M51008
Methyliminodiacetic acid
99%
Synonym(s):
MIDA, MIDA ligand
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All Photos(3)
About This Item
Linear Formula:
CH3N(CH2CO2H)2
CAS Number:
Molecular Weight:
147.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Certificates of Analysis (COA)
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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
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)
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
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)
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