M46705
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
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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
Signal Word
Danger
Hazard Statements
Precautionary 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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João M M Cordeiro et al.
The Journal of chemical physics, 138(4), 044502-044502 (2013-02-08)
The solvation of N-methylformamide (NMF) by dimethylsulfoxide (DMSO) in a 20% NMF/DMSO liquid mixture is investigated using a combination of neutron diffraction augmented with isotopic substitution and Monte Carlo simulations. The aim is to investigate the solute-solvent interactions and the
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
D O Futino et al.
Reproduction in domestic animals = Zuchthygiene, 45(2), 214-220 (2008-11-21)
The aim of the present work was to compare the efficiency of methyl-formamide (MF), dimethyl-formamide (DF) and glycerol (GL) as cryoprotectants in canine semen cryopreservation. For the experiment, pooled semen was submitted to one of the three cryoprotectants, with a
Shih-Min Wang et al.
The Science of the total environment, 388(1-3), 398-404 (2007-09-15)
N,N-dimethylformamide (DMF) could be readily absorbed via skin and inhalation routes. It is difficult, however, to separate the internal dose contribution from skin vapor and inhalation exposure. This study attempts to quantitatively determine the separate skin vapor and inhalation exposure
K Clagett-Carr et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 6(5), 906-918 (1988-05-01)
N-methylformamide (NMF), a polar solvent, is currently being evaluated by the National Cancer Institute (NCI) as an antineoplastic agent because of its activity against colon, mammary, and lung tumor xenografts. Results from preclinical studies suggest that it has radiosensitizing, chemosensitizing
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