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2403-88-5 molecular structure
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2,2,6,6-tetramethylpiperidin-4-ol

ChemBase ID: 91301
Molecular Formular: C9H19NO
Molecular Mass: 157.25326
Monoisotopic Mass: 157.14666423
SMILES and InChIs

SMILES:
N1C(C)(CC(CC1(C)C)O)C
Canonical SMILES:
OC1CC(C)(C)NC(C1)(C)C
InChI:
InChI=1S/C9H19NO/c1-8(2)5-7(11)6-9(3,4)10-8/h7,10-11H,5-6H2,1-4H3
InChIKey:
VDVUCLWJZJHFAV-UHFFFAOYSA-N

Cite this record

CBID:91301 http://www.chembase.cn/molecule-91301.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2,2,6,6-tetramethylpiperidin-4-ol
IUPAC Traditional name
2,2,6,6-tetramethylpiperidin-4-ol
Synonyms
2,2,6,6-Tetramethylpiperidin-4-ol
4-Hydroxy-2,2,6,6-tetramethylpiperidine 98%
4-Hydroxy-2,2,6,6-tetramethylpiperidine
2,2,6,6-Tetramethyl-4-piperidinol
2,2,6,6-Tetramethyl-4-piperidinol
4-Hydroxy-2,2,6,6-tetramethylpiperidine
2,2,6,6-Tetramethyl-4-hydroxypiperidine
Lastar A
NSC 16575
2,2,6,6-Tetramethyl-4-piperidinol
4-羟基-2,2,6,6-四甲基哌啶
2,2,6,6-四甲基-4-哌啶醇
4-羟基-2, 2, 6, 6-四甲氧基哌啶
CAS Number
2403-88-5
EC Number
219-291-2
MDL Number
MFCD00005983
Beilstein Number
105039
PubChem SID
162078005
24847236
PubChem CID
75471

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 15.144971  H Acceptors
H Donor LogD (pH = 5.5) -2.7033675 
LogD (pH = 7.4) -2.0619173  Log P 0.5194845 
Molar Refractivity 46.5317 cm3 Polarizability 18.725828 Å3
Polar Surface Area 32.26 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
methanol: soluble0.1 g/mL, clear expand Show data source
Melting Point
129-131 °C(lit.) expand Show data source
129-133°C expand Show data source
129-133°C expand Show data source
130-132 °C expand Show data source
Boiling Point
212-215 °C(lit.) expand Show data source
212-215°C expand Show data source
212-215°C expand Show data source
Flash Point
124°C(255°F) expand Show data source
Density
1.085 expand Show data source
Storage Warning
Corrosive expand Show data source
European Hazard Symbols
Corrosive Corrosive (C) expand Show data source
UN Number
UN3259 expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
1 expand Show data source
Hazard Class
8 expand Show data source
Packing Group
III expand Show data source
Risk Statements
34 expand Show data source
34-43 expand Show data source
Safety Statements
26-36/37/39-45 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS07 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H314-H317 expand Show data source
H314-H318 expand Show data source
H315-H317-H318-H413 expand Show data source
GHS Precautionary statements
P280-P305 + P351 + P338 expand Show data source
P280-P305 + P351 + P338-P310 expand Show data source
P280-P305+P351+P338-P309-P310 expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
Purity
≥99.0% (NT) expand Show data source
98% expand Show data source
Grade
purum expand Show data source
Certificate of Analysis
Download expand Show data source
Empirical Formula (Hill Notation)
C9H19NO expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich TRC TRC
Sigma Aldrich - 115746 external link
Packaging
10, 25 g in glass bottle
Application
Used as:
• An additive for polymer modified hindered amine light stabilizers1,2
• A light stabilizer for polyamide 66 fibers containing acid blue dyes3
Sigma Aldrich - 56515 external link
Application
Used as:
• An additive for polymer modified hindered amine light stabilizers1,2
• A light stabilizer for polyamide 66 fibers containing acid blue dyes3
Toronto Research Chemicals - T304625 external link
An intermediate in the preparation of Piperidinyloxy free radical derivatives.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Irie, O., et al.: Bioorg. Med. Chem. Lett., 18, 5280 (2008)
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PATENTS

PATENTS

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INTERNET

INTERNET

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