Document Type
Showing 1-19 of 19 results for "potassium sulfide"
Data Sheet - F5053
identified. The product is supplied in a solution of 100 mM potassium phosphate buffer, pH 7.4. Protein content, methyl p-tolyl sulfide oxidase activity, and FAD content1 are reported on a lot -to-
Data Sheet - F4928
identified. The product is supplied in a solution of 100 mM potassium phosphate buffer, pH 7.4. Protein content, methyl p-tolyl sulfide oxidase activity, and FAD content1 are reported on a lot-to-lot
Data Sheet - F5178
identified. The product is supplied in a solution of 100 mM potassium phosphate buffer, pH 7.4. Protein content, methyl p-tolyl sulfide oxidase activity, and FAD content1 are reported on a lot-to-lot
Quantitative Analysis of Active Metals and Metal Hydrides via Gas Buret
ether 1 R 19,211-2 Borane-methyl sulfide complex, 2.0M in diethyl ether G-W-M R 19,212-0 Borane-methyl sulfide complex, 2.0M in THF G-W-M R 19,482-4 Borane-methyl sulfide complex, 2.0M in toluene G-W-M R
Data Sheet - M0442
6β-hydroxytestosterone per minute at pH 7.4 at 37 °C. FMO Activity: Determined as methyl p-tolyl sulfide oxidase activity. Incubations are conducted at 0.8 mg/ml of protein with 1.3 mM NADP, 3.3 mM glucose 6-phosphate
Data Sheet - M0317
6β-hydroxytestosterone per minute at pH 7.4 at 37 °C. FMO Activity: Determined as methyl p-tolyl sulfide oxidase activity. Incubations were conducted at 0.8 mg/ml protein with 1.3 mM NADP, 3.3 mM glucose 6-phosphate
Data Sheet - M0692
6β-hydroxytestosterone per minute at pH 7.4 at 37 °C. FMO Activity: Determined as methyl p-tolyl sulfide oxidase activity. Incubations are conducted at 0.8 mg/ml protein with 1.3 mM NADP, 3.3 mM glucose 6-phosphate
Data Sheet - M0567
6β-hydroxytestosterone per minute at pH 7.4 at 37 °C. FMO Activity: Determined as methyl p-tolyl sulfide oxidase activity. Incubations were conducted at 0.8 mg/ml protein with 1.3 mM NADP, 3.3 mM glucose 6-phosphate
Data Sheet - 44782
thiosulphate are indicators of H2S formation. Cultures that produce hydrogen sulfide appear as black-brown colonies due to ferrous sulfide formation and precipitation. Proteus mirabilis in particular, displaying
Product Information Sheet - 11746081001
Label Function / description Content 1 Nitrite/Nitrate, Colorimetric Test, Potassium phosphate buffer Contains potassium phosphate buffer, pH 7.5 and stabilizers. 1 bottle, 22 ml 2 Nitrite/Nitrate
Spectral Viewer
MERCAPTANS & SULFIDES H14601 Hexyl sulfide NON-AROMATIC MERCAPTANS & SULFIDES O7007 Dioctyl sulfide NON-AROMATIC MERCAPTANS & SULFIDES D222801 Dodecyl sulfide NON-AROMATIC MERCAPTANS & SULFIDES I26809
Product Information Sheet - D8130
alpha-amylase, papain, and lysozyme10,11,12 Disulfide determination in peptides13 Hydrogen sulfide determination14 HPLC determination of alkylthiol using DTNB; EDTA to reduce metal ion interference14,15
Air Cleaner System Selection Guide
Carbon Chemical Name • Chromic Acids • Hydrochloric Acids • Hydrogen Chlorides • Hydrogen Sulfides • Hydrogen Fluorides • Methyl Formates • Nitric Acids • Phosphoric Acid • Sulfur Dioxides
ChemFiles 6.2
a collaborative effort to provide an array of potassium organotrifluoroborates, thereby expanding the toolbox of available boron reagents. Potassium organotrifluoroborates exhibit superb behavior
Chemfile vol.5 no 9
this transforma- tion, monochloroborane-dimethyl sulfide or catecholborane, both suffer from significant drawbacks. Monochloroborane-dimethyl sulfide exists in equilibrium with the BH3 and BHCl2 adducts
Acta Interactive Archive Vol 51
tolerance, producing the corresponding homoallyl sulfides selectively in up to 99% yield (eq 6).62 The same protocol was extended to benzyl phenyl sulfide, observing selective formation of the [1,2]-Stevens
Aldrichimica Acta Volume 50 Number 2
unintentionally synthesized iodoform and potassium formate from iodine, potassium metal, and ethanol.1 What he observed was the disproportionation of iodine in the presence of potassium ethoxide generated in situ
ChemFiles Vol. 6 No. 1
formal, stoichiometric oxygen atom transfer to organic reductants such as phosphines, alkenes, and sulfides.1 Re-catalyzed methodologies remained largely unexplored as a means of converting simple organic
Asymmetric Synthesis
indanol These chiral imine-ligands have recently been used in the vanadium- catalyzed oxidation of sulfides in conjunction with hydrogen peroxide. Optically active sulfoxides are obtained in high yields

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