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Merck
CN

357677

2,5-Dimethoxyphenethylamine

97%

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About This Item

Linear Formula:
(CH3O)2C6H3CH2CH2NH2
CAS Number:
3600-86-0
Molecular Weight:
181.23
NACRES:
NA.22
PubChem Substance ID:
24861933
UNSPSC Code:
12352100
MDL number:
MFCD00060614
Assay:
97%
Form:
liquid

Key Documents

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InChI

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

SMILES string

COc1ccc(OC)c(CCN)c1

InChI key

WNCUVUUEJZEATP-UHFFFAOYSA-N

assay

97%

form

liquid

drug control

USDEA Schedule I; regulated under CDSA - not available from Sigma-Aldrich Canada

refractive index

n20/D 1.5424 (lit.)

bp

160 °C/10 mmHg (lit.)

density

1.089 g/mL at 25 °C (lit.)

Gene Information

rat ... Htr2a(29595), Htr2c(25187)

General description

2,5-Dimethoxyphenethylamine is a phenethylamine-type designer drug and is commonly known as psychoactive drug. It was detected as psychostimulant in the urine using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Application

2,5-Dimethoxyphenethylamine may be used in the preparation of aminoketone hydrochloride.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBD1819
MKBD1735
01621CJ
02518JE
00922EE

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Sarah Kerrigan et al.
Journal of forensic sciences, 59(1), 175-183 (2013-12-10)
Designer psychostimulants are known by recreational drug users to produce a complex array of adrenergic and hallucinogenic effects. Many of these drugs are not targeted during routine toxicology testing and as a consequence, they are rarely reported. The purpose of
Simultaneous analysis of six phenethylamine-type designer drugs by TLC, LC-MS, and GC-MS.
Kanai K, et al.
Forensic Toxicology, 26(1), 6-12 (2008)
Amines Related to 2, 5-Dimethoxyphenethylamine. 1 II.
Baltzly R and Buck JS.
Journal of the American Chemical Society, 62(1), 164-167 (1940)
Eline Pottie et al.
Biochemical pharmacology, 182, 114251-114251 (2020-10-01)
Psychedelic new psychoactive substances (NPS), compounds exerting their main pharmacological effects through the activation of the serotonin 2A receptor (5-HT2AR), continuously comprise a substantial portion of the reported NPS. However, these substances and their exact mechanism of action, differentiating them

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