trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%
trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%
trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%
trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%
Thermo Scientific Chemicals

trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%

trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%, C14H24N2O9, CAS Number-125572-95-4 | CAS: 125572-95-4 | C14H20N2O8 | 344.32 g/mol
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Catalog NumberQuantity
ALFB22928.22100 g
Catalog number ALFB22928.22
Price (MYR)
1,134.00
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100 g
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Price (MYR)
1,134.00
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Specifications
Chemical Name or Materialtrans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate
CAS125572-95-4
Health Hazard 1H319
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P264b-P280i-P305+P351+P338
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trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate is an analytical reagent and a complexating agent for sodium. It acts as a ligand to prepare lanthanide shift reagents. It is involved in the separation and determination of iron(III)-dimethyldithiocarbamate, manganese(II)-ethylenebisdithiocarbamate and zinc(II)-ethylenebisdithiocarbamate by sensitive capillary electrophoretic ultraviolet method.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
trans-1,2-Diaminocyclohexane-N,N,N′,N′-tetraacetic acid monohydrate is an analytical reagent and a complexating agent for sodium. It acts as a ligand to prepare lanthanide shift reagents. It is involved in the separation and determination of iron(III)-dimethyldithiocarbamate, manganese(II)-ethylenebisdithiocarbamate and zinc(II)-ethylenebisdithiocarbamate by sensitive capillary electrophoretic ultraviolet method.

Solubility
Slightly soluble in water. Soluble in 1N sodium hydroxide and alkali solutions. Insoluble in most common organic solvents.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Complexing agent for metal ions.
  2. Gong, L.; McCullagh, J. S. Comparing ion-pairing reagents and sample dissolution solvents for ion-pairing reversed-phase liquid chromatography/electrospray ionization mass spectrometry analysis of oligonucleotides. Rapid Commun. Mass Spectrom. 2014, 28 (4), 339-350.
  3. Puggioni, V.; Dondi, A.; Folli, C.; Shin, I.; Rhee, S.; Percudani, R. Gene context analysis reveals functional divergence between hypothetically equivalent enzymes of the purine-ureide pathway. Biochemistry 2014, 53 (4), 735-745.