482-54-2

Basic information

• Product Name: 482-54-2
• Synonyms: Aceticacid, (1,2-cyclohexylenedinitrilo)tetra- (8CI);1,2-Cyclohexanediamine-N,N,N',N'-tetraacetic acid;1,2-Diaminocyclohexanetetraacetic acid;o-Cyclohexanediaminetetraacetic acid
• CAS NO: 482-54-2
• Molecular Formula: C₁₄H₂₂N₂O₈
• Molecular Weight: 346.14
• EINECS: 207-582-7
• Mol File: 482-54-2.mol

Chemical Properties

• Boiling Point: 670.8 °C at 760 mmHg
• Flash Point: 359.487 °C
• Appearance: /
• Density: 1.489 g/cm³
• Vapor Pressure: 1.9E-18mmHg at 25°C
• CAS DataBase Reference: 482-54-2(CAS DataBase Reference)
• NIST Chemistry Reference: 482-54-2(482-54-2)
• EPA Substance Registry System: 482-54-2(482-54-2)

Safety Data

• Hazardous Substances Data: 482-54-2(Hazardous Substances Data)

Usage

Uses

Used in Plasticizer Industry:
482-54-2 is used as a plasticizer for the production of synthetic rubber, resins, and plastic materials, enhancing their flexibility and workability.
Used in Chemical Synthesis:
482-54-2 is used as a corrosion inhibitor, a catalyst, and a solvent in various chemical synthesis processes, improving the efficiency and selectivity of reactions.
Used in Automotive Industry:
As a plasticizer, 482-54-2 is used in the production of automotive components, such as hoses, seals, and gaskets, providing durability and resistance to environmental factors.
Used in Construction Industry:
In the construction industry, 482-54-2 is used in the production of building materials, such as adhesives and sealants, ensuring their performance and longevity.
Used in Textile Industry:
482-54-2 is used as a plasticizer in the production of synthetic fibers and textiles, improving their flexibility, softness, and resistance to wear.
Used in Cosmetics and Personal Care Industry:
As a plasticizer, 482-54-2 is used in the formulation of cosmetics and personal care products, such as creams, lotions, and shampoos, providing improved texture and consistency.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 482-54-2 is used as a solvent in the synthesis of various drugs, facilitating the dissolution and absorption of active ingredients.

InChI:InChI=1/C6H14N2.4C2H4O2/c7-5-3-1-2-4-6(5)8;4*1-2(3)4/h5-6H,1-4,7-8H2;4*1H3,(H,3,4)

Upstream product

• 694-83-7 rac-diaminocyclohexane 
• 79-11-8 chloroacetic acid 

Downstream Products

• 15929-95-0 Eu⁽³⁺⁾*((OOCCH₂)2N)2C₆H₁₀^(4-)=Eu(((OOCCH₂)2N)2C₆H₁₀)^(1-) 
• 30641-74-8 Eu⁽³⁺⁾*((OOCCH₂)2N)2C₆H₁₀^(4-)*(OOCCH₂)2NH^(2-)=Eu((OOCCH₂)2NH)(((OOCCH₂)2N)2C₆H₁₀)^(3-) 
• 4870-57-9 1,2-cyclohexanediaminetetraacetic acid ammonium salt 

Relevant articles and documents

Imaging of Enzyme Activity

This invention relates to biochemistry and magnetic resonance imaging.

Preparation and purification of hydroxylamine stabilizers

The invention relates to the preparation of ultra-high purity 1,2-diaminocyclohexane-tetraacetic acid being essentially free of unwanted metal and metal ion contaminants and its use as a stabilizer for ultra-high purity hydroxylamine compounds used extensively in the production of high premium electronic components.

Iron chelate solutions

A method for the preparation of an aqueous solution of iron polyprotic acid chelate complexes, comprising reacting a solution of a mixture of a first polyprotic acid or a salt thereof, said first acid being capable of chelating iron, and a second polyprotic acid or a salt thereof, said second acid being capable of chelating iron and being different from the first acid, with iron in the presence of an oxidizing agent, with the proviso that at least part of the carboxylic acid groups in the first and second acids is present in salt form and at least part of the carboxylic acid groups in the first and second acids is present in acid form. Preferably, the first and second polyprotic acids may be selected from ethylenediaminetetraacetic acid (EDTA), N-hydroxyethyl-ethylenediaminetriacetic acid (HEDTA), and diethylenetriaminepentaacetic acid (DTPA), and the iron is selected from Fe-powder, Fe(OH)2 and FeCO3. Part of the polyprotic acid groups in the first and second acids is present in the salt form, the salt being selected from ammonium and alkali metal ions, in particular K , Na and mixtures thereof. The method makes it possible to obtain aqueous solutions containing high contents of iron, such as up to approximately 7% by weight of iron, for use as a plant nutrient, mainly in soil-free plant culturing.

Methods for controlling intraocular pressure with transition metal complexes

Methods for lowering elevated intraocular pressure resulting from the instillation to the eye of sodium hyaluronate during surgery by administration of transition metal complexes are disclosed.