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Merck
CN

D136204

3,4-Dimethoxyphenethylamine

97%

Synonym(s):

Homoveratrylamine, 2-(3,4-Dimethoxyphenyl)ethylamine

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About This Item

Linear Formula:
(CH3O)2C6H3CH2CH2NH2
CAS Number:
120-20-7
Molecular Weight:
181.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893271
EC Number:
204-376-9
Beilstein/REAXYS Number:
474393
MDL number:
MFCD00008188

Key Documents

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Product Name

3,4-Dimethoxyphenethylamine, 97%

InChI key

ANOUKFYBOAKOIR-UHFFFAOYSA-N

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

SMILES string

COc1ccc(CCN)cc1OC

assay

97%

form

liquid

drug control

USDEA Schedule I

refractive index

n20/D 1.546 (lit.)

bp

188 °C/15 mmHg (lit.)

density

1.074 g/mL at 25 °C (lit.)

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Application

Precursor for the synthesis of isoquinolines.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1B

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

257.0 °F

flash_point_c

125 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ1883
STBF2971V
STBD0331V
STBD7505V
STBD2645V

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Julia Fedotova et al.
American journal of translational research, 7(11), 2462-2473 (2016-01-26)
Novel anxiolytic medications are necessary to broaden treatment therapy. Thus, the aim of the present study was to compare the clinically effective anxiolytic, diazepam with the novel 3,4-dimethoxyphenylethylamine derivates. The novel 3,4-dimethoxyphenylethylamine derivates (PK, 0.1, 1.0, 10.0 mg/kg, i.p.) and
Organic preparations and procedures international, 25, 91-91 (1993)
Australian Journal of Chemistry, 47, 957-957 (1994)
Chem. Abstr., 119, 139040g-139040g (1993)
Siyu Wang et al.
Journal of agricultural and food chemistry, 65(2), 364-372 (2016-12-23)
Wolfberry or Goji berry, the fruit of Lycium barbarum, exhibits health-promoting properties that leads to an extensive study of their active components. We synthesized a set of hydroxycinnamic acid amide (HCCA) compounds, including trans-caffeic acid, trans-ferulic acid, and 3,4-dihydroxyhydrocinnamic acid
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