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Key Documents

M46705

Sigma-Aldrich

N-Methylformamide

99%

Synonym(s):

N-Formylmethylamine

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About This Item

Linear Formula:
HCONHCH3
CAS Number:
Molecular Weight:
59.07
Beilstein:
1098352
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

Assay

99%

form

liquid

refractive index

n20/D 1.432 (lit.)

bp

198-199 °C (lit.)

mp

−4 °C (lit.)

density

1.011 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)NC

InChI

1S/C2H5NO/c1-3-2-4/h2H,1H3,(H,3,4)

InChI key

ATHHXGZTWNVVOU-UHFFFAOYSA-N

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Legal Information

DuPont product

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Repr. 1B

Storage Class Code

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

WGK

WGK 1

Flash Point(F)

231.8 °F - closed cup

Flash Point(C)

111 °C - closed cup


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Jeppe S Spicker et al.
Toxicological sciences : an official journal of the Society of Toxicology, 102(2), 444-454 (2008-01-08)
A large number of databases are currently being implemented within toxicology aiming to integrate diverse biological data, such as clinical chemistry, expression, and other types of data. However, for these endeavors to be successful, tools for integration, visualization, and interpretation
Edward M Kosower et al.
The journal of physical chemistry. B, 113(16), 5622-5632 (2009-03-31)
N-methylformamide (NMF), the simplest model for peptides, exhibits hyperplectic (both simple and complex) behavior as revealed by thin film infrared spectroscopy on planar AgX [AgCl:AgBr] fiber. IR spectra (0.1 s scans) of 10 microg NMF/dichloromethane(DCM) under N(2) flow first show
Walther Caminati et al.
Physical chemistry chemical physics : PCCP, 12(35), 10230-10234 (2010-07-27)
We investigated the Fourier transform microwave spectra of the hydrated forms of N-methylformamide (NMF) in a supersonic expansion and assigned the rotational spectra of two mono-hydrated species. The conformation of each molecular complex was reliably determined on the basis of
Jolanta Swiergiel et al.
The journal of physical chemistry. B, 113(43), 14225-14228 (2009-10-07)
Impedance spectroscopy was used for studies of the frequency dependence of the electric conductivity of two highly conducting liquid amides: N-methylformamide (NMF), strongly self-associated via the hydrogen bonds C=O...N-H, and N,N-dimethylformamide (DMF), which is not able to self-organize by hydrogen
Merwe Albrecht et al.
The journal of physical chemistry. A, 112(33), 7530-7542 (2008-07-31)
Cold, isolated peptide model compounds and their aggregates are generated in pulsed supersonic jet expansions and detected by FTIR spectroscopy in the amide-A region, complemented by amide-I spectra. The most stable, symmetric dimer of formamide is unambiguously assigned in the

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