CAS 120-20-7

3,4-Dimethoxyphenethylamine

Description:

3,4-Dimethoxyphenethylamine, with the CAS number 120-20-7, is an organic compound belonging to the class of phenethylamines. It features a phenethylamine backbone, characterized by a two-carbon chain (ethyl) attached to a phenyl ring, which is further substituted with two methoxy groups at the 3 and 4 positions of the aromatic ring. This substitution pattern influences its chemical properties and biological activity. The compound is typically a white to off-white solid and is soluble in organic solvents. It has been studied for its potential psychoactive effects and is of interest in the field of medicinal chemistry, particularly for its possible applications in neuropharmacology. The presence of methoxy groups can enhance lipophilicity, potentially affecting its interaction with biological targets. As with many phenethylamines, it may exhibit stimulant properties, but specific effects can vary based on dosage and individual response. Safety and regulatory considerations are important, as substances in this class can have varying legal statuses and health implications.

Formula: C₁₀H₁₅NO₂

InChI: InChI=1S/C10H15NO2/c1-12-9-4-3-8(5-6-11)7-10(9)13-2/h3-4,7H,5-6,11H2,1-2H3

InChI key: InChIKey=ANOUKFYBOAKOIR-UHFFFAOYSA-N

SMILES: O(C)C1=C(OC)C=CC(CCN)=C1

Synonyms:

• 2-(3,4-Dimethoxyphenyl)-1-aminoethane
• 2-(3,4-Dimethoxyphenyl)ETHYLAMINE
• 2-(3,4-Dimethoxyphenyl)ethan-1-amine
• 2-(3,4-Dimethoxyphenyl)ethanamine
• 2-(3,4-Dimethoxyphenyl)ethaneamine
• 2-(3,4-Dimethyloxyphenyl)ethylamine Homoveratrylamine
• 3,4-Di-O-methyldopamine
• 3,4-Dimethoxy Phenylethylamine
• 3,4-Dimethoxy-β-phenylethylamine
• 3,4-Dimethoxybenzeneethanamine
• 3,4-Dimethoxyphenethylamin
• 3,4-Dimethoxyphenethylamine
• 3,4-Dimethyloxy Phenylethylamine
• 3,4-DimethyloxyPhenylethylamine
• 3,4-Dimetoxifenetilamina
• Akos 235-24
• Akos Bbs-00003591
• Akos Ncg1-0105
• Benzeneethanamine, 3,4-dimethoxy-
• Dimpea
• Dmpe
• Dmpea
• Dopamine dimethyl ether
• Ethylamine, 2-(3,4-Dimethoxyphenylene)-
• Homoveratrylamin
• Homoveratrylamine
• Nsc 16948
• Nsc 26152
• Nsc 6328
• O,O-Dimethyldopamine
• Phenethylamine, 3,4-dimethoxy-

Homoveratrylamine

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Red to Green clear liquid

Molecular weight: 181.24

Ref: 3B-D0678

Dopamine Related Compound C (2-(3,4-Dimethoxyphenyl)ethan-1-amine)

CAS: 120-20-7

Amino-naphthols and other amino-phenols, their ethers and esters, other than those cont more than one kind of oxygen function; salts thereof, nesoi

Formula: C₁₀H₁₅NO₂

Color and Shape: Yellow Brown Liquid

Molecular weight: 181.23

Ref: 45-1225237

2-(3,4-dimethoxyphenyl)ethan-1-amine

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 181.2316

Ref: IN-DA000Q05

Dopamine EP Impurity C (Dopamine USP Related Compound C)

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Color and Shape: Colorless Liquid

Molecular weight: 181.24

Ref: 4Z-D-3224

2-(3,4-Dimethoxyphenyl)ethanamine

Controlled Product

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Color and Shape: Neat

Molecular weight: 181.23

Ref: 86-MM0384.04

3,4-Dimethoxyphenethylamine

CAS: 120-20-7

3,4-Dimethoxyphenethylamine is a human endogenous metabolite.

Formula: C₁₀H₁₅NO₂

Purity: 95.19%

Color and Shape: Clear Yellowish Liquid Liquid

Molecular weight: 181.23

Ref: TM-T9326

Dopamine EP Impurity C

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Molecular weight: 181.2

Ref: ST-EA-CP-D55003

Homoveratrylamine

Controlled Product

CAS: 120-20-7

Applications A methylated metabolite of Dopamine (D533780); a potent inhibitor of brain mitochondrial respiration used in Parkinson’s disease studies.
References Gluck, M.R. et al.: J. Neurochem., 91, 788 (2004); Charlton, C.G. et al.: Life Sci., 66, 2159 (2000);

Formula: C₁₀H₁₅NO₂

Color and Shape: Light Yellow

Molecular weight: 181.23

Ref: TR-H669540

Homoveratrylamine

Controlled Product

CAS: 120-20-7

Homoveratrylamine is a dopamine-based analog of mivacurium chloride that is used as a pharmacological agent. Homoveratrylamine has been shown to be an effective blocker of the enzyme dopamine β-hydroxylase and is used to inhibit the synthesis of norepinephrine and epinephrine. It is also used in kinetic studies to produce stable complexes with dibutyltin oxide, which are then used to determine the kinetic energy of amines. Homoveratrylamine has been found in urine samples at concentrations of up to 4% and has shown no toxicological effects in animal studies or human clinical trials.

Formula: C₁₀H₁₅NO₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 181.23 g/mol

Ref: 3D-FH23862

Tetrabenazine Impurity 8

CAS: 120-20-7

Formula: C₁₀H₁₅NO₂

Molecular weight: 181.2

Ref: ST-EA-CP-T104016