Chemical Name: Piperazine-1,4-bis(2-hydroxy-3-propanesulfonic acid), dihydrate
Appearance: White crystalline powder
Purity: ≥99.0% (Titration)
MW: 398.45, C10H22N2O8S2, 2H2O
Storage Condition: ambient temperature
Shipping Condition: ambient temperatureChemical StructureIntroduction
biological experiments, it is important to maintain the pH of the
solutions used. Buffers, mixtures of appropriate weak acids, and their
conjugate bases, are usually used. Most biological reactions occur at a
neutral pH, from 6 to 8; the buffer needs to be effective in this range.
Furthermore, the acids and bases used in the buffer should not produce
chelates with metal ions, which are essential in biological systems. For
these reasons, Dr. Good developed several aminoethane and aminopropane
sulfonic acids that are now widely used for biological research and
analysis. Good’s buffers have the following characteristics:
1) High water-solubility
2) Low cell membrane permeability
3) Consistent acid-base dissociation constants
4) Low metal chelating capability
5) High chemical stability
6) Low absorption spectra in UV and visible regions.
1. N. E. Good, Uncoupling of the Hill reaction from photophosphorylation by anions. Arch Biochem Biophys. 1962;96:653-661.
2. N. E. Good, et al., Hydrogen ion buffers for biological research. Biochemistry. 1966;5:467-477.
3. C. Ceccarini, et al., Induction and reversal of contact inhibition of growth by pH modification. Nat New Biol. 1971;233:271-273.
E. L. Medzon, et al., Substitution of
4-(2-hydroxyethyl)-1-piperazineethane sulfonic acid (HEPES) for
bicarbonate in protein-free animal cell culture medium: application to
vaccinia virus quantitation and fluorogenic acetylesterase assay in
living LM cells. Can J Microbiol. 1971;17:651-653.
A. Itagaki, et al., TES and HEPES buffers in mammalian cell cultures
and viral studies: problem of carbon dioxide requirement. Exp Cell Res.
6. W. J. Ferguson, et al., Hydrogen ion buffers for biological research. Anal Biochem. 1980;104:300-310.
7. J. K. Grady, et al., Radicals from “Good’s” buffers. Anal Biochem. 1988;173:111-115.
8. J. W. Hanrahan, et al., Inhibition of an outwardly rectifying anion channel by HEPES and related buffers. J Membr Biol. 1990;116:65-77.
9. T. Kudo, et al., A simple and improved method to generate human hybridomas. J Immunol Methods. 1991;145:119-125.
Table 1 Active pH Range of Good’s Buffers
ADA, PIPES, POPSO
Solution A: 0.1 M solution
ADA 19.02 g + NaOH 4.0 g / 1 L
PIPES 30.24 g + NaOH 4.0 g / 1 L
POPSO 39.85 g + NaOH 4.0 g / 1 L
Solution B: 0.1 M NaOH solution
NaOH 4.0 g / 1 L