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/REAXYS Number:
1098352
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Pricing and availability is not currently available.
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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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Repr. 1B
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk_germany
WGK 1
flash_point_f
231.8 °F - closed cup
flash_point_c
111 °C - closed cup
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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
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
Diane Fournier et al.
Applied and environmental microbiology, 75(15), 5088-5093 (2009-06-23)
The propanotroph Rhodococcus ruber ENV425 was observed to rapidly biodegrade N-nitrosodimethylamine (NDMA) after growth on propane, tryptic soy broth, or glucose. The key degradation intermediates were methylamine, nitric oxide, nitrite, nitrate, and formate. Small quantities of formaldehyde and dimethylamine were
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