| PIPES | |
|---|---|
|
1,4-Piperazinediethanesulfonic acid (IUPAC) |
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Other names
PIPES |
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| Identifiers | |
| CAS number | 5625-37-6 |
| Properties | |
| Molecular formula | C8H18N2O6S2 |
| Molar mass | 302.37 |
| Appearance | White powder |
| Melting point |
Decomposes above 300 °C |
| Boiling point |
Decomposes |
| Solubility in water | 1 g/L (100 °C) |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | Irritant |
| NFPA 704 | |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
PIPES is the common name for piperazine-N,N′-bis(2-ethanesulfonic acid), and frequently used buffering agent in biochemistry. It is an ethanesulfonic acid buffer developed by Good et al. in the 1960s.[1]
PIPES has pKa (6.76 at 25°C) near the physiological pH which makes it useful in cell culture work. PIPES has been documented minimizing lipid loss when buffering glutaraldehyde histology in plant and animal tissues.[2][3] Fungal zoospore fixation for fluorescence microscopy and electron microscopy were optimized with a combination of glutaraldehyde and formaldehyde in PIPES buffer.[4] It has a negligible capacity to bind divalent ions.
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