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115746

Sigma-Aldrich

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

98%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C9H19NO
CAS Number:
2403-88-5
Molecular Weight:
157.25
Beilstein:
105039
EC Number:
219-291-2
MDL number:
MFCD00005983
UNSPSC Code:
12352100
PubChem Substance ID:
24847236
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

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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
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H317

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’.

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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
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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
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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
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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
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