2,2,6,6-Tetramethyl-4-piperidone monohydrate

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2,2,6,6-Tetramethyl-4-piperidone monohydrate Basic information
Product Name:2,2,6,6-Tetramethyl-4-piperidone monohydrate
Synonyms:TRIACETONEAMINE HYDRATE;2,2,6,6-Tetramethyl-4-Piperidone/Tripyruvalamine;4-Piperidinone, 2,2,6,6-tetramethyl-, monohydrate;2,2,6,6-TetraMethyl-4-piperidone Hydrate;Triacetonamine monohydrate;2,2,6,6-Tetramethyl-4-piperidone monohydrate
CAS:10581-38-1
MF:C9H19NO2
MW:173.25
EINECS:
Product Categories:
Mol File:10581-38-1.mol
2,2,6,6-Tetramethyl-4-piperidone monohydrate Structure
2,2,6,6-Tetramethyl-4-piperidone monohydrate Chemical Properties
Melting point 59 °C
storage temp. Inert atmosphere,2-8°C
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
TSCA Yes
MSDS Information
ProviderLanguage
ALFA English
2,2,6,6-Tetramethyl-4-piperidone monohydrate Usage And Synthesis
UsesTriacetonamine (2,2,6,6-Tetramethyl-4-piperidone) monohydrate is used as an intermediate for the synthesis of pharmaceutical products, pesticides and photostabilizers for polymers. Triacetonamine hydrochloride has oral activity and can induce acute liver failure (ALF) in rats[1][2].
in vivo

Triacetonamine (Purchased from MCE; 200 mg, 300 mg, 400 mg/Kg/day; gavage; 2 days) monohydrate shows typical hepatoenteropathology of ALF with 300 mg/Kg/day and 400 mg/Kg/day, while the group of 400 mg/Kg/day had higher mortality[2].

Animal Model:Rats (half male and female, 6-8 weeks old, 200±10 g)[2]
Dosage:200 mg, 300 mg, 400 mg/Kg
Administration:Gavage; daily; 2 days
Result:Showed typical hepatoenteropathology of ALF with 300 mg/Kg/day and 400 mg/Kg/day, while the group of 400 mg/Kg/day had higher mortality.
References[1] Cao JP, et al. Triacetonamine formation in a bio-oil from fast pyrolysis of sewage sludge using acetone as the absorption solvent. Bioresour Technol. 2010;101(11):4242-4245. DOI:10.1016/j.biortech.2010.01.031
[2] Cao JP, et al. Triacetonamine formation in a bio-oil from fast pyrolysis of sewage sludge using acetone as the absorption solvent. Bioresour Technol. 2010 Jun;101(11):4242-5. DOI:10.1016/j.biortech.2010.01.031
[3] Ting Jiang, et al. Application of Bone Marrow Mesenchymal Stem Cells Effectively Eliminates Endotoxemia to Protect Rat from Acute Liver Failure Induced by Thioacetamide. Tissue Eng Regen Med. 2022 Apr;19(2):403-415. DOI:10.1007/s13770-021-00421-5
2,2,6,6-Tetramethyl-4-piperidone monohydrate Preparation Products And Raw materials
Tag:2,2,6,6-Tetramethyl-4-piperidone monohydrate(10581-38-1) Related Product Information
Hexamidine piperidine 3-Methylpiperidin-3-ol HCl 4-Oxo-2,2,6,6-tetramethylpiperidine-1-15N-1-oxyl 1-Hydroxy-2 2 6 6-tetramethyl-4-piperi- 1-(Chloroacetyl)-2,2,6,6-tetramethylpiperidin-4-one 4-Oxo-2,2,6,6-tetramethylpiperidine-d16,1-15N-1-oxyl 2,2,6,6-Tetramethyl-4-piperidone monohydrate 4-OXO-2,2,6,6-TETRAMETHYLPIPERIDINE-D16-1-OXYL 3,5-Dibromo-4-oxo-2,2,6,6-tetramethylpiperidin-1-yl tempalgin 1-Benzoyloxy-2,2,6,6-tetramethyl-4-oxopiperidine SPECS AG-690/37009056 1-ACETYL-2,2,6,6-TETRAMETHYLTETRAHYDRO-4(1H)-PYRIDINONE 4-Oxo-2,2,6,6-tetramethylpiperidinooxy 1-Acetyloxy-2,2,6,6-tetramethyl-4-oxopiperidine 2,2,6,6-Tetramethylpiperidone-4-toluenesulfonate