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00375

4-Acetamino-TEMPO

greener alternative

purum, ≥98.0% (HPLC)

Synonym(e):

4-Acetamido-2,2,6,6-tetramethyl-piperidin-1-oxyl

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Über diesen Artikel

Empirische Formel (Hill-System):
C11H21N2O2
CAS-Nummer:
Molekulargewicht:
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)
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grade

purum

Quality Segment

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

SMILES string

CC(=O)NC1CC(C)(C)N([O])C(C)(C)C1

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)

InChI key

UXBLSWOMIHTQPH-UHFFFAOYSA-N

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Waste Prevention”, “Safer Solvents and Auxiliaries” and “Inherently Safer Chemistry for Accident Prevention”. Click here to view its DOZN scorecard.
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.

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.[1] 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

New oxidant for the mild oxidation of alcohols to carbonyls

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Dieser Artikel
1157548.40130705977
assay

≥98.0% (HPLC)

assay

≥99%

assay

≥95.0% (GC)

assay

97%

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

143-145 °C (lit.), 143-146 °C

mp

-

mp

67-71 °C

mp

70-75 °C

storage temp.

2-8°C

storage temp.

-

storage temp.

2-30°C

storage temp.

-

functional group

amide

functional group

-

functional group

-

functional group

aldehyde

sustainability

Greener Alternative Product

sustainability

-

sustainability

-

sustainability

Greener Alternative Product


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Lagerklasse

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



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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)
A Koceva-Chyła et al.
Anticancer research, 20(6B), 4611-4618 (2001-02-24)
The novel nitroxyl, Tempicol-3 (nitroxide-N-oxide) was synthesized and its capacity to act as a scavenger of hydroxyl radicals was tested. The concentration-dependent reducibility of this novel compound was also examined and compared with those of previously characterized nitroxides, Tempo and
Z. Ma et al.
The Journal of Organic Chemistry, 56, 6110-6110 (1991)



Global Trade Item Number

SKUGTIN
O2706-5G04061837594724
00375-1G04061826661239
00375-5G04061833354810

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