482-54-2

1,2-Cyclohexylenedinitrilotetraacetic acid Chemical Structure
482-54-2

Chemical Structure

1,2-Cyclohexylenedinitrilotetraacetic acid

Synonym(s): CDTA

  • CAS No.: 482-54-2
  • Formula:C14H22N2O8
  • Molecular Weight:346.33

IUPAC Name: 2,2',2'',2'''-(cyclohexane-1,2-diylbis(azanetriyl))tetraacetic acid

InChIKey: FCKYPQBAHLOOJQ-UHFFFAOYSA-N

SMILES: C1CCC(C(C1)N(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O

Biological Activity: 1,2-Cyclohexylenedinitrilotetraacetic acid (CDTA) is a chelating agent. 1,2-Cyclohexylenedinitrilotetraacetic acid has an ability to remove manganese from brain and liver (in vivo) and their sub-cellular fractions (in vitro), of rats pretreated with manganese sulphate[1].

Cat. No. Product Name Purity Description Pricing
HY-W102714
1,2-Cyclohexylenedinitrilotetraacetic acid 99.91% 1,2-Cyclohexylenedinitrilotetraacetic acid (CDTA) is a chelating agent. 1,2-Cyclohexylenedinitrilotetraacetic acid has an ability to remove manganese from brain and liver (in vivo) and their sub-cellular fractions (in vitro), of rats pretreated with manganese sulphate.
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HY-W102714R
1,2-Cyclohexylenedinitrilotetraacetic acid (Standard) ≥98% 1,2-Cyclohexylenedinitrilotetraacetic acid (Standard) is the analytical standard of 1,2-Cyclohexylenedinitrilotetraacetic acid (HY-W102714). This product is intended for research and analytical applications. 1,2-Cyclohexylenedinitrilotetraacetic acid (CDTA) is a chelating agent. 1,2-Cyclohexylenedinitrilotetraacetic acid has an ability to remove manganese from brain and liver (in vivo) and their sub-cellular fractions (in vitro), of rats pretreated with manganese sulphate.
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HY-138547
DHPTA 99.87% DHPTA (compound 3) can directly combine with lanthanide elements (Tb3+, Ho3+, Lu3+) to form a strong chelating effect,in aqueous solution with a pH of 2.0-7.0.
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HY-45290
trans-1,2-Cyclohexanediaminetetraacetic acid 97.0% trans-1,2-Cyclohexanediaminetetraacetic acid is an aminopolycarboxylic acid chelating agent, an EDTA derivative containing a phenyl group directly attached to the nitrogen atoms of the ethylenediamine moiety, and is used for the separation of rare earth elements.
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HY-W013178
DCTA monohydrate 98.0% DCTA monohydrate is an organic acid. DCTA refers to N,N,N',N' -tetraacetic acid, which has a strong chelating ability. DCTA monohydrate can be used as a chelating agent and coordination reagent for metal ions. DCTA monohydrate, for example, forms stable complexes with many metal ions, including calcium, magnesium and zinc. DCTA modified with ethylene glycol is selective to calcium ions in the presence of magnesium ions.
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HY-W013851
EDTA-OH 99.48% EDTA-OH is a chelating agent, which forms thermodynamically stable chelates with metal ions like calcium, magnesium, iron, zinc and copper. EDTA-OH exhibits ability of phytoremediation in heavy-metal-contaminated soils. EDTA-OH is able to cross brain-blood barrier.
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HY-W105700
Ethylenediaminetetraacetic acid sodium hydrate 98.0% Ethylenediaminetetraacetic acid (EDTA) sodium hydrate is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid sodium hydrate has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid sodium hydrate decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid sodium hydrate can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid sodium hydrate can be used for coronary artery disease and neural system disease research.
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HY-W127789
Ethylenediaminetetraacetic acid diammonium Ethylenediaminetetraacetic acid diammonium is a class of organic compounds containing both ammonium and carboxylic acid functional groups. It is commonly used as a chelating agent in various industrial and medical applications, especially in the food and pharmaceutical industries. Ethylenediaminetetraacetic acid diammonium has strong metal ion binding properties and can be used to chelate trace metals that may affect product quality or stability. In addition, it is used as an anticoagulant in blood collection tubes and as a clarifying agent in cosmetic and personal care products.
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HY-W128312
1,3-Diaminopropane-N,N,N',N'-tetraacetic acid 1,3-Diaminopropane-N,N,N',N'-tetraacetic acid (1,3-DAPTA) is a kind of biochemical reagent.
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HY-W140537
EDTA diammonium salt hydrate, 97% EDTA diammonium salt hydrate, 97% is a derivative of ethylenediaminetetraacetic acid (EDTA), commonly used as a chelating agent in various applications due to its ability to bind with various metal ions and form stable complexes.
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HY-W777365
Ethylenediaminetetraacetic acid-13C4 Ethylenediaminetetraacetic acid-13C4 (EDTA-13C4) is the 13C-labeled Ethylenediaminetetraacetic acid (HY-Y0682). Ethylenediaminetetraacetic acid (EDTA) is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid can be used for coronary artery disease and neural system disease research.
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HY-Y0682
Ethylenediaminetetraacetic acid 98.91% Ethylenediaminetetraacetic acid (EDTA) is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid can be used for coronary artery disease and neural system disease research.
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References