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Sodium N-(2-hydroxylethyl)ethylenediamine-N,N',N'-triacetate
[CAS# 139-89-9]

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Complete supplier list of Sodium N-(2-hydroxylethyl)ethylenediamine-N,N',N'-triacetate
Identification
Classification Organic raw materials >> Carboxylic compounds and derivatives
Name Sodium N-(2-hydroxylethyl)ethylenediamine-N,N',N'-triacetate
Synonyms N-(2-Hydroxyethyl)-N,N',N'-ethylenediaminetriacetic acid trisodium salt; N-(Carboxymethyl)-N'-(2-hydroxyethyl)-N,N'-ethylenediglycine trisodium salt; N-(2-hydroxyethyl)ethylenediaminetriacetate; Trisodium N-(hydroxyethyl)ethylenediaminetriacetate; Trisodium N-hydroxyethylethylenediamine-N,N',N'-triacetate
Molecular Structure CAS # 139-89-9, Sodium N-(2-hydroxylethyl)ethylenediamine-N,N',N'-triacetate, N-(2-Hydroxyethyl)-N,N',N'-ethylenediaminetriacetic acid trisodium salt, N-(Carboxymethyl)-N'-(2-hydroxyethyl)-N,N'-ethylenediglycine trisodium salt, N-(2-hydroxyethyl)ethylenediaminetriacetate, Trisodium N-(hydroxyethyl)ethylenediaminetriacetate, Trisodium N-hydroxyethylethylenediamine-N,N',N'-triacetate
Molecular Formula C10H15N2O7.3Na
Molecular Weight 344.21
CAS Registry Number 139-89-9
EC Number 205-381-9
SMILES C(CN(CC(=O)[O-])CC(=O)[O-])N(CCO)CC(=O)[O-].[Na+].[Na+].[Na+]
Properties
Density 1.300 g/mL (Expl.)
Melting point 288 ºC (Expl.)
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Serious eye damageEye Dam.1H318
Skin irritationSkin Irrit.2H315
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.4H302
Eye irritationEye Irrit.2H319
Eye irritationEye Irrit.2BH320
SDS Available
up Discovory and Applicatios
Sodium N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetate (commonly abbreviated as HEDTA-Na) is a chelating agent derived from ethylenediamine. It features a hydroxyethyl group and three acetate groups, which provide excellent metal-binding properties. The discovery of HEDTA-Na emerged from mid-20th-century research aimed at developing versatile ligands for industrial and agricultural applications.

HEDTA-Na is synthesized through the reaction of ethylenediamine with monochloroacetic acid, followed by hydroxyethylation. Its ability to chelate metal ions is attributed to the nitrogen and oxygen donor atoms in its structure, which form stable complexes with a wide range of metal cations. This feature makes it highly effective in applications where control over metal ions is critical.

One of the primary applications of HEDTA-Na is in industrial water treatment. It is used to sequester metal ions such as calcium, magnesium, and iron, preventing scale formation and improving the efficiency of boilers and cooling systems. Its stability under varying pH conditions enhances its utility in such systems.

In agriculture, HEDTA-Na serves as a micronutrient carrier in fertilizers. By forming soluble complexes with essential trace metals like iron, zinc, and manganese, it facilitates their availability to plants, thereby improving crop yield and health. It is particularly beneficial in soils with high alkalinity, where metal ions are typically less bioavailable.

HEDTA-Na is also employed in personal care products and detergents. In cosmetics, it stabilizes formulations by binding trace metals that could otherwise catalyze oxidative degradation. In cleaning products, it enhances performance by preventing metal-induced precipitation of active ingredients.

The discovery and diverse applications of HEDTA-Na underscore its significance as a versatile chelating agent. Its ability to manage metal ions effectively has made it indispensable in multiple industrial, agricultural, and consumer contexts.
Market Analysis Reports
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