InChI key
CJSZWOGCKKDSJG-UHFFFAOYSA-N
InChI
1S/C5H9NO2/c7-6(8)5-3-1-2-4-5/h5H,1-4H2
SMILES string
[O-][N+](=O)C1CCCC1
assay
99%
form
liquid
refractive index
n20/D 1.454 (lit.)
bp
180 °C (lit.)
density
1.086 g/mL at 25 °C (lit.)
functional group
nitro
General description
Nitrocyclopentane, a secondary nitroalkane, was examined for its ability to induce DNA repair in rat hepatocytes. The nitronate of nitrocyclopentane was mutagenic in Salmonella strains TA100 and TA102.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
152.6 °F - closed cup
flash_point_c
67 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
C C Conaway et al.
Mutation research, 261(3), 197-207 (1991-11-01)
The secondary nitroalkanes 2-nitropropane, 2-nitrobutane, 3-nitropentane and nitrocyclopentane, as well as their anionic forms (nitronates); the primary nitroalkanes 1-nitropropane, 1-nitrobutane, and 1-nitropentane and their respective nitronates; the nitrocarbinols 2-nitro-1-propanol, 2-nitro-1-butanol, 3-nitro-2-butanol, and 3-nitro-2-pentanol and their respective nitronates; 2-methyl-2-nitropropane, and 2-nitroso-2-nitropropane
E S Fiala et al.
Toxicology, 99(1-2), 89-97 (1995-05-05)
The secondary nitroalkanes, 2-nitropropane, 2-nitrobutane, 3-nitropentane, 2-nitroheptane, nitrocyclopentane and nitrocyclohexane, as well as the primary nitroalkanes, 1-nitropropane, 1-nitrobutane, 1-nitropentane and 1-nitroheptane, were examined for their ability to induce DNA repair in rat hepatocytes and to serve as substrates for activation
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