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Isobutyric acid

Isobutyric acid is a short-chain, branched-chain carboxylic acid with the chemical formula (CH3)2CHCOOH.
It is an isomer of butyric acid, with the methyl groups attached to the central carbon atom instead of the terminal carbon.
Isobutyric acid occurs naturally in various foods and is also used in the production of certain chemicals and pharmaceuticals.
It has a distinctive, pungent odor and can be found in trace amounts in some fermented foods, such as cheese and wine.
Isobutyric acid plays a role in the production of certain flavors and fragrances, and it may also have potential applications in the biofuels industry.
Researchers can use the PubCompare.ai platform to easily locate and compare protocols involving isobutyric acid from the scientific literature, preprints, and patents, helping to optimize research reproducibility and efficency.

Most cited protocols related to «Isobutyric acid»

Fecal SCFA content was determined by gas chromatography. Chromatographic
analysis was carried out using a Shimadzu GC14-A system with a flame ionization
detector (FID) (Shimadzu Corp, Kyoto, Japan). Fused silica capillary columns 30m
× 0.25 mm coated with 0.25um film thickness were used (Nukol™
for the volatile acids and SPB™-1000 for the nonvolatile acids (Supelco
Analytical, Bellefonte, PA). Nitrogen was used as the carrier gas. The oven
temperature was 170°C and the FID and injection port was set to
225°C. The injected sample volume was 2 µL and the run time for
each analysis was 10 minutes. The chromatograms and data integration was carried
out using a Shimadzu C-R5A Chromatopac. A volatile acid mix containing 10 mM of
acetic, propionic, isobutyric, butyric, isovaleric, valeric, isocaproic,
caproic, and heptanoic acids was used (Matreya, Pleasant Gap, PA). A
non-volatile acid mix containing 10 mM of pyruvic and lactic and 5 mM of
oxalacetic, oxalic, methy malonic, malonic, fumaric, and succinic was used
(Matreya, Pleasant Gap, PA). A standard stock solution containing 1%
2-methyl pentanoic acid (Sigma-Aldrich, St. Louis, MO) was prepared as an
internal standard control for the volatile acid extractions. A standard stock
solution containing 50 mM benzoic acid (Sigma-Aldrich, St. Louis, MO) was
prepared as an internal standard control for the non-volatile acid
extractions.
Samples were kept frozen at −80°C until analysis. The
samples were removed from the freezer and 1,200µL of water was added to
each thawed sample. The samples were vortexed for 1 minute until the material
was homogenized. The pH of the suspension was adjusted to 2–3 by adding
50 µL of 50% sulfuric acid. The acidified samples were kept at
room temperature for 5 minutes and vortexed briefly every minute. The samples
were centrifuged for 10 minutes at 5,000g. 500 µL of the clear
supernatant was transferred into two tubes for further processing. For the
volatile extraction 50 µL of the internal standard (1% 2-methyl
pentanoic acid solution) and 500 µL of ethyl ether anhydrous were added.
The tubes were vortexed for 30 seconds and then centrifuged at 5,000g for 10
minutes. 1 µL of the upper ether layer was injected into the
chromatogram for analysis. For the nonvolatile extraction 50 µL of the
internal standard (50 mM benzoic acid solution) and 500 µL of boron
trifluoride-methanol solution (Sigma-Aldrich St. Louis, MO) were added to each
tube. These tubes were incubated overnight at room temperature. 1 mL of water
and 500 µL of chloroform were added to each tube. The tubes were
vortexed for 30 seconds and then centrifuged at 5,000g for 10 minutes. 1
µL of the lower chloroform layer was injected into the chromatogram for
analysis. 500 µL of each standard mix was used and the extracts prepared
as described for the samples. The retention times and peak heights of the acids
in the standard mix were used as references for the sample unknowns. These acids
were identified by their specific retention times and the concentrations
determined and expressed as mM concentrations per gram of sample.
Publication 2013
Acids Benzoic Acid Capillaries Chloroform Ethers Feces ferrous fumarate Freezing Gas Chromatography Heptanoic Acids Methanol Neoplasm Metastasis Nitrogen Retention (Psychology) Silicon Dioxide Sulfuric Acids valeric acid
Volatile fatty acids and lactic acid, referred to in combination as short-chain fatty acids (SCFA), were analyzed in six replicate fermentation vessels per treatment at the 4-, 10-, and 24-h time-points. The SCFA were analyzed as free acids, using pivalic acid (Sigma-Aldrich, St. Louis, MO, USA) as an internal standard. For this, 400 μL of fermentation fluid and 2.4 mL of 1.0 mM pivalic acid solution were mixed, vigorously shaken for 5 min, and then centrifuged at 3,000 × g for 10 min. Then 800 μL of the supernatant and 400 μL of saturated oxalic acid solution were mixed, incubated at 4°C for 60 min, and centrifuged at 18,000 × g for 10 min. The supernatant was analyzed by gas chromatography (Agilent Technologies, Santa Clara, CA, USA) using a glass column packed with 80/120 Carbopack B-DA/4% Carbowax stationary phase, helium as a carrier gas, and a flame ionization detector. The acids quantified were acetic, propionic, butyric, valeric, isobutyric, 2-methylbutyric, isovaleric, and lactic acid.
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Publication 2019
Acids Blood Vessel Carbowax DNA Replication Fatty Acids, Volatile Fermentation Flame Ionization Gas Chromatography Helium Lactic Acid Oxalic Acids pivalic acid Vinegar
For structural analysis, lipid A was extracted by an ammonium hydroxide-isobutyric acid method as previously described23 (link), and subjected to MALDI-TOF MS analysis. Briefly, freshly washed cells (10 mg) were suspended in 400 μL of isobutyric acid-1M ammonium hydroxide mixture (5:3, vol/vol), and incubated for 2 h at 100 °C in a screw-cap test tube, with occasional vortexing. The mixture was then cooled on ice and centrifuged at 8000 g for 15 min. The supernatant was transferred to a new tube, mixed with an equal volume of water, and lyophilized overnight at −70 °C. The lyophilized sample was then washed twice with 400 μL of methanol, and centrifuged at 5000 rpm for 15 min. Finally, the insoluble lipid A was solubilized in 100 μL chloroform-methanol-water mixture (3:1.5:0.25, v/v/v). The lipid A structure was analyzed using MALDI-TOF mass spectrometry in the negative-ion mode8 (link),24 (link). All MALDI-TOF analyses were performed on a Bruker Ultraflex III TOF/TOF mass spectrometer (Bruker Daltonics, Coventry, UK) using the FlexControl 3.0 acquisition software. The matrix used for lipid A analysis was 2,5-dihydroxybenzoic acid (DHB; Sigma Chemical Co., St. Louis, MO, USA). The DHB solution (10 mg/mL) was prepared using a mixture of water and acetonitrile (1:4, vol/vol). All lipid A samples were premixed with the DHB solution (1:1, vol/vol) before MALDI measurements, and 1 μL of the resulting mixture was spotted on the MALDI metallic target. Lipid A from E. coli F583 was used as an external standard and mass calibrant.
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Publication 2017
2,3-dihydroxybenzoic acid acetonitrile Ammonium Hydroxide Cells Chloroform Escherichia coli isobutyric acid Lipid A Mass Spectrometry Metals Methanol Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Quantification of SCFAs in faecal samples was carried out using external calibration standard curves method. Seven calibration standards were prepared at six levels of concentration ranging from 0.005M to 0.03M for pyruvic acid, 0.01M to 0.06M for formic acid and acetic acid, and 0.02M to 0.12M for lactic acid, propionic acid, isobutyric acid and butyric acid. The reference samples were injected repeatedly for nine times to measure the retention time. The calibration curves were constructed by plotting the relative peak area versus the molarity of solution. Faecal SCFA concentrations were expressed as mean µmol per gram wet weight faeces using the following equation as described by Hoshi et al. [29 (link)] with modification.
Faecal SCFA (µmol/g) = [organic acid in faecal contents (mmol/ml) X Vd (ml) X 1000]/ Wet weight faeces (g)
Whereas: Vd = Total Volume of Dilution
Publication 2010
Acetic Acid Acids Butyric Acids Feces formic acid isobutyric acid Lactic Acid propionic acid Pyruvic Acid Retention (Psychology) Technique, Dilution
Right after evacuation, the stools were assigned a faecal quality score using a 5-points visual scale with 0.5 score interval ranging from 1 (hard and dry faeces) to 5 (liquid diarrhoea) [22 ]. Scores of 2–3 were considered the optimum, consisting in firm but not dry stool, with moderate segmentation visible, holding form when picked up leaving none or minimal residual on the ground.
After thawing, 2 g of faeces were mixed with 1/1 deionized water and pH measured using a Mettler Toledo InLab® Expert Pro pH meter. The analysis of short chain fatty acids (SCFA) (2:0, acetic; 3:0, propionic; 4:0, butyric; iso 4:0, isobutyric; 5:0, valeric; iso 5:0, isovaleric) and lactic acid of faecal samples was performed by HPLC according to the following procedures: 3 g of faeces was diluted with 150 mL of 0.1 N H2SO4 aqueous solution and homogenized for 2 min by UltraTurrax (IKA®-Werke GmbH & Co. KG, Staufen, Germany). The mix was centrifuged (5,000 × g for 15 min at 4 °C) to separate the liquid phase from the solid residuals and the liquid phase subsequently microfiltered (SLMV033RS, 0.45-μm Millex-HV, Merck-Millipore, Billerica, MA). The resulting sample was directly injected in the HPLC apparatus using an Aminex 85 HPX-87 H ion exclusion column (300 mm × 7.8 mm; 9-μm particle size; Bio-Rad, Milan, Italy) kept at 40 °C; the detection wavelength was 220 nm. The analyses were carried out applying an isocratic elution (flux 0.6 mL/min) with a 0.008 N H2SO4 solution as mobile phase; the injection loop was 20 μL. Individual SCFA and lactic acid were identified using a standard solution of 4.50 mg/mL of lactic acid, 5.40 mg/mL of acetic acid, 5.76 mg/mL of propionic acid, 7.02 mg/mL of butyric acid and isobutyric acid, 8.28 mg/mL of valeric acid and isovaleric acid in 0.1 N H2SO4 (69775, 338826, 402907, B103500, 58360, 75054, 129542, respectively; Sigma-Aldrich, Milano Italy). Quantification was done using an external calibration curve based on the standards described above.
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Publication 2016

Most recents protocols related to «Isobutyric acid»

Activated T cells (5 × 105 cells) were mixed with cancer cells (5 × 104 cells) that were previously seeded (at least 2 h before) in 6-well plates in iMediam for T medium or RPMI-1640 supplemented as the above medium in a total volume of 2 mL. After another 2 h, SCFAs (acetic, propionic, butyric, isobutyric, valeric, isovaleric, or hexanoic acids) (Merck KGaA, Darmstadt, Germany) were added to the co-culture in increasing concentrations (0.1, 3, or 10 mM). In order to make a pH similar with that of 10 mM isobutyric acid treatment, hydrochloric acid was added at a final concentration of 10 mM. The co-culture was maintained at 37 °C in 5% CO2 atmosphere for 72 h. The absolute numbers of cancer cells and T cells were determined using flow cytometry using fluorescent counting beads (Flow-Count, Beckman coulter, Brea, USA). After collecting floating cells, adherent cells were trypsinised and collected into the same tube. Fluorescent counting beads were added to each sample tube before staining cells with FITC or BV650-conjugated anti-CD45 antibody. CD45-positive cells were defined as T cells and all others as cancer cells. The numbers of T cells and cancer cells were corrected by the number of fluorophore beads counted in each sample (Supplementary Fig. S2).
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Publication 2024
All short-chain fatty acids standards ((acetic acid-AA (C2), propionic acid- PA (C3), butyric acid-BA (C4), isobutyric acid-IBA (C4), valeric acid- VA (C5), isovaleric acid-IVA (C5), caproic acid—CA (C6), isocaproic acid ICA (C6)) and short-chain fatty acid isotope-labeled standards (acetic acid-13C2, propionic acid-D6, butyric acid-13C2, isobutyric acid-D7, valeric acid-D9), pyridine anhydrous, 2-nitro phenylhydrazine (3NPH·HCl), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC·HCl)) were acquired from Sigma-Aldrich (St. Louis, MO, USA). All SCFAs stock solutions were prepared in 50% acetonitrile and stored at −20 °C. LC-MS grade acetonitrile, HPLC-grade acetonitrile, HPLC-grade methanol, and formic acid were obtained from J.T. Baker. Ultra-pure water (Mili-Q water) was produced using a water purification system (Mili-Q, Millipore, Milford, MA, USA).
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Publication 2024
BALB/C mice were obtained from CLEA Japan (Tokyo, Japan) and maintained at a constant temperature (23 ± 1 °C) with a 12 h light/dark cycle under specific pathogen-free conditions. The experimental protocols were approved by the Institutional Animal Care and Use Committee of the Showa University, and all experiments were conducted according to relevant guidelines and regulations. This study is a research report following the ARRIVE guidelines. Age-matched 8–12-week-old male mice were subcutaneously injected with 2 × 105 CT26 cells in the right flank. Mice received intraperitoneal injections of 150 μg of anti-PD-1 (clone RMP1-14; Lebanon, NH, USA) per injection or its isotype control (IgG2b; Lebanon, NH, USA) on days 4, 11, 18, and 25. Mice received isobutyric acid (100 mM) in the drinking water or pH-match water (control group) for 2 weeks prior to tumour inoculation, and the water solution was changed weekly. Tumour size was measured using a calliper twice a week until it reached the size that should be sacrificed, and tumour volume was determined as length × width2 × 0.5.
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Publication 2024
Fecal samples from mice in the PCa, ICA, CUR, and ICA + CUR groups were collected to detect changes in SCFAs (acetic, propionic, isobutyric, butyric, isovaleric, and valeric acid). An appropriate amount of feces (50 mg-100 mg) with magnetic beads and 300 µL saline (including 37.3 µg/mL d7 isobutyric acid) was homogenized at 60 Hz for 60 s. Supernatants were centrifuged at 4℃, and 200 µL was removed, acidified by adding 10 µL of 5 M HCl, and vortexed. Anhydrous ether (200 µL) was used for extraction, vortexed, and centrifuged at 4℃. The collected supernatant was subjected to analysis using an Agilent 7890B-5977B gas chromatograph.
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Publication 2024
Short-chain fatty acids (SCFAs) (acetic acid, propanoic acid, isobutyric acid, butyric acid, isovaleric acid, valeric acid, and caproic acid) were determined as described by Zhao et al. [16 (link)] with some modifications, which are given in Supplementary File S1. Gas chromatography–mass spectrometry was used to analyze SCFAs.
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Publication 2024

Top products related to «Isobutyric acid»

Sourced in United States, China, Germany, Italy, Sao Tome and Principe, Canada
Isobutyric acid is a colorless, flammable organic compound with a distinctive odor. It is a carboxylic acid with the chemical formula (CH3)2CHCOOH. Isobutyric acid is used as a chemical intermediate in various industrial applications.
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Isovaleric acid is a straight-chain carboxylic acid with the chemical formula CH3CH2CH(CH3)COOH. It is a colorless, oily liquid that is slightly soluble in water. Isovaleric acid is commonly used as a chemical intermediate in various industrial processes.
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Acetic acid is a colorless, vinegar-like liquid chemical compound. It is a commonly used laboratory reagent with the molecular formula CH3COOH. Acetic acid serves as a solvent, a pH adjuster, and a reactant in various chemical processes.
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Propionic acid is a widely used organic compound that serves as a key ingredient in various industrial and laboratory applications. It is a colorless, pungent liquid with a characteristic odor. Propionic acid is primarily utilized as a preservative and antimicrobial agent in food, animal feed, and pharmaceutical products.
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Butyric acid is a short-chain fatty acid that is commonly used in laboratory settings. It is a colorless liquid with a distinctive odor. Butyric acid is a key component in various biochemical and analytical processes, serving as a versatile tool for researchers and scientists.
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Valeric acid is a straight-chain, saturated carboxylic acid with the chemical formula CH3(CH2)3COOH. It is a colorless, oily liquid with a characteristic unpleasant odor. Valeric acid is commonly used as a chemical intermediate in the production of various pharmaceutical and industrial compounds.
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Hexanoic acid is a carboxylic acid with the chemical formula CH3(CH2)4COOH. It is a colorless liquid with a characteristic unpleasant odor. Hexanoic acid is used as a precursor in the synthesis of various organic compounds and as a component in certain industrial and laboratory applications.
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The DB-FFAP column is a gas chromatography column designed for the separation and analysis of polar compounds. It features a polyethylene glycol stationary phase, which provides high thermal stability and excellent peak shape for a wide range of polar analytes.
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Isobutyric is a chemical compound with the formula (CH3)2CHCOOH. It is a colorless liquid with a distinctive odor. Isobutyric is primarily used as a reagent in organic synthesis and laboratory applications.
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Acetic is a laboratory-grade chemical compound commonly used as a reagent in various scientific applications. It is the main component of vinegar and serves as a versatile solvent, buffer, and pH adjuster in laboratory settings. The core function of Acetic is to provide a consistent and reliable source of this widely used chemical for research and analytical purposes.

More about "Isobutyric acid"

Isobutyric acid, also known as 2-methylpropanoic acid, is a short-chain, branched-chain carboxylic acid with the chemical formula (CH3)2CHCOOH.
It is an isomer of butyric acid, with the methyl groups attached to the central carbon atom instead of the terminal carbon.
Isobutyric acid occurs naturally in various foods and is also used in the production of certain chemicals and pharmaceuticals.
Isobutyric acid has a distinctive, pungent odor and can be found in trace amounts in some fermented foods, such as cheese and wine.
It is closely related to other short-chain fatty acids like isovaleric acid, acetic acid, propionic acid, butyric acid, valeric acid, and hexanoic acid.
These compounds play important roles in the production of flavors and fragrances, and may also have potential applications in the biofuels industry.
Researchers can use the PubCompare.ai platform to easily locate and compare protocols involving isobutyric acid from the scientific literature, preprints, and patents.
This can help optimize research reproducibility and efficiency by identifying the best protocols and products.
By incorporating insights from related compounds and leveraging AI-driven comparisons, scientists can imrpove the quality and accuracy of their isobutyric acid research.