U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C14H22N2O8
Molecular Weight 346.3331
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOHEXANE-1,2-DIAMINE-N,N,N',N'-TETRAACETIC ACID, TRANS-

SMILES

OC(=O)CN(CC(O)=O)[C@@H]1CCCC[C@H]1N(CC(O)=O)CC(O)=O

InChI

InChIKey=FCKYPQBAHLOOJQ-NXEZZACHSA-N
InChI=1S/C14H22N2O8/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)/t9-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C14H22N2O8
Molecular Weight 346.3331
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Spectrophotometric determination of Pb(II), Fe(III) and Bi(III) in complexes with 1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (DACT).
2007-08-02
Application of pressurized fluid extraction to determine cadmium and zinc in plants.
2007-01-02
Alzheimer type II astrocytic changes following sub-acute exposure to manganese and its prevention by antioxidant treatment.
2006-04-03
Efficient expression of transgenes in adult zebrafish by electroporation.
2005-10-13
Metalloenzyme-like activity of Alzheimer's disease beta-amyloid. Cu-dependent catalytic conversion of dopamine, cholesterol, and biological reducing agents to neurotoxic H(2)O(2).
2002-10-25
The CDTA-soluble pectic substances from soybean meal are composed of rhamnogalacturonan and xylogalacturonan but not homogalacturonan.
2001-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:16:05 GMT 2025
Edited
by admin
on Mon Mar 31 21:16:05 GMT 2025
Record UNII
JD2BU42P20
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHELATON 4
Preferred Name English
CYCLOHEXANE-1,2-DIAMINE-N,N,N',N'-TETRAACETIC ACID, TRANS-
Common Name English
TRANS-CYCLOHEXANE-1,2-DIAMINE-N,N,N',N'-TETRAACETIC ACID
Common Name English
GLYCINE, N,N'-1,2-CYCLOHEXANEDIYLBIS(N-(CARBOXYMETHYL)-
Systematic Name English
TRANS-(±)-N,N'-1,2-CYCLOHEXANEDIYLBIS(N-(CARBOXYMETHYL)GLYCINE)
Systematic Name English
CYCLOHEXANEDIAMINE TETRAACETIC ACID
Systematic Name English
1,2-CYCLOHEXYLENEDIAMINETETRAACETIC ACID
Common Name English
GLYCINE, N,N'-(1R,2R)-1,2-CYCLOHEXANEDIYLBIS(N-(CARBOXYMETHYL)-, REL-
Common Name English
NSC-529593
Code English
CGTA
Common Name English
NSC-7339
Code English
CDTA
Common Name English
Code System Code Type Description
MESH
C005390
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
NSC
7339
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
FDA UNII
JD2BU42P20
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
CAS
13291-61-7
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID10889383
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
236-308-9
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
CAS
482-54-2
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
NSC
529593
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
PUBCHEM
2723845
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-582-7
Created by admin on Mon Mar 31 21:16:05 GMT 2025 , Edited by admin on Mon Mar 31 21:16:05 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY