3-Pentanol, 3-ethyl-
- Formula: C7H16O
- Molecular weight: 116.2013
- IUPAC Standard InChIKey: XKIRHOWVQWCYBT-UHFFFAOYSA-N
- CAS Registry Number: 597-49-9
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
View 3d structure (requires JavaScript / HTML 5) - Other names: Triethylcarbinol; Triethylmethanol; 3-Ethyl-3-pentanol; 3-Aethyl-pentanol-(3); 3-Ethyl-3-hydroxypentane; Ethyl-3 pentanol-3; 3-ethylpentan-3-ol
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Normal boiling 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
Tboil (K) | Reference | Comment |
---|---|---|
415.65 | Hillman, 1962 | Uncertainty assigned by TRC = 4. K; TRC |
414.15 | Viehe and Reinstein, 1962 | Uncertainty assigned by TRC = 3. K; TRC |
416.15 | Hamelin, 1961 | Uncertainty assigned by TRC = 3. K; TRC |
415.65 | Lanning and Moore, 1958 | Uncertainty assigned by TRC = 3. K; TRC |
415.15 | Dashkevich and Bratchanskii, 1957 | Uncertainty assigned by TRC = 3. K; TRC |
410.15 | Searles, Pollart, et al., 1957 | Uncertainty assigned by TRC = 5. K; TRC; Data excluded from overall average |
416. | Sager and Bradley, 1956 | Uncertainty assigned by TRC = 3. K; TRC |
414.65 | Sager, 1956 | Uncertainty assigned by TRC = 3. K; TRC |
414.15 | Soehring, Frey, et al., 1955 | Uncertainty assigned by TRC = 3. K; TRC |
415.25 | Pichler, Ziesecke, et al., 1950 | Uncertainty assigned by TRC = 2. K; TRC |
414.65 | Milas and Perry, 1946 | Uncertainty assigned by TRC = 3. K; TRC |
416.3 | Ginnings and Hauser, 1938 | Uncertainty assigned by TRC = 1. K; TRC |
413.15 | Boeseken and Wildschut, 1932 | Uncertainty assigned by TRC = 3. K; TRC |
413.65 | Moyer and Marvel, 1931 | Uncertainty assigned by TRC = 3. K; TRC |
414.15 | Edgar, Calingaert, et al., 1929 | Uncertainty assigned by TRC = 3. K; TRC |
414.15 | Davies and Kipping, 1911 | Uncertainty assigned by TRC = 3. K; TRC |
References
Go To: Top, Normal boiling point, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hillman, 1962
Hillman, M.E.D.,
J. Am. Chem. Soc., 1962, 84, 4715. [all data]
Viehe and Reinstein, 1962
Viehe; Reinstein,
Chem. Ber., 1962, 95, 2557. [all data]
Hamelin, 1961
Hamelin, R.,
Etude des solutions organomagnesiennes mixtures. (5e memoire) action des derives de grinard sur les aldehydes,
Bull. Soc. Chim. Fr., 1961, 1961, 926. [all data]
Lanning and Moore, 1958
Lanning; Moore,
J. Org. Chem., 1958, 23, 288. [all data]
Dashkevich and Bratchanskii, 1957
Dashkevich; Bratchanskii,
Nauk. Zap. Uzhgorod. Derzh. Univ., 1957, 22, 119. [all data]
Searles, Pollart, et al., 1957
Searles, S.; Pollart, K.A.; Lutz, E.F.,
Oxetanes: vi reductive cleavage and substituent effects,
J. Am. Chem. Soc., 1957, 79, 948-51. [all data]
Sager and Bradley, 1956
Sager, W.F.; Bradley, A.,
Oxidation of Trriethylmethane and Other Hydrocarbons by Acidified Dichromate,
J. Am. Chem. Soc., 1956, 78, 1187. [all data]
Sager, 1956
Sager, W.F.,
J. Am. Chem. Soc., 1956, 78, 4970. [all data]
Soehring, Frey, et al., 1955
Soehring, K.; Frey, H.H.; Endres, G.,
The correlation between structure and behavior of tertiary alcohols,
Arzneim.-Forsch., 1955, 5, 161-5. [all data]
Pichler, Ziesecke, et al., 1950
Pichler, H.; Ziesecke, K.H.; Traeger, B.,
The Oxygen-containing Compounds, Especially Alcohols, Formed in Isosynthesis,
Brennst.-Chem., 1950, 31, 361. [all data]
Milas and Perry, 1946
Milas, N.A.; Perry, L.H.,
J. Am. Chem. Soc., 1946, 68, 1938. [all data]
Ginnings and Hauser, 1938
Ginnings, P.M.; Hauser, M.,
Aqueous solubilities of some isomeric heptanols,
J. Am. Chem. Soc., 1938, 60, 2581-2582. [all data]
Boeseken and Wildschut, 1932
Boeseken, J.; Wildschut, A.J.,
The Action of Benzoyl Peroxide on Trimethylmethane,
Recl. Trav. Chim. Pays-Bas, 1932, 51, 168. [all data]
Moyer and Marvel, 1931
Moyer; Marvel,
Org. Synth., 1931, 11, 98. [all data]
Edgar, Calingaert, et al., 1929
Edgar, G.; Calingaert, G.; Marker, R.E.,
Preparation and Properties of the Isomeric Heptanes I. Preparation Preparation.,
J. Am. Chem. Soc., 1929, 51, 1483. [all data]
Davies and Kipping, 1911
Davies; Kipping,
J. Chem. Soc., 1911, 99, 296. [all data]
Notes
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- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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