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D136204

Sigma-Aldrich

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:
Molecular Weight:
181.23
Beilstein:
474393
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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.)

SMILES string

COc1ccc(CCN)cc1OC

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

ANOUKFYBOAKOIR-UHFFFAOYSA-N

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Application

Precursor for the synthesis of isoquinolines.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

257.0 °F

Flash Point(C)

125 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Chem. Abstr., 119, 139040g-139040g (1993)
Australian Journal of Chemistry, 47, 957-957 (1994)
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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