Description

3,4-Dimethoxyphenethyl alcohol (CAS No. 7417-21-2) is a high-purity aromatic alcohol with the molecular formula C₁₀H₁₄O₃. This compound, also known as Homoveratryl alcohol, is characterized by its two methoxy groups attached to the phenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a purity level of ≥98% (GC), it is supplied as a clear to pale-yellow liquid, ensuring consistency for sensitive applications. Ideal for researchers and scientists, this product is rigorously tested for quality, stability, and compliance with industry standards. Suitable for use in drug discovery, fragrance formulation, and as a precursor in the synthesis of complex molecules. Packaged under inert conditions to prevent degradation and stored in amber glass bottles to protect from light.

Properties

• CAS Number: 7417-21-2
• Complexity: 138
• IUPAC Name: 2-(3,4-dimethoxyphenyl)ethanol
• InChI: InChI=1S/C10H14O3/c1-12-9-4-3-8(5-6-11)7-10(9)13-2/h3-4,7,11H,5-6H2,1-2H3
• InChI Key: SRQAJMUHZROVHW-UHFFFAOYSA-N
• Exact Mass: 182.094294304
• Molecular Formula: C10H14O3
• Molecular Weight: 182.22
• SMILES: COC1=C(C=C(C=C1)CCO)OC
• Topological: 38.7
• Monoisotopic Mass: 182.094294304
• Synonyms: 3,4-Dimethoxyphenethyl alcohol, 2-(3,4-Dimethoxyphenyl)ethanol, 7417-21-2, 3,4-Dimethoxyphenethanol, Benzeneethanol, 3,4-dimethoxy-, Phenethyl alcohol, 3,4-dimethoxy-, EINECS 231-032-5, 3,4-Dimethoxy-.beta.-phenethyl alcohol, 1-(2-Hydroxyethyl)-3,4-dimethoxybenzene, AI3-39210, DTXSID80225138, Ethanol, 2-(3,4-dimethoxyphenyl), NSC 101852, NSC 179202, DTXCID80147629, 3,4-Dimethoxy-beta-phenethyl alcohol, 231-032-5, srqajmuhzrovhw-uhfffaoysa-n, 2-(3,4-Dimethoxyphenyl)Ethan-1-Ol, Homoveratryl alcohol, 3,4-Dimethoxybenzeneethanol, MFCD00002894, 3,4-Dimethoxyphenyl ethanol, Benzeneethanol,4-dimethoxy-, Phenethyl alcohol,4-dimethoxy-, 3,4-Dimethoxyphenethylalcohol, NCIOpen2_001861, SCHEMBL296592, SCHEMBL296593, SCHEMBL1099963, SCHEMBL8987432, 3,4-dimethoxy phenethyl alcohol, SCHEMBL27313293, 3,4-dimethoxyphenylethyl alcohol, 2-(3,4-dimethoxyphenyl)-ethanol, 2-(3,4-dimethoxy-phenyl)-ethanol, BCP30362, STR03669, NSC101852, NSC179202, AKOS000277428, AC-8719, FD54836, NSC-101852, NSC-179202, PS-5102, 2-(3,4-Dimethoxyphenyl)ethanol, 98%, SY051539, DB-021923, CS-0015314, D4107, NS00022743, ST45024076, EN300-117538, 2-(3,4-Dimethoxyphenyl)ethanol, >98.0%(GC), Q63399534, Z397587464, 2-(3,4-Dimethoxyphenyl)ethanol;3,4-Dimethoxyphenethyl alcohol, 2-(3,4-Dimethoxyphenyl)ethanol;2-(3,4-Dimethoxyphenyl)Ethan-1-Ol

3,4-Dimethoxyphenethyl alcohol is widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilators and CNS-active compounds. It serves as a precursor for the preparation of homoveratrylamine, an important building block in medicinal chemistry. In fragrance and flavor industries, it contributes to the formulation of aromatic esters and aldehydes. Researchers also utilize this compound in the study of neurotransmitter analogs and enzyme inhibition. Its stability and reactivity make it a versatile reagent for organic transformations.

Safety and Hazards

GHS Hazard Statements

• Not Classified
• Reported as not meeting GHS hazard criteria by 38 of 42 companies (only 9.5% companies provided GHS information). For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

• Not Classified

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