Triacetonamine monohydrate (Synonyms: 2,2,6,6-Tetramethyl-4-piperidone monohydrate)

Cat. No.: HY-N1131B: FAQs
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Triacetonamine (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.

For research use only. We do not sell to patients.

Triacetonamine monohydrate Chemical Structure

CAS No. : 10581-38-1

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5 mg	Get quote	Estimated Time of Arrival: December 31
10 mg	Get quote	Estimated Time of Arrival: December 31
25 mg	Get quote	Estimated Time of Arrival: December 31

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Other Forms of Triacetonamine monohydrate:

Triacetonamine In-stock
Triacetonamine hydrochloride Get quote

1 Publications Citing Use of MCE Triacetonamine monohydrate

•J Tissue Eng Regen Med. 2022 Feb 5. [Abstract]

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Description

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].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

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.

Molecular Weight

173.25

Formula

C₉H₁₉NO₂

CAS No.

10581-38-1

SMILES

O=C1CC(C)(C)NC(C)(C)C1.[H]O[H]

Structure Classification

Initial Source

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Handling Instructions (2659 KB)

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. [Content Brief]

[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. [Content Brief]

[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. [Content Brief]

Triacetonamine monohydrate Related Classifications

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The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Help & FAQs

Do most proteins show cross-species activity?
Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Triacetonamine10581-38-12,2,6,6-Tetramethyl-4-piperidoneBiochemical Assay ReagentsIntermediatepolymersacute liver failureALFTAAInhibitorinhibitorinhibit

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