1-Dodecanamine, N-dodecyl-
- Formula: C24H51N
- Molecular weight: 353.6684
- IUPAC Standard InChI: InChI=1S/C24H51N/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h25H,3-24H2,1-2H3
- IUPAC Standard InChIKey: MJCJUDJQDGGKOX-UHFFFAOYSA-N
- CAS Registry Number: 3007-31-6
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Didodecylamine; Alamine 204; Di-n-dodecylamine; Dilaurylamine
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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 |
|---|---|---|
| 328.65 | Schneider, Adkins, et al., 1952 | Uncertainty assigned by TRC = 2. K; TRC |
| 320.1 | Hoerr, Harwood, et al., 1946 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 320.05 | Hoerr, Harwood, et al., 1944 | Uncertainty assigned by TRC = 5. K; TRC |
| 325.15 | Ueno and Takase, 1941 | Uncertainty assigned by TRC = 6. K; TRC |
| 326.15 | Ueno, Takase, et al., 1941 | Uncertainty assigned by TRC = 6. K; TRC |
| 328.65 | Butterworth and Hey, 1940 | Uncertainty assigned by TRC = 8. K; TRC |
| 331.15 | Westphal and Jerchel, 1940 | Uncertainty assigned by TRC = 8. K; TRC |
| 317.55 | Wibaut, Heierman, et al., 1938 | Uncertainty assigned by TRC = 3. K; NOTE: This substance readily combines with carbonic acid when exposed to the air, giving impure substance which shows a higher freezing point.; TRC |
| 331.15 | Anonymous, 1937 | Uncertainty assigned by TRC = 6. K; TRC |
| 331.15 | Anonymous, 1935 | Uncertainty assigned by TRC = 8. K; TRC |
| 328.65 | Wojcik and Adkins, 1934 | Uncertainty assigned by TRC = 8. 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.
Schneider, Adkins, et al., 1952
Schneider, H.-J.; Adkins, H.; McElvain, S.M.,
The Hydrogenation of Amides and Ammonium Salts. The Transalkylation of Tertiary Amines,
J. Am. Chem. Soc., 1952, 74, 4287. [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]
Ueno, Takase, et al., 1941
Ueno, S.; Takase, S.; Tazima, Y.,
Reduction of Fatty Acid Amides Under High Pressure. III. Reduction of Anilides.,
Kogyo Kagaku Zasshi, 1941, 44, 58. [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]
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]
Wibaut, Heierman, et al., 1938
Wibaut, J.P.; Heierman, F.; Wagtendonk, H.M.,
Preparation of Dodecylamine and Didodecylamine From Dodecyl Chloride By Means of Anhydrous Liquid Ammonia.,
Recl. Trav. Chim. Pays-Bas, 1938, 57, 456. [all data]
Anonymous, 1937
Anonymous, P.,
, 1937. [all data]
Anonymous, 1935
Anonymous, P.,
, 1935. [all data]
Wojcik and Adkins, 1934
Wojcik, B.; Adkins, H.,
Catalytic Hydrogenation of Amides to Amines.,
J. Am. Chem. Soc., 1934, 56, 2419. [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
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