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Merck
CN

M46705

N-甲基甲酰胺

99%

别名:

甲基甲酰胺

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关于此项目

线性分子式:
HCONHCH3
化学文摘社编号:
分子量:
59.07
UNSPSC Code:
12352100
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-624-6
Beilstein/REAXYS Number:
1098352
MDL number:
Assay:
99%
Form:
liquid
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InChI key

ATHHXGZTWNVVOU-UHFFFAOYSA-N

InChI

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

SMILES string

[H]C(=O)NC

assay

99%

form

liquid

bp

198-199 °C (lit.)

mp

−4 °C (lit.)

density

1.011 g/mL at 25 °C (lit.)

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Legal Information

DuPont 产品

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Repr. 1B

存储类别

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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Johan Sjödahl et al.
Journal of separation science, 30(1), 104-109 (2007-02-23)
N-Methylformamide (NMF)-based matrices for capillary electrophoretic separation of nucleic acids have been developed. The use of an organic solvent as liquid base for the separation matrices allowed a hydrophobic polymer, C16-derivatized 2-hydroxyethyl cellulose (HEC), to be employed as structural element
Aleksandr B Sahakyan et al.
The journal of physical chemistry. A, 112(16), 3576-3586 (2008-03-28)
Electric field (EF) induced changes of one-bond indirect spin-spin coupling constants are investigated on a wide range of molecules including peptide models. EFs were both externally applied and internally calculated without external EF application by the hybrid density functional theory
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
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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