1,2-Cyclohexylenedinitrilotetraacetic acid

CAS: 13291-61-7

Ref. 3D-FC156321

Información del producto

• Nombre: 1,2-Cyclohexylenedinitrilotetraacetic acid
• Sinónimos: 1,2-Cyclohexylenedinitrilotetracetic acid, 2,2',2'',2'''-[(1R,2R)-cyclohexane-1,2-diyldinitrilo]tetraacetic acid, Acetic acid, (1,2-cyclohexylenedinitrilo)tetra-, trans-, Acide trans-cyclohexane-1,2-dinitrilotetraacetique, Acido Trans-Ciclohexano-1,2-Dinitrilotetraacetico, Cdta, Cdta Trans-1,2 Diaminocyclohexane-N,N,N'N-Tetraacetic Acid, Cgta, Chel 600, Chel CD, Chelaton 4, Chelaton IV, Complexon IV, CyDTA, Cyclohexane-trans-1,2-diamine tetra-acetate, Dcta, Glycine, N,N'-(1R,2R)-1,2-cyclohexanediylbis[N-(carboxymethyl)-, rel-, Glycine, N,N'-1,2-cyclohexanediylbis[N-(carboxymethyl)-, trans-, N,N'-1,2-Cyclohexanediylbis[N-(carboxymethyl)glycine], TRANS-1,2-DIAMINOCYCLOHEXANE-2,2',2'',2'''-(cyclohexane-1,2-diyldinitrilo)tetraacetic acid, Titriplex IV, Trans-1,2-Cyclohexanediamine-N,N,N',N'-tetraacetic acid, Trans-Cyclohexane-1,2-Dinitrilotetraacetic Acid, rel-N,N′-(1R,2R)-1,2-Cyclohexanediylbis[N-(carboxymethyl)glycine], trans-(.+-.)-N,N'-1,2-Cyclohexanediylbis[N-(carboxymethyl)glycine], trans-(1,2-Cyclohexylenedinitrilo)tetraacetic acid, trans-1,2-Cyclohexanediaminetetraacetic acid, trans-1,2-Diaminocyclohexanetetraacetic acid, trans-1,2-diaminocyclohexane-N,N,N,N-tetraacet, trans-Cyclohexan-1,2-dinitrilotetraessigsaure, trans-Cyclohexane-1,2-diamine-N,N,N′,N′-tetraacetic acid
• CAS: 13291-61-7

Descripción

1,2-Cyclohexylenedinitrilotetraacetic acid (CDTA) is a cyclic dianhydride with a malonic acid moiety that reacts with metal ions to form an acid complex. This compound has been used as a chelating agent in analytical chemistry and as an inhibitor of cellular transformation. CDTA has been shown to have an inhibitory effect on the growth of cultured cells at acidic pH and neutral pH, but not at alkaline pH. The mechanism for this inhibition is not fully understood, but it may be due to its ability to form complexes with metal ions.
CDTA's chemical structure consists of two cyclohexane rings linked by nitrile groups. In addition, the molecule contains two carboxylic acid groups, one hydroxyl group, and one amine group. The carboxylic acids in CDTA are labile under basic conditions and can be converted into amides or esters by treatment

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 346.33 g/mol
• Fórmula: C₁₄H₂₂N₂O₈
• Pureza: Min. 95%