Chemistry:CAPS (buffer)
From HandWiki
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| Names | |
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| Preferred IUPAC name
3-(Cyclohexylamino)propane-1-sulfonic acid | |
| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C9H19NO3S | |
| Molar mass | 221.32 g/mol |
| Melting point | >300 °C |
| Acidity (pKa) | 10.4[2] |
| Hazards | |
| GHS pictograms | 
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| GHS Signal word | Warning |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
CAPS is the common name for N-cyclohexyl-3-aminopropanesulfonic acid, a chemical used as buffering agent in biochemistry. The similar substance N-cyclohexyl-2-hydroxyl-3-aminopropanesulfonic acid (CAPSO) is also used as buffering agent in biochemistry. Its useful pH range is 9.7-11.1.
See also
References
- ↑ CAPS at Sigma-Aldrich
- ↑ Esplin, Taran L.; Cable, Morgan L.; Gray, Harry B.; Ponce, Adrian (2010). "Terbium-Macrocycle Complexes as Chemical Sensors: Detection of an Aspirin Metabolite in Urine Using a Salicylurate-Specific Receptor Site". Inorganic Chemistry 49 (10): 4643–4647. doi:10.1021/ic1003066.
Tabata, Masaaki; Habib, Ahsan; Watanabe, Keiichi (2005). "DNA Cleavage by Good’s Buffers in the Presence of Au(III)". Bulletin of the Chemical Society of Japan 78 (7): 1263–1269. doi:10.1246/bcsj.78.1263.
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