The largest database of trusted experimental protocols
> Chemicals & Drugs > Organic Chemical > Divinylbenzene

Divinylbenzene

Divinylbenzene is a chemical compound with the formula C6H4(CH=CH2)2.
It is a colorless liquid with a sweet odor and is used as a crosslinking agent in polymers and resins.
Divinylbenzene is also an important precursor in the synthesis of various organic compounds.
This versatile molecule has applications in fields such as polymer chemistry, materials science, and organic synthesis.
Researchers can optimize the use of divinylbenzene in their studies by utilizing the powerful AI-driven research protocol comparison tool offered by PubCompare.ai.
This cutting-edge tool streamlines the research process by effortlessly locating protocols from literature, preprints, and patents, while identifying the most reproducible and accurate methods.
With PubCompare.ai, scientists can achiev enhanced results in their divinylbenzene-related projects.

Most cited protocols related to «Divinylbenzene»

The urine samples analyzed for this study were selected from the Third National Health and Nutrition Examination Survey (NHANES III) callback cohort, a nonrepresentative subset of NHANES III composed of approximately 1,000 adults. The urine samples were all spot-urine samples, collected at different times throughout the day and were not necessarily first-morning voids. Creatinine adjustment was used to correct for urine dilution (Jackson 1966 (link)).
BPA and 4-n-nonylphenol (nNP), the linear chain NP isomer, were measured using a method based on an automated solid-phase extraction (SPE) coupled to isotope dilution-GC/MS (Kuklenyik et al. 2003 (link)). First, the urine samples were treated with β-glucuronidase to hydrolyze the glucuronide conjugates. Then, during the automated SPE process, BPA and nNP were both extracted from the deconjugated urine matrix and derivatized, using pentafluorobenzyl bromide, on commercial styrene-divinylbenzene copolymer-based SPE cartridges. After elution from the SPE column, the derivatized phenols in the SPE eluate were measured by isotope-dilution GC/MS. The limits of detection (LODs) for BPA and nNP in a 1-mL urine sample were 0.1 μg/L.
Quality control (QC) materials were analyzed along with the samples to assure the accuracy and reliability of the data. Low-concentration (QCL, 2–5 ng/mL) and high-concentration (QCH, 12–20 ng/mL) QC materials were prepared from a base urine pool—obtained from multiple anonymous donors as described previously (Kuklenyik et al. 2003 (link))—dispensed in 5-mL aliquots and stored at −20°C. Each QC material was characterized by repeated measurements, spanned over at least 4 weeks, to define the mean concentrations and the 95% and 99% control limits of BPA and nNP. Each analytical run consisted of 40 (2 QCH, 2 QCL, 4 blanks, and 32 unknown) samples. The concentrations of the two QCH and the two QCL, averaged to obtain one measurement of QCH and QCL for each run, were evaluated using standard statistical probability rules.
The samples used for this study were stored securely at −70°C and may have been subject to repeated thaw/freeze cycles. Before analysis, the samples and QC materials were left to thaw overnight at 5°C. The concentrations of the analytes in the QCs remained essentially constant under these experimental conditions. Furthermore, QC materials reanalyzed after the initial characterization showed that BPA and nNP remained stable in the QC materials at −20°C for at least 1 year. Although the long-term stability of the analytes in the urine samples stored for > 1 year is not known, the QC data suggest that the integrity of the specimens is likely maintained and that chemical degradation of the phenols was undetectable.
To estimate total sample size, we used a standard formula n = t2p(1 − p)/d2, where n is the estimated sample size, t is the critical value associated with the desired statistical confidence level, and d is the maximum allowable error above or below the estimate of the true proportion (p) of the target population with measurable levels of the analyte(s) of interest (Peavy 1996 ). Using a confidence level of 99% (t = 2.6), d = 0.065, and a 50% percentage of the population with measurable BPA and nNP levels (p = 0.5), the estimated total sample size was 400. Participants in this study were 20–59 years of age, of both sexes, and urban and rural residents. An arbitrary cutoff of 100,000 inhabitants per county was used to distinguish rural from urban areas. Each sample, defined by age (< 50 years or ≥50 years), residence (rural or urban), and sex (male or female), was categorized in eight subpopulation groups (e.g., < 50-year-old rural female).
Because samples were obtained from the NHANES III callback cohort, a nonrepresentative subset of NHANES III samples, the summary statistics are not representative of the U.S. population but serve as reference ranges for the three population breakdowns specified above (i.e., persons < 50 or ≥50 years of age; rural or urban residents; male or female). To improve the extent to which the results represent the U.S. population, we used sample weights. We developed our own weights for demographic groups, not for individual subjects. This approach is different from that used by the National Center for Health Statistics (NCHS) of the Centers for Disease Control and Prevention (CDC). The NCHS assigns a unique weight to each subject based on demographics, geographical data, and oversampling of certain population groups. Because we only had information on age group, sex, and residence (i.e., rural and urban), we could not assign weights to individual subjects, only to the demographic groups. We determined the weights by relating the sample sizes in each of the eight groups to the total numbers of persons in the U.S. population in the same groups defined by sex, residence, and age. From within these eight groups, we randomly selected 394 samples. The institutional review board of the NCHS approved the study.
We analyzed the weighted data using SAS software, version 8.2 (SAS Institute, Cary, NC). Because the base-10 logarithm of the concentrations (log-transformed concentrations) was less skewed than the nontransformed values, we used the log-transformed values in the analyses. We calculated GMs and distribution percentiles for both volume-based (micrograms per liter) and creatinine-corrected concentrations (micrograms per gram creatinine). The GMs were exponentiated results obtained from the means of the log-transformed concentrations. GMs were calculated when the frequency of detection of the analyte was > 60%. We did not use weights to obtain GM or percentile estimates for the various demographic groups because each subject in a demographic group had the same weight.
For exploratory purposes only, we compared BPA and NP levels among subgroups (by age, sex, and place of residence) even though we did not design the study to assure adequate statistical power for this type of hypothesis testing (i.e., the sample size was determined to answer only the question about the percentage of population with measurable urinary BPA and/or NP levels). We used weighted analysis of covariance models to study the effects of residence, sex, age group, and urinary creatinine on the urinary log-transformed concentrations of BPA and NP. The analyses were performed using SAS Proc GENMOD (SAS Institute) to model the log-transformed concentrations (dependent variable) as a function of sex, residence, age group (categorical covariates), and urinary creatinine (continuous covariate used to adjust for urine dilution). The purpose of our model adjustment was not to apply an individual adjustment to BPA and NP concentrations, but rather to enable us to determine whether there are differences in average BPA or NP urinary levels between individuals in the same demographic groups (e.g., men vs. women) after accounting for the differences due to urinary dilution. By adjusting for creatinine, we obtained a comparison that was not influenced by differences in creatinine levels. We also considered all possible two-way interactions between covariates. Type 3 equivalent sums of squares from the model were used to form likelihood ratio tests of model effects and various tests of hypotheses. Statistical significance was set at p < 0.05. We dealt with results < LOD by using a multiple imputation method (Lynn 2001 ) along with the SAS procedure PROC MIANALYZE, which summarizes parameter estimates and incorporates the resulting uncertainty associated with the multiple imputations used to obtain them.
Full text: Click here
Publication 2004
Bieleski buffer (60% methanol, 25% CHCl3, 10% HCOOH and 5% H2O) was used as extraction solvent (50 μl per sample). Tritium-labelled (105 dpm) or unlabelled (1 pmol) cytokinin standards were added to the sample extracts during the method optimization to determine the recoveries of the StageTip purification procedure. To validate the quantification of the endogenous cytokinin levels in A. thaliana seedlings, roots and shoots, the following stable isotope-labelled cytokinin internal standards (IS) were added as internal tracers at a concentration 0.5 pmol of each compound per 50 μl of Bieleski buffer: [13C5]cZ, [13C5]tZ, [2H5]tZR, [2H5]tZ7G, [2H5]tZ9G, [2H5]tZOG, [2H5]tZROG, [2H5]tZMP, [2H3]DHZ, [2H3]DHZR, [2H3]DHZ9G, [2H7]DHZOG, [2H3]DHZMP, [2H6]iP, [2H6]iPR, [2H6]iP7G, [2H6]iP9G, [2H6]iPMP. The plant material was placed in 2.0 ml microcentrifuge tubes and extracted in Bieleski solvent using a MM 301 vibration mill (Retsch GmbH & Co. KG, Haan, Germany) at a frequency of 27 Hz for 3 min after adding 3 mm tungsten carbide beads (Retsch GmbH & Co. KG, Haan, Germany) to increase the extraction efficiency. The tube content was ultrasonicated for 3 min and then stirred for 30 min at 4°C. After centrifugation (10 min, 15,000 rpm, 4°C) the supernatants (50 μl aliquots) were immediately transferred onto StageTips and purified according to the following protocol.
The PT-SPE was performed in self-packed StageTips by placing a very small disk of matrix in an ordinary pipette tip. Commercially available matrix of poly-tetrafluoroethylene containing reversed-phase octadecyl-bonded silica phase (C18) or poly(styrene-divinylbenzene) (SDB) copolymer modified with sulfonic acid groups to make it more hydrophilic (SDB-RPS Disk) was normally used. Alternatively, ion-exchange sorbent including sulfonic acid as cation exchanger (Cation-SR Disk) was also employed. The procedure shown in Additional file 5 was described by Rappsilber et al. [23 (link),26 (link)]. Small disks (approximately 1.0 mm diameter, 0.5 mm thickness) were cut out manually from the EmporeTM High Performance Extraction Disk placed on a clean surface (Petri dish) using a hollow tool cutter (blunt-ended syringe needle). The cutter was gently pressed into the Empore disk and the material penetrated to the inside of the needle. Subsequently, the cutter was placed inside a pipette tip (disposable GELoader® Tip, 100 μl, from Eppendorf). The small disk was then released using a plunger (rod) that fitted into the needle (both parts from Hamilton) and pressed gently repeatedly into place using the weight of the plunger. After removing the cutter and plunger, the single-StageTip was finished. Additional disks were added the same way to produce combined multi-StageTips.
The Empore sorbents were tested individually (C18, SDB-RPS, and Cation-SR) or in combination (C18/SDB-RPS, C18/Cation-SR, C18/SDB-RPS/Cation-SR). All solutions were loaded from the top of the tip in a volume of 50–100 μl using a pipette. The prepared StageTip was inserted into a hole at the centre of the lid of the microcentrifuge tube (1.5 ml) and placed in a centrifuge after solvent pipetting (Figure 2). Prior to loading the sample the StageTip sorbents were activated with 50 μl acetone (by centrifugation at 1,500 rpm, 15 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C), 50 μl methanol (1,500 rpm, 15 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C), equilibrated with 50 μl 50% (v/v) nitric acid (1,000 rpm, 20 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C) and 50 μl Bieleski solvent (1,500 rpm, 15 min, 4°C). Afterwards, the samples were loaded in extraction buffer (500 rpm, 45 min, 4°C). The tips were washed using 50 μl methanol (1,500 rpm, 15 min, 4°C) and elution of samples was performed with 50 μl of 0.5 M NH4OH in 60% MeOH (500 rpm, 45 min, 4°C). Eluates were collected into new clean microcentrifuge tubes and directly mixed with scintillation buffer prior to measurement of radioactivity or evaporated to dryness in a Speed-Vac concentrator RC1010 (Jouan, Winchester, UK) and dissolved in 20 μl of mobile phase prior to UHPLC-MS/MS analyses.
Full text: Click here
Publication 2012
RNA was purified by High performance liquid chromatography (HPLC) (Akta Purifier, GE Healthcare) using a column matrix of alkylated non-porous polystyrene-divinylbenzene copolymer microspheres (2.1 μm) (21 × 100 mm column). Buffer A contained 0.1 M triethylammonium acetate (TEAA), pH = 7.0 and Buffer B contained 0.1 M TEAA, pH = 7.0 and 25% acetonitrile (Transgenomics). Columns were equilibrated with 38% Buffer B, loaded with RNA and run with a single or 2 linear gradients to 55 or 65% Buffer B over 20–30 min at 5 ml/min. RNA analyses were performed with the same column matrix and buffer system using a 7.8 mm × 50 mm column at 1.0 ml/min.
Publication 2011
Acetate acetonitrile Buffers divinylbenzene-polystyrene copolymer High-Performance Liquid Chromatographies Microspheres
Lungs were perfused with PBS through the heart to remove blood. Then, ∼100 mg of total lung tissue (wet weight) was homogenized in 500 μl PBS (with protease inhibitor cocktail and EDTA) using an Ultra-turrax homogenizer. After centrifugation, the soluble proteins were collected and proteins were extracted from the insoluble pellet in three steps using buffers with increasing stringency [buffer 1: 150 mM NaCl, 50 mM Tris–HCl (pH 7.5), 5% glycerol, 1% IGEPAL® CA-630 (Sigma, #I8896), 1 mM MgCl2, 1× protease inhibitors (+EDTA), 1% benzonase (Merck, #70746-3), 1× phosphatase inhibitors (Roche, #04906837001); buffer 2: 50 mM Tris–HCl (pH 7.5), 5% glycerol, 150 mM NaCl, fresh protease inhibitor tablet (+EDTA), 1.0% IGEPAL® CA-630, 0.5% sodium deoxycholate, 0.1% SDS, 1% benzonase (Merck, #70746-3); and buffer 3: 50 mM Tris–HCl (pH 7.5), 5% glycerol, 500 mM NaCl, protease inhibitor tablet (+EDTA), 1.0% IGEPAL® CA-630, 2% sodium deoxycholate, 1% SDS, 1% benzonase (Merck, #70746-3)]. Insoluble pellets were resuspended in detergent-containing buffers and incubated for 20 min on ice (except for buffer 3, which was used at room temperature), followed by separation of soluble and insoluble material using centrifugation for 20 min at 16,000 g. The PBS from the tissue homogenate and the NP40-soluble fraction (buffer 1) was pooled, which together with the two fractions derived from ionic detergent extraction (buffers 2 and 3) resulted in a total of three soluble fractions and one insoluble pellet that were subjected to LC-MS/MS analysis. Soluble proteins were precipitated with 80% acetone and subjected to in-solution digestion using a modified published protocol (Kulak et al, 2014 (link)). In brief, protein reduction (10 mM TCEP) and alkylation (50 mM CAA) were performed at once in 6 M guanidinium hydrochloride (100 mM Tris–HCl pH 8.5) at 99°C for 15 min. Subsequent protein digestion was done in two steps. The first digestion was done at 37°C for 2 h with LysC (1:50 enzyme to protein ratio) in 10 mM Tris–HCl (pH 8.5) containing 2 M guanidinium hydrochloride (Gdm), 2.7 M urea, and 3% acetonitrile. The second digestion step was done using fresh LysC (1:50 enzyme to protein ratio) and trypsin (1:20 enzyme to protein ratio) in 600 mM Gdm, 800 mM urea, and 3% acetonitrile at 37°C overnight. For the insoluble protein pellet, which is strongly enriched for insoluble ECM proteins, we optimized the in-solution digestion protocol with additional steps involving extensive mechanical disintegration and ultrasonication-aided digestion. The insoluble material was cooked, reduced, and alkylated in 6 M Gdm for 15 min and then subjected to 200 strokes in a micro-Dounce device, which reduced the particle size of the insoluble protein meshwork. We then proceeded with the two-step digestion protocol described above, which was additionally aided by 15-min ultrasonication (Bioruptor, Diagenode) in the presence of the enzymes in both digestion steps.
For tissue proteome time course analysis, a similar sequential extraction procedure as described above was used. However, in these experiments, we employed slightly different buffers for extraction following a commercially available protein extraction kit (Compartment Protein Extraction Kit, Millipore). We collected three protein fractions for LC-MS analysis (two soluble fractions and one insoluble fraction). The first fraction measured was derived from proteins soluble in buffer M of the extraction kit [HEPES (pH 7.9), MgCl2, KCl, EDTA, sucrose, glycerol, sodium deoxycholate, NP-40, sodium orthovanadate]; the second fraction was derived from proteins soluble in buffer CS [PIPES (pH 6.8), MgCl2, NaCl, EDTA, sucrose, SDS, sodium orthovanadate], and finally, we also analyzed the proteins insoluble in buffer CS as described above for QDSP. To perform relative quantification of full proteomes in the various conditions, we summed up the peptide intensities of the three protein fractions in MaxQuant (Cox & Mann, 2008 (link)).
Peptides were purified using stage tips containing a poly-styrene-divinylbenzene copolymer modified with sulfonic acid groups (SDB-RPS) material (3M, St. Paul, MN, USA) as previously described (Kulak et al, 2014 (link)). For the QDSP experiments, we separated peptides in two fractions by sequentially eluting from the SDB-RPS stage tip material (buffer 1: 150 mM NH4HCO2, 60% acetonitrile, 0.5% FA; buffer 2: 5% ammonia and 80% acetonitrile).
Full text: Click here
Publication 2015
RNA was purified by HPLC using a Semi-Prep RNASep (100 × 21.1-mm) column packed with a matrix of C-18 alkylated non-porous polystyrene-divinylbenzene copolymer microspheres (Transgenomics, Omaha, NE) connected to an Äkta avant 25 system. Ion pair reversed-phase chromatography was performed according to a protocol described previously,17 (link), 18 (link) using a linear gradient of 38%–70% buffer B (0.1 M triethylammonium acetate [TEAA, pH 7.0] and 25% [v/v] acetonitrile) in buffer A (0.1 M TEAA [pH 7.0]) at a flow rate of 5 mL/min. The mRNA from the collected peak fractions was concentrated and desalted, by successive centrifugation using Amicon Ultra-15 centrifugal filter units (30 kDa molecular weight cut-off) (Merck Millipore, Darmstadt, Germany) and dilution with nuclease-free water, and finally it was recovered from the retentate by isopropanol precipitation.
Full text: Click here
Publication 2019
Acetate acetonitrile Buffers Centrifugation Chromatography, Reverse-Phase divinylbenzene-polystyrene copolymer High-Performance Liquid Chromatographies Isopropyl Alcohol Microspheres RNA, Messenger Technique, Dilution

Most recents protocols related to «Divinylbenzene»

Poplar wood (Populus spp.) was cut into blocks with the dimensions of 10 mm (longitudinal) × 20 mm (tangential) × 20 mm (radial). All wood blocks were ultrasonically cleaned with an ethanol/water mixture, and dried in an oven at 100 °C for 24 h until a constant weight was reached. 2-Isocyanatoethyl methacrylate (IEMA, 98%), divinylbenzene (DVB, 80%), 2,2′-azobis(2-methyl propionitrile) (AIBN, 98%), and dibutyltin dilaurate (DBTL, 95%) were purchased from Macklin Biochemical Co., Ltd (Shanghai, China). Ethyl acetate (99%), dimethylsulfoxide (DMSO, 99.8%), hydrochloric acid (HCl, 36–38%), sodium hydroxide (NaOH, 96%), sodium chloride (NaCl, 99.5%), toluene (99.5%), acetone (99.5%), n,n-dimethylformamide (DMF, 99.5%), decane (98%), 1,4-dioxane (99%), absolute ethanol were purchased from Sinopharm Chemical Reagent Co., Ltd (Shanghai, China).
Full text: Click here
Publication 2024
Styrene
(St), divinylbenzene (DVB), azobis(isobutyronitrile)
(AIBN), 2-ethylhexyl acrylate (EHA), and CaCl2·2H2O were purchased from Sigma-Aldrich. Polyurethane diacrylate
(PUDA) Ebecryl 8402 was kindly supplied by Allnex (Netherlands) and
the surfactant Hypermer B246 by Croda (Spain). All chemicals were
used as received.
Full text: Click here
Publication 2024
Fibers used in SPME volatile extraction including stable flex coated with divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS, 50/30 μm) or PDMS (polydimethylsiloxane) were purchased from Supelco (Oakville, ON, Canada). Volatile and alkane standards were provided from Sigma Aldrich (St. Louis, MO, USA).
Full text: Click here
Publication 2024
1,3-Di(9H-carbazol-9-yl)benzene
(mCP, 98%) was purchased from Aaron Chemicals. Hafnium(IV) chloride
(99%) was purchased from Acros Organics. Bis[2-(4,6-difluorophenyl)pyridinato-C2,N](picolinato)iridium(III) (FIrPic) was purchased from American
Dye Source. Ethanol was purchased from Decon Laboratories. EJ-550
optical grade silicone grease was purchased from Eljen. Trifluoroacetic
acid was purchased from EMD Millipore Corporation. Acetone (Certified
ACS), hydrogen peroxide (Certified ACS, 30%), sulfuric acid (Certified
ACS Plus), and toluene (Certified ACS) were purchased from Fisher
Chemical. Bis(2-(methacryloyloxy)ethyl) phosphate, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane (Luperox-231,
92%), cyclohexane (99.9%), divinylbenzene (technical grade, 80%),
inhibitor removers (Al2O3), methylstyrene (60% meta, 40% para, and 1% ortho, 99%), and oleylamine (technical grade, 70%) were purchased from
Sigma-Aldrich. 9,9-Dimethyl-9H-fluorene (MF, 97%)
was purchased from Synthonix. Chloroform (99.8%) was purchased from
Thermo Scientific. Trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl)silane was purchased from Tokyo Chemical Industry. Methylstyrene
and divinylbenzene were purified by a column packed with inhibitor
removers to remove tert-butylcatechol, then degassed
before use. Luperox-231 was also degassed before use. All other materials
were used as received.
Full text: Click here
Publication 2024
Special fibers used in extraction of volatiles by SPME are stable flex coated with divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS, 50 µm/30 µm, stable flex 24 Ga, fiber L 1 cm) or PDMS (polydimethylsiloxane) were purchased from Supelco (Oakville, ON, Canada). All volatile standards were purchased from Sigma-Aldrich (St. Louis, MO, USA)44 (link),45 (link).
Full text: Click here
Publication 2024

Top products related to «Divinylbenzene»

Sourced in United States, Canada, United Kingdom, Japan, Poland
DVB/CAR/PDMS is a type of stationary phase used in solid-phase extraction (SPE) and chromatographic techniques. It is composed of a mixture of divinylbenzene (DVB), carboxen (CAR), and polydimethylsiloxane (PDMS) materials. This stationary phase is designed to provide a diverse range of analyte retention capabilities, allowing for the extraction and separation of a wide variety of compounds.
Sourced in United States, Germany
Divinylbenzene is a chemical compound used in the manufacturing of various types of lab equipment. It is a clear, colorless liquid with a distinct aromatic odor. Divinylbenzene is primarily used as a crosslinking agent in the production of polymers and resins, which are essential components in the construction of various laboratory instruments and devices.
Sourced in United States, Germany
SPME fiber is a sampling device used for the extraction and concentration of analytes from various sample matrices. It consists of a fused silica fiber coated with a polymeric material that selectively absorbs target compounds. The SPME fiber can be used to extract and preconcentrate analytes from gas, liquid, or solid samples, improving the sensitivity and selectivity of analytical methods.
Sourced in Germany, United States, Italy, India, United Kingdom, China, France, Poland, Spain, Switzerland, Australia, Canada, Sao Tome and Principe, Brazil, Ireland, Japan, Belgium, Portugal, Singapore, Macao, Malaysia, Czechia, Mexico, Indonesia, Chile, Denmark, Sweden, Bulgaria, Netherlands, Finland, Hungary, Austria, Israel, Norway, Egypt, Argentina, Greece, Kenya, Thailand, Pakistan
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.
Sourced in United States, Switzerland
The DVB/CAR/PDMS fiber is a versatile laboratory equipment used in various analytical applications. It is a composite material made up of divinylbenzene (DVB), carboxen (CAR), and polydimethylsiloxane (PDMS) components. The fiber is designed to provide efficient extraction and concentration of a wide range of analytes, including volatile organic compounds, semivolatile organic compounds, and polar compounds, from complex matrices.
Sourced in United States, Germany, China
Styrene is a colorless liquid organic compound that is used as a chemical building block in the production of various polymers and copolymers. It serves as a precursor for the synthesis of polystyrene and other important industrial materials.
Sourced in United States
The SPME (Solid Phase Microextraction) device is a sample preparation tool used for the extraction and concentration of analytes from various matrices. It functions by utilizing a fiber coated with a selective sorbent material that can adsorb target compounds from the sample. The SPME device enables efficient sample preparation for subsequent analysis by techniques such as gas chromatography or liquid chromatography.
Sourced in United States, Spain
Divinylbenzene/carboxen/polydimethylsiloxane is a solid-phase microextraction (SPME) fiber coating used in gas chromatography. It is designed to effectively extract a wide range of volatile and semi-volatile organic compounds from various sample matrices.
Sourced in Germany, United States, Italy, India, China, United Kingdom, France, Poland, Spain, Switzerland, Australia, Canada, Brazil, Sao Tome and Principe, Ireland, Belgium, Macao, Japan, Singapore, Mexico, Austria, Czechia, Bulgaria, Hungary, Egypt, Denmark, Chile, Malaysia, Israel, Croatia, Portugal, New Zealand, Romania, Norway, Sweden, Indonesia
Acetonitrile is a colorless, volatile, flammable liquid. It is a commonly used solvent in various analytical and chemical applications, including liquid chromatography, gas chromatography, and other laboratory procedures. Acetonitrile is known for its high polarity and ability to dissolve a wide range of organic compounds.
Sourced in United States, Germany, France, United Kingdom, Italy, Morocco, Spain, Japan, Brazil, Australia, China, Belgium, Ireland, Denmark, Sweden, Canada, Hungary, Greece, India, Portugal, Switzerland
The Milli-Q system is a water purification system designed to produce high-quality ultrapure water. It utilizes a multi-stage filtration process to remove impurities, ions, and organic matter from the input water, resulting in water that meets the strict standards required for various laboratory applications.

More about "Divinylbenzene"

Divinylbenzene, also known as DVB, is a versatile chemical compound with the formula C6H4(CH=CH2)2.
This colorless liquid has a sweet odor and is widely used as a crosslinking agent in polymers and resins.
Divinylbenzene is an important precursor in the synthesis of various organic compounds, making it a crucial molecule in the fields of polymer chemistry, materials science, and organic synthesis.
One of the key applications of divinylbenzene is in the SPME (Solid-Phase Microextraction) technique, where it is often used in combination with carboxen (CAR) and polydimethylsiloxane (PDMS) to create the DVB/CAR/PDMS fiber.
This versatile fiber is employed in the extraction and analysis of a wide range of analytes, including volatile organic compounds (VOCs), pesticides, and other environmental pollutants.
The optimization of divinylbenzene-related research can be greatly enhanced by utilizing the AI-driven research protocol comparison tool offered by PubCompare.ai.
This cutting-edge platform streamlines the research process by effortlessly locating protocols from literature, preprints, and patents, while its intelligent system identifies the most reproducible and accurate methods.
With PubCompare.ai, scientists can achieve enhanced results in their divinylbenzene-related projects, whether they are working with methanol, acetonitrile, or other solvents and materials.
By tapping into the power of PubCompare.ai, researchers can streamline their workflow, improve the reproducibility of their experiments, and ultimately drive breakthroughs in the diverse applications of divinylbenzene, from polymer chemistry to environmental analysis and beyond.