Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

187305

Sigma-Aldrich

4-Methoxyphenethylamine

≥98%

Synonym(s):

2-(4-Methoxyphenyl)ethylamine, 4-Methoxyphenethylamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3OC6H4CH2CH2NH2
CAS Number:
55-81-2
Molecular Weight:
151.21
Beilstein:
508967
EC Number:
200-245-5
MDL number:
MFCD00008192
UNSPSC Code:
12352100
PubChem Substance ID:
24851266
NACRES:
NA.22

Quality Level

100

Assay

≥98%

form

liquid

refractive index

n20/D 1.538 (lit.)

bp

138-140 °C/20 mmHg (lit.)
254-256 °C

density

1.031 g/mL at 20 °C (lit.)

SMILES string

COc1ccc(CCN)cc1

InChI

1S/C9H13NO/c1-11-9-4-2-8(3-5-9)6-7-10/h2-5H,6-7,10H2,1H3

InChI key

LTPVSOCPYWDIFU-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

4-Methoxyphenethylamine inhibits the monoamine oxidase-catalyzed deamination of both tyramine and tryptamine.

4-Methoxyphenethylamine is used as a precursor for the synthesis of other organic compounds by the alkylation reaction.

Application

4-Methoxyphenethylamine was used in the synthesis of :
  • pyrrolo[3,2-c]carbazole
  • poly(4-methoxyphenethylamine), required for the immobilization of nitrogenated bases and oligonucleotides
  • organopolyphosphazenes such as poly[bis(4-methoxy benzylamino)polyphosphazene] and poly[bis(4-methoxyphenethylamino)polyphosphazene]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

3-Hydroxy-4-methoxyphenethylamine hydrochloride

Sigma-Aldrich

H3132

3-Hydroxy-4-methoxyphenethylamine hydrochloride

Synthesis and characterization of novel polyorganophosphazenes substituted with 4-methoxybenzylamine and 4-methoxyphenethylamine for in vitro release of indomethacin and 5-fluorouracil.
Gudasi KB, et al.
Reactive functional Polymers, 66(10), 1149-1157 (2006)
W J Keller et al.
Journal of pharmaceutical sciences, 65(10), 1539-1540 (1976-10-01)
It has been established that the oxidative deamination of tyramine by monoamine xodase is inhibited by (+/-)-4-methoxy-beta-hydroxyphenethylamine and its N-methylated derivatives. This particular series of compounds does not inhibit the action of monoamine oxidase when tryptamine is used as the
Francielle B Silva et al.
International journal of molecular sciences, 9(7), 1173-1188 (2009-03-28)
This work describes the immobilization of purine and pyrimidine bases and immobilization/hybridization of synthetic oligonucleotides on graphite electrodes modified with poly(4-methoxyphenethylamine) produced in acid medium. The immobilization of adenine, guanine, cytosine and thymine on these modified electrodes was efficient, producing
The Pummerer cyclization route to the ibophyllidine alkaloids. Total synthesis of (?)-deethylibophyllidine.
Catena J, et al.
Tetrahedron Letters, 35(25), 4433-4436 (1994)
T Kuramoto et al.
Journal of neuroscience research, 6(1), 37-48 (1981-01-01)
K+-sensitive liquid ion exchange electrode systems respond with a slow potential change to acetylcholine, choline, anticholinergic drugs, biogenic amines, and glutamic acid. The response threshold has been defined, and in most cases it is at extremely low concentrations (10(-7)-10(-5)M). The
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service