CAS 4408-64-4

N-Methyliminodiacetic acid

Description:

N-Methyliminodiacetic acid (CAS 4408-64-4) is an organic compound characterized by its structure, which includes two carboxylic acid groups and an imino group. It is a derivative of iminodiacetic acid, with a methyl group attached to the nitrogen atom. This compound is typically a white crystalline solid and is soluble in water, making it useful in various applications. N-Methyliminodiacetic acid is known for its chelating properties, allowing it to form stable complexes with metal ions, which is valuable in fields such as analytical chemistry and biochemistry. It is often utilized in the synthesis of pharmaceuticals, as well as in the formulation of detergents and agricultural products. Additionally, its ability to bind to metals makes it a candidate for use in environmental remediation processes. The compound is generally considered to have low toxicity, but safety data should always be consulted for handling and usage. Overall, N-Methyliminodiacetic acid is a versatile compound with significant industrial and research applications.

Formula: C₅H₉NO₄

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

InChI key: InChIKey=XWSGEVNYFYKXCP-UHFFFAOYSA-N

SMILES: C(N(CC(O)=O)C)C(O)=O

Synonyms:

• (Carboxymethyl-methyl-amino)-acetic acid
• (Methylimino)diacetic acid
• 2,2'-(Methylammonio)Diacetate
• 2,2'-(Methylimino)Diacetic Acid
• 2,2′-(Methylazanediyl)diacetic acid
• 2,2′-Methyliminodiacetic acid
• 2-[(Carboxymethyl)(methyl)amino]acetic acid
• Acetic acid, (methylimino)di-
• Glycine, N-(carboxymethyl)-N-methyl-
• Methylimidodiacetic acid
• Methyliminodiacetic acid
• Mida
• N-(Carboxymethyl)-N-methylglycine
• N-Methylaminodiacetic acid
• Nsc 11773
• Strombine

N-Methyliminodiacetic Acid

CAS: 4408-64-4

Formula: C₅H₉NO₄

Purity: >98.0%(GC)(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 147.13

Ref: 3B-M2090

N-Methyliminodiacetic acid, 99%

CAS: 4408-64-4

N-Methyliminodiacetic acid is used to prepare bis-(1H-benzoimidazol-2-ylmethyl)-methyl-amine by condensation with benzene-1,2-diamine. It is involved in Suzuki cross-coupling with N-methyliminodiacetic acid (MIDA) boronates. It acts as a reagent utilized for protecting boronic acids and as a chelati

Formula: C₅H₉NO₄

Purity: 99%

Color and Shape: White to pale cream to gray, Crystals or powder or crystalline powder or lumps

Molecular weight: 147.13

Ref: 02-L02589

N-Methyliminodiacetic acid

CAS: 4408-64-4

Formula: C₅H₉NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 147.1293

Ref: IN-DA0035EG

N-Methyliminodiacetic acid

CAS: 4408-64-4

N-Methyliminodiacetic acid

Purity: 98%

Molecular weight: 147.13g/mol

Ref: 54-OR51834

[(Carboxymethyl)(methyl)amino]acetic acid

CAS: 4408-64-4

Formula: C₅H₉NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 147.13

Ref: 10-F066640

N-Methyliminodiacetic Acid

Controlled Product

CAS: 4408-64-4

Applications N-Methyliminodiacetic Acid (cas# 4408-64-4) is a compound useful in organic synthesis.

Formula: C₅H₉NO₄

Color and Shape: Neat

Molecular weight: 147.13

Ref: TR-M313238

N-Methyliminodiacetic Acid

CAS: 4408-64-4

N-Methyliminodiacetic acid is a monosodium salt that is produced by the reaction of methylamine and malonic acid. It has been shown to have an inhibitory effect on enzymes and metabolic rates in the human body. The structure of N-methyliminodiacetic acid contains a hydroxyl group, which can form hydrogen bonding interactions with nitrogen atoms in proteins, forming a chelate ligand. This type of binding is thought to be responsible for its ability to inhibit enzyme activities and metabolic rate.

Formula: C₅H₉NO₄

Purity: Min. 95%

Molecular weight: 147.13 g/mol

Ref: 3D-FM60840