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Triacetonamine

Cat. No. M15010
Triacetonamine Structure
Synonym:

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

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Biological Activity

Triacetonamine is used as an intermediate for the synthesis of pharmaceutical products, pesticides and photostabilizers for polymers. Triacetonamine is an artifact of plant and fungal extracts using acetone and ammonium hydroxide or natural occurrence of ammonium salts in various steps of the isolation procedures. TAA is the main component of the pyrolysis oil.

Chemical Information
Molecular Weight 155.24
CAS Number 826-36-8
Solubility (25°C) Ethanol 50 mg/mL
Storage 2-8°C, protect from light
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Jude C Ikewuchi, et al. Heliyon. Nutrient and bioactive compounds composition of the leaves and stems of Pandiaka heudelotii: A wild vegetable

[2] Denis V Mishchenko, et al. Curr Cancer Drug Targets. Chemosensitizing Activity of Histone Deacetylases Inhibitory Cyclic Hydroxamic Acids for Combination Chemotherapy of Lymphatic Leukemia

[3] Jing-Pei Cao, et al. Bioresour Technol. Triacetonamine formation in a bio-oil from fast pyrolysis of sewage sludge using acetone as the absorption solvent

[4] C C Navajas, et al. J Comput Aided Mol Des. Theoretical models for the conformations and the protonation of triacetonamine

[5] L F Bjeldanes, et al. J Agric Food Chem. Triacetonamine formation in fungal extracts

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