Thiodiglycolic acid

CAS : 123-93-3

Ref. 3D-FT39370

Informations sur le produit

• Nom: Thiodiglycolic acid
• Synonymes: (Carboxymethylthio)Aceticacid, (Carboxymethylthio)acetic acid, 2,2'-Sulfanediylbis(Hydroxyacetic Acid), 2,2'-Sulfanediyldiacetate, 2,2'-Sulfanediyldiacetic Acid, 2,2-Mercaptodiacetic acid, 2,2-Thiodiglycolic acid, 2,2’-Thiobis-Aceticaci, 2,2’-Thiodiethanoicacid, 2,2′-Thiobis[acetic acid], 2,2′-Thiodiacetic acid, 2,2′-Thiodiethanoic acid, 2-(Carboxymethylsulfanyl)acetic acid, 2-[(Carboxymethyl)sulfanyl]acetic acid, Acetic acid, 2,2′-thiobis-, Acetic acid, thiobis-, Acetic acid, thiodi-, Beta,Beta’-Thiodiglycolicacid, Dicarboxymethyl sulfide, Dicarboxymethylsulfide, Dimethylsulfide-α,α′-dicarboxylic acid, Mercaptodiacetic acid, NSC 28743, NSC 40469, NSC 52326, Thiodi(Acetic, Thiodi-Aceticaci, Thiodiacetic acid, Thiodiglycollic Acid, Usafcb-36, β,β′-Thiodiglycolic acid
• CAS: 123-93-3

Description

Thiodiglycolic acid is a heterocyclic compound that is used as a reagent in organic synthesis. It is also used to prepare urinary thiodiglycolates, which are used as matrix effects in analytical chemistry. Thiodiglycolic acid reacts with disulfide bonds to form thiodiglycolate anions, which can be detected by the electron-capture gas chromatography/mass spectroscopy (GC/MS) technique. The LC-MS/MS method was used to measure the concentration of thiodiglycolate anions in urine samples from patients with autoimmune diseases and breast cancer. This compound also has been shown to have low toxicity in animal studies.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 150.15 g/mol
• Formule: C₄H₆O₄S
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C4H6O4S/c5-3(6)1-9-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)
• Code InChI: InChIKey=UVZICZIVKIMRNE-UHFFFAOYSA-N
• SMILES: O=C(O)CSCC(=O)O