N-(2-ACETAMIDO)IMINODIACETIC ACID

Details

Stereochemistry	ACHIRAL
Molecular Formula	C6H10N2O5
Molecular Weight	190.154
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of N-(2-ACETAMIDO)IMINODIACETIC ACID

Structure Search

SMILES

NC(=O)CN(CC(O)=O)CC(O)=O

InChI

InChIKey=QZTKDVCDBIDYMD-UHFFFAOYSA-N

InChI=1S/C6H10N2O5/c7-4(9)1-8(2-5(10)11)3-6(12)13/h1-3H2,(H2,7,9)(H,10,11)(H,12,13)

HIDE SMILES / InChI

Molecular Formula	C6H10N2O5
Molecular Weight	190.154
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: http://www.sigmaaldrich.com/catalog/product/sial/00307?lang=en®ion=RU | http://www.google.la/patents/US4521518

N-(2-Acetamido)iminodiacetic Acid is a biological buffer component with sodium hydroxide and sodium chloride (pH 5.67-7.57, useful pH range 6.4-7.4). N-(2-Acetamido)iminodiacetic Acid is used to prepare immobilized pH gradients. ADA, or N-(2-Acetamido)iminodiacetic acid, can be used to study biological buffers and zwitterionic compounds. ADA has been used in a study to describe the application of scanning capacitively coupled contactless conductivity detection (SC(4)D) for the determination of pH dependant behaviour of two aminopolycarboxylates immobilised onto the surface of a monolithic capillary column. Blood cell stabilizing agent.

Approval Year

Conditions

Condition	Modality	Targets	Highest Phase	Product
Unknown 2596

PubMed

Title	Date	PubMed
Monoanionic 99mTc-tricarbonyl-aminopolycarboxylate complexes with uncharged pendant groups: Radiosynthesis and evaluation as potential renal tubular tracers.	2017-04	28110124
High enrichment of MMP-9 and carboxypeptidase A by tweezing adsorptive bubble separation (TABS).	2010-11	20229282
On-column titration and investigation of metal complex formation for aminopolycarboxylate functionalised monoliths using scanning contactless conductivity detection.	2009-08	19585536

Patents

Sample Use Guides

In Vivo Use Guide

Unknown

Route of Administration: Unknown

In Vitro Use Guide

Crystals were grown at 20°C by hanging-drop vapor diffusion method by mixing equal volumes of protein samples with reservoir solutions containing 1.2 m sodium/potassium tartrate and 100 mm N-(2-acetamido)iminodiacetic acid, pH 6.5.

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:20:33 GMT 2025` Edited by `admin` on `Mon Mar 31 21:20:33 GMT 2025`
Record UNII	5C4R3O704E
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ACETIC ACID, ((CARBAMOYLMETHYL)IMINO)DI-

Preferred Name

English

N-(2-ACETAMIDO)IMINODIACETIC ACID

Common Name

English

N-(CARBAMOYLMETHYL)IMINODIACETATIC ACID

Common Name

English

N-(2-AMINO-2-OXOETHYL)-N-(CARBOXYMETHYL)GLYCINE

Systematic Name

English

ADA [MI]

Common Name

English

N-(CARBAMOYLMETHYL)IMINODIACETIC ACID

Systematic Name

English

Code System Code Type Description

PUBCHEM

117765