trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate

Catalog Number	ACM125572954-2
CAS	125572-95-4
Structure
Description	Trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate (abbreviated as tDACHTA) is a chelating agent that has been used in a wide variety of scientific research applications. It is a monomeric compound composed of a cyclohexane ring with four carboxylic acid groups attached. The compound is highly soluble in water and has been used in a variety of biochemical and physiological experiments, as well as in laboratory experiments. This paper will discuss the synthesis method of tDACHTA, its mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions.
IUPAC Name	2-[[(1R,2R)-2-[bis(carboxymethyl)amino]cyclohexyl]-(carboxymethyl)amino]acetic acid;hydrate
Molecular Weight	364.35 g/mol
Molecular Formula	C14H24N2O9
Canonical SMILES	C1CCC(C(C1)N(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O.O
InChI	InChI=1S/C14H22N2O8.H2O/c17-11(18)5-15(6-12(19)20)9-3-1-2-4-10(9)16(7-13(21)22)8-14(23)24;/h9-10H,1-8H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24);1H2/t9-,10-;/m1./s1
InChI Key	VASZYFIKPKYGNC-DHTOPLTISA-N
Application	TDACHTA has been used in a variety of scientific research applications. It has been used as a chelating agent for the isolation of metal ions from solution, as a reactant in organic synthesis, and as a substrate for enzymatic reactions. It has also been used in studies of protein-ligand interactions, as well as in studies of enzyme kinetics.
GHS Pictogram	Irritant
Isomeric SMILES	C1CC[C@H]([C@@H](C1)N(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O.O
Properties	TDACHTA has been used in a variety of biochemical and physiological experiments. It has been used to study the effects of metal ions on biological systems, as well as the effects of metal ions on enzyme activity. It has also been used to study the effects of metal ions on cellular processes, such as cell division and protein synthesis.