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Key Documents

270555

Sigma-Aldrich

N,N-Dimethylacetamide

suitable for HPLC, ≥99.9%

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About This Item

Linear Formula:
CH3CON(CH3)2
CAS Number:
Molecular Weight:
87.12
Beilstein:
1737614
EC Number:
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:
NACRES:
NA.21

vapor density

3 (vs air)

Quality Level

vapor pressure

2 mmHg ( 25 °C)
4 mmHg ( 38 °C)

Assay

≥99.9%

form

liquid

autoignition temp.

914 °F

expl. lim.

1.8 %, 100 °F
11.5 %, 160 °F

technique(s)

HPLC: suitable

impurities

<0.030% water

evapn. residue

<0.001%

refractive index

n20/D 1.437 (lit.)

pH

4 (20 °C, 200 g/L)

bp

164.5-166 °C (lit.)

mp

−20 °C (lit.)

density

0.937 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 270 nm Amax: 1.00
λ: 280 nm Amax: 0.30
λ: 290 nm Amax: 0.15
λ: 310 nm Amax: 0.05
λ: 320 nm Amax: 0.03
λ: 360-400 nm Amax: 0.01

application(s)

food and beverages

SMILES string

CN(C)C(C)=O

InChI

1S/C4H9NO/c1-4(6)5(2)3/h1-3H3

InChI key

FXHOOIRPVKKKFG-UHFFFAOYSA-N

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Application


  • Ternary Phase-Field Simulation of Poly(vinylidene fluoride) Microporous Membrane Structures Prepared by Nonsolvent-Induced Phase Separation with Different Additives and Solvent Treatments: This study highlights the use of N,N-Dimethylacetamide (DMAC) in the preparation of advanced poly(vinylidene fluoride) membranes, showcasing its critical role in enhancing polymer processing and membrane structures in material science (Zhang et al., 2024).

  • Improved Protein Removal Performance of PES Hollow-Fiber Ultrafiltration Membrane with Sponge-like Structure: Research demonstrates DMAC′s effectiveness in the production of high-performance ultrafiltration membranes, emphasizing its importance in biomedical applications and wastewater treatment (Zhao et al., 2024).

  • Poly(vinylidene fluoride) Aerogels with alpha, beta, and gamma; Crystalline Forms: Correlating Physicochemical Properties with Polymorphic Structures: This article showcases the versatility of DMAC as a solvent in the synthesis of poly(vinylidene fluoride) aerogels, linking its use to significant advancements in the understanding of polymer crystallinity and properties (Suresh et al., 2024).

  • Cellulose Esters: Synthesis for Further Formation of Films with Magnetite Nanoparticles Incorporated: The study leverages DMAC for the synthesis of advanced cellulose ester films integrated with magnetite nanoparticles, illustrating its potential in developing multifunctional materials for diverse industrial applications (Furlan Sandrini et al., 2024).

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Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

147.2 °F - closed cup

Flash Point(C)

64 °C - closed cup


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B Tosh et al.
Carbohydrate research, 327(3), 345-352 (2000-08-17)
Commercial rayon grade cellulose was dissolved in the lithium chloride-N,N-dimethylacetamide (LiCl-DMAc) solvent system and esterified with acetic anhydride using p-toluenesulfonyl chloride (p-TsCl) and pyridine as catalysts. The reaction temperature was varied from 28 to 70 degrees C and the time
Solution studies of cellulose in lithium chloride and N,N-dimethylacetamide.
McCormick CL, et al.
Macromolecules, 18(12), 2394-2401 (1985)
Solutions of cellulose in N, N-dimethylacetamide/lithium chloride studied by light scattering methods.
Roder T, et al.
Polymer, 42(16), 6765-6773 (2001)
Fen Ran et al.
Acta biomaterialia, 7(9), 3370-3381 (2011-06-11)
An amphiphilic triblock co-polymer of poly(vinyl pyrrolidone)-b-poly(methyl methacrylate)-b-poly(vinyl pyrrolidone) (PVP-b-PMMA-b-PVP) was synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization. The block co-polymer can be directly blended with polyethersulfone (PES) using dimethylacetamide (DMAC) as the solvent to prepare flat sheet and
André H Gröschel et al.
Nature communications, 3, 710-710 (2012-03-20)
Hierarchical self-assembly offers elegant and energy-efficient bottom-up strategies for the structuring of complex materials. For block copolymers, the last decade witnessed great progress in diversifying the structural complexity of solution-based assemblies into multicompartment micelles. However, a general understanding of what

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