Chemistry:1,3-Propanedisulfonic acid
From HandWiki
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| Names | |
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| Preferred IUPAC name
Propane-1,3-disulfonic acid | |
| Other names
Eprosidate
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| Identifiers | |
3D model (JSmol)
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| Properties | |
| C3H8O6S2 | |
| Molar mass | 204.21 g·mol−1 |
| Melting point | 120–125 °C (248–257 °F; 393–398 K)[1] |
| Boiling point | 157 °C (315 °F; 430 K)[1] |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H302, H312, H314, H332 | |
| P260, P261, P264, P270, P271, P280, P301+312, P301+330+331, P302+352, P303+361+353, P304+312, P304+340, P305+351+338, P310, P312, P321, P322, P330, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
1,3-Propanedisulfonic acid is a sulfonic acid containing two sulfonate units. Its salts are called eprodisates and have been evaluated as a protector of renal function in AA amyloidosis.[2]
See also
References
- ↑ 1.0 1.1 McElvain, S. M.; Jelinek, Arthur; Rorig, Kurt (September 1945). "Ethane-1,2- and Propane-1,3-disulfonic Acids and Anhydrides". Journal of the American Chemical Society 67 (9): 1578–1581. doi:10.1021/ja01225a053.
- ↑ Rumjon, Adam; Coats, Thomas; Javaid, Muhammad M (24 February 2012). "Review of eprodisate for the treatment of renal disease in AA amyloidosis". International Journal of Nephrology and Renovascular Disease 5: 37–43. doi:10.2147/IJNRD.S19165. ISSN 1178-7058. PMID 22427728.
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