Skip to Content
Merck
All Photos(2)

Documents

115746

Sigma-Aldrich

2,2,6,6-Tetramethyl-4-piperidinol

98%

Synonym(s):

4-Hydroxy-2,2,6,6-tetramethylpiperidine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H19NO
CAS Number:
Molecular Weight:
157.25
Beilstein:
105039
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

bp

212-215 °C (lit.)

mp

129-131 °C (lit.)

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

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Hirohisa Sato et al.
The Journal of toxicological sciences, 41(6), 793-799 (2016-11-18)
The present study aimed to evaluate the acute locally injurious property of our most current hydroxyl radical generation system by hydrogen peroxide (H2O2) photolysis. This system, which releases 3% H2O2 with a 405-nm laser, was developed in our laboratory for
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
Keisuke Nakamura et al.
PloS one, 8(3), e60053-e60053 (2013-03-26)
In the present study, the bactericidal effect of photo-irradiated proanthocyanidin was evaluated in relation to reactive oxygen species formation. Staphylococcus aureus suspended in proanthocyanidin aqueous solution was irradiated with light from a laser at 405 nm. The bactericidal effect of
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
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