| Identification | More | [Name]
4-BENZOYLOXY-TEMPO | [CAS]
3225-26-1 | [Synonyms]
4-BENZOYLOXY-2,2,6,6-TETRAMETHYLPIPERIDINE 1-OXYL
4-BENZOYLOXY-TEMPO
4-BENZOYLOXY-TEMPO FREE RADICAL
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE 1-OXYL BENZOATE
4-HYDROXY-TEMPO BENZOATE
4-HYDROXY-TEMPO BENZOATE, FREE RADICAL
4-Benzoyloxy-2,2,6,6-tetramethylpiperidinyloxy, free radical~4-Hydroxy-TEMPO benzoate, free radical
4-Benzyloxy-TEMPO,freeradical
4-HYDROXY-TEMPO-BENZOATE,97%
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE 1-OXYL BENZOATE (FREE RADICAL)
2,2,6,6-Tetramethyl-4-piperidinyl benzoate
4-HYDROXY-TEMPO BENZOATE FREE RADICAL 97%
4-BENZOYLOXY-TEMPO FREE RADICAL 97%
4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Benzoate Free Radical [Catalyst for Oxidation]
4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl benzoate, 4-Hydroxy-TEMPO benzoate | [EINECS(EC#)]
807-702-3 | [Molecular Formula]
C16H22NO3 * | [MDL Number]
MFCD00075563 | [Molecular Weight]
276.35 | [MOL File]
3225-26-1.mol |
| Chemical Properties | Back Directory | [Appearance]
orange crystalline powder | [Melting point ]
99-101 °C (lit.) | [density ]
0.001g/cm3 at 20℃ | [vapor pressure ]
11.5Pa at 20℃ | [form ]
Crystalline | [color ]
Light yellow to Brown | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [BRN ]
1431263 | [LogP]
3.13 at 20℃ and pH7.88 | [CAS DataBase Reference]
3225-26-1(CAS DataBase Reference) |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HS Code ]
29329990 |
| Hazard Information | Back Directory | [Chemical Properties]
orange crystalline powder | [Uses]
Recycling catalyst in hypochlorite/bromite-nitroxide oxidizing system for conversion of alcohols to aldehydes, ketones, and carboxylic acids. It circumvents the need to use a catalytic or stoichiometric heavy metal oxidant. | [Uses]
4-Hydroxy-TEMPO Benzoate, Free Radical is a recycling catalyst in a hypochlorite/bromite-nitroxide oxidizing system for conversion of alcohols to aldehydes, ketones, and carboxylic acids. It circumvents the need to use a catalytic or stoichiometric heavy metal oxidant. | [Definition]
ChEBI: 4-hydroxy-TEMPO benzoate is a member of the class of piperidines that is TEMPO carrying a benzoyloxy group at position 4. It has a role as a radical scavenger and a spin probe. It is a member of aminoxyls, a member of piperidines and a benzoate ester. It is functionally related to a 4-hydroxy-TEMPO. | [General Description]
4-Hydroxy-TEMPO benzoate is a 4-substituted 2,2,6,6-tetramethylpiperidyl-1-oxy (TEMPO) derivative. |
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