2,5-Dimethoxybenzaldehyde
CAS Number: 93-02-7
Chemical Formula: C9H10O3
Synonyms: 2,5-Dimethoxybenzaldehyde, 97%,2,5-Dimethoxybenzald, 5-DiMethoxy benzaldehyde
Appearance: Yellow Powder
MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)
2,5-Dimethoxybenzaldehyde serves as a key intermediate for synthesizing 2,5-dimethoxyphenethylamine. This compound is further used to manufacture psychoactive substances including 2,5-dimethoxy-4-bromophenethylamine, 2,5-dimethoxy-4-iodophenethylamine, and 4-Chloro-2,5-dimethoxy-phenethylamine. It functions as a building block for general organic synthesis.
Chemical Properties
| Property | Value |
| Melting point | 46-48 °C (lit.) |
| Boiling point | 146 °C/10 mmHg (lit.) |
| density | 1.1708 (rough estimate) |
| refractive index | 1.5260 (estimate) |
| Fp | >230 °F |
| storage temp. | Keep in dark place, Sealed in dry, Room Temperature |
| solubility | 795mg/l |
| form | Crystalline Powder, Crystals and/or Chunks |
| color | Yellow to beige |
| Water Solubility | Soluble in chloroform and methanol. Slightly soluble in water. |
| Sensitive | Air Sensitive |
| BRN | 509301 |
| InChI | 1S/C9H10O3/c1-11-8-3-4-9(12-2)7(5-8)6-10/h3-6H,1-2H3 |
| InChIKey | AFUKNJHPZAVHGQ-UHFFFAOYSA-N |
| SMILES | [H]C(=O)c1cc(OC)ccc1OC |
| LogP | 1.910 |
| CAS DataBase Reference | 93-02-7(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzaldehyde, 2,5-dimethoxy-(93-02-7) |
| EPA Substance Registry System | Benzaldehyde, 2,5-dimethoxy- (93-02-7) |
Safety Information
| Item | Details |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38-43 |
| Safety Statements | 26-36/37/39-24/25-36 |
| WGK Germany | 2 |
| RTECS | CU5740500 |
| Hazard Note | Irritant |
| TSCA | TSCA listed |
| HS Code | 29124900 |
| Storage Class | 11 – Combustible Solids |
| Hazard Classifications | Eye Irrit. 2 Resp. Sens. 1 Skin Irrit. 2 STOT SE 3 |
Product Application
2,5-Dimethoxybenzaldehyde, also referred to as 2C-H, is an organic derivative of benzaldehyde. It is widely employed in the production of 2,5-dimethoxyphenethylamine. Moreover, 2C-H acts as a precursor for numerous other substituted phenethylamines, such as 2C-B, 2C-I, and 2C-C.
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