Properties of Solvents Used in Organic Chemistry*
On 8/19/20, a compilation of boiling points, melting points, densities and refractive indices for 1000 organic compounds has been uploaded to http://murov.info/orgcmpds.htm . Please also note that on 3/30/20, a table with most of the data below has been uploaded that has sortable columns (click on the column heading). http://murov.info/orgsolvsort.htm . However the links below the tables on this site are not included on the sortable table site.
The values in the table below except as noted have been
extracted from online and hardbound compilations . Values for relative polarity, eluant strength, threshold
limits and vapor pressure have been extracted from: Christian Reichardt,
Solvents and Solvent Effects in Organic Chemistry, Wiley-VCH Publishers, 3rd ed., 2003, and the chemidplus site. For Spectra of
Solvents and other sites with properties of organic compounds, jump to the
bottom of the solvent tables. For an Organic Chemistry
Laboratory Manual with experiments and exercises, see: http://murov.info/orglab.htm .
*(Note: The
title of this site was changed from the original Properties of Organic Solvents
to the present title because the
"US
Patent and Trademark Office have relied on the document to assert that
water is an organic solvent.").
For those of you who conduct or organize
seminars, links to many Powerpoint Preshows, exercises and challenges that can
be used while audiences await the start of the seminar are available at:
http://murov.info/PPTPreshows.htm.
Please report any errors to
murovs@yosemite.edu.
For
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.
For recently posted sites,
please visit:
http://murov.info/orgchemres.htm
, http://murov.info/aufbaupt.htm ,
http://murov.info/timelines.htm ,
http://murov.info/organicmilestones.htm,
Photophysical
properties of organic compounds -
http://murov.info/photophys.htm
.
The tables below were posted (10/23/98), revised (07/28/09) and last modified (08/19/20) by Steve Murov, Professor Emeritus of
Chemistry, Modesto Junior College.
Table 1 arranged alphabetically
Table 2 arranged according to increasing polarity
Spectra
links
Chemical
Property links (and miscellaneous)
Solvent | formula | boiling point (oC) | melting point (oC) | density
(g/mL) |
solubility in H2O1 (g/100g) | relative polarity2 |
eluant strength3 | threshold limits4 (ppm) | vapor pressure 20oC (hPa) |
dipole moment (D) |
dielectric constant |
viscosity 10-3 Pa s |
acetic acid | C2H4O2 | 118 | 16.6 | 1.049 | M | 0.648 | >1 | 10 | 15.3 | 1.68 | 6.2 | 1.12 |
acetone | C3H6O | 56.2 | -94.3 | 0.786 | M | 0.355 | 0.56 | 500 | 240 | 2.85 | 21 | 0.30 |
acetonitrile | C2H3N | 81.6 | -46 | 0.786 | M | 0.460 | 0.65 | 20 | 97 | 3.5 | 37.5 | 0.34 |
acetyl acetone | C5H8O2 | 140.4 | -23 | 0.975 | 16 | 0.571 | 3 | 3.0 | 23 | 0.6 | ||
2-aminoethanol | C2H7NO | 170.9 | 10.5 | 1.018 | M | 0.651 | 3 | 0.53 | 2.3 - 2.6 | 37.7 | 20.8 | |
aniline | C6H7N | 184.4 | -6.0 | 1.022 | 3.4 | 0.420 | 2 | 0.4 | 1.6 | 6.8 | 3.8 | |
anisole | C7H8O | 153.7 | -37.5 | 0.996 | 0.10 | 0.198 | 3.5* | 1.4 | 4.3 | 0.98 | ||
benzene | C6H6 | 80.1 | 5.5 | 0.879 | 0.18 | 0.111 | 0.32 | 0.5 | 101 | 0 | 2.3 | 0.60 |
benzonitrile | C7H5N | 205 | -13 | 0.996 | 0.2 | 0.333 | 10 | 12 | 4.1 | 26 | 1.27 | |
benzyl alcohol | C7H8O | 205.4 | -15.3 | 1.042 | 3.5 | 0.608 | 0.094* | 1.7 | 13 | 5.47 | ||
1-butanol | C4H10O | 117.6 | -89.5 | 0.81 | 7.7 | 0.586 | 20 | 6.3 | 1.7 | 17.5 | 2.59 | |
2-butanol | C4H10O | 99.5 | -114.7 | 0.808 | 18.1 | 0.506 | 100 | 18.3* | 1.7 | 17.3 | 3.1 | |
i-butanol | C4H10O | 107.9 | -108.2 | 0.803 | 8.5 | 0.552 | 10.5* | 1.8 | 17.9 | 6.68 | ||
2-butanone | C4H8O | 79.6 | -86.3 | 0.805 | 25.6 | 0.327 | 0.51 | 200 | 105 | 2.8 | 18.6 | 0.41 |
t-butyl alcohol | C4H10O | 82.2 | 25.5 | 0.786 | M | 0.389 | 100 | 41 | 1.7 | 12.4 | 3.35 | |
carbon disulfide | CS2 | 46.3 | -111.6 | 1.263 | 0.2 | 0.065 | 0.15 | 10 | 400 | 0 | 2.6 | 0.36 |
carbon tetrachloride | CCl4 | 76.7 | -22.4 | 1.594 | 0.08 | 0.052 | 0.18 | 5 | 120 | 0 | 2.3 | 0.90 |
chlorobenzene | C6H5Cl | 132 | -45.6 | 1.106 | 0.05 | 0.188 | 0.30 | 10 | 12 | 1.54 | 5.7 | 0.75 |
chloroform | CHCl3 | 61.2 | -63.5 | 1.498 | 0.8 | 0.259 | 10 | 210 | 1.0 | 4.8 | 0.54 | |
cyclohexane | C6H12 | 80.7 | 6.6 | 0.779 | 0.005 | 0.006 | 0.04 | 100 | 104 | 0 | 2 | 0.89 |
cyclohexanol | C6H12O | 161.1 | 25.2 | 0.962 | 4.2 | 0.509 | 50 | 1.2 | 1.9 | 15 | ||
cyclohexanone | C6H10O | 155.6 | -16.4 | 0.948 | 2.3 | 0.281 | 25 | 5 | 2.9 | 15 | 2.00 | |
di-n-butylphthalate | C16H22O4 | 340 | -35 | 1.049 | 0.0011 | 0.272 | 16.6 | |||||
1,1-dichloroethane | C2H4Cl2 | 57.3 | -97.0 | 1.176 | 0.5 | 0.269 | 100 | 240 | 1.8 | 10 | 0.84 | |
1,2-dichloroethane | C2H4Cl2 | 83.5 | -35.4 | 1.235 | 0.87 | 0.327 | 79* | 1.8 | 10.4 | 0.78 | ||
diethylamine | C4H11N | 56.3 | -48 | 0.706 | M | 0.145 | 0.63 | 5 | 260 | 1.2 | 3.8 | 0.32 |
diethylene glycol | C4H10O3 | 245 | -10 | 1.118 | M | 0.713 | 0.027 | 2.3 | 31.8 | 30.2 | ||
diglyme | C6H14O3 | 162 | -64 | 0.945 | M | 0.244 | 1.9 | 7.23 | 1.88 | |||
dimethoxyethane (glyme) | C4H10O2 | 85 | -58 | 0.868 | M | 0.231 | 1.7 | 7.3 | 1.1 | |||
N,N-dimethylaniline | C8H11N | 194.2 | 2.4 | 0.956 | 0.14 | 0.179 | 1.40 | |||||
dimethylformamide (DMF) | C3H7NO | 153 | -61 | 0.944 | M | 0.386 | 10 | 3.5 | 3.8 | 37 | 0.80 | |
dimethylphthalate | C10H10O4 | 283.8 | 1 | 1.190 | 0.43 | 0.309 | ||||||
dimethylsulfoxide (DMSO) | C2H6OS | 189 | 18.4 | 1.092 | M | 0.444 | 0.75 | 0.61* | 3.9 | 46.7 | 2.00 | |
dioxane | C4H8O2 | 101.1 | 11.8 | 1.033 | M | 0.164 | 0.56 | 20 | 41 | 0.4 | 2 | 1.18 |
ethanol | C2H6O | 78.5 | -114.1 | 0.789 | M | 0.654 | 0.88 | 100 | 59 | 1.7 | 24 | 1.08 |
ether | C4H10O | 34.6 | -116.3 | 0.713 | 7.5 | 0.117 | 0.38 | 400 | 587 | 1.25 | 4.3 | 0.22 |
ethyl acetate | C4H8O2 | 77 | -83.6 | 0.894 | 8.7 | 0.228 | 0.58 | 400 | 97 | 1.78 | 6.0 | 0.43 |
ethyl acetoacetate | C6H10O3 | 180.4 | -80 | 1.028 | 2.9 | 0.577 | 0.78* | |||||
ethyl benzoate | C9H10O2 | 213 | -34.6 | 1.047 | 0.07 | 0.228 | 2.0 | 6.0 | ||||
ethylene glycol | C2H6O2 | 197 | -13 | 1.115 | M | 0.790 | 1.11 | 0.092* | 2.3 | 37.7 | 16.1 | |
glycerin | C3H8O3 | 290 | 17.8 | 1.261 | M | 0.812 | 2.7 | 42.5 | 934 | |||
heptane | C7H16 | 98 | -90.6 | 0.684 | 0.0003 | 0.012 | 400 | 48 | 0 | 1.9 | 0.39 | |
1-heptanol | C7H16O | 176.4 | -35 | 0.819 | 0.17 | 0.549 | 1.7 | 12 | 6.0 | |||
hexane | C6H14 | 69 | -95 | 0.655 | 0.0014 | 0.009 | 0.01 | 50 | 160 | 0 | 1.9 | 0.29 |
1-hexanol | C6H14O | 158 | -46.7 | 0.814 | 0.59 | 0.559 | 0.22* | 1.60 | 12.5 | 0.59 | ||
methanol | CH4O | 64.6 | -98 | 0.791 | M | 0.762 | 0.95 | 200 | 128 | 1.6 | 33 | 0.54 |
methyl acetate | C3H6O2 | 56.9 | -98.1 | 0.933 | 24.4 | 0.253 | 200 | 220 | 1.7 | 6.68 | 0.36 | |
methyl t-butyl ether (MTBE) | C5H12O | 55.2 | -109 | 0.741 | 4.8 | 0.124 | 0.20 | 250* | 1.4 | 2.6 | 0.36 | |
methylene chloride | CH2Cl2 | 39.8 | -96.7 | 1.326 | 1.32 | 0.309 | 0.42 | 50 | 475 | 1.6 | 9.0 | 0.42 |
1-octanol | C8H18O | 194.4 | -15 | 0.827 | 0.096 | 0.537 | 1.7 | 10.3 | 7.4 | |||
pentane | C5H12 | 36.1 | -129.7 | 0.626 | 0.004 | 0.009 | 0.00 | 600 | 573 | 0 | 1.84 | 0.23 |
1-pentanol | C5H12O | 138.0 | -78.2 | 0.814 | 2.2 | 0.568 | 2.2* | 1.7 | 14 | 3.5 | ||
2-pentanol | C5H12O | 119.0 | -50 | 0.810 | 4.5 | 0.488 | 6.1* | 1.7 | 13.7 | 3.5 | ||
3-pentanol | C5H12O | 115.3 | -8 | 0.821 | 5.1 | 0.463 | 8.8* | 1.7 | 13.3 | |||
2-pentanone | C5H10O | 102.3 | -76.9 | 0.809 | 4.3 | 0.321 | 35.4* | 2.7 | 15.4 | 0.50 | ||
3-pentanone | C5H12O | 101.7 | -39.8 | 0.814 | 3.4 | 0.265 | 200 | 37.7* | 2.8 | 17.0 | 0.44 | |
1-propanol | C3H8O | 97 | -126 | 0.803 | M | 0.617 | 0.82 | 21* | 1.68 | 22 | 1.95 | |
2-propanol | C3H8O | 82.4 | -88.5 | 0.785 | M | 0.546 | 0.82 | 400 | 44 | 1.66 | 19 | 2.07 |
pyridine | C5H5N | 115.5 | -42 | 0.982 | M | 0.302 | 0.71 | 5 | 20 | 2.2 | 13 | 0.88 |
tetrahydrofuran(THF) | C4H8O | 66 | -108.4 | 0.886 | 30 or M5 | 0.207 | 0.57 | 200 | 200 | 1.63 | 7.5 | 0.46 |
toluene | C7H8 | 110.6 | -93 | 0.867 | 0.05 | 0.099 | 0.29 | 50 | 29 | 0.36 | 2.4 | 0.55 |
water | H2O | 100.00 | 0.00 | 0.998 | M | 1.000 | >>1 | 17.5 | 1.85 | 80.1 | 0.89 | |
water, heavy | D2O | 101.3 | 4 | 1.107 | M | 0.991 | 15 | 1.84 | 78.3 | 1.10 | ||
p-xylene | C8H10 | 138.3 | 13.3 | 0.861 | 0.02 | 0.074 | 0.26 | 100 | 15 | 0 | 2.27 | 0.65 |
1 M =
miscible.
2 The values for
relative polarity are normalized from measurements of solvent shifts of
absorption spectra and were
extracted from Christian Reichardt, Solvents and Solvent Effects in
Organic Chemistry, Wiley-VCH Publishers, 3rd ed., 2003.
3 Snyder's
empirical eluant strength parameter for alumina. Extracted from Reichardt,
page 495.
4 Threshold limits for exposure. Extracted from
Reichardt, pages 501-502.
5
https://pubchem.ncbi.nlm.nih.gov/compound/tetrahydrofuran#section=Solubility
* 25oC
TABLE 2
Solvent | formula | boiling point (oC) | melting
point (oC) |
density
(g/mL) |
solubility in H2O1 (g/100g) |
relative polarity2 |
eluant strength3 | threshold limits4 (ppm) | vapor pressure 20oC (hPa) | dipole moment (D) |
dielectric constant |
viscosity 10-3 Pa s |
cyclohexane | C6H12 | 80.7 | 6.6 | 0.779 | 0.005 | 0.006 | 0.04 | 100 | 104 | 0 | 2 | 0.89 |
pentane | C5H12 | 36.1 | -129.7 | 0.626 | 0.0039 | 0.009 | 0.00 | 600 | 573 | 0 | 1.84 | 0.23 |
hexane | C6H14 | 69 | -95 | 0.655 | 0.0014 | 0.009 | 0.01 | 50 | 160 | 0 | 1.9 | 0.29 |
heptane | C7H16 | 98 | -90.6 | 0.684 | 0.0003 | 0.012 | 400 | 48 | 0 | 1.9 | 0.39 | |
carbon tetrachloride | CCl4 | 76.7 | -22.4 | 1.594 | 0.08 | 0.052 | 0.18 | 5 | 120 | 0 | 2.3 | 0.90 |
carbon disulfide | CS2 | 46.3 | -111.6 | 1.263 | 0.2 | 0.065 | 0.15 | 10 | 400 | 0 | 2.6 | 0.36 |
p-xylene | C8H10 | 138.3 | 13.3 | 0.861 | 0.02 | 0.074 | 0.26 | 100 | 15 | 0 | 2.27 | 0.65 |
toluene | C7H8 | 110.6 | -93 | 0.867 | 0.05 | 0.099 | 0.24 | 50 | 29 | 0.36 | 2.4 | 0.55 |
benzene | C6H6 | 80.1 | 5.5 | 0.879 | 0.18 | 0.111 | 0.32 | 0.5 | 101 | 0 | 2.3 | 0.60 |
ether | C4H10O | 34.6 | -116.3 | 0.713 | 7.5 | 0.117 | 0.38 | 400 | 587 | 1.25 | 4.3 | 0.22 |
methyl t-butyl ether (MTBE) | C5H12O | 55.2 | -109 | 0.741 | 4.8 | 0.124 | 0.20 | 250* | 1.4 | 2.6 | 0.36 | |
diethylamine | C4H11N | 56.3 | -48 | 0.706 | M | 0.145 | 0.63 | 5 | 260 | 1.2 | 3.8 | 0.32 |
dioxane | C4H8O2 | 101.1 | 11.8 | 1.033 | M | 0.164 | 0.56 | 20 | 41 | 0.4 | 2 | 1.18 |
N,N-dimethylaniline | C8H11N | 194.2 | 2.4 | 0.956 | 0.14 | 0.179 | 1.40 | |||||
chlorobenzene | C6H5Cl | 132 | -45.6 | 1.106 | 0.05 | 0.188 | 0.30 | 10 | 12 | 1.54 | 5.7 | 0.75 |
anisole | C7H8O | 153.7 | -37.5 | 0.996 | 0.10 | 0.198 | 3.5* | 1.4 | 4.3 | 0.98 | ||
tetrahydrofuran (THF) | C4H8O | 66 | -108.4 | 0.886 | 30 or M5 | 0.207 | 0.57 | 200 | 200 | 1.63 | 7.5 | 0.46 |
ethyl acetate | C4H8O2 | 77 | -83.6 | 0.894 | 8.7 | 0.228 | 0.57 | 400 | 97 | 1.78 | 6.0 | 0.43 |
ethyl benzoate | C9H10O2 | 213 | -34.6 | 1.047 | 0.07 | 0.228 | 2.0 | 6.0 | ||||
dimethoxyethane (glyme) | C4H10O2 | 85 | -58 | 0.868 | M | 0.231 | 1.7 | 7.3 | 1.1 | |||
diglyme | C6H14O3 | 162 | -64 | 0.945 | M | 0.244 | 1.9 | 7.23 | 1.88 | |||
methyl acetate | C3H6O2 | 56.9 | -98.1 | 0.933 | 24.4 | 0.253 | 200 | 220 | 1.7 | 6.68 | 0.36 | |
chloroform | CHCl3 | 61.2 | -63.5 | 1.498 | 0.8 | 0.259 | 0.40 | 10 | 210 | 1.0 | 4.8 | 0.54 |
3-pentanone | C5H12O | 101.7 | -39.8 | 0.814 | 3.4 | 0.265 | 200 | 37.7* | 2.8 | 17.0 | 0.44 | |
1,1-dichloroethane | C2H4Cl2 | 57.3 | -97.0 | 1.176 | 0.5 | 0.269 | 100 | 240 | 1.8 | 10 | 0.84 | |
di-n-butyl phthalate | C16H22O4 | 340 | -35 | 1.049 | 0.0011 | 0.272 | 16.6 | |||||
cyclohexanone | C6H10O | 155.6 | -16.4 | 0.948 | 2.3 | 0.281 | 25 | 5 | 2.9 | 15 | 2.00 | |
pyridine | C5H5N | 115.5 | -42 | 0.982 | M | 0.302 | 0.71 | 5 | 20 | 2.2 | 13 | 0.88 |
dimethylphthalate | C10H10O4 | 283.8 | 1 | 1.190 | 0.43 | 0.309 | ||||||
methylene chloride | CH2Cl2 | 39.8 | -96.7 | 1.326 | 1.32 | 0.309 | 0.42 | 50 | 475 | 1.6 | 9.0 | 0.42 |
2-pentanone | C5H10O | 102.3 | -76.9 | 0.809 | 4.3 | 0.321 | 35.4* | 2.7 | 15.4 | 0.50 | ||
2-butanone | C4H8O | 79.6 | -86.3 | 0.805 | 25.6 | 0.327 | 0.51 | 200 | 105 | 2.8 | 18.6 | 0.41 |
1,2-dichloroethane | C2H4Cl2 | 83.5 | -35.4 | 1.235 | 0.87 | 0.327 | 79* | 1.8 | 10.4 | 0.78 | ||
benzonitrile | C7H5N | 205 | -13 | 0.996 | 0.2 | 0.333 | 10 | 12 | 4.1 | 26 | 1.27 | |
acetone | C3H6O | 56.2 | -94.3 | 0.786 | M | 0.355 | 0.56 | 500 | 240 | 2.85 | 21 | 0.30 |
dimethylformamide (DMF) | C3H7NO | 153 | -61 | 0.944 | M | 0.386 | 10 | 3.5 | 3.8 | 37 | 0.80 | |
t-butyl alcohol | C4H10O | 82.2 | 25.5 | 0.786 | M | 0.389 | 100 | 41 | 1.7 | 12.4 | 3.35 | |
aniline | C6H7N | 184.4 | -6.0 | 1.022 | 3.4 | 0.420 | 2 | 0.4 | 1.6 | 6.8 | 3.8 | |
dimethylsulfoxide (DMSO) | C2H6OS | 189 | 18.4 | 1.092 | M | 0.444 | 0.75 | 0.61* | 3.9 | 46.7 | 2.00 | |
acetonitrile | C2H3N | 81.6 | -46 | 0.786 | M | 0.460 | 0.65 | 20 | 97 | 3.5 | 37.5 | 0.34 |
3-pentanol | C5H12O | 115.3 | -8 | 0.821 | 5.1 | 0.463 | 8.8* | 1.7 | 13.3 | |||
2-pentanol | C5H12O | 119.0 | -50 | 0.810 | 4.5 | 0.488 | 6.1* | 1.7 | 13.7 | 3.5 | ||
2-butanol | C4H10O | 99.5 | -114.7 | 0.808 | 18.1 | 0.506 | 100 | 18.3* | 1.7 | 17.3 | 3.1 | |
cyclohexanol | C6H12O | 161.1 | 25.2 | 0.962 | 4.2 | 0.509 | 50 | 1.2 | 1.9 | 15 | ||
1-octanol | C8H18O | 194.4 | -15 | 0.827 | 0.096 | 0.537 | 1.7 | 10.3 | 7.4 | |||
2-propanol | C3H8O | 82.4 | -88.5 | 0.785 | M | 0.546 | 0.82 | 400 | 44 | 1.66 | 19 | 2.07 |
1-heptanol | C7H16O | 176.4 | -35 | 0.819 | 0.17 | 0.549 | 1.7 | 12 | 6.0 | |||
i-butanol | C4H10O | 107.9 | -108.2 | 0.803 | 8.5 | 0.552 | 1.8 | 17.9 | 6.68 | |||
1-hexanol | C6H14O | 158 | -46.7 | 0.814 | 0.59 | 0.559 | 0.22* | 1.6 | 12.5 | 4.6 | ||
1-pentanol | C5H12O | 138.0 | -78.2 | 0.814 | 2.2 | 0.568 | 2.2* | 1.7 | 14 | 3.5 | ||
acetyl acetone | C5H8O2 | 140.4 | -23 | 0.975 | 16 | 0.571 | 3 | 3.0 | 23 | 0.6 | ||
ethyl acetoacetate | C6H10O3 | 180.4 | -80 | 1.028 | 2.9 | 0.577 | 0.78* | |||||
1-butanol | C4H10O | 117.6 | -89.5 | 0.81 | 7.7 | 0.586 | 20 | 6.3 | 1.7 | 17.5 | 2.59 | |
benzyl alcohol | C7H8O | 205.4 | -15.3 | 1.042 | 3.5 | 0.608 | 0.094* | 1.7 | 13 | 5.47 | ||
1-propanol | C3H8O | 97 | -126 | 0.803 | M | 0.617 | 0.82 | 21* | 1.68 | 22 | 1.95 | |
acetic acid | C2H4O2 | 118 | 16.6 | 1.049 | M | 0.648 | >1 | 10 | 15.3 | 1.68 | 6.2 | 1.12 |
2-aminoethanol | C2H7NO | 170.9 | 10.5 | 1.018 | M | 0.651 | 3 | 0.53 | 2.3 - 2.6 | 37.7 | 20.8 | |
ethanol | C2H6O | 78.5 | -114.1 | 0.789 | M | 0.654 | 0.88 | 1000 | 59 | 1.7 | 24 | 1.08 |
diethylene glycol | C4H10O3 | 245 | -10 | 1.118 | M | 0.713 | 0.027 | 2.3 | 31.8 | 30.2 | ||
methanol | CH4O | 64.6 | -98 | 0.791 | M | 0.762 | 0.95 | 200 | 128 | 1.6 | 33 | 0.54 |
ethylene glycol | C2H6O2 | 197 | -13 | 1.115 | M | 0.790 | 1.11 | 2.3 | 37.7 | 16.1 | ||
glycerin | C3H8O3 | 290 | 17.8 | 1.261 | M | 0.812 | 2.7 | 42.5 | 934 | |||
water, heavy | D2O | 101.3 | 4 | 1.107 | M | 0.991 | 15 | 1.84 | 78.3 | 1.10 | ||
water | H2O | 100.00 | 0.00 | 0.998 | M | 1.000 | >>1 | 17.5 | 1.85 | 80.1 | 0.89 |
A. Elements - Periodic Tables - WebElements -
http://www.webelements.com/
http://murov.info/aufbaupt.htm
http://murov.info/periodictables.htm
http://murov.info/pertabtrends.htm
http://murov.info/pertabtrends.pptx
Directory
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Periodic table with history of elements -
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Chronology of the development of the
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History of elements and periodic table -
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Properties of the elements -
http://www.knowledgedoor.com/
B. Compounds - Properties
1.
Tabulation
Murov - http://murov.info/orgcmpds.htm
WolframAlpha - http://www.wolframalpha.com/
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ChemSynthesis -
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Kaye and Laby - organic -https://web.archive.org/web/20190519191800/http://www.kayelaby.npl.co.uk/chemistry/3_3/3_3.html
inorganic -
https://web.archive.org/web/20190502165701/http://www.kayelaby.npl.co.uk/chemistry/3_2/3_2.html
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PubChem - https://pubchem.ncbi.nlm.nih.gov/
Osha -
https://www.osha.gov/chemicaldata/
Shriner,
et.al, Systematic Identification of Organic Compounds, manual for
identifying organic compounds especially with the use of derivatives,
includes tables of common organic compounds with melting or boiling points and
melting points of derivatives in tables at back.
https://celqusb.files.wordpress.com/2018/04/kupdf-com_systematic-identification-of-organic-compounds-wiley-shrinerhermannmorrillcurtinfuson.pdf
2.
Tabulation +
MSDS
Acros,
Fisher
-
https://www.fishersci.com/us/en/brands/I9C8LQ1I/acros-organics.html
Alpha Chemical
-
https://www.alfa.com/en/chemicals/
ChemExper Chem. Directory
- http://www.chemexper.com/
Chemidplus
-
https://chem.nlm.nih.gov/chemidplus/
https://chem.nlm.nih.gov/chemidplus/chemidlite.jsp
Chemindex - http://ccinfoweb.ccohs.ca/chemindex/search.html
Chemspider - http://www.chemspider.com/
http://www.chemspider.com/SimpleSearch.aspx
EMD Chemicals -
http://www.emdmillipore.com/US/en/documents/Z.qb.qB.tecAAAFDDJUsznLq,nav
TCI America -
http://www.tcichemicals.com/en/us/support-download/brochure/catalog.html
Wikipedia -
https://en.wikipedia.org/wiki/Dictionary_of_chemical_formulas
https://en.wikipedia.org/wiki/List_of_inorganic_compounds
Chemical Book - http://www.chemicalbook.com/
3.
MSDS or SDS
Aldrich, Sigma,-
https://www.sigmaaldrich.com/united-states.html
MSDS Solutions - http://www.msds.com/
Vermont Safety Information Resources, Inc. - http://hazard.com/msds/
MSDSprovider - http://www.msdsprovider.com/
MSDS online - https://www.msdsonline.com/
MSDS digital -
https://www.msdsdigital.com/msds-database
Fisher -
https://www.fishersci.com/us/en/catalog/search/sdshome.html
EHSO - http://ehso.com/msds-sds.php
C. Search for Compounds from
Properties
Aldrich -
http://www.sigmaaldrich.com/catalog/search/substructure/OldSubstructureSearchPage
accepts - formula, structure,
molecular mass, mp, bp, density
ChemExper Chem Directory - http://www.chemexper.com/advanced_search.shtml
accepts - formula,
structure, molecular mass, bp, mp, refractive index, density, ir,
nmr
ChemNet Data Base http://poc.chemnetbase.com/faces/chemical/ChemicalSearch.xhtml
accepts formula, melting point, boiling point
Chemspider -
http://www.chemspider.com/FullSearch.aspx
accepts - formula, molecular mass
Melting point and
molecular mass search:
https://chem.nlm.nih.gov/chemidplus/
accepts - formula, mp,
bp
Murov - http://murov.info/orgcmpds.htm
search by molecular mass, bp, mp, density, refractiive index
Organic Chemistry Data Base - http://www.colby.edu/chemistry/cmp/cmp.html
accepts -
formula, molecular
mass, mp, bp, density, refractive index, ir, ms
NIMC site -
http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng
accepts -
formula, molecular mass,
ir, nmr, ms
Polymers -
http://www.matweb.com/search/PropertySearch.aspx
Knovel Critical Tables (If using Explorer, it must be newest version)
(21824 compounds in sortable tables) - login required -
initial registration or login:
https://app.knovel.com/web/register.v
already registered login:
click on or copy and paste:
https://app.knovel.com/web/view/itable/show.v/rcid:kpKCTE000X/cid:kt002VLXT1/viewerType:itble/
To filter the listing, click on the triangle
following the desirred parameter, select filter and then enter the limits of the
desired parameter (<, > or =) and hit enter.
(7274 Compounds in sortable tables) -
https://app.knovel.com/web/view/itable/show.v/rcid:kpKS000009/cid:kt00395F16/viewerType:itble/
D. Solvent Properties
http://murov.info/orgsolvents.htm
http://murov.info/orgsolvsort.htm
https://www.organicdivision.org/ama/orig/organic_solvents.html
http://www.stenutz.eu/chem/
http://www.wiredchemist.com/chemistry/data/physical_character_solvents.html
https://www2.chemistry.msu.edu/faculty/reusch/OrgPage/solvent.htm
https://www.sigmaaldrich.com/chemistry/stockroom-reagents/learning-center/technical-library/solvent-properties.html
https://en.wikipedia.org/wiki/Solvent
https://www.ch.ic.ac.uk/williams/Solvent%20properties.pdf
Knovel Critical Tables (If using Explorer, it must be newest version)
(21824 compounds in sortable tables) - login required -
initial registration or login:
https://app.knovel.com/web/register.v
already registered login:
click on or copy and paste:
https://app.knovel.com/web/view/itable/show.v/rcid:kpKCTE000X/cid:kt002VLY34/viewerType:itble/
To filter the listing, click on the triangle
following the desirred parameter, select filter and then enter the limits of the
desired parameter (<, > or =) and hit enter.
ChemSynthesis -
https://www.chemsynthesis.com/
nmr of deuterated
solvents
http://www.wiredchemist.com/chemistry/data/common_nmr_solvents.html
http://www2.chem.umd.edu/nmr/reference/isotope_solvent.pdf
E. Chemical Education Journals
J. Chem. Ed.
- http://pubs.acs.org/journal/jceda8
http://pubs.acs.org/loi/jceda8
Education in Chemistry - http://www.rsc.org/eic/
http://www.rsc.org/eic/e-magazine
Chem13 News -
https://uwaterloo.ca/chem13-news-magazine/
F. Chemistry Directory -
https://organicchemistrydata.org/
http://murov.info/webercises.htm
G. Organic Chemistry Directory -
http://murov.info/orgchemres.htm
H. Reaction-Map of Organic Chemistry - http://murov.info/Reaction-Map.htm
Exercise based on the above -
http://murov.info/orgchemrxnexe.htm
I. Literature search -
http://www.researchgate.net/
J. Spectra
1. IR - Liquid or Solution
NIMC site -
http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi
NIST site - http://webbook.nist.gov/chemistry/
PSLC -
http://pslc.uwsp.edu/
Aldrich, Sigma -
https://www.sigmaaldrich.com/united-states.html
Gasmet -
https://www.gasmet.com/de/products/tools/spectrum-library/
2. IR - Gas Phase
NIST - http://webbook.nist.gov/chemistry/
Gasmet -
https://www.gasmet.com/de/products/tools/spectrum-library/
3.. HNMR - Experimental
NIMC site -
http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng
PSLC -
http://pslc.uwsp.edu/
Aldrich, Sigma -
https://www.sigmaaldrich.com/united-states.html
Solvents -
http://www2.chem.umd.edu/nmr/reference/isotope_solvent.pdf
Deuterated solvents - http://www.wiredchemist.com/chemistry/data/common_nmr_solvents.html
bioorganics - http://mmcd.nmrfam.wisc.edu/mmcdbrowse.html
4. HNMR - Calculated
ChemExper Chem Directory - http://www.chemexper.com/
nmrdb - http://www.nmrdb.org/
5. 13CNMR - Experimental
NIMC site -
http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng
PSLC -
http://pslc.uwsp.edu/
6. Mass
NIMC site - http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng
PSLC -
http://pslc.uwsp.edu/
Pherobase - http://www.pherobase.com/database/compound/compounds-index.php
human metabolites -
http://www.hmdb.ca/
7. UV-Vis
NIST site - http://webbook.nist.gov/chemistry/
OMLC - http://omlc.org/spectra/PhotochemCAD/html/alpha.html
8. Bibliography -
http://library.buffalo.edu/libraries/asl/guides/spectra.html
9. Polymer spectra - http://pslc.uwsp.edu/
10. Photophysical properties of organic compounds - http://murov.info/photophys.htm
11. Fee based KnowItAll spectral database - https://sciencesolutions.wiley.com/knowitall-u/
1. Acid Base Indicator properties
https://www.compoundchem.com/2014/04/04/the-colours-chemistry-of-ph-indicators/
https://en.wikipedia.org/wiki/PH_indicator
https://www.sciencecompany.com/ph_indicator_ranges.aspx
https://www.thoughtco.com/edible-ph-indicators-color-chart-603655
https://www.techknow.org.uk/wiki/index.php?title=PH
http://foundoutaboutchemistry.blogspot.com/2016/05/acid-base-indicator-charts.html
2. Electronegativities
http://www.meta-synthesis.com/webbook/36_eneg/electroneg.html
http://www.knowledgedoor.com/
https://periodictable.me/electronegativity-chart/
3. pKa values
https://www2.chem.wisc.edu/areas/reich/pkatable/index.htm
http://www.wiredchemist.com/chemistry/data/acid_constants.html
http://www.wiredchemist.com/chemistry/data/base_constants.html
http://www.zirchrom.com/organic.htm
http://ccc.chem.pitt.edu/wipf/MechOMs/evans_pKa_table.pdf
4. Hammett constants
http://www.wiredchemist.com/chemistry/data/hammett_sigma_constants.html
http://old.iupac.org/publications/pac/1997/pdf/6912x2497.pdf
Virtual Textbooks of Organic Chemistry
https://www.masterorganicchemistry.com/
https://www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/intro1.htm
https://www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/intro1a.htm
https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Book%3A_Virtual_Textbook_of_OChem_(Reusch)_UNDER_CONSTRUCTION
http://www.ochem.com
http://www.chemthes.com/rxn-type.php
http://www.chemguide.co.uk/orgpropsmenu.html
http://chemwiki.ucdavis.edu/Organic_Chemistry
http://en.wikibooks.org/wiki/Organic_Chemistry
http://www.stolaf.edu/depts/chemistry/courses/toolkits/247/
organic
lab book - http://murov.info/orglab/orglab.htm
Other websites by this author are available at: http://murov.info/
Organic chemistry web sites by this author include:
Organic chemistry milestones: http://murov.info/organicmilestones.htm
Organic chemistry directory: http://murov.info/orgchemres.htm
Online organic laboratory text: http://murov.info/orglab/orglab.htm
Organic chemistry exercises (also included in organic laboratory text): http://murov.info/orglab/exercises.htm
For a larger image and the keys for the Reaction-Map of Organic Chemistry, please visit: http://murov.info/Reaction-Map.htm . For exercise based on the reaction-map, please visit: http://murov.info/orgchemrxnexe.htm .
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