2,2,6,6-Tetramethyl-4-piperidinol - CAS 2403-88-5

Catalog:	BB018302
Product Name:	2,2,6,6-Tetramethyl-4-piperidinol
CAS:	2403-88-5
Synonyms:	2,2,6,6-tetramethylpiperidin-4-ol

Technical Data

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Computed Properties

IUPAC Name:	2,2,6,6-tetramethylpiperidin-4-ol
Description:	An intermediate in the preparation of Piperidinyloxy free radical derivatives.
Molecular Weight:	157.25
Molecular Formula:	C9H19NO
Canonical SMILES:	CC1(CC(CC(N1)(C)C)O)C
InChI:	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
Boiling Point:	212-215 °C
Purity:	98 %
Density:	0.891 g/cm³
Appearance:	White to slightly beige crystalline powder
MDL:	MFCD00005983
LogP:	1.61670

Publication Number	Title	Priority Date
CN-113429392-A	Method for preparing hindered amine nitroxide free radical compound by using alkaline heterogeneous catalysis system	20210726
CN-113477252-A	Preparation method and application of composite porous catalyst simultaneously containing titanium and other transition metals	20210630
CN-113475750-A	Cigarette filter stick capable of reducing gas-phase free radicals in cigarette smoke and preparation method thereof	20210629
CN-113337025-A	Combined ecological modified plastic enclosing wall	20210618
CN-113321796-A	High-transparency high-heat-resistance copolyester resin and preparation method thereof	20210526

PMID	Publication Date	Title	Journal
22617403	20120830	Tempol suppresses micronuclei formation in astrocytes of newborn rats exposed to 50-Hz, 10-mT electromagnetic fields under bleomycin administration	Mutation research
22420637	20120424	Chemoselective photodeoxidization of graphene oxide using sterically hindered amines as catalyst: synthesis and applications	ACS nano
22024718	20120301	Tempol inhibits growth of As4.1 juxtaglomerular cells via cell cycle arrest and apoptosis	Oncology reports
22337282	20120301	Two-week cast immobilization induced chronic widespread hyperalgesia in rats	European journal of pain (London, England)
22629466	20120101	Bactericidal action of photogenerated singlet oxygen from photosensitizers used in plaque disclosing agents	PloS one

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Related Functional Groups

Piperidines

[1035840-45-9]
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid
[874800-64-3]
1-(4-Chloro-2-nitrophenyl)piperidine-4-carboxylic acid
[2091301-46-9]
Tert-butyl 5-hydroxy-3,3-dimethylpiperidine-1-carboxylate
[758720-54-6]
1-(3-Nitropyridin-2-yl)piperidine-4-carboxylic acid
[2355617-42-2]
3-(1-(tert-Butoxycarbonyl)piperidin-4-yl)cyclobutane-1-carboxylic acid
[1189664-19-4]
Ethyl 1-(3-chlorobenzyl)piperidine-3-carboxylate hydrochloride

GHS Hazard Statement:	H302 (65.17%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P260, P261, P264, P270, P272, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P333+P313, P363, P405, and P501
Signal Word:	Danger

Complexity:	136
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	157.146664230
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	157.146664230
Rotatable Bond Count:	0
Topological Polar Surface Area:	32.3 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.9