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DL-MBDB:HCL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135795-90-3

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135795-90-3 Usage

Uses

Used in Scientific Research:
DL-MBDB:HCL is used as a research chemical for studying the effects and mechanisms of action of entactogens and psychoactive substances. It helps researchers understand the interactions between these compounds and the human brain, as well as their potential therapeutic applications.
Used in Recreational Settings:

Check Digit Verification of cas no

The CAS Registry Mumber 135795-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,9 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 135795-90:
(8*1)+(7*3)+(6*5)+(5*7)+(4*9)+(3*5)+(2*9)+(1*0)=163
163 % 10 = 3
So 135795-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-3-4-11(13-2)9-5-6-10-8-14-15-12(10)7-9/h5-7,11,13H,3-4,8H2,1-2H3

135795-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name MBDB

1.2 Other means of identification

Product number -
Other names 1-(1,3-benzodioxol-5-yl)-2-(methylamino)butane

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:135795-90-3 SDS

135795-90-3Downstream Products

135795-90-3Relevant academic research and scientific papers

Derivatives of 1-(1,3-benzodioxol-5-yl)-2-butanamine: Representatives of a novel therapeutic class

Nichols,Hoffman,Oberlender,Jacob III,Shulgin

, p. 2009 - 2015 (2007/10/02)

The α-ethyl phenethylamine derivative 1-(1,3-benzodioxol-5-yl)-2-butanamine was prepared. An asymmetric synthesis was used to prepare the enantiomers of this compound and the related α-methyl homologue (MDA). The racemates and enantiomers of both compounds were evaluated in the two-lever drug discrimination assay in rats trained to discriminate saline from 0.08 mg/kg of LSD tartrate. Stimulus generalization occurred with the racemate and the R-(-)enantiomer of the α-methyl homologue and the S-(+)enantiomer of the α-ethyl primary amine. No generalization occurred with the other enantiomers or with the N-methyl derivatives of either series. Human psychopharmacology studies revealed that the N-methyl derivative of the title compound was nonhallucinogenic and that it had a new, novel psychoactive effect. It is suggested that this compound is the prototype of a new pharmacologic class that may have value in facilitating psychotherapy and that this class be designated as entactogens.

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