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Merck
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187305

Sigma-Aldrich

4-Methoxyphenethylamine

≥98%

동의어(들):

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

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25 G
₩161,081
100 G
₩451,269

₩161,081

예상 입고일2025년 4월 14일세부사항

벌크 견적 요청
모든 사진(1)

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25 G
₩161,081
100 G
₩451,269

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 코드:
12352100
PubChem Substance ID:
24851266
NACRES:
NA.22

₩161,081

예상 입고일2025년 4월 14일세부사항

벌크 견적 요청

분석

≥98%

양식

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.)

작용기

amine

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

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관련 카테고리

일반 설명

4-Methoxyphenethylamine inhibits the monoamine oxidase-catalyzed deamination of both tyramine and tryptamine[1].

4-Methoxyphenethylamine is used as a precursor for the synthesis of other organic compounds by the alkylation reaction.[2]

애플리케이션

4-Methoxyphenethylamine was used in the synthesis of :
  • pyrrolo[3,2-c]carbazole[3]
  • poly(4-methoxyphenethylamine), required for the immobilization of nitrogenated bases and oligonucleotides[4]
  • organopolyphosphazenes such as poly[bis(4-methoxy benzylamino)polyphosphazene] and poly[bis(4-methoxyphenethylamino)polyphosphazene][5]

픽토그램

Corrosion
GHS05

신호어

Danger

유해 및 위험 성명서

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

개인 보호 장비

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

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시험 성적서(COA)

Lot/Batch Number
STBK9915
STBK4773
STBG7217
STBF0429V
STBC9460V

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문서 라이브러리 방문

이미 열람한 고객

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)
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
GC--MS analysis of N-(bromodimethoxybenzyl)-2-, 3-, and 4-methoxyphenethylamines: Inverse analogues of the psychoactive 25B-NBOMe drug
Almalki AJ, et al.
Forensic Chemistry, 21, 100277-100277 (2020)
F Peter Guengerich et al.
The Journal of biological chemistry, 277(37), 33711-33719 (2002-07-03)
Cytochrome P450 (P450) 2D6 is involved in the oxidation of a large fraction ( approximately 30%) of drugs used by humans and also catalyzes the O-demethylation of the model substrates 3- and 4-methoxyphenethylamine followed by subsequent ring hydroxylation to dopamine.
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
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