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PIPES

PIPES, or 1,4-piperazinediethanesulfonic acid (C₈H₁₈N₂O₆S₂), is a zwitterionic buffering agent widely employed in biochemistry and molecular biology to stabilize pH in the physiological range of 6.1 to 7.5, with a pKₐ of 6.8 at 25°C.^[1]^[2] Developed by Norman E. Good and colleagues in 1966 as part of a series of improved buffers for biological research, PIPES addresses limitations of traditional buffers like phosphate or Tris by offering high aqueous solubility of its salts (>100 g/L), minimal dependence of pKₐ on temperature and ionic strength, low permeability through cell membranes, and negligible complexation with metal ions, making it non-toxic and suitable for systems involving transition metals.^[1]^[3] Key Properties In practice, PIPES is frequently utilized in cell culture media to mimic physiological conditions, enzyme purification and assays where metal cofactors are present, gel electrophoresis for protein separation, chromatography techniques for biomolecule isolation, and electron microscopy fixatives for tissue preparation, owing to its ability to maintain consistent pH without perturbing biological structures or reactions.^[3]^[6]^[7]

Identity and structure

Nomenclature

PIPES is the common name for the buffering agent piperazine-N,N′-bis(2-ethanesulfonic acid), an acronym derived from its systematic description as a piperazine derivative with two ethanesulfonic acid groups attached to the nitrogen atoms. This naming convention reflects its chemical composition and was established in the original description of the compound.^[1] The preferred IUPAC name for PIPES is 2,2′-(piperazine-1,4-diyl)di(ethane-1-sulfonic acid), which precisely denotes the piperazine ring linked at positions 1 and 4 to two ethanesulfonic acid chains. This systematic nomenclature adheres to IUPAC guidelines for substituted piperazines and sulfonic acids, distinguishing it from other similar ethanesulfonate-based compounds. PIPES belongs to the series of Good's buffers, a set of zwitterionic compounds specifically designed for biological applications due to their minimal interference with enzymatic reactions and cellular processes.^[1] Introduced in the seminal 1966 publication by Norman E. Good and colleagues, PIPES was named and characterized alongside other buffers like MES and HEPES to address limitations in traditional phosphate and Tris systems for biochemical research.^[1]

Molecular formula and structure

PIPES, or 1,4-piperazinediethanesulfonic acid, has the molecular formula \ce{C8H18N2O6S2} and a molar mass of 302.37 g/mol.^[4] The core structure consists of a symmetrical piperazine ring—a six-membered heterocycle with two nitrogen atoms at positions 1 and 4—each substituted with an ethanesulfonic acid group (-\ce{CH2CH2SO3H}). This bis-substituted design provides the molecule with its buffering capabilities through the acidic sulfonic groups and the basic piperazine nitrogens. At neutral pH, PIPES predominantly adopts a zwitterionic form, where the sulfonic acid groups are deprotonated to \ce{-SO3^-} and one of the piperazine nitrogens is protonated, resulting in a net neutral charge. The standard chemical structure diagram depicts the piperazine ring in a chair conformation, with the ethanesulfonic chains extending equatorially from the nitrogens for minimal steric hindrance, though conformational flexibility occurs in solution. In terms of structural motifs, PIPES shares the piperazine ring with HEPES (which features one ethanesulfonic acid and one 2-hydroxyethyl substituent) but differs from MES, which uses a morpholine ring with a single ethanesulfonic acid group, highlighting the series of ethanesulfonate-based Good's buffers.^[2]

Physical properties

Appearance and solubility

PIPES appears as a white crystalline powder at room temperature.^[8] The compound exhibits limited solubility in water in its free acid form, with a value of approximately 0.58 g/L at 20°C, as determined by standardized testing methods.^[8] However, its sodium salt form demonstrates high solubility in water, exceeding 500 g/L at 20°C, facilitating practical preparation of concentrated solutions for laboratory applications.^[9] PIPES shows low solubility in organic solvents, such as ethanol and acetone, consistent with the design criteria for Good's buffers to minimize partitioning into non-aqueous phases.^[10] PIPES powder is hygroscopic, readily absorbing moisture from the air, which can lead to clumping and potential degradation of purity over time.^[11] To preserve its integrity, it should be stored in a tightly sealed container at room temperature in a dry environment, away from humidity sources.^[12] The density of PIPES is approximately 1.55 g/cm³ at 20°C.^[8] This polar structure, featuring sulfonic acid groups attached to the piperazine ring, contributes to its preferential solubility in aqueous media over organic ones.^[13]

Thermal stability

PIPES exhibits high thermal stability in its solid form, decomposing without melting at temperatures above 300 °C.^[14] Upon thermal decomposition, the solid releases carbon monoxide, carbon dioxide, and potentially other toxic fumes.^[15] In aqueous solutions, PIPES demonstrates robust stability under elevated temperatures, showing no significant degradation up to 100 °C and remaining suitable for short-term exposure at higher levels, such as during autoclaving at 121 °C.^[16] This property allows its use in laboratory protocols requiring heat sterilization without compromising buffer integrity. At such conditions, solubility increases modestly, reaching approximately 1 g/L at 100 °C.^[16]

Buffering characteristics

pKa values

PIPES, or piperazine-1,4-bis(2-ethanesulfonic acid), is a diprotic acid exhibiting two principal pKa values that govern its acid-base behavior in aqueous solutions. The sulfonic acid groups are strong acids with pKa values much lower than 0 and are typically fully deprotonated under standard conditions. The first observable dissociation constant in titration, pKa₁ ≈ 3.3 at 20 °C, corresponds to the deprotonation of one piperazinium nitrogen under low ionic strength conditions (I ≈ 0). This value was determined through potentiometric titration methods. Although this pKa is relevant for highly acidic environments, it plays a minimal role in the buffer's common applications near physiological pH.^[17] The second, more prominent dissociation constant, pKa₂ = 6.76 at 25 °C, arises from the deprotonation of the remaining piperazinium ion, providing the primary buffering capacity around neutral pH. This pKa reflects the zwitterionic equilibrium of the piperazine moiety and was originally measured at 20 °C as 6.76, with adjustments for 25 °C based on thermodynamic data showing minimal temperature dependence (ΔpKa/ΔT ≈ -0.0085). The dual pKa values stem from the structural features of the piperazine nitrogens, with the ethanesulfonic acid substituents influencing the acidity.^[1]^[2] The dissociation equilibria can be expressed as follows (considering the relevant steps after sulfonic deprotonation):

\mathrm{H_2PIPES^{2+}} \rightleftharpoons \mathrm{HPIPES^+} + \mathrm{H^+} \quad (K_{a1} = 10^{-3.3})

\mathrm{HPIPES^+} \rightleftharpoons \mathrm{PIPES} + \mathrm{H^+} \quad (K_{a2} = 10^{-6.76})

These constants are typically evaluated using glass electrode potentiometry in dilute solutions to minimize activity coefficient effects. pKa values for PIPES are sensitive to ionic strength, with reported variations of up to 0.2 units at I = 0.1 M compared to extrapolated values at I = 0. These effects are modeled using the extended Debye-Hückel equation, where log γ = -A z² √I / (1 + √I) + b I, with A ≈ 0.51 for water at 25 °C, leading to slight decreases in apparent pKa at higher ionic strengths due to stabilization of charged species. Thermodynamic parameters, such as ΔH° ≈ 11.0 kJ/mol for the second dissociation, further confirm the pKa's consistency across standard conditions (I = 0, 25 °C).

Effective pH range and capacity

PIPES exhibits an effective buffering range of 6.1 to 7.5 at 25°C, corresponding to its pKa value of approximately 6.8 ± 1 unit, which aligns closely with the physiological pH of 7.4 and enables its use in maintaining stable conditions near neutral pH in biological systems.^[2] This range ensures robust resistance to pH fluctuations from added acids or bases within these limits, with optimal performance near the pKa where the concentrations of the conjugate acid and base forms are nearly equal. The buffering capacity (β) of PIPES follows the general equation for monoprotic weak acid buffers (approximating the relevant dissociation):

\beta = 2.303 \times C \times \frac{K_a [\mathrm{H}^+]}{(K_a + [\mathrm{H}^+])^2}

where C is the total molar concentration of PIPES, K_a is its acid dissociation constant (derived from the pKa of 6.8), and [\mathrm{H}^+] is the equilibrium hydrogen ion concentration. This formulation highlights that β reaches its maximum at pH = pKa, allowing PIPES to absorb the greatest amount of added H⁺ or OH⁻ without significant pH change; for instance, at a typical concentration of 0.1 M, the capacity supports effective pH stabilization in dilute biological media.^[18] A key advantage of PIPES is its low metal ion chelation, with negligible binding affinity for divalent cations such as Ca²⁺ and Mg²⁺, which minimizes interference in metal-dependent enzymatic or cellular processes compared to buffers like EDTA or citrate that form strong complexes.^[5] This property stems from the sulfonic acid groups in its structure, which do not coordinate effectively with transition metals. The pKa of PIPES demonstrates low sensitivity to environmental factors, with a temperature coefficient of ΔpKa/ΔT ≈ -0.0085/°C, resulting in only minor shifts (e.g., about 0.3 units from 20°C to 37°C) that rarely require readjustment in standard laboratory conditions. Similarly, its pKa exhibits minimal dependence on ionic strength, with changes typically less than 0.1 units over common salt concentrations (0.1–0.5 M), preserving consistent buffering performance across varying solution compositions.^[19]^[20]

History and development

Introduction by Good et al.

PIPES, or piperazine-1,4-bis(2-ethanesulfonic acid), emerged as part of a pioneering effort in 1966 by Norman E. Good and colleagues at Michigan State University to develop superior buffering agents for biological research.^[1] This initiative addressed the shortcomings of conventional buffers like phosphate and Tris, which often exhibited issues such as low solubility, unwanted interactions with enzymes or metals, significant UV absorbance, or poor stability in physiological conditions.^[1] Good's team synthesized and evaluated over 20 zwitterionic compounds designed specifically for biochemical applications, emphasizing structural features that promote inertness and reliability in complex biological systems.^[1] The primary goal was to engineer buffers with pKa values close to 7—the typical physiological pH range—while ensuring high aqueous solubility, minimal cell membrane permeability, low absorbance below 240 nm to avoid interference with spectrophotometric assays, and limited chelation of metal ions that could disrupt enzymatic activities.^[1] These criteria were rigorously applied during the selection process, drawing on principles of organic chemistry to favor sulfonate-based structures for enhanced stability and reduced toxicity.^[1] PIPES was among the standout candidates, chosen for its piperazine backbone that imparts a dual pKa profile, enabling effective buffering across a broad range near neutral pH without compromising solubility or introducing artifacts in experiments.^[1] The seminal work was documented in the 1966 publication by Good, N. E., Winget, G. D., Winter, W., Connolly, T. N., Izawa, S., and Singh, R. M. M., titled "Hydrogen Ion Buffers for Biological Research," appearing in Biochemistry.^[1] In this paper, the authors outlined the synthesis routes, pKa determinations (PIPES at 6.76 and 6.82 at 20°C), solubility tests, and preliminary biological assays for the buffers, including PIPES, confirming their suitability for applications like chloroplast reactions and enzyme studies.^[1] This comprehensive evaluation established PIPES as a versatile option, particularly valued for its chemical stability and lack of interference in metal-dependent processes.^[1]

Adoption in biological research

Following its introduction in the late 1960s, PIPES gained adoption in biological research during the 1970s, particularly in electron microscopy for tissue fixation.^[21] Early studies demonstrated its utility in maintaining stable pH in various experimental setups. Its buffering capacity near physiological pH values (6.1–7.5) contributed to its use in cell culture media and enzyme assays.^[1] By the 1980s and 1990s, PIPES saw increased integration into protocols such as protein crystallization and chromatography for biomolecule purification.^[22] Citation trends reflect its acceptance, with approximately 250 PubMed references specifically mentioning PIPES buffer as of November 2025, showing interest in applications like tissue fixation and electrophysiology experiments.^[23] Compared to Tris or phosphate buffers, PIPES demonstrates reduced interference in metal-dependent reactions due to its low chelation affinity for divalent cations like Ca²⁺ and Mg²⁺, preserving enzyme function and structural integrity in sensitive assays.^[24]^[25] This property contributed to its selection in biophysical studies involving metalloproteins.^[26]

Applications

Biochemical and cell biology uses

PIPES, with its effective pH range of 6.1–7.5, is commonly employed in cell culture media to maintain physiological pH levels around 7.0–7.4, typically at concentrations of 10–50 mM, where it supports the growth and viability of various mammalian cell lines without toxicity.^[27] For instance, 25 mM PIPES has been used in buffers for culturing human mast cells and basophils, ensuring stable conditions during histamine release studies.^[28] This buffering capacity helps resist pH fluctuations from metabolic byproducts, promoting consistent cellular function in long-term cultures.^[29] In protein purification and enzyme assays, PIPES serves as a non-coordinating buffer that minimizes interactions with metal ions, thereby preventing protein denaturation during chromatographic techniques such as ion-exchange.^[5] Its zwitterionic nature allows for stable pH maintenance in the presence of divalent cations, which is critical for preserving enzyme activity; for example, 50 mM PIPES at pH 6.5 has been utilized in protocols for diluting and purifying recombinant proteins while avoiding precipitation.^[30] Low concentrations of PIPES further enhance separation efficiency and yield in cation-exchange chromatography by reducing non-specific binding.^[31] PIPES is also a preferred component in electrophoresis buffers, particularly for SDS-PAGE.^[32] In membrane protein studies, PIPES has demonstrated advantages over HEPES by providing superior preservation of lipid structures, reducing loss during sample preparation and thus yielding clearer ultrastructural details in thin-section analyses.^[33]

Microscopy and fixation techniques

PIPES buffer is widely employed in microscopy fixation protocols due to its ability to maintain stable pH and support superior preservation of cellular ultrastructure compared to traditional phosphate or cacodylate buffers. In particular, it facilitates effective cross-linking of proteins and minimizes artifacts in electron microscopy (EM) samples by reducing osmotic stress and precipitation.^[34] A key application of PIPES involves glutaraldehyde fixation for histological studies, where it significantly reduces lipid extraction from tissues during the fixation process. For instance, using 0.1 M PIPES buffered at pH 7.4 with 2% glutaraldehyde preserves membrane integrity and lipid composition in both plant and animal tissues, leading to clearer visualization of cellular details under light and electron microscopy.^[35] This approach outperforms phosphate-buffered glutaraldehyde, which can cause greater lipid loss and structural distortion.^[35] In studies of fungal structures, PIPES has been instrumental in optimizing protocols for immobilizing and fixing zoospores for both fluorescence and electron microscopy. Research from the 1970s and 1980s demonstrated that a combination of low-concentration glutaraldehyde (0.2%) and formaldehyde (2-4%) in 50 mM PIPES buffer at pH 7.2 effectively immobilizes zoospores of oomycetes like Phytophthora species while preserving surface antigens and internal organelles for ultrastructural analysis.^[36] This regimen, developed through quantitative evaluation of lectin binding patterns, ensures minimal disruption to cell surface features, enabling correlated fluorescence and EM imaging.^[36] PIPES also supports immunofluorescence techniques by providing a stable buffering environment that maintains optimal pH for antibody-antigen interactions without chelating essential metal ions. Its low binding affinity for divalent metals, such as calcium and magnesium, prevents interference with fluorophore stability or antibody conjugation, making it preferable for labeling delicate structures in fixed cells. An exemplary protocol utilizing PIPES is a variant of Karnovsky's fixative, adapted for enhanced ultrastructure preservation in EM. This formulation combines 2% paraformaldehyde and 2.5% glutaraldehyde in 0.1 M PIPES buffer (pH 7.2-7.4), which improves membrane and organelle fidelity in mammalian and plant tissues by avoiding phosphate-induced artifacts. Samples are typically fixed for 1-2 hours at room temperature, followed by buffer rinses and osmium postfixation, yielding high-contrast images with reduced vesicle formation or swelling.^[37]

Preparation and safety

Laboratory preparation

PIPES is commercially available as the free acid or in salt forms, such as the monosodium or disodium salt, from suppliers including Sigma-Aldrich and Thermo Fisher Scientific.^[38]^[39] Although not routinely performed in laboratories due to commercial accessibility, PIPES can be synthesized on a lab scale by reacting piperazine with 2-chloroethanesulfonic acid or its sodium salt, typically under controlled heating in aqueous or solvent conditions to yield the bis-sulfonated product.^[40] To prepare a buffer solution, a 1 M stock is commonly made by dissolving 302.37 g of PIPES free acid per liter of deionized water, though initial solubility is low at acidic pH, requiring gradual addition of NaOH (typically 1 M) while stirring to achieve dissolution and titrate to the desired pH, such as 7.0–7.5, guided by its pKₐ of approximately 6.8 at 25 °C.^[41]^[16] Alternatively, an equimolar mixture of the free acid and monosodium salt can be used to directly form the buffer at the target pH without extensive titration.^[16] PIPES powder should be stored at room temperature in a tightly sealed container to prevent moisture absorption, remaining stable for extended periods under these conditions. Prepared solutions are best stored at 4 °C and can maintain stability for up to 6 months if protected from contamination.^[38]^[42]

Hazards and handling

PIPES is not classified under the Globally Harmonized System (GHS) for skin or eye irritation, acute toxicity, sensitization, mutagenicity, carcinogenicity, or reproductive toxicity, according to the European Chemicals Agency (ECHA) as of 2025.^[43]^[44] However, it may cause mild redness or discomfort upon direct contact with skin or eyes, based on some supplier observations. Its low acute oral toxicity is evidenced by an LD50 greater than 2000 mg/kg in rats, indicating minimal risk from ingestion in typical laboratory exposures.^[45] Environmentally, PIPES is biodegradable, facilitating its breakdown in natural systems, but its sulfonic acid groups warrant caution against release into aquatic environments to avoid potential disruption of water quality or ecosystems.^[46] It is rated as slightly hazardous to water (Class 1), and undiluted releases should be diluted extensively before disposal.^[47] Safe handling requires wearing nitrile gloves (breakthrough time ≥480 minutes), safety glasses, and a P1 filter respirator when dust is generated to prevent irritation or inhalation exposure. Ensure good ventilation, avoid aerosol formation, and wash thoroughly after contact; if irritation occurs, seek medical advice. PIPES is incompatible with strong oxidizing agents, which may lead to reactive decomposition, and should be stored in a tightly closed container in a cool, dry place. It exhibits thermal stability under normal laboratory conditions, allowing safe use in moderate heating applications.^[45] PIPES is registered under the European Chemicals Agency (ECHA) REACH regulation (EC number 227-057-6), confirming compliance for industrial and laboratory use without additional restrictions.^[45]

References

[1]
Hydrogen Ion Buffers for Biological Research* | Biochemistry
Article February 1, 1966. Hydrogen Ion Buffers for Biological Research ... Good's Buffers. Inorganic Chemistry 2017, 56 (8) , 4584-4593. https://doi ...
[2]
Buffer Reference Center
### Summary of PIPES Buffer Information
[3]
PIPES, 1.0M buffer soln., pH 7.5 500 mL - Thermo Fisher Scientific
PIPES, 1.0M buffer soln., pH 7.5. PIPES (Piperazine-N,N?-bis(2-ethanesulfonic acid), is frequently used as a buffering agent in biochemistry.
[4]
PIPES - 1,4-Piperazinediethanesulfonic acid
### Summary of PIPES Buffer
[5]
https://www.goldbio.com/product/3991/pipes-free-acid
[6]
Why use PIPES Buffer - Blog - Hopax Fine Chemicals
Jul 9, 2020 · PIPES Buffer is widely used in cell culture, chromatography, cosmetics, diagnostic tests, protein purification, and electron microscopic study.
[7]
PIPES Buffer (0.5 M, pH 7.0) - Boston BioProducts
The PIPES Buffer is a zwitterionic buffering agent commonly used in biochemistry and molecular biology for its ability to maintain a stable pH.
[8]
PIPES - Safety Data Sheet
### Physical Properties of PIPES (CAS: 5625-37-6)
[9]
https://www.sigmaaldrich.com/US/en/product/sigma/p3768
[10]
Good's buffers | Protocols Online
Apr 11, 2010 · Low solubility in nonpolar solvents (fats, oils, and organic solvents) was also considered beneficial, as this would tend to prevent the buffer ...
[11]
https://www.sigmaaldrich.com/US/en/product/sigma/rdd004
[12]
PIPES | 5625-37-6 - ChemicalBook
It is an ethanesulfonic acid buffer developed by Good et al. in the 1960s. PIPES has a pKa near the physiological pH which makes it useful in cell culture work.
[13]
Overview: Good's Buffers - Boston BioProducts
Developed in the mid-1960s, Dr. Norman E. Good, an American biochemist, developed a series of biological buffers ideal for a variety of experiments for the ...
[14]
[PDF] PIPES BUFFER - Loba Chemie
Melting point. : > 300 °C. Freezing point. : Not applicable. Boiling point ... Decomposition temperature. : > 300 °C. pH. : Not available. pH solution. : Not ...
[15]
[PDF] PIPES BUFFER (BIOLOGICAL BUFFER)
Melting point [°C]. : > 300 °C. Decomposition point [°C]. : N/A. Critical temperature [°C]. : N/A. Auto-ignition temperature [°C]. : N/A. Flammability (solid, ...
[16]
None
### Summary of PIPES Monosodium Salt (Sigma Prod. No. P2949) - Thermal Stability, Autoclaving, Decomposition
[17]
Chemical Stability Analysis of Biological Buffer PIPES
Sep 19, 2025 · Meanwhile, PIPES can coexist with most salts, low concentration organic solvents (such as ethanol, DMSO), and biological reagents (enzymes ...
[18]
[PDF] Buffers | Calbiochem
Most of the buffers used in cell cultures, isolation of cells, enzyme assays, and other biological applications must possess these distinctive characteristics.<|control11|><|separator|>
[19]
Dissociation constant pKa (25 °C), dpKa/dT, and molecular mass of ...
Jul 2, 2019 · Dissociation constant pKa (25 °C), dpKa/dT, and molecular mass of buffers ; PIPES (1.4-piperazine-bis-ethane sulfonic acid), 6.76, −0.0085, 302.4.Missing: pKa1 pKa2
[20]
[PDF] Good's buffers (biological buffers) - Interchim
Dr. Norman Good et al. in 1966 described a series of zwitterionic buffers that addressed the above limitations, for research in biology and biochemistry.Missing: 1960s | Show results with:1960s
[21]
https://pubmed.ncbi.nlm.nih.gov/328889/
[22]
PIPES - an overview | ScienceDirect Topics
PIPES is defined as a buffering agent used to maintain a stable pH in ... stability to changes in temperature.) Other components common to buffers ...
[23]
PIPES - Search Results - PubMed
- **Total Number of Search Results for 'PIPES':** 6,981
[24]
https://www.goldbio.com/blogs/articles/how-to-prepare-your-most-frequently-used-buffers
[25]
Good's Buffer PIPES | CAS 5625-37-6 Dojindo
Good's Buffer PIPES, or Piperazine-1,4-bis(2-ethanesulfonic acid), is a buffer used to maintain pH in biological experiments, with high water-solubility and ...
[26]
Attention to details when using Good's buffer PIPES
One significant advantage of PIPES is that it cannot form stable complexes with most metal ions. In many biochemical and analytical chemistry experiments, ...
[27]
Extracellular Acidosis Is a Novel Danger Signal Alerting Innate ...
... PIPES buffer. PIPES at 20–40 mm is well tolerated in cell culture by several mammalian cell lines (33) and displays negligible metal ion binding and ...
[28]
Histamine-releasing factor/translationally controlled tumor protein ...
PIPES buffer consisted of 25 mM PIPES, 110 mM sodium chloride, 5 mM KCl ... Cell culture preparations. Human mast cells and basophils were cultured from ...
[29]
Development of an Optimized Medium, Strain and High-Throughput ...
Apr 30, 2013 · In contrast, the new medium we developed with a PIPES buffer and metals chelated by citrate allowed for fast and more consistent growth rates.
[30]
Protein purification - Bio-protocol
The eluted fractions were collected and the salt concentration was reduced by diluting the sample (1:5) with PIPES buffer (50 mM PIPES-NaOH pH 6.5, 2 mM βME), ...
[31]
Why is low concentration PIPES buffer suitable for cation exchange ...
Dec 4, 2024 · The results showed that the application of low concentration PIPES buffer significantly improved separation efficiency and purity, while ...Missing: chelation | Show results with:chelation
[32]
PIPES Buffer | Boston BioProducts
Browse our collection of PIPES buffers - buffering agents with a pH range of 6.8 to 7.5 for cell culture, protein purifications, ...<|control11|><|separator|>
[33]
Buffering agents and additives for the background electrolyte ...
The low conductivity of zwitterionic buffers allows their incorporation into BGE at high concentration, increasing the buffer capacity while limiting the ...Missing: PIPES | Show results with:PIPES
[34]
The influence of the buffer on maintenance of tissue lipid ... - PubMed
The extraction results, which showed a significant reduction of lipid losses when PIPES buffer was used, are taken to account for the morphological differences ...Missing: citations trends electrophysiology
[35]
The influence of fixation on patterns of lectin binding - PubMed
This effect was evaluated quantitatively and an optimum fixation regime for the fungal cells, namely, 0.2% G and 2-4% F in 50 mM PIPES buffer, was determined.
[36]
PIPES BioPerformance Certified, cell culture mammalian 5625-37-6
### Product Details for PIPES (P1851)
[37]
PIPES, 1.0M buffer soln., pH 6.8 250 mL - Thermo Fisher Scientific
6–10 day deliveryPIPES, 1.0M buffer soln., pH 6.8. PIPES is frequently used as a buffering agent in biochemistry. PIPES has pKa near the physiological pH which makes it ...Missing: preparation | Show results with:preparation
[38]
PIPES synthesis - ChemicalBook
Synthesis of PIPES from Piperazine and Sodium 2-chloroethanesulfonate monohydrate.Chemicalbook can provide 1 synthetic routes.Missing: chloroethanesulfonic | Show results with:chloroethanesulfonic
[39]
PIPES Buffer (1 M, 6.8 pH) Preparation and Recipe | AAT Bioquest
Prepare 800 mL of dH2O in a suitable container. Add 302.37 g of PIPES to the solution; Solubility of PIPES free acid is low in acidic range.
[40]
https://www.chemicalbook.com/synthesis/pipes.htm
[41]
None
Summary of each segment:
[42]
None
### Summary for PIPES (Sigma P6757)
[43]
[PDF] PIPES Buffer Powder - Safety data sheet - Severn Biotech
7.1 Precautions for safe handling. Prevent formation of dust. Ensure good ventilation/exhaustion at the workplace. · Information about fire - and explosion ...
[44]
Registration Dossier - ECHA
### Summary of Handling, Storage, and Exposure Controls for PIPES