4-Acetamido-TEMPO, free radical

Modify Date: 2024-01-06 10:11:19

4-Acetamido-TEMPO, free radical Structure
4-Acetamido-TEMPO, free radical structure
Common Name 4-Acetamido-TEMPO, free radical
CAS Number 14691-89-5 Molecular Weight 213.297
Density N/A Boiling Point 368.8ºC at 760 mmHg
Molecular Formula C11H21N2O2 Melting Point 143-145 °C(lit.)
MSDS Chinese USA Flash Point 176.8ºC
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 4-acetamido-tempo
Synonym More Synonyms

 Chemical & Physical Properties

Boiling Point 368.8ºC at 760 mmHg
Melting Point 143-145 °C(lit.)
Molecular Formula C11H21N2O2
Molecular Weight 213.297
Flash Point 176.8ºC
Exact Mass 213.160309
PSA 32.34000
LogP 1.81840
Vapour Pressure 1.9E-06mmHg at 25°C
Index of Refraction 1.506
Storage condition 2-8°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S26-S36-S24/25
RIDADR NONH for all modes of transport
WGK Germany 1

 Synthetic Route

~99%

4-Acetamido-TEMPO, free radical Structure

4-Acetamido-TEM...

CAS#:14691-89-5

Literature: Bobbitt, James M. Journal of Organic Chemistry, 1998 , vol. 63, # 25 p. 9367 - 9374

~98%

4-Acetamido-TEMPO, free radical Structure

4-Acetamido-TEM...

CAS#:14691-89-5

Literature: Ma, Zhenkun; Bobbitt, James M. Journal of Organic Chemistry, 1991 , vol. 56, # 21 p. 6110 - 6114

~%

4-Acetamido-TEMPO, free radical Structure

4-Acetamido-TEM...

CAS#:14691-89-5

Literature: Monatshefte fur Chemie, , vol. 134, # 6 p. 843 - 850

~94%

4-Acetamido-TEMPO, free radical Structure

4-Acetamido-TEM...

CAS#:14691-89-5

Literature: Kashparova; Kagan; Kashparov; Zhukova Russian Journal of Applied Chemistry, 2002 , vol. 75, # 4 p. 667 - 668

~%

4-Acetamido-TEMPO, free radical Structure

4-Acetamido-TEM...

CAS#:14691-89-5

Literature: Carbohydrate research, , vol. 89, # 2 p. 211 - 220

 Articles14

More Articles
Tempace and troxyl-novel synthesized 2,2,6,6-tetramethylpiperidine derivatives as antioxidants and radioprotectors.

Biochem. Mol. Biol. Int. 40(6) , 1211-9, (1996)

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...

Rutoxyl [rutin/4-acetamide-1-hydroxy-2,2,6,6-tetramethylpiperidinium] is a new member of the class of semi-natural products of high pharmacological potency.

Biochem. Mol. Biol. Int. 42(6) , 1261-70, (1997)

A novel complex, Rutoxyl [rutin/4-acetamide-1-hydroxy-2,2,6,6-tetramethylpiperidinium] was synthesized and its structure and anticancer activity were investigated. The results reported here are consis...

Different effectiveness of piperidine nitroxides against oxidative stress induced by doxorubicin and hydrogen peroxide.

Cell Biol. Toxicol. 24(1) , 101-12, (2008)

The piperidine nitroxides Tempamine and Tempace have been studied for their effect on doxorubicin (DOX) and hydrogen peroxide (H(2)O(2)) cytotoxicity in immortalized B14 cells, a model for neoplastic ...

 Synonyms

4-acetmamido-TEMPO
4-Acetamido-TEMPO, free radical
4-Acetamido-2,2,6,6-tetramethylpiperidinyloxy
4-acetylamino 2,2,6,6-tetramethylpiperidin-N-oxyl
4-Acetamido-2,2,6,6-tetramethylpiperidinooxy
tempace
1-Piperidinyloxy, 4-(acetylamino)-2,2,6,6-tetramethyl-
T6NJ AO B1 B1 DMV1 F1 F1 &&Free radical
4-Acetylamino-2,2,6,6-tetramethylpiperidin-1-oxyl
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl
(4-Acetamido-2,2,6,6-tetramethyl-1-piperidinyl)oxidanyl
(4-Acetamido-2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl
ACETAMINO-TEMPO
EINECS 423-840-3
4-ACETAMIDO-2,2,6,6-TEMPO
MFCD00043593
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl free radical
4-N-acetyl-amino-TEMPO
4-acetamide-TEMPO
4-acetamidoTEMPO
4-Acetylamino-2,2,6,6-tetramet
4-Acetamido-2,2,6,6-tetramethyl-1-piperidinyloxy, free radical
4-Acetamido-TEMPO Free Radical
4-Acetamino-Tempo
4-ACETAMIDO-2,2,6,6-TETRAMETHYL-N-PIPERI