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1082-23-1

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1082-23-1 Usage

Description

1-(2,3,4-trimethoxyphenyl)propan-2-amine, also known as TMA-6 and 2,4,5-trimethoxyamphetamine, is a chemical compound belonging to the phenethylamine and amphetamine classes. With the molecular formula C11H17NO3, it is structurally similar to the psychedelic drug mescaline. 1-(2,3,4-trimethoxyphenyl)propan-2-amine has been studied for its potential psychoactive effects and is believed to act as a serotonin receptor agonist. It has the capacity to alter perception, mood, and cognition, and is classified as a Schedule I controlled substance in the United States. Further research is necessary to fully comprehend its effects and safety profile.

Uses

Used in Pharmaceutical Research:
1-(2,3,4-trimethoxyphenyl)propan-2-amine is used as a research compound for its potential psychoactive effects. Its structural similarity to mescaline and its action as a serotonin receptor agonist make it a valuable subject for studying the mechanisms of psychedelic substances and their impact on human perception, mood, and cognition.
Used in Drug Regulation and Policy:
As a Schedule I controlled substance in the United States, 1-(2,3,4-trimethoxyphenyl)propan-2-amine is used in the context of drug regulation and policy to understand the classification and control of novel psychoactive substances. This helps in developing strategies for managing the risks associated with these compounds and ensuring public safety.
Please note that the provided materials do not specify any industrial applications for 1-(2,3,4-trimethoxyphenyl)propan-2-amine. The uses listed above are based on the information given and are primarily focused on research and regulatory aspects.

Check Digit Verification of cas no

The CAS Registry Mumber 1082-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1082-23:
(6*1)+(5*0)+(4*8)+(3*2)+(2*2)+(1*3)=51
51 % 10 = 1
So 1082-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H19NO3/c1-8(13)7-9-5-6-10(14-2)12(16-4)11(9)15-3/h5-6,8H,7,13H2,1-4H3

1082-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3,4-trimethoxyphenyl)propan-2-amine

1.2 Other means of identification

Product number -
Other names 2,3,4-trimethoxyphenylisopropylamine

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:1082-23-1 SDS

1082-23-1Downstream Products

1082-23-1Relevant articles and documents

Discrimination and identification of the six aromatic positional isomers of trimethoxyamphetamine (TMA) by gas chromatography-mass spectrometry (GC-MS)

Zaitsu, Kei,Katagi, Munehiro,Kamata, Hiroe,Kamata, Tooru,Shima, Noriaki,Miki, Akihiro,Iwamura, Tatsunori,Tsuchihashi, Hitoshi

, p. 528 - 534 (2008/09/20)

A reliable and accurate GC-MS method was developed that allows both mass spectrometric and chromatographic discrimination of the six aromatic positional isomers of trimethoxyamphetamine (TMA). Regardless of the trifluoroacetyl (TFA) derivatization, chromatographic separation of all the investigated isomers was achieved by using DB-5ms capillary columns (30 m x 0.32 mm i.d.), with run times less than 15 min. However, the mass spectra of the nonderivatized TMAs, except 2,4,6-trimethoxyamphetmine (TMA-6), showed insufficient difference for unambiguous discrimination. On the other hand, the mass spectra of the TFA derivatives of the six isomers exhibited fragments with significant intensity differences, which allowed the unequivocal identification of all the aromatic positional isomers investigated in the present study. This GC-MS technique in combination with TFA derivatization, therefore, is a powerful method to discriminate these isomers, especially useful to distinguish the currently controlled 3,4,5-trimethoxyamphetmine (TMA-1) and 2,4,5-trimethoxyamphetmine (TMA-2) from other uncontrolled TMAs. Copyright

The six trimethoxyphenylisopropylamines (trimethoxyamphetamines).

Shulgin

, p. 445 - 446 (2007/10/05)

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