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Thiothinone
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Buy Thiothinone Online
Thiothinone is a thiophene-based beta-ketone compound for lab research. Ideal for monoamine studies and SAR mapping. ≥98% purity.
Product Information Table
Property | Value |
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Product Name | Thiothinone |
IUPAC Name | 1-(thiophen-2-yl)-2-(pyrrolidin-1-yl)pentan-1-one |
Molecular Formula | C13H19NOS |
Molecular Weight | ~237.36 g/mol |
Form | Crystalline powder |
Appearance | Off-white to white crystals |
Purity | ≥98% |
Storage | Cool, dry place, sealed container |
Legal Status | Research use only |
Applications | Monoamine transport, SAR, pharmacological research |
Buy Thiothinone – High-Purity Beta-Ketone Research Chemical
Thiothinone is a lesser-known yet highly promising compound in the beta-ketone class of research chemicals, structurally similar to compounds like a-PVP and MDPV. Known for its unique thiophene substitution, Thiothinone has gained interest in scientific studies involving monoamine transporters and dopaminergic activity.
This compound is offered in high-purity crystalline form and is intended exclusively for laboratory research and forensic analysis. Its molecular profile provides researchers with an exciting opportunity to study thiophene-based analogs in a controlled, replicable format.
Key Product Details
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Chemical Name: Thiothinone (β-keto-thiophenyl compound)
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IUPAC Name: 1-(thiophen-2-yl)-2-(pyrrolidin-1-yl)pentan-1-one
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Common Name: Thiothinone
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Form: Crystalline powder
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CAS Number: [Pending or Unlisted]
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Molecular Formula: C13H19NOS
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Molecular Weight: ~237.36 g/mol
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Purity: ≥98%
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Appearance: Off-white crystalline powder
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Storage: Store in airtight container, away from moisture and sunlight
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Application: Analytical, chemical, and forensic research
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Legal Status: Not for human or animal consumption
How It Works
Thiothinone operates as a dopamine-norepinephrine reuptake inhibitor (DNRI), similar to other cathinone derivatives, but with distinct properties due to its thiophene ring substitution.
The thiophene group alters electron distribution, potentially affecting binding affinity to monoamine transporters such as DAT, NET, and possibly SERT. These unique electronic properties make Thiothinone a compound of interest in structure-activity relationship (SAR) studies, especially when compared with traditional phenyl-substituted cathinones.
In laboratory settings, it is examined for:
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Reuptake inhibition kinetics
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Receptor binding profiles
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Metabolic pathway mapping
This makes it suitable for pharmacological simulations, enzyme assays, and transporter binding models.
⚠️ Safety and Warning Guidelines
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Lab Use Only: Not for human ingestion, medical, or veterinary use.
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Personal Protective Equipment: Always wear gloves, goggles, and lab coats.
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Handling Procedures: Avoid direct contact or inhalation. Handle under fume hood with certified lab equipment.
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Storage Instructions: Store in original sealed container in a dry, cool, and dark environment.
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Disposal: Dispose of in compliance with institutional chemical waste protocols.
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Legal Notice: Thiothinone may fall under analog laws in some regions. Researchers must verify local legal status before purchase.
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Emergency Protocol: In case of accidental exposure, wash with soap and water, and seek professional medical guidance.
Research Applications of Thiothinone
Thiothinone is widely explored in:
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Receptor binding affinity tests
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Comparative beta-ketone analog studies
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CNS interaction simulations
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Pharmacokinetics modeling
Its thiophene backbone makes it chemically distinct, offering unique insights for SAR profiling and cross-referencing with popular stimulants.
Usage Disclaimer
For laboratory research only. Not for human consumption or household use. Only certified professionals should handle this substance in controlled environments.
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