Sodium thiosulfate or thiosulfate or thiosulphate

General description Thioglycolic acid is a mercaptocarboxylic acid that serves as a stabilizer, reducing agent, and ligand. Application Thioglycolic acid may be used as a sulfur source for the synthesis of metal sulfide nanostructures via

Thioglycolic acid protects tryptophan in amino acid analysis,and also mediates formation of ATP from ADP. It lowers the oxidation-reduction potential and neutralises mercurial preservatives.

Applications: Thiophilic affinity purification is based on the ability of some proteins, particularly immunoglobulins, to bind to this immobilized ligand. The term &quotThiophilic&quot refers to an affinity for sulfone groups that lie in close

Applications: Thiophilic affinity purification is based on the ability of some proteins, particularly immunoglobulins, to bind to this immobilized ligand. The term &quotThiophilic&quot refers to an affinity for sulfone groups that lie in close

Applications: Thiophilic affinity purification is based on the ability of some proteins, particularly immunoglobulins, to bind to this immobilized ligand. The term &quotThiophilic&quot refers to an affinity for sulfone groups that lie in close

Application Thiosalicylic acid can be used as: A nucleophilic trapping agent for the desulfenylation of 3-indolyl sulfides to obtain 3-unsubstituted indoles. A starting material to prepare 2&#8242:-mercaptoacetophenone, which is used in the

Application Thiosalicylic acid can be used as: A nucleophilic trapping agent for the desulfenylation of 3-indolyl sulfides to obtain 3-unsubstituted indoles. A starting material to prepare 2&#8242:-mercaptoacetophenone, which is used in the

Application Thiosalicylic acid can be used as: A nucleophilic trapping agent for the desulfenylation of 3-indolyl sulfides to obtain 3-unsubstituted indoles. A starting material to prepare 2&#8242:-mercaptoacetophenone, which is used in the

Thiosemicarbazide is an environmentally toxic compound, which is usually derived from thiourea. Its ability to chelate trace metals promotes its biological activity against certain tumors, protozoa, influenza, pesticides, and fungicides.

Thiosemicarbazide is an environmentally toxic compound, which is usually derived from thiourea. Its ability to chelate trace metals promotes its biological activity against certain tumors, protozoa, influenza, pesticides, and fungicides.

THIOSULFATE N/10,2 OZ,DB

Analyte: Sodium thiosulfate (as thiosulfate), CAS Number: 7772-98-7 InChl: AKHNMLFCWUSKQB-UHFFFAOYSA-L.