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M51008

Sigma-Aldrich

Methyliminodiacetic acid

99%

Sinónimos:

MIDA, MIDA ligand

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About This Item

Fórmula lineal:
CH3N(CH2CO2H)2
Número de CAS:
4408-64-4
Peso molecular:
147.13
EC Number:
224-557-6
MDL number:
MFCD00004284
UNSPSC Code:
12352100
PubChem Substance ID:
24896977
NACRES:
NA.22

Quality Level

100

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
SHBM0764
SHBL9171
SHBL0872
SHBH1876V
SHBF6763V

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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)
Juan Lorenzo Hagad et al.
Sensors (Basel, Switzerland), 21(5) (2021-04-04)
Two of the biggest challenges in building models for detecting emotions from electroencephalography (EEG) devices are the relatively small amount of labeled samples and the strong variability of signal feature distributions between different subjects. In this study, we propose a
Gas-liquid chromatography and enzymatic determination of alanopine and strombine in tissues of marine invertebrates.
K B Storey et al.
Analytical biochemistry, 125(1), 50-58 (1982-09-01)
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