537373

N,N-Dimethylacetoacetamide solution

80% in H₂O

• Synonym(s): DMAA, N,N-Dimethyl-3-oxobutyramide
• Linear Formula: CH₃COCH₂CON(CH₃)₂
• CAS Number: 2044-64-6
• Molecular Weight: 129.16
• Beilstein/REAXYS Number: 1755038
• MDL number: MFCD00038243
• UNSPSC Code: 12352100
• PubChem Substance ID: 24878216
• NACRES: NA.22

Properties

• Quality Level: 100
• concentration: 80% in H₂O
• refractive index: n20/D 1.447
• bp: 105 °C
• density: 1.067 g/mL at 25 °C
• functional group: amide; ketone
• SMILES string: CN(C)C(=O)CC(C)=O
• InChI: 1S/C6H11NO2/c1-5(8)4-6(9)7(2)3/h4H2,1-3H3
• InChI key: YPEWWOUWRRQBAX-UHFFFAOYSA-N

Description

General description

The product is an 80% solution of N,N-dimethylacetoacetamide (DMAA) in water.

Application

• Disposition and metabolism of N,N-dimethylacetoacetamide in male F344 and Wistar-Han rats and female B6C3F1 mice.: The research examines the metabolic pathways and disposition of N,N-dimethylacetoacetamide in different rat and mouse models, providing insights into its pharmacokinetic properties (Fennell T et al., 2011).
• Reduction of ketones and alkyl iodides by SmI(2) and Sm(II)-HMPA complexes. Rate and mechanistic studies.: Explores the use of N,N-dimethylacetoacetamide in the reduction of ketones and alkyl iodides using samarium iodide complexes, providing detailed mechanistic insights into the reactions (Prasad E, Flowers RA 2nd, 2002).
• Mechanistic study of beta-substituent effects on the mechanism of ketone reduction by SmI(2).: This study delves into the effects of beta-substituents on the reduction mechanisms of ketones using samarium iodide in the presence of N,N-dimethylacetoacetamide, elucidating critical aspects of the reaction dynamics (Prasad E, Flowers RA 2nd, 2002).

Safety Information

• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 1
• flash_point_f: 251.6 °F - closed cup
• flash_point_c: 122 °C - closed cup
• ppe: Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)