Diphenylmethane
- Formula: C13H12
- Molecular weight: 168.2344
- IUPAC Standard InChIKey: CZZYITDELCSZES-UHFFFAOYSA-N
- CAS Registry Number: 101-81-5
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Benzene, 1,1'-methylenebis-; Methane, diphenyl-; Benzene, (phenylmethyl)-; Benzylbenzene; Ditan; Ditane; Benzene, benzyl-; Toluene, α-phenyl-; 1,1'-Dimethylenebis(benzene); NSC 4708
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Data at other public NIST sites:
- Options:
Data at NIST subscription sites:
NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.
Normal melting point
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
Tfus (K) | Reference | Comment |
---|---|---|
571.4 | Lee, Chen, et al., 1999 | Uncertainty assigned by TRC = 0.3 K; TRC; Data excluded from overall average |
298.21 | Powell and Swinton, 1968 | Uncertainty assigned by TRC = 0.15 K; TRC |
298.170 | Duff and Everett, 1956 | Crystal phase 1 phase; Uncertainty assigned by TRC = 0.1 K; TRC |
300.2 | Al-Mahdi and Ubbelohde, 1953 | Uncertainty assigned by TRC = 0.7 K; TRC |
298.2 | Bright, 1951 | Uncertainty assigned by TRC = 1. K; TRC |
298.35 | Serijan and Wise, 1951 | Uncertainty assigned by TRC = 0.15 K; TRC |
298.8 | Wender, Greenfield, et al., 1951 | Uncertainty assigned by TRC = 3. K; TRC |
299.2 | Wender, Greenfield, et al., 1951 | Uncertainty assigned by TRC = 3. K; TRC |
299.65 | Kurbatov, 1950 | Crystal phase 1 phase; Uncertainty assigned by TRC = 0.5 K; TRC |
298.3 | Parks and Mosley, 1950 | Uncertainty assigned by TRC = 0.3 K; TRC |
25.20 | Wise, Serijan, et al., 1950 | Uncertainty assigned by TRC = 0.2 K; TRC; Data excluded from overall average |
299. | Foehr and Fenske, 1949 | Uncertainty assigned by TRC = 2. K; TRC |
299.8 | Smith, Alderman, et al., 1949 | Uncertainty assigned by TRC = 0.5 K; TRC |
298.25 | Parks, West, et al., 1946 | Uncertainty assigned by TRC = 0.3 K; TRC |
298. | Vavon, Chaminade, et al., 1945 | Uncertainty assigned by TRC = 3. K; TRC |
300.15 | Nazarova and Tsukervanik, 1944 | Uncertainty assigned by TRC = 2. K; TRC |
298.40 | Hennion and Kurtz, 1943 | Uncertainty assigned by TRC = 3. K; TRC |
301. | Wibaut, Overhoff, et al., 1943 | Uncertainty assigned by TRC = 3. K; TRC |
298.0 | Ju, Wood, et al., 1942 | Uncertainty assigned by TRC = 0.7 K; TRC |
299. | Bredereck, Lehmann, et al., 1939 | Uncertainty assigned by TRC = 2. K; TRC |
298.24 | De Vries and Strow, 1939 | Uncertainty assigned by TRC = 0.02 K; TRC |
297.7 | Ardaliani, 1938 | Uncertainty assigned by TRC = 2. K; TRC |
299. | Wolf and Weghofer, 1938 | Uncertainty assigned by TRC = 2. K; TRC |
299. | Busch and Weber, 1936 | Uncertainty assigned by TRC = 2. K; TRC |
299. | Lal and Dutt, 1935 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Sharma and Dutt, 1935 | Uncertainty assigned by TRC = 3. K; TRC |
298.7 | Sreerangachar and Sreenivasulu, 1935 | Uncertainty assigned by TRC = 0.2 K; TRC |
299. | Hurd, Christ, et al., 1933 | Uncertainty assigned by TRC = 2. K; TRC |
300. | Bergman, Engel, et al., 1932 | Uncertainty assigned by TRC = 2. K; TRC |
298.0 | Hare and Mack, 1932 | Uncertainty assigned by TRC = 1. K; TRC |
298.4 | Parks and Huffman, 1931 | Uncertainty assigned by TRC = 0.5 K; TRC |
298.20 | Smith and Andrews, 1931 | Uncertainty assigned by TRC = 0.5 K; melt. pt with Hg therm.; TRC |
298.30 | Smith and Andrews, 1931 | Uncertainty assigned by TRC = 0.3 K; f. p. by thermocouple; TRC |
297. | Vanscheidt and Moldavski, 1931 | Uncertainty assigned by TRC = 3. K; TRC |
297.7 | Wittig, 1931 | Uncertainty assigned by TRC = 3. K; TRC |
300. | Zelinskii and Gaverdovskaya, 1931 | Uncertainty assigned by TRC = 2. K; TRC |
298.40 | Huffman, Parks, et al., 1930 | Uncertainty assigned by TRC = 0.1 K; TRC |
299.7 | Sornet, 1929 | Uncertainty assigned by TRC = 2. K; TRC |
300.15 | Adams and Marshall, 1928 | Uncertainty assigned by TRC = 1. K; TRC |
297. | Foeldi, 1928 | Uncertainty assigned by TRC = 3. K; TRC |
297. | Foldi, 1928 | Uncertainty assigned by TRC = 3. K; TRC |
298. | Stadnikov and Kashtanov, 1928 | Uncertainty assigned by TRC = 3. K; TRC |
298.7 | Castille, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
299. | Kubota and Hayashi, 1926 | Uncertainty assigned by TRC = 2. K; TRC |
297.7 | Olivier, 1926 | Uncertainty assigned by TRC = 3. K; TRC |
298.7 | Shorygin, 1926 | Uncertainty assigned by TRC = 2. K; TRC |
298.7 | Zelinskii, Tits, et al., 1926 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Staudinger and Rheiner, 1924 | Uncertainty assigned by TRC = 2. K; TRC |
297.40 | Stratton and Partington, 1924 | Uncertainty assigned by TRC = 3. K; TRC |
297. | Steinkopf and Wolfram, 1923 | Uncertainty assigned by TRC = 3. K; TRC |
299.3 | Mortimer, 1922 | Uncertainty assigned by TRC = 2. K; TRC |
299.7 | Von Auwers and Fruhling, 1921 | Uncertainty assigned by TRC = 3. K; TRC |
297.1 | Kremann and Fritsch, 1920 | Uncertainty assigned by TRC = 3. K; TRC |
297. | Kremann and Fritsch, 1920 | Uncertainty assigned by TRC = 3. K; TRC |
297.0 | Kremann and Fritsch, 1920 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Kotyukov, 1915 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Kurnakov, Oksmann, et al., 1915 | Uncertainty assigned by TRC = 3. K; TRC |
300. | Sabatier and Murat, 1915 | Uncertainty assigned by TRC = 2. K; TRC |
300. | Sabatier and Murat, 1914 | Uncertainty assigned by TRC = 2. K; TRC |
298.7 | Biltz and Seydel, 1913 | Uncertainty assigned by TRC = 2. K; TRC |
300. | Sabatier and Murat, 1913 | Uncertainty assigned by TRC = 2. K; TRC |
299.3 | Tammann, 1913 | Uncertainty assigned by TRC = 1. K; TRC |
300.19 | Block, 1912 | Uncertainty assigned by TRC = 0.5 K; TRC |
300. | Hilditch and Dunstan, 1912 | Uncertainty assigned by TRC = 1.5 K; TRC |
299.15 | Wolff, 1912 | Uncertainty assigned by TRC = 1. K; TRC |
299. | Mascarelli and Musatty, 1911 | Uncertainty assigned by TRC = 2. K; TRC |
300. | Busch and Fleischmann, 1910 | Uncertainty assigned by TRC = 2. K; TRC |
299. | Mascarelli and Musatty, 1910 | Uncertainty assigned by TRC = 2. K; TRC |
299.40 | Von Meyer, 1910 | Uncertainty assigned by TRC = 2. K; TRC |
299. | Vorlander and Siebert, 1906 | Uncertainty assigned by TRC = 2. K; TRC |
299.5 | Centnerszwer, 1903 | Uncertainty assigned by TRC = 1. K; TRC |
299.7 | Schmidlin, 1903 | Uncertainty assigned by TRC = 1.5 K; TRC |
297.60 | Paterno and Ampola, 1897 | Uncertainty assigned by TRC = 1. K; TRC |
299.6 | Anderlini, 1895 | Uncertainty assigned by TRC = 1. K; TRC |
298.8 | Miolati, 1892 | Uncertainty assigned by TRC = 1.5 K; TRC |
299.5 | Eykman, 1889 | Uncertainty assigned by TRC = 1.5 K; TRC |
299.8 | Eykman, 1889 | Uncertainty assigned by TRC = 1.5 K; TRC |
298. | Friedel and Crafts, 1887 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Engler, 1878 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Stadel, 1878 | Uncertainty assigned by TRC = 3. K; TRC |
299. | Doer, 1872 | Uncertainty assigned by TRC = 3. K; TRC |
297.7 | Zincke, 1871 | Uncertainty assigned by TRC = 3. K; TRC |
299.7 | Zincke, 1871, 2 | Uncertainty assigned by TRC = 3. K; TRC |
298. | Zincke, 1871, 2 | Uncertainty assigned by TRC = 2. K; TRC |
299.6 | Jena, 1870 | Uncertainty assigned by TRC = 2. K; TRC |
References
Go To: Top, Normal melting point, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Lee, Chen, et al., 1999
Lee, M.J.; Chen, C.-H.; Lin, H.-M.,
Solid-Liquid Equilibria for Binary Mixtures Composed of Acenaphthene, Dibenzofuran, Fluorene, Phenanthrene, and Diphenylmethane,
J. Chem. Eng. Data, 1999, 44, 1058-62. [all data]
Powell and Swinton, 1968
Powell, R.J.; Swinton, F.L.,
Excess Volumes of Mixing: Benzene-Cyclohexane and Benzene-Diphenylmethane Systems,
J. Chem. Eng. Data, 1968, 13, 260-2. [all data]
Duff and Everett, 1956
Duff, G.M.; Everett, D.H.,
The Heat Capacity of the System Benzene + Diphenylmethane,
Trans. Faraday Soc., 1956, 52, 753. [all data]
Al-Mahdi and Ubbelohde, 1953
Al-Mahdi, A.A.K.; Ubbelohde, A.R.,
Proc. R. Soc. London, A, 1953, 220, 143. [all data]
Bright, 1951
Bright, N.F.,
The Vapor Pressure of Biphenyl, Bibenzyl, and Diphenylmethane,
J. Chem. Soc., 1951, 1951, 624. [all data]
Serijan and Wise, 1951
Serijan, K.T.; Wise, P.H.,
Dicylic Hydrocarbons. III. Diphenyl- and Dicyclohexylalkanes through C15,
J. Am. Chem. Soc., 1951, 73, 4766. [all data]
Wender, Greenfield, et al., 1951
Wender, I.; Greenfield, H.; Orchin, M.,
Chemistry of Oxo and Related Reactions IV. Reductions in the Aromatic Series,
J. Am. Chem. Soc., 1951, 73, 2656. [all data]
Kurbatov, 1950
Kurbatov, V.Y.,
Specific heat of liquids. III. Specific heat of hydrocarbons with several noncondensed rings,
Zh. Obshch. Khim., 1950, 20, 1139. [all data]
Parks and Mosley, 1950
Parks, G.S.; Mosley, J.R.,
Redetermination of the heat of combustion of diphenylmethane,
J. Am. Chem. Soc., 1950, 72, 1850. [all data]
Wise, Serijan, et al., 1950
Wise, P.H.; Serijan, K.T.; Goodman, I.A.,
Correlation of Physical Properties with Molecular Structre for Dicyclic Hydrocarbons. I. 2-n-Alakylbiphenyl-1,1-alkane, α,ω-dicyclohexylalkane Series, Nat. Advis. Comm. Aeronaut., Tech. Notes, No. 2081, Lewis Flight Propulsion Lab., Cleveland, OH, 1950. [all data]
Foehr and Fenske, 1949
Foehr, E.G.; Fenske, M.R.,
Magneto-optic Rotation of Hydrocarbons,
Ind. Eng. Chem., 1949, 41, 1956. [all data]
Smith, Alderman, et al., 1949
Smith, H.A.; Alderman, D.M.; Shacklett, C.D.; Welch, C.M.,
The Catalytic Hydrogenation of the Benzene Nucleus VI. The Hydrogenation of Compounds with Two Benzene Rings,
J. Am. Chem. Soc., 1949, 71, 3772. [all data]
Parks, West, et al., 1946
Parks, G.S.; West, T.J.; Naylor, B.F.; Fujii, P.S.; McClaine, L.A.,
Thermal Data on Organic Compounds XXIII. Modern Combustion Data for Fourteen Hydrocarbons and Five Polyhydric Alcohols,
J. Am. Chem. Soc., 1946, 68, 2524. [all data]
Vavon, Chaminade, et al., 1945
Vavon, G.; Chaminade, C.; Quesnel, G.,
Action of Benzyl Bromide Upon (organic) Magnesium Compoundes,
C. R. Hebd. Seances Acad. Sci., 1945, 220, 850. [all data]
Nazarova and Tsukervanik, 1944
Nazarova, Z.N.; Tsukervanik, I.P.,
Alkylation of Aromatic Compounds with Alcohols in the Presence of Anhydrouys FeCl3,
Zh. Obshch. Khim., 1944, 14, 77. [all data]
Hennion and Kurtz, 1943
Hennion, G.F.; Kurtz, R.A.,
Some Friedel-Crafts Type ALkylations with Boron Trifluoride,
J. Am. Chem. Soc., 1943, 65, 1001. [all data]
Wibaut, Overhoff, et al., 1943
Wibaut, J.P.; Overhoff, J.; Jonker, E.W.,
On the Preparation of Some Hydrocarbons of the Mixed Aliphatic-Aromatic and Aliphatic-Alicyclic Type Containing 22 to 30 C-atoms,
Recl. Trav. Chim. Pays-Bas, 1943, 62, 31. [all data]
Ju, Wood, et al., 1942
Ju, T.Y.; Wood, C.E.; Garner, F.H.,
J. Inst. Pet., 1942, 28, 159. [all data]
Bredereck, Lehmann, et al., 1939
Bredereck, H.; Lehmann, G.; Schonfeld, C.; Fritzsche, E.,
Beryllium chloride in organic reactions,
Chem. Ber., 1939, 72, 1414. [all data]
De Vries and Strow, 1939
De Vries, T.; Strow, H.A.,
Diphenylmethane as a Thermometric Standeard,
J. Am. Chem. Soc., 1939, 61, 1796. [all data]
Ardaliani, 1938
Ardaliani, D.,
Zh. Obshch. Khim., 1938, 8, 1887. [all data]
Wolf and Weghofer, 1938
Wolf, K.L.; Weghofer, H.Z.,
Z. Phys. Chem. Abt. B, 1938, 39, 194. [all data]
Busch and Weber, 1936
Busch; Weber,
J. Prakt. Chem., 1936, 146, 1. [all data]
Lal and Dutt, 1935
Lal, J.B.; Dutt, S.,
J. Indian Chem. Soc., 1935, 12, 389. [all data]
Sharma and Dutt, 1935
Sharma, V.N.; Dutt, S.,
J. Indian Chem. Soc., 1935, 12, 774. [all data]
Sreerangachar and Sreenivasulu, 1935
Sreerangachar, H.B.; Sreenivasulu, M.,
Biochem. J., 1935, 29, 295. [all data]
Hurd, Christ, et al., 1933
Hurd, C.D.; Christ, R.; Thomas, C.L.,
J. Am. Chem. Soc., 1933, 55, 2589. [all data]
Bergman, Engel, et al., 1932
Bergman; Engel, E.L.; Wolff, H.A.,
Z. Phys. Chem., Abt. B, 1932, 17, 81. [all data]
Hare and Mack, 1932
Hare, W.A.; Mack, E., Jr.,
J. Am. Chem. Soc., 1932, 54, 4272. [all data]
Parks and Huffman, 1931
Parks, G.S.; Huffman, H.M.,
Some fusion and transition data for hydrocarbons,
Ind. Eng. Chem., 1931, 23, 1138-9. [all data]
Smith and Andrews, 1931
Smith, R.H.; Andrews, D.H.,
Thermal Energy Studies I. Phenyl Derivatives of Methane, Ethane and Some Related Compounds,
J. Am. Chem. Soc., 1931, 53, 3644. [all data]
Vanscheidt and Moldavski, 1931
Vanscheidt; Moldavski,
Chem. Ber., 1931, 64, 917. [all data]
Wittig, 1931
Wittig, G.,
Chem. Ber., 1931, 64, 437. [all data]
Zelinskii and Gaverdovskaya, 1931
Zelinskii, N.D.; Gaverdovskaya, M.V.,
Chem. Ber., 1931, 64, 435. [all data]
Huffman, Parks, et al., 1930
Huffman, H.M.; Parks, G.S.; Daniels, A.C.,
Thermal Data on Organic Compounds: VII The Heat Capacities, Entropies and Free Energies of Twelve Aromatic Hydrocarbons,
J. Am. Chem. Soc., 1930, 52, 1547-58. [all data]
Sornet, 1929
Sornet, R.,
Rev. Chim. Ind., 1929, 38, 8-10. [all data]
Adams and Marshall, 1928
Adams, R.; Marshall, J.R.,
The Use of Platinum-Oxide Platinum Black in the Catalytic Reduction of Aromatic Hydrocarbons XVII.,
J. Am. Chem. Soc., 1928, 50, 1970. [all data]
Foeldi, 1928
Foeldi, Z.,
Introduction of the Benzyk Group into the Benzene Nucleus with the Aid of Sulfonic Acid Esters,
Chem. Ber., 1928, 61B, 1609-16. [all data]
Foldi, 1928
Foldi, Z.,
Chem. Ber., 1928, 61, 1609. [all data]
Stadnikov and Kashtanov, 1928
Stadnikov, G.L.; Kashtanov, L.,
Chem. Ber., 1928, 61, 1389. [all data]
Castille, 1926
Castille, A.,
Bull. Cl. Sci., Acad. R. Belg., 1926, 12, 498. [all data]
Kubota and Hayashi, 1926
Kubota, B.; Hayashi, T.,
Bull. Chem. Soc. Jpn., 1926, 1, 67. [all data]
Olivier, 1926
Olivier, S.C.J.,
Recl. Trav. Chim. Pays-Bas, 1926, 45, 817. [all data]
Shorygin, 1926
Shorygin, P.,
Chem. Ber., 1926, 59, 2510. [all data]
Zelinskii, Tits, et al., 1926
Zelinskii, N.D.; Tits, I.N.; Gaverdovskaya, M.,
Chem. Ber., 1926, 59, 2590. [all data]
Staudinger and Rheiner, 1924
Staudinger; Rheiner,
Helv. Chim. Acta, 1924, 7, 8. [all data]
Stratton and Partington, 1924
Stratton, K.; Partington, J.R.,
Philos. Mag., 1924, 48, 1085. [all data]
Steinkopf and Wolfram, 1923
Steinkopf, W.; Wolfram, A.,
Justus Liebigs Ann. Chem., 1923, 430, 113. [all data]
Mortimer, 1922
Mortimer, F.S.,
J. Am. Chem. Soc., 1922, 44, 1416. [all data]
Von Auwers and Fruhling, 1921
Von Auwers, K.; Fruhling, A.,
The spectrochemistry of benzene derivatives, II Phenol & phenol ester,
Justus Liebigs Ann. Chem., 1921, 422, 192. [all data]
Kremann and Fritsch, 1920
Kremann; Fritsch,
Sitzungsber. Akad. Wiss. Wien, Math.-Naturwiss. Kl., Abt. 2B, 1920, 129, 633. [all data]
Kotyukov, 1915
Kotyukov, I.,
Zh. Russ. Fiz.-Khim. O-va., Chast Khim., 1915, 47, 1087. [all data]
Kurnakov, Oksmann, et al., 1915
Kurnakov, N.S.; Oksmann, M.; Beketov, I.; Perelmutter, S.I.; Kanov, F.P.; Finkel, I.,
Zh. Russ. Fiz.-Khim. O-va., Chast Khim., 1915, 47, 558. [all data]
Sabatier and Murat, 1915
Sabatier, P.; Murat, M.,
Ann. Chim. (Paris), 1915, 4, 253. [all data]
Sabatier and Murat, 1914
Sabatier, P.; Murat, M.,
C. R. Hebd. Seances Acad. Sci., 1914, 158, 760. [all data]
Biltz and Seydel, 1913
Biltz, H.; Seydel, K.,
Chem. Ber., 1913, 46, 138. [all data]
Sabatier and Murat, 1913
Sabatier, P.; Murat, M.,
C. R. Hebd. Seances Acad. Sci., 1913, 157, 1496. [all data]
Tammann, 1913
Tammann, G.,
Nachr. Ges. Wiss. Goettingen, Math.-Phys. Kl., 1913, 1913, 335. [all data]
Block, 1912
Block, H.,
Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1912, 78, 385. [all data]
Hilditch and Dunstan, 1912
Hilditch, T.P.; Dunstan, A.E.,
Ber. Bunsen-Ges. Phys. Chem., 1912, 18, 881. [all data]
Wolff, 1912
Wolff, L.,
Methods of Substituting An Oxygen Atom with Hydrogen in Ketones and Aldehydes,
Justus Liebigs Ann. Chem., 1912, 394, 86. [all data]
Mascarelli and Musatty, 1911
Mascarelli, L.; Musatty, I.,
Gazz. Chim. Ital., 1911, 1911, I, 103. [all data]
Busch and Fleischmann, 1910
Busch, M.; Fleischmann, M.,
Chem. Ber., 1910, 43, 740. [all data]
Mascarelli and Musatty, 1910
Mascarelli, L.; Musatty, I.,
Atti Accad. Naz. Lincei, Cl. Sci. Fis., Mat. Nat., Rend., 1910, 19, 213. [all data]
Von Meyer, 1910
Von Meyer, E.,
J. Prakt. Chem., 1910, 82, 538. [all data]
Vorlander and Siebert, 1906
Vorlander, D.; Siebert, C.,
Chem. Ber., 1906, 39, 1024. [all data]
Centnerszwer, 1903
Centnerszwer, M.,
About the Critical Temperatures of Solutions.,
Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1903, 46, 427. [all data]
Schmidlin, 1903
Schmidlin, J.,
Thermochemistry the substitution of phenyl in the phenylmethanes, their carbinols and chlorides,
C. R. Hebd. Seances Acad. Sci., 1903, 136, 1560-2. [all data]
Paterno and Ampola, 1897
Paterno, E.; Ampola, G.,
Gazz. Chim. Ital., 1897, 27, 481. [all data]
Anderlini, 1895
Anderlini, F.,
Gazz. Chim. Ital., 1895, 25, 127. [all data]
Miolati, 1892
Miolati, A.,
Z. Phys. Chem. (Leipzig), 1892, 9, 649. [all data]
Eykman, 1889
Eykman, J.F.,
Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1889, 4, 497. [all data]
Friedel and Crafts, 1887
Friedel, C.; Crafts, J.M.,
Ann. Chim. Phys., 1887, 11, 263. [all data]
Engler, 1878
Engler, C.,
Chem. Ber., 1878, 11, 926. [all data]
Stadel, 1878
Stadel, W.,
Justus Liebigs Ann. Chem., 1878, 194, 307. [all data]
Doer, 1872
Doer, W.H.,
Chem. Ber., 1872, 5, 795. [all data]
Zincke, 1871
Zincke, T.,
Chem. Ber., 1871, 4, 298. [all data]
Zincke, 1871, 2
Zincke, T.,
Justus Liebigs Ann. Chem., 1871, 159, 367. [all data]
Jena, 1870
Jena, A.,
Justus Liebigs Ann. Chem., 1870, 155, 77. [all data]
Notes
Go To: Top, Normal melting point, References
- Symbols used in this document:
Tfus Fusion (melting) point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.