2-Naphthalenamine
- Formula: C10H9N
- Molecular weight: 143.1852
- IUPAC Standard InChIKey: JBIJLHTVPXGSAM-UHFFFAOYSA-N
- CAS Registry Number: 91-59-8
- 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: 2-Naphthylamine; β-Naphthylamine; C.I. 37270; Fast Scarlet Base B; 2-Aminonaphthalene; 2-Aminonaftalen; β-naftyloamina; β-Naftalamin; β-Naftilamina; 2-Naftylamin; 2-Naftylamine; 2-Naphthalamine; β-Naftylamin; β-Naphthylamin; 2-Naphthylamin; 6-Naphthylamine; RCRA waste number U168; UN 1650; USAF CB-22
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Normal melting point
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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 |
---|---|---|
386.15 | Khetarpal, Lal, et al., 1979 | Uncertainty assigned by TRC = 1.5 K; TRC |
385.15 | Karyakin, Rabinovich, et al., 1968 | Uncertainty assigned by TRC = 1. K; TRC |
381.15 | Snyder, Elston, et al., 1953 | Uncertainty assigned by TRC = 2. K; TRC |
383.15 | Bastic and Pushin, 1947 | Uncertainty assigned by TRC = 2. K; TRC |
383. | Butterworth and Hey, 1940 | Uncertainty assigned by TRC = 5. K; TRC |
383.15 | Cowley and Partington, 1938 | Uncertainty assigned by TRC = 0.4 K; TRC |
382.7 | Skau, 1935 | Uncertainty assigned by TRC = 0.2 K; TRC |
383.3 | Lee and Jones, 1922 | Uncertainty assigned by TRC = 0.25 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.
Khetarpal, Lal, et al., 1979
Khetarpal, S.C.; Lal, K.; Bhatnagar, H.L.,
Thermodynamic Studies on Melting of Some α- and β-Derivitives of Naphthalene,
Aust. J. Chem., 1979, 32, 49. [all data]
Karyakin, Rabinovich, et al., 1968
Karyakin, N.V.; Rabinovich, I.B.; Pakhomov, L.G.,
Heats of sublimation of naphthalene and its monosubstituted beta-derivative,
Zh. Fiz. Khim., 1968, 42, 1814-6. [all data]
Snyder, Elston, et al., 1953
Snyder, H.R.; Elston, C.T.; Kellom, D.B.,
Phosphoric acid as a reagent in organic chemistry. IV conversion of aromatic acids and their derivatives to amines.,
J. Am. Chem. Soc., 1953, 75, 2014. [all data]
Bastic and Pushin, 1947
Bastic, B.L.; Pushin, N.A.,
Melting diagrams of mixtures of formic acid,
Glas. Hem. Drus. Beograd, 1947, 128, 109. [all data]
Butterworth and Hey, 1940
Butterworth, E.C.; Hey, D.H.,
Nuclear Alkylation of Aromatic Bases. IV. The Action of Dodecyl Alcohol on the Hydrochlorides of alpha- and beta- Naphthylamine.,
J. Chem. Soc., 1940, 1940, 388. [all data]
Cowley and Partington, 1938
Cowley, E.G.; Partington, J.R.,
Studies in Dielectric Polarisations. Part XXIV. The Solvent Effect on the Dipole Moments of Some Amines.,
J. Chem. Soc., 1938, 1938, 1598. [all data]
Skau, 1935
Skau, E.L.,
Purification and physical properties of organic compounds. IX. Some binary freezing point diagrams and a study of their ideality.,
J. Phys. Chem., 1935, 39, 761. [all data]
Lee and Jones, 1922
Lee, H.R.; Jones, D.O.,
The Analysis of beta-naphthylamine.,
J. Ind. Eng. Chem., 1922, 14, 961. [all data]
Notes
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- Symbols used in this document:
Tfus Fusion (melting) point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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