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M51008

Sigma-Aldrich

Methyliminodiacetic acid

99%

Synonym(s):

MIDA, MIDA ligand

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About This Item

Linear Formula:
CH3N(CH2CO2H)2
CAS Number:
4408-64-4
Molecular Weight:
147.13
EC Number:
224-557-6
MDL number:
MFCD00004284
UNSPSC Code:
12352100
PubChem Substance ID:
24896977
NACRES:
NA.22

Assay

99%

mp

220 °C (dec.) (lit.)

SMILES string

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

InChI

1S/C5H9NO4/c1-6(2-4(7)8)3-5(9)10/h2-3H2,1H3,(H,7,8)(H,9,10)

InChI key

XWSGEVNYFYKXCP-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Mengping Guo et al.
Organic & biomolecular chemistry, 12(36), 7136-7139 (2014-08-12)
N-Methyliminodiacetic acid (MIDA) as a simple, air stable and water-soluble ligand has been used in the palladium-catalyzed Hiyama cross-coupling reaction of trimethoxyphenylsilane with aryl halides. The yield of the corresponding Hiyama coupling products is high up to around 90% in
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 25(10), 1144-1149 (1984-10-01)
A new approach to radiopharmaceutical design is demonstrated, in which small chelating groups capable of binding gamma-emitting radiometals are attached to biologically active molecules, thus producing radiopharmaceuticals based on bifunctional drug and biochemical analogs. The chelating group iminodiacetic acid has
Alanopine and strombine are novel imino acids produced by a dehydrogenase found in the adductor muscle of the oyster, Crassostrea gigas.
J H Fields et al.
Archives of biochemistry and biophysics, 201(1), 110-114 (1980-04-15)
M Sato et al.
Analytical biochemistry, 174(2), 623-627 (1988-11-01)
A new method for the quantitative analysis of acidic opines--alanopine, strombine, tauropine, and beta-alanopine--is presented. The method is based on formation of phenylthiocarbamyl (PTC) derivatives of the acidic opines after partial purification by ion-exchange chromatography. The PTC acidic opines are
Wan-Yu Deng et al.
IEEE transactions on neural networks and learning systems, 30(4), 1180-1190 (2018-09-04)
In most domain adaption approaches, all features are used for domain adaption. However, often, not every feature is beneficial for domain adaption. In such cases, incorrectly involving all features might cause the performance to degrade. In other words, to make
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