CAS 2564-83-2

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Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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Also known as: 2564-83-2, 2,2,6,6-tetramethyl-1-piperidinyloxy, 2,2,6,6-tetramethylpiperidoxyl, 2,2,6,6-tetramethylpiperidine 1-oxyl, 2,2,6,6-tetramethylpiperidinyloxy, Vqn7359icq

Molecular Formula

C₉H₁₈NO

Molecular Weight

156.25 g/mol

InChI Key

QYTDEUPAUMOIOP-UHFFFAOYSA-N

FDA UNII

VQN7359ICQ

1 2D Structure

CAS 2564-83-2

2 Identification

2.1 Computed Descriptors

2.1.1 InChI

InChI=1S/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3

2.1.2 InChI Key

QYTDEUPAUMOIOP-UHFFFAOYSA-N

2.1.3 Canonical SMILES

CC1(CCCC(N1[O])(C)C)C

2.2 Other Identifiers

2.2.1 UNII

VQN7359ICQ

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 2,2,6,6-tetramethyl-1-piperidinyloxyl

2. 2,2,6,6-tetramethyl-4-piperidine-n-oxide

3. 2,2,6,6-tetramethylpiperidine-1-oxyl

4. Oxoammonium Tpo

2.3.2 Depositor-Supplied Synonyms

1. 2564-83-2

2. 2,2,6,6-tetramethyl-1-piperidinyloxy

3. 2,2,6,6-tetramethylpiperidoxyl

4. 2,2,6,6-tetramethylpiperidine 1-oxyl

5. 2,2,6,6-tetramethylpiperidinyloxy

6. Vqn7359icq

7. (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl

8. Chebi:32849

9. Piperidinooxy, 2,2,6,6-tetramethyl-

10. 2,2,6,6-tetramethyl Piperidine-n-oxyl

11. 2,2,6,6-tetramethylpiperidinyl-1-oxide

12. Tanane

13. (2,2,6,6-tetramethylpiperidin-1-yl)oxyl

14. 1-piperidinyloxy, 2,2,6,6-tetramethyl- (9ci)

15. 2,2,6,6-tetramethylpiperidine 1-oxyl Free Radical

16. Tanan

17. Tetramethylpiperidinooxy

18. 2,2,6,6-tetramethylpiperidine-1-oxyl Free Radical, 98%

19. Tetramethylpiperidine Nitroxide

20. 2,2,6,6-tetramethylpiperidinooxyl

21. Einecs 219-888-8

22. Tempo, Free Radical

23. Mfcd00009599

24. Brn 1422418

25. Tempo [mi]

26. Unii-vqn7359icq

27. Ccris 8316

28. Chembl606971

29. Tempo, 98%

30. Dtxsid2073300

31. Amy23375

32. Akos015902714

33. Tempo, Purified By Sublimation, 99%

34. Ccg-207968

35. Cs-w001187

36. Hy-w001187

37. 2,2,6,6-tetramethyl-1-oxylpiperidine

38. 2,2,6,6-tetramethylpiperidine-1-yloxy

39. 2,2,6,6-tetramethylpiperindyl-1-oxide

40. 2,2,6,6-tetramethylpiperidinooxy Radical

41. Bp-20268

42. 1,1,5,5-tetramethylpentamethylene Nitroxide

43. Ft-0609130

44. T1560

45. En300-125971

46. Z-1024

47. 1-piperidinyloxy,2,2,6,6-tetramethyl-,

48. A817947

49. 1-$l^{1}-oxidanyl-2,2,6,6-tetramethylpiperidine

50. 1-oxy-2,2,6,6-tetramethylpiperidine, Free Radical

51. 2,2,6,6-tetramethylpentamethylene Nitroxide

52. 1-$l^{1}-oxidanyl-2,2,6,6-tetramethyl-piperidine

53. Z1255386734

54. 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl-

55. 2,2,6,6-tetramethylpiperidine 1-oxyl, Free Radical - Solid Melt

56. 125012-91-1

57. 126517-51-9

58. 25657-03-8

59. 26933-82-4

2.4 Create Date

2004-09-16

3 Chemical and Physical Properties

Molecular Formula	C₉H₁₈NO
Molecular Weight	156.25 g/mol
XLogP3	1.4
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	g/mol
Monoisotopic Mass	g/mol
Topological Polar Surface Area	4.2
Heavy Atom Count	11
Formal Charge	0
Complexity	136
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Antioxidants

Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)

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