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N,N-Diethyltryptamine Methanol Solution is a chemical compound that consists of N,N-diethyltryptamine (DET) dissolved in methanol. DET is a synthetic psychedelic drug and a member of the tryptamine class, which is structurally similar to the neurotransmitter serotonin. It is known for its psychoactive effects, including hallucinations, altered perceptions, and changes in mood. The methanol solution serves as a solvent, which helps to dissolve the DET and facilitate its absorption when used. This solution is typically used in research settings to study the effects of DET on the central nervous system and to understand its potential therapeutic applications. It is important to note that DET is a controlled substance in many countries due to its psychoactive properties and potential for abuse, and its use outside of a research context is illegal and can be dangerous.

61-51-8

61-51-8 Suppliers

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61-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61-51-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61-51:
(4*6)+(3*1)+(2*5)+(1*1)=38
38 % 10 = 8
So 61-51-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2/c1-3-16(4-2)10-9-12-11-15-14-8-6-5-7-13(12)14/h5-8,11,15H,3-4,9-10H2,1-2H3

61-51-8SDS

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 N,N-DIETHYLTRYPTAMINE METHANOL SOLUTION

1.2 Other means of identification

Product number -
Other names diethyl-(2-indol-3-yl-ethyl)-amine

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:61-51-8 SDS

61-51-8Downstream Products

61-51-8Relevant academic research and scientific papers

Well-Defined Phosphine-Free Iron-Catalyzed N-Ethylation and N-Methylation of Amines with Ethanol and Methanol

Lator, Alexis,Gaillard, Sylvain,Poater, Albert,Renaud, Jean-Luc

supporting information, p. 5985 - 5990 (2018/10/02)

An iron(0) complex bearing a cyclopentadienone ligand catalyzed N-methylation and N-ethylation of aryl and aliphatic amines with methanol or ethanol in mild and basic conditions through a hydrogen autotransfer borrowing process is reported. A broad range of aromatic and aliphatic amines underwent mono- or dimethylation in high yields. DFT calculations suggest molecular hydrogen acts not only as a reducing agent but also as an additive to displace thermodynamic equilibria.

Benzocarbazoles heterocyclic compound and its preparation and use (by machine translation)

-

Paragraph 0106; 0108, (2016/10/07)

The present invention provides a class of non-nucleoside anti-viral inhibitors, in particular to such as shown in formula I benzo heterocyclic compound or its pharmaceutically acceptable salt or hydrate, the invention also provides the compound or its pharmaceutically acceptable salt or hydrate of the preparation method. Pharmacological test indicates that the compound or its pharmaceutically acceptable salt or hydrate can effectively inhibit hepatitis b virus DNA replication and hepatitis c virus RNA replication, therefore, the invention also provides the compounds in the preparation of preventing and/or the treatment of viral infections, particularly hepatitis b virus (HBV) infection, hepatitis c virus (HCV) infection of use of the medicament. (by machine translation)

Tryptamine derivatives as novel non-nucleosidic inhibitors against hepatitis B virus

Qu, Shi-Jin,Wang, Gui-Feng,Duan, Wen-Hu,Yao, Shan-Yan,Zuo, Jian-Ping,Tan, Chang-Heng,Zhu, Da-Yuan

experimental part, p. 3120 - 3127 (2011/06/24)

A series of tryptamine derivatives were synthesized and evaluated for their anti-hepatitis B virus (HBV) activity and cytotoxicity in the HepG2.2.15 cell line. The preliminary SAR was discussed. Compounds 2e and 4a showed potent antiviral activity (IC50 = 0.4 and 50 = 40.6 and >25 μM, respectively).

Investigations into the mechanism of lactamization of lactones yielding in a novel route to biologically active tryptamine derivatives

Decker, Michael,Nguyen, Thi Thanh Huyen,Lehmann, Jochen

, p. 4567 - 4578 (2007/10/03)

The mechanism of lactamization of corresponding lactones was investigated by means of gas chromatography and synthesis of possible intermediates as references. Lactones react with amines via the amino acid with subsequent elimination of water to the corresponding lactams. In the first step, also hydroxyamides are in equilibrium with the lactones and amines, respectively, which are not able to form the amide though. This mechanism opens a new approach for the synthesis of Nβ-disubstituted tryptamines.