115746
2,2,6,6-Tetramethyl-4-piperidinol
98%
Synonym(s):
4-Hydroxy-2,2,6,6-tetramethylpiperidine
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C9H19NO
CAS Number:
Molecular Weight:
157.25
Beilstein/REAXYS Number:
105039
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
98%
bp
212-215 °C (lit.)
mp
129-131 °C (lit.)
functional group
hydroxyl
SMILES string
CC1(C)CC(O)CC(C)(C)N1
InChI
1S/C9H19NO/c1-8(2)5-7(11)6-9(3,4)10-8/h7,10-11H,5-6H2,1-4H3
InChI key
VDVUCLWJZJHFAV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
2,2,6,6-Tetramethyl-4-piperidinol has been used to study the green and efficient method for chemoselective deoxidization of graphene oxide via the ultraviolet irradiation.
2,2,6,6-tetramethyl-4-piperidinol has been used to study the irradiation of Camptothecin (CPT) in aerated dimethylsulfoxide (DMSO) solution that leads to formation of singlet oxygen.
Used as:
- An additive for polymer modified hindered amine light stabilizers
- A light stabilizer for polyamide 66 fibers containing acid blue dyes
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 1
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Fei Zhao et al.
ACS nano, 6(4), 3027-3033 (2012-03-17)
We report a green and efficient method for chemoselective deoxidization of graphene oxide via the ultraviolet irradiation catalyzed with 2,2,6,6-tetramethyl-4-piperidinol. While the sp(2)-hybridized oxygen functional groups are removed after the reduction, the epoxy and hydroxyl groups are retained in the
Shunichi Shishido et al.
Scientific reports, 8(1), 12888-12888 (2018-08-29)
In the present study, we evaluated the prooxidative mode of action of photoirradiated (+)-catechin at 400 nm in relation to reactive oxygen species generation and its possible application to disinfection. Photoirradiation of (+)-catechin at a concentration of 1 mg/mL yielded not only
Vlasta Brezová et al.
Molecular biotechnology, 37(1), 48-51 (2007-10-05)
Camptothecin (CPT) is an anticancer drug that inhibits topoisomerase I (Topo I) by forming a ternary DNA-CPT-Topo I complex. However, it has also been shown that UVA-irradiated CPT in the absence of Topo I produces significant DNA damage to cancer
Caicai Wang et al.
Journal of environmental sciences (China), 99, 249-259 (2020-11-14)
A series of Sr-doped BiFeO3 perovskites (Bi1-xSrxFeO3, BSFO) fabricated via sol-gel method was applied as peroxydisulfate (PDS) activator for ciprofloxacin (CIP) degradation. Various technologies were used to characterize the morphology and physicochemical features of prepared BSFO samples and the results
S X Liu et al.
Proceedings of the National Academy of Sciences of the United States of America, 98(4), 1643-1648 (2001-02-15)
Although arsenic is a well-established human carcinogen, the mechanisms by which it induces cancer remain poorly understood. We previously showed arsenite to be a potent mutagen in human-hamster hybrid (A(L)) cells, and that it induces predominantly multilocus deletions. We show
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service