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69496-75-9

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69496-75-9 Usage

Description

5-methoxy DPT is a substituted form of DPT that is also an analog of 5-methoxy DiPT , a psychoactive monoamine re-uptake inhibitor. The physiological and toxicological properties of this compound are not known. 5-methoxy DPT is regulated as a Schedule I compound in the United States. This product is intended for forensic and research applications.

Uses

5-Methoxy-N'',N''-dipropyltryptamine is a derivative of N,N-Dipropyl-1H-indole-3-ethanamine (D678870, HCl salt) which is a psychedelic drug of the tryptamine class. DPT inhibits the re-uptake of dopamine, serotonin, and norepinephrine.

Check Digit Verification of cas no

The CAS Registry Mumber 69496-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,9 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69496-75:
(7*6)+(6*9)+(5*4)+(4*9)+(3*6)+(2*7)+(1*5)=189
189 % 10 = 9
So 69496-75-9 is a valid CAS Registry Number.

69496-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-propylpropan-1-amine

1.2 Other means of identification

Product number -
Other names N,N-di-n-propyl-5-methoxytryptamine

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:69496-75-9 SDS

69496-75-9Upstream product

69496-75-9Downstream Products

69496-75-9Relevant articles and documents

METHOD OF INHIBITING GASTRIC ACID SECRETION WITH BENZODIOXANES

-

, (2008/06/13)

The present invention provides a method of inhibiting gastric acid secretion in mammals by administering a 5-HT1A agonist compound or a pharmaceutically acceptable salt thereof.

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