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M51008

Sigma-Aldrich

Methyliminodiacetic acid

99%

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Synonym(s):
MIDA, MIDA ligand
Linear Formula:
CH3N(CH2CO2H)2
CAS Number:
4408-64-4
Molecular Weight:
147.13
EC Number:
224-557-6
MDL number:
MFCD00004284
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

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729221675067450561
Methyliminodiacetic acid 99%

Sigma-Aldrich

M51008

Methyliminodiacetic acid

trans-2-(Pinacol boronate)vinylboronic acid MIDA ester 96%

Sigma-Aldrich

729221

trans-2-(Pinacol boronate)vinylboronic acid MIDA ester

12-Mercaptododecanoic acid 96%

Sigma-Aldrich

675067

12-Mercaptododecanoic acid

11-Mercaptoundecanoic acid 95%

Sigma-Aldrich

450561

11-Mercaptoundecanoic acid

mp

220 °C (dec.) (lit.)

mp

254-260 °C

mp

45-50 °C

mp

46-50 °C (lit.)

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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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
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
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
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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
Christian Starkenmann et al.
Journal of agricultural and food chemistry, 57(17), 7938-7943 (2009-08-12)
A broth of dried scallop adductor muscles was prepared. Tasters appreciated the typical seafood, sweet, slightly umami taste of scallop, which is difficult to reproduce with common ingredients. Therefore, the broth was fractionated and, guided by multiple tastings, we isolated
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