2,4,5-Trimethoxybenzaldehyde
Analyze the control, ≥98%(GC)
- Product Code: 239883
Alias:
2,4,5-trimethoxybenzaldehyde;asonic aldehyde
CAS:
4460-86-0
| Molecular Weight: | 196.2 g./mol | Molecular Formula: | C₁₀H₁₂O₄ |
|---|---|---|---|
| EC Number: | 224-713-3 | MDL Number: | MFCD00003312 |
| Melting Point: | 112-114 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature |
Product Description:
Used in the synthesis of psychoactive substances, particularly in the production of hallucinogenic phenethylamines such as TMA-2 and related compounds. It serves as a key intermediate in organic chemistry for constructing substituted amphetamines due to the reactivity of the aldehyde group and the electron-rich aromatic ring. Its methoxy substituents enhance the compound's stability and influence the pharmacological profile of the final products. Also employed in research settings for studying structure-activity relationships in psychedelic drugs. Not used in commercial pharmaceuticals or industrial applications due to its restricted nature and controlled substance precursors.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to brown powder, crystals and/or chunks |
| Purity (GC) | 98%-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | €32.15 |
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| 0.050 | 10-20 days | €68.02 |
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2,4,5-Trimethoxybenzaldehyde
Used in the synthesis of psychoactive substances, particularly in the production of hallucinogenic phenethylamines such as TMA-2 and related compounds. It serves as a key intermediate in organic chemistry for constructing substituted amphetamines due to the reactivity of the aldehyde group and the electron-rich aromatic ring. Its methoxy substituents enhance the compound's stability and influence the pharmacological profile of the final products. Also employed in research settings for studying structure-activity relationships in psychedelic drugs. Not used in commercial pharmaceuticals or industrial applications due to its restricted nature and controlled substance precursors.
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