00375
4-乙酰氨-2,2,6,6-四甲基哌啶-1-氧
purum, ≥98.0% (HPLC)
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关于此项目
经验公式（希尔记法）:
C11H21N2O2
化学文摘社编号:
分子量:
213.30
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
423-840-3
Beilstein/REAXYS Number:
3546225
MDL number:
Assay:
≥98.0% (HPLC)
InChI key
UXBLSWOMIHTQPH-UHFFFAOYSA-N
InChI
1S/C11H21N2O2/c1-8(14)12-9-6-10(2,3)13(15)11(4,5)7-9/h9H,6-7H2,1-5H3,(H,12,14)
SMILES string
CC(=O)NC1CC(C)(C)N([O])C(C)(C)C1
grade
purum
assay
≥98.0% (HPLC)
greener alternative product score
old score: 9
new score: 8
Find out more about DOZN™ Scoring
greener alternative product characteristics
Waste Prevention
Safer Solvents and Auxiliaries
Inherently Safer Chemistry for Accident Prevention
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
143-145 °C (lit.), 143-146 °C
functional group
amide
greener alternative category
storage temp.
2-8°C
Quality Level
相关类别
General description
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl undergoes one-electron oxidation and reduction reactions. Reaction products were analyzed by 1H, 13C and 15N NMR spectral data.
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Application
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl radical may be employed in the catalytic system used for the regioselective oxidation of curdlan. It may be employed as model nitroxyl radical to study its reaction with thiophosgene. Reaction afforded 2,2,6,6-tetramethylpiperidine and 2,2,6,6-tetramethyl-1-hydroxypiperidine as major products.
Other Notes
将醇轻度氧化成羰基的新型氧化剂
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
ppe
dust mask type N95 (US), Eyeshields, Gloves
flash_point_f
No data available
flash_point_c
No data available
Z. Ma et al.
The Journal of Organic Chemistry, 56, 6110-6110 (1991)
A 1H, 13C and 15N NMR study of oxidation and reduction products of 4-acetamido-2, 2, 6, 6-tetramethylpiperidine-1-oxyl.
Schilf W, et al.
Journal of Molecular Structure, 407(1), 1-3 (1997)
Reaction of Nitroxides with Sulfur Containing Compounds II [1]. Preparation of Nitroxides Bearing an Isothiocyanate Substituent in View of the Nitroxyl Group Reduction with Thiophosgene.
Zakrzewski J, et al.
Monatshefte fur Chemie / Chemical Monthly, 134(6), 843-850 (2003)
D Metodiewa et al.
Biochemistry and molecular biology international, 40(6), 1211-1219 (1996-12-01)
Two novel 2,2,6,6-tetramethylpiperidine derivatives (Tempace and Troxyl) were synthesized and their capacity to act as scavengers of superoxide, inhibitors of iron and ascorbate-driven Fenton reaction and radioprotectors was tested. The possibility for one-electron oxidation of novel compounds by heme-ferryl species
D Metodiewa et al.
Anticancer research, 19(2A), 1255-1260 (1999-06-16)
Since flavanone oximes derivatives (ethers) have been shown to modulate the growth of Yoshida Sarcoma cells in vivo and to induce apoptosis, the effects of these substances on immortalized cell lines growth were examined. Cell viability and sensitivity to investigated
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