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4-(Acetamidophenylsulfonyl)acetonitrile
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4-(Acetamidophenylsulfonyl)acetonitrile
Catalog Number:
(10044-496)
Supplier:
Thermo Scientific
Description:
For exceptionally high resolution and efficiency anion-exchange separation of protein variants, use Thermo Scientific™ ProPac SAX and WAX strong and weak anion-exchange columns.
Supplier:
Thermo Scientific
Description:
For separations of proteins and their variants using Thermo Scientific™ ProPac SCX and WCX strong and weak cation-exchange columns, which provide exceptionally high resolution.
Supplier:
Adipogen
Description:
Hordenine is a phenethylamine type alkaloid found naturally in various plants such as barley and cacti. Hordenine may be used as an analytical reference material and in research on the activities of phenethylamine type alkaloids. Quorum-sensing inhibitor (QSI).
Supplier:
AMBEED, INC
Description:
Phenylsulfonylacetonitrile, Purity: 98%, CAS Number: 7605-28-9, Appearance: White to yellow powder or crystals, Storage: Sealed in dry, Room Temperature, Size: 1g
Supplier:
Adipogen
Description:
(Aminostyryl)pyridinium hemicyanine dye with solvent-dependent one- and two-photon emission1.
Catalog Number:
(75835-544)
Supplier:
Restek
Description:
The mix consists of acetonitrile, acrylonitrile, allyl chloride , benzene, bromobenzene, bromochloromethane, bromodichloromethane, bromoform, n-butylbenzene, sec-butylbenzene, tert-butylbenzene, carbon disulfide, carbon tetrachloride, chlorobenzene, 2-chloroethanol, chloroform, chloroprene , 2-chlorotoluene, 4-chlorotoluene, dibromochloromethane, 1,2-dibromo-3-chloropropane , 1,2-dibromoethane , dibromomethane, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, cis-1,4-dichloro-2-butene, trans-1,4-dichloro-2-butene, 1,1-dichloroethane, 1,2-dichloroethane, 1,1-dichloroethene, cis-1,2-dichloroethene, trans-1,2-dichloroethene, 1,2-dichloropropane, 1,3-dichloropropane, 2,2-dichloropropane, 1,1-dichloropropene, cis-1,3-dichloropropene, trans-1,3-dichloropropene, diethyl ether , 1,4-dioxane, ethylbenzene, ethyl methacrylate, hexachloro-1,3-butadiene, iodomethane , isobutyl alcohol , isopropylbenzene , 4-isopropyl toluene , methacrylonitrile, methyl acrylate, methyl methacrylate, methylene chloride , naphthalene, nitrobenzene, 2-nitropropane, propionitrile, n-propylbenzene, styrene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, tetrachloroethene, tetrahydrofuran, toluene, 1,2,3-trichlorobenzene, 1,1,1-trichloroethane, 1,1,2-trichloroethane, trichloroethene, 1,2,3-trichloropropane, 1,1,2-trichlorotrifluororethane , 1,2,4-trimethylbenzene, 1,3,5-trimethylbenzene, m-xylene, o-xylene, p-xylene.
Supplier:
Adipogen
Description:
New class of highly photostable, water soluble fluorescent labels with large Stoke's shift, high QY in aqueous media and pH tolerance. Major disadvantage: rel. low extinction coefficient.
Supplier:
Adipogen
Description:
Widely used blue fluorescent thiol-reactive dye (Ex/Em: 384/470nm). This maleimide derivative of coumarin is essentially non-fluorescent until it reacts with thiols, making it possible to quantify thiols without a separation step. Good energy acceptor from tryptophan and a good energy donor to fluorescein. Used to monitor release of thiols and to distinguish proliferating cancer cells by nucleolar protein staining.
Supplier:
Adipogen
Description:
Redox indicator. Blue fluorescence until oxidized to ethidium. Can be used for detecting superoxide radical in cells, tissues and organisms.
Catalog Number:
(TCP1014-025G)
Supplier:
TCI America
Description:
CAS Number: 2739-97-1
MDL Number: MFCD00006346 Molecular Formula: C7H6N2 Molecular Weight: 118.14 Purity/Analysis Method: >98.0% (GC) Form: Crystal Color: Very Pale Yellow Flash Point (°C): 94 Freezing point (°C): 25
Supplier:
Adipogen
Description:
Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.
Supplier:
Adipogen
Description:
Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.
Supplier:
Adipogen
Description:
4-(4,5-diphenyl-1H-imidazol-2-yl)benzoyl chloride (DIB-Cl) as reagent for amine labelling was used successfully for derivatization and fluorescence detection of enantiomers of methamphetamin and p-hydroxymethamphetamin, in urine samples. It has also been used for 3,4-Methylendioxy-N-methylamphetamin in blood, morpholine and orther compounds. DIB-Cl as a label was used on fluorescent derivatization some hydroxyl group containing endocrine disruptors, including bisphenol A (BPA), bisphenol B (BPB), bisphenol E (BPE), bisphenol F (BPF) and 4-nonylphenol (4-NP). DIB-Cl showed superior fluorescence intensity (FI) to other commercially available reagents, excellent stability in solution and high reactivity with primary and secondary amines under mild conditions.
Supplier:
Adipogen
Description:
An amine-reactive blue fluorescent probe that provides a distinguishable contrast when used with longer-wavelength probes in certain multicolor fluorescence applications such as nucleic acid and protein microarrays, in situ hybridization and immunofluorescence. This carboxylic acid derivative of 7-methoxycoumarin can be used for coupling to amines, hydrazines or hydroxylamines on biomolecules of interest. Spectral data: Ex=336nm, Em=402nm (Buffer, pH9).
Catalog Number:
(75835-788)
Supplier:
Restek
Description:
The compund consists of components such as, acenaphthene (100 μg/ml), acenaphthylene (100 μg/ml), anthracene (100 μg/ml), benz(a)anthracene (10 μg/ml), benzo(a)pyrene (10 μg/ml), benzo(b)fluoranthene (10 μg/ml), benzo(ghi)perylene (10 μg/ml), benzo(k)fluoranthene (5 μg/ml), chrysene (10 μg/ml), dibenz(a,h)anthracene (10 μg/ml), fluoranthene (10 μg/ml), fluorene (100 μg/ml), indeno(1,2,3-cd)pyrene (10 μg/ml), 1-methylnaphthalene (100 μg/ml), 2-methylnaphthalene (100 μg/ml), naphthalene (100 μg/ml), phenanthrene (100 μg/ml), pyrene (10 μg/ml).
Supplier:
MP Biomedicals
Description:
Arachidonic Acid is an essential fatty acid. Occurs in liver, brain, glandular organs, and depot fats of animals, in small amounts in human depot fats, and is a constituent of animal phosphatides.
Arachidonic Acid is a precursor in the biosynthesis of prostaglandins, thromboxanes, and leukotrienes. Arachidonic acid plays a key role in cellular regulation and is controlled through multiple interconnected pathways. Arachidonic acid (AA) is an unsaturated ω6 fatty acid constituent of the phospholipids of cell membranes. Phospholipase A2 releases AA from the membrane phospholipids in response to inflammation. AA is subsequently metabolized to prostaglandins and thromboxanes by at least two cyclooxygenase (COX) isoforms, to leukotrienes and lipoxins by lipoxygenases, and to epoxyeicosatrienoic acids via cytochrome p450-catalyzed metabolism. AA and its metabolites play important roles in a variety of biological processes, including signal transduction, smooth muscle contraction, chemotaxis, cell proliferation and differentiation, and apoptosis. AA has been demonstrated to bind to the a subunit of G protein and inhibit the activity of Ras GTPase-activating proteins (GAPs). Cellular uptake of AA is energy dependent and involves protein-facilitated transport across the plasma membrane. If ethanol is undesirable, arachidonic acid may be dissolved in acetonitrile, DMF, or DMSO. Simply evaporate the ethanol under a gentle stream of nitrogen (be certain not to evaporate the material to dryness) and redissolve the arachidonic acid in the solvent of choice.Just prior to use, make dilutions of the stock solution into aqueous buffer or isotonic saline to bring the arachidonic acid to the desired concentration. Ensure that the residual amount of organic solvent is insignificant, since organic solvents may have physiologic effects at low concentrations. A control using the solvent in the absence of the prostaglandin will address this potential variable. We do not recommend storing the aqueous solution for more than one day. It is difficult to obtain aqueous solutions of arachidonic acid directly. However, an organic solvent free solution of arachidonic acid can be prepared using concentrated basic buffers (pH > 8.0 and ionic strength not less than 0.1 M). Add 400 μL of cold buffer (0 °C) per mg of arachidonic acid and agitate vigorously and/or ultrasonicate.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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