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安全信息

357677

Sigma-Aldrich

2,5-二甲氧基苯乙胺

97%

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About This Item

线性分子式:
(CH3O)2C6H3CH2CH2NH2
CAS号:
3600-86-0
分子量:
181.23
MDL编号:
MFCD00060614
UNSPSC代码:
12352100
PubChem化学物质编号:
24861933
NACRES:
NA.22

方案

97%

表单

liquid

药品控制

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

折射率

n20/D 1.5424 (lit.)

沸点

160 °C/10 mmHg (lit.)

密度

1.089 g/mL at 25 °C (lit.)

SMILES字符串

COc1ccc(OC)c(CCN)c1

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

InChI key

WNCUVUUEJZEATP-UHFFFAOYSA-N

基因信息

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

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一般描述

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).

应用

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

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

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

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Amines Related to 2, 5-Dimethoxyphenethylamine. 1 II.
Baltzly R and Buck JS.
Journal of the American Chemical Society, 62(1), 164-167 (1940)
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)
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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