Propyl mercaptan
- Formula: C3H8S
- Molecular weight: 76.161
- IUPAC Standard InChIKey: SUVIGLJNEAMWEG-UHFFFAOYSA-N
- CAS Registry Number: 107-03-9
- 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: 1-Propanethiol; n-Propyl mercaptan; Propanethiol; 1-Propyl mercaptan; n-C3H7SH; Propane-1-thiol; 1-Mercaptopropane; 1-Propylthiol; n-Propylthiol; Propylthiol
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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
Tboil (K) | Reference | Comment |
---|---|---|
340.7 | Weast and Grasselli, 1989 | BS |
340.9 | Majer and Svoboda, 1985 | |
338. | Cossar, Fournier, et al., 1962 | Uncertainty assigned by TRC = 2. K; TRC; Data excluded from overall average |
340.95 | Morris, Lanum, et al., 1960 | Uncertainty assigned by TRC = 0.2 K; TRC |
340.7 | Coleman, Adams, et al., 1956 | Uncertainty assigned by TRC = 1. K; TRC |
341. | Dunbar and Bolstad, 1955 | Uncertainty assigned by TRC = 3. K; TRC |
341.0 | Anonymous, 1954 | Uncertainty assigned by TRC = 0.2 K; TRC |
340.97 | Birch, 1953 | Uncertainty assigned by TRC = 0.3 K; TRC |
342. | Zinner, 1953 | Uncertainty assigned by TRC = 3. K; TRC |
340.97 | Denyer, Fidler, et al., 1949 | Uncertainty assigned by TRC = 0.2 K; TRC |
340.5 | Lecat, 1947 | Uncertainty assigned by TRC = 0.5 K; TRC |
340.9 | Trotter and Thompson, 1946 | Uncertainty assigned by TRC = 0.7 K; TRC |
340.7 | Vaughan and Rust, 1942 | Uncertainty assigned by TRC = 3. K; TRC |
341. | Bottomley, 1941 | Uncertainty assigned by TRC = 1.38 K; TRC |
389. | Jones and Reid, 1938 | Uncertainty assigned by TRC = 3. K; TRC; Data excluded from overall average |
341.4 | Bezzi, 1935 | Uncertainty assigned by TRC = 1. K; TRC |
335. | Mann and Purdie, 1935 | Uncertainty assigned by TRC = 3. K; TRC; Data excluded from overall average |
341. | Ingold, Jessop, et al., 1933 | Uncertainty assigned by TRC = 3. K; TRC |
341. | Backer and Dijkstra, 1932 | Uncertainty assigned by TRC = 3. K; TRC |
340. | Sabatier and Mailhe, 1910 | Uncertainty assigned by TRC = 2. K; TRC |
341. | Roemer, 1873 | Uncertainty assigned by TRC = 5. 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.
Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]
Majer and Svoboda, 1985
Majer, V.; Svoboda, V.,
Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
Cossar, Fournier, et al., 1962
Cossar, B.C.; Fournier, J.O.; Fields, D.L.; Reynolds, D.D.,
Prepartion of Thiols,
J. Org. Chem., 1962, 27, 93. [all data]
Morris, Lanum, et al., 1960
Morris, J.C.; Lanum, W.J.; Helm, R.V.; Haines, W.E.; Cook, G.L.; Ball, J.S.,
Purification and Properties of Ten Organic Sulfur Compounds,
J. Chem. Eng. Data, 1960, 5, 112-6. [all data]
Coleman, Adams, et al., 1956
Coleman, H.J.; Adams, B.H.; Eccleston, R.L.; Hopkins, R.L.; Mikkelsen, L.; Rall, H.T.; Richardson, D.; Thompson, C.J.; Smith, H.M.,
Anal. Chem., 1956, 28, 1380. [all data]
Dunbar and Bolstad, 1955
Dunbar, R.E.; Bolstad, A.N.,
The Acetylation of Mercaptans with Ketene,
J. Am. Chem. Soc., 1955, 77, 4672. [all data]
Anonymous, 1954
Anonymous, R.,
, Am. Pet. Inst. Res. Proj. 45, Tech. Rep. 13, Ohio State Univ., 1954. [all data]
Birch, 1953
Birch, S.F.,
Sulphur Compounds in Petroleum,
J. Inst. Pet., 1953, 39, 185. [all data]
Zinner, 1953
Zinner, H.,
Perparation of Mercaptans,
Chem. Ber., 1953, 86, 825. [all data]
Denyer, Fidler, et al., 1949
Denyer, R.L.; Fidler, F.A.; Lowry, R.A.,
Azeotrope Formation Between Thiols and Hydrocarbons,
Ind. Eng. Chem., 1949, 41, 2727-37. [all data]
Lecat, 1947
Lecat, M.,
Orthobaric Azeotropes of Sulfides,
Bull. Cl. Sci., Acad. R. Belg., 1947, 33, 160-82. [all data]
Trotter and Thompson, 1946
Trotter, I.F.; Thompson, H.W.,
Infrared SPectra of Thiols, Sulfides, and Disulfides,
J. Chem. Soc., 1946, 1946, 481. [all data]
Vaughan and Rust, 1942
Vaughan, W.E.; Rust, F.F.,
The Photoaddition of Hydrogen Sulfide to Olefinic Bonds,
J. Org. Chem., 1942, 7, 472. [all data]
Bottomley, 1941
Bottomley, H.,
Ref. Nat. Gas. Mfg., 1941, 20, 526-9. [all data]
Jones and Reid, 1938
Jones, S.O.; Reid, E.E.,
The Addition of Sulfurl, Hydrogen Sulfide and Mercaptans to Unsaturated Hydrocarbons,
J. Am. Chem. Soc., 1938, 60, 2452. [all data]
Bezzi, 1935
Bezzi, S.,
The Consitution of Polysulfides,
Gazz. Chim. Ital., 1935, 65, 693. [all data]
Mann and Purdie, 1935
Mann, F.G.; Purdie, D.,
The Constitution of Complex Metallic Salts III. The Parachors of Palladium and Mercury in Simple and Complex Compounds,
J. Chem. Soc., 1935, 1935, 1549. [all data]
Ingold, Jessop, et al., 1933
Ingold; Jessop; Kuriyam; Mandour,
Influence of Poles and Polar Linkages on the Course Pursued by Elimination Reactions XVIII. Thermal Decompostion of Sulphoniumm Hydroxides,
J. Chem. Soc., 1933, 1933, 3455. [all data]
Backer and Dijkstra, 1932
Backer, H.J.; Dijkstra, N.D.,
The Thioethers of Pentaerythritol,
Recl. Trav. Chim. Pays-Bas, 1932, 51, 289. [all data]
Sabatier and Mailhe, 1910
Sabatier, P.; Mailhe, A.,
General Methods for Direct Preparation of Thiols by Catalysic Splitting of Alcohols,
C. R. Hebd. Seances Acad. Sci., 1910, 150, 1217. [all data]
Roemer, 1873
Roemer, H.,
Derivatives of Normal Propyl Alcohol,
Chem. Ber., 1873, 6, 784. [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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