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M51008
Methyliminodiacetic acid
99%
Synonyme(s) :
MIDA, MIDA ligand
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5 G
42,90 €
25 G
48,00 €
42,90 €
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5 G
42,90 €
25 G
48,00 €
About This Item
Formule linéaire :
CH3N(CH2CO2H)2
Numéro CAS:
Poids moléculaire :
147.13
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
42,90 €
Veuillez contacter notre Service Clients pour connaître la disponibilité de ce produit.
Devis pour commande en gros
Produits recommandés
Niveau de qualité
Essai
99%
Pf
220 °C (dec.) (lit.)
Chaîne SMILES
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)
Clé InChI
XWSGEVNYFYKXCP-UHFFFAOYSA-N
Catégories apparentées
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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B Siegmund et al.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 364(7), 807-812 (1983-07-01)
meso-Alanopine and D-strombine are separated by high pressure liquid chromatography using a cation exchange resin and 2.5 X 10(-5) M sulfuric acid as eluant, at a flow rate of 1.0 ml/min, 20 degrees C column temperature and a pressure of
María Eugenia García-Rubiño et al.
Journal of inorganic biochemistry, 200, 110801-110801 (2019-08-30)
The study of the metal binding pattern of N-methyladenines (1-, 3-, 7- or 9-Meade) towards CuII-iminodiacetate-like chelates is addressed on the basis of XRD crystal structures of sixteen novel ternary compounds. Except for three compounds, all others feature an square-based
M E Haque et al.
Acta medica Okayama, 54(1), 1-8 (2000-03-10)
We present here a reliable and sensitive method for the determination of acidic opines such as meso-alanopine, beta-alanopine, tauropine and strombine in biological samples. Interfering primary amino acids were eliminated by reaction with o-phthalaldehyde, and the derivatized compounds were passed
G B Fiore et al.
Analytical biochemistry, 139(2), 413-417 (1984-06-01)
A method for the separation and quantification of the levels of alanopine and strombine in neutralized, perchloric acid extracts of tissues of marine invertebrates is presented. The method is based on high-performance liquid chromatographic (HPLC) separation, postcolumn derivatization using o-phthaldialdehyde
G Meinardus-Hager et al.
Experimental biology, 45(2), 91-110 (1986-01-01)
The cockle Cardium tuberculatum responds with a typical escape movement (jumping by foot contractions) when touched by a starfish. In addition, this species can survive anoxic conditions for up to 20 h at 22 degrees C. The maximum activities of
Articles
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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What is the solubility for Product M51008, Methyliminodiacetic acid?
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Unfortunately, we do not test solubility for product M51008. However, this product should be soluble in 25 mg/mL, 1 N acetic acid and deuterated water.
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What is the particle size of Product M51008, Methyliminodiacetic acid?
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Unfortunately, neither Sigma-Aldrich nor the supplier has determined the particle size.
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