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22204-89-3

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22204-89-3 Usage

Description

4-hydroxy Diethyltryptamine (4-hydroxy DET) is a substituted tryptamine which is structurally related to the natural hallucinogen psilocin (4-hydroxy dimethyltryptamine). 4-hydroxy DET is a designer drug of abuse. The physiological and toxicological properties of this compound are poorly studied. This product is intended for forensic and research purposes.

Uses

4-Hydroxy-N,N-diethyltryptamine (4-HO-DET) is a hallucinogenic tryptamine of moderate duration; a psychedelic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 22204-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22204-89:
(7*2)+(6*2)+(5*2)+(4*0)+(3*4)+(2*8)+(1*9)=73
73 % 10 = 3
So 22204-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O/c1-3-16(4-2)9-8-11-10-15-12-6-5-7-13(17)14(11)12/h5-7,10,15,17H,3-4,8-9H2,1-2H3

22204-89-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-N,N-diethyltryptamine

1.2 Other means of identification

Product number -
Other names 3-[2-(diethylamino)ethyl]-1H-indol-4-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22204-89-3 SDS

22204-89-3Downstream Products

22204-89-3Relevant articles and documents

H-D exchange of psilocin and its analogs

Sogawa, Kazuyo,Hashimoto, Kimiko,Shirahama, Haruhisa

, p. 657 - 660 (1999)

H-D exchange experiments were performed on psilocin (1) and its analogs in MeOH-d4. The various exchange rates depending on their C3-substituents were observed. The exchange of bufotenine (5) and 5-hydroxyindole (7) is much slower than psilocin (1) and its analogs (2 ~ 4).