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Merck
CN

03951

N-乙基甲酰胺

≥99.0% (GC)

别名:

N-甲酰乙胺

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关于此项目

线性分子式:
HCONHC2H5
化学文摘社编号:
分子量:
73.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-001-2
Beilstein/REAXYS Number:
1737860
MDL number:
Assay:
≥99.0% (GC)
Form:
liquid
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Quality Level

assay

≥99.0% (GC)

form

liquid

refractive index

n20/D 1.432

bp

202-204 °C

density

0.950 g/mL at 20 °C (lit.)

functional group

amide

SMILES string

CCNC=O

InChI

1S/C3H7NO/c1-2-4-3-5/h3H,2H2,1H3,(H,4,5)

InChI key

KERBAAIBDHEFDD-UHFFFAOYSA-N



存储类别

10 - Combustible liquids

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H Cross et al.
Chemical research in toxicology, 3(4), 357-362 (1990-07-01)
Hepatotoxic formamides such as N-methylformamide (NMF) and N,N-dimethylformamide (DMF) are metabolized in vivo to N-acetyl-S-(N-methylcarbamoyl)cysteine via oxidation at the formyl carbon, which yields a reactive intermediate. The hypothesis was tested that this biotransformation route can be studied in vitro with
M R Del Carratore et al.
Environmental and molecular mutagenesis, 36(2), 97-104 (2000-10-03)
A cDNA coding for rat cytochrome P450 2E1 was cloned into the multicopy vector pYeDP60 and expressed in haploid RSY6 and diploid RS112 yeast strains of Saccharomyces cerevisiae under control of the GAL10-CYC1 promoter. Spectral and catalytic properties of the
S P Langdon et al.
Toxicology, 43(3), 239-249 (1987-03-01)
The induction of terminal differentiation in tumour cells represents a possible therapeutic strategy for treating cancer. The alkylformamides are 1 group of experimental compounds which have been shown to induce terminal differentiation in human HL-60 leukemia and murine Friend erythroleukemia



全球贸易项目编号

货号GTIN
27130-10G04061826143759
03951-50ML04061836690793