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N-(2-Hydroxyethyl)iminodiacetic Acid, with the chemical formula C6H11NO5, is an organic compound that plays a significant role in various chemical processes and applications. It is characterized by its unique structure, which includes a hydroxyethyl group attached to an iminodiacetic acid backbone, providing it with versatile functional groups for chemical reactions and interactions.

93-62-9

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93-62-9 Usage

Uses

Used in Organic Synthesis:
N-(2-Hydroxyethyl)iminodiacetic Acid is used as a key intermediate in the synthesis of various organic compounds. Its presence in the molecular structure allows for the formation of new bonds and the creation of complex molecules that can be utilized in a wide range of applications.
Used in Chelating Agents:
In the chemical industry, N-(2-HYDROXYETHYL)IMINODIACETIC ACID is used as a chelating agent for metal ions. Its ability to form stable complexes with metal ions makes it an effective component in various industrial processes, such as water treatment, where it helps in removing metal contaminants.
Used in Pharmaceutical Industry:
N-(2-Hydroxyethyl)iminodiacetic Acid is used as a building block in the development of pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications, making it a valuable asset in the field of medicinal chemistry.
Used in Environmental Applications:
In environmental applications, N-(2-Hydroxyethyl)iminodiacetic Acid is used for its ability to bind and remove heavy metals from contaminated sites. Its chelating properties make it a useful tool in environmental remediation efforts, helping to clean up polluted areas and protect ecosystems.
Used in Analytical Chemistry:
N-(2-Hydroxyethyl)iminodiacetic Acid is employed in analytical chemistry as a reagent for the detection and quantification of various metal ions. Its selective binding properties enable precise measurements and analysis in laboratory settings.

Flammability and Explosibility

Notclassified

Purification Methods

Crystallise HIMDA from water. [Beilstein 4 IV 2432.]

Check Digit Verification of cas no

The CAS Registry Mumber 93-62-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93-62:
(4*9)+(3*3)+(2*6)+(1*2)=59
59 % 10 = 9
So 93-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO5/c8-2-1-7(3-5(9)10)4-6(11)12/h8H,1-4H2,(H,9,10)(H,11,12)/p-1

93-62-9 Well-known Company Product Price

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  • Aldrich

  • (54345)  N-(2-Hydroxyethyl)iminodiaceticacid  ≥98.0% (T)

  • 93-62-9

  • 54345-5G

  • 790.92CNY

  • Detail

93-62-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Hydroxyethyl)iminodiacetic Acid

1.2 Other means of identification

Product number -
Other names N-(2-HYDROXYETHYL)IMINODIACETIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:93-62-9 SDS

93-62-9Relevant academic research and scientific papers

Synthesis of metal-chelating polymerizable phospholipids

Singh,Tsao,Puranik

, p. 573 - 586 (2007/10/02)

Two routes for the synthesis of metal chelating phospholipids are reported. An iminodiacetic acid functionality served as metal chelating site in the polar headgroup region of a phospholipid while a tricosa-10,12-diynoyl group linked to the glycerol backbone, made up the polymerizable hydrocarbon region.

Iron chelate solutions

-

, (2008/06/13)

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.

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