7
0.82
1.6
0.70
2.2
0.0041
54
0.0130
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
6
6
25
0.093
25
25
20
25
50
20
25
20
30
25
25
25
25
0
25
40
25
45
0
25
40
0
25
40
25
25
29
25
25
25
25
40
25
25
25
25
25
25
0.013
0.00050
0.187
0.025
0.046
0.145
0.55
0.21
0.74
0.247
0.89
0.52
0.34
0.020
0.0169
0.0200
0.0173
0.021
0.0203
0.016
0.022
0.0160
0.018
0.022
0.12
0.787
0.62
0.005
0.0024
0.00027
0.00079
0.00066
0.00060
0.000384
0.00020
0.00037
0.113
0.0798
8
2
6
4
4
6
-8-
Przyp
10
10
8
2
2
2
4
4
4
4
4
4
4
4
4
4
4
10
10
10
4
4
4
4
4
4
4
4
4
10
10
kH/kPa m3 mol1
Przyp.
0.3
0.30
15
13
0.887
11
0.565
13
0.730
13
0.578
13
7.87
96.3
10.7
36
88.2
90.2
159
13
13
13
5
5
5
5
Nazwa
C8H16O2
C8H16O2
C8H16O2
C8H17Cl
C8H18
Octan heksylu
Octan sec-heksylu
Izobutanian izobutylu
3-(Chlorometylo)heptan
Oktan
C8H18
C8H18
C8H18
C8H18O
C8H18O
C8H18O
C8H18O
C8H18O
C8H19N
C8H19N
C8H20Si
C9H7N
C9H7N
C9H9N
C9H10
C9H10O2
C9H12
C9H12
C9H12
C9H12
C9H12
C9H12
C9H12
C9H12
C9H14O6
C9H16
C9H18
C9H18O
C9H18O2
C9H20
3-Metyloheptan
2,2,4-Trimetylopentan
2,3,4-Trimetylopentan
Eter dibutylowy
1-Oktanol
2-Oktanol
2-Metylo-2-heptanol
2-Etylo-1-heksanol
Dibutyloamina
2-Etyloheksylamina
Tetraetylosilan
Chinolina
Izochinolina
3-Metylo-1H-indol
Indan
Benzoesan etylu
1,8-Nonadiyn
Propylobenzen
Izopropylobenzen
o-Etylotoluen
p-Etylotoluen
1,2,3-Trimetylobenzen
1,2,4-Trimetylobenzen
1,3,5-Trimetylobenzen
Triacetyna
1-Nonyn
1,1,3-Trimetylocykloheksane
Keton diizobutylowy
Kwas nonanowy
Nonan
C9H20
C9H20
C9H20O
C9H20O
C9H20O
C9H20O
C9H20O
C9H20O
C10H7Cl
C10H7Cl
C10H8
4-Metyloktan
2,2,5-Trimetyloheksan
3,5-Dimetylo-4-heptanol
1-Nonanol
2-Nonanol
3-Nonanol
4-Nonanol
5-Nonanol
1-Chloronaftalen
2-Chloronaftalen
Naftalen
C10H9N
C10H10O4
C10H14
C10H14
C10H14
C10H14
C10H14
C10H14
C10H16
3-Metyloizochinolina
Ftalan dimetylu
Butylobenzen
sec-Butylobenzen
tert-Butylobenzen
Izobutylobenzen
p-Cymen
1,2,4,5-Tetrametylobenzen
d-Limonen
t/C
20
20
20
20
25
50
25
25
25
20
25
25
30
25
20
20
25
20
20
20
25
25
25
25
25
25
25
25
25
25
25
25
25
25
20
25
50
25
25
15
25
15
15
15
15
25
25
10
25
50
20
25
25
25
25
25
25
25
0
25
S/mas %
0.02
0.13
0.5
0.01
0.000071
0.00010
0.000079
0.00022
0.00018
0.03
0.054
0.4
0.25
0.01
0.47
0.25
0.0000325
0.633
0.452
0.050
0.010
0.083
0.0125
0.0055
0.0056
0.0093
0.0094
0.0069
0.0056
0.00489
5.8
0.00072
0.000177
0.043
0.0284
0.000017
0.000022
0.0000115
0.00008
0.072
0.014
0.026
0.032
0.0026
0.0032
0.00224
0.00117
0.0019
0.0031
0.0082
0.092
0.40
0.0015
0.0014
0.0032
0.0010
0.00234
0.000348
0.00097
0.00138
-9-
Przyp
10
10
10
10
4
4
4
4
4
10
1
1
1
1
10
10
10
6
6
6
4
20
4
4
4
5
5
4
4
4
10
4
4
10
10
4
4
4
4
1
1
1
1
1
1
5
5
4
4
4
6
15
4
4
4
4
4
4
4
4
kH/kPa m3 mol1
Przyp.
311
13
376
307
206
0.48
5
13
13
13
1.04
1.47
0.529
0.500
0.343
0.569
0.781
11
11
13
13
11
11
11
105
13
333
13
1000
246
5
13
0.0430
1.33
1.89
1.28
3.32
0.80
2.55
11
11
11
11
5
11
Nazwa
C10H16O
C10H18
C10H20
C10H20
C10H22
C10H22O
C10H22O
C11H10
C11H10
C11H16
C12Cl10
C12HCl9
C12H2Cl8
C12H3Cl7
C12H4Cl6
C12H4Cl6
C12H4Cl6
C12H5Cl5
C12H5Cl5
C12H6Cl4
C12H6Cl4
C12H7Cl3
C12H7Cl3
C12H8Cl2
C12H8Cl2
C12H8O
C12H8S
C12H9Cl
C12H9N
C12H10
Kamfora
trans-Decahydronaftalen
Pentylocyklopentan
1-Deken
Dekan
Eter diizopentylowy
1-Dekanol
1-Methylnaftalen
2-Metylonaftalen
Pentylobenzen
Decachlorobifenyl
2,2,3,3,4,5,5,6,6-Nonachlorobifenyl
2,2,3,35,5,6,6-Octachlorobifenyl
2,2,3,3,4,4,6-Heptachlorobifenyl
2,2,3,3,4,4-Heksachlorobifenyl
2,2,4,4,6,6-Heksachlorobifenyl
2,2,3,3,6,6-Heksachlorobifenyl
2,3,4,5,6-Pentachlorobifenyl
2,2,4,5,5-Pentachlorobifenyl
2,3,4,5-Tetrachlorobifenyl
2,2,4,5-Tetrachlorobifenyl
2,4,5-Trichlorobifenyl
2,4,6-Trichlorobifenyl
2,5-Dichlorobifenyl
2,6-Dichlorobifenyl
Dibenzofuran
Dibenzofiofen
2-Chlorobifenyl
Karbazol
Acetonaften
C12H10
Bifenyl
C12H10N2O
C12H10O
C12H12
C12H12
C12H12
C12H12
C12H12
C12H12
C12H12
C12H18
C12H26
C12H26O
C12H27O4P
C13H9N
C13H9N
C13H10
N-Nitrozodifenyloamina
Eter difenylowy
1-Ethylnaftalen
2-Ethylnaftalen
1,3-Dimethylnaftalen
1,4-Dimethylnaftalen
1,5-Dimethylnaftalen
2,3-Dimethylnaftalen
2,6-Dimetylonaftalen
Heksylobenzen
Dodekan
1-Dodekanol
Fosforan tributylu
Akrydyna
Benzo[f]chinolina
9H-Fluoren
C13H12
C13H14
C14H10
Difenylometan
1,4,5-Trimetylonaftalen
Antracen
C14H10
Fenantren
t/C
20
25
25
25
0
20
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
22
0
25
50
0
25
50
25
25
25
25
25
25
25
25
25
25
25
25
25
25
25
0
25
50
25
25
0
25
10
25
50
S/mas %
0.01
0.000089
0.0000115
0.00057
0.0000015
0.02
0.0037
0.0028
0.0025
0.00105
0.00000000012
0.0000000018
0.0000003
0.0000002
0.00000006
0.00000007
0.00000008
0.0000008
0.000001
0.000002
0.0000016
0.000014
0.00002
0.0002
0.00014
0.000656
0.000103
0.00055
0.000120
0.00015
0.00038
0.00092
0.000272
0.00072
0.0022
0.0035
0.00180
0.00101
0.00080
0.0008
0.00114
0.00031
0.00025
0.00017
0.00021
0.00000037
0.0004
0.039
0.00466
0.0079
0.00007
0.00019
0.00063
0.000141
0.00021
0.0000022
0.0000062
0.000050
0.00011
0.00041
-10-
Przyp
10
4
4
4
4
10
1
4
4
5
7
7
7
7
7
7
7
7
7
7
9
7
7
7
7
6
6
7
6
4
4
4
4
4
4
17
6
4
4
4
4
4
4
4
4
4
1
10
6
6
4
4
4
4
4
4
4
4
4
4
kH/kPa m3 mol1
Przyp.
3
185
13
5
479
13
0.0450
0.051
1.69
0.0208
12
12
11
7
0.0381
0.0054
0.0119
0.818
7
7
7
7
0.0355
0.0243
0.0495
0.0201
7
7
7
0.011
12
0.0701
0.012
12
0.028
0.027
0.039
0.078
13
12
12
750
0.0079
12
0.001
12
0.0040
12
0.0032
12
Nazwa
C14H12
C14H14
C14H14O
C14H30
C14H30O
C15H12
C15H12
C15H12
C15H32O
C16H10
C16H10
trans-Stylben
1,2-Difenyletan
Eter dibenzylowy
Tetradekan
1-Tetradekanol
2-Metyloantracen
9-Metyloantracen
1-Metylofenantren
1-Pentadekanol
Fluoranten
Piren
C16H14
C16H22O4
C16H34O
C17H12
C17H12
C18H12
C18H12
C18H12
C18H12
C18H12N2
C18H34O4
C19H14
C19H14
C19H14
C20H12
C20H12
C20H12
C20H13N
C20H14
C20H42
C21H13N
C21H16
C22H12
C22H14
C22H14
C22H14
C22H14
C22H44O2
C24H12
9,10-Dimetylantracen
Ftalan dibutylu
1-Heksadekanol
11H-Benzo[a]fluoren
11H-Benzo[b]fluoren
Benzo[a]antracen
Chryzen
Naftacen
Trifenylen
2,2-Bichinolina
Sebacynian dibutylu
5-Metylochryzen
9-Metylbenzo[a]antracen
10-Metylobenzo[a]antracen
Benzo[a]piren
Perylen
Benzo[e]piren
13H-Dibenzo[a,i]karbazol
1,2-Dihydrobenz[j]aceantrylen
Ejkozan
Dibenz[a,j]akrydina
1,2-Dihydro-3-meylbenzo[j]aceantrylen
Benzo[ghi]perylen
Picen
Benzo[b]trifenylen
Dibenzo[a,h]antracen
Dibenzo[a,j]antracen
Stearynian butylu
Koronen
t/C
25
25
35
25
25
25
25
25
25
25
25
50
25
25
25
25
25
25
25
25
25
24
20
27
27
25
25
25
20
24
25
25
25
25
25
25
25
25
25
25
25
S/mas %
0.000029
0.00044
0.0040
0.000012
0.000031
0.0000030
0.000026
0.0000269
0.000010
0.000024
0.0000132
0.00009
0.0000056
0.00112
0.000003
0.0000045
0.0000002
0.0000011
0.00000019
0.00000006
0.0000041
0.000102
0.004
0.0000062
0.0000066
0.0000055
0.00000038
0.00000004
0.00000046
0.00000104
0.00000036
0.00000019
0.000016
0.00000022
0.000000026
0.00000025
0.0000027
0.00000006
0.0000012
0.2
0.000000014
-11-
Przyp
4
6
10
5
1
4
4
4
1
4
4
4
4
15
1
4
4
4
4
4
4
6
10
4
4
4
4
4
4
6
6
4
6
6
4
4
4
4
4
10
4
kH/kPa m3 mol1
Przyp.
0.040
0.017
12
12
0.0010
0.00092
12
12
0.00058
0.006
0.000004
0.00001
12
12
12
12
0.000046
0.000003
0.00002
12
12
12
0.000075
12