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Potassium phosphate, dibasic

Potassium phosphate, dibasic is an inorganic salt with a wide range of applications in scientific research and industrial processes.
It serves as a buffering agent, pH regulator, and nutrient in cell culture media, biochemical assays, and various other laboratory procedures.
This compound is also used in the production of fertilizers, detergents, and food preservatives.
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One typo: 'literatuer' instead of 'literature'.

Most cited protocols related to «Potassium phosphate, dibasic»

Cultivation and Genetic Manipulation of Escherichia coli and Clostridium Species

Cited 19 times

Escherichia coli TOP10 (Invitrogen) and E. coli CA434 [39] (link) were cultured in Luria-Bertani (LB) medium, supplemented with chloramphenicol (25 µg/ml), where appropriate. Routine cultures of C. difficile 630 Δerm[40] (link) and C. difficile R20291 were carried out in BHIS medium (brain heart infusion medium supplemented with 5 mg/ml yeast extract and 0.1% [wt/vol] L-cysteine) [41] (link). C. difficile medium was supplemented with D-cycloserine (250 µg/ml), cefoxitin (8 µg/ml), lincomycin (20 µg/ml), and/or thiamphenicol (15 µg/ml) where appropriate. A defined minimal media [18] (link) was used as uracil-free medium when performing genetic selections. A basic nutritive mannitol broth for growth assays of C. difficile strains were prepared as follows : Proteose peptone no. 2 4% [wt/vol] (BD Diagnostics, USA), sodium phosphate dibasic 0.5%[wt/vol], potassium phosphate monobasic 0.1%[wt/vol], sodium chloride, 0.2% [wt/vol], magnesium sulfate, 0.01% [wt/vol], mannitol, 0.6% [wt/vol] with final pH at +/−7.35. For solid medium, agar was added to a final concentration of 1.0% (wt/vol). Clostridium sporogenes ATCC 15579 was cultivated in TYG media [7] (link). All Clostridium cultures were incubated in an anaerobic workstation at 37°C (Don Whitley, Yorkshire, United Kingdom). Uracil was added at 5 µg/ml, and 5-Fluoroorotic acid (5-FOA) at 2 mg/ml. All reagents, unless noted, were purchased from Sigma-Aldrich.

Ng Y.K., Ehsaan M., Philip S., Collery M.M., Janoir C., Collignon A., Cartman S.T, & Minton N.P. (2013). Expanding the Repertoire of Gene Tools for Precise Manipulation of the Clostridium difficile Genome: Allelic Exchange Using pyrE Alleles. PLoS ONE, 8(2), e56051.

Publication 2013

5-fluoroorotic acid Agar Biological Assay Brain Cefoxitin Chloramphenicol Clostridium Clostridium sporogenes Cycloserine Cysteine Diagnosis Escherichia coli Genetic Selection Heart Lincomycin Mannitol potassium phosphate proteose-peptone Sodium Chloride sodium phosphate Strains Sulfate, Magnesium Thiamphenicol Uracil Yeast, Dried

pH-Sensitive Fluorescent Protein Assays

Cited 12 times

Excitation scans were generated using a Deltascan dual-wavelength fluorimeter from Photon Technology International (PTI; Birmingham, NJ) and the associated Felix software. Standard HEK293 cells were plated on 10 cm dishes and transiently transfected with 5 µg each of the soluble forms of GFP2, pHluorin and pHluorin2 using Fugene HD (Roche, Indianapolis, IN). Forty-eight hours post transfection, cells were washed with Hank’s Balanced Salt solution lacking calcium and magnesium ions and containing 2 mM EDTA. Cells were lifted from the plates using the same solution after a 10 minute incubation at 37°C and placed in a quartz cuvette with a stir bar. Excitation scans were performed between wavelengths 370 nm to 490 nm with the emission set at 510 nm. For the pH clamp experiments, cells were resuspended in a buffer containing 140 mM potassium chloride, 10 mM sodium phosphate with molar ratios of mono- and dibasic forms appropriate for the given pH and 30 mM nigericin (EMD Biosciences, Gibbstown, NJ). For the florescence plate reader studies, black, 96-well plates (Perkin-Elmer, Boston, MA) were loaded with 25,000 cells per well from the transfections described above and analyzed with dual excitation at 405 nm/8 nm and 485 nm/25 nm with a 535 nm/25 nm emission filter in an EnVision plate reader (Perkin-Elmer, Boston, MA). The narrow bandwidth of the 405 nm filter of 8 nm reduces the relative florescence compared to the larger bandwidth of the 485 nm filter. Despite this effect, the 405/485 nm ratios are still responsive to changes in intracellular pH.
For the hPTH1R endocytosis studies, HEK293 cells were sparsely plated into culture slides and transiently transfected with 100 ng of the hPTH1R-pHluorin2 construct using Fugene HD. Forty-eight hours post-transfection, cells were treated with either vehicle (acetic acid) or 100 nM parathyroid hormone containing amino acids 1 to 34 for 20 minutes. Cells were fixed with 3.7% paraformaldehyde and analyzed by confocal microscopy using a Radiance 2100 confocal microscope and the associated LaserSharp 2000 software (Bio-Rad Laboratories, Inc., Hercules, CA).

, & Mahon M.J. (2011). pHluorin2: an enhanced, ratiometric, pH-sensitive green florescent protein. Advances in bioscience and biotechnology (Print), 2(3), 132-137.

Publication 2011

Acetic Acid Amino Acids Buffers Calcium Cells Edetic Acid Endocytosis FuGene HEK293 Cells Hyperostosis, Diffuse Idiopathic Skeletal Ions Magnesium Microscopy, Confocal Molar Nigericin paraform Parathyroid Hormone PHluorin Potassium Chloride Protoplasm Quartz Radionuclide Imaging Sodium Chloride sodium phosphate Transfection

Isolation and Characterization of Anaerobic Gut Bacteria

Cited 10 times

The chickens were sacrificed under chloroform anesthesia by cervical dislocation. Whole caeca with their contents originating from 18 random healthy chickens or hens 4 to 40 weeks of age were removed during necropsy, chilled on ice and transported to an anaerobic chamber for further processing within one hour. The caeca were opened in an anaerobic chamber (10% CO₂, 5% H₂ and 85% N₂ atmosphere; Concept 400, Baker Ruskinn, USA) and 0.5 g of content was squeezed into 4.5 ml pre-reduced PRAS dilution blank (0.1 g magnesium sulfate heptahydrate, 0.2 g monobasic potassium phosphate, 0.2 g potassium chloride, 1.15 g dibasic sodium phosphate, 3.0 g sodium chloride, 1.0 g sodium thioglycolate, 0.5 g L-cysteine, 1000 ml distilled water; final pH 7.5 +/− 0.2 at 25 °C) and mixed thoroughly. All samples were serially diluted in pre-reduced PRAS dilution blank and plated on Wilkins-Chalgren anaerobe agar (WCHA) (Oxoid) supplemented with 30% of rumen fluid. The rumen fluid was collected from cows by an oral probe, filtered through cheesecloth, centrifuged at 8000 g for 30 min and sterilised by filtration through a 0.22 μm filter. Aliquots of rumen fluid were stored at − 20 °C. WCHA was additionally supplemented with 5 mg/l hemin, 1 mg/l cellobiose, 0.5 g/l soluble starch, 1 mg/ml maltose, 0.2 ml vitamin K1 solution (0.1 ml of filter sterilized vitamin K1 in 20 ml 95% ethanol) and 0.5 mg/ml L-cysteine. Approx. 10 well-separated colonies of different morphology were selected from each agar plate after a five-day incubation at 37 °C and purified by subculture on WCHA. All isolates were stored at − 80 °C in pre-reduced PRAS dilution blank containing glycerol at 20% concentration and equal volume of sterile sheep blood. Sensitivity of pure anaerobe cultures to air oxygen exposure was tested exactly as described elsewhere [6 (link)]. Briefly, bacterial cultures were serially diluted in anaerobic chamber and plated on 4 copies of WCHA. One copy of WCHA was left in the anaerobic chamber to determine initial counts of each anaerobe. The remaining 3 copies of WCHA plates were placed into a standard aerobic 37 °C incubator and after 1, 8 and 24 h, a single copy of agar plate was returned back to the anaerobic chamber to check for growth restoration.

Medvecky M., Cejkova D., Polansky O., Karasova D., Kubasova T., Cizek A, & Rychlik I. (2018). Whole genome sequencing and function prediction of 133 gut anaerobes isolated from chicken caecum in pure cultures. BMC Genomics, 19, 561.

Publication 2018

2-N-propylamine-cyclo-hexanethiol Agar Anesthesia Atmosphere Autopsy Bacteria Bacteria, Aerobic Bacteria, Anaerobic Blood Volume Cattle Cecum Cellobiose Chickens Chloroform Cysteine Ethanol Filtration Glycerin Hemin Heptahydrate Magnesium Sulfate Hypersensitivity Joint Dislocations Maltose Neck Oxygen Potassium Chloride potassium phosphate, monobasic Rumen S100A6 protein, human Sheep Sodium Chloride sodium phosphate, dibasic sodium thioglycolate Starch Sterility, Reproductive Technique, Dilution Vitamin K1

Cell-Free Extract Preparation for Cell-Free Protein Synthesis

Cited 10 times

Refer to the detailed extract preparation protocol included in the Supplemental Note. Briefly, cell-free extract was prepared based on the protocol in the literature.^{58 (link)} Rosetta 2 cells were streaked onto chloramphenicol agar plates overnight, then inoculated into 30 mL LB supplemented with antibiotic and grown in a 250 mL baffled flask at 37 °C. After 16 h, 20 mL of the stationary culture was used to inoculate one liter of autoclaved growth media 2× YT + P (16 g/Ltryptone, 10 g/L yeast extract, 5 g/L sodium chloride, 7 g/L potassium phosphate dibasic, 3 g/L potassium phosphate monobasic) in a 2.5 L baffled Tunair flask. A separate bottle containing 7.2% glucose solution was autoclaved and added at the time of inoculation for 2× YTP + G experiments to a final glucose concentration of 1.8%.
Cultures were grown to the exponential phase optical density (OD6OO) 3.0 ± 0.2 for approximately 4 h at 37 °C and 200 rpm. The culture was divided in two and centrifuged for 15 min at 5000g at 4 °C to pellet the cells. The cell pellets were washed three times in 25 mL wash buffer (50 mM Tris, 14 mM Mg-glutamate, 60 mM K-glutamate, 2 mM DTT, brought to pH 7.7 with acetic acid) and recentrifuged between each wash at 5000g at 4 °C for 10 min. After the fourth and final centrifugation at 7000g at 4 °C for 10 min, pellets were resuspended in 1 mL wash buffer/g pellet and transferred to 1.6 mL microcentrifuge tubes. For the flash freeze experiments, cell pellets were submersed in liquid nitrogen before this step and thawed the next day.
The cell suspensions were then lysed by sonication on a QSonica Q125 sonicator with a 3.175 mm diameter probe at a frequency of 20 kHz and 50% amplitude by 10 s ON/OFF pulses for a total of 60 s (delivering ~350 J). The lysate was centrifuged for 10 min at 4 °C and 12 OOOg, and the supernatant was removed. For preparations including a runoff reaction, the tubes of crude lysate were covered in aluminum foil and were incubated shaking with lids on for 80 min at 37 °C and 200 rpm. The extract was recentrifuged for 10 min at 4 °C and 12 000g and the supernatant was removed. For preparations including a dialysis, the extract was injected into a 10K MWCO Slide-a-Lyzer dialysis cassette (ThermoFisher, 66380) and dialyzed against 600 mL of dialysis buffer (5 mM Tris, 14 mM Mg-glutamate, 60 mM K-glutamate, 1 mM DTT, pH 8.2) at 4 °C for 3 h. The dialyzed extract was removed from the cassette and centrifuged once more for 10 min at 4 °C and 12 00Og. The supernatant was removed, aliquoted, and snap-frozen in liquid nitrogen.

Silverman A.D., Kelley-Loughnane N., Lucks J.B, & Jewett M.C. (2019). Deconstructing Cell-Free Extract Preparation for in Vitro Activation of Transcriptional Genetic Circuitry. ACS synthetic biology, 8(2), 403-414.

Publication 2019

Evaluating Inhibitory Compounds on Xylose Utilization

Cited 7 times

Cultures were grown in RM medium (10 g/L yeast extract, 2 g/L KH₂PO₄) supplemented with either 2% (w/v) glucose (RMG) or 2% (w/v) xylose (RMX) for inhibitor studies. The pH of all media was adjusted to pH5.8 and was filter sterilized. Media were prepared from stock solutions of yeast extract and monobasic potassium phosphate, and when possible, inhibitor stock solutions were prepared and titrated to pH 5.8. Two compounds (4-hydroxycinnamic acid and syringaldehyde) were prepared from stock solutions in 100% DMSO due to their low solubility in water. The total amount of DMSO in the final medium ranged from 0.1-5.0% (v/v) for 4-hydroxycinnamic acid and 0.1%-3% (v/v) in syringaldehyde. Inhibitor studies with DMSO alone did not detect notable inhibitions on growth or final cell mass (data not shown).
Ammonium salts were prepared by titrating the acids with concentrated ammonium hydroxide, except for the anions: sulfate, chloride, nitrate, acetate, phosphate. Calcium formate was prepared by titrating formic acid with lime. Phosphate stocks were made by preparing 1 M stock solutions of monobasic phosphate and titrating the medium to pH of 5.8 with 1 M dibasic solution.
As a consequence of precipitation of monobasic potassium phosphate with calcium, it was not included in medium containing calcium. In this case, 50 mM MES, pH 5.8, was provided to supply some buffering capacity. Growth rates in RMG or RMX with 50 mM MES, pH 5.8, and no potassium phosphate were similar to those obtained in media with potassium phosphate which indicated that yeast extract in rich media could supply sufficient phosphorous for growth at the 2% sugar level (data not shown).
Overnight cultures in RMG medium were either started from single colonies or from glycerol stocks. Optical densities were measured using a Beckman DU-640 spectrophotometer (Beckman Coulter, Inc., Brea, CA) for inoculation. Growth rates were obtained from the Bioscreen C analyzer purchased from Growth Curves USA (Piscataway, NJ). Procedures for inoculation, growth conditions, measurement, recording of final cell densities and calculations used to correct for non-linear response at high cell densities were previously reported [22 (link)]. In brief, log phase cultures of Z. mobilis 8b (a recombinant xylose-utilizing strain of ZM4) were obtained by inoculating overnight cultures in RMG at 30°C and allowing the cells to grow to an OD₆₀₀ ~ 1.0. Cells were then spun down at 3840 × g, for 10 min at RT and resuspended in RMG or RMX with inhibitor at the desired concentration such that the starting cell density distributed to Bioscreen C microplates after appropriate dilutions with inhibitors was OD₆₀₀ = 0.05 (~5 × 10⁶ cells/mL⁼) in a total volume of 300 μL. Incubations were performed at 30°C and absorbance readings were taken every 10 min. Operation of the Bioscreen C and collection of turbidity measurements (OD_420–580) were computer automated with EZ Experiment. Data were collected and exported to Microsoft Excel spreadsheets.
Cultures for mini-fermentation studies at 1X MIC were inoculated with Z. mobilis 8b from seed cultures at an OD₆₀₀ of 1.0 described above, in 4.5 mL of RM medium containing 5% glucose or 5% xylose and inhibitor compounds at a concentration which would cause 100% inhibition of growth rates (1X MIC) in 6 mL HPLC vials at 30°C, 150 rpm, and were vented with an 18 gauge needle and 0.2 micron syringe filter. Samples (0.5 mL) were removed at 0, 24 and 48 hours post inoculation for OD₆₀₀ and HPLC analysis.
Cultures for aldehyde conversion studies were inoculated with Z. mobilis 8b at an OD₆₀₀ of 1.0 in 100 mL of RMG containing 5% glucose in 125 mL unbaffled shake flasks containing aldehyde inhibitors at a concentration that would cause 50% inhibition of growth rates at 30°C, 125 rpm. Samples were removed at 0, 24 and 48 hours for HPLC and growth analysis. Flasks containing inhibitor medium without cells were included to assess abiotic loss due to instability or volatility.

Franden M.A., Pilath H.M., Mohagheghi A., Pienkos P.T, & Zhang M. (2013). Inhibition of growth of Zymomonas mobilis by model compounds found in lignocellulosic hydrolysates. Biotechnology for Biofuels, 6, 99.

Publication 2013

Most recents protocols related to «Potassium phosphate, dibasic»

Preparation of Biological Buffers

Not available on PMC !

Potassium dihydrogen phosphate (Merck Group), Potassium phosphate dibasic (SPECTRUM), sodium acetate (Merck Group), Tris Base (Fisher Bioreagents), Bis-Tris Hydrochloride (Sigma Aldrich), and sodium chloride (BioLab) were used for buffer preparation.

Golan N., Parizat A., Tabachnikov O., Barnea E., Olsen W.P., Otzen D.E., & Landau M. (2024). Resilience and Charge-Dependent Fibrillation of Functional Amyloids: Interactions ofPseudomonasBiofilm-Associated FapB and FapC.

Publication 2024

Solvent and Reagent Preparation

LC-MS grade water, methanol, acetonitrile, and isopropanol were all purchased from Merck (Darmstadt, Germany). Formic acid, dimethyl sulfoxide (DMSO), potassium phosphate dibasic (K₂HPO₄), potassium phosphate monobasic (KH₂PO₄), and bovine serum albumin (BSA) were acquired from Sigma-Aldrich (Buchs, Switzerland).

Thomann J., Kolaczynska K.E., Stoeckmann O.V., Rudin D., Vizeli P., Hoener M.C., Pryce C.R., Vollenweider F.X., Liechti M.E, & Duthaler U. (2024). In vitro and in vivo metabolism of psilocybin’s active metabolite psilocin. Frontiers in Pharmacology, 15, 1391689.

Publication 2024

Sodium Alginate-Based Paracetamol Formulation

Not available on PMC !

Sodium alginate (SA) (low viscosity and medium viscosity) was obtained from Sigma Aldrich.
Paracetamol, Carboxymethyl cellulose (CMC) (7M1FPH) was a gift from Ashland, Türkiye. Calcium chloride dehydrates, potassium phosphate dibasic (K HPO ) and potassium phosphate monobasic (KH PO ) were from ISO LAB chemicals and ethanol from LiChrosolv.

Ullah H., Akram M., Khan H., Irfan M., & Hassan A. (2024). Sodium Alginate Carboxymethyl Cellulose Composite Hydrogel beads for Oral Drug Delivery.

Publication 2024

Recombinant H3N2 Influenza Protein Production

Recombinant truncated NA protein from the A/Perth/16/2009 H3N2 strain of influenza virus was produced in Chinese hamster ovary (CHO) cell line. The recombinant protein was secreted and purified from clarified supernatants, yielding a homogeneous SEC profile with a major peak corresponding to the molecular size of the tetramer.
Sodium phosphate monobasic and dibasic, potassium phosphate dibasic (all ACS reagents) and monobasic (molecular grade), sodium chloride and sucrose (both BioXtra, ≥ 99.5%), were purchased from Sigma.

Li B., Ustyugova I.V., Szymkowicz L., Zhu S., Ming M., Fung K.Y., Cortés G., James D.A., Hrynyk M., Rahman N., Brookes R.H, & Ausar S.F. (2024). Formulation development of a stable influenza recombinant neuraminidase vaccine candidate. Human Vaccines & Immunotherapeutics, 20(1), 2304393.

Publication 2024

Preparation of Bacterial Culture Media

Ammonium chloride (NH₄Cl), magnesium sulfate heptahydrate (MgSO₄·7H₂O), calcium chloride dihydrate (CaCl₂·2H₂O), Sodium phosphate dibasic (Na₂HPO₄), potassium dihydrogen phosphate (KH₂PO₄), iron (III) chloride hexahydrate (FeCl₃·6H₂O), sodium hydroxide (NaOH), sodium bicarbonate (NaHCO₃), potassium chloride (KCl), potassium hydroxide (KOH), ethanol, Luria-Bertani medium, agarose gel, osmium acid were purchased from Aladdin Industrial Corporation, China. Anhydrophosphoric acid, 4-aminobenzoic acid, hydrochloric acid, glutaraldehyde, acetone, potassium hexacyanoferrate (III) (K₃[Fe(CN)₆]), sodium acetate were purchased from Sinopharm Chemical Reagent Co. Ltd. China.

Zheng Y., Wang H., Liu Y., Liu P., Zhu B., Zheng Y., Li J., Chistoserdova L., Ren Z.J, & Zhao F. (2024). Electrochemically coupled CH4 and CO2 consumption driven by microbial processes. Nature Communications, 15, 3097.

Publication 2024

Top products related to «Potassium phosphate, dibasic»

Potassium phosphate monobasic by Merck Group

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Potassium phosphate monobasic is a chemical compound used in various laboratory applications. It is a colorless, crystalline solid that is soluble in water. The primary function of potassium phosphate monobasic is to serve as a buffer in pH-sensitive experiments and to maintain specific pH levels in various biological and chemical systems.

Sodium phosphate dibasic by Merck Group

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Sodium phosphate dibasic is a chemical compound that is commonly used in laboratory settings. It is a crystalline, white solid that is soluble in water and has a neutral to basic pH. The compound's primary function is to serve as a buffering agent, helping to maintain a specific pH level in various chemical reactions and processes.

Sodium chloride (nacl) by Merck Group

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NaCl is a chemical compound commonly known as sodium chloride. It is a white, crystalline solid that is widely used in various industries, including pharmaceutical and laboratory settings. NaCl's core function is to serve as a basic, inorganic salt that can be used for a variety of applications in the lab environment.

Potassium phosphate dibasic by Merck Group

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Potassium phosphate dibasic is a chemical compound that is commonly used in various laboratory applications. It is a white crystalline powder that is soluble in water and has a neutral to slightly alkaline pH. The core function of potassium phosphate dibasic is to serve as a buffer agent, helping to maintain a specific pH range in aqueous solutions.

Potassium chloride (kcl) by Merck Group

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Potassium chloride (KCl) is an inorganic compound that is commonly used as a laboratory reagent. It is a colorless, crystalline solid with a high melting point. KCl is a popular electrolyte and is used in various laboratory applications.

Sodium hydroxide (naoh) by Merck Group

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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.

Hydrochloric acid (hcl) by Merck Group

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Hydrochloric acid is a commonly used laboratory reagent. It is a clear, colorless, and highly corrosive liquid with a pungent odor. Hydrochloric acid is an aqueous solution of hydrogen chloride gas.

Methanol by Merck Group

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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.

Sodium phosphate monobasic by Merck Group

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Sodium phosphate monobasic is a chemical compound commonly used as a lab reagent. It is a white, crystalline solid that is soluble in water. The primary function of sodium phosphate monobasic is to act as a pH buffer in various laboratory applications, helping to maintain a specific pH level in solutions.

Dimethyl sulfoxide (dmso) by Merck Group

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What are the common uses and applications of Potassium phosphate, dibasic?

Potassium phosphate, dibasic is a versatile inorganic salt with a wide range of applications in scientific research and industrial processes. It is commonly used as a buffering agent, pH regulator, and nutrient in cell culture media, biochemical assays, and various other laboratory procedures. This compound is also utilized in the production of fertilizers, detergents, and food preservatives. Its unique properties make it an essential ingredient in many diverse industries and research fields.

How can Potassium phosphate, dibasic help optimize my experiments and research?

PubCompare.ai's AI-driven platform can assist you in leveraging the power of Potassium phosphate, dibasic for your research and experiments. The platform allows you to screen protocol literatuer more efficiently, and its AI-driven analysis can help you identify the most effective protocols related to Potassium phosphate, dibasic for your specific research goals. By pinpointing critical insights, the platform enables you to choose the best option for reproducibility and accuracy, ultimately optimizing your experiments and findings.

Are there different types or variations of Potassium phosphate, dibasic?

Yes, there are different forms and variations of Potassium phosphate, dibasic. The most common forms include the anhydrous and dihydrate versions. The anhydrous form is a white, crystalline powder, while the dihydrate version appears as colorless crystals. These variations can have slightly different properties and may be suitable for different applications, so it's important to select the appropriate form for your specific needs.

How can I troubleshoot any challenges or issues when using Potassium phosphate, dibasic?

When working with Potassium phosphate, dibasic, you may encounter some common usage challenges. For instance, the salt can be hygroscopic, meaning it can absorb moisture from the air, which may affect its solubility and handling. To mitigate this, ensure proper storage conditions and consider using the anhydrous form if moisture is a concern. Additionally, the pH of solutions containing Potassium phosphate, dibasic can be sensitive, so careful monitoring and adjustments may be necessary to maintain the desired pH levels. PubCompare.ai's platform can provide guidance on optimizing the use of this compound and troubleshooting any issues that may arise.

Potassium phosphate, dibasic

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