1-Octanamine, n-octyl-

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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
287.65Sudaricov, Phrolov, et al., 1963Metastable crystal phase; Uncertainty assigned by TRC = 2. K; TRC
296.65Sudaricov, Phrolov, et al., 1963Uncertainty assigned by TRC = 1.4 K; TRC
283.45Carroll and Wright, 1948Uncertainty assigned by TRC = 2. K; TRC
287.77Hoerr, Harwood, et al., 1946Uncertainty assigned by TRC = 0.3 K; TRC
287.75Hoerr, Harwood, et al., 1944Uncertainty assigned by TRC = 0.5 K; TRC
307.15Ueno and Takase, 1941Uncertainty assigned by TRC = 5. K; TRC
308.15Westphal and Jerchel, 1940Uncertainty assigned by TRC = 5. K; TRC
309.15Von Braun, 1937Uncertainty assigned by TRC = 5. K; TRC
309.65Merz and Gasiorowski, 1884Uncertainty assigned by TRC = 5. K; TRC

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


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.

Sudaricov, Phrolov, et al., 1963
Sudaricov, B.N.; Phrolov, U.G.; Ilichev, V.A.I.; Pushcov, A.A.; Zaharov-Narcissov, O.I.; Ochkin, A.B., Physicochemical Properties of Certain n-Aliphatic Amines, Tr. Inst. - Mosk. Khim. -Tekhnol. Inst. im. D. I. Mendele- eva, 1963, 43, 21. [all data]

Carroll and Wright, 1948
Carroll, K.K.; Wright, G.F., Catalyzed Nitration of Amines. VI. Nitration of Dioctylamine., Can. J. Res., Sect. B, 1948, 26, 271. [all data]

Hoerr, Harwood, et al., 1946
Hoerr, C.W.; Harwood, H.J.; Ralston, A.W., Dimorphism of Symmetrical Normal Aliphatic Secondary Amines of High Molecular Weight., J. Org. Chem., 1946, 11, 199. [all data]

Hoerr, Harwood, et al., 1944
Hoerr, C.W.; Harwood, H.J.; Ralston, A.W., Solubilities of High-Molecular-Weight Symmetrical Normal Aliphatic Secondary Amines., J. Org. Chem., 1944, 9, 201-10. [all data]

Ueno and Takase, 1941
Ueno, S.; Takase, S., Reduction of Aliphatic Acid Amides Under High Pressure., Kogyo Kagaku Zasshi, 1941, 44, 30. [all data]

Westphal and Jerchel, 1940
Westphal, O.; Jerchel, D., Reaction of Higher 1-Chloroparaffins With Ammonia, Primary, Secondary, and Tertiary Amines., Chem. Ber., 1940, 73, 1002. [all data]

Von Braun, 1937
Von Braun, J., Chem. Ber., 1937, 70, 983. [all data]

Merz and Gasiorowski, 1884
Merz, V.; Gasiorowski, K., Chem. Ber., 1884, 17, 623. [all data]


Notes

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