Hetastarch/sodium chloride

Application 1-Naphthoyl chloride has been used: as derivatization reagent in analysis of short-chained dodecyl alcohol ethoxylates and dodecyl alcohol by solid-phase extraction combined with dispersive liquid-liquid microextraction method as

Application 1-Naphthoyl chloride has been used: as derivatization reagent in analysis of short-chained dodecyl alcohol ethoxylates and dodecyl alcohol by solid-phase extraction combined with dispersive liquid-liquid microextraction method as

Application 2-Naphthoyl chloride has been used in: preparation of amide derivatives of the amphetamine enantiomers synthesis of 7-dimethylamino-2-methyl-3-naphthamido-phenothiazinium salt modification of self-assembled monolayer formed on silica

Application 2-Naphthoyl chloride has been used in: preparation of amide derivatives of the amphetamine enantiomers synthesis of 7-dimethylamino-2-methyl-3-naphthamido-phenothiazinium salt modification of self-assembled monolayer formed on silica

Pt(NH₃)₂Cl₂ CAS#: 15663-27-1 F.W.: 300.06 cis-Platin

The Sephadex &#174 ion exchangers contain a cross-linked dextran matrix with functional groups. These groups are linked by stable ether linkages to the glucose units in the matrix.

The Sephadex &#174 ion exchangers contain a cross-linked dextran matrix with functional groups. These groups are linked by stable ether linkages to the glucose units in the matrix.

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Analysis Note Assay (HClO&#8324): &#8805 98.0 % Sulfated ash: &#8804 0.

Geranyl chloride undergoes palladium-catalyzed cross-coupling reaction with aryl and alkenylgold(I) phosphanes to afford the &#945-substitution product. Application Geranyl chloride was used as starting reagent in the synthesis of: C 25 compound

Analysis Note Assay (acidimetric): &#8805 99,0 %(m) Melting range (lower value): &#8805 95 &#176C Melting range (upper value): &#8804 99 &#176C Identity (IR): conforms

Glutaric acid monoethyl ester chloride (ethyl glutaryl chloride) is a higher acyl chloride homolog. Its reaction with calix[4]arene to form ester group-containing calix[4]arenes has been reported.